Perfumes for Linear Citrus Release in Rinse-Off Systems

Information

  • Patent Application
  • 20100087351
  • Publication Number
    20100087351
  • Date Filed
    September 24, 2009
    15 years ago
  • Date Published
    April 08, 2010
    14 years ago
Abstract
Perfume compositions and method of formulating perfume composition are designed for use in wash-off system with a linear citrus perfume release and either any of the following effects: a desired initial release with minimal residual perfume on the targeted system, a long sustained release of fragrance, or a residual deposition of fragrance after use.
Description
FIELD OF THE INVENTION

This invention relates to the method of the design and engineering of a perfume using odorants' mass transfer properties in order to control the optimization and predicted kinetic progression and/or release of a citrus hedonic profile with time in the presence of high levels of water.


The present invention relates to perfume systems. More particularly, the present inventions relates to the optimization of perfumes used in high water dilution conditions and/or rinse off applications, which will provide a linear continuous citrus hedonic note.


In addition to citrus, this invention provides method to design a predominantly linear citrus hedonic note coupled with a linear secondary nuance of either one of the following odors: fruity, green and floral.


BACKGROUND OF THE INVENTION

Fragrances are an important part of cosmetic compositions since their primary role is to create an agreeable sensory experience for the consumer, in addition to providing malodor coverage or other more functional roles.


Perfumes are composed of odorants with a wide range of molecular weights, vapor pressures and diffusivities as well as different polarities and chemical functionalities. Using these different properties, an individual skilled in the art could create different hedonic profiles describing the fragrance.


Fragrance materials are generally small molecular weight substances with a vapor pressure that allows their molecules to evaporate, become airborne, and eventually reach the olfactory organ of a living entity. There are a variety of different fragrance materials with different functional groups and molecular weights, 67% both of which affect their vapor pressures, and hence, the ease with which they can be sensed.


Odorants used in perfumery offer a wide array of polarity ranging from the somewhat water miscible to the water immiscible chemical compounds. Perfumery in the various rinse-off applications spanning from cosmetic to industrial and household have different functionalities and must be engineered to fulfill certain needs and objectives. Perfumes' effect and quality during use plays a big role in the consumer's purchase intent as well and the desire of the consumer to purchase the product again.


Fragrances have been designed based upon the selection of odorants with certain properties. For instance, U.S. Pat. No. 6,143,707 directed to automatic dishwashing detergent discloses blooming fragrance compositions by which were chosen based on their clogP and boiling point values. Hydrophobicity is usually gauged by the clogP values of these odorants. The logP value of an odorant is defined as the ratio between its equilibrium concentration in octanol and in water. The logP value of many of the fragrance materials have been reported and are available in databases such as the Pomona92 database, the Daylight Chemical Information Systems, Inc, Irvine, Calif. The logP can also be very conveniently calculated using the fragment approach of Hansch and Leo. See A. Leo, Comprehensive Medicinal Chemistry, Vol 4, C. Hansch et al. p 295, Pergamon press, 1990. These logP values are referred to as clogP values. Odorants thought to result in bloom in water dilutions are thought to have clogP of at least 3.0 and boiling points of less than 26° C. The same rationale for dishwashing liquids with blooming perfumes is also disclosed in U.S. Patent Application Publication No. 2004/0138078. EP Patent No. 0888440B1 relates to a glass cleaning composition containing “blooming perfumes” based on criteria mentioned above. U.S. Pat. No. 6,601,789 discloses toilet bowl cleaning compositions also containing “blooming perfumes” made of odorants chosen based on their clogP values of at least 3.0 and boiling points of less that 260° C. Generally, odorants with delayed bloom are thought to have a clogP of less than 3.0 and boiling point values of less than 250° C.


While the above-mentioned references disclose methods of selecting odorants based upon some of their physical properties, i.e. clogP and boiling point values, they do not encompass and identify all odorants which have superior release properties in heavy water dilutions nor do they provide a quantifying method to define bloom.


Furthermore, descriptors for “blooming odorants” and “delayed blooming odorants” described in the above prior art remain general and do not take in consideration the kinetic aspect of odorants' release in high water dilutions. Predictive quantification of odorants partitioning in headspace based on quantity and various other physico-kinetic aspects are included in the method described herein this invention.


SUMMARY OF THE INVENTION

A method of formulating a perfume composition for wash-off systems, comprising values of odor detection threshold, an acceleration term (γ) and water release (Ω) values for a group of odorants and engineering the perfume composition in a wash-off system to provide a continuous citrus note upon water dilution.


In addition to citrus, the method enclosed in the herein invention permits the engineering of a linear predominantly citrus perfume in rinse-off coupled with a linear release of secondary, less prominent note of either of the following odor categories: fruity, green, and floral.


The general physical properties of perfume odorants as currently known in the art (e.g., U.S. Pat. No. 6,143,707 U.S. Patent Application Pub. No. 2004/0138078, EP Patent No.0888440 B1 and U.S. Pat. No. 6,601,789) do not provide a complete picture when creating perfumes for rinse-off systems.


Odorants such as ethyl formate, ethyl acetoacetate, ethyl acetate, diethyl malonate, fructone, ethyl propionate, toluic aldehyde, leaf aldehyde, trans-2-hexenal, trans-2-hexenol, cis-3-hexenol, prenyl acetate, ethyl butyrate, hexanal, butyl acetate, 2-phenylpropanal, cis-4-heptenal, cis-3-hexenyl formate, propyl butyrate, amyl acetate, ethyl-2-methylbutyrate, ethyl amyl ketone, hexyl formate, 3-phenyl butanal, cis-3-hexenyl methyl carbonate, methyl phenyl carbinyl acetate, methyl hexyl ether, methyl cyclopentylidene acetate, 1-octen-3-ol, cis-3-hexenyl acetate, amyl vinyl carbinol, 2,4-dimethyl-3-cyclohexen-1-carbaldehyde, ethyl 2-methylpentanoate, 1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane, 3,7-dimethyl-7-methoxyoctan-2-ol etc. are considered by the authors of the herein invention to have superior release properties in heavy water dilutions. Yet, the above mentioned odorants are considered “delayed release” odorants according to the previously mentioned patents, which is counter to both empirical and experimental observations when used in wash-off products.


Prior art mentioned above does not provide ways to quantify bloom or the presence of odorants in headspace in highly diluted water partitions nor do they present a person skilled in the art the ability to predict the kinetic progression of the perfume during rinse-off.


A direct relationship between the quantity of an odorant in a perfume and its ability to be released from the water partition under heavy water dilution is generally observed by perfumers skilled in the art. The opposite can also hold true when using very small amounts of an odorant in a perfume. Above mentioned patents do not account for the change in an odorant's ability to release or bloom due to its concentration or quantity.


A mathematical relationship relating release of odorants from water partitions to their quantity in perfumes as well as their mass transfer properties needs to be established in order to predict their order of elution when exposed to heavy water dilutions.


For example, thiogeraniol (clogP 4.88, boiling point 250° C.) is considered a blooming odorant according to prior art mentioned above. Due to its very low odor detection threshold and overwhelming odor intensity, it is often used as a dilution within a perfume. It can have very delayed water release properties when used in parts per trillion in a perfume although considered a “blooming” material based on its physical properties, according to existing literature and above mentioned patents.


By establishing an approximate correlation mass transfer properties and perceived odorants' hedonic quality and intensity, one can design and further improve water release hedonic perception of perfume materials. The result is the new optimization and applied perfumery for wash off applications.


U.S. Pat. No. 6,858,574 relates odorants release properties in heavy water dilution to a relationship with components of the formulation in which the perfume is delivered, more notably, the surfactant system. The so-called perfume burst index (PBI) is defined by:







P





B





I

=


φ
-


1.4
/
C






M





C


K





where φ is water/oil partition


coefficient (an equivalent to clogP mentioned above), K is the volatility constant of perfumes in air (in direct relationship to boiling point values) and CMC is the critical micellization concentration of the surfactant systems (wt/wt). A burst release in water dilutions is thought to happen when there is at least 20% increase of the odorant in headspace. Examples provided by the author are done in dilutions not exceeding 60 and mostly between 0 and 30. Yet, in consumer usage of formulations in wash off conditions, especially in applications such as body wash, conditions, shampoos, and surface cleaners, the conditions far exceed the dilution values used in U.S. Pat. No. 6,858,574 for the calculations. For example, a typical usage of water during a shower exceeds 25 gallons of water and can reach 50 gallons of water when considering a typical household shower pressure dispensing 5-10 gallons a minute (See


http://www.engr.uga.edu/service/extension/publications/c819-1.html).


Values for water dilutions in a typical household, cosmetic, industrial wash-off application therefore far exceeds the dilution values used in U.S. Pat. No. 6,858,574. One can therefore argue that under these extreme dilution conditions of a typical wash-off application (1/100 and above), the release partitions become essentially water, water-air and air, with surfactants' contributions very minimal, almost non-existent.


In the present invention, mass transfer properties of odorants in water as well as their odor detection threshold values and hedonic descriptors are used to design fragrances optimized for rinse-off.


Descriptors of fragrance ingredients are designated under two categories (“Descriptor 1” and “Descriptor 2”) independently by a panel of in-house expert perfumers. Descriptor 1 is used to describe the overall dominating hedonic perception whilst descriptor 2 is mostly for nuances of the odorant. By definition, citrus or fruity, green, and floral odorants will be defined as such, preferably based on either one or the other of the descriptors, and more preferably “Descriptor 1”.


Specific physico-chemical properties of odorants are utilized in methods described in this invention to control and engineer linear citrus hedonic perfumes during use or alternatively linear citrus-fruity, citrus-floral and citrus-green.


According to the present invention, a perfume composition is optimized for various cosmetic, household and industrial applications in water systems and/or in presence of water based on specific physico-kinetic properties. In addition, methods are included to estimate odorants' hedonic contribution (odor being defined by the said odorants' odor descriptors) out of a total odor value within specifically designated water release groupings.


The perfumes of this invention are also designed to potentially give the consumer the perception of sustained and more prolonged release of a citrus perfume or citrus-fruity, citrus-green and citrus-floral during wash-off. Methods to create such superior sustained citrus release in high water dilutions are used for perfumes used in cosmetic and household applications.


The perfumes created using methods described herein this invention also have the ability provide a linear release of a citrus fragrance or a predominantly citrus fragrance with a secondary fruity or floral or green odor also in a linear manner without substantial residual perfume left behind on a surface upon the completion of the wash-off experience. This desired effect will target certain applications such surface cleaners and dish washing liquids.


Perfumes engineered according to methods described in this invention can also provide the person skilled in the art with a method to create a sustained release of a perfume with a constant perceived intense citrus background upon heavy dilution with linear nuances of fruit, green and floral. Such perfumes are intended for household and cosmetic applications such as shampoo, conditioners, body wash and soaps.


Finally, other important categories of cosmetic, household and industrial rinse-off products must result in a substantial deposition of perfumes upon rinse-off. Methods to create such perfumes with an additional intense background of a citrus perfume throughout the rinse-of experience are shown herein. These perfumes can also be designed as mentioned in the above cases to include linear nuances of floral, green or fruity perfumes against a strong citrus background during rinse-off.


This invention deals primarily with the method to optimize a citrus fragrance diffusion and behavior in high water dilutions based on calculated mass transfer and transport properties of odorants in water, water vapor and air partitions according to methods described herein.


The object of this patent is to improve a citrus fragrance released perception during delivery or release in presence of large volumes of water.


In water-based systems, choosing fragrance molecules based on specific mass-transfer values for release out of a matrix optimizes the perfume's intensity and perceived hedonic quality. These values are calculated according to these odorants' physico-chemical properties based on principles of mass transfer as well as odorants calculated odor contributions within defined water release groups.


Water release value (Ω) is defined by the authors as being the product of quantity of an odorant in a perfume totaling 100 parts used arbitrarily at 1% in rinse-off application with the odorant's flux (φ) and its estimated pseudo-acceleration value (γ) out of the water-air partitions.


These Ω values are used to separate the fragrance into water release groups, therefore predicting the kinetic release of odorants out the water, water/air into the air partitions.


Within these defined water-release groups, odorants are then further described based on their experimentally determined odor detection thresholds (ODT) to further characterize the odor impact or olfactive intensity of a citrus and other olfactive types within the herein-described released group of odorants.


Based on the application considered, the perfume considered will be optimized using odorants' mass transfer and physico kinetic properties as well as their odor intensity and description. “Water release groups” for water partitions are defined in more details in the invention and are engineered specifically to result in fragrances with an impactful citrus background during the entire rinse-off experience.


Perfumes designed for surface cleaners and dishwashing detergents are composed of at least 20%, preferably at least 30% of total perfume odorants with characteristic flash water release values: γ values more than 900 and in addition, no more than 30%, more preferably no more than 15% of the composing odorants must have γ values below 100.


Perfumes engineered for shampoos, conditioners, body wash etc. will on the other hand be optimized using primarily sustained release odorants based on the optimal residence time in headspace. Fragrances constructed with at least 30% and preferably at least 40% of odorants with acceleration values for sustained release: γ values between 900 and 100.


More residual fragrances for wash-off applications such as laundry can be engineered based on a majority of fragrance at least 30%, preferably 40% of odorants, more preferably 50%, referred to by the authors as “deposition odorants,” based on their mass transfer properties: γ values lower than 100.


According to the present invention, all perfumes engineered for intended functionalities described above will provide a continuous citrus fragrance during rinse-off or in the presence of large quantities of water. Green, fruity and floral nuances may also be built in the linear release of the perfume out of the rinse-off partitions, essentially creating what the inventors refer to as linear “citrus-green”, “citrus-fruity”, and “citrus-floral” blooming perfumes.


A continuous, sustained citrus hedonic background during rinse off can be achieved designing at least three, preferably four different release groups as described in this invention with at least 30%, preferably at least 40% of their total odor contributed by one or a group of citrus odorants.


In addition, linear release of olfactive floral, green and fruity nuances may be added to a dominating citrus background during rinse off. To achieve secondary linearity of either floral, green or fruity nuances, one or a group of the corresponding floral, green or fruity odorants must contribute to at least 20%, of at least three, preferably four different water release groups as described in the invention herein.


Water Release Value, Ω

Water based formulations are usually oil in water or water in oil emulsions with a varied concentration of water. By emulsifying these partitions, fragrances are dispersed and solubilized. Upon heavy water dilutions typical for the average household, industrial and cosmetic rinse-off in-use, odorants making up perfumes need to diffuse through what is considered to be mostly water, a vapor phase above the liquid phase and finally the air phase.


To increase the water release impact of these fragrances in these systems, properties of odorants based on their mass transfer characteristics were used. These odorants' release properties in water (Ω1,2) will determine the order of elution of these odorants in the partitions considered: water, water-air and air





Ω=n·φ·γ  [1]


φ=Flux of odorant in a system considering the partitions: water, water-air and air, expressed in






mg


cm
2

×
sec





and

  • γ=Pseudo-acceleration factor of odorant in water, water-air and air expressed in







cm

sec
2


,




n is the parts quantity of an odorant in a total 100 parts of a perfume used arbitrarily at 1% in a formulation.


This value of water release is indicative of the kinetic order of elution of the odorants involved in the composition of the perfume diluted in water. As discussed later in this document, it is intimately linked to various thermodynamic and calculated mass transfer properties obtained by the authors but also based on quantity of the odorant considered within the entire formula.


Below is the description of the terms used to derive equation [1]


Flux (φ12)

Flux of an odorant in partitions water, water-air and air, (φ) is defined as the ratio of the quantity of odorant being transferred in the media considered divided by the time and area of the contained medium. Flux values can also be defined in relation to a concentration gradient of the odorant throughout a partition according to:










φ
12

=

-


D
12



(




(

c
1

)




z


)







[
2
]







D12 is the diffusion constant of odorant (1) in partition (2) and dC1/dZ is the concentration gradient of odorant (1) throughout the partition.


D12 is calculated using the “Slattery Kinetic Theory” with non-polar odorants using odorants' critical parameters, unsteady state evaporation and measurement of binary diffusion coefficient. (Chem. Eng. Sci. 52, 1511-1515). The concentration gradients of the odorants composing the perfumes throughout the partitions considered (water, water-air and air) are calculated by solving for the dimensionless velocity value determined using the Arnold equation. (See Arnold, J. H. Studies in Diffusion: III. Unsteady State Vaporization and Absorption. Trans. Am. Inst. Chem Eng., 40, 361-378.). Some flux values for a variety of odorants out of a water partition are listed in the Table 1 below.









TABLE 1







Examples of flux values for some perfume odorants.








Odorant
φ (mg/cm2 · sec)





Ethyl 2-methylbutyrate
0.004361536


d-1-Methyl-4-isopropenyl-1-cyclohexene
0.001571820


2,2-Dimethyl-3-(p-ethylphenyl)propanal
0.000006157


4-Methyl-3-decen-5-ol
0.000004491


5-Hexyldihydro-2(3H)-furanone
0.000005070


1-(5,5-Dimethyl-1-cyclohexen-1-yl)-pent-4-en-1-one
0.000005501


6,6-Dimethyl-2-methylenebicyclo-(3.1.1)-heptane
0.001912106


6-sec-Butylquinoline
0.000006754


Octahydro-4,7-methano-1H-indene-5-yl acetate
0.000009115


Ethyl 2,3-epoxy-3-methyl-3-phenylpropionate
0.000010182


2(6)-methyl-8-(1-methylethyl)-bicyclo[2.2.2]octe-5-en-2(3)-yl-1,3-dioxolane
0.000003792


Isopropyl-methyl-2-butyrate;
0.002632239


Tricyclo-decenyl propionate
0.000003150


2,6,10-Trimethyl-9-undecenal
0.000001843


Methyl-2-hexyl-3-oxocyclopetanedecarboxylate
0.000000204


2-Phenylethyl phenylacetate
0.000000080


3,7-Dimethyl-1,6-octadien-3-yl 3-phenyl-2-propenoate
0.000000039


Ethyl octyne carbonate
0.000007735


3,7-Dimethyl-2,6-octadien-1-thiol
0.000046576


(1R-(1a,4b,4aa,6b,8aa))-Octahydro-4,8a,9,9-tetramethyl-1,6-methano-1(2H)-naphtol
0.000001119









Pseudo-Acceleration, γ12

In the analysis of the volatility of odorants, several variables are found to be important. First, the vapor pressure of the odorant is an important measure of its volatility. The product of the odorant's activity coefficient γ in the partition, its mole fraction X and its pure vapor pressure value Pv, gives the odorant's relative vapor pressure. A second important factor for volatility is the diffusivity D12 of the odorant in the considered media: water, vapor phase and subsequently air.


Other important variables to consider are the molecular weight Mw, of the odorant and its density in the partition pi and in the solvent vapor state ρv. The final variable to consider is an energy parameter in the partition state. The energy difference ε1212(polar)−ε12o(non-polar) is proportional to the partition coefficient of an odorant in a polar solvent such as water, and a water immiscible solvent such as octanol, benzene and paraffin liquid. The energy ε12 is called the partition energy and can be correlated to the clogP value of odorants. By definition: clogP proportional to








(


ɛ

12


(
water
)



-

ɛ

12


(
octanol
)




)

RT

;




R=1.987 cal/(mole-°K); T=temperature (Kelvin).


The five variables D12, Pv, Mw, ρv, and ε12 and the three dimensional variables indicate that there can be 5−3=2 dimensional variables which describe Newton's law. The easiest separation is to break the acceleration vector into 2 dimensional quantities: a frequency or first order rate constant (1/time) and a velocity (distance/time) term.


The velocity group can be formed from the vapor pressure and density. Since pressure has units of (mass*distance)/(distance2*time2), and density has units of mass/distance3, the ratio of the two has units of velocity squared. The square root gives the desired velocity. This velocity group is therefore defined as:










Velocity
=


(


γ
*
X
*

P
v



ρ
v


)


1
2









(

Units


:






length


/


time

)





[
3
]







The first order rate constant can be formed from the variables Mw, D12 and ε12. Since the partition energy ε12 has dimensions of calories per mole (mass.length2/mole.time2) and the diffusivity coefficient D12 has a dimension of distance2 per time, the ratio yields exactly a molecular weight unit per time t. The energy can be made dimensionless by dividing by the gas constant k and temperature T. The remaining variable D12 can be made to a frequency by dividing by a cross sectional area L2. A molecular area calculated from the liquid molar volume could represent this area. The frequency term or first order rate constant is therefore defined as:










Frequency
=


ɛ
12


MW
*

D
12










(

Units


:







1
/
time


)





[
4
]







Some γ values for a variety of odorants are listed below in Table 2.









TABLE 2







Calculated pseudo-acceleration values for some perfume odorants








Odorant
γ (cm/sec2)











Ethyl 2-methylbutyrate
12827.56


d-1-Methyl-4-isopropenyl-1-cyclohexene
8200.76


2,2-Dimethyl-3-(p-ethylphenyl)propanal
121.17


4-Methyl-3-decen-5-ol
116.38


5-Hexyldihydro-2(3H)-furanone
115.36


1-(5,5-Dimethyl-1-cyclohexen-1-yl)-pent-4-en-1-one
109.12


6,6-Dimethyl-2-methylenebicyclo-(3.1.1)-heptane
9007.51


6-sec-Butylquinoline
135.34


Octahydro-4,7-methano-1H-indene-5-yl acetate
144.06


Ethyl 2,3-epoxy-3-methyl-3-phenylpropionate
147.67


2(6)-methyl-8-(1-methylethyl)-bicyclo[2.2.2]octe-5-en-2(3)-yl-1,3-dioxolane
57.74


Isopropyl-methyl-2-butyrate;
8722.05


Tricyclo-decenyl propionate
60.58


2,6,10-Trimethyl-9-undecenal
43.58


Methyl-2-hexyl-3-oxocyclopetanedecarboxylate
6.71


2-Phenylethyl phenylacetate
2.29


3,7-Dimethyl-1,6-octadien-3-yl 3-phenyl-2-propenoate
0.71


Ethyl octyne carbonate
156.29


3,7-Dimethyl-2,6-octadien-1-thiol
659.09


(1R-(1a,4b,4aa,6b,8aa))-Octahydro-4,8a,9,9-tetramethyl-1,6-methano-1(2H)-naphtol
25.57









Pseudo acceleration values are also closely linked to the ability of an odorant to travel through headspace once it is airborne in addition to its ability to migrate through the water and water-air partitions. This value is predictive of what the authors consider “flash release”, “sustained release” and “deposition” of odorants in heavy water dilutions.


“Flash release” is defined as fast migration through water and subsequent very low residence time in headspace, resulting in a short hedonic experience of initial release and very minimal deposition on a treated surface. “Sustained release” is characterized by good water release properties along with a longer residence time in the water vapor and subsequently, the air phase. “Deposition” or also “delayed-release” is a term used to categorize odorants with very poor water/air release properties and consequently remain available for superior deposition on the surfaces treated.


Flash release odorants are considered by the authors to have acceleration, γ values above 900 cm/sec2, sustained release odorants are thought to have γ values between 900 and 100 and finally deposition odorants have acceleration values of less than 100.


As an illustration, some odorants with characteristic acceleration values for all three release categories defined by the authors are shown below. Water release properties are observed in 1 to 100 water dilution of a typical formulation containing these odorants as shown in the following procedure. The odorants chosen for this illustrative example are as follow in Table 3.









TABLE 3







Release properties and predicted residence


time for some perfume odorants.









Γ (acceleration water/air)














Flash Release
ethyl formate
46183.23
cm/sec2



ethyl-2-methyl butyrate
12827.56



melonal
2655.52



cyclacet
1687.87


Sustained Release
linalool
644.41



aldehyde c-11 moa
401.44



alpha ionone
283.60



lilial
104.63


Deposition Odorants
cyclamen aldehyde
99.64



jasmolactone
76.30



hexyl cinnamic aldehyde
21.01



acetal cd
0.08










The partition release value Ω is defined as the product of the pseudo acceleration γ and the flux value Φ and the quantity of odorant in a total 100 parts of the perfume diluted in water. The expression of water release out of the water, water-air and air partitions can then be physically equated to a value of







(

force
area

)



1
sec





or in other words, units of pressure per time out partition. It is important to establish that water release values are a way to predict the kinetic release profile of a perfume out the partitions considered into headspace when subject to extreme aqueous dilutions. This predictive value for elution time allows a person skilled in the art to establish groupings of odorants as they kinetically elute from the water dilutions. Keys or hedonic profile can be constructed, achieving better engineering control of their creative process. By designing these groupings of odorants and their order of elution, a perfumer can construct optimized perfumes for water release systems, since most of these odorants will behave differently in aqueous dilutions as compared to emulsions with various surfactant proportions.


Water release values, Ω for the corresponding odorants is a kinetic expression of water release. Once in headspace, acceleration values as well as odor detection thresholds (discussed in more details further) will dictate the intensity and odor contribution as well as residence time of each odorant in the water vapor and air.


An empirical relationship using real time headspace analysis was established by the authors between elution times of odorants and Ω values. This empirical relationship is shown in Table 5.









TABLE 5







Water Release Groups Definitions.









Water Release Values














Water Release Group 1
  Ω ≧ 10



Water Release Group 2
 10 > Ω ≧ 0.07



Water Release Group 3
0.07 > Ω ≧ 0.007



Water Release Group 4
0.007 > Ω ≧ 0.0005



Water Release Group 5
0.0005 > Ω ≧ 0.00003



Water Release Group 6
0.00003 > Ω     











Examples of odorants having an acceleration value greater than 900 include:
  • ethyl formate
  • ethyl acetate
  • ethyl propionate
  • ethyl 2-methylpropanoate
  • methyl hexyl ether
  • 2,6,6-Trimethylbicyclo-(3,1,1)-2-heptene
  • butyl butyrate
  • ethyl isovalerate
  • ethyl butyrate
  • ethyl 2-methylbutyrate
  • butyl acetate
  • hexanal
  • isopropyl-methyl-2-butyrate;
  • β-methyl butyl acetate
  • 6,6-dimethyl-2-methyleneorpinene
  • pentyl acetate
  • propyl butyrate
  • 7-methyl-3-methylene-1,6-octadiene
  • (R)-(+)-p-Mentha-1,8-diene
  • 2,6-Dimethyl-2-heptanol
  • 2-ethenyl-2,6,6-trimethyltetrahydropyran
  • E-2-hexenal
  • 4-isopropyl-1-methyl-1,5-cyclohexadiene
  • cis-4-heptenal;
  • methyl phenyl ether
  • 1-methyl-4-isopropyl-1,4-cyclohexadiene
  • ethyl-2-methylbentanoate
  • 3-methyl-2-butenyl acetate
  • hexyl formate
  • 1-methyl-4-isopropylidene-1-cyclohexene
  • 1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane
  • 2,3-butanedione
  • 3,7-dimethyl-1,3,6-octatrene
  • ethyl hexanoate
  • cis-3-hexenyl formate
  • 6-methyl-5-hepten-2-one
  • 3-octanone
  • trans-2-hexenyl acetate
  • 2,2-Dimethyl-3-(3-methyl-2,4-pentadienyl)-oxirane
  • 2-(2′-methyl-1′-propenyl)-4-methyltetrahydropyran
  • octanal
  • hexyl acetate
  • methyl-2,2-dimethyl-6-methylene-1-cyclohexanecarboxylate
  • phenylethyl methyl ether
  • methyl phenyl carbinyl acetate
  • 3,3-dimethyl-8,9-dinorbornan-2-one
  • isobutyl cis-2-methyl-2-butenoate
  • cis-4-(isopropyl)-cyclohexane methanol
  • isoamyl butyrate
  • 2,6-dimethyl-2hepten-7-al
  • pentyl butyrate
  • tricyclo decenyl acetate
  • 5-methyl-2-(2-methylpropyl)-cis-3-Propylbicyclo(2.2.1)hept-5-ene-2-carbaldehyde
  • Methyl trans-1,4-dimethylcyclohexanecarboxylate
  • 1,3-Dimethylbutyl 2-butenoate
  • 4-(1-Methoxy-1-methylethyl)-1methylcyclohexene
  • 2-Methyl-1,5-dioxaspiro[5,5]undecane
  • 3,6-Dihydro-4methyl-2-(2-methylopropen-1-yl)-2H-pyran;
  • 2-Propenyl hexanoate
  • cis-3-hexenyl isobutyrate
  • ethyl heptanoate
  • 2,4dimethyl-3-cyclohexen-1-carbaldehyde
  • cis-3hexenyl methyl carbonate;
  • 1-Ethyl-3-methoxytricyclo[2.2.1 02,6]heptane
  • 1-(3,3-Dimethylcyclohexyl)ethan-1-one
  • nonanal
  • trans-2-hexenol
  • dl-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one
  • 1,3Dimethylbut-3-enyl isobutyrate
  • cis-3-hexenol
  • 3,7-dimethyl-7-methoxyocian-2-ol
  • Methyl cyclopentylidene acetate
  • benzaldehyde
  • Aldehyde C-8 dimethyl acetal
  • 3,7-Dimethyl-1,6-octadien-3-yl formate
  • 3,7-Dimethyloctanal
  • 2,6-dimethyl-2-heptanol
  • 4,5,6,7-Tetrahydro-3,6-dimethylbenzofuran
  • 1,3,5-Undecatriene
  • 2,5-dimethyl-2-octen-6-one
  • cis-3-hexenyl acetate
  • butyl 2-methyl pentanoate
  • 3,7-Dimethyl-6-octenal
  • dimethyloctenone;
  • 2,4-Dimethyltetrahydro benzaldehyde
  • cis-3-hexanyl propionate
  • 2-isopropyl-5-methylcyclohexanone (isomer unspecified;
  • 2-(1-Ethylpentyl)-1,3-dioxolane
  • 3-octanol
  • 2-phenylpropanal
  • 3,5,5-trimethyl hexanal
  • 1,3-undecadein-5-yne
  • 1p-menthene-8-thiol;
  • 1Phenyl-4-methyl-3-oxapentane
  • 3,7-Dimethyl-3,6-octadienal
  • 3-Octenol
  • E-4-Decenal
  • cis-4-decenal
  • phenylacetaldehyde
  • 2-(1-methylpropyl) cyclohexanone
  • 2-Butyl-4,4,6-trimethyl-1,3-dioxane
  • cyclohexyl ethyl acetate
  • 1-octen-3-ol
  • tricyclodecenyl propionate
  • 6-Butyl-2,4-dimethyldihydropyrene
  • 2,6-nonadienal
  • 3-phenyl butanal
  • 3,7-dimethyl-2,6-octadiene-1-nitrile
  • Z-6-nonenal


    Examples of odorants having an acceleration value less than 100 include:
  • 2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol
  • o-Amino methylbenzoate
  • 1-(2,6,6-Trimethyl-2-cyclohexene-1-yl)-1,6-heptadien-3-one
  • 3,7-Dimethyl-6-octenyl 3-methylbutanoate
  • 4-Methoxybenzaldehyde diethyl acetal
  • [2-(Cyclohexyloxy)ethyl]benzene
  • AGARBOIS
  • 2-Methoxy-4-(2-propenyl)phenol
  • 2(6)-methyl-8-(1-methylethyl)bicyclo[2.2.2]ocle-5-en-2(3)-yl-1,3-dioxoiane
  • 2-Methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol
  • 3-Phenylpropyl alcohol
  • 2-(Phenylmethylene)heptanal
  • Ethyl (2E,4Z)-decadienoate
  • 7-Methyl-2H-benzo-1,5-dioxepin-3(4H)-one
  • Ethyl 2-hexylacetoacetate
  • 4,4a,5,9b-Tetrahydroindeno[1,2-d]-1,3-dioxine
  • 3-Methyl-5-phenylpentanenitrile
  • 3,4-Dihydro-2H-1-benzopyran-2-one
  • 2-Phenoxyethyl isobutyrate-Dodecanenitrile
  • 2-(3-Phenylpropyl)pyridine
  • 2,6,19-trimethyl-5,9-undecadienal
  • p-isobutyl-a-methyl hydrocinnamaldehyde
  • trans-3,7-Dimethyl-2,8-octadien-1yl 3-methylbutanoate
  • 8-β-H-Cedran-8-ol acetate
  • VETHYMINE
  • Tricyclo(5.2.1.02.6)dec-3-en-9-yl isobutyrate
  • Trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene
  • 3,7-Dimethyl-7-hydroxyoctanan
  • 2-Benzyl-4,4,6-trimethyl-1,3-dioxene
  • amberketal;
  • 2,6,10-Trimethyl-9-undecenal
  • γ-undecalacione
  • 10-undecen-1-ol
  • 1,2-Benzopyrone
  • 4-(p-Methoxyphenyl)-2-butanone
  • 3-Butyltetrahydro-5-methyl-2H-pyran-4-ylacetate
  • 3(Or 4)-(4-methylpenten-3-yl)cyclohex-3-ene-1-methyl acetate
  • 6,10-dimethyl-9-undecen-2-one
  • carbonic acid:4-cyclootene-1-ylmethyl ester;
  • 2-(2-Methylphenyl)ethanol
  • a,a-Dimethylphenethyl butyrate
  • 4-Hydroxy-3-methoxy-1-propenylbenzene
  • 1,5,5,9-Tetramethyl-13-oxatricyclo(8,3,0,0(4,9))iridecanel
  • 2-Methyl-4-(2,2,3-trimethyl-3-cyclopentenyl)butanol
  • 2-isobutoxynaphtalene
  • 3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol
  • Methoxy dicyclopentadiene carboxaldehyde
  • 1,1′-Bicyclopentyl]-2-yl2-buteneate; 2-Cyclopentylcyclopentyl cretonate;
  • methyl-2-naphtyl ketone
  • 1,2,3,4,4a,5,6,7-Octahydro-2,5,5-trimethyl-2-naphthol
  • 2H-Pyran-2-one, tetrahydro-8-(3-pentenyl)
  • FRESCILE
  • Dihydro-5-octylfuran-2(3H)-one
  • 1,2,3,4,4a,7,8,8a-Octahydro-2,4a5,8a-tetramethyl-1-naphthyl formate
  • FRUTONILE
  • magnolan;
  • 3-Methyl-5-phenylbentanol
  • (E) and (Z) 6,10-Dimethylundeca-5,9-den-2-yl acetate
  • alcohol C-12, dodecanol
  • 5,6-Dimethyl-β-isopropenylbicyclo(4.4.0)dec-1-en-3-one
  • 2-methyl-5-phenlpentanol
  • 3-methyl-5-phenlpentanol
  • 2-Methoxy-4-propenylphenyl acetate
  • 1-(1,2,3,4,5,6,7,8-Octahyro-2,3,8,8-tetramethyl-2-naphthalenyl)ethanone
  • Tricyclo[6.3.1.02.5]dodecan-1-ol, 4,4,8-trimethyl-, acetate, [1R-(1a, 2a,5b,8b)]-;
  • PIVACYCLENE
  • Ethyl a,b-epoxy-b-phenylpropionate
  • 3-(4-ethyl phenyl)-2,2-dimethylproapanenitrile
  • (1R-(1a,4b,4aa,6b,8aa))-Octahydro-4,8a,9,9-tetramethyl-1,6-methano-1(2H)-naphthol
  • 2-methyl-3-(3,4-methylenedioxyphenyl)propanal
  • 3-Methylbutyl o-hydroxybenzoate
  • 2-Ethyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol
  • 1,3-Benzodioxole-5-carboxaldehyde;
  • benzyl alcohol
  • 1-Phenyl-3-methyl-3-pentanol;
  • 2-Ethyl-2-prenyl-3-hexenol
  • 4-Acetyl-6-t-butyl-1,1-dimethylindan;
  • α-hexylcinnamic aldehyde;
  • 2-Oxo-1,2-benzopyran,
  • 3aR-(3aa,5ab,9aa,9bb)Dodecahydro-3a,6,6,9a-tetramethylhaphtho(2,1-b)furan,
  • hydroxycitronellal dimethyl acetal
  • 2-Methyl-4-phenylpentanol;
  • 3,7,11-Trimethyldodeca-1,6,10-trien-3-ol mixed isomers
  • a,b,2,2,3-Pentamethylcyclopent-3ene-1-butanol
  • 3,12-tridecadien-nitrile
  • 3a,4,5,6,7,7a-Hexahydro-2,6(3,6)-dimethyl-4,7-methano-1H-inden-5-ol
  • 3-Phenyl-2-propen-1-ol
  • 4-(2,6,6-Trimethylcyclohexyl)-3-methylbutan-2-ol;
  • 4-(3,4-Methylenedioxyphenyl)-2-butanone;
  • 3,4-dimethoxybenzaldehyde,
  • SINODOR
  • 3-Methyl-5-(2,2,3-trimethyl-3-cyclopenien-1-yl)pent-4-en-2-ol
  • Ethoxymethoxy)cyclodecane;
  • 2-ethoxy-4-methoxymethylphenol,
  • 2-[2-(4-Methylcyclohex-3-en-1yl)propyl]cyclopentanone;
  • 4-(4,8-Dimethylnona-3,7-dienyl)pyridine
  • (E,E,E)-2,6,10-Trimethyldodeca-2,6,9,11-tetraen-1-al
  • DUPICAL
  • Methyl 3-phenylpropenoate
  • 7-Methyl-2H-benzo-1,5-dioxepin-3(4H)-one
  • amber core;
  • 3-(2-bornyloxy)-2methyl-1-propanol (exo)
  • 3Phenyl-2-propen-1-yl 3-methylbutanoate
  • trans-2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolan
  • a-Cyclohexylidene benzeneacetonitrile,
  • 3-(Hydroxymethyl)nonan-2-one;
  • Benzoic acid, 2-hydroxy-, 3-methyl-2-butenyl ester
  • cedryl methyl ketone
  • cis-4-Cyclopentadecanone;
  • 6-Ethylidineociahydro-5,8-methano-2H-1-benzopyran-2-one;
  • 5-cyclohexadecen-1-one;
  • cyclopentadecanone;
  • MEVANTRAAL
  • 3,3-Dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-4-penten-2-ol
  • methyl dihydrojasmonate
  • cyclopentadecanoide
  • 1,3-Dioxane, 2-(2,4-dimethyl-3-cyclohexene-1-yl)-5-methyl-5-(1-methylpropyl)-3,7-dimethyl-1,6-octadien-3-yl benzoate.
  • Methyl(2-pent-2-enyl-3-oxo-1-cyclopentyl) acetate
  • 2-tert-butylcyclohexyl carbonate;
  • 4-(4-hydroxyphenyl)-2-butanone
  • 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyctopenia-γ-2-benzopyran
  • methyl-2-hexyl-3-oxocyclopetanedecarboxylate
  • 3-methylcyclopentadecanone;
  • 4-(4-Hydroxy-4-methylpentyl)cyclohex-3-enecarbaldehyde
  • 1,12-dodecanedioic acid ethylene ester;
  • 2-tridecenenitrile;
  • hexyl salicylate,
  • 15-pentadecanolide,
  • 2-Phenylethyl benzoate
  • 3-Ethoxy-4-hydroxybenzaldehyde
  • hexadecanolide
  • 9-cycloheptadecen-1-one
  • 3-(5,5,6-Trimethylbicyclo[2.2.1]hept-2-yl)cyclohexan-1-ol
  • Pentyl-2-hydroxybenzoate,
  • 3,7-Dimethyloctane-1,7-diol
  • p-cresyl phenylacetate
  • 1-Methyl-1-(3S,8S)-1,2,3,4,5,6,7,8-octahydro-3,8-dimethylazulen-5-yl)ethyl acetate
  • 3-Hexenyl 2-hydroxybenzoate
  • 1,4-Dioxacycloheptadecane-5,17-dione
  • 2,5-Dimethyl-4-hydroxy-2,3-dihydrofuran-3-one
  • 2-Phenylethyl phenylacetate
  • TRASEOLIDE
  • 4-methoxybenzyl alcohol
  • Benzyl o-hydroxybenzoate
  • 2-Ethyl-3-hydroxy-4-pyrone
  • DECEN 1 AL 9
  • 4-Hydroxy-3-methoxybenzaldehyde
  • Ethyl 2-methyl-4-oxo-6-pentylcyclohex-2-ene-1-carboxylate
  • 4-(4-Hydroxy-3-methoxyphenyl)-2-butanone
  • 3,7,11,15-Tetramethyl-1-hexadecen-3-ol
  • oxacycloheptadec-10-en-2-one
  • 3,7-dimethyl-1,6-octadien-3-yl 3-phenyl-2-propenoate
  • 2-Phenylethyl 2-hydroxybenzoate
  • Methyl 2,4-dihydroxy-3,6-dimethylbenzoate
  • 5-Hydroxy-2-benzyl-1,3-doxan
  • PARADISAMIDE


    Examples of odorants having an acceleration value between 100 and 900 include:
  • 3-phenyl butanal
  • 3,7-dimethyl-6-octenol
  • 2,6-dimethyl-7-octen-2-ol
  • 6-Butyl-2,4-dimethyldihydropyrane
  • 3,7-Dimethyl-2,6-octadienal
  • cyclohexyl ethyl acetate
  • 3a,4,5,6,7,7a-Hexahydro-5-methoxy-4,7-methano-1H-indene
  • methyl-2-octynoate
  • decanal
  • 3,7-Dimethyl-1-octen-7-ol
  • (Z)-1-(1-Methoxypropoxy)hex-3-ene
  • Nonen acid nitrile
  • (Z)-3,4,5,6,6-Pentamethylhept-3-en-2-one
  • 2-Butyl-4,4,6-trimethyl-1,3-dioxane
  • 2-Heptyltetrahydrofuran
  • hexyl butyrate
  • Ethyl octanoate
  • 2,2,5-Trimethyl-4-hexanal dimethyl acetal
  • tricyclodecenyl propionate
  • p-cresyl acetate
  • 2-propenyl heptanoate
  • 2-methyl-3-(4-methoxyphenyl)propanal
  • Exo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acetate
  • benzyl acetate
  • 2,6-dimethyl-2-octanol
  • 3,7-Dimethyl-2,6-octadien-1-thiol
  • Methyl 2-nonenoate
  • 4-Methyl-1-oxaspiro[5.5]undecan-4-ol
  • 2-Pentylcyclopentan-1-one
  • 3,7-Dimethyl-1,6-octadien-3-ol
  • ethyl acetoacetate
  • Decyl methyl ether
  • 1-Methyl-4-isopropenyl-6-cyclohexen-2-one
  • n-Hexyl 2-butenoate
  • 3,7-Dimethyl-1,6-octadien-3-ol acetate
  • p-Menth-1-en-8-yl acetate
  • 3,7-Dimethyloctan-3yl acetate
  • 2-Methyl-4-propyl-1,3-oxathiene
  • α,3,3-Trimethylcyclohexylmethyl acetate
  • α,3,3-Trimethylcyclohexylmethyl formate
  • 3-phenylpropanal
  • 1,3,3-Trimethylbicyclo(2,2,1)heptan-2-ol
  • 2-Pentyl-3-methyl-2-cyclopenten-1-one
  • 3,7-Dimethyl-6-octen-3-ol
  • o-t-butylyl-cyclohexyl acetate
  • 4-(1,1-Dimethylpropyl)cyclohexanone
  • Ethylacetoacetate ethylene glycol ketal
  • 3-Methylene-7-methyl-1-octen-7-yl acetate
  • 4-methylphenylacetaldehyde
  • 3,5,5-trimethylhexl acetate
  • 4-Methoxy-1-propenylbenzene (E)
  • p-Menthan-8-yl acetate
  • nonyl acetate
  • isolongifolene oxide
  • methyl-2-nonynoate
  • benzyl propionate
  • 4-methoxyacetophenone
  • 3,7-dimethyloctan-3-ol
  • 1,7,7-Trimethylbicyclo(2,2,1)heptan-2-ol
  • 3,7-Dimethyl-2-methylenocta-6-enal
  • phenylacetaldehyde dimethyl acetal
  • 1-Methyl-4-isopropyl-3-cyclohexan-1-ol
  • ethyl 2,6,6-trimethyl-1,3cycloheadiene-1-carboxylate
  • 2,4-Dimethyl-4-phenyltetrahydrofuran
  • Ethyl propanedioate
  • 2,6-dimethyl-7-octenyl-2-yl acetate
  • (Z)-3,7-Dimethylocta-2,6-dienenitrile
  • exo-1,7,7-Trimethylbicyclo(2,2,1)hept-2-ylpropionate
  • cis-3,7-Dimethyl-2,6-octadien-1-yl ethanoate
  • 3-Methyl-4-(2,6,6-trimethylcyclohex-1-enyl)out-3-en-2-one
  • 2-isopropenyl-5-methylhex-4-enyl acetate
  • 2,4-Dimethylcyclohexylmethyl acetate
  • 3,5-Dimethylcyclohex-3-ene-1-methyl acetate
  • VERDORACINE
  • 1-Phenylethyl propionate
  • 2,4-Demethylcyclohex-3-ene-1-methanol
  • p-isopropylbenzaldehyde,
  • undecanal
  • 2-ethylidene-6-isopropoxy-bicyclo[2.2.1] heptane
  • 3-Methyl-5-propyl-2-cyclohexan-1-one
  • 8,8-dimethyl-7-[1-methylethyl]-6,10-dioxaspiro[4,5]decane
  • 3,7-Dimethyl-1,6-octadien-3-yl propionate
  • 2-Methyldecanal
  • 1,1-Dimethoxy-2-phenylpropane
  • o-tertiary butyl cyclohexanol
  • VIOLET NITRILE CI (Q)
  • 4n-Butyl-4-hydroxybutyric acid lactone
  • CRESSANTHER
  • 3,7-dimethyl-6-octen-1-yl formate
  • 2-Phenylethyl acetate
  • 3,7-dimethyl-6-octen-1-yl acetate
  • 8,9-epoxy cedrane
  • p-isopropylcyclohexanol
  • 2,6-dimethyl-2-octanol
  • 4-isopropyl cyclohexanol
  • p-tert-Butylcyclohexl acetate
  • cis-6-nonenol
  • 5-Methyl-2-(1-methylethyl)cyclohexanol
  • γ-methylonone
  • Ethyl 2,4-dimethyldioxolane-2-acetate
  • 1-Methyl-4-isopropylcyclohexane-8-ol
  • JASMATONE
  • 3,7-Dimethyl-1-octen-7-ol
  • cis-3-hexenyl methylbutyrate
  • phenylethyl formate
  • trans-3,7-Dimethyl-2,6-octadien-1-yl acetate
  • 4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-3-buten-2-one
  • ROSSITOL
  • 2,4-dimethyl cyclohexane methanol
  • cis-8-Methyl-1-oxaspiro[4.5]decan-2-one
  • 2-Methylpent-2-en-1-oic acid
  • 1a,3a,6a)-2′,2′,3,7,7-Pentamethylspiro(biclo[4.1.0]heptane-2,5′-[1,3]dioxane
  • g-nonalactone
  • 10-undecenal
  • α-ionone
  • 1-methyl-1-methoxycyclododecane
  • 3,7-Dimethyl-1,6-octadien-3yl 2-methylpropanoate
  • 2,2,5-trimethyl-5-pentylcyclopentanone
  • CUMIN NITRILE
  • 4-Methoxybenzyl acetate
  • 3,7-Dimethyl-1,6-nonadien-3-ol
  • cis-2,6-Dimethyl-2,6-octadien-8-ol
  • spiro[furan-2(3H), 5′-(4,7-methano-5H-indene)], decahydro
  • ethyl safranate
  • 1-p-Menthen-8-ol, 1-Methyl-4-isopropyl-1-cyclohexen-8-ol
  • 5,9-Dimethyl-4,8-decadienal
  • benzyl-n-butyrate
  • (E)-3,7-Demethyl-2,6-octadienyl 2-methylcrotonate
  • 2-Methyl-3-phenyl-2-propanal
  • o-t-amyl-cyclohexanyl acetate
  • ROSYRANE SUPER
  • Octyl-2-methylpropanoate
  • dimethyl benzyl carbinyl acetate
  • 3-Methyl-1,4-octalactone
  • 2-Methyl-4-phenyl-2-butanol
  • 2,6-Nonadienol
  • isobutyl phenylacetate
  • (R-(E)-1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one
  • LEVISTAMEL
  • 3,7-dimethyl-1,6-nonadien-3yl acetate
  • 1-(2,4-Dimethyl-3-cyclohexenyl)-2,2-dimethylpropan-1-one
  • α,α-Dimethylphenethyl alcohol
  • (E)-1-2,4,4-Trimethyl-2-cyclohexen-1-yl)-2-buten-1-one
  • 1-(2,6,6-Trimethyl-1-cyclohexen-1-yl)pent-1-en-3-one
  • 2,4,6-Trimethyl-3-cyclohexene-1methanol
  • trans-3,7-Dimethyl-2,7-octadien-1-ol
  • 1,1-Diethoxy-3,7-dimethyl-2,6-octadiene
  • 1-Phenyl-4-penien-1-one
  • cedryl methyl ether
  • 1-Methyl-4-isopropanylcyclohexen-3-ol
  • phenylethyl isoamyl ether
  • 3-Methylene-7-methyl-1-octen-7-yl acetate
  • 6-ethylideneoctahydro-5,8-methano-2H-benznopyran
  • 3,7-Dimethyl-1-octanol
  • 3,7-Dimethyl-1,6-octadien-3-yl butyrate
  • 2-hexyl-2-cyclopenten-1-one
  • methoxycyclodecan
  • 1-Cyclohexylethyl-2-butenoate
  • 5,6-epoxy-2,6,10,10-tetramethyl bicyclo[7,2,0]undecane
  • Tetrahydro-4-methyl-2phenyl-2H-pyran
  • acetaldehyde ethyl phenylethyl acetal
  • trans-3,7-Dimethyl-2,6-octadien-1-yl propionate
  • 6,10-dimethyl-5,9-undecadien-2-one
  • 6-Methyl-2-(4-methylcyclohex-3-enyl)hept-1,5-diene
  • 3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-one isomers
  • 2-ethoxy-9methylen-2,6,6-trimethylbicyclo[3,3,1]nonane
  • Tetrahydro-4-methyl-2-propyl-2H pyran-4-yl acetate
  • trans-3,7-Dimethyl-2,6-octadien-1-yl isobutyrate
  • p-Methyltetrahydroquinoline
  • decahydro-b-naphtyl acetate
  • dodecanal
  • 1-phenylethyl alcohol
  • (E)-7,11-Dimethyl-3-methylenedodeca-1,6,10-diene
  • 3-(isopropylphenyl)butanal
  • ethyl-2-ethyl-6,6-dimethyl-2-cyclohexene
  • 3,7-dimethyl-2(3), 6-nonadienenitrile
  • 6-methyl-β-ionone
  • 7-methoxy-3,7-dimethyloctanal
  • (Z)-1-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-2-buten-1-one
  • Allyl (3-methylbutoxy)acetate
  • 4-(2,5,6,6-Tetramethyl-2-cyclohexen-1-yl)-3-buten-2-one
  • 3-Methyl-2-butenyl benzoate
  • 3-(4-ethyl(phenyl)-2,2-dimethylpropanal
  • 3,5,6,6-Tetramethyl-4-methyleneheptan-2-ol
  • δ-1-(2,6,6-Trimethyl-3-cyclohexen-1-yl)-2-buten-1-one
  • ethyl tricyclo [5.2.1.02.6] decan-2-carboxylate
  • α-1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-2-buten-1-one
  • 9-decenol
  • UNDECENE 2 NITRILE
  • Ethyl 2-nonynoate
  • 3,4,4a,5,8,8a-Hexahydro-3′,7-dimethylspiro[1,4-methanonaphthalene-2-(1H), 2′-oxirane]
  • MARENIL
  • Ethyl 2,3-epoxy-3-methyl-3-phenylpropionate
  • 3,6-Dihydro-2,4-dimethyl-6-phenyl-2H-pyran
  • cis-trans-2-Methyl-2-vinyl-5(2-hydroxy-2-propyl)tetrahydrofuran
  • 4-methyl-3decenn-5-ol
  • Octahydro-4,7-methano-1H-indene-5-yl acetate
  • 2-Methylundecanal
  • 2-heptyl cyclopentanone
  • HERBANATE
  • 6-sec-Butylquinoine
  • allyl cyclohexyloxyacetate
  • 5-phenyl-5-methyl-3-hexanone
  • DISPIRONE
  • BOURGEONAL
  • 3,7-Dimethyl-6-octen-1-yl propanoate
  • phenylethyl isobutyrate
  • 1,2,3,4,5,6,7,8-Octahydro-8,8-dimethyl-2-naphthaldehyde
  • 1-(5,5-Dimethyl-1cyclohexen-1-yl)pent-4-en-1-one
  • Methyl 2-hydroxybenzoate
  • ELINTAAL Forte
  • allyl cyclohexyl propionate
  • 3,7-Dimethyl-6-octen-1-yl 2-methylpropanoate
  • INDOCLEAR
  • AZARBRE
  • 2-Phenoxyethyl propionate;
  • Ethyl 2-methoxybenzoate
  • 3-Phenyl-2-propanal
  • 2,2-Dimethyl-3-(p-ethylphenylpropanal
  • 2,7-Dimethyl-10-(1-methylethyl)-1-oxaspiro[4,5]deca-3,6-diene
  • 1,3,4,6,7,8a-1,1,5,5-tetramethyl-2H-2,4a-methanonaphthalen-8)5H)-one
  • 5-methyl-3-heptanone oxime
  • cis-3-hexenyl benzoate
  • 2,3,4,5,6,7,8-Octahydro-8,8-dimethyl-2-naphthaldehyde
  • 5-Hydroxyundecanoic acid lactone
  • 4-methoxybenzaldehyde
  • 4-methyl-3-decen-5-ol
  • 4-n-Hexyl-4-hydroxybutanoic acid lactone
  • Allyl (2-methylbutoxy)acetate
  • p-Mentha-8-thio-3-one
  • dodecahydro-3a,6,6,9a-tetramethylnaphto(2,1-b)-furan
  • 5-methyl-3-heptanone oxime
  • 4-(1-ethoxyvinyl)-3,5,5,5-tetramethylcyclo-hexanone
  • 2-(4-tert-Butylbenzyl)propionaldehyde
  • Cyclohexyl lactone
  • decanol
  • 1-(2,6,6-Trimethylcyclohexa-1,3-denyl)-2-buten-1-one
  • 2-methyl-3-(4-isopropylphenyl)propanal
  • 1-(4-ISOPROPYLCYCLOHEXYL)-ETHANOL


Odorant's Hedonic Contributions

It is also important to construct the fragrance with a balanced olfactive intensity in order not to overwhelm the consumer or to be aesthetically unappealing. Constructing each segment for the targeted application or intended effect must be based on balanced impact in accordance to odor detection threshold values (ODT) while at the same time answering to certain physico-kinetic rules to give a well-rounded experience to the consumer.


Upon their release in headspace, odorants are detected based on their odor detection threshold values. Odor detection thresholds are defined as the lowest concentration of odorants in a selected medium (air or water) to be detected. By including odor values of odorants in the model, one can further improve on the values for predicted performance of once odorants are released from the partition into the air.


Various databases for experimental odor detection threshold values in various partitions such as water and air are available. See Compilation of Odor and Taste Threshold Values Data, American Society for Testing and Materials, F. A. Fazzalari Editor; Booleans Aroma Chemical Information Service (BACIS)).


In order to create a linear citrus fragrance upon dilution, the authors further hedonically define each kinetic “water release group” based on the odor detection threshold values and concentration of its composing odorants along with their odor descriptors as defined by a panel of expert perfumers. Once the odorants are grouped in a “water release group” based on their Ω values, their hedonic contribution is estimated using the following equation:










Odor





Impact

=


Parts





in





formula


O





D





T






[
5
]







Within each water release group, the odor contributions for each composing odorant are then added to calculate the overall odor contribution of each “water release group”. This not only provides the person skilled in the art with the capability of estimating the odor intensity of each “water release group” but also the hedonic bloom contribution of each odorant within the “water release group”. A simple percentage calculation can then be performed to obtain the percent contribution of each odorant within the “water release group” as shown below:











(

%





odor





contribution

)

odorant

=



(

Odor





Impact

)

odorant



(

Total





Odor





Impact

)


water





release





group







[
6
]







Odorants are described according to a classification given by a panel of expert perfumers. The odorants composing each water release group is defined hedonically according to two descriptors given by the panelists. For example, odorants are defined as green if either one of the two descriptors contains a “green” or “grass” definition as shown below:
















Odor Descriptor 1
Odor Descriptor 2









Green
Cucumber



Green
Cuminic



Green
Earthy



Green
Fatty/Greasy



Green
Floral



Green
Fruity



Green
Citrus



Green
Hay



Green
Herbal



Green
Honeysuckle



Green
Hyacinth



Green
Lavender



Green
Leaf



Green
Lilac



Green
Metallic



Green
Mushroom



Green
Musty



Green
Narcissus



Green
Nutty



Green
Pine



Green
Rose



Green
Violet



Grass
Green



Grass
Fruity



Grass
Violet



Grass
Green



Grass
Fruity



Aldehydic
Green



Amber/Woody
Green



Aniseed
Green



Apple
Green



Balsamic
Green



Blackcurrant
Green



Citrus
Green



Earthy
Green



Tropical
Green



Fruity
Green



Galbanum
Green



Hyacinth
Green



Jamin
Green



Leather
Green



Marine
Green



Mimosa
Green



Muguet
Green



Mushroom
Green



Narcissus
Green



Pine
Green



Rose
Green



Sandalwood
Green



Tuberose
Green



Violet
Green



Woody
Green










Odorants are described as either citrus, floral, fruity or green based on odor definitions in contained in either Descriptor 1 or Descriptor 2 but more preferably, based on attributes found in Descriptor 1.







APPLIED PERFUME EXAMPLES

As an illustration, linear citrus fragrances for rinse-off were designed according to the rationale described in the invention to fit the application needs of three different wash-off categories: dish-washing and surface cleaners, body wash and shampoos, conditioners, and finally laundry detergents.


Examples of perfumes engineered for linear citrus, citrus/fruity, citrus/floral and citrus/green release during rinse-off are shown in the following examples.


I. Linear Citrus

The following general examples are to illustrate linear citrus release during rinse-off conditions.


A. Dish Washing and Surface Cleaners

The fragrance designed for these types of application are intended to give a superior impact to the consumer whilst avoiding any hedonics or streak residual on the targeted cleaned surface. One can design a pleasant and full experience for the user of the market product with the engineered perfume while at the same time minimizing substantivity.


Formulations for these types of household and/or industrial applications must contain perfumes that answer to the following criteria: at least 20%, preferably at least 30% of the odorant constituents must have γ values characteristic of flash release in aqueous dilutions, as described above (γ≧900).


In addition to the required content of flash release odorants mentioned above, the percentage of delayed release (or deposition) odorants must not exceed 30%, preferably not exceed 15% of the perfume's total content.


In order to have an impactful citrus released background, at least three, preferably four of the water release groups constructed based on odorants' Ω values must have at least 30%, preferably at least 40% of their overall odor contributed by one or more citrus odorants.


As an illustrative example, a fragrance (“Flash Release Type Citrus”) was designed to give maximum linear citrus impact during rinse-off with minimal deposition on targeted surface. The perfume is shown below:









TABLE 9







Flash Release Type Citrus


















Odor
% Odor



parts
γ
Ω
ODT (ppb)
Descriptor
Contribution

















Water Release Group 1








d-LIMONINE
50.00
8200.7592
586.22897
430
CITRUS
99.40


ETHYL 2-METHYL BUTYRATE
0.30
14512.2887
21.185694
20
APPLE
0.60


total parts
50.30



% Citrus Odor
99.40


Water Release Group 2


HEXYL ACETATE
0.90
3115.7849
1.3050809
950
FRUITY
2.18


DIHYDROMYRCENOL
20.00
844.4125
0.2646234
810
CITRUS
56.73


CIS-3-HEXENYL ACETATE
0.90
1364.2710
0.1522188
170
GREEN
12.16


ETHYL ACETOACETATE
0.50
840.3492
0.1081678
54
APPLE
21.27


CIS-3-HEXEN-1-OL
0.30
1589.1101
0.0789638
90
GREEN
7.66


total parts
22.60



% Citrus Odor
56.73


Water Release Group 3


CITRONELLYL NITRILE
1.40
913.0422
0.0881181
71
CITRUS
17.38


APPLINAL
1.40
554.7882
0.0485108
55
APPLE
22.43


TETRAHYDROLINALOOL
5.40
503.4877
0.0151079
380
FLORAL
12.52


ROSSITOL
2.90
303.8040
0.0182541
440
CITRUS
5.81


ETHYL LINALOOL
5.70
275.6310
0.0121484
120
CITRUS
41.88


total parts
16.80



% Citrus Odor
65.04


Water Release Group 4


OXANE
0.06
810.1552
0.0019673
58
CITRUS
0.48


GARDAMIDE
5.00
88.4744
0.0019517
24
CITRUS
94.48


ALLYL CYCLOHXYL PROPIONATE
0.90
126.7982
0.0008514
81
FRUITY
5.04


total parts
5.96



% Citrus Odor
94.96


Water Release Group 5


MEFRANAL
0.30
84.7562
0.0000885
17
CITRUS
100.00


total parts
0.30



% Citrus Odor
100.00


Water Release Group 6


METHYL DIHYDRO JASMONATE
1.60
8.3984
0.00000381
0.23
FLORAL
95.82


EBANOL
0.14
15.5977
0.00000108
54
SANDALWOOD
0.04


CIS-3-HEXENYL SALICYLATE
0.60
2.8507
0.00000015
1.9
GREEN
4.34


total parts
2.34



% Citrus Odor
0.00


DIPROPYLENE GLYCOL
1.70


total perfume parts
100.00









The odor profile of each water release group is expressed in percentage contribution according to odor type. This kinetic odor progression of the perfume in rinse-off conditions is shown in FIG. 1.


The perfume odorants determined by the inventors to result in flash release in water dilutions are: d-limonene, ethyl 2-methylbutyrate, hexyl acetate, cis-3-hexenol, cis-3-hexenyl acetate, and citronellyl nitrile. The fragrance odorants' physico-kinetics properties are as follow:












TABLE 10







parts
γ


















Flash Release Odorants




ETHYL 2-METHYL BUTYRATE
0.30
14612.2887


d-LIMONENE
50.00
8200.7592


HEXYL ACETATE
0.90
3118.7849


CIS-3-HEXEN-1-OL
0.30
1569.1101


CIS-3-HEXENYL ACETATE
0.90
1384.2710


CITRONELLYL NITRILE
1.40
913.0422


total
53.80


Sustained Release Odorants


DIHYDROMYRCENOL
20.00
644.4128


ETHYL ACETOACETATE
0.50
640.3492


OXANE
0.06
610.1552


APPLINAL
1.40
554.7882


TETRAHYDOLINALOOL
5.40
503.4877


ROSSITOL
2.90
303.8040


ETHYL LINALOOL
5.70
275.6310


ALLYL CYCLOHEXYL PROPIONATE
0.90
126.7982


total
36.86


Delayed Release Odorants


MEFRANAL
0.30
84.7562


GARDAMIDE
5.00
66.4744


EBANOL
0.14
15.5977


METHYL DIHYDRO JASMONATE
1.60
8.3964


CIS-3-HEXENYL SALICYLATE
0.60
2.8007


total
7.64


DIPROPYLENE GLYCOL
1.70


total perfume parts
100.00









These flash release odorants and the deposition odorants (also referred to as delayed release odorants) are calculated to make up respectively 54% and 8% of the total perfume.


The above perfume (Flash Release Citrus Type) provides a released citrus linear hedonic impact in use while also leaving a minimum amount of residual fragrance or streaks upon completing the cycle or the cleaning experience.


B. Body-Wash, Soap, Shampoo and Conditioners

It is important to establish that a perfume during a wash off experience in household, cosmetic and industrial applications such as body wash, shampoo, conditioners etc. must provide a well rounded, impactful hedonic experience that will last throughout the entire rinsing process. In most instances, the performance attributes of the product are largely dependent on the impact, intensity and overall hedonic quality of its perfume in use. For instance, consumers often base their liking of the product to a diffuser-type of fragrance release in use. In other words, a long sustained perfume residence profile during and after use in an enclosed are (bathroom, shower room etc.).


Residence time of the chosen odorants within the perfume formula must therefore be optimally based on their acceleration γ values out of the water partition. Since γ is derived partly based on the vapor pressure and the diffusion coefficients in water as well as in the vapor phase, it is an indication of the residence time of odorants.


Grouping odorants in a perfume according to their mass correlated water release values and optimizing specific release groups will serve to result in a longer residence time in headspace and a more rounded hedonic experience for the user during the wash-off.


Rinse-off experience of wash-off systems such as shampoo, conditioners, body wash etc. should provide the consumer with a sustained hedonic release.


Perfumes for wash-off systems such as shampoos, conditioners and body-wash lotions and gels must have at least 30%, preferably at least 40% of the total perfume with γ values between 900 and 100, as defined earlier within this patent.


In addition, linear citrus release can be engineered based on odorants' odor detection threshold values and concentration within a perfume. Using methods described earlier, at least three, preferably four release groups defined by Ω values of their composing odorants must have an overall citrus odor value of at least 30%, preferably 40% of the overall release group odor from one or more odorants within the release group.


Below in Table 11 is an illustrative example (“Citrus Sustained Release-Type”) of a fragrance engineered for sustained release of a citrus note in high water dilutions.









TABLE 11







Citrus Sustained Release Type Fragrance


















Odor
% Odor



Parts
γ
Ω
odt
Descriptor
Contribution

















Water Release Group 1








d-LIMONINE
12.00
8200.7592
154.881433937
430.00
CITRUS
85.04


ETHYL 2-METHYL BUTYRATE
0.30
12827.5826
18.784383082
20.00
FRUITY
34.98







% Citrus Odor
65.04


Water Release Group 2


LIGUSTRAL
4.90
1704.6486
1.537120485
110.00
GREEN
7.01


DIHYDROMYRCENOL
25.00
865.6450
1.538238177
819.00
CITRUS
4.85


HEXYL ACETATE
0.50
3118.7849
1.305060933
550.00
FRUITY
0.15


CITRONELLAL
5.00
1345.8902
0.838905732
33.00
CITRUS
23.84


CITRONELLOL
5.00
865.5602
0.289877934
29.00
FLORAL
27.12


CIS-3-HEXENYL ACETATE
0.90
1384.2710
0.182218814
170.00
GREEN
0.83


CITRAL
2.50
857.0901
0.133615808
12.00
CITRUS
32.77


TETRAHYDROLINALOOL
7.00
503.4877
0.117505958
380.00
FLORAL
2.96


CIS-3-HEXEN-1-OL
0.30
1569.1101
0.075983597
90.00
CITRUS
0.52







% Citrus Odor
81.99


Water Release Group 3


CITRONELLYL NITRILE
1.40
913.0422
0.065115111
71.00
CITRUS
19.46


ROSSITOL
10.00
303.8040
0.083048652
440.00
CITRUS
22.45


APPLINAL
1.40
554.7882
0.048510807
55.00
FRUITY
25.14


RHUBAFURAN
1.50
475.0599
0.025835530
440.00
CITRUS/GREEN
3.37


ETHYL ACETOACETATE
0.50
540.3492
0.023075908
55.00
FRUITY
8.98


ETHYL LINALOOL
2.50
275.6310
0.010472748
120.00
CITRUS
20.58







% Citrus Odor
85.58


Water Release Group 4


OXANE
0.08
510.1652
0.001957274
58.00
CITRUS
0.49


GARDAMIDE
5.00
65.4744
0.001051679
24.00
CITRUS
94.48


ALLYL CYCLOHXYL PROPIONATE
0.90
128.7982
0.000851449
81.00
FRUITY
5.04







% Citrus Odor
94.96


Water Release Group 5


MEFRANAL
1.50
84.7562
0.000443184
17.00
CITRUS
100.00







% Citrus Odor
100.00


Water Release Group 6


METHYL DIHYDRO JASMONATE
5.00
8.3964
0.000012010
0.23
FLORAL
90.17


CIS-3-HEXENYL SALICYLATE
4.50
2.5007
0.000001122
1.90
FLORAL
9.52


EBANOL
0.14
15.5977
0.000001077
54.00
SANDALWOOD
0.81







% Citrus Odor
0.00


DIPROPYLENE GLYCOL
1.80


total perfume parts
100.00









The odor profile of each water release group is expressed in percentage contribution according to odor type. This kinetic odor progression of the perfume in rinse-off conditions is shown in FIG. 2


The perfume odorants determined by the inventors to result in sustained release in water dilutions are: citronellol, dihydromyrcenol, citral, ethyl acetoacetate, oxane, applinal, tetrahydrolinalool, rhubafuran, rossitol, ethyl linalool, allyl cyclohexyl propionate. The physico-kinetic properties of the perfume composing odorants are as follow:












TABLE 12







parts
γ


















Flash Release Odorants




ETHYL 2-METHYL BUTYRATE
0.30
12827.5626


d-LIMONENE
12.00
8200.7592


HEXYL ACETATE
0.90
3118.7849


LIGUSTRAL
4.90
1704.6486


CIS-3-HEXEN-1-OL
0.30
1569.1101


CIS-3-HEXENYL ACETATE
0.90
1384.2710


CITRONELLAL
5.00
1345.0902


CITRONELLYL NITRILE
1.40
913.0422


Total
25.70


Sustained Release Odorants


CITRONELLOL
5.00
866.5602


DIHYDROMYRCENOL
25.00
866.5450


CITRAL
2.50
857.0901


ETHYL ACETOACETATE
0.50
640.3492


OXANE
0.06
610.1552


APPLINAL
1.40
554.7882


TETRAHYDOLINALOOL
7.00
503.4877


RHUBAFURAN
1.50
476.0599


ROSSITOL
10.00
303.6040


ETHYL LINALOOL
2.50
275.6310


ALLYL CYCLOHEXYL PROPIONATE
0.90
126.7982


Total
56.36


Delayed Release Odorants


MEFRANAL
1.50
84.7562


GARDAMIDE
5.00
66.4744


EBANOL
0.14
15.5977


METHYL DIHYDRO JASMONATE
5.00
8.3964


CIS-3-HEXENYL SALICYLATE
4.50
2.8007


Total
16.14


DIPROPYLENE GLYCOL
1.80


total perfume parts
100.00









The above perfume provides a linear sustained release citrus hedonic impact during the process of rinse-off in formulations such as shampoo, conditioners and body wash amongst others.


C. Laundry Products

At the end of a typical wash cycle, perfume deposition is often minimal due to the relative solubility and water-release values of a number of odorants making up a typical perfume in addition to the large amount of water used during a typical household wash cycle whether automated or manual. It is therefore important to engineer fragrances with maximum deposition on woven and non-woven surfaces for obvious commercial and environmental reasons when considering these types of household and industrial applications.


Furthermore, many parts of the world still rely on hand-washing of laundry rather than using automated appliances as often found in Western countries. It is therefore important to provide the consumer with an agreeable impactful hedonic experience during the wash-off whilst also resulting with a significant amount of fragrance deposition on the woven and non-woven surfaces at the end of the process.


Since water release values are derived based on activity and water diffusion coefficients of odorants in water, as well as partition energies of these odorants for polar and non polar partitions, vapor pressure etc., it is possible to predict quantitatively the substantivity of the individual odorants considered in the perfume in water.


Based on the Ω values of odorants and their subsequent grouping in various release groups as shown in methods above, this invention provides a person skilled in the art with the possibility to engineer the release of a citrus hedonic note or perfumes to be perceived by the consumer during a manual or automated laundry cycle. In addition to a linear release of a citrus hedonic note, the method mentioned in this invention will allow a significant amount of fragrance to be deposited on the woven and non-woven surfaces upon completion of the wash cycle. In addition, fragrances designed according to methods described herein for laundry applications will limit unnecessary environmental waste of perfumes.


Perfumes intended for maximum deposition in wash-off systems must have at least 40% and preferably at least 50% of the total perfume with delayed release type of odorants (depositors) as defined in the herein invention.


In addition to criteria for maximum deposition of perfume defined above, at least three, preferably four of the water release groups constructed based on odorants' Ω values must have at least 30%, preferably at least 40% of their overall odor contributed by one or more citrus odorants. These fragrances will therefore also provide the consumer with a perception of linear sustained citrus perfume throughout the process of rinse-off.


A perfume (Deposition/Linear Release Citrus Perfume) for laundry detergents designed to provide maximum deposition of fragrance as well as a linear release of a citrus note during the process of rinse-off is shown below in Table 13.














TABLE 13








Parts
γ
φ
φ · γ
Ω





Water Release Group 1


d-LIMONINE
3.50
8200.7592
0.001571820
12.896119495
45.115418232


ETHYL 2-METHYL BUTYRATE
0.25
12027.5828
0.004361536
55.947878874
13.958569218


Water Release Group 2


HEXYL ACETATE
1.48
3118.7849
0.000454948
1.450067703
2.140498258


LIGUSTRAL
0.82
1704.6488
0.000195997
0.334108221
0.273992309


DIHYDROMYRCENOL
3.28
886.5450
0.000073316
0.083531527
0.208402502


CITRONELLAL
0.62
1345.0902
0.000124439
0.187331348
0.137285332


CITRONELLOL
1.23
888.5802
0.000066703
0.057935587
0.171287328


Water Release Group 3


ALDEHYDE C11
4.10
420.7513
0.000026178
0.011014407
0.045183224


CIS-3-HEXENYL ACETATE
0.25
1384.2710
0.000130208
0.180243127
0.044343889


RHUBAFURAN
2.46
476.0589
0.000037580
0.017890353
0.044014318


TETRAHYDROLINALOOL
2.46
503.4877
0.000033341
0.018788566
0.041298751


CITRONELLYL NITRILE
0.82
913.8422
0.000053290
0.048655794
0.039901422


ROSSITOL
4.10
303.8040
0.000020753
0.005304865
0.025852326


CIS-3-HEXEN-1-OL
0.08
1569.1101
0.000163540
0.258611990
0.021044119


ETHYL ACETOACETATE
0.25
640.3492
0.000072026
0.048159815
0.011358369


ETHYL LINALOOL
2.46
275.8310
0.000015196
0.004189096
0.010306130


ALLYL CYCLOHEXYL PROPIONATE
9.02
126.7962
0.000007481
0.000946055
0.006534198


APPLINAL
0.25
554.7832
0.000052457
0.034850577
0.008524626


Water Release Group 4


MEFRANAL
12.30
84.7562
0.000003468
0.000295458
0.003834447


GARDAMIDE
16.40
86.4744
0.000003164
0.000210338
0.003449823


OXANE
0.10
810.1562
0.000053737
0.032787903
0.003228827


MANDARIN ALDEHYDE
8.20
90.2674
0.000003454
0.000311846
0.002557369


CITRAL
0.03
857.0801
0.000062358
0.053448322
0.001753201


EMPETAL
2.48
95.5058
0.000004462
0.000433836
0.001057335


Water Release Group 5


LAURONITRILE
4.10
52.2181
0.000001569
0.000081912
0.000135870


Water Release Group 6


METHYL DIHYDRO JASMONATE
8.20
3.3054
0.000000285
0.000002402
0.000015850


PARADISAMIDE
2.90
7.7893
0.000000242
0.000001880
0.000005453


EBANOL
0.30
15.5977
0.000000492
0.000007590
0.000002505


CIS-3-HEXENYL SALICYLATE
7.38
2.8007
0.000000068
0.000006248
0.000001841



100.00

















Odor
% Odor




odt
Descriptor
Contribution







Water Release Group 1



d-LIMONINE
430.00
CITRUS
39.44



ETHYL 2-METHYL BUTYRATE
20.00
FRUITY
80.58





% Citrus Odor
39.44



Water Release Group 2



HEXYL ACETATE
950.00
FRUITY
1.93



LIGUSTRAL
110.00
GREEN
9.26



DIHYDROMYRCENOL
810.00
CITRUS
5.04



CITRONELLAL
33.00
CITRUS
30.54



CITRONELLOL
29.00
FLORAL
52.01





% Citrus Odor
36.98



Water Release Group 3



ALDEHYDE C11
7.70
CITRUS
75.15



CIS-3-HEXENYL ACETATE
170.00
GREEN
0.20



RHUBAFURAN
440.00
CITRUS
0.79



TETRAHYDROLINALOOL
380.00
FLORAL
0.91



CITRONELLYL NITRILE
71.00
CITRUS
1.83



ROSSITOL
440.00
CITRUS
1.52



CIS-3-HEXEN-1-OL
90.00
GREEN
0.13



ETHYL ACETOACETATE
55.00
FRUITY
0.63



ETHYL LINALOOL
120.00
CITRUS
2.85



ALLYL CYCLOHEXYL PROPIONATE
61.00
FRUITY
15.72



APPLINAL
55.00
FRUITY
0.83





% Citrus Odor
81.77



Water Release Group 4



MEFRANAL
17.00
CITRUS
10.43



GARDAMIDE
24.00
CITRUS
9.90



OXANE
58.00
CITRUS
0.03



MANDARIN ALDEHYDE
1.50
CITRUS
79.18



CITRAL
12.00
CITRUS
0.04



EMPETAL
6.00
CITRUS
0.40





% Citrus Odor
100.00



Water Release Group 5



LAURONITRILE
6.70
CITRUS
100.00





% Citrus Odor
100.00



Water Release Group 6



METHYL DIHYDRO JASMONATE
0.23
FLORAL
80.34



PARADISAMIDE
0.80
CITRUS
10.89



EBANOL
54.00
SANDALWOOD
0.01



CIS-3-HEXENYL SALICYLATE
1.80
FLORAL
8.75





% Citrus Odor
10.89










The odor profile of each water release group is expressed in percentage contribution according to odor type. This kinetic odor progression of the perfume in rinse-off conditions is shown in FIG. 3:


A total of 62% of the above perfume is composed of delayed-release odorants (also equivalent to surface depositing odorants) in high water dilutions as calculated using these odorants' γ values. These delayed release odorants are: empetal, mandarin aldehyde, mefranal, gardamide, lauronitrile, ebanol, methyl dihydro jasmonate, paradisamide and cis-3-hexenyl salicylate.


The perfume's odorants' physico-kinetic properties are shown below in table 14:
















parts
γ


















Flash release Odorants




ETHYL 2-METHYL BUTYRATE
0.49
12827.5626


d-LIMONENE
3.28
8200.7592


HEXYL ACETATE
1.48
3118.7849


LIGUSTRAL
0.82
1704.6486


CIS-3-HEXEN-1-OL
0.08
1589.1101


CIS-3-HEXENYL ACETATE
0.25
1384.2710


CITRONELLAL
0.82
1345.0902


CITRONELLYL NITRILE
0.82
913.0422


total
8.04


Sustained Release Odorants


CITRONELLOL
1.23
868.5602


DIHYDROMYRCENOL
3.28
866.5450


CITRAL
0.03
857.0901


ETHYL ACETOACETATE
0.25
640.3492


OXANE
0.10
610.1552


APPLINAL
0.25
544.7882


TETRAHYDOLINALOOL
2.46
503.4877


RHUBAFURAN
2.46
476.0599


ALDEHYDE C11
4.10
420.7513


ROSSITOL
4.10
303.8040


ETHYL LINALOOL
2.46
275.6310


ALLYL CYCLOHEXYL PROPIONATE
9.02
126.7982


total
29.74


Delayed Release Odorants


EMPETAL
2.46
96.8058


MANDARIN ALDEHYDE
8.20
90.2874


MEFRANAL
12.30
64.7562


GARDAMIDE
16.40
66.4744


LAURONITRILE
4.10
52.2161


EBANOL
0.23
15.5977


METHYL DIHYDRO JASMONATE
8.20
8.3964


PARADISAMIDE
2.95
7.7693


CIS-3-HEXENYL SALICYLATE
7.38
2.8007


total
62.23









The above description is for the purposes of teaching the person of ordinary skill in the art how to practice the present invention, and it is not intended to detail all those obvious modifications and variations of it which will become apparent to the skilled worker upon reading the description.


The next examples are to illustrate perfumes intended to result in a impactful, prominent linear citrus odor during the process of rinse-off while also introducing linear release of a less dominating nuance of either one of the following hedonic groups: fruit, floral and green.


Citrus-Green Release Perfumes

As an illustration, a citrus-green type fragrance was designed according to the rationale described in the invention to fit the application needs of three different wash-off categories: dish-washing and surface cleaners, body wash and shampoos, conditioners, and finally laundry detergents. The perfume is intended to result in a linear release of a citrus and/or green odor during rinse-off conditions.


A. Dish Washing and Surface Cleaners

The fragrance designed for these types of application are intended to give a superior impact to the consumer whilst avoiding any hedonics or streak residual on the targeted cleaned surface. One can design a pleasant and full experience for the user of the market product with the engineered perfume while at the same time minimizing substantivity. Fragrances for this type of application are based on the physico-chemical rationale used in the preceding illustrative example: at least 30%, preferably at least 40% of the total perfume with y values between 900 and 100 coupled with the percentage of delayed release (or deposition) odorants must not exceed 30%, preferably not exceed 15% of the perfume's total content


In order to have an impactful citrus perfume released predominantly, at least three, preferably four of the water release groups constructed based on odorants' Ω values must have at least 30%, preferably at least 40% of their overall odor contributed by one or more citrus odorants.


In addition a linear release of a secondary green nuance along with the predominant citrus release may be built by having at least three, preferably four of the water release groups constructed based on odorants' Ω values must have at least 20%, of their overall odor contributed by one or more green odorants.


As an illustrative example, a flash release fragrance (“Flash Release Citrus-Cucumber”) was designed to give maximum linear citrus impact with a linear cucumber nuance during rinse-off with minimal deposition on targeted surface. The perfume is shown below in table 15. Odorants are grouped in water release groups according to their water release values. They are further characterized based on their odor descriptors and subsequently their contribution to each of the release groups' total odor.









TABLE 15





“Flash Release Type Citrus - Cucumber”






















Odor
Odor





Parts
Descriptor 1
Descriptor 2
γ
φ





Water Release Group 1


d-LIMONINE
42.2500
CITRUS
ORANGE
8200.75
0.001571820


Water Release Group 2


STRALLYL ACETATE
1.5000
GREEN
FRUITY
2576.59
0.000383964


DIHYDRO MYRCENOL
15.0000
CITRUS
METALLIC
868.55
0.000073318


MELONAL
0.5000
GREEN
ALDEHYDIC
2555.52
0.000309918


LIGUSTRAL
0.7700
GREEN
LEAF
1764.55
0.000196597


CITRONELLAL
1.5000
CITRUS
CITRONELLA
1345.08
0.000124439


CITRONELLYL NITRILE
4.5000
CITRUS
NITRILE
913.04
0.000053290


CIS 3 HEXENYL ACETATE
0.5000
GRASS
FRUITY
1384.27
0.000138208


LINALOOL
2.5000
LINALOOL

644.41
0.000047749


ALDEHYDE C 8 (OCTANAL)
0.0450
ALDEHYDIC
CITRUS
3630.08
0.000455096


ALDEHYDE C 10 (DECANAL)
1.4300
ALDEHYDIC
ORANGE
818.28
0.000080573


Water Release Group 3


RHUBAFURAN
3.0000
GREEN
GRAPEFRUIT
475.05
0.000037580


ETHYL LINALOOL
5.7000
CITRUS
FLORAL
275.53
0.000015198


ROSSITOL
3.0000
NUGUET
CITRUS
303.80
0.000020753


CIS 3 HEXENOL
0.0500
GRASS
GREEN
1569.11
0.000183540


METHYL OCTINE CARBONATE
0.4000
GREEN
VIOLET
525.10
0.000036464


Water Release Group 4


TRANS 2 CIS 6 NONADENOL
0.4500
GREEN
CUCUMBER
245.87
0.000012085


GARDAMIDE
5.0000
CITRUS
WOODY
86.47
0.000002154


UNDECAVERTOL
1.5000
GREEN
FRUITY
118.38
0.000004491


ALDEHYDE C12 (DODECANAL)
0.4000
ALDEHYDIC
FATTY/GREASY
183.88
0.000008217


Water Release Group 5


CIS 4 DECENAL
0.0043
ALDEHYDIC
CARDAMOM
1078.65
0.000090457


TRANS 2 CIS 6 NONADENAL
0.0040
GREEN
CUCUMBER
1010.87
0.000075353


MEFRANAL
0.4000
ALDEHYDIC
CITRUS
87.76
0.000003486


CITRATHAL
1.5000
LIME
CITRUS
39.32
0.000001915


Water Release Group 6


PARADISAMIDE
7.0000
CITRUS
FRUITY
7.77
0.000000242


TRIDECEN 2 NITRILE
0.5000
NITRILE
CITRUS
6.43
0.000000137


CIS-3-HEXENYL SALICYLATE
0.5000
GRASS
SALICYLATE
2.30
0.000000069


Perfume Total
100.0033


















% Odor




Ω
odt
Contribution







Water Release Group 1



d-LIMONINE
544.607548652
430
100.00





% Citrus
100.00





% Green
0.00



Water Release Group 2



STRALLYL ACETATE
1.483977879
110
1.54



DIHYDRO MYRCENOL
0.952972906
810
2.22



MELONAL
0.411493829
1.5
40.04



LIGUSTRAL
0.257251791
110
0.84



CITRONELLAL
0.251072029
33
5.46



CITRONELLYL NITRILE
0.215951073
71
7.81



CIS 3 HEXENYL ACETATE
0.090121564
170
0.36



LINALOOL
0.076925400
20
15.02



ALDEHYDE C 8 (OCTANAL)
0.074341612
4.8
1.18



ALDEHYDE C 10 (DECANAL)
0.070875843
8.7
25.84





% Citrus
42.11





% Green
42.52



Water Release Group 3



RHUBAFURAN
0.053871058
440
8.82



ETHYL LINALOOL
0.023577881
120
48.16



ROSSITOL
0.018914598
440
8.82



CIS 3 HEXENOL
0.012830600
90
0.54



METHYL OCTINE CARBONATE
0.007658962
9.7
40.08





% Citrus
52.77





% Green
47.23



Water Release Group 4



TRANS 2 CIS 6 NONADENOL
0.001327108
1.5
50.89



GARDAMIDE
0.001051879
24
35.34



UNDECAVERTOL
0.000784043
28
9.79



ALDEHYDE C12 (DODECANAL)
0.000677932
17
3.99





% Citrus
35.34





% Green
60.67



Water Release Group 5



CIS 4 DECENAL
0.000418780
3.1
0.42



TRANS 2 CIS 6 NONADENAL
0.000304629
0.2
8.10



MEFRANAL
0.000118183
17
7.16



CITRATHAL
0.000115109
5.3
88.30





% Citrus
93.48





% Green
8.10



Water Release Group 6



PARADISAMIDE
0.000013163
0.6
95.75



TRIDECEN 2 NITRILE
0.000000441
8.7
0.52



CIS-3-HEXENYL SALICYLATE
0.000000150
1.9
2.82





% Citrus
97.38





% Green
2.28



Perfume Total










The odor profile of each odorant in each water release group is expressed in percentage contribution according to odor type. This kinetic odor progression of the perfume in rinse-off conditions based on each odorant's odor contribution is shown in FIG. 4.


The flash release odorants (γ values more than 900) and the deposition odorants (also referred to as delayed release odorants: γ values less than 100) are calculated to make up respectively 52% and 15% of the total perfume. The acceleration (γ) values of the fragrance odorants are shown in table 16:












TABLE 16







Parts
γ




















Flash Release Materials





d-LIMONENE
42.2500
8200.76



ALDEHYDE C 8 (OCTANAL)
0.0450
3630.08



MELONAL
0.5000
2655.52



STYRALLYL ACETATE
1.5000
2576.59



LIGUSTRAL
0.7700
1704.65



CIS 3 HEXENOL
0.0500
1569.11



CIS 3 HEXENYL ACETATE
0.5000
1384.27



CITRONELLAL
1.5000
1345.09



CIS 4 DECENAL
0.0043
1076.65



TRANS 2 CIS 6 NONADIENAL
0.0040
1010.67



CITRONELLYL NITRILE
4.5000
913.04



Total
51.6233



Sustained Release Materials



DIHYDRO MYRCENOL
15.0000
866.55



ALDEHYDE C10 (DECANAL)
1.4300
816.26



LINALOOL
2.5000
644.41



METHYL OCTINE CARBONATE
0.4000
525.10



RHUBAFURAN
3.0000
476.08



ROSSITOL
3.0000
303.80



ETHYL LINALOOL
5.7000
275.63



TRANS 2 CIS 6 NONADIENOL
0.4500
245.87



ALDEHYDE C12 (DODECANAL)
0.4000
183.88



UNDECAVERTOL
1.5000
116.38



Total
33.3800



Delayed Release Materials



MEFRANAL
0.4000
84.76



GARDAMIDE
5.0000
66.47



CITRATHAL
1.5000
39.32



PARADISAMIDE
7.0000
7.77



TRIDECEN 2 NITRILE
0.5000
6.43



CIS-3-HEXENYL SALICYLATE
0.6000
2.80



Total
15.0000










The above perfume example provides a citrus linear hedonic with a secondary linear cucumber odor while also leaving a minimum amount of residual fragrance of streaks upon completing the cycle or cleaning experience.


B. Body-Wash, Soap, Shampoo and Conditioners

Below in Table 17 is an illustrative example (“Citrus Cucumber Sustained Release-Type”) of a fragrance engineered for sustained release of a dominating citrus with a secondary linear green cucumber note in high water dilutions.


As in the earlier example for “Flash Release Citrus-Cucumber”, a linear citrus note can be constructed by ensuring that least three, preferably four of the water release groups constructed based on odorants' Ω values must have at least 30%, preferably at least 40% of their overall odor contributed by one or more citrus odorants. In addition a linear release of a secondary green nuance along with the predominant citrus release may be built by having at least three, preferably four of the water release groups to have at least 20%, of their overall odor contributed by one or more green odorants


The Citrus-Cucumber Sustained Release perfume is designed based on the same criteria defined earlier for sustained release in water: at least 30%, preferably at least 40% of the total perfume with γ values between 900 and 100. The perfume is shown in the table below:









TABLE 17





Citrus-Cucumber Sustained Release Type Fragrance





















Odor
Odor




Parts
Descriptor 1
Descriptor 2
γ





Water Release Group 1


d-LIMONINE
10.0000
CITRUS
ORANGE
8200.76


Water Release Group 2


STRALLYL ACETATE
1.5000
GREEN
FRUITY
2576.59


DIHYDRO MYRCENOL
15.0000
CITRUS
METALLIC
888.55


MELONAL
0.5000
GREEN
ALDEHYDIC
2555.52


LIGUSTRAL
0.7700
GREEN
LEAF
1704.65


CITRONELLAL
1.5000
CITRUS
CITRONELLA
1345.08


CITRONELLYL NITRILE
4.5000
CITRUS
NITRILE
913.04


LINALOOL
0.5000
LINALOOL

844.41


ALDEHYDE C 10 (DECANAL)
2.3600
ALDEHYDIC
ORANGE
615.25


CIS 3 HEXENYL ACETATE
0.5000
GRASS
FRUITY
1384.27


RHUBAFURAN
5.0000
GREEN
GRAPEFRUIT
478.05


ALDEHYDE C 8 (OCTANAL)
0.0450
ALDEHYDIC
CITRUS
3830.08


Water Release Group 3


ROSSITOL
15.0000
CITRUS
FLORAL
276.63


ETHYL LINALOOL
0.5000
MUGUET
CITRUS
303.86


CIS 3 HEXENOL
0.0500
GRASS
GREEN
1569.11


METHYL OCTINE CARBONATE
0.4000
GREEN
VIOLET
525.10


Water Release Group 4


GARDAMIDE
10.0000
CITRUS
WOODY
86.47


UNDECAVERTOL
3.5000
GREEN
FRUITY
118.38


TRANS 2 CIS 6 NONADENOL
0.4500
GREEN
CUCUMBER
245.87


ALDEHYDE C12 (DODECANAL)
0.4000
ALDEHYDIC
FATTY/GREASY
183.88


Water Release Group 5


CITRATHAL
5.5000
LIME
CITRUS
29.32


CIS 4 DECENAL
0.0043
ALDEHYDIC
CARDAMOM
1075.68


TRANS 2 CIS 6 NONADENAL
0.0040
GREEN
CUCUMBER
1010.67


Water Release Group 6


MEFRANAL
0.4000
ALDEHYDIC
CITRUS
94.78


PARADISAMIDE
3.0000
CITRUS
FRUITY
7.77


TRIDECEN 2 NITRILE
0.5000
NITRILE
CITRUS
8.43


CIS-3-HEXENYL SALICYLATE
0.6000
GRASS
SALICYLATE
2.80


Perfume Total
100.0033


















% Odor



φ
Ω
odt
Contribution





Water Release Group 1


d-LIMONINE
0.001571820
128.901194947
430
100.00





% Citrus
100.00





% Green
0.00


Water Release Group 2


STRALLYL ACETATE
0.000383964
1.483977879
110
1.23


DIHYDRO MYRCENOL
0.000073216
0.952972908
810
1.87


MELONAL
0.000309918
0.411493829
1.5
30.01


LIGUSTRAL
0.000196597
0.257251791
110
0.63


CITRONELLAL
0.000124439
0.251072020
33
4.09


CITRONELLYL NITRILE
0.000053290
0.218951073
71
5.71


LINALOOL
0.000047748
0.153850800
20
22.51


ALDEHYDE C 10 (DECANAL)
0.000060573
0.117962667
6.7
31.97


CIS 3 HEXENYL ACETATE
0.000130208
0.696121584
170
0.28


RHUBAFURAN
0.000037530
0.089451785
440
1.02


ALDEHYDE C 8 (OCTANAL)
0.000456095
0.074341812
4.5
0.85





% Citrus
44.33





% Green
33.16


Water Release Group 3


ROSSITOL
0.000015198
0.062636476
120
87.18


ETHYL LINALOOL
0.000020753
0.053591356
440
10.38


CIS 3 HEXENOL
0.000183540
0.012830800
90
0.30


METHYL OCTINE CARBONATE
0.000035454
0.007858962
8.7
22.18





% Citrus
77.64





% Green
22.46


Water Release Group 4


GARDAMIDE
0.000003164
0.002103357
24
47.83


UNDECAVERTOL
0.000004491
0.001829435
28
15.39


TRANS 2 CIS 6 NONADENOL
0.000012085
0.001337108
1.5
34.28


ALDEHYDE C12 (DODECANAL)
0.000009217
0.000577933
17
2.69





% Citrus
47.63





% Green
49.88


Water Release Group 5


CITRATHAL
0.000001915
0.000422065
5.3
97.98


CIS 4 DECENAL
0.000000457
0.000418780
3.1
0.13


TRANS 2 CIS 6 NONADENAL
0.000075353
0.000304829
0.2
1.89





% Citrus
97.98





% Green
2.02


Water Release Group 6


MEFRANAL
0.000003488
0.000013133
17
0.17


PARADISAMIDE
0.000000242
0.000015044
0.6
98.98


TRIDECEN 2 NITRILE
0.000000137
0.000000441
6.7
0.54


CIS-3-HEXENYL SALICYLATE
0.000000069
0.000000150
1.9
2.30





% Citrus
97.70


Perfume Total


% Green
2.30









The odor profile of each odorant in each water release group is expressed in percentage contribution according to odor type. This kinetic odor progression of the perfume in rinse-off conditions based on each odorant's odor contribution is shown in FIG. 5.


Odorants from the “Citrus-Cucumber Linear Sustained Release” type are also grouped according to their type of release based on the γ values as shown below in table 18:
















Parts
γ




















Flash Release Odorants





d-LIMONENE
10.0000
8200.76



ALDEHYDE C 8 (OCTANAL)
0.0450
3630.08



MELONAL
0.5000
2655.52



STYRALLYL ACETATE
1.5000
2578.59



LIGUSTRAL
0.7700
1704.65



CIS 3 HEXENOL
0.0500
1569.11



CIS 3 HEXENYL ACETATE
0.5000
1384.27



CITRONELLAL
1.5000
1345.09



CIS 4 DECENAL
0.0043
1076.85



TRANS 2 CIS 6 NONADIENAL
0.0040
1010.67



CITRONELLYL NITRILE
4.5000
913.04




19.3733



Sustained Release Odorants



DIHYDRO MYRCENOL
15.0000
866.55



ALDEHYDE C10 (DECANAL)
2.3800
818.26



LINALOOL
5.0000
644.41



METHYL OCTINE CARBONATE
0.4000
525.10



RHUBAFURAN
5.0000
476.06



ROSSITOL
8.5000
303.80



ETHYL LINALOOL
15.0000
275.63



TRANS 2 CIS 6 NONADIENOL
0.4500
245.87



ALDEHYDE C12 (DODECANAL)
0.4000
183.88



UNDECAVERTOL
3.5000
116.38




55.6300



Delayed Release Odorants



MEFRANAL
0.4000
84.76



GARDAMIDE
10.0000
66.47



CITRATHAL
5.5000
39.32



PARADISAMIDE
8.0000
7.77



TRIDECEN 2 NITRILE
0.5000
6.43



CIS-3-HEXENYL SALICYLATE
0.6000
2.80




25.0000










The above perfume example provides a linear sustained citrus dominating odor with a secondary cucumber release during rinse-off.


C. Laundry Products

The following example is illustrative of a linear dominating citrus release with a secondary linear cucumber hedonic note for leave-on applications. Perfumes intended for maximum deposition in wash-off systems must have at least 40% and preferably at least 50% of the total perfume with delayed release type of odorants (depositors) as defined in the invention.


In addition to criteria for maximum deposition of perfume defined above, at least three, preferably four of the water release groups constructed based on odorants' Ω values must have at least 30%, preferably at least 40% of their overall odor contributed by one or more citrus odorants. In addition, to construct a secondary linear green note, at least three water release groups based on Ω values, must have at least 20% of their overall odor contributed by a single or a group of green odorants. These fragrances will therefore also provide the consumer with a perception of linear sustained predominantly citrus perfume with a linear nuance of cucumber throughout the process of rinse-off.


A perfume (Delayed Linear Release Cucumber-Citrus Perfume) for laundry detergents designed to provide maximum deposition of fragrance as well as a linear release of a citrus/green note during the process of rinse-off is shown below in Table 19.


















TABLE 19








Odor
Odor




% Odor



Parts
Descriptor 1
Descriptor 2
γ
φ
Ω
odt
Contribution
























Water Release Group 1










d-LIMONINE
2.5
CITRUS
ORANGE
8200.76
0.0015718
32.2252987
430
100.00









% Citrus
100.00









% Green
0.00


Water Release Group 2


STRALLYL ACETATE
1.5
GREEN
FRUITY
2576.58
0.0003840
1.4838779
110
1.42


MELONAL
0.5
GREEN
ALDEHYDIC
2655.52
0.0003099
0.4114938
1.5
34.76


LIGUSTRAL
0.77
GREEN
LEAF
1704.85
0.0001950
0.2572618
110
0.73


CITRONELLAL
1.5
CITRUS
CITRONELLA
1345.09
0.0001244
0.2510720
33
4.74


CITRONELLYL NITRILE
4.5
CITRUS
NITRILE
913.04
0.0000523
0.2189511
71
5.61


DIHYDRO MYRCENOL
2.5
CITRUS
METALLIC
868.55
0.0000733
0.1588288
810
0.32


ALDEHYDE C10 (DECANAL)
2.38
ALDEHYDIC
CITRUS
818.26
0.0000808
0.1179829
6.7
37.05


CIS 3 HEXENYL ACETATE
0.5
GRASS
FRUITY
1384.27
0.0001302
0.0901218
170
0.31


LINALOOL
2.5
LINALOOL

544.41
0.0000477
0.0759254
20
13.04


ALDEHYDE C 8 (OCTANAL)
0.045
ALDEHYDIC
CITRUS
3630.08
0.0004551
0.0743418
4.8
1.02









% Citrus
49.74









% Green
37.22


Water Release Group 3


ETHYL LINALOOL
15
CITRUS
FLORAL
276.63
0.0000152
0.0528356
120
65.96


ROSSITOL
8.5
MUGUET
CITRUS
303.86
0.0000206
0.0535914
440
10.18


RHUBAFURAN
1.6
GREEN
GRAPEFRUIT
475.08
0.0000375
0.0258365
440
1.80


CIS 3 HEXENOL
0.05
GRASS
GREEN
1569.11
0.0001835
0.0128308
90
0.29


METHYL OCTINE CARBONATE
0.4
GREEN
VIOLET
525.10
0.0000356
0.0075690
9.7
21.75









% Citrus
76.15









% Green
23.85


Water Release Group 4


MEFRANAL
12
ALDEHYDIC
CITRUS
84.76
0.0000035
0.0035455
17
39.46


GARDAMIDE
15
CITRUS
WOODY
56.47
0.0000032
0.0031550
24
34.94


UNDECAVERTOL
3.5
GREEN
FRUITY
116.38
0.0000045
0.0012294
28
7.52


TRANS 2 CIS 6 NONADENOL
0.45
GREEN
CUCUMBER
245.57
0.0000121
0.0013371
1.5
16.77


ALDEHYDE C12 (DODECANAL)
0.4
ALDEHYDIC
FATTY/GREASY
183.88
0.0000092
0.0005779
17
1.32









% Citrus
74.39









% Green
24.29


Water Release Group 5


CIS 4 DECENAL
0.0043
ALDEHYDIC
CARDAMOM
1078.65
0.0000905
0.0004186
3.1
0.28


TRANS 2 CIS 6 NONADENAL
0.004
GREEN
CUCUMBER
1010.87
0.0000754
0.0003046
0.2
4.08


CITRATHAL
2.5
LIME
CITRUS
39.32
0.0000019
0.0001918
5.3
95.68









% Citrus
95.68









% Green
4.06


Water Release Group 6


PARADISAMIDE
8
CITRUS
FRUITY
7.77
0.0000002
0.0000156
0.8
33.85


METHYL DIHYDRO JASMONATE
5
FLORAL

8.40
0.0000003
0.0000120
0.23
55.23


CIS-3-HEXENYL SALICYLATE
8
GRASS
SALICYLATE
2.80
0.0000001
0.0000020
1.9
10.70


TRIDECEN 2 NITRILE
0.5
NITRILE
CITRUS
6.43
0.0000001
0.0000004
8.7
0.18









% Citrus
34.07









% Green
10.70









The odor profile of each odorant in each water release group is expressed in percentage contribution according to odor type. This kinetic odor progression of the perfume in rinse-off conditions based on each odorant's odor contribution is shown in FIG. 6.


The odorants in the illustrative example are also grouped according to their type of release based on the acceleration (γ) values as shown in table 20 below.












TABLE 20







Parts
γ




















Flash Release





d-LIMONENE
2.5000
8200.76



ALDEHYDE C 8 (OCTANAL)
0.0450
3630.08



MELONAL
0.5000
2655.52



STYRALLYL ACETATE
1.5000
2576.59



LIGUSTRAL
0.7700
1704.65



CIS 3 HEXENOL
0.0500
1569.11



CIS 3 HEXENYL ACETATE
0.5000
1384.27



CITRONELLAL
1.5000
1345.09



CIS 4 DECENAL
0.0043
1078.65



TRANS 2 CIS 6 NONADIENAL
0.0040
1010.67



CITRONELLYL NITRILE
4.5000
913.04



total
11.8733



Sustained Release



DIHYDRO MYRCENOL
2.5000
866.55



ALDEHYDE C10 (DECANAL)
2.3800
818.26



LINALOOL
2.5000
644.41



METHYL OCTINE CARBONATE
0.4000
525.10



RHUBAFURAN
1.5000
476.06



ROSSITOL
8.5000
303.80



ETHYL LINALOOL
15.0000
275.63



TRANS 2 CIS 6 NONADIENOL
0.4500
245.87



ALDEHYDE C12 (DODECANAL)
0.4000
183.88



UNDECAVERTOL
3.5000
116.36



total
37.1300



Delayed Release



MEFRANAL
12.0000
84.76



GARDAMIDE
15.0000
66.47



CITRATHAL
2.5000
39.32



METHYL DIHYDRO JASMPNATE
5.0000
6.40



PARADISAMIDE
8.0000
7.77



TRIDECEN 2 NITRILE
0.5000
6.43



CIS-3-HEXENYL SALICYLATE
8.0000
2.80



total
51.0000










“Delayed Linear Release Cucumber-Citrus Perfume” for laundry detergents provides maximum deposition of fragrance as well as a linear release of a citrus/green note during the process of rinse-off in use.


In addition to the Citrus-Green examples provided above, examples below will in turn, provide illustrations of perfumes for linear citrus release with linear nuances of floral and fruity odors in rinse-off.


The method to construct these Citrus-Fruity and Citrus-Floral perfumes is the same as the ones shown for Citrus-Green.


Citrus-Fruity Perfumes

All the following perfumes will result in a predominantly linear citrus odor during rinse off whilst also providing the consumer with a linear perception of a secondary fruity nuance.


A. Flash Release Citrus-Fruity

The following provided example “Flash Release Citrus Fruity” perfume is for applications intended to result in minimal deposition of fragrance upon rinse-off such as dishwashing liquid and glass cleaners. The example of Flash Release Citrus Fruity is shown below in table 21.
















TABLE 21







Parts
γ
φ
Ω
ODT
% Odor






















Water Release Group 1








d-LIMONINE
35
8200.7592
0.0015718
451.15418
430
76.50


ETHYL 2-METHYLBUTYRATE
0.5
12827.563
0.0043615
27.973938
20
23.50







% Citrus
76.50







% Fruity
23.50


Water Release Group 2


MANZANATE
0.5
5288.4237
0.00111863
2.9518233
50
0.76


CITRONELLAL
7.5
1345.0902
0.0001244
1.2553601
33
17.16


DIHYDROMYRCENOL
10
888.54502
7.332E−05
0.6353153
810
0.93


ALDEHYDE C 8 (OCTANAL)
0.3
3830.0763
0.0004551
0.4956107
290
0.06


CITRONELLYL NITRILE
6
913.04218
5.329E−05
0.2919348
71
6.39


ORTHOLATE
9.5
584.56181
6.262E−05
0.2828299
58
12.38


CITRAL
5
857.09011
6.236E−05
0.2672318
12
31.50


ALLYL CAPROATE
0.5
1738.6656
0.0002108
0.183027
4.6
8.22


ALDEHYDE C10
2
818.26196
8.057E−05
0.0991285
6.7
22.57







% Citrus
78.65







% Fruity
21.35


Water Release Group 3


LINALYL ACETATE
1.5
617.71622
8.451E−05
0.059773
450
2.07


APPLINAL
1.5
554.78818
8.246E−05
0.0519759
55
16.97


HEXYL ACETATE
0.8
3118.7849
0.0004649
0.0464022
950
0.52


RHUBAFURAN
2
478.05986
3.758E−05
0.0357807
440
2.83


ALLYL HEPTANOATE
0.5
711.57994
8.076E−05
0.0216168
58
5.36


APHERMATE
0.5
589.61679
5.808E−05
0.0165332
100
3.11


DIMETHYL BENZYL CARBINYL ACETATE
2
249.9309
1.784E−05
0.0089185
18
89.13







% Citrus
4.90







% Fruity
95.10


Water Release Group 4


OXANE
0.1
294.09802
3.802E−05
0.0011181
58
4.82


CIS 4 DECENAL
0.008
1076.6476
9.046E−05
0.0005843
3.1
5.22


PHENOXY ETHYL ISOBUTYRATE
4
52.666397
2.538E−05
0.0005346
120
89.98







% Citrus
10.04







% Fruity
89.96


Water Release Group 5


GRAPEFRUIT MERCAPTAN
0.003
1043.221
0.0001031
0.0003227
0.00002
98.99


CITRATHAL
4
39.32
1.915E−06
0.000307
5.3
0.50


alpha-DAMASCONE
0.1
157.3017
9.183E−06
0.0001444
3.6
0.02


DIMETHYL BENZYL CARBINYL BUTYRATE
1.5
39.667071
1.85E−06
0.0001106
42
0.02


GAMMA UNDECALACTONE
0.5
42.962736
1.513E−06
3.251E−05
0.7
0.47







% Citrus
99.49







% Fruity
0.51


Water Release Group 6


ISO E SUPER
0.75
27.835581
1.397E−06
2.915E−05
0.6
16.27


NECTARYL
1.55
13.535512
5.134E−07
1.077E−05
0.4
50.42


PARADISAMIDE
1.5
7.7363238
2.42E−07
2.821E−06
0.6
32.53


TRIDECEN 2 NITRILE
0.4
6.426612
1.372E−07
3.527E−07
6.7
0.78







% Citrus
83.73







% Fruity
0.00









The above perfume results in an impactful citrus linear note during dilution coupled with linear nuances of apple throughout usage.


B. Sustained Release Citrus-Fruity Perfume

The following perfume “Sustained Release Citrus-Fruity Perfume” is an example of a perfume resulting in a sustained linear predominantly citrus note with clear linear nuances of fruit in high water dilutions. This perfume is intended for applications such as shampoo, conditioners, soap etc. and is designed based on methods discussed in great details earlier in the herein invention.


The perfume “Sustained Release Citrus-Fruity” analysis along with its composition is shown below in table 22:




















Parts
γ
φ
Ω
ODT
% Odor






















Release Group I








d-LIMONINE
15.2500
8200.76
0.001571820
195.574322295
430
73.94


ETHYL 2-METHYLBUTYRATE
0.2500
12827.56
0.004361536
13.986969219
20
26.06







% Citrus
73.94







% Fruity
26.06


Release Group II


MANZANATE
0.5000
5288.42
0.001116334
2.951823345
50
0.70


CITRONELLAL
10.0000
1345.09
0.000124439
1.673813464
33
21.25


DIHYDROMYRCENOL
15.0000
866.55
0.000073316
0.952972906
810
1.30


ALDEHYDE C 8 (OCTANAL)
0.3000
3630.08
0.000455096
0.495810745
290
0.07


CITRONELLYL NITRILE
6.0000
913.04
0.000053290
0.291934763
71
5.93


ORTHOLATE
9.5000
564.56
0.000062622
0.282829871
58
11.49


CITRAL
5.0000
857.09
0.000062358
0.267231617
12
29.22


ALLYL CAPROATE
0.5000
1738.67
0.000217080
0.183027006
4.8
7.52


LINALYL ACETATE
4.5000
617.72
0.000054510
0.179319015
450
0.70


ALDEHYDE C10
2.0000
818.28
0.000060573
0.099128451
6.7
20.93


RHUBAFURAN
5.0000
478.08
0.000037580
0.089451765
440
0.50







% Citrus
80.19







% Fruity
19.81


Release Group III


APPLINAL
1.5000
554.79
0.000062457
0.051975865
55
16.75


APHERMATE
1.5000
589.82
0.000058081
0.049599731
100
9.21


HEXYL ACETATE
0.5000
3118.78
0.000464946
0.045402167
950
0.52


ALLYL HEPTANOATE
0.5000
711.58
0.000060757
0.021616782
58
5.29


DIMETHYL BENZYL CARBINYL ACETATE
2.0000
249.93
0.000017842
0.008918540
18
88.23







% Citrus
0.00







% Fruity
100.00


Release Group IV


OXANE
0.5000
294.10
0.000038018
0.005590490
56
4.88


alpha-DAMASCONE
0.5000
157.30
0.000009183
0.000722246
3.6
75.86


CIS 4 DECENAL
0.0080
1078.85
0.000090457
0.000584344
3.1
1.06


PHENOXY ETHYL ISOBUTYRATE
4.0000
52.67
0.000002538
0.000534648
120
18.21







% Citrus
5.93







% Fruity
94.07


Water Release Group V


GRAPEFRUIT MERCAPTAN
0.0030
1043.22
0.000103096
0.000322655
0.00002
99.01


CITRATHAL
4.0000
39.32
0.000001915
0.000308956
5.3
0.50


DIMETHYL BENZYL CARBINYL BUTYRATE
1.5000
39.87
0.000001850
0.000110829
42
0.02


GAMMA UNDECALACTONE
0.5000
4.98
0.000001513
0.000032513
0.7
0.47







% Citrus
99.50







% Fruity
0.50


Release Group VI


NECTARYL
3.0000
13.54
0.000000513
0.000020848
0.4
44.84


ISO E SUPER
0.5000
27.84
0.000001397
0.000019436
0.6
4.98


PARADISAMIDE
5.0000
7.77
0.000000242
0.000009402
0.6
49.82


TRIDECEN 2 NITRILE
0.4000
6.43
0.000000137
0.000000353
6.7
0.36







% Citrus
95.02







% Fruity
0.00









The perfume “Sustained Release Citrus-Fruity” provides a linear sustained citrus note during rinse-off along with a less dominant linear fruity nuance as well in various applications such as body-wash, conditioners etc.


C. Delayed Citrus-Fruity Linear Release Perfume

The perfume “Delayed Citrus-Fruity Linear Release” is intended to maximize deposition of fragrance whilst providing the consumer with an impactful release of a citrus fragrance along with a less dominant, secondary linear fruity note during rinse-off.


It is engineered based on odorants' physico kinetic properties as described in the preceding examples for Delayed Citrus-Green Perfume. The analysis of Delayed Citrus-Fruity Linear Release Perfume is shown below in table 23:
















TABLE 23







Parts
γ
φ
Ω
ODT
% Odor






















Water Release I








d-LIMONINE
2.0000
8200.76
0.00157182
25.78023899
430
100.00







% Citrus
100.00







% Fruity
0.00


Water Release II


MANZANATE
0.5000
5288.42
0.00111633
2.95182335
50
1.13


ETHYL 2-METHYLBUTYRATE
0.0500
12827.56
0.00436154
2.79739384
20
0.28


CITRONELLAL
10.0000
1345.09
0.00012444
1.67381346
33
34.14


CITRONELLYL NITRILE
7.5000
913.04
0.00005329
0.29193475
71
11.90


ORTHOLATE
8.0000
564.56
0.00006262
0.28282987
58
15.54


ALLYL CAPROATE
0.5000
1736.67
0.00021070
0.15302701
4.6
12.25


CITRAL
2.5000
857.09
0.00006235
0.13361561
12
23.47


RHUBAFURAN
5.0000
476.06
0.00003758
0.05945177
440
1.28







% Citrus
70.80







% Fruity
29.20


Water Release III


APPLINAL
1.5000
554.79
0.00008246
0.05197587
55
1.02


APHERMATE
1.5000
589.82
0.00005808
0.04959973
100
0.58


ALDEHYDE C10
1.0000
818.28
0.00008057
0.04966423
8.7
5.58


LINALYL ACETATE
1.1000
617.72
0.00006451
0.04383354
450
0.09


ALLYL HEPTANOATE
0.5000
711.58
0.00008076
0.02161678
58
0.32


MEFRANAL
8.5000
84.76
0.00000349
0.01300043
3.5
88.27


DIMETHYL BENZYL CARBINYL ACETATE
2.0000
249.93
0.00001784
0.00891854
18
4.15







% Citrus
93.94







% Fruity
6.06


Water Release IV


OXANE
0.5000
294.10
0.00003802
0.00559049
58
0.04


GARBAMIDE
12.0000
27.84
0.00000140
0.00058309
0.5
99.79


PHENOXY ETHYL ISOBUTYRATE
4.0000
52.67
0.00000254
0.00053465
120
0.17







% Citrus
99.83







% Fruity
0.17


Water Release IV


OXANE
0.5000
294.10
0.00003802
0.00559049
58
0.04


GARBAMIDE
12.0000
27.84
0.00000140
0.00058309
0.5
99.79


PHENOXY ETHYL ISOBUTYRATE
4.0000
52.67
0.00000254
0.00053465
120
0.17







% Citrus
99.83







% Fruity
0.17


Water Release V


CITRATHAL
5.5000
39.32
0.00000192
0.00042206
5.3
4.03


DIMETHYL BENZYL CARBINYL BUTYRATE
3.0000
39.87
0.00000185
0.00022126
42
0.28


GAMMA UNDECALACTONE
5.0000
42.98
0.00000151
0.00009754
0.7
27.74


NECTARYL
7.0000
13.54
0.00000051
0.00004885
0.4
87.98







% Citrus
71.99







% Fruity
28.01


Water Release VI


PARADISAMIDE
8.5000
7.77
0.00000024
0.00001880
0.6
48.36


TRIDECEN 2 NITRILE
0.8500
8.43
0.00000014
0.00000075
6.7
0.43


ETHYL METHYL PHENYL GLYCIDATE
1.5000
28.35
0.000000116
0.00001533
0.1
51.21







% Citrus
48.79



100.0000



% Fruity
51.21









The above perfume Delayed Citrus-Fruity Linear Release provides the consumer with a perceived impactful citrus linear release during rinse-off along with a secondary linear fruity nuance whilst resulting in maximum deposition of fragrance as well.


Citrus-Floral Perfumes

The following examples are for Citrus-Fragrance family of perfumes which result in a linear impactful release of a citrus note along with a secondary floral fragrance in the presence of large water quantities.


Following the rationale provided in earlier examples, perfumes were engineered for flash release, sustained release and delayed release according to their intended application and usage.









TABLE 24







Flash Release Citrus-Floral



















% Odor



Parts
γ
φ
Ω
odt
Contribution

















Water Release Group 1








d-LIMONINE
42.25
8200.76
0.00157182
544.60754865
430
100.00







% Citrus
100.00







% Floral
0.00


Water Release Group 2


LINALOOL
12.00
844.41
0.00004775
0.36924192
20
63.75


DIHYDRO MYRCENOL
5.00
866.55
0.00007332
0.31765764
810
0.66


CITRONELLAL
1.50
1345.09
0.00012444
0.25107202
33
4.83


CITRONELLYL NITRILE
4.50
913.04
0.00004329
0.21895107
71
8.73


CIS 3 HEXENYL ACETATE
0.50
1384.27
0.00013021
0.09012156
170
0.31


ALDEHYDE C 8 (OCTANAL)
0.05
3630.08
0.00045510
0.07434161
4.6
1.04


ALDEHYDE C10 (DECANAL)
1.43
818.26
0.00006057
0.07087684
6.7
22.68







% Citrus
35.94







% Floral
63.75


Water Release Group 3


RHUBAFURAN
3.00
476.06
0.00003758
0.05367106
440
0.16


ETHYL LINALOOL
5.70
275.63
0.00001520
0.02387786
120
1.12


ROSSITOL
3.00
303.80
0.00002075
0.01891460
440
0.16


IONONE-BETA
2.50
311.32
0.00002357
0.01834091
0.6
98.31


PHENYL ETHYL ACETATE
1.50
384.06
0.00002819
0.01624022
150
0.24


CIS 3 HEXENOL
0.05
1569.11
0.00016354
0.01283060
90
0.01







% Citrus
1.44







% Floral
98.31


Water Release Group 4


LILIAL
7.50
104.63
0.00000569
0.00446800
0.93
100.00







% Citrus
0.00







% Floral
100.00


Water Release Group 5


GARDAMIDE
1.50
88.47
0.00000316
0.00031550
24
16.62


MEFRANAL
0.52
84.76
0.00000349
0.00015364
17
8.13


CITRATHAL
1.50
39.32
0.00000192
0.00011511
5.3
75.25







% Citrus
100.00







% Floral
0.00


Water Release Group 6


PARADISAMIDE
2.50
7.77
0.00000024
0.00000470
0.6
38.40


METHYL DIHYDRO JASMONA
1.50
8.40
0.00000029
0.00000360
0.23
60.10


TRIDECEN 2 NITRILE
0.50
6.43
0.00000014
0.00000044
8.7
0.69


CALYXOL
1.50
1.23
0.00000004
0.00000008
17
0.81







% Citrus
39.09







% Floral
60.918


Perfume Total
100.00
















TABLE 25







Sustained Citrus-Floral Linear Release



















% Odor



Parts
γ
φ
Ω
odt
Contribution

















Water Release Group 1








d-LIMONINE
10.00
8200.76
0.001571820
128.901194947
430
100.00







% Citrus
100.00







% Floral
0.00


Water Release Group 2


CITRONELLOL
12.00
888.56
0.000088703
0.895227041
29
53.41


DIHYDRO MYRCENOL
5.00
866.55
0.000073318
0.317657635
810
0.80


CITRONELLAL
1.50
1345.09
0.000124439
0.251072020
33
5.87


CITRONELLYL NITRILE
4.50
913.04
0.000053290
0.218951073
71
8.18


BENZYL ACETATE
5.00
884.29
0.000059238
0.196748700
252
2.58


CIS 3 HEXENYL ACETATE
0.50
1384.27
0.000130208
0.090121564
170
0.38


ALDEHYDE C 8 (OCTANAL)
0.05
3630.08
0.000455096
0.074341612
4.6
1.28


ALDEHYDE C10 (DECANAL)
1.43
818.26
0.000080573
0.070876843
6.7
27.55







% Citrus
43.65







% Floral
55.97


Water Release Group 3


RHUBAFURAN
3.00
476.06
0.000037580
0.053871059
440
0.16


GERANYL ACETATE
5.00
314.92
0.000022992
0.038203472
89
1.88


ETHYL LINALOOL
5.00
275.63
0.000015198
0.020945492
120
0.97


ROSSITOL
3.00
303.30
0.000020753
0.018914596
440
0.18


IONONE-BETA
2.50
311.32
0.000023566
0.018340905
0.6
96.79


PHENYL ETHYL ACETATE
1.50
384.06
0.000028191
0.018240221
150
0.23


CIS 3 HEXENOL
0.05
1569.11
0.000183540
0.012830600
90
0.01







% Citrus
1.28







% Floral
98.70


Water Release Group 4


LILIAL
5.00
104.63
0.000005694
0.002978669
0.93
99.39


HYDROXYCITRONELLAL
8.95
45.82
0.000001620
0.000664438
270
0.61







% Citrus
0.61







% Floral
99.39


Water Release Group 5


GARDAMIDE
1.50
66.47
0.000003184
0.000315504
24
16.62


MEFRANAL
0.52
84.76
0.000003486
0.000153837
17
8.13


CITRATHAL
1.50
39.32
0.000001915
0.000115109
5.3
75.25







% Citrus
100.00







% Floral
0.00


Water Release Group 6


METHYL DIHYDRO JASMONATE
10.00
8.40
0.000000286
0.000024021
0.23
74.03


PARADISAMIDE
9.00
7.77
0.000000242
0.000016924
0.6
25.54


TRIDECEN 2 NITRILE
0.50
6.43
0.000000137
0.000000441
6.7
0.13


CALYXOL
3.00
1.23
0.000000041
0.000000151
17
0.30


Perfume Total
100.00



% Citrus
25.67







% Floral
74.33
















TABLE 27







Delayed Citrus-Floral Linear Release



















% Odor



Parts
γ
φ
Ω
odt
Contribution

















Water Release Group 1








d-LIMONINE
2.50
8200.76
0.001571820
32.22529874
430
100.00







% Citrus
100.00







% Floral
0.00


Water Release Group 2


CITRONELLOL
5.50
868.56
0.000066703
0.31884573
29
70.80


DIHYDRO MYRCENOL
2.50
866.55
0.000073316
0.15882882
810
1.15


CITRONELLAL
1.50
1345.09
0.000124439
0.25107202
33
18.97


CITRONELLYL NITRILE
0.50
913.04
0.000053290
0.02432790
71
2.83


BENZYL ACETATE
2.50
664.29
0.000059238
0.09837435
252
3.70


CIS 3 HEXENYL ACETATE
0.50
1384.27
0.000130208
0.09012158
170
1.10


ALDEHYDE C 8 (OCTANAL)
0.05
3630.08
0.000455096
0.07434161
4.6
3.85







% Citrus
74.50







% Floral
24.40


Water Release Group 3


ALDEHYDE C10 (DECANAL)
0.50
818.26
0.000060573
0.02478211
8.7
1.70


RHUBAFURAN
3.00
475.05
0.000037580
0.05367106
440
0.18


GERANYL ACETATE
5.00
314.92
0.000022992
0.03620347
69
1.65


ETHYL LINALOOL
5.00
275.63
0.000015198
0.02094549
120
0.95


ROSSITOL
3.00
303.80
0.000020753
0.01891460
440
0.18


IONONE-BETA
2.50
311.32
0.000023566
0.01834091
0.6
95.14


PHENYL ETHYL ACETATE
1.50
384.05
0.000028191
0.01624022
150
0.23


CIS 3 HEXENOL
0.05
1569.11
0.000163540
0.01283060
90
0.01







% Citrus
2.97







% Floral
97.02


Water Release Group 4


LILIAL
5.00
104.63
0.000005894
0.00297867
0.93
90.12


HYDROXYCITRONELLAL
10.00
45.82
0.000001620
0.00074239
270
0.62


GARDAMIDE
5.50
55.47
0.000003164
0.00115685
24
3.84


MEFRANAL
5.50
84.76
0.000003485
0.00182501
17
5.42







% Citrus
9.88







% Floral
90.12


Water Release Group 5


CITRATHAL
5.00
39.32
0.000001915
0.00038370
5.3
1.43


METHYL DIHYDRO JASMONATE
15.00
8.40
0.000000286
0.00003603
0.23
98.57







% Citrus
1.43







% Floral
98.57


Water Release Group 6


PARADISAMIDE
4.00
7.77
0.000000242
0.00000752
0.5
88.08


TRIDECEN 2 NITRILE
3.50
6.43
0.000000137
0.00000309
6.7
6.75


BENZYL SALICYLATE
5.00
1.73
0.000000070
0.00000059
21
3.07


CALYXOL
5.40
1.23
0.000000041
0.00000027
17
4.10







% Citrus
92.82







% Floral
7.18








Claims
  • 1.-12. (canceled)
  • 13. A method of formulating a citrus perfume composition for use in rinse-off systems such that said composition provides a continuous citrus note during rinse-off or upon water dilution, said composition comprising odorants in at least three different water release groups, each water release group comprising at least 30% citrus descriptor for its overall odour, said method comprising calculating values of odour threshold detection, acceleration and water release values for a group of odorants, to provide water release groups including a flash water release group having an acceleration value greater than 900, a sustained water release group having an acceleration value of 100 to 900; and a delayed water release group having an acceleration value of less than 100 and selecting odorants from said water release groups to provide a citrus perfume composition (a) containing at least 20 wt % of the flash release group and not more than 30 wt % of delayed water release group;(b) at least 30 wt % of sustained water release group; or(c) at least 30 wt % of delayed water release group.
  • 14. The method of claim 13 wherein said composition comprises odorants in the different water release groups such that each water release group comprises at least 20% green descriptor for its overall odour.
  • 15. The method of claim 13 wherein said composition comprises odorants in the different water release groups such that each water release group comprises at least 20% fruity descriptor for its overall odour.
  • 16. The method of claim 13 wherein said composition comprises odorants in the different water release groups such that each water release group comprises at least 20% floral descriptor for its overall odour.
  • 17. The method of claim 13 wherein the odorants are selected so that said composition includes 30% odorant with an acceleration value of greater than 900, and no more than 15 wt % of odorants with an acceleration value of less than 100.
  • 18. The method of claim 13 wherein the composition comprises at least 40 wt % of odorants with an acceleration value of from 100 to 900.
  • 19. The method of claim 13 wherein the composition comprises at least 40 wt % of odorants with an acceleration value of less than 100.
  • 20. The method of claim 13 wherein said composition is included in a rinse-off consumer composition.
  • 21. The method of claim 13 wherein the composition is added to a surface cleaner, detergent, shampoo or conditioner.
  • 22. A method of formulating a perfume composition for wash-off systems comprising determining an odor detection threshold, an acceleration term and water release values for a group of odorants and selecting from these values the appropriate combination of odorants to provide a continuous citrus note upon water dilution, optionally with a linear release of a secondary, less prominent note of fruity, green or floral odor.
Priority Claims (1)
Number Date Country Kind
0701173.7 Jan 2007 GB national
Divisions (1)
Number Date Country
Parent 11657698 Jan 2007 US
Child 12565868 US