US3758411A - Aerosol composition compatible with excess propellant - Google Patents
Aerosol composition compatible with excess propellant Download PDFInfo
- Publication number
- US3758411A US3758411A US00191541A US3758411DA US3758411A US 3758411 A US3758411 A US 3758411A US 00191541 A US00191541 A US 00191541A US 3758411D A US3758411D A US 3758411DA US 3758411 A US3758411 A US 3758411A
- Authority
- US
- United States
- Prior art keywords
- lather
- aerosol
- propellant
- compositions
- fatty acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title abstract description 103
- 239000000443 aerosol Substances 0.000 title abstract description 54
- 239000003380 propellant Substances 0.000 title description 54
- 239000000194 fatty acid Substances 0.000 abstract description 45
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 44
- 229930195729 fatty acid Natural products 0.000 abstract description 44
- -1 FATTY ACID ESTER AMIDE Chemical class 0.000 abstract description 43
- 239000004615 ingredient Substances 0.000 abstract description 17
- 239000008149 soap solution Substances 0.000 abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000000344 soap Substances 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 239000000463 material Substances 0.000 description 17
- 239000006260 foam Substances 0.000 description 15
- 150000004665 fatty acids Chemical class 0.000 description 13
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 150000008282 halocarbons Chemical class 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 235000021355 Stearic acid Nutrition 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 8
- 239000008117 stearic acid Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 238000013019 agitation Methods 0.000 description 6
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 229960004418 trolamine Drugs 0.000 description 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 230000002939 deleterious effect Effects 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000001856 aerosol method Methods 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 229940077388 benzenesulfonate Drugs 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- LHSGMFNKICSRPI-UHFFFAOYSA-N ethanol octadecanoic acid Chemical compound CCO.CCO.CCO.CCCCCCCCCCCCCCCCCC(O)=O LHSGMFNKICSRPI-UHFFFAOYSA-N 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000001282 iso-butane Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- UKVYVYQRDUUCBK-UHFFFAOYSA-N morpholin-4-ium;octadecanoate Chemical compound C1COCCN1.CCCCCCCCCCCCCCCCCC(O)=O UKVYVYQRDUUCBK-UHFFFAOYSA-N 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 239000008257 shaving cream Substances 0.000 description 2
- 235000015424 sodium Nutrition 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical class [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 2
- 229940029614 triethanolamine stearate Drugs 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- PWVUXRBUUYZMKM-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOCCO PWVUXRBUUYZMKM-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 101001065065 Aspergillus awamori Feruloyl esterase A Proteins 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 101100027898 Homo sapiens OCR1 gene Proteins 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 102100026725 Ovarian cancer-related protein 1 Human genes 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- IHUMNXSBUOIDQI-UHFFFAOYSA-N Triethanolamine myristate Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCCC(O)=O IHUMNXSBUOIDQI-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- ZHALDANPYXAMJF-UHFFFAOYSA-N octadecanoate;tris(2-hydroxyethyl)azanium Chemical compound OCC[NH+](CCO)CCO.CCCCCCCCCCCCCCCCCC([O-])=O ZHALDANPYXAMJF-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000000246 remedial effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q9/00—Preparations for removing hair or for aiding hair removal
- A61Q9/02—Shaving preparations
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/30—Materials not provided for elsewhere for aerosols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0043—For use with aerosol devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/526—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 are polyalkoxylated
Definitions
- RCONHCH CH OOCR wherein R and R independently represent alkyl containing from 12 to carbon atoms.
- the present invention relates in general to compositions beneficially and advantageously adapted for use in connection with aerosol applications and in particular to the provision of improved lather-producing compositions for such purposes.
- aerosol methods of dispensing latherproducing compositions have met with a considerable measure of commercial success, e.g., compositions specifically adapted for the production of lather for shaving, shampooing or other and related Washing, cleansing, etc., operations.
- aerosol, lather-producing compositions make possible a much more highly efficient means for product application to, for example, human skin.
- significant increase in areacoverage efiiciency is attainable with aerosol methods of dispensing.
- the aerosol containers be subjected to vigorous agitation, e.g., shaking, during shipping in order to insure the requisite product stability. Moreover, maintaining the aerosol containers under constant agitation serves to arrest or otherwise retard any tendency of the product composition to deemulsify.
- latherproducing compositions specifically adapted for aerosol applications can be synergistically modified to advantage by the inclusion therein of a further additive selected from a relatively delimited class of compounds.
- a primary object of the present invention resides in the provision of aerosol, lather-producing compositions wherein the foregoing and related disadvantages are eliminated or at least mitigated to a substantial extent.
- Another object of the present invention resides in the provision of aerosol, lather-producing compositions capable of providing a foam or lather product upon aerosol dispensing having optimum properties as regards texture, feel, and the like.
- a further object of the present invention resides in the provision of aerosol, lather-producing compositions compatible with propellant quantities substantially in excess of those conventionally employed.
- a still further object of the present invention resides in the provision of aerosol, lather-producing compositions wherein any necessity for extended heat-curing operations, the maintaining of agitation conditions during transit, etc., is completely obviated.
- Yet another object of the present invention resides in the provision of aerosol, lather-producing compositions possessed of a high degree of exhaustion efficiency leading to manifold increase in volume of product foam.
- aerosol compositions comprising: (I) a propellant selected from the group consisting of saturated aliphatic hydrocarbons containing from 2-4 carbon atoms, halogenated hydrocarbons containing from l-2 carbon atoms and mixtures thereof, and (II) a lather-producing component containing as essential ingredients: (a) a water soluble soap selected from the group consisting of C C saturated and unsaturated fatty acids, sodium C -C alkyl benzene sulfonate, sodium lauryl sulfate and mixtures thereof, present in an amount of about 3-30% by weight (b) water present in an amount of at least 70% by weight, and (c) a fatty acid ester amide of the following structural formula:
- R and R independently represent alkyl containing from 12 to 20 carbon atoms and present in an amount of about 01-10% by weight of the lather-producing composition, the weight ratio of (II) to (I) being within the range of from about 5:1 to about 70:1 said composition exhibiting higher foam volume and compatibility with larger amounts of propellant than similar compositions not containing said ester-amide.
- the fatty acid ester amides contemplated for use in accordance with the present invention are uniquely typified in that their use in compositions of the type herein described permit the incorporation of propellant materials in unusually high quantities in the total absence of the deleterious effects characterizing compositions heretofore promulgated in the art such as sputtering, inferior product texture, feel, etc.
- concentration of propellant in the compositions herein described can be of such magnitude as to permit the 0btention of foam volume which approximately double those heretofore obtainable utilizing the identical amounts of lather-forming ingredients.
- aerosol products commercially available in nominal six ounce containers generally provide from about 1400 to about 1700 cubic centimeters of lather with the use of a feasible maximum of 5.1 grams of hydrocarbon propellant to about 180 grams of lather-producing composition, the latter being comprised primarily of an aqueous soap solution.
- aerosol products formulated in accordance with the present invention are capable of yielding approximately 3400 centimeters of superior quality lather or foam by increasing the quantity of propellant employed, the lather being made feasible by the presence of the fatty acid ester amide.
- compositions of the present invention likewise offer significant advantage when prepared using conventional propellant quantities.
- the lather product obtainable possesses superior properties as regards texture, feel, etc.
- the presence of the fatty acid ester amide eliminates entirely any need for agitation-in-transit or extensive heat curing prior to shipment. Without intending to be bound by any theory, it is postulated in explanation of the foregoing that the presence of the fatty acid ester amide serves to augment or otherwise promote compatibility of the involved ingredients, e.g., propellant, soap solution, as well as any other auxiliary ingredients which might be present.
- the increased compatibility is manifested in the form of a more stable aerosol product, i.e., the tendency of the ingredients to de-emulsify or otherwise separate is minimized if not eliminated. In this manner there is obtained a more uniform product throughout the aerosol container.
- the present invention proves particularly beneficial in connection with aerosol compositions formulated with propellants of the aliphatic hydrocarbon type.
- fatty acid ester amides contemplated for use in accordance with the present invention may be employed either singly or in admixture. Suitable for use are monoethanol amide esters of straight and branched chain, saturated and unsaturated C C more preferred C to C fatty acids or mixtures thereof. For example, one such compound found to be particularly effective is a monoethanol amide ester of a mixture of saturated straight chain G to C fatty acids.
- the fatty acid ester amide compound may be readily and conveniently prepared by reacting, for example, ethanol amide (H NCH CH OH) with the fatty acid material whereby to form the corresponding fatty acid ester amide derivative.
- this manner of preparation involves the acylation of both the amino and hydroxyl groups, i.e., simultaneous amidification and esterification.
- This method of synthesis is preferable in those instances wherein it is desired that the R and R moieties in the above depicted structural formula be identical.
- the amidification and esterification reactions may be carried out separately, i.e., sequentially; this particular procedure is preferable in the preparation of fatty acid ester amides having different acyl moieties.
- the particular fatty acid selected must be one having the requisite number of carbon atoms in accordnace with the structural formula hereinbefore given.
- the amount of fatty acid ester amide employed may be rather minimal in comparison to the other ingredients comprising the essential components of the subject compositions.
- optimum realization of the improvements described herein can be obtained with the use of the fatty acid acide in concentrations ranging from about 0.1% to about 10% by weight of the soap solution, the latter comprising the soap and water components, with a range of about 0.5% to about 5.0% being particularly preferred.
- Selection of a specific concentration within the aforestated range will be influenced to a great extent by, for example, the type of propellant material employed.
- hydrocarbon propellants increased quantities of atty acid ester amide are usually preferable while in the case of halogenated hydrocarbon propellants, it is usually found that lesser amounts suflice.
- departures from the aforestated ranges may be dictated in a particular circumstance depending upon the requirements of the formulator.
- soap or detergent material employed in the compositions described herein is not particularly critical and thus may be selected from any of those water soluble soap materials conventionally employed in the preparation of lather-producing compositions of the type utilized in shaving creams, shampoos, etc., such as the water soluble soaps of higher fatty acids.
- Suitable for use are water soluble soaps selected from the group consisting of sodium, potassium, ammonium, triethanol amine, morpholine C C fatty acids and mixtures thereof. More suitable soaps include the soluble stearate soaps such as the sodium, potassium, ammonium and soluble amine soaps of commercial stearic acid with particularly preferred representatives including the sodium-potassium soaps of commercial, double-pressed stearic acid, e.g.,
- the stearates may be produced by neutralization of stearic acid with alkali or alternatively may be introduced in the form of animal fats such as tallow, the latter containing high quantities of stearic acid. Mixtures of stearate soaps may also be used if desired in Order to assure the obtention of a soap material having the desired consistency. The latter is particularly significant in connection with the preparation of shaving lather compositions. Vegetable oil soaps may likewise be employed and in fact are particularly recommended for use in the preparation of shampoo compositions.
- vegetable oil soaps may be employed to advantage in admixture with soluble soaps of the stearic acid type in the preparation of shaving lather compositions, the presence of the vegetable oil soap serving to minimize any tendency of the resulting soap solution to gel or otherwise undergo undesired increases in viscosity at low temperatures.
- the amount of soap employed in the preparation of compositions described herein may vary within relatively wide limits, this aspect comprising a relatively non-critical factor in the practice of the present invention, apart from the obvious requirement that the soap material be employed in amounts sufiicient to yield a Satisfactory lather.
- the minimum amount of soap employed will be governed by the latter mentioned factor.
- the maximum amount of soap employed is governed primarily be economic considerations. However, the use of excess quantities of soap may very likely give rise to problems associated with gel formation at lower temperature ranges. Accordingly, the maximum amount of soap employed should be such as to substantially resist any tendency to form a gel at the temperature ranges likely to be encountered in use.
- soap in amounts approximating from about 3 to about 30 percent by weight of the soap in water solution sufiice for the vast majority of applications contemplated with a range of from about 5 to about 20% being particularly preferred.
- soap materials found to be eminently suitable for use in the present invention there may be mentioned without necessary limitation the following:
- the amount of water employed will, of course, be determined by the concentration of soap desired in the lather-producing composition. For most applications, the water will usually comprise at least about 70% by weight of the composition.
- the propellant materials suitable for use in the practice of the present invention comprise in general any of those conventionally employed in the formulation of aerosol products, i.e., non-toxic, liquefied, normally gaseous, saturated, low molecular weight hydrocarbon and halogenated hydrocarbons.
- Suitable aliphatic hydrocarbon propellants include, for example, ethane, propane, butane, isobutane, etc.
- aliphatic hydrocarbon propellants containing from 2 to 4 carbon atoms are preferred for use.
- halogenated hydrocarbon propellants there may be mentioned in particular and without necessary limitation, dichlorodifluoromethane, 1,2-dichloro-1,1,2,2-tetraiiuoromethane; monofluorotrichloromethane; trichlorotrifiuoroethane, etc.
- the propellant material whether of the hydrocarbon or halogenated hydrocarbon type is employed in concentrations sufiicient to yield a lather-producing composition/ propellant weight ratio in the range of from about 5:1 to :1.
- concentrations sufiicient to yield a lather-producing composition/ propellant weight ratio in the range of from about 5:1 to :1.
- the presence of the fatty acid ester amide material makes possible the provision of superior lather or foam producing compositions whether the propellant material be employed in excess or conventional quantities.
- the selection of a particular concentration of propellant capable of providing optimum advantage for the application at hand can be readily determined by one having reasonable skill in the art.
- the propellant, fatty acid ester amide and aqueous soap solution comprises the essential ingredients of the composition described herein.
- Ingredients of this type are, of course, well known in the art and include, for example, skin fresheners, lather stabilizers and the like such as glycerine, lanolin, lecithin, coconut oil, fatty acids, fatty amides, etc.; perfume, etc.
- lower molecular Weight aliphatic alcohols and preferably lower monohydric alcohols e.g., methanol, ethanol, normal propanol, isopropanol, etc., may be employed for such purposes.
- Auxiliary ingredients of the aforedescribed type may be added in any desired amount with the obvious limitation that their proportions be confined within limitations Whch assures the absence of deleterious effects. In any event, it is conventional practice to include such materials in amounts sufficient to yield a concentration within the range of from about 0.1 to about 10% by weight of the total composition.
- the lather-producing compositions described herein may be prepared in any suitable manner.
- one satisfactory method comprising dissolving the soap or detergent material in water and thereafter adding the fatty acid ester amide compound.
- the latter composition is thereafter introduced into the aerosol container.
- the propellant, under pressure, may then be admitted to the container through a valve or other appropriate means, the container preferably being slightly chilled during the addition.
- the diethanol amide of a 70 :30 (by Weight) mixture or lauric and myristic acids The diethanol amide of a 70 :30 (by Weight) mixture or lauric and myristic acids.
- Coconut oil fatty acid is a mixture of Ca to C13 fatty acids comprising approximately 48% lauric acid, a myristic acid, 9% palmitic, 2.1% stearic, 5.7 oleic, 2.6% linoleic, 7.9% caprylic, and 7.2% capric.
- the stearic monoethanol amide ester employed in this example is a mixture of monoethanol amide esters of straight chain, saturated CLO-C15 fatty acids of which stearic acid is one. It is marketed by Van Dyk and Company under the trade name Cerasynt D and has an acid number of 10-20, free stearic acid of 36-72%, saponification number 98-108 and an iodine value of 0.5 maximum.
- the aerosol container is cured at 130 F. for a period of 20 minutes and thereafter subjected to vigorous shaking. Expulsion of the aerosol contents resulted in the formation of a rubbery, sputtery product which proved to be highly unsuitable 8 evaluated in terms of texture, feel, uniformity of composition as well as total volume of foam available for a given quantity of composition.
- the quantity of lather obtainable with the compositions of the present invention at least double in volume the quantity of foam obtainable with corresponding control compositions.
- the lather products obtained with the compositions of Examples 215 were of excellent texture and feel, being smooth, aesthetically pleasing and non-rubbery to the touch.
- EXAMPLES 2-15 A series of lather-producing compositions for shaving cream applications is prepared utilizing a simple mixture of fatty acid ester amide, aqueous soap solution and propellant in varying quantities as indicated in the following table.
- the composition in question contains the fatty acid ester amide, soap and propellant in the proportions stated with the balance of the composition comprising water, i.e., sufiicient to make 100 parts of total formula.
- each of the compositions thus prepared is charged to a six ounce hermetically sealed container and thereafter pressurized with propellant in the manner described in Example 1.
- the lather product obtained is The results obtained tend to indicate that the halogenated hydrocarbon propellant materials may be more readily incorporated in greater amounts than is possible with propellants of the hydrocarbon type.
- the presence of the fatty acid ester amide proves highly beneficial since it obviates completely any requirement for mechanical agitation of the aerosol container for purposes of expediting the attainment of a satisfactory aerosol foam.
- halogenated hydrocarbon propellants in increased quantities in compositions devoid of the fatty acid ester amide fails to obviate the agition requirement as a condition to the obtention of a satisfactory product.
- improvements as regards quality of lather, volume of foam obtainable with a predetermined quantity of lather-producing composition, etc. are readily obtainable despite the employment of the fatty acid ester amide in relatively minor proportions.
- the present invention as is evident from the above description relates in one of its aspects to an improved lather-producing composition comprising propellant, water soluble soap, and water, wherein the improvement comprises that also present is a fatty acid ester amide of the following structural formula:
- the fatty acid ester amide provides a lather composition of superior quality compatible with propellant in excess of amounts permitted in the absence of said fatty acid ester amide.
- the lather compositions containing additional propellant supply larger volumes of superior lather.
- An aerosol composition consisting essentially of:
- a propellant selected from the group consisting of saturated aliphatic hydrocarbons containing from 2-4 caruon atoms, halogenated hydrocarbons containing from 12 carbon atoms and mixtures thereof;
- a lather-producing component containing as essential ingredients: (a) a water soluble soap selected from the group consisting of C -C saturated and unsaturated fatty acids, sodium C -C alkyl benzene sulfonates sodium lauryl sulfate, and mixtures thereof, present in an amount of about 15-30% by Weight (b) Water present in an amount of at least 70% by weight, and (c) a fatty acid ester amide of the following structural formula:
- RCONHCH CH OOCR wherein R and R independently represent alkyl containing from 12 to 20 carbon atoms and present in an amount of about 0.1-10% by weight of the latherproducing composition, the weight ratio of (II) to (I) being within the range of from about 5:1 to about 70:1 said composition exhibiting higher foam volume and compatibility with larger amounts of propellant than similar compositions not containing said ester-amide.
- An aerosol composition according to claim 1 wherein said water soluble soap is selected from the group consisting of sodium, potassium, ammonium, trielhanol amine, and morpholine C C fatty acids.
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46858865A | 1965-06-30 | 1965-06-30 | |
US19154171A | 1971-10-21 | 1971-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3758411A true US3758411A (en) | 1973-09-11 |
Family
ID=26887150
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00191541A Expired - Lifetime US3758411A (en) | 1965-06-30 | 1971-10-21 | Aerosol composition compatible with excess propellant |
Country Status (4)
Country | Link |
---|---|
US (1) | US3758411A (enrdf_load_stackoverflow) |
BE (1) | BE683288A (enrdf_load_stackoverflow) |
DE (1) | DE1617049A1 (enrdf_load_stackoverflow) |
GB (1) | GB1103818A (enrdf_load_stackoverflow) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0205553A4 (en) * | 1984-12-07 | 1988-08-04 | Lloyd I Osipow | SHAVING COMPOSITION WITH AUTOMATIC FOAM PRODUCTION. |
US5560859A (en) * | 1989-07-26 | 1996-10-01 | Pfizer Inc. | Post foaming gel shaving composition |
KR100460949B1 (ko) * | 2001-12-11 | 2004-12-09 | 주식회사 태평양 | 에어로졸 타입의 클렌징 폼 조성물 |
US20130150244A1 (en) * | 2011-12-12 | 2013-06-13 | Diversified Cpc International, Inc. | Ethane as an Aerosol Propellant |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1125457A (en) * | 1978-08-09 | 1982-06-15 | James J. Albanese | Aerosol preparation |
US4439342A (en) * | 1979-07-23 | 1984-03-27 | United Industries Corporation | Aerosol preparation |
US4439343A (en) * | 1979-07-23 | 1984-03-27 | United Industries Corporation | Aerosol preparation |
-
1966
- 1966-04-16 DE DE19661617049 patent/DE1617049A1/de active Pending
- 1966-06-22 GB GB27858/66A patent/GB1103818A/en not_active Expired
- 1966-06-28 BE BE683288D patent/BE683288A/xx unknown
-
1971
- 1971-10-21 US US00191541A patent/US3758411A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0205553A4 (en) * | 1984-12-07 | 1988-08-04 | Lloyd I Osipow | SHAVING COMPOSITION WITH AUTOMATIC FOAM PRODUCTION. |
US5560859A (en) * | 1989-07-26 | 1996-10-01 | Pfizer Inc. | Post foaming gel shaving composition |
US5902778A (en) * | 1989-07-26 | 1999-05-11 | Pfizer Inc | Post foaming gel shaving composition |
KR100460949B1 (ko) * | 2001-12-11 | 2004-12-09 | 주식회사 태평양 | 에어로졸 타입의 클렌징 폼 조성물 |
US20130150244A1 (en) * | 2011-12-12 | 2013-06-13 | Diversified Cpc International, Inc. | Ethane as an Aerosol Propellant |
Also Published As
Publication number | Publication date |
---|---|
GB1103818A (en) | 1968-02-21 |
DE1617049A1 (de) | 1971-02-11 |
BE683288A (enrdf_load_stackoverflow) | 1966-12-01 |
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