Synergistic deodorant compositions

Information

  • Patent Grant
  • 4305930
  • Patent Number
    4,305,930
  • Date Filed
    Monday, November 19, 1979
    44 years ago
  • Date Issued
    Tuesday, December 15, 1981
    42 years ago
Abstract
The disclosure teaches a synergistic deodorant combination of citronellyl senecioate with 3-trifluoromethyl-4,4'-dichlorocarbanilide or 3,4,4'trichlorocarbanilide. The disclosure also teaches synergistic combinations of the foregoing ingredients with 2,4,4'-trichloro-2'-hydroxy diphenyl ether. The foregoing ingredients show synergistic activity as deodorants in various combinations and concentrations as set out in the disclosure. The structures of the ingredients are shown below. ##STR1##
Description

BACKGROUND OF THE INVENTION
This invention relates to the personal care field, particularly to preparations for use by humans as underarm deodorants.
Underarm deodorant preparations are convenient chemical aids to keeping the human body's odors unobtrusive and the owner socially acceptable. Deodorant ingredients that are safe and efficacious are known; however, they are expensive ingredients and a continuing need exists for less expensive active ingredients or ways of making existing ingredients go farther.
BRIEF SUMMARY OF THE INVENTION
From among the numerous deodorant substances known in the art, I have discovered that a combination of citronellyl senecioate (sometimes hereafter referred to as CS), having the structure: ##STR2## with carbanilides having the general structure: ##STR3## wherein R is selected from the group consisting of CF.sub.3 and Cl, which are 3-trifluoromethyl-4, 4'-dichlorocarbanilide (sometimes hereafter referred to as TDC) and 3,4,4' trichlorocarbanilide (sometimes hereafter referred to as TCC) respectively, or mixtures of the two, yields an unexpected synergestic potentiation of the deodorant capabilities of the ingredients; and further, that a combination of citronellyl senecioate, 3,4,4' trichlorocarbanilide and/or 3-trifluoromethyl-4,4'-dichlorocarbanilide and a compound having the structure: ##STR4## which is 2,4,4'-trichloro-2'-hydroxy diphenyl ether (sometimes hereinafter referred to as DPE) also has synergistic deodorant properties. Owing to the synergistically enhanced efficacy, less of the combined active ingredients is required to obtain the effect of a greater quantity of the prior art active ingredients used separately.
The synergistic results of this invention occur in such compositions containing the following concentrations: from about 25 to 500 parts per million of citronellyl senecioate, from about 10 to 500 parts per million of TCC or from about 0.1 to 10 parts per million of TDC. Any of the foregoing combinations with the addition of about 0.1 to 1 part per million DPE is also synergistic.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
The ingredients of the synergistic deodorant combination of this invention can be combined at ambient temperatures and atmospheric pressures by simple mixing.





The resulting composition can be incorporated into product formulations by state of the art methods known to those skilled in the art. The following are examples of products which can be made by incorporating the composition of this invention.
EXAMPLE I
Deodorant Cleansing Bar
Soap pellets are mixed with a synergistic combination of this invention according to the ranges in Schedule A below. Additional optional ingredients such as, without limitation: brighteners, dispersing agents, colors and preservatives, may be added as desired. The optional ingredients and TCC are mixed together in water and the resulting slurry is added to the soap pellets in the amalgamator. Then the CS and perfume are mixed together and added to the soap pellets. The ingredients are processed into finished soap bars in the usual manner of making soap bars.
______________________________________Schedule A85/15 % %tallow/coco Synthetic TCC/CS % Option- Per-8% Moisture Detergent 1:2 Water al fume______________________________________A. 50 28.5 5.0 14 0.5 2.0B. 90 0 0.5 8.9 0.1 0.5C. 70 19.1 2.0 8.0 0.2 0.7D. 70 19.3 1.0 8.0 0.2 1.5______________________________________
EXAMPLE II
Stick Deodorant
Expressing parts by weight:
1st moiety: Mix 42 parts ethyl alcohol, 3 parts propylene glycol, 6 parts sodium stearate and 0.01 part TDC together and heat to 50.degree. C. and until a clear solution is obtained.
2nd moiety: Add 0.5 parts CS to perfume q.s. and mix
Add the 2nd moiety to the 1st moiety at 50.degree. C. and mix well. Let product cool to about 35.degree. C. and place in container to cool to ambient temperature.
EXAMPLE III
Water-in-Oil Deodorant Cream
______________________________________A Mineral Oil 20.00 Petrolatum 8.50 Ceresin Wax 6.00 Lanolin 4.50 ARLACEL 83 4.00B Magnesium Sulfate 0.15 Water 21.85C Zinc Oxide 15.00 Zinc Stearate 10.00D CS/TCC/DPE (100:50:1) 10.00E Perfume q.s.______________________________________
Procedure: Heat (A) to 80.degree. C. Add (B) to (A) with stirring and continue to stir until emulsion reaches 50.degree. C. Add (C) slowly with stirring and cool slowly to 40.degree. C., continuing to stir during the cooling process. Add TDC plus DPE slowly with stirring. Mix the perfume with CS to get a uniform mixture, and then add and perfume and CS mixture to the formulation with stirring.
EXAMPLE IV
Aerosol Deodorant Powder
______________________________________Ingredients:______________________________________A Talc 11.65 Zinc Oxide 0.80 Magnesium Stearate 1.20B Isopropyl Myristate 0.50 Sorbitan sesquioleate 0.50 CS/TDC (50:1) 0.25C Freon 11 55.05 Freon 12 30.05D Perfume q.s.______________________________________
Mix ingredients of (A). Dissolve CS/TDC in warm isopropyl myristate; Cool and add Sorbitan sesquioleate, perfume. Then add (A) to (B) with constant stirring to form a slurry. Cold or pressure fill container with (C) using powder spray head.
EXAMPLE V
Deodorant Aerosol
Dissolve the following ingredients in alcohol:
______________________________________ % in AerosolConcentrate: 40.0______________________________________1. SDA 40 Anhydrous 93.202. Zinc Phenolsulfonate 4.253. CS/TDC (10:1) 0.304. Propylene Glycol USP 2.005. Perfume 0.25Propellent: 60.0Isotron 12 40.00Isotron 114 60.00______________________________________
The compositions of this invention were tested for efficacy at various concentrations and ratios, and compared to the efficacies of the single ingredients at various concentrations, explanations and examples of which follow.
In Vitro Deodorant Test
The synergistic odor-inhibiting properties of this invention were evaluated by in vitro deodorant tests. The in vitro test method involves the preparation of odor generating medium which evolves a strong body type odor upon inoculation with appropriate bacteria followed by incubation at 37.degree. C. for 72 hours or longer. An incubation time of at least forty hours is generally needed for detection of odor generation.
EXAMPLE VI
Following the protocol of the in vitro deodorant test, varying ratios of CS:TDC were incorporated into the sweat medium as a DMF solution or suspension before inoculation and incubation. After incubation for periods of 43 and 110 hours on the average, a comparison of the odor generated in the medium-plus-active material with the odor generated in the medium-without-active indicated effectiveness against "body type" odors of bacterial origin at 43 hours (average) and 110 hours (average). The results are tabulated in Table I below. In Table I a comparison of (a) and (b) to (c) for example indicates that a 50:1 ratio does reduce odor dramatically.
The relationships in Table I are illustrated in FIGS. 1 and 2 of the drawings.
TABLE I______________________________________Concentration Odor*CS TDC 43 Hr. Avg. 110 Hr. Avg.______________________________________(a) 0 0 +1.6 +2.4(b) 500 ppm 0 +1.0 +1.0(c) 0 10 ppm +1.6 +2.0(d) 500 ppm 10 ppm -0.5** +0.3(e) 0 5 ppm +1.1 +2.7(f) 500 ppm 5 ppm -0.3 +1.3(g) 100 ppm 0 +1.5 +2.2(h) 100 ppm 10 ppm +0 +1.3(i) 100 ppm 5 ppm +0 +1.2______________________________________ *The maximum odor possible is +3.0 on our scale. **The negative scores mean that the sample containing test chemical but uninoculated had more odor than the corresponding samples that were inoculated.
EXAMPLE VII
The protocol of Example VI was followed (with the exception noted below) using compounds CS:TCC with the results shown in Table II. The relationships in Table II are illustrated in FIGS. 3 and 4 of the drawings.
TABLE II______________________________________ConcentrationCS TCC Odor Score*______________________________________0 0 1.8250 ppm 0 0.8100 ppm 0 1.40 50 ppm 1.6250 ppm 50 ppm 0100 ppm 50 ppm 0.10 25 ppm 1.3250 ppm 25 ppm 0100 ppm 25 ppm 00 10 ppm 1.9250 ppm 10 ppm 1.4100 ppm 10 ppm 1.6______________________________________ *These values are for 72 hour evaluations. The maximum odor score possibl (water plus medium only) is +3.0. The tubes were innoculated with S. epidermidis (24 hour culture).
Ratios of the combination CS:TCC:DPE were tested in vitro and the results appear in the next example. The data from Table III therein indicate synergism in the combinations CS:TCC:DPE at the ratios 100:10:0.5; 50:10:0.5; 100:10:0.1; 100:25:0.5; 50:25:0.5; 100:25:1; and 50:25:1. The best ratios are at 100:10:0.5 and 50:10:0.5.
EXAMPLE VIII
The protocol of Example VI was followed (with the exception noted below) using compounds CS:TCC:DPE with the results shown in Table III.
TABLE III______________________________________ConcentrationCS TCC DPE Odor Score*______________________________________0 0 0 2.1100 ppm 0 0 1.4 50 ppm 0 0 1.20 25 1 0.8100 ppm 25 1 0.250 ppm 25 1 0.10 10 1 0.6100 ppm 10 1 0.3 50 ppm 10 1 0.30 25 0.5 0.8100 ppm 25 0.5 0.1 50 ppm 25 0.5 0.10 10 0.5 1.4100 ppm 10 0.5 0.2 50 ppm 10 0.5 0.20 25 0.1 0.3100 ppm 25 0.1 0.20 10 0.1 0.6100 ppm 10 0.1 00 0 1 1.50 0 0.5 2.20 0 0.1 2.0 50 ppm 0 1 0.7 50 ppm 0 0.5 1.4 50 ppm 0 0.1 0.7______________________________________ *These values are for 72 hour evaluations. The maximum odor score possibl (water plus medium only) is +3.0. The tubes were innoculated with S. epidermidis (24 hour culture).
EXAMPLE IX
An in vivo deodorancy test of the composition of this invention in a 10:1 ratio of CS:TDC was conducted according to the following:
This test panel is carried out over a three week period and requires only one panelist per deodorant candidate. The final odor reduction attributable to each deodorant material is obtained by averaging all 6 hour and/or 24 hour period odor reduction values. The actual calculations used are illustrated below. The results as shown below are given additional significance by comparing them with similar values obtained by treating both axillae with placebo only under the same protocol.
__________________________________________________________________________Hours AfterInitial Treatment 6 24 30 48 54 72 78 96__________________________________________________________________________Week One Scores.sup.a 13-13 16-13 16-13 19-13 19-14 19-12 20-14 20-11Week Two Scores.sup.a 13-13 20-14 18-13 22-13 20-14 22-13 21-14 20-12Total Scores 26-26 36-27 34-26 41-26 39-28 41-25 41-28 40-23Reduction Ratio.sup.b 0/26 9/36 8/34 15/41 11/39 16/41 13/41 17/40% Odor Reduction 0% 25% 24% 37% 28% 39% 32% 43%__________________________________________________________________________ .sup.a These scores are the sum of all judges employed. They also represent untreated side treated side scores respectively. .sup.b This ratio is untreated score minus treated score divided by untreated score. ##STR5## ##STR6##
Over a two week active test period the CS:TDC combination effected a consistent and definite reduction in body odor.
The results of the test conducted are set forth below as Table IV.
TABLE IV______________________________________Time after CS + TDC Placebo treatmentfirst active % Odor of both axillaeapplication Reduction (a) % Odor Reduction______________________________________O hr. - -* 6 hr. -5% (b) +12%** 24 hr. -1% -20%* 30 hr. +12% +10%** 48 hr. +20% -8%* 54 hr. +18% -7%** 72 hr. +24% -13%* 78 hr. +15% -12%** 96 hr. - (c) +7%______________________________________ (a) This ratio is untreated score minus treated score divided by untreate score. (b) A negative value indicates that the treated axilla had a higher odor than the untreated axilla. (c) No value was taken for this time period.
* 6 hour odor Reduction Average +10% +1%** 24 hour odor Reduction Average +14% -9%
Claims
  • 1. A composition of matter comprising the synergistic, deodorant combination, by weight, of about 100 to 250 parts citronellyl senecioate and about 25 to 50 parts 3,4,4' trichlorocarbanilide.
  • 2. The composition of claim 1 wherein citronellyl senecioate comprises about 250 parts and 3,4,4' trichlorocarbanilide comprises about 50 parts.
  • 3. The composition of claim 1 wherein citronellyl senecioate comprises about 100 parts and 3,4,4' trichlorocarbanilide comprises about 50 parts.
  • 4. The composition of claim 1 wherein citronellyl senecioate comprises about 100 parts and 3,4,4' trichlorocarbanilide comprises about 25 parts.
  • 5. A composition of matter comprising the synergistic, deodorant combination, by weight, of about 100 to 500 parts citronellyl senecioate and about 5 to 10 parts 3-trifluoromethyl-4, 4'-dichlorocarbanilide.
  • 6. The composition of claim 5 wherein citronellyl senecioate comprises about 500 parts and 3-trifluoromethyl-4, 4'-dichlorocarbanilide comprises about 10 parts.
  • 7. The composition of claim 5 wherein citronellyl senecioate comprises about 100 parts and 3-trifluoromethyl-4, 4'-dichlorocarbanilide comprises about 10 parts.
  • 8. The composition of claim 5 wherein citronellyl senecioate comprises about 100 parts and 3-trifluoromethyl-4, 4'-dichlorocarbanilide comprises about 5 parts.
Parent Case Info

This is a continuation of application Ser. No. 843,904, filed Oct. 20, 1977, now abandoned.

US Referenced Citations (2)
Number Name Date Kind
3288681 Goldberg et al. Nov 1966
3493650 Dunkel Feb 1970
Foreign Referenced Citations (1)
Number Date Country
2351927 Apr 1975 DEX
Non-Patent Literature Citations (1)
Entry
La Parfumerie Moderne, Nov.-Dec. 1952, vol. 44:30, pp. 64 to 74.
Continuations (1)
Number Date Country
Parent 843904 Oct 1977