1. Field of the Invention
The present invention relates to benzoic acid esters, and more particularly to the use of phenylethyl benzoate as a cosmetic ingredient for toiletry, cosmetic and anti-perspirant formulations, particularly as an emollient additive in view of its high refractive index.
2. Description of the Related Art
Esters are known for a variety of different applications for cosmetic, pharmaceutical and medicinal purposes. Numerous references describe the production and use of benzoic acid esters. None of these references teach or suggest the specific uses of the benzoate ester of this invention in cosmetics, toiletries and personal care products such as antiperspirants for other than perfume fragrance purposes.
For example, benzoate esters of certain alcohols and alcohol mixtures and their uses are disclosed in assignee's U.S. Pat. Nos. 4,323,694; 4,322,545; and 4,275,222, all to Scala; and U.S. Pat. Nos. 4,791,097; 5,270,461; and 5,271,930, all to Walele et al. U.S. Pat. Nos. 5,500,138; 5,668,094 and 6,491,728 to Bacon et al. discloses liquid and solid fabric softener compositions and liquid laundry detergent compositions, combined with enduring perfumes, such as phenylethyl benzoate.
U.S. Pat. Nos. 5,843,881 and 6,126,930 to Dubois et al. disclose a composition for use on the skin, hair or mucosa comprising an alcohol, a personal care polymer, and an alcohol-masking perfume component, such as phenylethyl benzoate, which reduces the alcohol aroma and the stinging sensation in the nose or throat due to the alcohol when the compositions are sprayed or atomized.
U.S. Pat. Nos. 5,540,853; 5,833,999; 5,849,310 and 6,086,903 to Trinh et al. disclose personal treatment compositions containing from about 0.001% to about 50% enduring perfume compositions selected from the group including phenylethyl benzoate.
Phenylethyl benzoate is known to have utility as a perfume ingredient for use in perfumes, colognes, eye and throat oils, stick rouge, skin moisturizers, cleansing creams, and after-bath splash and lotions.
However, among the foregoing patents, none have the unique properties of the ester compositions described and claimed herein for use in antiperspirants. None disclose or suggest phenylethyl benzoate that is substantially non-greasy and non-oily, has very low cloud point and pour point, has a high refractive index, a bland odor, low toxicity and is stable. These are vital properties in numerous applications, as the esters may be incorporated into personal care products, cosmetics and toiletries, including anti-perspirants.
3. Object and summary of the Invention
It is an object of the invention to provide phenylethyl benzoate for use as an emollient additive in cosmetics, toiletries, and personal care products, such as anti-perspirants.
It has now been found that phenylethyl benzoate has unique properties in that it is substantially non-greasy and non-oily, has a very low cloud point and pour point, has a bland odor, low toxicity, a high refractive index, and is stable. These properties make the ester useful as an emollient additive for toiletry and cosmetic formulations and personal care products, such as hair creams, hand cleaners, bath oils, cold creams, electric preshaves, finger nail polish, topical pharmaceutical ointments, lipsticks, skin lotions and creams, as well as other formulations. The foregoing list is only exemplary of the type of compositions in which the esters of this invention may be used, and, as such, is not to be considered limiting.
The benzoate ester of the invention is represented by the following formula:
C6H5-CH2-CH2-O—C—
The chemical name and proposed INCI name of the compound is Phenylethyl benzoate.
The phenylethyl benzoate ester of the invention has the following featured properties:
The phenylethyl benzoate of the invention is prepared as described in Examples 1 and 2 below. The processes of Examples 1 and 2 differ in the catalyst used.
The phenylethyl benzoate of the invention is advantageous in that it is non-oily, tasteless, inert, essentially nontoxic and non-sensitizing, and is stable. Phenylethyl benzoate is useful as an emollient, moisturizer, plasticizer, and de-oiler/degreaser. Further, phenylethyl benzoate possesses other unusual physico-chemical properties, in particular, a higher spreading coefficient and high refractive index that can make it a beneficial and unique component of a sophisticated delivery system such as in hand, face, and body creams and lotions, and for anti-perspirants. The foregoing list is only exemplary of the type of composition in which phenylethyl benzoate may be used and as such, is not to be considered limiting.
The amount of phenylethyl benzoate used as an emollient additive, in an aqueous surfactant or antiperspirant composition is dependent on the type of composition, the type and quantity of other ingredients used, and the amount and type of functional additives that are utilized. Typically, the amount of phenylethyl benzoate used ranges from about 0.5% to about 50%, by weight, of the personal care compositions. Preferably, from about 0.5% to about 10% of phenylethyl benzoate is used. Phenylethyl benzoate ester may be used in skin care and personal care compositions. The amount used in skin care compositions is dependent on the type of skin care composition, the type and quantity of cosmetic ingredients used, and the amount and type of functional additives. Typically, the amount ranges from about 0.5% to about 80% by weight of the skin care composition. For example, a facial cream may have only about 0.5% of the phenylethyl benzoate ester, whereas a massage oil may have up to about 80% by weight. Still higher amounts may be used in other compositions; for example, up to 95% of the ester may be used in bath oils.
The ester of the invention also functions as a plasticizer for polymers contained in skin care compositions, and acts as an auxiliary suspending agent capable of assisting in the suspension of ingredients in skin care compositions. Thus, the phenylethyl benzoate ester when used in skin care compositions serves not only as an emollient but also exhibits one or more other functions. The skin care compositions may take the form of a liquid, cream, gel, paste, bar, granules, stick, emulsion, dispersion, suspension, powder, foam or spray, or other forms.
A particularly useful composition of this invention is for use in anti-perspirant compositions. Typically, the amount of phenylethyl benzoate used in anti-perspirants ranges from about 0.5% to about 25% by weight of the antiperspirant composition, and preferably from about 1% to about 10% by weight of the antiperspirant composition. The most commonly used antiperspirant actives are aluminum chlorohydrate and aluminum zirconium tetrachloro-glycine.
Typical adjunct ingredients in skin care compositions are selected from the group consisting of conditioning agents, fatty substances, organic solvents, thickening agents, emollients, emulsifiers, humectants, softeners, lubricants, penetrants, plasticizers, antioxidants, agents for combating free radicals, opacifiers, stabilizers, emollients, solvents and co-solvents, dispersants, silicones, alpha-hydroxy acids, buffers, chelating agents, foaming agents, antifoaming agents, moisturizing agents, vitamins, insect repellents, fragrances, preservatives, surfactants, anti-inflammatories, pH adjusters, chelating agents, fillers, polymers, propellants, basifying or acidifying agents, odor masking agents, tanning agents, colorants and mixtures thereof.
The following are non-limiting examples of uses of the ester of the invention in specific cosmetic or personal care anti-perspirant products as an emollient additive. In the Examples, as well as throughout this application, the chemical and scientific symbols have their customary meanings and all percents are weight percents unless otherwise specified.
Example Nos. 1 and 2 describe preparation of a Benzoate ester of phenylethyl alcohol, referred to herein as Finsolv SUN. Examples 3 through 6 identify anti-perspirant formulations using the ester of the invention. For ease of identification, each ester is identified by both an Example Number and a Reference No., where applicable. Color in the Examples below is measured using ASTM D-1209 on the APHA scale of the American Public Health Association. APHA scores less than 20 denote good color, with scores of 5 to 10 signifying superior color, i.e., clear color or absence of color. APHA scores over 20 are not good, as a yellow tint is visible, becoming progressively more colored as the APHA scores increase.
Preparation of Benzoate Ester of Phenylethyl Alcohol (FINSOLV SUN)
In a 2,000 ml. four neck round bottom flask equipped with glass stirrer, distillation head, condenser, thermometer and receiver, added 488.61 grams (1.0 moles) of Phenylethyl alcohol and 511.84 grams (1.05 moles) of Benzoic Acid. The temperature was raised to 60° C. with a good flow of Nitrogen. At 60° C. added 0.9 grams of Stannous Oxalate and continued to heat to 240° C. maintaining a good flow of Nitrogen over 120 minutes and held for 2 hours. The distillate as water of reaction collected was 70 grams against theoretical estimates of 76 grams. The ester had the acidity of 20 mg KOH/g and it was cooled to 40° C. under nitrogen. The crude ester was treated with 200 grams of deionized water containing 20 grams of Potassium Carbonate and 20.00 grams of Potassium Chloride at 80° C. When acidity of ester was <0.1 mg KOH/gram, it was treated with 5.0 grams of Hydrogen Peroxide. The top layer containing the benzoate ester was collected. It was vacuum stripped at 115° C.-120° C. and 20-25 mm of Hg vacuum. The liquid benzoate of this reaction was then treated with 0.2 grams each of magnesol, celaton FW 60 (diatomaceous earths) at 50° C. The product was filtered through a Filter Press with Whatman Paper #4. The net yield of the benzoate ester product was 935 grams.
Preparation of Benzoate Ester of Phenylethyl Alcohol (FINSOLV SUN)
In a 2,000 ml. four neck round bottom flasks equipped with glass stirrer, distillation head, condenser and receiver, added 488.61 grams (1.0 moles) of Phenylethyl alcohol and 511.84 grams (1.05 moles) of Benzoic acid. The temperature was raised to 60° C. with a good flow of Nitrogen. At 60° C. added 3.0 grams of Methane sulfonic acid and continued to heat to 150° C. maintaining a good flow of nitrogen over 60 minutes and held for 2 hours. The distillate collected was 70 grams against theoretical estimates of 76 grams. The ester had the acidity of 20 mg KOH/g. The reaction product was treated with 200 grams of deionized water containing 20.0 grams of sodium carbonate, 3 grams hydrogen peroxide and 20 grams of sodium sulfate at 80° C. The top layer containing the Benzoate ester was collected. It was vacuum stripped at 115° C.-120° C. and 20-25 mm of Hg vacuum. The liquid Benzoate of this reaction was then treated with 0.2 grams each of magnesol, celetom FW 60 (diatomaceous earths) at 50° C. The product was filtered through a Filter Press with Whatman Paper #4. The net yield of the Benzoate ester product was 946 grams. An analysis of the phenylethyl benzoate ester was conducted. Table I sets forth the typical physical and chemical properties that were observed.
Solubility of Phenylethyl Benzoate (Finsolv SUN)
The solubility characteristics of Phenylethyl Benzoate (Finsolv SUN) are tabulated in Table 2 below. It is soluble in most commonly used solvents, emollients and vehicles employed in cosmetic product formulations.
Soap Bar Evaluation
An evaluation of the use of phenylethyl benzoate in bar soaps was conducted as described below. The results show improvements in the properties of bar soaps upon inclusion of the phenylethyl benzoate ester of the invention.
Control bars: A soap bar containing 100% Syndet Base 96-143-1 available from Finetex, Inc. and a Combo Bar comprising 25% Syndet Base 96-143-1 and 75% Bradford soap base 80/20 have the following features during processing of the soap bars and after washing with said bars:
To the above control soap bar containing 100% Syndet Base 96-143-1 and to the above control combo bar comprising 25% Syndet Base and 75% Bradford soap base 80/20, was added 1% Finsolv SUN. The typical processing was followed, i.e., Syndet Base 96-143-1 or combo bar (25% Syndet Base 96-143-1 and 75% Bradford Tallow/coco soap base 80/20) was added to the amalgamator with Finsolv SUN, fragrance was incorporated and the bar colored and refined as usual. The resulting bar was found to have the following additional beneficial properties in addition to those properties described above for the control bars:
Syndet and combo bars containing Finsolv SUN were found to run excellently in the extruder, have excellent body with better consistency than the control bars, have excellent transparent or pearlescent effect, and have excellent body texture. When washed with water, the bars produce dense bubbles, and a slippery feel was observed when the bars were wet. After drying, no stickiness was found on the skin. It had a nice, soft, silky feel and excellent shine and gloss were observed. The skin felt well moisturized.
Transparent Combo Bar
Procedure:
Add the ingredients listed in Table III from Glycerin to water in sequence, heat to 60° C. with mixing. Add coco fatty acid and stearic acid and mix. Heat to 70° C. and allow to dissolve. Add sodium stearate and soap base and mix. When it becomes clear, add Tauranol I 78 C. Mix and adjust moisture until clear liquid is formed. Discharge after deaeration.
Non-Whitening Antiperspirant Stick
Procedure:
Formulations A to C so prepared were tested for emolliency, skin feel, slip and stick structure, on a scale of 1 to 5 with 1 representing the best and 5 representing poor. Results are as follows.
Clear Deodorant Stick
Procedure: Charge all ingredients into a suitable vessel. Heat to 80° C., with mixing, allowing all to dissolve. Cool to 60° C. and cast into stick molds. Formulations A to C so prepared were tested for skin feel, slip, stick structure, emolliency and tackiness on a scale of 1 to 5, with 1 representing the best and 5 representing poor. Results are as follows:
Pump Spray Deodorant
Procedure:
Combine alcohol, water and Triclosan. Mix well. Add balance of ingredients with mixing. Formulations A, B and C so prepared were tested for skin feel, slip, dryness, emolliency and tackiness on a scale of 1 to 5, with 1 representing the best and 5 representing poor. Results are as follows:
Cream Antiperspirant
Procedure:
Formulations A, B and C so prepared were tested for skin feel, slip, dryness, emoliiency and tackiness on a scale of 1 to 5, with 1 representing the best and 5 representing poor. Results are as follows:
Emollient Cleansing Lotion
Procedure:
Disperse carbopol into water. Add balance of I ingredients and heat to 75° C. Mix II Ingredients together and heat to 75° C. Add II to I with mixing. Combine III ingredients, then add to balance and begin cooling. At 40° C., add ingredients of IV and continue cooling to 30° C. Formulations A, B and C so prepared were tested for slip, skin feel, and emolliency, on a scale of 1 to 5, with 1 representing the best and 5 representing poor. Results are as follows:
Hand and Body Lotion
Procedure:
Disperse carbomer in water. Heat to 70° C. Add sorbitol 70% and tetrasodium EDTA. Weigh all II ingredients together and heat to 70° C. Add the ingredients of II to I with mixing. Add triethanoamine, continue mixing until 45° C. Add Germaben II as a preservative.
Formulations A, B and C so prepared were tested for skin feel, slip and emolliency on a scale of 1 to 5 with 1, representing the best and 5 representing poor. Results are as follows:
Light Body Lotion
Procedure:
Mix ingredients of I and heat to 65° C. Mix ingredients of II and heat to 70° C. Add ingredients of I to ingredients of II with mixing, maintaining temperature of 70° C. Mix 15 minutes. Cool with mixing to 25° C.
Formulations A, B and C so prepared were tested for skin feel, slip and emolliency on a scale of 1 to 5, with 1 representing the best and 5 representing poor. Results are as follows:
2 in 1 Conditioning Shampoo (Opaque Cream Type)
Procedure:
Table 12-A compares the properties of shampoo preparations of Formulations A, B and C of Example 13. Table 12-B compares foam results for shampoo of formulations A, B and C of Example 13. Table 12-C compares the effects of shampoo of formulations A, B and C of Example 13.
Procedure: 1% of each formulation was dissolved in 200 mls. of water and shaken in a 500 mls. cylinder with 10 sets of shakes.
All measurements are on a scale of 1-10, with I representing the best and 10 representing the worst.
Procedure: Rinsed hair tresses under tap water for 15 seconds. Rinsed hair tresses were Treated with shampoo. Mixed for 5 minutes. Removed the tresses and rinsed with tap water running on it for 15 seconds. Air dried. Performed wet and dry comb tests.
Clear Conditioning Shampoo
Procedure:
Charge water and heat to 75° C. Add all ingredients in order except DMDM Hydantoin, mixing well. Cool to 45° C. and add DMDM Hydantoin. Cool to room temperature.
Table 13-A compares the properties of shampoo preparations of formulations A, B & C of Example 14. Table 13-B compares properties of clear conditioning shampoo formulations A, B & C of Example 14. Table 13-C compares the effects of shampoo of formulations A, B & C on hair tresses.
Procedure: 1% of the respective formulation was dissolved in 200 mls of water and shaken in a 500 ml. cylinder with 10 sets of shakes.
All measurements are on a scale of 1 to 10, with 1 representing the best and 10 representing the worst.
Procedure: Rinsed hair tresses under tap water for 15 seconds. Rinsed hair tresses were treated with shampoo, mixed for 5 minutes. Removed the tresses and rinsed with tap water running on it for 15 seconds, then air dried. Performed wet and dry comb.
Shower and Bath Gel
Procedure:
Heat water to 50° C. and add all part I ingredients in order, allowing each to mix well. Raise temperature to 70° C. and add part II ingredients allowing each to mix well. Cool to 45° C. and add ingredients of part III. Cool to below 35° C. and adjust pH to 6.2. Pour warm.
Table 15-A compares the properties of shower & bath gel preparations of formulations A, B and C of Example 15.
Foaming Facial Cleanser Cream
Procedure:
Combine the contents of I and heat to 75° C. with gentle stirring until an homogeneous system is formed. Avoid aeration, separately combine II and heat with mixing to 60° C.
Add the molten II slowly to the vortex of I and continue stirring until cooled below 40° C. Resultant product builds viscosity and pearlescence in 48 hrs.
Table 16-A compares the properties of facial cleanser cream of formulations A, B and C of Example 16.
Table 17 identifies the trade or generic names of the ingredients used in the examples set forth above.
The examples demonstrate the uses of the ester of the invention in personal care products, specifically, non-whitening antiperspirant stick, deodorant stick, pump spray deodorant, cream antiperspirant, emollient cleansing lotion, hand and body lotion, light body lotion, 2 in 1 conditioning shampoo (opaque cream type) clear conditioning shampoo, shower and bath gel, and foaming facial cleanser cream. These are considered to be representative of formulations wherein the ester of the invention finds application.
The formulations prepared using the compositions of the present invention have outstanding attributes in that the phenylethyl benzoate ester of the invention functions as an emollient and to raise the refractive index properties of the compositions to which it is added.
It will be understood that the embodiments described herein are merely exemplary and that a person skilled in the art may make many variations and modifications without departing from the spirit and scope of the invention. All such variations and modifications are intended to be included in the scope of the invention as described herein.
Number | Date | Country | |
---|---|---|---|
Parent | 10757012 | Jan 2004 | US |
Child | 11141706 | May 2005 | US |