PERFUMING COMPOSITIONS

Information

  • Patent Application
  • 20240301319
  • Publication Number
    20240301319
  • Date Filed
    May 20, 2024
    7 months ago
  • Date Published
    September 12, 2024
    3 months ago
Abstract
The present disclosure provides fragrance compositions having an olfactive profile that changes with time. The fragrance compositions include at least two contrasting perfume accords. The at least two contrasting perfume accords provide an olfactory modulating effect, such that the fragrance compositions deliver a desirable scent with increased perceived intensity and improved longevity of perception.
Description
FIELD OF THE INVENTION

The present invention relates to the field of perfumery. In particular, fragrance compositions having an olfactive profile that changes with time, wherein the fragrance compositions comprise at least two contrasting perfume accords that provide an olfactory modulating effect, wherein the perfume formulation delivers a desirable scent with increased perceived intensity and improved longevity of perception.


BACKGROUND

Consumers are looking for different sensory experiences, and the perfume industry is constantly seeking for solutions to answer that demand and in particular for ways to prolong the perfume experience over time. The industry is also keen on finding solutions to phenomenon referred to as perfume habituation and perfume adaptation resulting in a decrease of perceived intensity over time.


SUMMARY

One aspect presented herein provides a perfume composition comprising at least two perfuming accords,

    • wherein a first perfume accord of the at least two perfuming accords comprises perfuming compounds dominated by a first olfactive note,
    • wherein a second perfume accord of the at least two perfuming accords comprises perfuming compounds dominated by a second olfactive note,
    • wherein the first and second olfactive notes are contrasting notes,
    • wherein the first perfume accord is present in the perfume composition in an amount sufficient for the first olfactive note to be perceived by a subject at a first time,
    • wherein the second perfume accord is present in the perfume composition in an amount sufficient for the second olfactive note to be perceived by a subject at a second time, and
    • wherein the perception of the first olfactive note and the second olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In one aspect, the second time is after the first time.


In one aspect, the first perfume accord comprises perfuming compounds having a volatility ranging from 70,000 to 100 μg/l in air.


In one aspect, the second perfume accord comprises perfuming compounds having a volatility ranging from 99 to 50 μg/l in air.


In one aspect, the sufficient amount of the first perfume accord is from 30% to 70% by weight of the perfume composition.


In one aspect, the sufficient amount of the second perfume accord is from 30% to 70% by weight of the perfume composition.


In one aspect, the first perfume accord and the second perfume accord are present in the perfume composition in a weight ratio ranging from 3:1 to 1:3.


In one aspect, the first perfume accord and the second perfume accord are present in the perfume composition at a weight ratio of 1:1.


In one aspect, the perception of the second olfactive note after the first olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In one aspect, the perfume composition further comprises a third perfume accord comprising perfuming compounds dominated by a third olfactive note, wherein the third perfume accord is present in the perfume composition in an amount sufficient for the third olfactive note to be perceived by a subject at a third time.


In one aspect, the sufficient amount of the third perfume accord is from 30% to 70% by weight of the perfume composition.


In one aspect, the first perfume accord the second perfume accord, and the third perfume accord are present in the perfume composition at a weight ratio of 1:1:1.


In one aspect, the third olfactive note and the second olfactive note are contrasting notes.


In one aspect, the first perfume accord further comprises a mixture comprising the first perfume accord encapsulated within a matrix material.


In one aspect, the second perfume accord further comprises a mixture comprising the second perfume accord encapsulated within a matrix material.


In one aspect, the third perfume accord further comprises a mixture comprising the third perfume accord encapsulated within a matrix material.


In one aspect, the third olfactive note and the first olfactive note are contrasting notes.


In one aspect, the third time is after the second time.


In one aspect, the third perfume accord comprises perfuming compounds having a volatility ranging from 49 to 0.1 μg/l in air.


In one aspect, the first time is less than one hour after exposure of the subject to the perfuming composition.


In one aspect, the second time is from one to six hours after exposure of the subject to the perfuming composition.


In one aspect, the second time is from one to four hours after exposure of the subject to the perfuming composition.


In one aspect, the third time is from four to six hours after exposure of the subject to the perfuming composition.


In one aspect, the perception of the first olfactive note, the second olfactive note, and the third olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In one aspect, the perception of the third olfactive note after the second olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In one aspect, the first olfactive note is selected from the group consisting of floral, water, green, fruity and citrus olfactive notes.


In one aspect, the second olfactive note is selected from the group consisting of floral, fruity, citrus, sweet, oriental, woody and meringue olfactive notes.


In one aspect, the third olfactive note is selected from the group consisting of floral, fruity, citrus, sweet, oriental, woody and meringue olfactive notes.


In one aspect, the first perfume accord is dominated by an olfactive note consisting of lemon and the second perfume accord is dominated by a second olfactive note consisting of oriental.


In one aspect, the first perfume accord is dominated by an olfactive note consisting of lemon and the second perfume accord is dominated by an olfactive note consisting of meringue.


In one aspect, the first perfume accord is dominated by an olfactive note consisting of citrus, floral, fruity and green, and the second perfume accord is dominated by an olfactive note consisting of a floral, fruity and sweet.


In one aspect, the first perfume accord is dominated by an olfactive note consisting of citrus and green, the second perfume accord is dominated by an olfactive note consisting of a floral, and fruity, and the third perfume accord is dominated by an olfactive note consisting of floral, fruity, citrus and sweet.


In one aspect, the perfume composition is a pre-formulated perfume composition, and the first perfume accord is added to the pre-formulated perfume composition in an amount sufficient for the first olfactive note to be perceived by the subject at the first time.


In one aspect, the perfume composition is a pre-formulated perfume composition, and the second perfume accord is added to the pre-formulated perfume composition in an amount sufficient for the second olfactive note to be perceived by the subject at the second time.


In one aspect, the perfume composition is a pre-formulated perfume composition, and the third perfume accord is added to the pre-formulated perfume composition in an amount sufficient for the third olfactive note to be perceived by the subject at the third time.


One aspect presented herein provides a manufactured product comprising the perfume composition according to an aspect presented herein.


In one aspect, the manufactured product is selected from the group consisting of a perfume, eau de toilette, home care product and a personal care product.


One aspect presented herein provides a method to reduce, prevent, or suppress a reduced perception of the perfume composition by a subject over time, comprising exposing the subject to a perfume composition according an aspect presented herein.


One aspect presented herein provides a method to reduce, prevent, or suppress a reduced perception of the perfume composition by a subject over time, comprising dispensing sequentially at least partly in the air, the first perfume accord dominated by a first olfactive note followed by the second perfume comprising perfuming compounds forming a second perfume accord dominated by a second olfactive note.


In one aspect, the sequential dispensing is performed using a device.


In one aspect, the first accord and the second accord are physically separated within the device.





BRIEF DESCRIPTION OF THE FIGURES


FIG. 1 shows a fragrance wheel showing the inferred relationships among olfactory groups based upon similarities and differences in their odor according to some aspects presented herein.



FIG. 2 shows a graph of perceived perfume intensities after sequential exposure to contrasting and non-contrasting accords, according to some aspects presented herein.



FIG. 3 shows a graph of perceived perfume intensities after sequential exposure to contrasting and non-contrasting accords, according to some aspects presented herein.



FIG. 4 shows a graph of perceived perfume intensities after sequential exposure to contrasting and non-contrasting accords, according to some aspects presented herein.



FIG. 5 shows the olfactive profile of a reference fine fragrance at the times indicated. The bars at each time point, moving from left to right, represent the number of subjects that perceived green, citrus, fruity, floral, woody, musk, or sweet/gourmand notes, or lack of any note.



FIG. 6 shows the olfactive profile of a reference fine fragrance at the times indicated, after a subject has been exposed to the fine fragrance for two minutes. The bars at each time point, moving from left to right, represent the number of subjects that perceived green, citrus, fruity, floral, woody, musk, or sweet/gourmand notes, or lack of any note.



FIG. 7 shows the olfactive profile of fine fragrance according to one aspect presented herein at the times indicated. The bars at each time point, moving from left to right, represent the number of subjects that perceived green, citrus, fruity, floral, woody, musk, or sweet/gourmand notes, or lack of any note.



FIG. 8 shows the olfactive profile of a fine fragrance according to one aspect presented herein at the times indicated, after a subject has been exposed to the fine fragrance for two minutes. The bars at each time point, moving from left to right, represent the number of subjects that perceived green, citrus, fruity, floral, woody, musk, or sweet/gourmand notes, or lack of any note.



FIG. 9 shows the olfactive profile of fine fragrance according to one aspect presented herein at the times indicated. The bars at each time point, moving from left to right, represent the number of subjects that perceived green, citrus, fruity, floral, woody, musk, or sweet/gourmand notes, or lack of any note.



FIG. 10 shows the olfactive profile of a fine fragrance according to one aspect presented herein at the times indicated, after a subject has been exposed to the fine fragrance for two minutes. The bars at each time point, moving from left to right, represent the number of subjects that perceived green, citrus, fruity, floral, woody, musk, or sweet/gourmand notes, or lack of any note.



FIG. 11 shows the mean decrease in perceived intensity of the fine fragrances evaluated in Example 4.



FIG. 12 shows the perceived fragrance intensity following sequential exposure to a perfume composition according to some aspects presented herein.



FIG. 13 shows the mean panel scores of a first test utilizing a shower gel composition according to some aspects presented herein.



FIG. 14 shows the mean panel scores of a second test utilizing a shower gel composition according to some aspects presented herein.





DETAILED DESCRIPTION

In the following description, reference is made to specific embodiments which may be practiced, which is shown by way of illustration. These embodiments are described in detail to enable those skilled in the art to practice the invention described herein, and it is to be understood that other embodiments may be utilized and that logical changes may be made without departing from the scope of the aspects presented herein. The following description of example embodiments is, therefore, not to be taken in a limited sense, and the scope of the various aspects presented herein is defined by the appended claims.


The Abstract is provided to comply with 37 C.F.R. § 1.72(b) to allow the reader to quickly ascertain the nature and gist of the technical disclosure. The Abstract is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims.


Consumers are looking for different sensory experiences, and the perfume industry is constantly seeking for solutions to answer that demand and in particular for ways to prolong the perfume experience over time. The industry is also keen on finding solutions to phenomenon referred to as perfume habituation and perfume adaptation resulting in a decrease of perceived intensity over time. The present disclosure provides a solution to the above-mention problems in particular to the decrease of perfume perception over time and offers a novel solution to improve fragrance longevity and satisfy the consumer needs for new sensory experience.


Odor descriptors are well known and widely use to describe the odor character of a fragrance. Several procedures for describing odor characters are known and have been the object of many publications, and sensory maps for odor descriptors (olfactive note) are largely known and used by the perfumery industry. In 2009 an approach to reach a standard sensory map of perfumery odor perception has been described by M. Zarzo and David Stanton in Attention, Perception and Psychophysicy, 2009, 71(2) 225-247. Therefore, in some aspects, a perfume accord can be defined with a number of descriptors.


As used herein, the term “contrasting accords”, “contrasting notes” or “contrasting pairs” is meant to designate accords for which the respective dominant olfactive notes are belonging to odor families that are distant from one another. Tools such as the fragrance wheel for instance can be used to define those fragrance families. An exemplar fragrance wheel is shown in FIG. 1.


Referring to the classification shown in FIG. 1, olfactive notes adjacent to each other on the fragrance wheel are not considered contrasting olfactive notes. However, olfactive notes separated by at least one adjacent olfactive note are considered contrasting olfactive notes, wherein the degree of contrast is directly proportional to the degree of separation. For example, by way of illustration, a dry woods olfactive note is opposite to a soft floral olfactive note, and therefore the degree of contrast is considered to be greater than the contrast between a soft floral olfactive note and a soft oriental olfactive note.


Contrasting accords in the context of the invention can be defined as accords for which there is no more than one descriptor shared between the two accords, preferably for which there is no descriptor shared between the two accords. As an example, “sweet” and “aromatic” are strongly correlated and share more than one descriptor. Sweet is also correlated with powdery. Aromatic and powdery are not directly correlated with one another but they both share the correlation with sweet, so they are not contrasting in the context of the invention.


An alternate way to look at contrasting accords is to use the notion of cross-adaptation. Cross-adaptation is well-known in the perfumery technical field and accords for which there is no perceptual cross-adaptation between the accords constitutes contrasting accords.


Alternatively, in some aspects, olfactive notes may be classified as contrasting according to the methods disclosed in Zarzo, J. Sensory Studies, 23 (2008), μg 354-376.


Alternatively, in some aspects, olfactive notes may be classified as contrasting according to the methods disclosed in Zarzo, J. Chemical Senses (2015), μg 305-313.


Alternatively, in some aspects, olfactive notes may be classified as contrasting according to the methods disclosed in Zarzo, J. Chemical Senses 31 (2006), μg 713-724.


Alternatively, in some aspects, olfactive notes may be classified as contrasting according to the methods disclosed in Abe et al, Analytica Chimica 239 (1990), pg 73-85.


Alternatively, in some aspects, olfactive notes may be classified as contrasting according to the methods disclosed in Chastrette et al, Chemical Senses 16 (1991), pg 81-93. Compositions According to Some Aspects Presented Herein:


Subjects' perceptions of perfume compositions may decline over time. The compositions described herein address the subjects' decline in perception of fragrance in several ways.


Compositions Comprising Contrasting Perfuming Accords: It has been now surprisingly found that combining contrasting fragrance accords into a single composition may accentuate the differences in the pairing. In particular, the inventors found that the perceived intensity of the resulting mixture of such dissimilar fragrance accords was significantly higher than predicted, based on the intensities of the individual accords; and, that attention to the odor of a mixture of contrasting accords was enhanced and prolonged versus the accords alone.


Accordingly, some aspects described herein provide a perfume composition comprising perfuming compounds forming a first perfume accord dominated by a first olfactive note; and perfuming compounds forming a second perfume accord dominated by a second olfactive note, wherein the first and second olfactive notes are contrasting notes. Additionally, some aspects provide a method to improve perfume intensity perceived by a subject over time, which method comprises, exposing said subject to a composition as defined herein.


A perfume accord is meant to designate a mixture of perfuming ingredients. As used herein, the term “perfuming ingredient” it is meant a compound, which is used for the primary purpose of conferring or modulating an odour. In other words such an ingredient, to be considered as being a perfuming one, must be recognized by a person skilled in the art as being able to at least impart or modify in a positive or pleasant way the odor of a composition, and not just as having an odor. For the purpose of the present disclosure, perfume accord also includes combination of perfuming ingredients with substances which together improve, enhance or modify the delivery of the perfuming ingredients, such as perfume precursors, emulsions or dispersions, as well as combinations which impart an additional benefit beyond that of modifying or imparting an odor, such as long-lasting, blooming, malodour counteraction, antimicrobial effect, microbial stability, insect control.


The nature and type of the perfuming ingredients do not warrant a more detailed description here, which in any case would not be exhaustive, the skilled person being able to select them on the basis of its general knowledge and according to intended use or application and the desired organoleptic effect. In general terms, these perfuming ingredients belong to chemical classes as varied as alcohols, aldehydes, ketones, esters, ethers, acetates, nitriles, terpenoids, nitrogenous or sulphurous heterocyclic compounds and essential oils, and said perfuming co-ingredients can be of natural or synthetic origin. Many of these co-ingredients are in any case listed in reference texts such as the book by S. Arctander, Perfume and Flavor Chemicals, 1969, Montclair, New Jersey, USA, or its more recent versions, or in other works of a similar nature, as well as in the abundant patent literature in the field of perfumery. It is also understood that said ingredients may also be compounds known to release in a controlled manner various types of perfuming compounds.


The perfuming ingredients may be dissolved in a solvent of current use in the perfume industry. In some embodiments, the solvent is not an alcohol. Examples of such solvents are diethyl phthalate, isopropyl myristate, Abalyn® (rosin resins, available from Eastman), benzyl benzoate, ethyl citrate, limonene or other terpenes, or isoparaffins. In some aspects, the solvent is very hydrophobic and highly sterically hindered, like for example Abalyn® or benzyl benzoate.


In some aspects, the perfume comprises less than 30% of solvent. In some aspects, the perfume comprises less than 20%, alternatively less than 10% of solvent, all these percentages being defined by weight relative to the total weight of the perfume. In some aspects, the perfume is essentially free of solvent.


In some aspects, the first perfume comprising perfuming compounds forming a first perfume accord dominated by a first olfactive note, when dispersed into a surrounding space has a given profile. In some aspects, the given profile does not change over time. Similarly, in some aspects the second perfume comprising perfuming compounds forming a second perfume accord dominated by a second olfactive note has a given profile. In some aspects, the given profile does not change over time.


Referring to Examples 1 to 3, the compositions according to the present disclosure advantageously proved to increase the perceived intensity of a perfume, when comparing with the perceived intensity of the individual accords as shown in the examples below. Contrary to what would be expected, namely an intensity for the composition comprising the two accords between the respective intensities of the accord evaluated individually, the composition according to the invention shows increased intensity. Therefore another object of the invention consists of a method to improve perfume intensity perceived by a subject over time, which method comprises exposing said subject to a first perfume accord dominated by a first olfactive note followed by exposure to a second perfume accord dominated by a second olfactive note wherein the first and second olfactive note are contrasting notes.


Moreover, the compositions described herein have also shown to impact noticeability of a perfume when the consumer is exposed to the contrasting accords sequentially. Therefore, a method to improve noticeability of a perfume which comprises dispensing sequentially at least partly in the air, a first perfume comprising perfuming compounds forming a first perfume accord dominated by a first olfactive note followed by a second perfume comprising perfuming compounds forming a second perfume accord dominated by a second olfactive note, wherein the first olfactive and second olfactive notes are contrasting notes, is also an object of the present invention.


In some aspects, the first perfume accord is dominated by an olfactive note selected from the group consisting of floral, water, green, fruity and citrus and the second perfume accord is dominated by an olfactive note selected from the group consisting of oriental, woody and meringue. In an alternate aspect, the first perfume accord is dominated by an olfactive note consisting of lemon and the second perfume accord is dominated by a second olfactive note consisting of an oriental note. In an alternate aspect, the first perfume accord is dominated by an olfactive note consisting of lemon and the second perfume accord is dominated by an olfactive note consisting of a meringue note.


In some aspects, the perfume composition comprises a third contrasting accord. This accord, if used, must contrast with the other two accords in the composition. There must be no perceptual cross-adaptation (reciprocal or non-reciprocal) between either pair of accords in the composition; at least one pair of accords must show either reciprocal or non-reciprocal perceptual enhancement; and, the three accords must be used in the fragrance composition at approximately the same intensity as one another.


In some aspects, the perfume composition further comprises additional ingredients.


Compositions Comprising Contrasting Perfuming Accords Having Different Temporal Release Profiles: Without intending to be limited to any particular theory, in some aspects, the likelihood of a subject's decreased perception of a fragrance (also referred to herein as habituation) may be greater if the olfactive profile (i.e. the olfactive notes of the perfume composition) does not change, or changes only slightly with time.


By way of illustration, Example 4 describes a perfume composition having an olfactive profile that was consistently reported to be floral, musk and woody for up to 6 hours following application to a surface. It was found that subjects adapted to the perfume composition, in that the perception of the perfume composition decline over time.


In contrast, again referring to Example 4, less adaptation was observed to perfume compositions having an olfactive profile that changes over time.


Accordingly, some aspects provide a perfume composition comprising at least two perfuming accords,

    • wherein a first perfume accord of the at least two perfuming accords comprises perfuming compounds dominated by a first olfactive note,
    • wherein a second perfume accord of the at least two perfuming accords comprises perfuming compounds dominated by a second olfactive note,
    • wherein the first and second olfactive notes are contrasting notes,
    • wherein the first perfume accord is present in the perfume composition in an amount sufficient for the first olfactive note to be perceived by a subject at a first time,
    • wherein the second perfume accord is present in the perfume composition in an amount sufficient for the second olfactive note to be perceived by a subject at a second time, and
    • wherein the perception of the first olfactive note and the second olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In some aspects, the second time is after the first time.


In some aspects, the perfume composition further comprises a third perfume accord comprising perfuming compounds dominated by a third olfactive note, wherein the third perfume accord is present in the perfume composition in an amount sufficient for the third olfactive note to be perceived by a subject at a third time.


In some aspects, the third time is after the second time.


In some embodiments, the perfume composition is the perfume composition described in Table 2.


In some embodiments, the perfume composition is the perfume composition described in Table 3.


In some aspects, the perfume composition further comprises additional ingredients.


In some aspects, the perfume composition is a pre-formulated perfume composition, and the first perfume accord is added to the pre-formulated perfume composition in an amount sufficient for the first olfactive note to be perceived by the subject at the first time.


In some aspects, the perfume composition is a pre-formulated perfume composition, and the second perfume accord is added to the pre-formulated perfume composition in an amount sufficient for the second olfactive note to be perceived by the subject at the second time.


In some aspects, the perfume composition is a pre-formulated perfume composition, and the third perfume accord is added to the pre-formulated perfume composition in an amount sufficient for the third olfactive note to be perceived by the subject at the third time.


In some aspects, the third olfactive note and the second olfactive note are contrasting notes.


In some aspects, the third olfactive note and the first olfactive note are contrasting notes.


In some aspects, there are no perceptual cross-adaptation (reciprocal or non-reciprocal) between either pair of accords in the composition (either between the first and second, or the second and third)


In some embodiments, at least one pair of accords show either reciprocal or non-reciprocal perceptual enhancement.


In some aspects, the first olfactive note is selected from the group consisting of floral, water, green, fruity and citrus olfactive notes.


In some aspects, the second olfactive note is selected from the group consisting of floral, fruity, citrus, sweet, oriental, woody and meringue olfactive notes.


In some aspects, the third olfactive note is selected from the group consisting of floral, fruity, citrus, sweet, oriental, woody and meringue olfactive notes.


In some aspects, the first perfume accord is dominated by an olfactive note consisting of lemon and the second perfume accord is dominated by a second olfactive note consisting of oriental.


In some aspects, the first perfume accord is dominated by an olfactive note consisting of lemon and the second perfume accord is dominated by an olfactive note consisting of meringue.


In some aspects, the first perfume accord is dominated by an olfactive note consisting of citrus, floral, fruity and green, and the second perfume accord is dominated by an olfactive note consisting of a floral, fruity and sweet.


In some aspects, the first perfume accord is dominated by an olfactive note consisting of citrus and green, the second perfume accord is dominated by an olfactive note consisting of a floral, and fruity, and the third perfume accord is dominated by an olfactive note consisting of floral, fruity, citrus and sweet.


In some aspects, the sufficient amount of the first perfume accord is from 30% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the first perfume accord is from 40% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the first perfume accord is from 50% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the first perfume accord is from 60% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the first perfume accord is from 30% to 60% by weight of the perfume composition. In some aspects, the sufficient amount of the first perfume accord is from 30% to 50% by weight of the perfume composition. In some aspects, the sufficient amount of the first perfume accord is from 30% to 40% by weight of the perfume composition.


In some aspects, the sufficient amount of the first perfume accord is 30%, or 40%, or 50%, or 60%, or 70% by weight of the perfume composition.


In some aspects, the sufficient amount of the second perfume accord is from 30% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the second perfume accord is from 40% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the second perfume accord is from 50% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the second perfume accord is from 60% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the second perfume accord is from 30% to 60% by weight of the perfume composition. In some aspects, the sufficient amount of the second perfume accord is from 30% to 50% by weight of the perfume composition. In some aspects, the sufficient amount of the second perfume accord is from 30% to 40% by weight of the perfume composition.


In some aspects, the sufficient amount of the second perfume accord is 30%, or 40%, or 50%, or 60%, or 70% by weight of the perfume composition.


In some aspects, the first perfume accord and the second perfume accord are present in the perfume composition in a weight ratio ranging from 3:1 to 1:3. In some aspects, the first perfume accord and the second perfume accord are present in the perfume composition at a weight ratio of 1:1.


In some aspects, the sufficient amount of the third perfume accord is from 30% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the third perfume accord is from 40% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the third perfume accord is from 50% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the third perfume accord is from 60% to 70% by weight of the perfume composition. In some aspects, the sufficient amount of the third perfume accord is from 30% to 60% by weight of the perfume composition. In some aspects, the sufficient amount of the third perfume accord is from 30% to 50% by weight of the perfume composition. In some aspects, the sufficient amount of the third perfume accord is from 30% to 40% by weight of the perfume composition.


In some aspects, the sufficient amount of the third perfume accord is 30%, or 40%, or 50%, or 60%, or 70% by weight of the perfume composition.


In some aspects, the first perfume accord the second perfume accord, and the third perfume accord are present in the perfume composition at a weight ratio of 1:1:1.


Without intending to be limited to any particular theory, the perception of a particular perfume accord depends on a number of factors, such as, for example, the particular mixture of perfuming ingredients, the volatility of the perfuming ingredients, the odor detection threshold of the perfuming ingredients, the concentration of the perfuming ingredients that a subject is exposed to, and the like.


In some embodiments, the first, second, and third perfuming accords, when perceived, are perceived at the same intensity by the subject.


In some embodiments, the time at which a given perfume accord is perceived by the user may be controlled by the relative volatility of a given perfume accord compared to the others in the perfume composition. For example, in some embodiments, the first perfuming accord comprises perfuming ingredients that are more volatile than the perfuming ingredients comprising the second, or third perfume accords. Consequently, the first perfume accord is perceived by the subject at a first time that is before the time the second perfume accord is perceived. Similarly, in some embodiments, the second perfuming accord comprises perfuming ingredients that are more volatile than the perfuming ingredients comprising the third perfume accord. Consequently, the second perfume accord is perceived by the subject at a time second time that is before the time the third perfume accord is perceived. Similarly, the third perfuming accord comprises perfuming ingredients that are less volatile than the perfuming ingredients comprising the second perfume accord. Consequently, the third perfume accord is perceived by the subject at a time second time that is after the time the second perfume accord is perceived.


In some aspects, the first perfume accord comprises perfuming compounds having a volatility ranging from 70,000 to 100 μg/l in air. In some aspects, perfuming compounds having a volatility ranging from 70,000 to 100 μg/l in air are referred to as “top notes”.


In some aspects, the second perfume accord comprises perfuming compounds having a volatility ranging from 99 to 50 μg/l in air. In some aspects, perfuming compounds having a volatility ranging from 99 to 50 μg/l in air are referred to as “middle notes”.


In some aspects, the third perfume accord comprises perfuming compounds having a volatility ranging from 49 to 0.1 μg/l in air. In some aspects, perfuming compounds having a volatility ranging from 49 to 0.1 μg/l in air are referred to as “bottom notes”.


In some aspects, the first perfume accord comprises perfuming compounds having a vapor pressure greater than 0.1 mm Hg. In some aspects, perfuming compounds having a vapor pressure greater than 0.1 mm Hg are referred to as “top notes”.


In some aspects, the second perfume accord comprises perfuming compounds having a vapor pressure between 0.1 mm Hg and 0.001 mm Hg. In some aspects, perfuming compounds having a vapor pressure between 0.1 mm Hg and 0.001 mm Hg are referred to as “middle notes”.


In some aspects, the third perfume accord comprises perfuming compounds having a vapor pressure less than 0.001 mm Hg. In some aspects, perfuming compounds having a vapor pressure less than 0.001 mm Hg are referred to as “bottom notes”.


Tables 4 to 10 describe top, middle and bottom note perfuming compounds for watery, green, fruity, citrus, sweet, gourmand and woody notes respectively.


In some aspects, the perception of the second olfactive note after the first olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In some aspects, the perception of the first olfactive note, the second olfactive note, and the third olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


In some aspects, the perception of the third olfactive note after the second olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.


Accordingly, some aspects provide a method to reduce, prevent, or suppress a reduced perception of the perfume composition by a subject over time, comprising exposing the subject to a perfume composition according an aspect presented herein.


In some aspects, the first time is less than one hour after exposure of the subject to the perfuming composition. In some aspects, the first time is 60, or 55, or 50, or 45, or 40, or 35, or 30, or 25, or 20, or 15 minutes after exposure of the subject to the perfuming composition.


In some aspects, the second time is from one to six hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from one to five hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from one to four hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from one to three hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from one to two hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from two to six hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from three to six hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from four to six hours after exposure of the subject to the perfuming composition. In some aspects, the second time is from five to six hours after exposure of the subject to the perfuming composition. In some aspects, the second time is 1, or 1.5, or 2, or 2.5, or 3, or 3.5, or 4, or 4.5, or 5, or 5.5, or 6 six hours after exposure of the subject to the perfuming composition.


In some aspects, the second time is from one to four hours after exposure of the subject to the perfuming composition.


In some aspects, the third time is from four to six hours after exposure of the subject to the perfuming composition. In some aspects, the third time is from four to five hours after exposure of the subject to the perfuming composition. In some aspects, the third time is from five to six hours after exposure of the subject to the perfuming composition. In some aspects, the third time is 4, or 4.5, or 5, or 5.5, or 6 six hours after exposure of the subject to the perfuming composition.


Encapsulated Perfume accords: In some aspects, the first perfume accord further comprises a mixture comprising the first perfume accord encapsulated within a matrix material.


In some aspects, the second perfume accord further comprises a mixture comprising the second perfume accord encapsulated within a matrix material.


In some aspects, the third perfume accord further comprises a mixture comprising the third perfume accord encapsulated within a matrix material.


Without intending to be limited to any particular theory, the matrix material forms a shell, encapsulating and retaining the perfume accord. The matrix material may be permeable to the perfuming accord, and accordingly, in some aspects, the matrix material may release the retained perfuming accord slowly over time, by a mechanism, such as, for example, diffusion.


Alternatively, the matrix material may be impermeable to the perfuming accord. Accordingly, in some aspects, the matrix material may release the retained perfuming accord when the encapsulating matrix material is ruptured.


In some aspects, the rate of release of the first perfuming accord from the encapsulating matrix material defines the first time.


In some aspects, the rate of release of the second perfuming accord from the encapsulating matrix material defines the second time.


In some aspects, the rate of release of the third perfuming accord from the encapsulating matrix material defines the third time.


The matrix material may be any material capable of retaining fragrance. Examples include core-shell type capsules composed of a polymeric rupturable external wall enclosing a perfume accord; a spray-dried matrix type wherein the matrix comprises a water-soluble material; an extrusion granulation type; and, a composite type comprising a plurality of core-shell microcapsules dispersed in a spray-dry carrier.


Examples of the core-shell capsules include but are not limited to PopScent® M, PopScent® MG, PopScent® P and PolyBloom™.


An example of the spray-dried capsules include but is not limited to Fircaps®.


Examples of the extrusion granulation capsules include but are not limited to Flexarome® and Durarome®.


Examples of the composite capsules include but are not limited to PopScent® M-Dry, PopScent® P-Dry and PopScent® M-Dry Plus.


Another example of a capsule suitable for use in the present disclosure are the capsules disclosed in U.S. Pat. No. 5,135,747.


Another example of a capsule suitable for use in the present disclosure are the capsules disclosed in U.S. Pat. No. 5,508,259 A.


Another example of a capsule suitable for use in the present disclosure are the capsules disclosed in U.S. Pat. No. 6,200,949 B1.


Another example of a capsule suitable for use in the present disclosure are the capsules disclosed in U.S. Pat. No. 7,208,463 B2.


Another example of a capsule suitable for use in the present disclosure are the capsules disclosed in U.S. Patent Application Publication No. 2003/0194416 A1.


Referring to Examples 5 and 6, without intending to be limited to any particular theory, in a consumer product, it is often required to use a combination of non-confined (free) fragrance and encapsulated fragrance to provide the desired sensorial benefit. For example, if a fragrance is encapsulated, it may provide little contribution to the odor of a product at point-of-purchase, or when dispensing the product from its container. Therefore, a non-confined fragrance may be added to optimize both odor intensity and hedonics during these stages of product use.


At later times in product use, however, it may be desirable to release a second fragrance to optimize both odor and intensity. “At later times” means some time after experiencing the non-confined fragrance. This may be a short time (for example less than 5 minutes or even less than 1 minute), if the aim is to provide a fragrance blooming effect such as might be desired in the case of a shower gel, liquid hand soap, shampooing product or hand-wash detergent powder; or, it may be a long time (for example more than 6 hours or even more than 1 day), if the aim is to provide a long-lasting fragrance effect such as might be desired in a body lotion, fabric softener, liquid and/or powder fabric detergent.


In some aspects, the subject may become adapted to the non-confined (free) fragrance. In these instances, the perception of the encapsulated fragrance may be enhanced if it is contrasting with respect to the non-confined fragrance.


Devices and Applications

In some aspects, the time at which a given perfume accord is perceived by the user may be controlled by dispensing the given perfume accord at a given time. For example, the first perfume accord may be dispensed at the first time, the second perfume accord may be dispensed at the second time, and so on. In some embodiments, the subject does not perceive a given perfume accord until it is dispensed.


Accordingly, some aspect presented herein provide a method to reduce, prevent, or suppress a reduced perception of the perfume composition by a subject over time, comprising dispensing sequentially at least partly in the air, the first perfume accord dominated by a first olfactive note followed by the second perfume comprising perfuming compounds forming a second perfume accord dominated by a second olfactive note.


In some aspects, the sequential dispensing is performed using a device configured to sequentially emanate separate fragrances at timed intervals from each other. Devices suitable for this include the AIRWICK® SYMPHONIA device which is configured to receive two separate bottles of fragrance and sequentially direct heat toward each bottle to accelerate the evaporation of fragrance therefrom. In such a device the fragrances contained in each bottle can be different to facilitate a consumer being able to notice the sequential nature of the fragrance emanation.


U.S. Patent Application Publication No. 2013/0156408 A1 discloses an example of a device configured to sequentially emanate separate fragrances at timed intervals from each other.


U.S. Patent Application Publication No. 2013/0156408 A1 discloses an example of methods to sequentially emanate separate fragrances at timed intervals from each other.


U.S. Patent Application Publication No. 2015/0098860 A1 discloses an example of methods to sequentially emanate separate fragrances at timed intervals from each other.


In some aspects, the device comprises dispensing means for dispersing sequentially in the air volatile compositions and a composition as defined in any of the above-described aspects. In some aspects, the device is such that the first accord and the second accord are physically separated by separating means. According to one aspect, the device is an air-freshener. By sequentially diffusing contrasting accords, the intensity of the perfume can be improved over time.


In some aspects, the first time is 60, or 55, or 50, or 45, or 40, or 35, or 30, or 25, or 20, or 15 minutes.


In some aspects, the second time is 1, or 1.5, or 2, or 2.5, or 3, or 3.5, or 4, or 4.5, or 5, or 5.5, or 6 six hours.


In some aspects, the third time is 4, or 4.5, or 5, or 5.5, or 6 six hours.


The compositions of the present disclosure can be used for different applications. According to some aspects, the perfume composition according to the invention consists of an air freshener.


One aspect presented herein provides a manufactured product comprising the perfume composition according to an aspect presented herein. In one aspect, the manufactured product is selected from the group consisting of a perfume, eau de toilette, home care product and a personal care product.


The present invention is best illustrated but is not limited to the following examples.


EXAMPLES
Example 1: Sensory Evaluation of Perceived Perfume Intensity with Sequential Exposure to Contrasting Accords vs Non Contrasting Accords

For this example, 3 perfume accords were prepared: a lemon accord (A1); a lime accord (A2); and, an oriental accord (C1). The lemon accord and lime accords are non-contrasting accords, whereas the lemon and oriental accords are contrasting accords.


Protocol: Each accord was applied to a cellulose type air freshener and placed in an evaluation booth. A panel was then asked to rate the intensity of the odor in each booth. The test was repeated later the same day. The sample preparation and set-up was identical to the first test but there was one important difference: each assessor was asked to wear a small device for 15 minutes prior to the evaluation. The device was a small plastic holder that could be clipped onto the assessors clothing, the holder contained a cellulose pad that was impregnated with the lemon accord. In this way we were able to adapt the assessors to the lemon accord.


The results of the two tests are illustrated in FIG. 2 and are markedly different. The perceived intensity of the lemon accord was significantly suppressed after adaptation to the lemon accord (self-adaptation). The perceived intensity of the lime accord (non-contrasting accord if compared to lemon) was also strongly suppressed after adaptation to the lemon accord (significant cross-adaptation*). On the other hand, the perceived intensity of the oriental accord (contrasting accord compare to lemon) was increased/enhanced after adaptation to the lemon accord. The lemon accord and oriental accord would meet the definition of “contrasting fragrance accords”—there is no cross-adaptation and there is a perceptual enhancement.


Example 2: Sensory Evaluation of Perceived Perfume Intensity with Sequential Exposure to Contrasting Accords vs Non Contrasting Accords

The protocol described in Example 1 was repeated using a larger panel and different accords. Accords used were a berry accord (A1) and a coconut accord (C1). There was also used an accord that would be “complementary” to the berry accord, that is one that is noticeably different (more different than lime from lemon) but which shares some olfactive quality—there was used an apple accord for this purpose (B1). Results are illustrated in FIG. 3. The berry accord showed a strong self-adapting effect, cross-adaptation with the apple accord and no cross-adaptation with the coconut accord. Furthermore, there was an enhancement of the coconut accord after adaptation to the berry.


Example 3: Sensory Evaluation of Perceived Perfume Intensity of a Perfume Composition According to Some Aspects Presented Herein

A sensory test was conducted with 24 panelists. Two contrasting fragrance accords were used, namely “LEMON” (A1) and “MERINGUE” (C1). Three identical odor evaluation booths were set up as follows: one booth contained two 5 cm×5 cm cellulose pads, each impregnated with 2 g of the “LEMON” accord; a second booth contained two 5 cm×5 cm cellulose pads, each impregnated with 2 g of the “MERINGUE” accord; a third booth contained one 5 cm×5 cm cellulose pad impregnated with 2 g of the “LEMON” accord and one 5 cm×5 cm cellulose pad impregnated with the “MERINGUE” accord. Panelists were asked to rate the intensity of the odors in each booth. Normally, it could have been expected that the intensity of the mixture “LEMON+MERINGUE” would fall between the intensity of the LEMON only and MERINGUE only; however, surprisingly the intensity of the mixture was significantly stronger than the intensity of either single accord. Results are illustrated in FIG. 3.


Also, it was mentioned by panelist that the citrus aspects were more noticeable when paired with the “meringue” than when smelled alone. This view was echoed by several of the professional evaluators that smelled the samples.


Example 4: Sensory Evaluation of Perceived Perfume Intensity of a Fine Fragrance Perfume Composition According to Some Aspects Presented Herein

A sensory test was conducted with 22 to 24 panelists in each session, comparing the three fine fragrances shown in three different sesasions, set forth in Tables 1-3 below:









TABLE 1







Test Attention Modulation Fragrance “HAF A”:










Ingredient Name
Parts













Naphtho[2,1-b]furan,dodecahydro-3a,6,6,9a-
15



tetramethyl-,[3aR-(3a.alpha.,5a.beta.,




9a.alpha.,9b.beta)] @10% DIPG




Benzyl Acetate
5



Ethoxymethyl-cyclododecyl ether
10



3-(4-tert-butylphenyl)propanal
5



(Z)-3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-
1



one




3,7-dimethyl-2,6-octadienal @ 10% DIPG
3



3,7-dimethyloct-6-enyl acetate
10



1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-3-
3



en-1-one @ 10% DIPG




(E)-1-(2,6,6-trimethyl-1-cyclohexa-1,3-
3



dienyl)but-2-en-l-one @10% DIPG




5-hexyloxolan-2-one
2



(6E)-3,7-dimethylnona-1,6-dien-3-ol
35



1,4-dioxacycloheptadecane-5,17-dione
50



1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-
50



hexamethylcyclopenta(g)-2-benzopyran 70




MIP EXTRA




(Z)-3,7-Dimethyl-2,6-octadien-1-ol
7



GRAPEFRUIT OIL
10



methyl 3-oxo-2-pentylcyclopentaneacetate
100



3-(1,3-benzodioxol-5-yl)-2-methylpropanal
20



HYDROXYCITRONELLAL SYNTH P FAB
25



INDOLE @ 1% DIPG
5



7-acetyl, 1,2,3,4,5,6,7,8-octahydro-1,1,6,7-
35



tetramethyl naphthalene




JASMIN PAYS FIR ABSOLUE @ 10%
3



DIPG




6-[(E)-pent-2-enyl]oxan-2-one @10% DIPG
14



LEMON OIL SFUMA PRIMOFIORE
10



3-(4-tert-butylphenyl)butanal
40



MANDARIN INCOL DM
15



METHYL ANTHRANILATE DIST @1%
4



DIPG




methyl 2,4-dihydroxy-3,6-dimethylbenzoate
3



@10 DIPG




TAGETES OIL @10% DIPG
2



5-heptyloxolan-2-one
5



(E)-4-methyldec-3-en-5-ol
6



2,4-dimethylcyclohex-3-ene-1-carbaldehyde
4



@10% DIPG





500
















TABLE 2







Test Attention Modulation Fragrance “HAF A2”:










Ingredient Name
Parts













Naphtho[2,1-b]furan,dodecahydro-3a,6,6,9a-
15



tetramethyl-,[3aR-




(3a.alpha.,5a.beta.,9a.alpha.,9b.beta)]




@10% DIPG




Benzyl Acetate
5



Ethoxymethyl-cyclododecyl ether
10



3-(4-tert-butylphenyl)propanal
5



(Z)-3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-
1



one




3,7-dimethyl-2,6-octadienal @ 10% DIPG
3



3,7-dimethyloct-6-enyl acetate
10



1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-3-
3



en-1-one @ 10% DIPG




(E)-1-(2,6,6-trimethyl-1-cyclohexa-1,3-
3



dienyl)but-2-en-1-one @10% DIPG




5-hexyloxolan-2-one
2



(6E)-3,7-dimethylnona-1,6-dien-3-ol
35



ETHYL PRANILE @10% DIPG
5



1,4-dioxacycloheptadecane-5,17-dione
50



1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-
50



hexamethylcyclopenta(g)-2-benzopyran 70




MIP EXTRA




(Z)-3,7-Dimethyl-2,6-octadien-1-ol
7



GRAPEFRUIT OIL
10



methyl 3-oxo-2-pentylcyclopentaneacetate
100



3-(1,3-benzodioxol-5-yl)-2-methylpropanal
20



HYDROXYCITRONELLAL SYNTH P FAB
38



INDOLE @ 1% DIPG
5



7-acetyl,1,2,3,4,5,6,7,8-octahydro-1,1,6,7-
35



tetramethyl naphthalene




JASMIN PAYS FIR ABSOLUE @ 10%
3



DIPG




6-[(E)-pent-2-enyl]oxan-2-one @10% DIPG
14



LEMON OIL SFUMA PRIMOFIORE
10



3-(4-tert-butylphenyl)butanal
40



MANDARIN INCOL DM
15



METHYL ANTHRANILATE DIST @1%
4



DIPG




methyl 2,4-dihydroxy-3,6-dimethylbenzoate
3



@10 DIPG




TAGETES OIL @10% DIPG
2



5-heptyloxolan-2-one
5



(E)-4-methyldec-3-en-5-ol
6



VANILLIN NAT NFB LC @ 10% DIPG
2



2,4-dimethylcyclohex-3-ene-1-carbaldehyde
4



@10% DIPG





520
















TABLE 3







Reference Fragrance “HAF 1”:










Ingredient Name
Parts













Ambrettolide
5



3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-
10



octahydro-1H-benzo[e][1]benzofuran




Benzyl Salicylate
40



Ethoxymethyl-cyclododecyl ether
20



Dartanol
15



1,4-dioxacycloheptadecane-5,17-dione
77



Firsantol
10



1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-
120



hexamethylcyclopenta(g)-2-benzopyran 70




MIP EXTRA




methyl 3-oxo-2-pentylcyclopentaneacetate
80



Hydroxycitronellal Synth P FAB
30



Indole @ 10% DIPG
2



7-acetyl,1,2,3,4,5,6,7,8-octahydro-1,1,6,7-
180



tetramethyl naphthalene




Jasmin Sambac Fir absolue @ 10% DIPG
5



5-Ethyl-5-phenylhydantoin
10



Pipol Salicylate
10



(E)-3,3-dimethyl-5-(2,2,3-trimethyl-3-
25



cyclopenten-1-yl)-4-penten-2-ol




3-methyl-5-(2,2,3-trimethyl-1-cyclopent-3-
30



enyl)pentan-2-ol




1-(2,6,10-TRIMETHYL-1(2),5,9-
30



CYCLODODECATRIEN-1-YL)-1-




ETHANONE + 1-(6,10-DIMETHYL-2-




METHYLENE-5,9- . . .)-1-E . . .




5-heptyloxolan-2-one
1




700









The fine fragrances were applied to glass slides, which were maintained at 32 degrees Celsius. The olfactive profile and perceived global intensity of the fragrances were evaluated at 15 min, 1 hour, 2 hours, 4 hours, and 6 hours after application to the glass surfaces, by randomly presenting the slides.


The panelists were asked to describe the olfactive profile by selecting the three most dominant descriptors (out of 7 presented: Green, Citrus, Fruity, Floral, Woody, Musk, Sweet/Gourmand). Panelists were also able to mention when they perceived nothing (i.e., were not able to describe the olfactive profile).


The panelists were asked to rate the perceived global intensity of the fragrances at 15 min, 1 hour, 2 hours, 4 hours, and 6 hours after application to the glass surfaces, by randomly presenting the slides.


Adaptation was determined by applying the fragrance to a cellulose pad, and presenting the fragrance to the panelist for two minutes before the glass slides were presented again to the panelists.


The Reference Fine Fragrance: Referring to FIG. 5, the olfactive profile did not appear to change over time, wherein the panelists reported a Floral, Musk, and Woody profile at all time points. The horizontal line depicts the limit of a random selection of the terms. 46% of the panelists reported no change in olfactive profile, whilst 46% of the panelists reported 2 to 4 changes in olfactive profile, and none of the panelists reported a maximum of 4 changes in olfactive profile.


Referring to FIG. 6, the perception of the reference fine fragrance declined significantly following a two minute exposure to the fragrance. Before exposure, 65% of the selected terms were above chance, compared to 15% after exposure.


The Attention Modulation Fragrance “HAF A”: Referring to FIG. 7, the olfactive profile changed or switched, wherein the panelists reported a Citrus/Green profile at 15 min, a Floral/Fruity profile at 1 to 4 hours, and a Floral/Fruity/Citrus/Sweet profile at 6 hours. The horizontal line depicts the limit of a random selection of the terms. Only 18% of the panelists reported no change in olfactive profile, whilst 73% of the panelists reported 2 to 4 changes in olfactive profile, and 23% of the panelists reported a maximum of 4 changes in olfactive profile.


Referring to FIG. 8, the perception of the attention modulation fine fragrance did not decline as much, compared to the decline observed with the reference fragrance following a two minute exposure to the fragrance. After exposure, 38% of the selected terms were above chance compared to only 15% for the reference fragrance.


The Attention Modulation Fragrance “HAF A2”: Referring to FIG. 9, the olfactive profile changed or switched, wherein the panelists reported a Citrus/Floral/Fruity/Green profile at 15 min, and a Floral/Fruity/Sweet profile at 1 to 6 hours. The horizontal line depicts the limit of a random selection of the terms. Only 9% of the panelists reported no change in olfactive profile, whilst 82% of the panelists reported 2 to 4 changes in olfactive profile, and 34% of the panelists reported a maximum of 4 changes in olfactive profile.


Referring to FIG. 10, the perception of the attention modulation fine fragrance did not decline as much, compared to the decline observed with the reference fragrance following a two minute exposure to the fragrance. After exposure, 51% of the selected terms were above chance compared to only 15% for the reference fragrance.



FIG. 11 shows the effect of adaptation on the percent intensity decrease of perception following adaptation of the reference and two test fragrances. A greater decrease in intensity following adaptation was observed in the reference fragrance, particularly at 2 and 4 hours.


Taken together, these data suggest that the olfactive profiles of perfume compositions according to some aspects presented herein change more over time, compared to a reference composition. Additionally, less adaptation is observed by subjects for perfume compositions according to some aspects presented herein change more over time, compared to a reference composition. Finally, the perfume compositions according to some aspects presented herein are more long lasting than reference compositions, as evidenced by a lower decrease in perceived intensity after a 2 minute adaptation.









TABLE 4







Perfuming Compounds Having a Watery Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















TOP
(+−)-2,6-
140
1889.68
3.15
2.11E−04
8.96E+06



DIMETHYL-5-








HEPTENAL







TOP
(2E,6Z)-2,6-
138
632.43
2.56
1.46E−04
4.34E+06



NONADIENAL″







TOP
(2E,6Z)-2,6-
138
632.43
2.56
1.46E−04
4.34E+06



NONADIENAL″







TOP
METHYL 2-
154
472.01
2.90
8.31E−04
5.68E+05



OCTYNOATE″







TOP
DECANAL″
156
466.56
3.99
1.92E−03
2.43E+05


TOP
(+−)-2-
170
297.74
3.73
9.00E−04
3.31E+05



methyldecanal″







TOP
undecanal
170
178.29
4.56
1.65E−03
1.08E+05


TOP
DODECANAL
184
144.79
4.94
9.90E−04
1.46E+05


TOP
10-undecenal
168
136.73
3.93
3.15E−03
4.34E+04


TOP
10-undecenal (A) +
168
131.95
4.26
3.77E−05
3.50E+06



(9E)-9-








undecenal (B) +








(9Z)-9-undecenal








(C)







TOP
8-ISOPROPYL-
192
131.02
3.81
7.11E−05
1.84E+06



6-METHYL-








BICYCLO[2.2.2]








OCT-








5-ENE-2-








CARBALDEHYDE







TOP
(2Z)-3,7-
196
123.21
3.81
6.02E−02
2.05E+03



dimethyl-2,6-








octadien-1-yl








acetate







middle
(2E,6Z)-2,6-
140
98.76
2.68
3.22E−06
3.07E+07



NONADIEN-1-








OL







middle
METHYL 2-
168
91.76
3.51
1.60E−03
5.74E+04



NONYNOATE







middle
7-methyl-2H-1,5-
142
89.26
3.40
5.05E−04
1.77E+05



benzodioxepin-








3(4H)-one







middle
(+−)-
172
79.79
2.22
1.35E−02
5.91E+03



TETRAHYDRO-








2-ISOBUTYL-4-








METHYL-4(2H)-








PYRANOL







middle
(+−)-2-
184
75.55
5.01
7.24E−05
1.04E+06



methylundecanal







middle
(2R)-2-methyl-4-
206
63.49
4.25
2.22E−03
2.86E+04



[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-4-pentenal (A) +








(2S)-2-methyl-








4-[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-4-pentenal (B)







middle
7-methyl-2H-1,5-
178
56.74
1.61
3.20E−06
1.77E+07



benzodioxepin-








3(4H)-one







middle
7-ISOPROPYL-
178
56.74
1.61
3.20E−06
1.77E+07



2H,4H-1,5-








BENZODIOXEPIN-








3-ONE







middle
DODECANENITRILE
178
56.74
1.61
3.20E−06
1.77E+07


bottom
3-(4-
190
48.69
3.56
5.33E−03
9.14E+03



ETHYLPHENYL)-








2,2-








DIMETHYLPROPANAL








(A) + 3-








(2-








ETHYLPHENYL)-








2,2-








DIMETHYLPROPANAL








(B)







bottom
7-methyl-2H-1,5-
190
32.27
3.53
6.05E−05
5.33E+05



benzodioxepin-








3(4H)-one







bottom
(+−)-1-METHYL-
206
26.54
5.14
2.72E−02
9.76E+02



4-(4-METHYL-3-








PENTENYL)-3-








CYCLOHEXENE-








1-








CARBALDEHYDE







bottom
(+−)-3-(4-
190
24.85
3.59
3.00E−03
8.28E+03



isopropylphenyl)-








2-methylpropanal







bottom
(+−)-3-(4-methyl-
192
21.54
4.11
3.68E−03
5.85E+03



3-penten-1-yl)-3-








cyclohexene-1-








carbaldehyde (A) +








(+−)-4-(4-








methyl-3-penten-








1-yl)-3-








cyclohexene-1-








carbaldehyde (B)







bottom
(+−)-3-(4-
178
18.99
2.80
9.79E−03
1.94E+03



methoxyphenyl)-








2-methylpropanal







bottom
(+−)-2,6,10-
210
18.23
5.20
1.59E−02
1.15E+03



TRIMETHYL-9-








UNDECENAL







bottom
1,5,9-
238
14.74
5.28
3.28E−04
4.49E+04



TRIMETHYL-








4,8-








DECADIENYL








ACETATE







bottom
(+−)-3-(3-
194
14.74
2.01
7.71E−04
1.91E+04



ISOPROPYL-1-








PHENYL)BUTANAL







bottom
3-(3,3-dimethyl-
206
13.73
2.58
1.32E−05
1.04E+06



2,3-dihydro-1H-








inden-5-








yl)propanal (A) +








3-(1,1-dimethyl-








2,3-dihydro-1H-








inden-5-








yl)propanal (B)







bottom
3-(3,3-dimethyl-
181
13.68
4.63
4.00E−03
3.42E+03



2,3-dihydro-1H-








inden-5-








yl)propanal (A) +








3-(1,1-dimethyl-








2,3-dihydro-1H-








inden-4-








yl)propanal (B) +








3-(1,1-dimethyl-








2,3-dihydro-1H-








inden-5-








yl)propanal (C)







bottom
(+−)-2-methyl-3-
204
12.86
3.90
2.39E−04
5.38E+04



[4-(2-methyl-2-








propanyl)phenyl]propanal







bottom
(+−)-7-hydroxy-
172
12.81
2.00
6.98E−03
1.84E+03



3,7-








dimethyloctanal







bottom
CYCLOSIA
172
10.34
2.00
6.98E−03
1.48E+03



BASE








(POLYMER)








(MAIN CPD = 7-








HYDROXY-3,7-








DIMETHYLOCTANAL)







bottom
(Z)-6-NONEN-1-
202
6.91
3.44
6.10E−04
1.13E+04



OL







bottom
(1S,4S,9S,10R,13R)-
278
6.77
4.59
4.36E−04
1.55E+04



5,5,9,13-








tetramethyl-








14,16-








dioxatetracyclo








[11.2.1.0~1,10~.0~4,9~]








hexadecane








(A) +








(1R,4S,9S,10R,13S)-








5,5,9,13-








tetramethyl-








14,16-








dioxatetracyclo








[11.2.1.0~1,10~.0~4,9~]








hexadecane








(B)







bottom
8(9)-METHOXY-
193
5.87
5.00
4.02E−05
1.46E+05



TRICYCLO[5.2.1.0(2,6)]DECANE-








3(4)-








CARBALDEHYDE







bottom
(+−)-2,5-
176
4.86
3.12
1.28E−04
3.79E+04



DIMETHYL-2-








INDANMETHANOL







bottom
7-PROPYL-
206
4.85
2.79
6.43E−05
7.54E+04



2H,4H-1,5-








BENZODIOXEPIN-








3-ONE







bottom
7-(2-methyl-2-
220
4.37
2.97
1.53E−04
2.85E+04



propanyl)-2H-








1,5-








benzodioxepin-








3(4H)-one







bottom
(+−)-3-(1,3-
192
3.57
1.28
2.23E−04
1.60E+04



BENZODIOXOL-








5-YL)-2-








METHYLPROPANAL







bottom
METHYL 2,4-
196
1.52
2.30
4.89E−06
3.11E+05



DIHYDROXY-








3,6-








DIMETHYLBENZOATE







bottom
(+−)-3-(4-
210
0.70
2.19
8.81E−05
7.92E+03



hydroxy-4-








methylpentyl)-3-








cyclohexene-1-








carbaldehyde (A) +








(+−)-4-(4-








hydroxy-4-








methylpentyl)-3-








cyclohexene-1-








carbaldehyde (B)
















TABLE 5







Perfuming Compounds Having a Green Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















Top
ETHYL
116
142519.74
2.03
3.68E−04
3.87E+08



BUTANOATE







Top
(+−)-ethyl 2-
130
83769.16
2.58
1.26E−04
6.67E+08



methylbutanoate







Top
hexanal
100
68294.85
2.00
1.76E−03
3.88E+07


Top
3-
130
51307.81
2.65
5.92E−02
8.67E+05



METHYLBUTYL








ACETATE (A) +








(+−)-2-








METHYLBUTYL








ACETATE (B)







Top
(+−)-ETHYL 2-
144
35090.18
3.05
3.84E−05
9.14E+08



METHYLPENTANOATE







Top
(−)-(1S)-2,6,6-
136
33722.60
5.43
1.02E−01
3.31E+05



TRIMETHYL-








BICYCLO[3.1.1]








HEPT-








2-ENE







Top
beta-PINENE
136
33722.60
5.43
1.02E−01
3.31E+05



89% (A) + alpha-








PINENE 11% (B)







Top
(2E)-2-
98
33708.26
1.62
2.53E−03
1.33E+07



HEXENAL







Top
(+−)-3-
88
33382.87
−1.03
1.46E−02
2.28E+06



HYDROXY-2-








BUTANONE







Top
3-methyl-2-buten-
128
27705.98
2.19
5.58E−02
4.97E+05



1-yl acetate







Top
METHYL
130
23345.90
2.65
8.43E−02
2.77E+05



HEXANOATE







Top
(+−)-2-ethenyl-
154
23116.66
3.59
1.64E−01
1.41E+05



2,6,6-








trimethyltetrahydro-








2H-pyran







Top
HEPTANAL
114
22184.00
2.15
2.03E−03
1.09E+07


Top
1-BUTANOL
74
17700.00
0.88
8.70E−02
2.03E+05


Top
1,1-DIETHOXY-
226
16590.69
4.59
3.57E−03
4.65E+06



3,7-DIMETHYL-








2,6-OCTADIENE







Top
(+−)-3,5,5-
142
12045.92
3.02
9.37E−03
1.29E+06



TRIMETHYLHEXANAL







Top
(Z)-3-HEXENYL
128
9873.53
2.17
2.11E−03
4.68E+06



FORMATE







Top
ETHYL
145
9675.10
3.12
9.11E−04
1.06E+07



HEXANOATE







Top
BENZALDEHYDE
106
8207.00
1.33
4.26E−02
1.93E+05


Top
(1R,5R)-4,7,7-
168
6351.47
4.48
7.99E−05
7.95E+07



trimethyl-6-








thiabicyclo[3.2.1]








oct-3-ene (A) +








(1R,4R,5R)-4,7,7-








trimethyl-6-








thiabicyclo[3.2.1]








octane (B)







Top
(E)-2-HEXENYL
142
6062.68
2.59
2.08E−01
2.92E+04



ACETATE







Top
(Z)-3-HEXEN-1-
100
5986.62
1.65
1.13E−02
5.30E+05



OL







Top
6-METHYL-5-
126
5775.94
2.05
1.06E−01
5.45E+04



HEPTEN-2-ONE







Top
1-ISOBUTYL-3-
186
5265.61
4.19
1.62E+00
3.24E+03



METHYLBUTYL








ACETATE







Top
OCTANAL
128
4147.61
2.94
2.77E−04
1.50E+07


Top
(2Z)-3-methyl-2-
156
4131.05
3.11
2.73E−02
1.51E+05



hexen-1-yl








acetate (A) +








(2E)-3-methyl-2-








hexen-1-yl








acetate (B)







Top
(1RS,6RS)-3,6-
138
3770.43
2.24
2.69E−04
1.40E+07



dimethyl-3-








cyclohexene-1-








carbaldehyde (A) +








(1RS,6RS)-4,6-








dimethyl-3-








cyclohexene-1-








carbaldehyde (B) +








(1RS,6SR)-4,6-








dimethyl-3-








cyclohexene-1-








carbaldehyde (C)







Top
(E)-2-HEXEN-1-
100
3752.17
1.73
1.29E−01
2.92E+04



OL







Top
3,7-DIMETHYL-
136
3480.57
4.91
2.57E−02
1.35E+05



1,3,6-








OCTATRIENE







Top
(Z)-3-HEXENYL
142
3398.34
2.62
1.00E−02
3.40E+05



ACETATE







Top
(+−)-1-octen-3-ol
128
3030.11
2.33
1.77E−03
1.71E+06


Top
ETHYL 3-
130
2885.67
0.35
5.83E−02
4.95E+04



OXOBUTANOATE








(A) <=> (2Z)-








ETHYL 3-








HYDROXY-2-








BUTENOATE








(B)







Top
nonanal
142
2777.63
3.42
8.14E−03
3.41E+05


Top
DIBUTYL
146
2766.10
4.86
2.34E−02
1.18E+05



SULFIDE







Top
(3Z)-1-[(2E)-2-
154
2673.47
3.77
2.05E−02
1.31E+05



buten-1-yloxy]-3-








hexene (A) +








(3Z)-1-[(2Z)-2-








buten-1-yloxy]-3-








hexene (B)







Top
(+−)-1-
148
2534.77
3.06
1.92E−07
1.32E+10



METHOXY-3-








HEXANETHIOL







Top
TETRAHYDRO-
154
2483.93
3.49
8.77E−04
2.83E+06



4-METHYL-2-(2-








METHYL-1-








PROPENYL)-








2H-PYRAN







Top
(+−)-
154
2483.93
3.49
8.77E−04
2.83E+06



TETRAHYDRO-








4-METHYL-2-(2-








METHYL-1-








PROPENYL)-








2H-PYRAN (A) +








3,6-DIHYDRO-








4-METHYL-2-(2-








METH-.(B)







Top
(Z)-6-NONENAL
140
2431.73
2.88
2.91E−05
8.36E+07


Top
HEXYL
144
2316.04
3.09
1.32E−01
1.75E+04



ACETATE







Top
(+−)-ETHYL 3-
158
2276.17
1.96
5.06E−04
4.50E+06



METHYL-2-








OXOPENTANOATE







Top
1-hexanol
102
2070.00
2.20
1.17E−01
1.77E+04


Top
(+−)-METHYL
182
2010.91
3.16
1.06E−02
1.90E+05



2,6,6-








TRIMETHYL-2-








CYCLOHEXENE-








1-








CARBOXYLATE







Top
3,5,6-
152
1951.74
3.23
6.17E−03
3.16E+05



TRIMETHYL-3-








CYCLOHEXENE-








1-








CARBALDEHYDE








(A) + 2,4,6-








TRIMETHYL-3-








CYCLOHEXENE-








1-








CARBALDEHYDE








(B)







Top
(2-
164
1714.82
3.15
1.65E−03
1.04E+06



ISOPROPOXYETHYL)BENZENE







Top
(3Z)-3-hexen-1-yl
170
1674.15
3.59
7.85E−02
2.13E+04



butyrate







Top
hexyl 2-
172
1661.18
4.31
7.15E−01
2.32E+03



methylpropanoate







Top
PYRAZOBUTYLE
166
1617.21
2.88
7.20E−07
2.25E+09


Top
(3Z)-hex-3-en-1-
158
1506.33
2.97
4.58E−02
3.29E+04



yl methyl








carbonate







Top
BENZYL
136
1339.53
1.76
3.23E−01
4.15E+03



FORMATE







Top
(3E,5Z)-1,3,5-
150
1247.28
5.68
3.76E−05
3.32E+07



UNDECATRIENE







Top
(2-
136
1239.07
2.33
6.32E−04
1.96E+06



METHOXYETHYL)BENZENE







Top
ALLYL
170
1235.24
4.16
1.75E−02
7.06E+04



HEPTANOATE







Top
(+−)-1-(3,3-
154
1214.93
2.99
1.44E−02
8.44E+04



dimethylcyclohexyl)ethanone








(A) +








(+−)-2,6,6-








trimethylcycloheptanone








(B)







Top
(2RS,4SR)-2-
160
1113.06
3.11
1.47E−03
7.57E+05



methyl-4-propyl-








1,3-oxathiane (A) +








(2RS,4RS)-2-








methyl-4-propyl-








1,3-oxathiane (B)







Top
(Z)-3-HEXENYL
170
1073.97
3.57
4.54E−02
2.36E+04



ISOBUTYRATE







Top
(+)-(R)-4-(2-
168
993.39
4.59
1.99E−01
5.00E+03



methoxypropan-








2-yl)-1-








methylcyclohex-








1-ene







Top
(3Z)-1,3-
148
990.87
5.11
3.32E−03
2.98E+05



undecadien-5-yne








(A) + (3E)-1,3-








undecadien-5-yne








(B)







Top
(+−)-(Z)-3-
184
833.05
3.84
1.96E−02
4.24E+04



HEXENYL 2-








METHYLBUTANOATE







Top
ethyl octanoate
172
800.05
4.20
5.30E−03
1.51E+05


Top
2-METHYL-3-
129
687.75
2.08
4.81E−04
1.43E+06



HEXANONE








OXIME







Top
(2E,6Z)-2,6-
138
632.43
2.56
1.46E−04
4.34E+06



NONADIENAL







Top
(Z)-4-DECENAL
154
629.54
1.11
3.78E−05
1.67E+07


Top
(+−)-(3-methoxy-
164
587.76
3.57
1.51E−02
3.89E+04



2-








methylpropyl)benzene







Top
2-
150
567.67
1.90
8.34E−04
6.81E+05



PHENYLETHYL








FORMATE







Top
ETHYL 2-
174
479.20
1.12
1.62E−03
2.95E+05



METHYL-1,3-








DIOXOLANE-2-








ACETATE







Top
METHYL 2-
154
472.01
2.90
8.31E−04
5.68E+05



OCTYNOATE







Top
(2,2-
166
456.97
2.10
4.55E−02
1.00E+04



DIMETHOXYETHYL)BENZENE







Top
2-
200
450.33
5.13
2.41E−01
1.87E+03



METHYLPENTYL








2-








METHYLPENTANOATE







Top
(+−)-3,7-
158
421.15
3.78
3.45E−03
1.22E+05



DIMETHYL-3-








OCTANOL







Top
(+−)-3-
176
421.09
2.64
2.72E−06
1.55E+08



mercaptohexyl








acetate







Top
3-(4,4-dimethyl-
166
417.92
3.30
2.06E−03
2.03E+05



1-cyclohexen-1-








yl)propanal







Top
(1RS,2RS)-2-(2-
198
402.03
4.40
2.12E−02
1.90E+04



methyl-2-








propanyl)cyclohexyl








acetate (A) +








(1RS,2SR)-2-(2-








methyl-2-








propanyl)cyclohexyl








acetate (B)







Top
1,1-
180
376.94
2.50
1.42E−02
2.65E+04



DIMETHOXY-2-








PHENYLPROPANE







Top
(+−)-1,5-
196
339.21
4.04
7.40E−02
4.58E+03



DIMETHYL-1-








VINYL-4-








HEXENYL








ACETATE







Top
(+−)-1,5-
196
339.21
4.04
7.40E−02
4.58E+03



DIMETHYL-1-








VINYL-4-








HEXENYL








ACETATE (A) +








1-P-MENTHEN-








8-YL ACETATE








(B)







Top
(+−)-
182
330.48
3.92
5.32E−06
6.21E+07



PERHYDRO-








4alpha,8Abeta-








DIMETHYL-4A-








NAPHTHALENOL







Top
(+−)-3,7-
184
322.28
3.79
5.28E−04
6.10E+05



dimethyl-6-octen-








1-yl formate (A) +








(2E)-3,7-








dimethyl-2,6-








octadien-1-yl








formate (B)







Top
(+−)-ethyl 2-
184
295.22
2.15
3.64E−03
8.10E+04



acetyl-4-methyl-








4-pentenoate







Top
(+−)-(4Z)-4-
184
278.83
3.02
3.69E−04
7.56E+05



cycloocten-1-yl








methyl carbonate







Top
methyl (2E)-2-
170
264.84
4.05
5.84E−02
4.53E+03



nonenoate







Top
(+−)-2,4-
176
263.73
3.02
5.04E−04
5.23E+05



dimethyl-4-








phenyltetrahydrofuran







Top
(+−)-3,7-
184
262.84
4.16
1.72E−03
1.53E+05



DIMETHYL-6-








OCTENYL








FORMATE







Top
ALLYL (3-
186
261.90
2.79
9.89E−05
2.65E+06



METHYLBUTOXY)ACETATE








(A) + (+−)-








ALLYL (2-








METHYLBUTOXY)ACETATE








(B)







Top
hexyl (2E)-2-
184
256.81
4.80
1.16E−02
2.22E+04



methyl-2-








butenoate







Top
(2RS,5SR)-6-
206
252.44
5.07
7.71E−03
3.27E+04



ethyl-2,10,10-








trimethyl-1-








oxaspiro[4.5]deca-








3,6-diene (A) +








(2RS,5RS)-6-








ethyl-2,10,10-








trimethyl-1-








oxaspiro[4.5]deca-








3,6-diene (B)







Top
(+−)-3-
148
227.83
2.34
3.89E−04
5.86E+05



PHENYLBUTANAL







Top
(3Z)-3-hexen-1-yl
196
210.68
4.22
5.17E−02
4.08E+03



(3Z)-3-hexenoate







Top
(Z)-3,7-
152
202.66
2.68
4.12E−03
4.92E+04



DIMETHYL-2,6-








OCTADIENAL








(A) + (E)-3,7-








DIMETHYL-2,6-








OCTADIENAL








(B)







Top
HEXANOIC
116
197.90
1.92
1.82E−02
1.09E+04



ACID







Top
2-METHOXY-3-
194
195.24
4.27
1.18E−07
1.65E+09



(4-








METHYLPENTYL)PYRAZINE







Top
2-METHOXY-4-
172
189.74
2.60
2.85E−02
6.66E+03



PROPYL-1-








CYCLOHEXANOL







Top
(+−)-CIS-
188
189.16
3.95
1.73E−05
1.09E+07



TETRAHYDRO-








METHYL-4-








METHYLENE-6-








PHENYL-2H-








PYRAN (A) + (+−)-








CIS-3,6-








DIHYDRO-4,6-








DIMETHYL-2-








PHENYL-2H-








PYRAN (B) + (+−)-








CIS-3,6-








DIHYDRO-2,4-








DIMETHYL-6-








PHENYL-2H-








PYRAN (C)







Top
4-PHENYL-2-
148
176.55
1.79
2.22E−04
7.95E+05



BUTANONE







Top
(3Z)-3-hexen-1-yl
182
168.78
3.96
9.92E−03
1.70E+04



(2E)-2-methyl-2-








butenoate







Top
10-undecenal (A) +
168
167.56
4.20
3.56E−04
4.71E+05



9-undecenal (B)







Top
(1R,4R)-8-
186
155.12
2.99
3.43E−05
4.52E+06



MERCAPTO-3-








P-








MENTHANONE







Top
(+−)-2-phenyl-1-
136
142.19
1.74
3.62E−02
3.93E+03



propanol







Top
(+)-(3S)-3-[(1R)-
166
134.08
3.51
1.11E−03
1.21E+05



4-methyl-3-








cyclohexen-1-








yl]butanal (A) +








(+)-(3R)-3-[(1R)-








4-methyl-3-








cyclohexen-1-








yl]butanal







Top
8-ISOPROPYL-
192
131.02
3.81
7.11E−05
1.84E+06



6-METHYL-








BICYCLO[2.2.2]








OCT-5-ENE-2-








CARBALDEHYDE







Top
5-METHYL-3-
143
128.04
2.45
8.80E−03
1.45E+04



HEPTANONE








OXIME







Top
BENZYL
164
113.60
2.35
2.81E−02
4.04E+03



PROPANOATE







Top
ETHYL
208
111.67
4.32
6.87E−05
1.63E+06



TRICYCLO[5.2.1.0.(2,6)]DECANE-








2-








CARBOXYLATE







Top
(+−)-(2E)-1-
192
110.53
3.65
1.04E−04
1.06E+06



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-2-buten-1-one







Middle
(1RS,2RS,7SR,8SR)-
162
99.95
2.53
1.23E−02
8.13E+03



tricyclo[6.2.1.0~2,7~]undec-








9-en-3-








one (A) +








(1RS,2SR,7RS,8SR)-








tricyclo[6.2.1.0~2,7~]undec-








9-en-3-








one (B)







Middle
(2E,6Z)-2,6-
140
98.76
2.68
3.22E−06
3.07E+07



NONADIEN-1-








OL







Middle
4-
135
98.47
1.56
1.81E−05
5.44E+06



METHOXYBENZALDEHYDE







Middle
4-
136
98.47
1.56
1.81E−05
5.44E+06



METHOXYBENZALDEHYDE







Middle
METHYL 2-
168
91.76
3.51
1.60E−03
5.74E+04



NONYNOATE







Middle
(4-METHYLPHENOXY)
150
89.41
1.99
6.46E−05
1.38E+06



ACETALDEHYDE







Middle
7-methyl-2H-1,5-
142
89.26
3.40
5.05E−04
1.77E+05



benzodioxepin-








3(4H)-one







Middle
(E)-3,7-
196
85.23
3.99
3.57E−02
2.39E+03



DIMETHYL-2,6-








OCTADIENYL








ACETATE (A) +








3,7-DIMETHYL-








6-OCTENYL








ACETATE (B)







Middle
GERANYL
196
85.23
3.99
3.57E−02
2.39E+03



ACETATE (A) +








NERYL








ACETATE (B)







Middle
(E)-3,7-
196
79.23
3.99
3.57E−02
2.22E+03



DIMETHYL-2,6-








OCTADIENYL








ACETATE







Middle
3,7-DIMETHYL-
163
78.89
3.17
3.10E−04
2.55E+05



2,6-








NONADIENENITRILE








(A) + 3,7-








DIMETHYL-3,6-








NONADIENENITRILE








(B)







Middle
ALLYL 3-
196
75.80
4.51
7.96E−03
9.53E+03



CYCLOHEXYLPROPANOATE







Middle
(+−)-4-methylene-
174
70.50
3.33
6.64E−06
1.06E+07



2-








phenyltetrahydro-








2H-pyran (A) +








(+−)-4-methyl-6-








phenyl-3,6-








dihydro-2H-pyran








(B) + (+−)-4-








methyl-2-phenyl-








3,6-dihydro-2H-








pyran (C)







Middle
(+−)-(3E)-4-
192
68.11
4.06
5.30E−04
1.29E+05



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-3-buten-2-one







Middle
(+−)-(E)-4-
170
64.15
3.63
6.78E−04
9.46E+04



METHYL-3-








DECEN-5-OL







Middle
6(8)-
171
60.10
3.44
1.24E−04
4.84E+05



ISOPROPYLQUINOLINE







Middle
1-PHENYL-2-(1-
208
59.63
3.58
1.52E−03
3.93E+04



PROPOXYETHOXY)ETHANE







Middle
(+−)-1,3-
220
50.65
3.02
1.06E−02
4.77E+03



DIMETHYL-3-








PHENYLBUTYL








ACETATE







Middle
1-(4-
150
50.21
1.76
1.41E−04
3.57E+05



METHOXYPHENYL)-








1-








ETHANONE″







Bottom
(+−)-
208
48.90
5.24
8.15E−04
6.00E+04



(1S,4aR,8S,8aR)-








2,2,6,8-








tetramethyl-








1,2,3,4,4a,5,8,8a-








octahydro-1-








naphthalenol







Bottom
1-(3,3-dimethyl-
192
47.01
3.89
1.64E−06
2.87E+07



1-cyclohexen-1-








yl)-4-penten-1-








one (A) + 1-(5,5-








dimethyl-1-








cyclohexen-1-yl)-








4-penten-1-one








(B)







Bottom
ALLYL
198
47.01
2.62
4.66E−05
1.01E+06



(CYCLOHEXYLOXY)ACETATE







Bottom
1-(5,5-dimethyl-
192
38.43
3.89
1.64E−06
2.34E+07



1-cyclohexen-1-








yl)-4-penten-1-








one







Bottom
ethyl (2E,4Z)-2,4-
196
36.76
4.69
3.07E−04
1.20E+05



decadienoate







Bottom
(+−)-3,4′-
204
36.76
4.58
9.93E−04
3.70E+04



dimethylspiro[oxirane-








2,9′-








tricyclo[6.2.1.0~2,7~]undec[4]ene







Bottom
(−)-(S)-1,8-P-
152
33.78
2.68
2.07E−02
1.63E+03



MENTHADIEN-








7-OL







Bottom
7-methyl-2H-1,5-
190
32.27
3.53
6.05E−05
5.33E+05



benzodioxepin-








3(4H)-one







Bottom
1-DECANOL
158
31.90
4.10
1.13E−02
2.83E+03


Bottom
2-BENZYL-
220
29.99
3.39
5.26E−02
5.70E+02



4,4,6-








TRIMETHYL-








1,3-DIOXANE







Bottom
ETHYL (2E)-
194
25.34
4.25
1.49E−02
1.70E+03



2,4,7-








DECATRIENOATE







Bottom
(2S,5R)-5-
169
22.29
2.81
5.52E−05
4.04E+05



methyl-2-(2-








propanyl)cyclohexanone








oxime







Bottom
(+−)-3-(4-
178
18.99
2.80
9.79E−03
1.94E+03



methoxyphenyl)-








2-methylpropanal







Bottom
(+−)-3-(3-
194
14.74
2.01
7.71E−04
1.91E+04



ISOPROPYL-1-








PHENYL)BUTANAL







Bottom
(1RS,2SR,8RS)-
236
11.75
5.51
1.51E−01
7.78E+01



2-(8-








ISOPROPYL-6-








METHYL-








BICYCLO[2.2.2]








OCT-5-EN-2-








YL)-1,3-








DIOXOLANE







Bottom
(3Z)-3-hexen-1-yl
204
11.05
4.21
4.37E−02
2.53E+02



benzoate







Bottom
2-phenoxyethyl
208
10.05
2.82
3.01E−02
3.34E+02



2-








methylpropanoate







Bottom
ALLYL
192
9.94
2.04
1.22E−03
8.13E+03



PHENOXYACETATE







Bottom
(+−)-8-sec-
185
8.73
4.06
1.93E−04
4.53E+04



butylquinoline








(A) + (+−)-6-sec-








butylquinoline








(B)







Bottom
diethyl cis-1,4-
228
8.51
2.65
2.87E−03
2.97E+03



cyclohexanedicarboxylate








(A) +








diethyl trans-1,4-








cyclohexanedicarboxylate








(B)







Bottom
(Z)-6-NONEN-1-
202
6.91
3.44
6.10E−04
1.13E+04



OL







Bottom
7-PROPYL-
206
4.85
2.79
6.43E−05
7.54E+04



2H,4H-1,5-








BENZODIOXEPIN-








3-ONE







Bottom
7-(2-methyl-2-
220
4.37
2.97
1.53E−04
2.85E+04



propanyl)-2H-








1,5-








benzodioxepin-








3(4H)-one







Bottom
(3Z)-3-hexen-1-yl
220
4.34
4.83
3.23E−04
1.34E+04



salicylate







Bottom
2-(3-
197
3.83
2.87
1.29E−06
2.98E+06



PHENYLPROPYL)PYRIDINE







Bottom
HEXYL 2-
222
3.82
5.55
5.50E−03
6.95E+02



HYDROXYBENZOATE







Bottom
(+−)-(1E)-1-
232
3.01
4.86
7.14E−03
4.22E+02



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1,6-heptadien-








3-one (A) + (1E)-








1-(2,6,6-








trimethyl-1-








cyclohexen-1-yl)-








1,6-heptadien-3-








one (B)







Bottom
(2E)-2-
216
1.15
4.86
1.91E−03
6.01E+02



benzylideneoctanal







Bottom
CYCLOHEXYLIDENE(PHENYL)
197
0.96
3.24
3.31E−04
2.88E+03



ACETONITRILE
















TABLE 6







Perfuming Compounds Having a Fruity Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















TOP
ETHYL
88
404705.61
0.80
7.26E−01
5.58E+05



ACETATE







TOP
ETHYL
116
142519.74
2.03
3.68E−04
3.87E+08



BUTANOATE







TOP
ETHYL
116
132964.09
2.03
1.14E−04
1.17E+09



ISOBUTYRATE







TOP
BUTYL
116
117207.52
2.11
4.18E−01
2.80E+05



ACETATE







TOP
(+−)-ethyl 2-
130
83769.16
2.58
1.26E−04
6.67E+08



methylbutanoate







TOP
(+−)-ISOPROPYL
144
51367.63
2.85
8.42E−03
6.10E+06



2-








METHYLBUTANOATE







TOP
3-
130
51307.81
2.65
5.92E−02
8.67E+05



METHYLBUTYL








ACETATE (A) +








(+−)-2-








METHYLBUTYL








ACETATE (B)







TOP
(+−)-ETHYL 2-
144
35090.18
3.05
3.84E−05
9.14E+08



METHYLPENTANOATE







TOP
(2E)-2-
98
33708.26
1.62
2.53E−03
1.33E+07



HEXENAL







TOP
3-methyl-2-buten-
128
27705.98
2.19
5.58E−02
4.97E+05



1-yl acetate







TOP
2-HEPTANONE
114
26409.73
2.09
5.85E−02
4.52E+05


TOP
METHYL
130
23345.90
2.65
8.43E−02
2.77E+05



HEXANOATE







TOP
7-METHYL-3-
136
15094.56
5.33
4.12E−02
3.66E+05



METHYLENE-








1,6-OCTADIENE







TOP
5-METHYL-3-
128
14141.42
2.43
9.87E−02
1.43E+05



HEPTANONE







TOP
(+)-LIMONENE
136
10216.93
5.40
1.29E−01
7.92E+04


TOP
(+−)-4-methyl-4-
170
9902.98
3.57
2.26E−01
4.39E+04



penten-2-yl 2-








methylpropanoate







TOP
(Z)-3-HEXENYL
128
9873.53
2.17
2.11E−03
4.68E+06



FORMATE







TOP
ETHYL
144
9675.10
3.12
9.11E−04
1.06E+07



HEXANOATE







TOP
ETHYL
145
9675.10
3.12
9.11E−04
1.06E+07



HEXANOATE







TOP
3-OCTANONE
128
6787.60
2.56
4.53E−02
1.50E+05


TOP
(+−)-methyl 2-
158
6677.64
3.37
1.74E−01
3.84E+04



ethylhexanoate







TOP
2-OCTANONE
128
6639.71
2.60
5.37E−02
1.24E+05


TOP
(1R,5R)-4,7,7-
168
6351.47
4.48
7.99E−05
7.95E+07



trimethyl-6-








thiabicyclo[3.2.1]








oct-3-ene (A) +








(1R,4R,5R)-4,7,7-








trimethyl-6-








thiabicyclo[3.2.1]








octane (B)







TOP
(1R,5R)-4,7,7-
167
6351.47
4.48
7.99E−05
7.95E+07



trimethyl-6-








thiabicyclo[3.2.1]








oct-3-ene (A) +








(1R,4R,5R)-4,7,7-








trimethyl-6-








thiabicyclo[3.2.1]








octane (B)







TOP
(1R,5R)-4,7,7-
168
6351.47
4.48
7.99E−05
7.95E+07



trimethyl-6-








thiabicyclo[3.2.1]








oct-3-ene (A) +








(1R,4R,5R)-4,7,7-








trimethyl-6-








thiabicyclo[3.2.1]








octane (B)







TOP
(E)-2-HEXENYL
142
6062.68
2.59
2.08E−01
2.92E+04



ACETATE







TOP
6-METHYL-5-
126
5775.94
2.05
1.06E−01
5.45E+04



HEPTEN-2-ONE







TOP
1-ISOBUTYL-3-
186
5265.61
4.19
1.62E+00
3.24E+03



METHYLBUTYL








ACETATE







TOP
(+−)-2,6-
154
4203.89
3.12
2.78E−01
1.51E+04



DIMETHYL-7-








OCTEN-4-ONE







TOP
(2Z)-3-methyl-2-
156
4131.05
3.11
2.73E−02
1.51E+05



hexen-1-yl








acetate (A) +








(2E)-3-methyl-2-








hexen-1-yl








acetate (B)







TOP
3,7-DIMETHYL-
136
3480.57
4.91
2.57E−02
1.35E+05



1,3,6-








OCTATRIENE







TOP
ethyl heptanoate
158
3052.89
3.58
7.17E−03
4.26E+05


TOP
ETHYL 3-
130
2885.67
0.35
5.83E−02
4.95E+04



OXOBUTANOATE








(A) <=> (2Z)-








ETHYL 3-








HYDROXY-2-








BUTENOATE








(B)







TOP
heptyl acetate
158
2814.34
3.69
1.32E−01
2.14E+04


TOP
3-
158
2611.71
3.52
2.08E−01
1.26E+04



METHYLBUTYL








BUTANOATE








(A) + 2-








METHYLBUTYL








BUTANOATE








(B)







TOP
PENTYL
158
2611.71
3.52
2.08E−01
1.26E+04



BUTANOATE








(A) + 2-








METHYLBUTYL








BUTANOATE








(B)







TOP
PENTYL
159
2611.71
3.52
2.08E−01
1.26E+04



BUTANOATE








(A) + 2-








METHYLBUTYL








BUTANOATE








(B)







TOP
(+−)-4-
100
2355.15
−0.12
6.62E−01
3.56E+03



PENTANOLIDE







TOP
HEXYL
144
2316.04
3.09
1.32E−01
1.75E+04



ACETATE







TOP
(+−)-2,6-
140
1889.68
3.15
2.11E−04
8.96E+06



DIMETHYL-5-








HEPTENAL







TOP
methyl
182
1879.01
3.63
9.00E−03
2.09E+05



(1RS,2SR)-2,6,6-








trimethyl-3-








cyclohexene-1-








carboxylate (A) +








methyl








(1RS,2RS)-2,6,6-








trimethyl-3-








cyclohexene-1-








carboxylate (B)







TOP
(3Z)-3-hexen-1-
170
1674.15
3.59
7.85E−02
2.13E+04



yl butyrate







TOP
hexyl 2-
172
1661.18
4.31
7.15E−01
2.32E+03



methylpropanoate







TOP
ethyl (2E)-2,4-
156
1618.37
3.35
9.55E−03
1.69E+05



dimethyl-2-








pentenoate







TOP
3-
102
1530.76
1.49
2.23E−04
6.87E+06



METHYLBUTANOIC








ACID







TOP
(+−)-1-PENTYL-
170
1506.95
3.79
4.84E−02
3.12E+04



2-PROPENYL








ACETATE







TOP
(3Z)-hex-3-en-1-
158
1506.33
2.97
4.58E−02
3.29E+04



yl methyl








carbonate







TOP
3,5,5-
186
1461.80
4.17
1.28E+00
1.14E+03



TRIMETHYLHEXYL








ACETATE







TOP
ETHYL
150
1285.12
2.51
1.54E−02
8.34E+04



BENZOATE







TOP
ALLYL
170
1235.24
4.16
1.75E−02
7.06E+04



HEPTANOATE







TOP
1-(3,3-
184
1129.46
4.01
2.05E−01
5.50E+03



DIMETHYL-1-








CYCLOHEXYL)








ETHYL








FORMATE







TOP
(2RS,4SR)-2-
160
1113.06
3.11
1.47E−03
7.57E+05



methyl-4-propyl-








1,3-oxathiane (A) +








(2RS,4RS)-2-








methyl-4-propyl-








1,3-oxathiane (B)







TOP
methyl
140
1091.46
2.02
2.80E−02
3.90E+04



cyclopentylideneacetate







TOP
(+−)-methyl 2,2-
182
1089.25
3.93
5.78E−04
1.88E+06



dimethyl-6-








methylidenecyclohexanecarboxylate







TOP
(Z)-3-
170
1073.97
3.57
4.54E−02
2.36E+04



HEXENYL








ISOBUTYRATE







TOP
(−)-PROPYL (S)-
202
995.16
3.17
4.98E−01
2.00E+03



2-(1,1-DIMETHYLPROPOXY)








PROPANOATE







TOP
ALLYL
156
941.49
3.62
4.58E−02
2.06E+04



HEXANOATE







TOP
(+−)-3,7-
154
896.72
2.94
8.89E−05
1.01E+07



dimethyl-1,6-








octadien-3-ol







TOP
(+−)-(Z)-3-
184
833.05
3.84
1.96E−02
4.24E+04



HEXENYL 2-








METHYLBUTANOATE







TOP
octyl acetate
172
666.51
4.29
1.76E−01
3.78E+03


TOP
(A) + (+−)-
182
659.22
3.71
7.24E−02
9.11E+03



3,5,6,6-








tetramethyl-4-








methylidene-2-








heptanone (B) +








(+−)-(4E)-








3,4,5,6,6-








pentamethyl-4-








hepten-2-one (C) +








(+−)-(3Z)-








3,4,5,6,6-








pentamethyl-3-








hepten-2-one (D) +








(+−)-(3E)-








3,4,5,6,6-








pentamethyl-3-








hepten-2-one (E)







TOP
1-METHOXY-4-
150
629.29
4.02
5.37E−04
1.17E+06



PROPYLBENZENE







TOP
(+−)-(3-methoxy-
164
587.76
3.57
1.51E−02
3.89E+04



2-








methylpropyl)benzene







TOP
2-
150
567.67
1.90
8.34E−04
6.81E+05



PHENYLETHYL








FORMATE







TOP
(+−)-2-
154
560.22
3.62
1.28E−03
4.38E+05



pentylcyclopentanone







TOP
METHYL
150
555.30
1.98
3.21E−04
1.73E+06



PHENYLACETATE







TOP
(+)-(1R)-1,7,7-
153
555.04
2.50
1.72E−01
3.23E+03



TRIMETHYL-








BICYCLO[2.2.1]








HEPTAN-








2-ONE







TOP
3-(2,2-
149
516.21
3.17
2.82E−03
1.83E+05



DIMETHYLPROPYL)PYRIDINE







TOP
benzyl acetate
150
507.38
2.04
5.24E−03
9.68E+04


TOP
2-
170
489.45
4.25
4.49E−02
1.09E+04



CYCLOHEXYL








ETHYL








ACETATE







TOP
ETHYL 2-
174
479.20
1.12
1.62E−03
2.95E+05



METHYL-1,3-








DIOXOLANE-2-








ACETATE







TOP
1-PHENYL-1-
122
470.00
1.42
2.98E−01
1.58E+03



ETHANOL







TOP
2-
200
450.33
5.13
2.41E−01
1.87E+03



METHYLPENTYL








2-








METHYLPENTANOATE







TOP
(+−)-2-
153
439.00
3.67
7.83E−02
5.61E+03



propylheptanenitrile







TOP
(+−)-3-
175
421.09
2.64
2.72E−06
1.55E+08



mercaptohexyl








acetate







TOP
(+−)-3-
176
421.09
2.64
2.72E−06
1.55E+08



mercaptohexyl








acetate







TOP
(+−)-1,5-
196
409.40
4.04
7.40E−02
5.53E+03



DIMETHYL-1-








VINYL-4-








HEXENYL








ACETATE







TOP
(1RS,2RS)-2-(2-
198
402.03
4.40
2.12E−02
1.90E+04



methyl-2-








propanyl)cyclohexyl








acetate (A) +








(1RS,2SR)-2-(2-








methyl-2-








propanyl)cyclohexyl








acetate (B)







TOP
(+−)-1-
164
387.96
2.22
4.43E−02
8.75E+03



PHENYLETHYL








ACETATE







TOP
(2RS,5SR,9RS,10SR)-
192
379.51
4.29
2.79E−02
1.36E+04



2,6,9,10-








tetramethyl-1-








oxaspiro[4.5]deca-








3,6-diene (A) +








(2RS,5RS,9SR,10RS)-








2,6,9,10-








tetramethyl-1-








oxaspiro[4.5]deca-








3,6-diene (B) +








(2RS,5RS,9RS,10SR)-








2,6,9,10-








tetramethyl-1-








oxaspiro[4.5]deca-








3,6-diene (C) +








(2RS,5SR,9SR,10RS)-








2,6,9,10-








tetramethyl-1-








oxaspiro[4.5]deca-








3,6-diene (D)







TOP
ETHYL 2,6,6-
195
368.81
3.16
4.40E−03
8.38E+04



TRIMETHYL-








1,3-








CYCLOHEXADIENE-








1-








CARBOXYLATE







TOP
(+−)-1,5-
196
339.21
4.04
7.40E−02
4.58E+03



DIMETHYL-1-








VINYL-4-








HEXENYL








ACETATE







TOP
(+−)-3,7-
184
322.28
3.79
5.28E−04
6.10E+05



dimethyl-6-octen-








1-yl formate (A) +








(2E)-3,7-








dimethyl-2,6-








octadien-1-yl








formate (B)







TOP
(+−)-ethyl 2-
184
295.22
2.15
3.64E−03
8.10E+04



acetyl-4-methyl-








4-pentenoate







TOP
cis-4-(2-methyl-
198
291.85
4.47
5.43E−02
5.37E+03



2-








propanyl)cyclohexyl








acetate (A) +








trans-4-(2-








methyl-2-








propanyl)cyclohexyl








acetate (B)







TOP
ETHYL
164
269.77
2.10
4.19E−04
6.44E+05



PHENYLACETATE







TOP
(+−)-2,2,5-
196
265.42
4.63
3.25E−02
8.16E+03



trimethyl-5-








pentylcyclopentanone







TOP
methyl (2E)-2-
170
264.84
4.05
5.84E−02
4.53E+03



nonenoate







TOP
(+−)-2,4-
176
263.73
3.02
5.04E−04
5.23E+05



dimethyl-4-








phenyltetrahydrofuran







TOP
(+−)-3,7-
184
262.84
4.16
1.72E−03
1.53E+05



DIMETHYL-6-








OCTENYL








FORMATE







TOP
ALLYL (3-
186
261.90
2.79
9.89E−05
2.65E+06



METHYLBUTOXY)ACETATE








(A) + (+−)-








ALLYL (2-








METHYLBUTOXY)ACETATE








(B)







TOP
hexyl (2E)-2-
184
256.81
4.80
1.16E−02
2.22E+04



methyl-2-








butenoate







TOP
(2RS,5SR)-6-
206
252.44
5.07
7.71E−03
3.27E+04



ethyl-2,10,10-








trimethyl-1-








oxaspiro[4.5]deca-








3,6-diene (A) +








(2RS,5RS)-6-








ethyl-2,10,10-








trimethyl-1-








oxaspiro[4.5]deca-








3,6-diene (B)







TOP
cis-4-(2-methyl-
198
229.76
4.18
2.33E−02
9.87E+03



2-








propanyl)cyclohexyl








acetate (A) +








trans-4-(2-








methyl-2-








propanyl)cyclohexyl








acetate (B)







TOP
(3Z)-3-hexen-1-
196
210.68
4.22
5.17E−02
4.08E+03



yl (3Z)-3-








hexenoate







TOP
(Z)-3,7-
152
202.66
2.68
4.12E−03
4.92E+04



DIMETHYL-2,6-








OCTADIENAL








(A) + (E)-3,7-








DIMETHYL-2,6-








OCTADIENAL








(B)







TOP
2-
164
201.26
2.49
2.14E−03
9.38E+04



PHENYLETHYL








ACETATE







TOP
1,1-DIMETHYL-
192
198.02
3.45
5.16E−02
3.84E+03



2-








PHENYLETHYL








ACETATE







TOP
1-methoxy-4-
148
184.60
3.58
1.23E−03
1.51E+05



[(1E)-1-propen-1-








yl]benzene







TOP
4-PHENYL-2-
148
176.55
1.79
2.22E−04
7.95E+05



BUTANONE







TOP
4-
178
167.81
3.03
1.66E−05
1.01E+07



METHYLPHENYL








ISOBUTYRATE







TOP
2-
122
159.75
1.41
1.02E−04
1.56E+06



PHENYLETHANOL







TOP
(1R,4R)-8-
186
155.12
2.99
3.43E−05
4.52E+06



MERCAPTO-3-








P-








MENTHANONE







TOP
(+−)-(E)-1-(2,2-
192
152.99
4.11
3.73E−03
4.10E+04



DIMETHYL-6-








METHYLENE-1-








CYCLOHEXYL)-








2-BUTEN-1-








ONE







TOP
(2E)-1-
192
143.53
4.13
1.70E−05
8.44E+06



[(1RS,2SR)-








2,6,6-trimethyl-3-








cyclohexen-1-yl]-








2-buten-1-one







TOP
[2-(1-
270
136.67
2.96
1.59E−03
8.59E+04



ETHOXYETHOXY)ETHYL]








BENZENE (A) +








1,1-BIS(2-








PHENYLETHOXY)ETHANE








(B)







TOP
3,7-DIMETHYL-
198
128.72
4.22
2.75E−02
4.68E+03



6-OCTENYL








ACETATE







TOP
5-METHYL-3-
143
128.04
2.45
8.80E−03
1.45E+04



HEPTANONE








OXIME







TOP
(2Z)-3,7-
196
123.21
3.81
6.02E−02
2.05E+03



dimethyl-2,6-








octadien-1-yl








acetate







TOP
(2E)-1-(2,6,6-
190
119.10
3.27
1.68E−05
7.09E+06



trimethyl-1,3-








cyclohexadien-1-








yl)-2-buten-1-one







TOP
2,4,6-
206
113.83
2.90
7.82E−03
1.46E+04



TRIMETHYL-4-








PHENYL-1,3-








DIOXANE







TOP
BENZYL
164
113.60
2.35
2.81E−02
4.04E+03



PROPANOATE







TOP
(+−)-(2E)-1-
192
113.31
3.65
1.04E−04
1.09E+06



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-2-buten-1-one







TOP
ETHYL
208
111.67
4.32
6.87E−05
1.63E+06



TRICYCLO[5.2.1.0.(2,6)]








DECANE-2-








CARBOXYLATE







TOP
(+−)-(2E)-1-
192
110.53
3.65
1.04E−04
1.06E+06



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-2-buten-1-one







TOP
3-
192
110.11
4.31
1.38E−02
7.96E+03



METHYLBUTYL








2-








PHENYLETHYL








ETHER







TOP
(+−)-4-
142
108.41
1.80
2.32E−05
4.67E+06



OCTANOLIDE







TOP
HEXYL
200
105.52
5.56
9.98E−02
1.06E+03



HEXANOATE







Middle
(2RS,4SR)-4-
176
99.84
3.47
1.04E−03
9.61E+04



methyl-2-








phenyltetrahydro-








2H-pyran (A) +








(2RS,4RS)-4-








methyl-2-








phenyltetrahydro-








2H-pyran (B)







Middle
tricyclo[5.2.1.0~2,6~]dec-
192
96.53
3.73
7.19E−04
1.34E+05



3-en-8-yl








acetate (A) +








tricyclo[5.2.1.0~2,6~]dec-








4-en-8-yl








acetate (B)







Middle
3-HYDROXY-2-
126
92.42
0.11
4.17E−04
2.22E+05



METHYL-4(4H)-








PYRANONE







Middle
(2E)-1-(2,6,6-
190
91.38
3.33
3.00E−06
3.04E+07



trimethyl-1,3-








cyclohexadien-1-








yl)-2-buten-1-one







Middle
(E)-3,7-
196
85.23
3.99
3.57E−02
2.39E+03



DIMETHYL-2,6-








OCTADIENYL








ACETATE (A) +








3,7-DIMETHYL-








6-OCTENYL








ACETATE (B)







Middle
GERANYL
196
85.23
3.99
3.57E−02
2.39E+03



ACETATE (A) +








NERYL








ACETATE (B)







Middle
(E)-3,7-
196
85.23
3.99
3.57E−02
2.39E+03



DIMETHYL-2,6-








OCTADIENYL








ACETATE







Middle
(2E)-1-(2,6,6-
192
81.66
3.63
2.18E−04
3.75E+05



trimethyl-1-








cyclohexen-1-yl)-








2-buten-1-one







Middle
4-
170
79.34
3.93
2.83E−02
2.81E+03



CYCLOHEXYL-








2-METHYL-2-








BUTANOL







Middle
(E)-3,7-
196
79.23
3.99
3.57E−02
2.22E+03



DIMETHYL-2,6-








OCTADIENYL








ACETATE







Middle
ALLYL 3-
196
75.80
4.51
7.96E−03
9.53E+03



CYCLOHEXYLPROPANOATE







Middle
2-
206
71.44
3.69
3.85E−02
1.86E+03



PHENYLETHYL








PIVALATE







Middle
2-
192
67.38
3.16
6.70E−03
1.01E+04



PHENYLETHYL








ISOBUTYRATE







Middle
(+−)-(E)-4-
170
64.15
3.63
6.78E−04
9.46E+04



METHYL-3-








DECEN-5-OL







Middle
(+−)-(3E)-4-
192
64.00
4.22
5.08E−04
1.26E+05



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-3-buten-2-one








(A) + (3E)-4-








(2,6,6-trimethyl-








1-cyclohexen-1-








yl)-3-buten-2-one








(B);







Middle
BENZYL 3-
192
63.56
3.45
7.31E−03
8.70E+03



METHYLBUTANOATE







Middle
METHYL (E)-3-
162
61.65
2.56
3.13E−03
1.97E+04



PHENYL-2-








PROPENOATE







Middle
(+−)-6-
142
57.43
1.47
2.17E−04
2.65E+05



propyltetrahydro-








2H-pyran-2-one







Middle
(+−)-1,3-
220
50.65
3.02
1.06E−02
4.77E+03



DIMETHYL-3-








PHENYLBUTYL








ACETATE







Bottom
(+−)-
208
48.90
5.24
8.15E−04
6.00E+04



(1S,4aR,8S,8aR)-








2,2,6,8-








tetramethyl-








1,2,3,4,4a,5,8,8a-








octahydro-1-








naphthalenol







Bottom
2-ETHYL-3-
141
48.86
0.76
6.45E−05
7.57E+05



HYDROXY-








4(4H)-








PYRANONE







Bottom
ALLYL
198
47.01
2.62
4.66E−05
1.01E+06



(CYCLOHEXYL








OXY)ACETATE







Bottom
1-(3,3-dimethyl-
192
47.01
3.89
1.64E−06
2.87E+07



1-cyclohexen-1-








yl)-4-penten-1-








one (A) + 1-(5,5-








dimethyl-1-








cyclohexen-1-yl)-








4-penten-1-one








(B)







Bottom
1-(5,5-dimethyl-
192
38.43
3.89
1.64E−06
2.34E+07



1-cyclohexen-1-








yl)-4-penten-1-








one







Bottom
(+−)-2-
206
37.73
3.64
8.56E−03
4.41E+03



PHENYLETHYL








2-








METHYLBUTANOATE







Bottom
ethyl (2E,4Z)-2,4-
196
36.76
4.69
3.07E−04
1.20E+05



decadienoate







Bottom
(+−)-3,4′-
204
36.76
4.58
9.93E−04
3.70E+04



dimethylspiro[oxirane-








2,9′-








tricyclo[6.2.1.0~2,7~]undec[4]ene







Bottom
(+−)-(3E)-3-
206
36.33
4.83
1.92E−04
1.89E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
(+−)-(E)-3-
206
36.33
4.83
1.92E−04
1.89E+05



METHYL-4-








(2,6,6-








TRIMETHYL-2-








CYCLOHEXEN-








1-YL)-3-BUTEN-








2-ONE







Bottom
TRICYCLO[5.2.1.0(2,6)]DEC-3-
206
35.82
4.38
2.44E−04
1.47E+05



EN-8-YL








PROPANOATE








(A) +








TRICYCLO[5.2.1.0(2,6)]DEC-4-








EN-8-YL








PROPANOATE








(B)







Bottom
1,1-DIMETHYL-
220
34.65
4.42
2.68E−02
1.29E+03



2-








PHENYLETHYL








BUTANOATE







Bottom
(+−)-(3E)-3-
206
34.44
4.28
1.70E−04
2.03E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
BENZYL (E)-2-
190
33.88
3.32
3.07E−04
1.11E+05



METHYL-2-








BUTENOATE







Bottom
(+−)-4-
156
27.42
2.45
1.45E−04
1.89E+05



NONANOLIDE







Bottom
(1RS,2RS,6RS,7RS,8SR)-
220
26.90
4.79
2.26E−03
1.19E+04



tricyclo[5.2.1.0~2,6~]








dec-4-en-8-yl








2-








methylpropanoate








(A) +








(1RS,2SR,6RS,7RS,8SR)-








tricyclo[5.2.1.0~2,6~]








dec-3-en-8-yl








2-








methylpropanoate








(B)







Bottom
9-DECEN-1-OL
156
26.88
3.70
8.92E−03
3.01E+03


Bottom
ETHYL (2E)-
194
25.34
4.25
1.49E−02
1.70E+03



2,4,7-








DECATRIENOATE







Bottom
5-
156
23.87
1.82
1.16E−05
2.06E+06



NONANOLIDE







Bottom
(+−)-(E)-TRANS-
206
22.11
4.05
9.26E−04
2.39E+04



alpha-IRONE (A) +








(+−)-(E)-CIS-








alpha-IRONE (B) +








(+−)-(E)-beta-








IRONE (C)







Bottom
(+−)-TRANS-3-
170
21.05
2.59
8.33E−04
2.53E+04



METHYL-4-








NONANOLIDE







Bottom
ETHYL (E)-3-
176
20.55
3.00
2.38E−05
8.62E+05



PHENYL-2-








PROPENOATE







Bottom
(E)-3-PHENYL-
176
20.47
2.52
1.87E−04
1.10E+05



2-PROPENYL








ACETATE







Bottom
4-
180
17.59
2.18
9.24E−05
1.90E+05



METHOXYBENZYL








ACETATE







Bottom
1,5,9-
238
14.74
5.28
3.28E−04
4.49E+04



TRIMETHYL-








4,8-








DECADIENYL








ACETATE







Bottom
ETHYL 2,3-
206
12.97
2.30
2.28E−05
5.68E+05



EPDXY-3-








PHENYLBUTANOATE







Bottom
(+−)-2,2,2-
268
11.96
3.20
1.15E−03
1.04E+04



TRICHLORO-1-








PHENYLETHYL








ACETATE







Bottom
(3Z)-3-hexen-1-yl
204
11.05
4.21
4.37E−02
2.53E+02



benzoate







Bottom
(+−)-4-
170
10.49
3.02
1.61E−04
6.51E+04



DECANOLIDE







Bottom
2-phenoxyethyl
208
10.05
2.82
3.01E−02
3.34E+02



2-








methylpropanoate







Bottom
ALLYL
192
9.94
2.04
1.22E−03
8.13E+03



PHENOXYACETATE







Bottom
(+−)-6-
170
9.61
2.22
3.72E−05
2.58E+05



pentyltetrahydro-








2H-pyran-2-one







Bottom
diethyl cis-1,4-
228
8.51
2.65
2.87E−03
2.97E+03



cyclohexanedicarboxylate








(A) +








diethyl trans-1,4-








cyclohexanedicarboxylate








(B)







Bottom
(E)-3-PHENYL-
190
8.14
3.09
1.28E−04
6.35E+04



2-PROPENYL








PROPANOATE







Bottom
(+−)-(E)-8-
168
6.89
2.70
5.14E−04
1.34E+04



DECEN-5-








OLIDE (A) + (+−)-








(Z)-8-DECEN-








5-OLIDE (B)







Bottom
8(9)-METHOXY-
193
5.87
5.00
4.02E−05
1.46E+05



TRICYCLO[5.2.1.0(2,6)]








DECANE-3(4)-








CARBALDEHYDE







Bottom
4-(4-
178
5.58
2.06
5.88E−06
9.49E+05



METHOXYPHENYL)-








2-








BUTANONE







Bottom
6-
184
4.64
3.00
5.85E−05
7.93E+04



hexyltetrahydro-








2H-pyran-2-one







Bottom
(+)-(1S,1′R)-2-[1-
284
4.39
5.46
3.69E−04
1.19E+04



(3′,3′-








DIMETHYL-1′-








CYCLOHEXYL)ETHOXY]-








2-








METHYLPROPYL








PROPANOATE







Bottom
(+)-
218
4.14
4.39
6.32E−04
6.54E+03



(1S,2S,3S,5R)-








2,6,6-








trimethylspiro[bicyclo[3.1.1]








heptane-3,1′-








cyclohexane]-2′-








en-4′-one







Bottom
HEXYL 2-
222
3.82
5.55
5.50E−03
6.95E+02



HYDROXYBENZOATE







Bottom
(+−)-5-
184
3.67
3.32
3.16E−05
1.16E+05



heptyldihydro-








2(3H)-furanone







Bottom
(+−)-(1E)-1-
232
3.01
4.86
7.14E−03
4.22E+02



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1,6-heptadien-








3-one (A) + (1E)-








1-(2,6,6-








trimethyl-1-








cyclohexen-1-yl)-








1,6-heptadien-3-








one (B)







Bottom
9-
192
2.10
2.29
1.42E−04
1.48E+04



ETHYLIDENE-








3-








OXATRICYCLO[6.2.1.0(2,7)








UNDECAN-








4-ONE








(A) + 10-








ETHYLIDENE-








3-








OXATRICYCLO[6.2.1.0(2,7)] . . .








(B)







Bottom
(1′R)-2-[2-(4′-
220
2.05
5.19
1.66E−04
1.24E+04



METHYL-3′-








CYCLOHEXEN-








1′-








YL)PROPYL]CYCLOPENTANONE







Bottom
(E)-2-
206
1.85
2.56
4.08E−07
4.54E+06



METHOXY-4-(1-








PROPENYL)PHENYL








ACETATE







Bottom
(+−)-4,6,6,7,8,8-
258
1.59
6.57
2.62E−04
6.08E+03



hexamethyl-








1,3,4,6,7,8-








hexahydrocyclopenta[g]isochromene







Bottom
methyl
224
1.59
2.33
5.56E−03
2.86E+02



{(1RS,2RS)-3-








oxo-2-[(2Z)-2-








penten-1-








yl]cyclopentyl}acetate







Bottom
(+−)-5-
198
1.44
3.82
2.85E−05
5.05E+04



octyldihydro-








2(3H)-furanone







Bottom
(2E)-2-
216
1.15
4.86
1.91E−03
6.01E+02



benzylideneoctanal







Bottom
4-formyl-2-
222
1.01
1.90
7.33E−05
1.38E+04



methoxyphenyl 2-








methylpropanoate







Bottom
(+−)-6-
198
0.90
3.42
1.27E−04
7.06E+03



heptyltetrahydro-








2H-pyran-2-one







Bottom
BENZYL
212
0.85
3.64
3.67E−02
2.31E+01



BENZOATE







Bottom
BENZYL
213
0.85
3.64
3.67E−02
2.31E+01



BENZOATE







Bottom
(10E)-
252
0.74
6.15
4.77E−04
1.55E+03



oxacycloheptadec-








10-en-2-one







Bottom
(E)-2-PENTYL-
202
0.68
4.30
3.64E−04
1.87E+03



3-PHENYL-2-








PROPENAL







Bottom
4-(4-HYDROXY-
164
0.36
0.93
2.05E−07
1.75E+06



1-PHENYL)-2-








BUTANONE







Bottom
2-
240
0.20
3.59
9.08E−04
2.24E+02



PHENYLETHYL








PHENYLACETATE
















TABLE 7







Perfuming Compounds Having a Citrus Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















Top
hexanal
100
68294.85
2.00
1.76E−03
3.88E+07


Top
(+−)-ISOPROPYL
144
51367.63
2.85
8.42E−03
6.10E+06



2-








METHYLBUTANOATE







Top
(2E)-2-
98
33708.26
1.62
2.53E−03
1.33E+07



HEXENAL







Top
(+)-LIMONENE
136
10216.93
5.40
1.29E−01
7.92E+04


Top
1-methyl-4-(2-
136
4298.67
5.87
1.16E−01
3.70E+04



propanyl)-1,4-








cyclohexadiene







Top
(+−)-2,6-
154
4203.89
3.12
2.78E−01
1.51E+04



DIMETHYL-7-








OCTEN-4-ONE







Top
heptyl acetate
158
2814.34
3.69
1.32E−01
2.14E+04


Top
nonanal
142
2777.63
3.42
8.14E−03
3.41E+05


Top
(+−)-4-
100
2355.15
−0.12
6.62E−01
3.56E+03



PENTANOLIDE







Top
1-(3,3-
184
1129.46
4.01
2.05E−01
5.50E+03



DIMETHYL-1-








CYCLOHEXYL)








ETHYL








FORMATE







Top
(−)-PROPYL (S)-
202
995.16
3.17
4.98E−01
2.00E+03



2-(1,1-








DIMETHYLPROPOXY)








PROPANOATE







Top
(3Z)-1,3-
148
990.87
5.11
3.32E−03
2.98E+05



undecadien-5-yne








(A) + (3E)-1,3-








undecadien-5-yne








(B)







Top
(+−)-3,7-
154
896.72
2.94
8.89E−05
1.01E+07



dimethyl-1,6-








octadien-3-ol







Top
(+−)-3,7-
154
896.72
2.94
8.89E−05
1.01E+07



dimethyl-1,6-








octadien-3-ol







Top
(+−)-3,7-
154
896.72
2.94
8.89E−05
1.01E+07



dimethyl-1,6-








octadien-3-ol







Top
(E)-4-DECENAL
154
691.34
3.73
7.59E−05
9.11E+06


Top
octyl acetate
172
666.51
4.29
1.76E−01
3.78E+03


Top
(A) + (+−)-
182
659.22
3.71
7.24E−02
9.11E+03



3,5,6,6-








tetramethyl-4-








methylidene-2-








heptanone (B) +








(+−)-(4E)-








3,4,5,6,6-








pentamethyl-4-








hepten-2-one (C) +








(+−)-(3Z)-








3,4,5,6,6-








pentamethyl-3-








hepten-2-one (D) +








(+−)-(3E)-








3,4,5,6,6-








pentamethyl-3-








hepten-2-one (E)







Top
(+−)-(3-methoxy-
164
587.76
3.57
1.51E−02
3.89E+04



2-








methylpropyl)benzene







Top
2-
150
567.67
1.90
8.34E−04
6.81E+05



PHENYLETHYL








FORMATE







Top
(+−)-2-
153
439.00
3.67
7.83E−02
5.61E+03



propylheptanenitrile







Top
(+−)-1,5-
196
409.40
4.04
7.40E−02
5.53E+03



DIMETHYL-1-








VINYL-4-








HEXENYL








ACETATE







Top
(+−)-1-
164
387.96
2.22
4.43E−02
8.75E+03



PHENYLETHYL








ACETATE







Top
(+−)-1,5-
196
339.21
4.04
7.40E−02
4.58E+03



DIMETHYL-1-








VINYL-4-








HEXENYL








ACETATE







Top
cis-4-(2-methyl-
198
291.85
4.47
5.43E−02
5.37E+03



2-








propanyl)cyclohexyl








acetate (A) +








trans-4-(2-








methyl-2-








propanyl)cyclohexyl








acetate (B)







Top
(Z)-3,7-
168
283.43
3.54
1.38E−03
2.05E+05



DIMETHYL-1,6-








NONADIEN-3-








OL (A) + (E)-3,7-








DIMETHYL-1,6-








NONADIEN-3-








OL (B)







Top
ALLYL (3-
186
261.90
2.79
9.89E−05
2.65E+06



METHYLBUTOXY)








ACETATE








(A) + (+−)-








ALLYL (2-








METHYLBUTOXY)








ACETATE








(B)







Top
(Z)-3,7-
152
202.66
2.68
4.12E−03
4.92E+04



DIMETHYL-2,6-








OCTADIENAL








(A) + (E)-3,7-








DIMETHYL-2,6-








OCTADIENAL








(B)







Middle
(2RS,4SR)-4-
176
99.84
3.47
1.04E−03
9.61E+04



methyl-2-








phenyltetrahydro-








2H-pyran (A) +








(2RS,4RS)-4-








methyl-2-








phenyltetrahydro-








2H-pyran (B)







Middle
tricyclo[5.2.1.0~2,6~]
192
96.53
3.73
7.19E−04
1.34E+05



dec-3-en-8-yl








acetate (A) +








tricyclo[5.2.1.0~2,6~]








dec-4-en-8-yl








acetate (B)







Middle
3,7-DIMETHYL-
154
89.88
2.97
7.69E−04
1.17E+05



2,6-OCTADIEN-








1-OL







Middle
(E)-3,7-
154
89.88
2.97
7.69E−04
1.17E+05



DIMETHYL-2,6-








OCTADIEN-1-








OL







Middle
CITRONELLOL
154
89.88
2.97
7.69E−04
1.17E+05



(A) +








GERANIOL (B)







Middle
(E)-3,7-
154
89.88
2.97
7.69E−04
1.17E+05



DIMETHYL-2,6-








OCTADIEN-1-








OL







Middle
(Z)-3,7-
154
86.02
2.91
1.56E−02
5.51E+03



DIMETHYL-2,6-








OCTADIEN-1-








OL







Middle
4-
170
79.34
3.93
2.83E−02
2.81E+03



CYCLOHEXYL-








2-METHYL-2-








BUTANOL







Middle
(+−)-3,7-
158
76.57
4.24
4.59E−02
1.67E+03



DIMETHYL-1-








OCTANOL







Middle
3,7-DIMETHYL-
154
67.92
2.97
7.69E−04
8.83E+04



2,6-OCTADIEN-








1-OL







Middle
(+−)-6-
142
57.43
1.47
2.17E−04
2.65E+05



propyltetrahydro-








2H-pyran-2-one







Bottom
(+−)-(3E)-3-
206
36.33
4.83
1.92E−04
1.89E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
TRICYCLO[5.2.1.0(2,6)]
206
35.82
4.38
2.44E−04
1.47E+05



DEC-3-








EN-8-YL








PROPANOATE








(A) +








TRICYCLO[5.2.1.0(2,6)]








DEC-4-








EN-8-YL








PROPANOATE








(B)







Bottom
(+−)-(3E)-3-
206
34.44
4.28
1.70E−04
2.03E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
9-DECEN-1-OL
156
26.88
3.70
8.92E−03
3.01E+03


Bottom
2-
172
22.67
3.82
3.57E−03
6.35E+03



ETHOXYNAPHTHALENE







Bottom
3-(3,3-dimethyl-
181
13.68
4.63
4.00E−03
3.42E+03



2,3-dihydro-1H-








inden-5-








yl)propanal (A) +








3-(1,1-dimethyl-








2,3-dihydro-1H-








inden-4-








yl)propanal (B) +








3-(1,1-dimethyl-








2,3-dihydro-1H-








inden-5-








yl)propanal (C)







Bottom
(+−)-2,2,2-
268
11.96
3.20
1.15E−03
1.04E+04



TRICHLORO-1-








PHENYLETHYL








ACETATE







Bottom
(3Z)-3-hexen-1-yl
204
11.05
4.21
4.37E−02
2.53E+02



benzoate







Bottom
8(9)-METHOXY-
193
5.87
5.00
4.02E−05
1.46E+05



TRICYCLO[5.2.1.0(2,6)]








DECANE-3(4)-








CARBALDEHYDE







Bottom
(+−)-(3,7-
198
4.70
4.33
8.95E−04
5.26E+03



DIMETHYL-6-








OCTENYLOXY)








ACETALDEHYDE







Bottom
(+−)-(3,7-
198
4.70
4.33
8.95E−04
5.26E+03



DIMETHYL-6-








OCTENYLOXY)








ACETALDEHYDE







Bottom
HEXYL 2-
222
3.82
5.55
5.50E−03
6.95E+02



HYDROXYBENZOATE







Bottom
methyl 2-
226
2.12
2.92
5.77E−04
3.67E+03



((1RS,2RS)-3-








oxo-2-








pentylcyclopentyl)acetate







Bottom
9-
192
2.10
2.29
1.42E−04
1.48E+04



ETHYLIDENE-








3-








OXATRICYCLO








[6.2.1.0(2,7)]UNDECAN-








4-ONE








(A) + 10-








ETHYLIDENE-








3-








OXATRICYCLO








[6.2.1.0(2,7)] . . . (B)







Bottom
(E)-2-
206
1.85
2.56
4.08E−07
4.54E+06



METHOXY-4-(1-








PROPENYL)PHENYL








ACETATE







Bottom
BENZYL
213
0.85
3.64
3.67E−02
2.31E+01



BENZOATE







Bottom
(10E)-
252
0.74
6.15
4.77E−04
1.55E+03



oxacycloheptadec-








10-en-2-one







Bottom
(E)-2-PENTYL-
202
0.68
4.30
3.64E−04
1.87E+03



3-PHENYL-2-








PROPENAL







Bottom
2-
240
0.20
3.59
9.08E−04
2.24E+02



PHENYLETHYL








PHENYLACETATE
















TABLE 8







Perfuming Compounds Having a Sweet Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















Top
ETHYL
88
404705.61
0.80
7.26E−01
5.58E+05



ACETATE







Top
BUTYL
116
117207.52
2.11
4.18E−01
2.80E+05



ACETATE







Top
3-
130
51307.81
2.65
5.92E−02
8.67E+05



METHYLBUTYL








ACETATE (A) +








(+−)-2-








METHYLBUTYL








ACETATE (B)







Top
(+−)-3-
88
33382.87
−1.03
1.46E−02
2.28E+06



HYDROXY-2-








BUTANONE







Top
2-
114
29677.31
1.70
1.43E−09
2.08E+13



FURANMETHANETHIOL







Top
1-BUTANOL
74
17700.00
0.88
8.70E−02
2.03E+05


Top
(+−)-4-methyl-4-
170
9902.98
3.57
2.26E−01
4.39E+04



penten-2-yl 2-








methylpropanoate







Top
ETHYL
145
9675.10
3.12
9.11E−04
1.06E+07



HEXANOATE







Top
BENZALDEHYDE
106
8207.00
1.33
4.26E−02
1.93E+05


Top
2,3,5-
122
7897.31
1.27
2.82E−04
2.80E+07



TRIMETHYLPYRAZINE







Top
5-METHYL-2-
126
5525.83
1.98
7.62E−07
7.26E+09



HEPTEN-4-ONE







Top
DIALLYL
146
5487.52
3.30
3.98E−05
1.38E+08



DISULFIDE







Top
(+−)-ETHYL 3-
158
2276.17
1.96
5.06E−04
4.50E+06



METHYL-2-








OXOPENTANOATE







Top
1-phenylethanone
120
1728.98
1.59
6.61E−03
2.62E+05


Top
ALLYL
170
1235.24
4.16
1.75E−02
7.06E+04



HEPTANOATE







Top
(+−)-4-
114
841.23
0.48
2.63E−02
3.20E+04



HEXANOLIDE







Top
(+−)-2-
154
560.22
3.62
1.28E−03
4.38E+05



pentylcyclopentanone







Top
METHYL
150
555.30
1.98
3.21E−04
1.73E+06



PHENYLACETATE







Top
2-
170
489.45
4.25
4.49E−02
1.09E+04



CYCLOHEXYL








ETHYL








ACETATE







Top
ETHYL 2-
174
479.20
1.12
1.62E−03
2.95E+05



METHYL-1,3-








DIOXOLANE-2-








ACETATE







Top
2-HYDROXY-3-
112
396.50
0.08
3.82E−04
1.04E+06



METHYL-2-








CYCLOPENTEN-








1-ONE







Top
2-METHOXY-4-
138
306.61
1.52
6.96E−04
4.41E+05



METHYLPHENOL







Top
(+−)-4-
128
295.34
1.16
5.18E−04
5.70E+05



HEPTANOLIDE







Top
hexyl (2E)-2-
184
256.81
4.80
1.16E−02
2.22E+04



methyl-2-








butenoate







Top
(3Z)-3-hexen-1-yl
196
210.68
4.22
5.17E−02
4.08E+03



(3Z)-3-hexenoate







Top
2-
164
201.26
2.49
2.14E−03
9.38E+04



PHENYLETHYL








ACETATE







Top
HEXANOIC
116
197.90
1.92
1.82E−02
1.09E+04



ACID







Top
1-methoxy-4-
148
184.60
3.58
1.23E−03
1.51E+05



[(1E)-1-propen-1-








yl]benzene







Top
2-
122
159.75
1.41
1.02E−04
1.56E+06



PHENYLETHANOL







Top
(+−)-(E)-1-(2,2-
192
152.99
4.11
3.73E−03
4.10E+04



DIMETHYL-6-








METHYLENE-1-








CYCLOHEXYL)-








2-BUTEN-1-








ONE







Top
(2E)-1-
192
143.53
4.13
1.70E−05
8.44E+06



[(1RS,2SR)-








2,6,6-trimethyl-3-








cyclohexen-1-yl]-








2-buten-1-one







Top
[2-(1-
270
136.67
2.96
1.59E−03
8.59E+04



ETHOXYETHOXY)ETHYL]








BENZENE








(A) +








1,1-BIS(2-








PHENYLETHOXY)ETHANE








(B)







Top
5-METHYL-3-
143
128.04
2.45
8.80E−03
1.45E+04



HEPTANONE








OXIME







Top
(+−)-(2E)-1-
192
110.53
3.65
1.04E−04
1.06E+06



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-2-buten-1-one







Top
3-
192
110.11
4.31
1.38E−02
7.96E+03



METHYLBUTYL








2-








PHENYLETHYL








ETHER







Middle
(+−)-2-PENTYL-
156
97.79
3.59
5.43E−03
1.80E+04



1-








CYCLOPENTANOL







Middle
(1RS,2SR)-2-
156
97.79
3.59
5.43E−03
1.80E+04



pentylcyclopentanol








(A) +








(1RS,2RS)-2-








pentylcyclopentanol








(B)







Middle
3-HYDROXY-2-
126
92.42
0.11
4.17E−04
2.22E+05



METHYL-4(4H)-








PYRANONE







Middle
ALLYL 3-
196
75.80
4.51
7.96E−03
9.53E+03



CYCLOHEXYLPROPANOATE







Middle
2-
206
71.44
3.69
3.85E−02
1.86E+03



PHENYLETHYL








PIVALATE







Middle
2-
192
67.38
3.16
6.70E−03
1.01E+04



PHENYLETHYL








ISOBUTYRATE







Middle
4-(2,6,6-
194
63.61
3.99
8.51E−03
7.48E+03



trimethyl-1-








cyclohexen-1-yl)-








2-butanone







Middle
BENZYL 3-
192
63.56
3.45
7.31E−03
8.70E+03



METHYLBUTANOATE







Middle
3-methyl-2-[(2Z)-
165
56.72
2.61
2.16E−04
2.63E+05



2-penten-1-yl]-2-








cyclopenten-1-








one







Middle
(+−)-6-METHYL-
159
52.47
1.10
2.53E−06
2.07E+07



7-OXA-1-THIA-








4-








AZASPIRO[4.4]








NONANE







Middle
2-
158
51.04
3.29
1.02E−05
5.00E+06



METHOXYNAPHTHALENE







Bottom
2-ETHYL-3-
141
48.86
0.76
6.45E−05
7.57E+05



HYDROXY-








4(4H)-








PYRANONE







Bottom
1,1-DIMETHYL-
220
34.65
4.42
2.68E−02
1.29E+03



2-








PHENYLETHYL








BUTANOATE







Bottom
5-
156
23.87
1.82
1.16E−05
2.06E+06



NONANOLIDE







Bottom
(+−)-TRANS-3-
170
21.05
2.59
8.33E−04
2.53E+04



METHYL-4-








NONANOLIDE







Bottom
2,6-
154
19.23
1.02
8.01E−06
2.40E+06



DIMETHOXYPHENOL







Bottom
(1E)-1-(2,6,6-
206
15.81
4.47
1.16E−04
1.37E+05



trimethyl-1-








cyclohexen-1-yl)-








1-penten-3-one







Bottom
3-
188
14.37
3.12
8.65E−04
1.66E+04



BUTYLIDENE-








1-








BENZO[C]FURANONE







Bottom
2-methoxy-4-
164
11.28
2.15
6.63E−06
1.70E+06



[(1E)-1-propen-1-








yl]phenol







Bottom
(+−)-4-
170
10.49
3.02
1.61E−04
6.51E+04



DECANOLIDE







Bottom
(+−)-6-
170
9.61
2.22
3.72E−05
2.58E+05



pentyltetrahydro-








2H-pyran-2-one







Bottom
2-
185
8.73
4.06
1.93E−04
4.53E+04



ISOBUTYLQUINOLINE







Bottom
diethyl cis-1,4-
228
8.51
2.65
2.87E−03
2.97E+03



cyclohexanedicarboxylate








(A) +








diethyl trans-1,4-








cyclohexanedicarboxylate








(B)







Bottom
(+−)-(E)-8-
168
6.89
2.70
5.14E−04
1.34E+04



DECEN-5-








OLIDE (A) + (+−)-








(Z)-8-DECEN-








5-OLIDE (B)







Bottom
4-(4-
178
5.58
2.06
5.88E−06
9.49E+05



METHOXYPHENYL)-








2-








BUTANONE







Bottom
6-
184
4.64
3.00
5.85E−05
7.93E+04



hexyltetrahydro-








2H-pyran-2-one







Bottom
4-hydroxy-3-
152
4.24
0.72
6.75E−06
6.28E+05



methoxybenzaldehyde







Bottom
(+−)-5-
184
3.67
3.32
3.16E−05
1.16E+05



heptyldihydro-








2(3H)-furanone







Bottom
2-(4-METHYL-
143
2.36
0.22
2.43E−04
9.71E+03



1,3-THIAZOL-5-








YL)-1-








ETHANOL







Bottom
(1′R)-2-[2-(4′-
220
2.05
5.19
1.66E−04
1.24E+04



METHYL-3′-








CYCLOHEXEN-








1′-








YL)PROPYL]








CYCLOPENTANONE







Bottom
4-formyl-2-
222
1.01
1.90
7.33E−05
1.38E+04



methoxyphenyl 2-








methylpropanoate







Bottom
(+−)-6-
198
0.90
3.42
1.27E−04
7.06E+03



heptyltetrahydro-








2H-pyran-2-one







Bottom
2-
146
0.51
1.35
1.62E−05
3.16E+04



CHROMENONE







Bottom
1,4-
256
0.46
3.83
7.05E−04
6.55E+02



dioxacyclohexadecane-








5,16-dione







Bottom
2-
240
0.20
3.59
9.08E−04
2.24E+02



PHENYLETHYL








PHENYLACETATE







Bottom
3-ethoxy-4-
166
0.11
1.27
2.10E−05
5.25E+03



hydroxybenzaldehyde
















TABLE 9







Perfuming Compounds Having a Gourmand Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















Top
BUTYL
116
117207.52
2.11
4.18E−01
2.80E+05



ACETATE







Top
3-
130
51307.81
2.65
5.92E−02
8.67E+05



METHYLBUTYL








ACETATE (A) +








(+−)-2-








METHYLBUTYL








ACETATE (B)







Top
(+−)-3-
88
33382.87
−1.03
1.46E−02
2.28E+06



HYDROXY-2-








BUTANONE







Top
1-BUTANOL
74
17700.00
0.88
8.70E−02
2.03E+05


Top
(+−)-4-methyl-4-
170
9902.98
3.57
2.26E−01
4.39E+04



penten-2-yl 2-








methylpropanoate







Top
ETHYL
145
9675.10
3.12
9.11E−04
1.06E+07



HEXANOATE







Top
DIALLYL
146
5487.52
3.30
3.98E−05
1.38E+08



DISULFIDE







Top
ALLYL
170
1235.24
4.16
1.75E−02
7.06E+04



HEPTANOATE







Top
(+−)-2-
154
560.22
3.62
1.28E−03
4.38E+05



pentylcyclopentanone







Top
METHYL
150
555.30
1.98
3.21E−04
1.73E+06



PHENYLACETATE







Top
2-
170
489.45
4.25
4.49E−02
1.09E+04



CYCLOHEXYL








ETHYL








ACETATE







Top
ETHYL 2-
174
479.20
1.12
1.62E−03
2.95E+05



METHYL-1,3-








DIOXOLANE-2-








ACETATE







Top
(3Z)-3-hexen-1-yl
196
210.68
4.22
5.17E−02
4.08E+03



(3Z)-3-hexenoate







Top
2-
164
201.26
2.49
2.14E−03
9.38E+04



PHENYLETHYL








ACETATE







Top
HEXANOIC
116
197.90
1.92
1.82E−02
1.09E+04



ACID







Top
1-methoxy-4-
148
184.60
3.58
1.23E−03
1.51E+05



[(1E)-1-propen-1-








yl]benzene







Top
2-
122
159.75
1.41
1.02E−04
1.56E+06



PHENYLETHANOL







Top
(+−)-(E)-1-(2,2-
192
152.99
4.11
3.73E−03
4.10E+04



DIMETHYL-6-








METHYLENE-1-








CYCLOHEXYL)-








2-BUTEN-1-








ONE







Top
(2E)-1-
192
143.53
4.13
1.70E−05
8.44E+06



[(1RS,2SR)-








2,6,6-trimethyl-3-








cyclohexen-1-yl]-








2-buten-1-one







Top
[2-(1-
270
136.67
2.96
1.59E−03
8.59E+04



ETHOXYETHOXY)ETHYL]








BENZENE








(A) +








1,1-BIS(2-








PHENYLETHOXY)ETHANE








(B)







Top
5-METHYL-3-
143
128.04
2.45
8.80E−03
1.45E+04



HEPTANONEOXIME







Top
3-
192
110.11
4.31
1.38E−02
7.96E+03



METHYLBUTYL








2-








PHENYLETHYL








ETHER







Top
(+−)-4-
142
108.41
1.80
2.32E−05
4.67E+06



OCTANOLIDE







Middle
(3RS,3ARS,6SR,
168
80.76
2.14
1.84E−06
4.39E+07



7ASR)-








PERHYDRO-3,6-








DIMETHYL-








BENZO[B]FURAN-








2-ONE (A) +








(3SR,3ARS,6SR,








7ASR)-








PERHYDRO-3,6-








DIMETHYL-








BENZO[B]FURAN-








2-ONE (B)







Middle
ALLYL 3-
196
75.80
4.51
7.96E−03
9.53E+03



CYCLOHEXYLPROPANOATE







Middle
(3S,3aS,6R,7aR)-
168
74.03
2.11
3.46E−05
2.14E+06



3,6-








dimethylhexahydro-








1-benzofuran-








2(3H)-one







Middle
2-
206
71.44
3.69
3.85E−02
1.86E+03



PHENYLETHYL








PIVALATE







Middle
2-
192
67.38
3.16
6.70E−03
1.01E+04



PHENYLETHYL








ISOBUTYRATE







Middle
1-
154
62.86
1.66
2.90E−04
2.17E+05



oxaspiro[4.5]decan-








2-one







Middle
benzo[d][1,3]dioxole-
150
61.82
1.52
1.01E−04
6.12E+05



5-








carbaldehyde







Middle
3-methyl-2-[(2Z)-
165
56.72
2.61
2.16E−04
2.63E+05



2-penten-1-yl]-2-








cyclopenten-1-








one







Middle
2-
158
51.04
3.29
1.02E−05
5.00E+06



METHOXYNAPHTHALENE







Bottom
1,1-DIMETHYL-
220
34.65
4.42
2.68E−02
1.29E+03



2-








PHENYLETHYL








BUTANOATE







Bottom
(+−)-4-
156
27.42
2.45
1.45E−04
1.89E+05



NONANOLIDE







Bottom
5-
156
23.87
1.82
1.16E−05
2.06E+06



NONANOLIDE







Bottom
(+−)-TRANS-3-
170
21.05
2.59
8.33E−04
2.53E+04



METHYL-4-








NONANOLIDE







Bottom
2,6-
154
19.23
1.02
8.01E−06
2.40E+06



DIMETHOXYPHENOL







Bottom
(1E)-1-(2,6,6-
206
15.81
4.47
1.16E−04
1.37E+05



trimethyl-1-








cyclohexen-1-yl)-








1-penten-3-one







Bottom
3-
188
14.37
3.12
8.65E−04
1.66E+04



BUTYLIDENE-








1-








BENZO[C]FURANONE







Bottom
2-methoxy-4-
164
11.28
2.15
6.63E−06
1.70E+06



[(1E)-1-propen-1-








yl]phenol







Bottom
(+−)-4-
170
10.49
3.02
1.61E−04
6.51E+04



DECANOLIDE







Bottom
(+−)-6-
170
9.61
2.22
3.72E−05
2.58E+05



pentyltetrahydro-








2H-pyran-2-one







Bottom
diethyl cis-1,4-
228
8.51
2.65
2.87E−03
2.97E+03



cyclohexanedicarboxylate








(A) +








diethyl trans-1,4-








cyclohexanedicarboxylate








(B)







Bottom
(+−)-(E)-8-
168
6.89
2.70
5.14E−04
1.34E+04



DECEN-5-








OLIDE (A) + (+−)-








(Z)-8-DECEN-








5-OLIDE (B)







Bottom
4-(4-
178
5.58
2.06
5.88E−06
9.49E+05



METHOXYPHENYL)-








2-








BUTANONE







Bottom
6-
184
4.64
3.00
5.85E−05
7.93E+04



hexyltetrahydro-








2H-pyran-2-one







Bottom
4-hydroxy-3-
152
4.24
0.72
6.75E−06
6.28E+05



methoxybenzaldehyde







Bottom
(+−)-5-
184
3.67
3.32
3.16E−05
1.16E+05



heptyldihydro-








2(3H)-furanone







Bottom
(1′R)-2-[2-(4′-
220
2.05
5.19
1.66E−04
1.24E+04



METHYL-3′-








CYCLOHEXEN-








1′-








YL)PROPYL]








CYCLOPENTANONE







Bottom
4-formyl-2-
222
1.01
1.90
7.33E−05
1.38E+04



methoxyphenyl 2-








methylpropanoate







Bottom
(+−)-6-
198
0.90
3.42
1.27E−04
7.06E+03



heptyltetrahydro-








2H-pyran-2-one







Bottom
2-
146
0.51
1.35
1.62E−05
3.16E+04



CHROMENONE







Bottom
2-
240
0.20
3.59
9.08E−04
2.24E+02



PHENYLETHYL








PHENYLACETATE
















TABLE 10







Perfuming Compounds Having a Woody Note

















Log P
Odor





Molecular
Volatility
(n-octanol/
Threshold
Odor


Type
Name
Weight
(μg/l air)
water)
(μg/l air)
Value
















Top
1-BUTANOL
74
17700.00
0.88
8.70E−02
2.03E+05


Top
(+−)-methyl 2-
158
6677.64
3.37
1.74E−01
3.84E+04



ethylhexanoate







Top
3-
102
1530.76
1.49
2.23E−04
6.87E+06



METHYLBUTANOIC








ACID







Top
6,6-
186
1311.32
3.90
1.26E−02
1.04E+05



DIMETHOXY-








2,5,5-








TRIMETHYL-2-








HEXENE







Top
4-(2-methyl-2-
154
755.28
2.77
1.15E−01
6.57E+03



propanyl)cyclohexanone







Top
(1R,2R)-1,7,7-
196
735.37
4.13
4.46E−02
1.65E+04



TRIMETHYL-








BICYCLO[2.2.1]








HEPT-








2-YL








ACETATE







Top
(A) + (+−)-
182
659.22
3.71
7.24E−02
9.11E+03



3,5,6,6-








tetramethyl-4-








methylidene-2-








heptanone (B) +








(+−)-(4E)-








3,4,5,6,6-








pentamethyl-4-








hepten-2-one (C) +








(+−)-(3Z)-








3,4,5,6,6-








pentamethyl-3-








hepten-2-one (D) +








(+−)-(3E)-








3,4,5,6,6-








pentamethyl-3-








hepten-2-one (E)







Top
(+−)-(3Z)-
182
659.22
3.71
7.24E−02
9.11E+03



3,4,5,6,6-








PENTAMETHYL-








3-HEPTEN-2-








ONE







Top
cis-4-(2-methyl-
198
229.76
4.18
2.33E−02
9.87E+03



2-








propanyl)cyclohexyl








acetate (A) +








trans-4-(2-








methyl-2-








propanyl)cyclohexyl








acetate (B)







Top
(1S,2S,4S)-1,7,7-
210
216.42
4.66
4.55E−02
4.76E+03



trimethylbicyclo[2.2.1]hept-








2-yl








propanoate







Top
(+−)-1-(2-TERT-
228
205.05
4.65
3.53E−02
5.81E+03



BUTYL-1-








CYCLOHEXYLOXY)-








2-








BUTANOL







Top
(+−)-ALPHA-
154
172.78
2.91
1.03E−01
1.68E+03



TERPINEOL







Top
(+−)-2-ETHOXY-
222
135.00
6.50
1.37E−01
9.83E+02



2,6,6-








TRIMETHYL-9-








METHYLENE-








BICYCLO[3.3.1]








NONANE







Top
(+−)-(2E)-1-
192
110.53
3.65
1.04E−04
1.06E+06



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-2-buten-1-one







Top
(+−)-(E)-3-
206
106.28
4.09
5.03E−05
2.11E+06



METHYL-4-








(2,6,6-








TRIMETHYL-2-








CYCLOHEXEN-








1-YL)-3-BUTEN-








2-ONE







Middle
(2E)-1-(2,6,6-
190
91.38
3.33
3.00E−06
3.04E+07



trimethyl-1,3-








cyclohexadien-1-








yl)-2-buten-1-one







Middle
(5RS,6RS)-
212
84.04
3.51
5.15E−04
1.63E+05



2,6,10,10-








TETRAMETHYL-








1-








OXASPIRO[4.5]DECAN-








6-OL







Middle
2-TERT-BUTYL-
194
82.95
4.00
1.65E−02
5.02E+03



1,4-








DIMETHOXYBENZENE







Middle
(2E)-1-(2,6,6-
192
81.66
3.63
2.18E−04
3.75E+05



trimethyl-1-








cyclohexen-1-yl)-








2-buten-1-one







Middle
(+−)-3ENDO-
208
79.45
5.73
4.82E−03
1.65E+04



METHOXY-7,7-








DIMETHYL-10-








METHYLENE-








BICYCLO[4.3.1]








DECANE








(A) +








(+−)-3EXO-








METHOXY-7,7-








DIMETHYL-10-








METHYLENE-








BICYCLO[4.3.1]








DECANE








(B)







Middle
(E)-3-PHENYL-
132
70.14
1.50
1.36E−03
5.16E+04



2-PROPENAL







Middle
(Z)-3-PHENYL-
132
70.14
1.50
1.36E−03
5.16E+04



2-PROPENAL








(A) + (E)-3-








PHENYL-2-








PROPENAL (B)







Middle
(E)-3-PHENYL-
132
70.14
1.50
1.36E−03
5.16E+04



2-PROPENAL







Middle
(E)-3-PHENYL-
129
66.00
1.98
8.97E−05
7.36E+05



2-








PROPENENITRILE







Middle
4-(2,6,6-
194
63.61
3.99
8.51E−03
7.48E+03



trimethyl-1-








cyclohexen-1-yl)-








2-butanone







Middle
(2R)-2-methyl-4-
206
63.49
4.25
2.22E−03
2.86E+04



[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-4-pentenal (A) +








(2S)-2-methyl-








4-[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-4-pentenal (B)







Middle
2-(6,6-
208
60.02
4.41
1.10E−01
5.45E+02



DIMETHYL-








BICYCLO[3.1.1]








HEPT-








2-EN-2-








YL)ETHYL








ACETATE







Middle
1,2,3,4,5,6,7,8-
192
55.09
3.65
3.91E−03
1.41E+04



OCTAHYDRO-








8,8-DIMETHYL-








2-








NAPHTHALENE








CARBALDEHYDE








(A) + (B,C,D) +








OCTAHYDRO-








5,5-DIMETHYL-








2-








NAPHTHALENE








CARBALDEHYDE







Bottom
(+−)-(3E)-3-
206
43.62
4.22
6.30E−05
6.92E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
(+−)-8-
236
42.22
7.59
2.09E−02
2.02E+03



methoxycedrane







Bottom
(+−)-(3E)-3-
206
36.33
4.83
1.92E−04
1.89E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
(+−)-7-
188
35.54
2.19
2.66E−02
1.34E+03



METHOXY-3,7-








DIMETHYL-2-








OCTANOL







Bottom
(3E)-4-(2,6,6-
192
35.41
3.88
3.58E−05
9.89E+05



trimethyl-1-








cyclohexen-1-yl)-








3-buten-2-one







Bottom
(+−)-(E)-3-
206
34.78
4.09
2.15E−04
1.62E+05



METHYL-4-








(2,6,6-








TRIMETHYL-2-








CYCLOHEXEN-








1-YL)-3-BUTEN-








2-ONE (A) + (E)-








1-(2,6,6-








TRIMETHYL-2-








CYCLOHEXEN-








1-YL)-1-








PENTEN-3-ONE








(B) + (+−)-(E)-1-








(2,2-








DIMETHYL-6-








METHYLENE-1-








CYCLOHEXYL)-








1-PENTEN-3-








ONE (C) + (E)-1-








(2,6,6-








TRIMETHYL-1-








CYCLOHEXEN-








1-YL)-1-








PENTEN-3-ONE








(D)







Bottom
(+−)-(3E)-3-
206
34.44
4.28
1.70E−04
2.03E+05



methyl-4-(2,6,6-








trimethyl-2-








cyclohexen-1-yl)-








3-buten-2-one (A) +








(+−)-(1E)-1-








(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1-penten-3-








one (B)







Bottom
BENZYL (E)-2-
190
33.88
3.32
3.07E−04
1.11E+05



METHYL-2-








BUTENOATE







Bottom
(+−)-2,4-
204
32.53
2.44
2.43E−04
1.34E+05



dimethyl-








4,4a,5,9b-








tetrahydroindeno[1,2-








d][1,3]dioxine








(ISOMER A) +








(+−)-2,4-








dimethyl-








4,4a,5,9b-








tetrahydroindeno[1,2-








d][1,3]dioxine








(ISOMER B) (A +








B)







Bottom
1,2,3,5,6,7-
207
29.81
3.65
4.57E−03
6.52E+03



HEXAHYDRO-








1,1,2,3,3-








PENTAMETHYL-








4-INDENONE







Bottom
(+−)-(6RS,10RS)-
220
22.40
5.40
5.59E−03
4.01E+03



2,2,8,10-








tetramethylspiro[5.5]undec-








8-en-1-








one (A) + (+−)-








(6RS,10SR)-








2,2,8,10-








tetramethylspiro[5.5]undec-








8-en-1-








one (B) +








(6RS,7RS)-








2,2,7,9-








tetramethylspiro[5.5]undec-








8-en-1-








one (C) +








(6RS,7SR)-








2,2,7,9-








tetramethylspiro[5.5]undec-








8-en-1-








one (D)







Bottom
(+−)-(E)-4-(2,2,C-
208
20.50
4.62
5.14E−04
3.99E+04



3,T-6-








TETRAMETHYL-








R-1-








CYCLOHEXYL)-








3-BUTEN-2-








ONE







Bottom
(+−)-(E)-4-(2,2,C-
208
20.50
4.62
5.14E−04
3.99E+04



3,T-6-








TETRAMETHYL-








R-1-








CYCLOHEXYL)-








3-BUTEN-2-








ONE (A) + (+−)-








(E)-4-(2,2,T-3,T-








6-








TETRAMETHYL-








R-1-








CYCLOHEXYL)-








3-BUTEN-2-








ONE (B)







Bottom
(E)-3-METHYL-
208
20.41
4.33
9.56E−05
2.13E+05



5-(2,2,3-








TRIMETHYL-3-








CYCLOPENTEN-








1-YL)-4-








PENTEN-2-OL







Bottom
(2R,4E)-3,3-
222
16.31
4.77
7.11E−05
2.29E+05



dimethyl-5-[(1R)-








2,2,3-trimethyl-3-








cyclopenten-1-








yl]-4-penten-2-ol








(A) + (2S,4E)-








3,3-dimethyl-5-








[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-4-penten-2-ol








(B)







Bottom
5,5,8a-
238
14.41
5.50
4.19E−04
3.44E+04



trimethyldecahydro-








2-naphthalenyl








acetate







Bottom
(2RS,4aRS,8aSR)-
238
14.41
5.50
4.19E−04
3.44E+04



5,5,8a-








trimethyldecahydro-








2-naphthalenyl








acetate







Bottom
(+−)-3,6,8,8-
222
11.83
5.39
3.38E−02
3.51E+02



tetramethyloctahydro-








1H-3a,7-








methanoazulen-6-








ol







Bottom
(+−)-1-
234
10.59
5.55
2.59E−04
4.09E+04



(OCTAHYDRO-








2,3,8,8-








TETRAME-2-








NAPHTHALEN








YL)-1-








ETHANONE








(DOUBLE








BOND: 4A,5 (A) +








4,4A (B) +








4A,8A (C)







Bottom
3aRS,5aSR,9aSR,
236
9.23
6.93
2.16E−03
4.28E+03



9bSR)-3a,6,6,9a-








tetramethyldodecahydronaphtho








[2,1-b]furan







Bottom
(1RS,6RS,11RS)-
264
8.25
6.44
3.79E−03
2.18E+03



2,2,9,11-








tetramethylspiro[5.5]undec-








8-en-1-








yl acetate







Bottom
(−)-
236
8.02
6.87
1.08E−05
7.45E+05



(3aR,5aS,9aS,9bR)-








3a,6,6,9a-








tetramethyldodecahydronaphtho








[2,1-b]furan







Bottom
(+−)-1-
234
7.59
5.24
4.24E−04
1.79E+04



(OCTAHYDRO-








2,3,8,8-








TETRAME-2-








NAPHTHALENYL)-








1-








ETHANONE








(DOUBLE








BOND: 4A,5 (A) +








4,4A (B) +








4A,8A (C)







Bottom
(+−)-(4Z,8E)-
220
7.11
4.88
7.14E−03
9.96E+02



1,5,8-trimethyl-








13-








oxabicyclo[10.1.0]trideca-








4,8-diene








(A) + (+−)-








(4Z,8E)-1,4,8-








trimethyl-13-








oxabicyclo[10.1.0]trideca-








4,8-diene








(B)







Bottom
(1S,4S,9S,10R,13R)-
278
6.77
4.59
4.36E−04
1.55E+04



5,5,9,13-








tetramethyl-








14,16-








dioxatetracyclo








[11.2.1.0~1,10~.0~4,9~]








hexadecane








(A) +








(1R,4S,9S,10R,13S)-








5,5,9,13-








tetramethyl-








14,16-








dioxatetracyclo








[11.2.1.0~1,10~.0~4,9~]








hexadecane








(B)







Bottom
(ETHOXYMETHOXY)
242
6.63
6.59
8.90E−02
7.45E+01



CYCLODODECANE







Bottom
(+−)-3-methyl-5-
210
5.22
4.68
1.52E−03
3.43E+03



(2,2,3-trimethyl-








3-cyclopenten-1-








yl)-2-pentanol







Bottom
(2S)-2-methyl-4-
208
5.04
4.43
1.70E−05
2.97E+05



[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-4-penten-1-ol








(A) + (2R)-2-








methyl-4-[(1R)-








2,2,3-trimethyl-3-








cyclopenten-1-








yl]-4-penten-1-ol








(B)







Bottom
(+−)-(1-
256
5.04
6.68
2.51E−02
2.01E+02



ethoxyethoxy)cyclododecane







Bottom
(+)-(1R,7R)-
190
4.86
3.00
2.86E−05
1.70E+05



10,10-








DIMETHYL-








TRICYCLO[7.1.1.0(2,7)]








UNDEC-2-EN-4-ONE







Bottom
(+)-
218
4.14
4.39
6.32E−04
6.54E+03



(1S,2S,3S,5R)-








2,6,6-








trimethylspiro[bicyclo[3.1.1]








heptane-3,1′-








cyclohexane]-2′-








en-4′-one







Bottom
2-(2,4-
266
3.82
6.50
1.67E−03
2.28E+03



DIMETHYL-3-








CYCLOHEXEN-








1-YL)-5-








METHYL-5-(1-








METHYLPROPYL)-








1,3-








DIOXANE







Bottom
(+−)-2-ETHYL-4-
208
3.69
4.39
7.80E−05
4.73E+04



(2,2,3-








TRIMETHYL-3-








CYCLOPENTEN-








1-YL)-2-








BUTEN-1-OL







Bottom
(+−)-1-(2,2,3,6-
240
3.42
5.96
4.05E−04
8.44E+03



TETRAMETHYL-








CYCLOHEXYL)-








3-HEXANOL







Bottom
9-ACETYL-8-
246
3.21
5.84
1.43E−03
2.25E+03



CEDRENE +








CEDARWOOD








SESQUITERPENES







Bottom
(+−)-(1E)-1-
232
3.01
4.86
7.14E−03
4.22E+02



(2,6,6-trimethyl-








2-cyclohexen-1-








yl)-1,6-heptadien-








3-one (A) + (1E)-








1-(2,6,6-








trimethyl-1-








cyclohexen-1-yl)-








1,6-heptadien-3-








one (B)







Bottom
(−)-(2E)-2-ethyl-
208
2.75
4.44
2.41E−05
1.14E+05



4-[(1R)-2,2,3-








trimethyl-3-








cyclopenten-1-








yl]-2-buten-1-ol







Bottom
1-[(1RS,6SR)-
226
2.34
5.42
5.92E−04
3.95E+03



2,2,6-








trimethylcyclohexyl]-








3-hexanol







Bottom
(3R)-1-[(1R,6S)-
226
2.20
5.52
4.40E−04
5.00E+03



2,2,6-








trimethylcyclohexyl]-








3-hexanol (A) +








(3S)-1-








[(1R,6S)-2,2,6-








trimethylcyclohexyl]-








3-hexanol (B) +








(3R)-1-








[(1S,6S)-2,2,6-








trimethylcyclohexyl]-








3-hexanol (C)







Bottom
(−)-
236
2.19
6.88
1.31E−05
1.68E+05



(3aR,5aS,9aS,9bR)-








3a,6,6,9a-








tetramethyldodecahydronaphtho








[2,1-b]furan







Bottom
(3aRS,5aSR,9aSR,9bRS)-
236
2.19
5.95
6.49E−05
3.37E+04



3a,6,6,9a-








tetramethyldodecahydronaphtho








[2,1-b]furan (A) +








(3aRS,5aSR,9aSR,9bSR)-








3a,6,6,9a-








tetramethyldodecahydronaphtho








[2,1-b]furan (B)







Bottom
(−)-
236
2.19
6.85
3.94E−05
5.56E+04



(3aR,5aS,9aS,9bR)-








3a,6,6,9a-








tetramethyldodecahydronaphtho








[2,1-b]furan







Bottom
(+−)-1-
234
1.85
5.82
5.57E−04
3.33E+03



(OCTAHYDRO-








2,3,8,8-








TETRAME-2-








NAPHTHALENYL)-








1-








ETHANONE








(DOUBLE








BOND: 4A,5 (A) +








4,4A (B) +








4A,8A (C)







Bottom
(1′S,3′R)-{1-
222
1.74
4.82
2.18E−06
8.01E+05



METHYL-2-








[(1′,2′,2′-








TRIMETHYLBICYCLO[3.1.0]








HEX-3′-








YL)METHYL]CYCLOPROPYL}








METHANOL







Bottom
(+)-METHYL
226
1.71
2.95
2.82E−04
6.06E+03



(1R)-CIS-3-








OXO-2-








PENTYL-1-








CYCLOPENTANEACETATE







Bottom
2/3/4-(5,5,6-
236
1.38
5.23
7.70E−04
1.79E+03



TRIMETHYLBICYCLO[2.2.1]








HEPT-2-YL)-1-








CYCLOHEXANOL








(A/B/C) + 2-








(1,7,7-








TRIMETHYLBICYCLO[2.2.1]








HEPT-2-YL)-1-








CYCLOHEXANOL








(D)







Bottom
1-(2,6,10-
246
1.24
5.94
3.88E−04
3.19E+03



TRIMETHYL-








1(2),5,9-








CYCLODODECATRIEN-








1-YL)-








1-ETHANONE +








1-(6,10-








DIMETHYL-2-








METHYLENE-








5,9-. . . )-1-E . . .







Bottom
(−)-
278
0.00
4.23
3.90E−06
6.26E+02



(1R,3S,7R,8R,10S,13R)-








5,5,7,9,9,13-








HEXAMETHYL-








4,6-








DIOXATETRACYCLO








[6.5.1.0(1,10).0(3,7)]








TETRADECANE









Example 4: Sensory Evaluation of Perceived Fragrance Intensity with Sequential Exposure to Contrasting Fragrance vs Non Contrasting Fragrance

For this example, 3 fragrances were prepared: an almond/coconut/woody fragrance, suitable for direct addition to a consumer product base (ACM1); an almond/coconut/woody fragrance, suitable for encapsulation in a poly-urea core-shell capsule (ACM2); and, a fruity/mango/passion-fruit fragrance, suitable for encapsulation in a poly-urea core-shell capsule (FMP1). The almond/coconut/woody fragrance (ACM1) and the almond/coconut/woody fragrance (ACM2) are non-contrasting fragrances; whereas, the almond/coconut/woody fragrance (ACM1) and the fruity/mango/passion-fruit fragrance (FMP1) are contrasting fragrances.


A first test was performed as follows. 1.00 g of fragrance ACM1 and 1.00 g of fragrance ACM2 were applied to separate 2″×2″ cellulose pads (Carlson Filtration Ltd., product reference EE3.0) and placed in glass petri-dishes. 0.25 g fragrance FMP1 was applied to a 1″×1″ cellulose pad (Carlson Filtration Ltd., product reference EE3.0) and place in a glass petri-dish. The cellulose pads comprising fragrance were then placed in to three identical odor evaluation booths with volume of 390 cu. ft set to 3 air changes per hour. The environmental conditions in the cabins during the test were 72° F., 35% RH with 3 air changes per hour. A portable desk fan, set on low, was placed in each cabin to circulate the air within.


After one hour the fragrance intensity in the cabins was assessed by 16 untrained but experienced assessors. The term “untrained but experienced assessors” refers to individuals who have not received formal olfactive training but who are used to participating in such sensory panels and have experience in rating fragrance intensity.


The assessors were instructed to smell the odor the cabins and rate the fragrance intensity using a 1 to 7 category scale, where 1 indicates no perceivable odor and 7 indicates very strong odor. Presentation of the test cabins was blind, balanced, randomized, and sequential monadic. Assessors were instructed to wait 60 seconds between successive assessments.


The results of this first test are shown in Table 11.


A second test was performed later the same day. The sample preparation and test set-up was identical to the first test but there was one important difference: each assessor was asked to wear a small device for 15 minutes prior to the assessing the intensity of fragrances in the cabins. The device was a small plastic holder that could be clipped onto the assessors clothing, the holder contained a 2″×2″ cellulose pad that was impregnated with 1.00 g of the almond/coconut/woody fragrance (ACM1). In this way we were able to adapt the assessors to the almond/coconut/woody fragrance (ACM1).


17 untrained but experienced assessors participated in the second test, the results of which are shown in Table 12.


The mean panelist intensities of the two tests are shown together in FIG. 12, and are markedly different. The perceived intensity of the almond/coconut/woody fragrance (ACM1) was significantly suppressed after adaptation to itself (self-adaptation). The perceived intensity of the almond/coconut/woody fragrance (ACM2) was also strongly suppressed after adaptation to ACM1 (significant cross-adaptation). On the other hand, the perceived intensity of the fruity/mango/passion-fruit fragrance (FMP1) was unaffected after adaptation to ACM1. The almond/coconut/woody fragrance (ACM1) and fruity/mango/passion-fruit fragrance (FMP1) would meet the definition of “contrasting fragrances” as there is no cross-adaptation between them.









TABLE 11







Rating of fragrance intensity (without adaptation to ACM1)









Panelist Intensity Rating











almond/coconut/
almond/coconut/
fruity/mango/



woody
woody
passion-fruit


Assessor
(ACM1)
(ACM2)
(FMP1)













Panelist #1
5
6
6


Panelist #2
5
4
7


Panelist #3
5
4
7


Panelist #4
4
4
5


Panelist #5
3
4
6


Panelist #6
5
6
7


Panelist #7
5
5
6


Panelist #8
5
6
7


Panelist #9
5
4
6


Panelist #10
4
4
5


Panelist #11
5
5
6


Panelist #12
4
5
5


Panelist #13
5
6
7


Panelist #14
4
4
6


Panelist #15
4
3
5


Panelist #16
5
4
5


Mean (n = 16)
4.56
4.63
6.00
















TABLE 12







Rating of fragrance intensity (after adaptation to ACM1)









Panelist Intensity Rating











almond/coconut/
almond/coconut/
fruity/mango/



woody
woody
passion-fruit


Assessor
(ACM1)
(ACM2)
(FMP1)













Panelist #1
3
2
7


Panelist #2
2
2
6


Panelist #3
2
4
6


Panelist #4
3
4
6


Panelist #5
3
4
5


Panelist #6
4
6
6


Panelist #7
4
4
6


Panelist #8
4
2
5


Panelist #9
2
3
6


Panelist #10
4
3
6


Panelist #11
2
5
6


Panelist #12
2
4
5


Panelist #13
4
3
6


Panelist #14
3
2
6


Panelist #15
4
3
7


Panelist #16
4
4
6


Panelist #17
6
5
6


Mean (n = 17)
3.29
3.53
5.94









Example 5: Sensory Evaluation of Perceived Fragrance Intensity in a Shower Gel of a Contrasting Fragrance/Capsule System Versus a Non-Contrasting Fragrance/Capsule System

The consumer product used in this example was a structured transparent shower gel, the composition of which was as follows:
















% by


Ingredient/Commercial Name
INCI Name
weight

















De-ionized water

49.35


Tetrasodium EDTA

0.05


CARBOPOL AQUA SF-1
Acrylates Copolymer
6.00


POLYMER




ZETESOL AO 328 U
Sodium C12-C15 Pareth
35.00



Sulfate



SODIUM HYDROXIDE

1.00


(20% soln.)




TEGO-BETAIN F 50
Cocamidopropyl Betaine
8.00


KATHON CG
Methylchloroisothiazolinone
0.10



(and) Methylisothiazolinone



CITRIC ACID (40% soln.)

0.50









A first shower gel formulation (SG1) comprising a reference (non-contrasting) fragrance/capsule system was prepared as follows. 3.00 g of the almond/coconut/woody fragrance (ACM1, see Example 4) was admixed with 294.0 g of the structured, transparent shower gel composition. To this was added 3.00 g of a poly-urea core-shell capsule suspension that comprised a mean particle diameter of between 300 and 400 microns and comprised approximately 30% by weight of the almond/coconut/woody fragrance (ACM2, see example 4). The sample was gently stirred using a glass rod until the capsules were evenly distributed throughout the shower gel.


A second shower gel formulation (SG2) comprising a contrasting fragrance/capsule system according to the present invention was prepared as follows. 3.00 g of the almond/coconut/woody fragrance (ACM1, see Example 4) was admixed with 296.25 g of the structured, transparent shower gel composition. To this was added 0.75 g of a poly-urea core-shell capsule suspension that comprised a mean particle diameter of between 300 and 400 microns and comprised approximately 30% by weight of the fruity/mango/passion-fruit fragrance (FMP1, see example 4). The sample was gently stirred using a glass rod until the capsules were evenly distributed throughout the shower gel.


A third shower gel formulation (SG3), comprising only a non-confined (free) fragrance was prepared as follows. 2.00 g of the almond/coconut/woody fragrance (ACM1, see Example 4) was admixed with 198.00 g of the structured, transparent shower gel composition.


A first test was performed as follows. 50 g of shower gel (SG1) was added to each of two 4 oz amber glass jars. One of the glass jars was capped. The contents of the second glass jar were vigorously mixed for 10 seconds and then capped (the mixing results in rupture of some of the fragrance capsules, which mimics the breakage of the capsules that the consumer experiences when using the shower gel). Two 4 oz amber glass jars were prepared in the same way using shower gel (SG2).


A panel of assessors was asked to smell the odor in the jars and rate the fragrance intensity using a 1 to 7 scale, where 1 indicates no perceivable odor and 7 indicates very strong odor intensity. Samples were presented blind, labelled with 3-digit random codes. Sample presentation to the panelists was balanced according to the following four orders of presentation:

    • 1. SG1 Unmixed; followed by SG2 Unmixed; followed by SG1 Mixed; followed by SG2 Mixed
    • 2. SG1 Unmixed; followed by SG2 Unmixed; followed by SG2 Mixed; followed by SG1 Mixed
    • 3. SG2 Unmixed; followed by SG1 Unmixed; followed by SG1 Mixed; followed by SG2 Mixed
    • 4. SG2 Unmixed; followed by SG1 Unmixed; followed by SG2 Mixed; followed by SG1 Mixed


The results of the first test are shown in Table 13. The panelist data was analyzed using a repeated measures ANOVA with Tukey post-hoc analysis of the differences between means with a confidence interval of 95%.









TABLE 13







Rating of fragrance intensity (without


adaptation to non-confined fragrance)










Panelist Intensity Rating













SG1
SG2
SG1
SG2


Assessor
Unmixed
Unmixed
Mixed
Mixed














Panelist #1
5
4
4
3


Panelist #2
4
4
4
5


Panelist #3
5
4
3
4


Panelist #4
4
6
5
6


Panelist #5
4
6
4
7


Panelist #6
4
5
4
4


Panelist #7
4
6
5
5


Panelist #8
4
5
5
6


Panelist #9
4
5
5
7


Panelist #10
5
5
5
4.5


Panelist #11
4
4
5
6


Mean (n = 11)
4.27
4.91
4.45
5.23









A second test was repeated later the same day. The sample preparation and set-up was identical to the first test but there was one important difference: after rating the fragrance intensity of the two unmixed shower gels, assessors were instructed to continuously smell (but not rate) the odor in a fifth jar for between approximately 30 seconds and 1 minute. This fifth jar comprised 50 g of shower gel (SG3). In this way we were able to adapt the assessors to the non-confined almond/coconut/woody fragrance (ACM1). Thus, sample presentation to the panelists was approximately balanced according to the following four orders of presentation:

    • 1. SG1 Unmixed; followed by SG2 Unmixed; followed by adaptation to SG3; followed by SG1 Mixed; followed by SG2 Mixed
    • 2. SG1 Unmixed; followed by SG2 Unmixed; followed by adaptation to SG3; followed by SG2 Mixed; followed by SG1 Mixed
    • 3. SG2 Unmixed; followed by SG1 Unmixed; followed by adaptation to SG3; followed by SG1 Mixed; followed by SG2 Mixed
    • 4. SG2 Unmixed; followed by SG1 Unmixed; followed by adaptation to SG3; followed by SG2 Mixed; followed by SG1 Mixed


The results of the first test are shown in Table 14. The panelist data was analyzed using a repeated measures ANOVA with Tukey post-hoc analysis of the differences between means with a confidence interval of 95%.



FIG. 13 shows the mean panel scores of the first test. The unmixed shower gels (SG1 and SG2) provide similar fragrance intensity. After mixing both shower gels (SG1 and SG2) show slight increases in perceived intensity versus the corresponding unmixed samples that is consistent with breakage of the capsules caused by the mixing step. The difference between mean intensity ratings of the four samples is not significant at the 95% confidence interval.



FIG. 14 shows the mean panel scores of the second test. As in the first test, the unmixed shower gels (SG1 and SG2) provide similar fragrance intensity; however, after mixing there is a marked difference between the samples. There is a slight decrease in perceived intensity of mixed SG1 versus the corresponding unmixed sample. The mixed SG2 sample shows a significant increase in perceived intensity versus the unmixed sample. The intensity boost afforded by breakage of the capsules in SG1 was suppressed after adaptation to the unmixed sample. On the other hand, the contrasting fragrance/capsule system used in SG2 was more resistant to adaptation and showed a statistically significant intensity boost upon breakage of the capsules. The fragrance/capsule system comprising the almond/coconut/woody fragrance (fragrance) and fruity/mango/passion-fruit fragrance (capsule) would meet the definition of “contrasting fragrance/capsule system” as there is no cross-adaptation between them.









TABLE 14







Rating of fragrance intensity (after


adaptation to non-confined fragrance)










Panelist Intensity Rating













SG1
SG2
SG1
SG2


Assessor
Unmixed
Unmixed
Mixed
Mixed














Panelist #1
4
5
4
6


Panelist #2
5
5
6
4


Panelist #3
5
5
3
4


Panelist #4
4
5
4
6


Panelist #5
4.5
4
5
7


Panelist #6
4
5
3
5


Panelist #7
4
5
4
5


Panelist #8
4
5
4
7


Panelist #9
5
4
4
7


Panelist #10
4.5
5
4.5
6


Panelist #11
4
5
4
7


Mean (n = 11)
4.36
4.82
4.14
5.82









Publications cited throughout this document are hereby incorporated by reference in their entirety. Although the various aspects of the invention have been illustrated above by reference to examples and preferred embodiments, it will be appreciated that the scope of the invention is defined not by the foregoing description but by the following claims properly construed under principles of patent law.

Claims
  • 1. A perfume composition comprising at least two perfuming accords, wherein a first perfume accord of the at least two perfuming accords comprises perfuming compounds dominated by a first olfactive note,wherein a second perfume accord of the at least two perfuming accords comprises perfuming compounds dominated by a second olfactive note,wherein the first and second olfactive notes are contrasting notes,wherein the first perfume accord is present in the perfume composition in an amount sufficient for the first olfactive note to be perceived by a subject at a first time,wherein the second perfume accord is present in the perfume composition in an amount sufficient for the second olfactive note to be perceived by a subject at a second time, andwherein the perception of the first olfactive note and the second olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.
  • 2. The perfume composition of claim 1, wherein the second time is after the third time.
  • 3. The perfume composition of claim 1, wherein the first perfume accord comprises perfuming compounds having a volatility ranging from 70,000 to 100 μg/l in air.
  • 4. The perfume composition of claim 1, wherein the second perfume accord comprises perfuming compounds having a volatility ranging from 99 to 50 μg/l in air.
  • 5. The perfume composition of claim 1, wherein the perfume composition further comprises a third perfume accord comprising perfuming compounds dominated by a third olfactive note, wherein the third perfume accord is present in the perfume composition in an amount sufficient for the third olfactive note to be perceived by a subject at a third time.
  • 6. The perfume composition of claim 5, wherein the third time is after the second time.
  • 7. The perfume composition of claim 5, wherein the third perfume accord comprises perfuming compounds having a volatility ranging from 49 to 0.1 μg/l in air.
  • 8. The perfume composition of claim 1, wherein the sufficient amount of the first perfume accord is from 30% to 70% by weight of the perfume composition.
  • 9. The perfume composition of claim 1, wherein the sufficient amount of the second perfume accord is from 30% to 70% by weight of the perfume composition.
  • 10. The perfume composition of claim 5, wherein the sufficient amount of the third perfume accord is from 30% to 70% by weight of the perfume composition.
  • 11. The perfume composition of claim 1, wherein the first perfume accord and the second perfume accord are present in the perfume composition in a weight ratio ranging from 3:1 to 1:3.
  • 12. The perfume composition of claim 1, wherein the first perfume accord and the second perfume accord are present in the perfume composition at a weight ratio of 1:1.
  • 13. The perfume composition of claim 5, wherein the first perfume accord the second perfume accord, and the third perfume accord are present in the perfume composition at a weight ratio of 1:1:1.
  • 14. The perfume composition of claim 1, wherein the perception of the second olfactive note after the first olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.
  • 15. The perfume composition of claim 5, wherein the perception of the first olfactive note, the second olfactive note, and the third olfactive note is at a level sufficient to reduce, prevent, or suppress a reduced perception of the perfume composition by the subject over time.
  • 16. The perfume composition of claim 5, wherein the first perfume accord further comprises a mixture comprising the first perfume accord encapsulated within a matrix material.
  • 17. The perfume composition of claim 5, wherein the second perfume accord further comprises a mixture comprising the second perfume accord encapsulated within a matrix material.
  • 18. The perfume composition of claim 5, wherein the third perfume accord further comprises a mixture comprising the third perfume accord encapsulated within a matrix material.
Priority Claims (1)
Number Date Country Kind
18162659.9 Mar 2018 EP regional
CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. provisional patent application 62/609,653, filed 22 Dec. 2017, and EP application no. 18162659.9, filed 19 Mar. 2018, the contents of which are hereby incorporated by reference in their entirety.

Provisional Applications (1)
Number Date Country
62609653 Dec 2017 US
Divisions (1)
Number Date Country
Parent 16757938 Apr 2020 US
Child 18668323 US