US2853423A - Aerosol sun-screening composition - Google Patents
Aerosol sun-screening composition Download PDFInfo
- Publication number
- US2853423A US2853423A US510050A US51005055A US2853423A US 2853423 A US2853423 A US 2853423A US 510050 A US510050 A US 510050A US 51005055 A US51005055 A US 51005055A US 2853423 A US2853423 A US 2853423A
- Authority
- US
- United States
- Prior art keywords
- acids
- sun
- aerosol
- propellent
- vehicle
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 45
- 239000000443 aerosol Substances 0.000 title claims description 14
- 238000012216 screening Methods 0.000 title description 4
- 239000002253 acid Substances 0.000 claims description 22
- 150000002148 esters Chemical class 0.000 claims description 21
- 239000000516 sunscreening agent Substances 0.000 claims description 17
- 150000007513 acids Chemical class 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 5
- 239000003380 propellant Substances 0.000 claims description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 4
- 239000000600 sorbitol Substances 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 239000005871 repellent Substances 0.000 claims description 3
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 2
- 229930195725 Mannitol Natural products 0.000 claims description 2
- 239000000594 mannitol Substances 0.000 claims description 2
- 235000010355 mannitol Nutrition 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 description 34
- 239000004480 active ingredient Substances 0.000 description 18
- -1 propellent Substances 0.000 description 18
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 7
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 7
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 7
- 125000005907 alkyl ester group Chemical group 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- 206010042496 Sunburn Diseases 0.000 description 5
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 5
- WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 description 4
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229960004881 homosalate Drugs 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- 125000003944 tolyl group Chemical group 0.000 description 4
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 4
- 229940029284 trichlorofluoromethane Drugs 0.000 description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 description 3
- 229960004050 aminobenzoic acid Drugs 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 2
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 2
- WGIMXKDCVCTHGW-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOCCO WGIMXKDCVCTHGW-UHFFFAOYSA-N 0.000 description 2
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 2
- AMEMLELAMQEAIA-UHFFFAOYSA-N 6-(tert-butyl)thieno[3,2-d]pyrimidin-4(3H)-one Chemical compound N1C=NC(=O)C2=C1C=C(C(C)(C)C)S2 AMEMLELAMQEAIA-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N Nonanedioid acid Natural products OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229960004909 aminosalicylic acid Drugs 0.000 description 2
- 150000001733 carboxylic acid esters Chemical class 0.000 description 2
- XFKBBSZEQRFVSL-UHFFFAOYSA-N dipropan-2-yl decanedioate Chemical compound CC(C)OC(=O)CCCCCCCCC(=O)OC(C)C XFKBBSZEQRFVSL-UHFFFAOYSA-N 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 2
- MMKRHZKQPFCLLS-UHFFFAOYSA-N ethyl myristate Chemical compound CCCCCCCCCCCCCC(=O)OCC MMKRHZKQPFCLLS-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 229940033357 isopropyl laurate Drugs 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- AOHAPDDBNAPPIN-UHFFFAOYSA-N myristicinic acid Natural products COC1=CC(C(O)=O)=CC2=C1OCO2 AOHAPDDBNAPPIN-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N n-hexadecanoic acid Natural products CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000001593 sorbitan monooleate Substances 0.000 description 2
- 229940035049 sorbitan monooleate Drugs 0.000 description 2
- 235000011069 sorbitan monooleate Nutrition 0.000 description 2
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- NWGAAWUUGRXXSC-UHFFFAOYSA-N 1-(2-hydroxypropoxy)propan-2-yl 2-hydroxybenzoate Chemical compound CC(O)COCC(C)OC(=O)C1=CC=CC=C1O NWGAAWUUGRXXSC-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- LNYTUARMNSFFBE-UHFFFAOYSA-N 4-(diethylazaniumyl)benzoate Chemical compound CCN(CC)C1=CC=C(C(O)=O)C=C1 LNYTUARMNSFFBE-UHFFFAOYSA-N 0.000 description 1
- WUBBRNOQWQTFEX-UHFFFAOYSA-M 4-aminosalicylate(1-) Chemical compound NC1=CC=C(C([O-])=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-M 0.000 description 1
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 229940031569 diisopropyl sebacate Drugs 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 229940113120 dipropylene glycol Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 230000002014 erythemogenic effect Effects 0.000 description 1
- XPKFLEVLLPKCIW-UHFFFAOYSA-N ethyl 4-(diethylamino)benzoate Chemical compound CCOC(=O)C1=CC=C(N(CC)CC)C=C1 XPKFLEVLLPKCIW-UHFFFAOYSA-N 0.000 description 1
- 229940067592 ethyl palmitate Drugs 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 229940075495 isopropyl palmitate Drugs 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- AYOOGWWGECJQPI-NSHDSACASA-N n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-3-(3-propan-2-yloxy-1h-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine Chemical compound N1C(OC(C)C)=CC(N2C3=NC(N[C@@H](C)C=4N=CC(F)=CN=4)=CC=C3N=C2)=N1 AYOOGWWGECJQPI-NSHDSACASA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- 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
- A61K8/445—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof aromatic, i.e. the carboxylic acid directly linked to the aromatic ring
Definitions
- This invention relates to compositions of matter and more particularly to aerosol compositions useful in protecting against sunburn.
- compositions Prior to this invention, various compositions were known which were effective in minimizing or preventing erythema solare, commonly known as sunburn. These compositions can be divided into three classes: greaseless compositions having an alcoholic base; greasy compositions containing vegetable or mineral oil or other tacky components; and water-based emulsions of any suitable oil. More recently, aerosol compositions have been formulated for protection against sunburn. These compositionsinvariably were of the greaseless type employing as a solvent for the sun screening agent, propellent, and other components, an alcohol such as ethanol or isopropanol. The use of an alcoholic solvent, however, is subject to several disadvantages. When such compositions are sprayed, the liquid components, including the alcohol, are dispersed in the form of fine droplets.
- the alcohol represents a fire hazard, so that all previously known aerosol sunburn preparations were subject to this disadvantage. Furthermore, since the alcohol solvent was highly volatile and evaporated quickly, a second film-forming ingrediout had to be incorporated into the composition in order to assure even distribution of the sun screening agent and protection thereby of the skin.
- An object of this invention is the provision of an aerosol preparation for the prevention of sunburn, which is non-inflammable, easily applied, and which produces on the skin a continuous, substantially invisible, elastic film which provides elfective protection against excessive exposure to erethernogenic actinic light.
- Suitable film-forming, liquid carboxylic acid ester vehicles utilizable in the compositions of this invention, are those which have high flash points (e. g. flash points above about 300 F), are water-repellant, so that they are not readily removed on bathing, form thin films on contact with the skin, so that relatively large areas of skin are covered with the minimum amount of Vehicle and sun screening agent, and Which dissolve at least some and preferably all the other active ingredients of the compositions of this invention.
- esters of higher aliphatic carboxylic acids such as the esters of higher allcanoic acids (e. g. the mono and polyhydric alcohol esters of capric, lauric, myristic, palmitic, and stearic acid), the esters of higher alkenoic acids (e. g. the mono and polyhydric alcohol esters of citronellic, undecyleni-c, and oleic acid), and the esters of higher alkanedioic acids (e. g. the mono and polyhydric alcohol esters of azelaic and sebacic acid). These esters may be used either singly or in combination as the vehicle of this invention.
- the esters of higher allcanoic acids e. g. the mono and polyhydric alcohol esters of capric, lauric, myristic, palmitic, and stearic acid
- the esters of higher alkenoic acids e. g. the mono and polyhydric alcohol esters of citronellic, undecy
- Suitable sun screening agents are those which are capable of absorbing and dissipating erythemogenic actinic light and preferably are soluble in the vehicle.
- examples of such agents are the esters of p-arninobenzoic acid and p-(lower alkyl substituted)aminobenzoic acid (e. g. the ethyl, propyl, isobutyl, butyl, glyceryl and other higher alcohol esters of p-aminobenzo-ic acid, p-dimethylarninobenzoic acid, and p-diethylaminobenzoic acid) and the esters of salicylic acid and p-arninosalicylic acid (e. g.
- the alcohol moiety of the ester has little effect on the screening activity of the ester, so that virtually any esterifying group may be used.
- any other of the known sunscreening agents can be used in the compositions of this invention, although those soluble in the vehicle are preferred because they permit the formation of a homogeneous solution.
- a silicone or other additional film-forming substance is not absolutely essential in the compositions of this invention, since the novel vehicles of this invention serve the dual purpose of solvent and Water-repellent filmformer on the skin.
- a silicone particularly a silicone fluid, also be incorporated in the compositions of this invention. Any relatively water-insoluble silicone is utilizable, as long as it is dermatologically acceptable and preferably soluble in the vehicle.
- Utilizable silicones include the silicone fluids such as aryl polysiloxanes (e. g. phenyl polysiloxanes), cyclic alkyl polysiloxanes (e. g.
- cyclic ethyl silicone tetramer cyclic ethyl silicone tetramer
- alkyl polysiloxanes e. g. ethyl polysiloxanes and methyl polysiloxanes
- mixed polysiloxanes e. g. methyl phenyl polysiloxanes.
- the viscosity of these preferred silicone fluids can range anywhere from about 25 to 15,000 centistrokes.
- Suitable propellents are those which individually or in mixture have a gauge pressure less than about 50 pounds per square inch at 70 F.
- the propellent preferably is one which has a gauge pressure in the range of about: 20 to 35 lbs/in. at 70 F. (optimally about 25 to 30 lbs/in? at 70 F.).
- Suitable propellents which can be used either alone or in mixture to give a gauge pressure in the hereinbefore recited ranges include the halogenated lower alkanes, such as trichlorornonofluoromethane, dichlorodifluoromethane, monochloridifluoromethane, trichlorotrifiuoroethane, and dichlorctetrafluoroethane.
- a particularly preferred propellent for the active ingredients in the compositions of this invention is one consisting of about equal proportions of trichloromonofluoromethane and dichlorodifluoromethane.
- the proportion of active ingredients to propellent is not critical, but preferably should be such that there is sulficient propellent present to expel substantially the entire amount of active ingredients from the container as a spray.
- the propellent is added in the proportion of about one to about 20 parts of propellent by weight per one part of active ingredients (an optimal composition being one wherein the propellent is present in a ratio of 1 to 5 parts of propellent per part of active ingredients).
- Example 1 To 100.0 g. of homomenthyl salicylate is added with stirring 7.5 g. of a perfuming agent, such as Perfume G. D. 6763, Givaudan-Delawanna, 50.0 g. of a silicone fluid (e. g. a methyl phenyl polysiloxane of 75 ctsks. viscosity), and finally enough isopropyl palmitate to bring the mixture to a weight of 1,000.0 g., the mixture having a fiash point above 310 F.
- a perfuming agent such as Perfume G. D. 6763, Givaudan-Delawanna
- a silicone fluid e. g. a methyl phenyl polysiloxane of 75 ctsks. viscosity
- the finished mixture is then strained through a fine muslin and filled into 6 ounce valved pressure cans using a ratio of 20% by Weight of the solution to 80% by weight of a propellent, the propellent being an equal mixture of trichloromonofluoromethane and dichlorodifluoromethane.
- the cans are then sealed to give a final composition having a gauge pressure of about 28 lbs/in. at 70 F.
- the perfurning agent is, of course, an optional ingredient and may be eliminated if desired. Furthermore, the specific ingredients and pro portions may be changed Within the limits hereinbefore noted Without qualitatively affecting the nature of the final composition.
- Example 1 illustrate other utilizable compositions, which are mixed and formulated as in Example 1:
- Example 2 One part of active ingredients consisting of:
- a propellent consisting of 40% dichlorodifluoromethane and 60% dichlorotetrafluoroethane.
- Example 3 One part of active ingredients consisting of:
- Percent Dipropyleneglycol salicylate 50.0 A methyl phenyl polysiloxane of 50 ctsks, viscosity [Silicone 81431 (G. E.)] 5.0 isopropyl palmitate 15.0 Isopro-pyl myristrate 15.0 isopropyl laurate -1 15.0
- a propellent consisting of an equal mixture of dichlorodifluoromethane and trichlorotrifluoroethane.
- Example 4 One part of active ingredients consisting of:
- Percent Ethyl p-diethylaminobenzoate 10.0 A methyl. phenyl polysiloxane of 75 ctsks. viscosity [Silicone DC 555] 25.0 Diisopropyl sebacate 65.0
- a propellent consisting of 10% monochlorodifiuoromethane and dichlorotetrafiuoroethane.
- a propellent consisting of 40% dichlorodifluoromethane and 60% trichlorotrifluoroethane.
- Percent Solprotex digalloyloleate 25.0 A methyl polysiloxane of 12,000 ctsks. viscosity [Silicone D0200] 25.0
- a propellent consisting of an equal mixture of trichloromonofluoromethane and dichlorodifluoromethane.
- Example7 One part of active ingredients consisting of:
- a propellent consisting of 10% monochlorodifluoromethane and 90% trichloromonofluoromethane.
- An aerosol composition consisting essentially of: a sun-screening agent; a propellant; and a water-repellent, film-forming liquid ester vehicle of high flash point, said ester having an acid moiety selected from the group consisting of higher alkanoic acids, higher alkenoic acids and higher alkanedioic acids, said acids having not more than 18 carbon atoms, and an alcohol moiety selected from the group consisting of saturated, unsubstituted lower aliphatic monohydric alcohols, lower alkylene glycols of low molecular weight, sorbitol and mannitol.
- composition of claim 1 which also contains a polysiloxane fluid.
- composition of claim 1 wherein the vehicle is a lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms.
- composition of claim 4 wherein the vehicle is a lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms. 7
- composition of claim 5 wherein the sun-screening agent is selected from the group consisting of the esters of p-aminobenzoic acid, p-(lower-alkyl-substituted) aminobenz-oic acid, salicylic acid and p-aminosalicylic acid.
- composition of claim 6 wherein the propellant comprises a halogenated lower alkane.
- composition of claim 5 wherein the sun-screening agent is homomenthyl salicylate.
- An aerosol composition consisting essentially of a halogenated lower alkane propellant and sun-screeningfilm-forming active ingredients consisting essentially of homomenthyl salicylate, a mono-lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms, and a polysiloxane fluid, wherein said homo- References Cited in the file of this patent UNITED STATES PATENTS 2,257,106 Christiansen Sept. 30, 1941 2,446,272 Farris Aug. 3, 1948 2,639,213 Barth May 19, 1953 FOREIGN PATENTS 84,595 Argentina May 22, 1947 OTHER REFERENCES Soap and Sanitary Chem., Sept. 1953, pp. 142, 143, 145, 147, 153 and 155.
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Description
AEROSOL SUN-SCREENING COMPOSITION Anthony L. La Via, Brooklyn, N. Y., assignor to Olin Mathieson Qhemical Corporation, New York, N. Y., a corporation of Virginia No Drawing. Application May 20, 1955 Serial No. 510,050
Claims. (Cl. 167-90) This invention relates to compositions of matter and more particularly to aerosol compositions useful in protecting against sunburn.
Prior to this invention, various compositions were known which were effective in minimizing or preventing erythema solare, commonly known as sunburn. These compositions can be divided into three classes: greaseless compositions having an alcoholic base; greasy compositions containing vegetable or mineral oil or other tacky components; and water-based emulsions of any suitable oil. More recently, aerosol compositions have been formulated for protection against sunburn. These compositionsinvariably were of the greaseless type employing as a solvent for the sun screening agent, propellent, and other components, an alcohol such as ethanol or isopropanol. The use of an alcoholic solvent, however, is subject to several disadvantages. When such compositions are sprayed, the liquid components, including the alcohol, are dispersed in the form of fine droplets. Under these conditions, and because of the large surface area of the droplets, the alcohol represents a fire hazard, so that all previously known aerosol sunburn preparations were subject to this disadvantage. Furthermore, since the alcohol solvent was highly volatile and evaporated quickly, a second film-forming ingrediout had to be incorporated into the composition in order to assure even distribution of the sun screening agent and protection thereby of the skin.
I have now discovered that these disadvantages can be obviated by the compositions of this invention, which essentially comprise a sun screening agent, a water-repellant, film-forming, liquid carboxylic acid ester vehicle of high flash point (hereinafter referred to simply as the vehicle), a propellent, and optionally but preferably a silicone. I have further discovered that by the use of the vehicles of this invention, not only is the aerosol composition rendered fire proof, but further, since the vehicle serves the dual purpose of a carrier for the various active ingredients of the composition-and a water-repelling film-former on the skin, the quantity of silicone or other film-former previously employed may be reduced or eliminated.
An object of this invention, therefore, is the provision of an aerosol preparation for the prevention of sunburn, which is non-inflammable, easily applied, and which produces on the skin a continuous, substantially invisible, elastic film which provides elfective protection against excessive exposure to erethernogenic actinic light.
Suitable film-forming, liquid carboxylic acid ester vehicles, utilizable in the compositions of this invention, are those which have high flash points (e. g. flash points above about 300 F), are water-repellant, so that they are not readily removed on bathing, form thin films on contact with the skin, so that relatively large areas of skin are covered with the minimum amount of Vehicle and sun screening agent, and Which dissolve at least some and preferably all the other active ingredients of the compositions of this invention.
- esters of higher aliphatic carboxylic acids, such as the esters of higher allcanoic acids (e. g. the mono and polyhydric alcohol esters of capric, lauric, myristic, palmitic, and stearic acid), the esters of higher alkenoic acids (e. g. the mono and polyhydric alcohol esters of citronellic, undecyleni-c, and oleic acid), and the esters of higher alkanedioic acids (e. g. the mono and polyhydric alcohol esters of azelaic and sebacic acid). These esters may be used either singly or in combination as the vehicle of this invention. Specific examples of suitable esters utilizable in the compositions of this invention, include the lower alkyl esters of higher fatty acids (e. g. isopropyl laurate, ethyl myristate, isopropyl myristate, ethyl palmitate, isopropyl palmitate, and butyl stearate), the polyhydric alcohol esters of higher fatty acids (e. g. diglycol laurate, sorbitol monolaurate, mannide monoleate, sorbitan monooleate, sorbitan sesquioleate, and diglycol oleate), and esters of higher alkanedioic acids, such as di-isopr-opyl sebacate. The particularly preferred esters are the mono-lower alkyl esters of higher fatty acids (optimally the lower alkyl esters of higher alkanoic acids).
Suitable sun screening agents are those which are capable of absorbing and dissipating erythemogenic actinic light and preferably are soluble in the vehicle. Examples of such agents are the esters of p-arninobenzoic acid and p-(lower alkyl substituted)aminobenzoic acid (e. g. the ethyl, propyl, isobutyl, butyl, glyceryl and other higher alcohol esters of p-aminobenzo-ic acid, p-dimethylarninobenzoic acid, and p-diethylaminobenzoic acid) and the esters of salicylic acid and p-arninosalicylic acid (e. g. the ethyl, propyl, isobutyl, benzyl, phenyl, dipropylene glycol and especially the menthyl and homomenthyl esters of salicylic acid and p-aminosalicylic acid). It should be noted, however, that the alcohol moiety of the ester has little effect on the screening activity of the ester, so that virtually any esterifying group may be used. Furthermore, any other of the known sunscreening agents can be used in the compositions of this invention, although those soluble in the vehicle are preferred because they permit the formation of a homogeneous solution.
In contrast to previously known aerosol preparations,
the use of a silicone or other additional film-forming substance is not absolutely essential in the compositions of this invention, since the novel vehicles of this invention serve the dual purpose of solvent and Water-repellent filmformer on the skin. However, to prevent any frothing upon contact of the aerosol spray with the skin, it is desirable that a silicone, particularly a silicone fluid, also be incorporated in the compositions of this invention. Any relatively water-insoluble silicone is utilizable, as long as it is dermatologically acceptable and preferably soluble in the vehicle. Utilizable silicones include the silicone fluids such as aryl polysiloxanes (e. g. phenyl polysiloxanes), cyclic alkyl polysiloxanes (e. g. cyclic ethyl silicone tetramer), alkyl polysiloxanes (e. g. ethyl polysiloxanes and methyl polysiloxanes) and mixed polysiloxanes (e. g. methyl phenyl polysiloxanes). The viscosity of these preferred silicone fluids can range anywhere from about 25 to 15,000 centistrokes.
To prepare the sun-screening film-forming active ingredients of the aerosols of this invention, the vehicle, sun screening agent, and silicone (if any) are intermixed in any order or together. Other ingredients such as a perfume or an insect repellent may also be added if desired. The proportion of sun screening agent to vehicle is not critical, but rather depends on the efiicacy of the sun screening agent and hence the maximum dilution of the agent which is possible Without making the composition ineffective. The preferred ratio of sun screening agent to vehicle, however, is in the order of one part by Weight of the former to about one to about fifty parts by weight of the latter (optimally one part of sun screening agent to about seven to about ten parts of vehicle). If a silicone is used, it is preferably present in relatively small amounts, not exceeding about 40% (preferably less than about 25%) of the total weight of active ingredients.
The active ingredients are then mixed with a suitable propellent in a valved pressure container, such as one customarily employed in the aerosol industry. Suitable propellents are those which individually or in mixture have a gauge pressure less than about 50 pounds per square inch at 70 F. For use with the active ingredients of this invention, the propellent preferably is one which has a gauge pressure in the range of about: 20 to 35 lbs/in. at 70 F. (optimally about 25 to 30 lbs/in? at 70 F.). Suitable propellents which can be used either alone or in mixture to give a gauge pressure in the hereinbefore recited ranges include the halogenated lower alkanes, such as trichlorornonofluoromethane, dichlorodifluoromethane, monochloridifluoromethane, trichlorotrifiuoroethane, and dichlorctetrafluoroethane. A particularly preferred propellent for the active ingredients in the compositions of this invention is one consisting of about equal proportions of trichloromonofluoromethane and dichlorodifluoromethane.
The proportion of active ingredients to propellent is not critical, but preferably should be such that there is sulficient propellent present to expel substantially the entire amount of active ingredients from the container as a spray. For this purpose, the propellent is added in the proportion of about one to about 20 parts of propellent by weight per one part of active ingredients (an optimal composition being one wherein the propellent is present in a ratio of 1 to 5 parts of propellent per part of active ingredients).
The following examples illustrate the invention:
Example 1 To 100.0 g. of homomenthyl salicylate is added with stirring 7.5 g. of a perfuming agent, such as Perfume G. D. 6763, Givaudan-Delawanna, 50.0 g. of a silicone fluid (e. g. a methyl phenyl polysiloxane of 75 ctsks. viscosity), and finally enough isopropyl palmitate to bring the mixture to a weight of 1,000.0 g., the mixture having a fiash point above 310 F. The finished mixture is then strained through a fine muslin and filled into 6 ounce valved pressure cans using a ratio of 20% by Weight of the solution to 80% by weight of a propellent, the propellent being an equal mixture of trichloromonofluoromethane and dichlorodifluoromethane. The cans are then sealed to give a final composition having a gauge pressure of about 28 lbs/in. at 70 F.
In the formulation of Example 1, the perfurning agent is, of course, an optional ingredient and may be eliminated if desired. Furthermore, the specific ingredients and pro portions may be changed Within the limits hereinbefore noted Without qualitatively affecting the nature of the final composition.
The following examples illustrate other utilizable compositions, which are mixed and formulated as in Example 1:
Example 2 One part of active ingredients consisting of:
Percent Homomenthyl salicylate 10.0 Isopropyl palmitate 90.0
is mixed with three parts of a propellent consisting of 40% dichlorodifluoromethane and 60% dichlorotetrafluoroethane.
4 Example 3 One part of active ingredients consisting of:
Percent Dipropyleneglycol salicylate 50.0 A methyl phenyl polysiloxane of 50 ctsks, viscosity [Silicone 81431 (G. E.)] 5.0 isopropyl palmitate 15.0 Isopro-pyl myristrate 15.0 isopropyl laurate -1 15.0
is mixed with nine parts of a propellent consisting of an equal mixture of dichlorodifluoromethane and trichlorotrifluoroethane.
Example 4 One part of active ingredients consisting of:
Percent Ethyl p-diethylaminobenzoate 10.0 A methyl. phenyl polysiloxane of 75 ctsks. viscosity [Silicone DC 555] 25.0 Diisopropyl sebacate 65.0
is mixed with one part of a propellent consisting of 10% monochlorodifiuoromethane and dichlorotetrafiuoroethane.
Example 5 One part of active ingredients consisting of:
Percent lsobutyl p-aminosalicylate 10.0
A methyl phenyl polysiloxane of 35 ctsks. viscosity [Silicone DC 701] 5.0 Diglycol laurate 40.0 Isopropyl palmitate 45.0
is mixed with three parts of a propellent consisting of 40% dichlorodifluoromethane and 60% trichlorotrifluoroethane.
Example6 One part of active ingredients consisting of:
Percent Solprotex (digalloyloleate) 25.0 A methyl polysiloxane of 12,000 ctsks. viscosity [Silicone D0200] 25.0
Sorbitol monolaurate 50.0
is mixed with eight parts of a propellent consisting of an equal mixture of trichloromonofluoromethane and dichlorodifluoromethane.
Example7 One part of active ingredients consisting of:
Percent Ethyl p-dimethylaminobenzoate 20.0 A methyl polysiloxane of 500 ctsks. viscosity [Silicone 8-96 (G. E.)] 10.0 Sorbitan monooleate 35.0 Sorbitan sesquioleate 35.0
is mixed with three part of a propellent consisting of 10% monochlorodifluoromethane and 90% trichloromonofluoromethane.
The compositions of Examples 2 through 7 may be perfumed if desired.
The invention may be variously otherwise embodied within the scope of the appended claims.
I claim:
1. An aerosol composition consisting essentially of: a sun-screening agent; a propellant; and a water-repellent, film-forming liquid ester vehicle of high flash point, said ester having an acid moiety selected from the group consisting of higher alkanoic acids, higher alkenoic acids and higher alkanedioic acids, said acids having not more than 18 carbon atoms, and an alcohol moiety selected from the group consisting of saturated, unsubstituted lower aliphatic monohydric alcohols, lower alkylene glycols of low molecular weight, sorbitol and mannitol.
2. The composition of claim 1 which also contains a polysiloxane fluid.
3. The composition of claim 1 wherein the vehicle is a lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms.
4. The composition of claim 1 in which the film-forming vehicle is present in the proportion of about one to about fifty parts by weight per part by weight of sun-screening agent, and in which the propellant is present in the proportion of about one to about twenty parts by weight per part by weight of combined sun-screening agent and filmforming vehicle.
5. The composition of claim 4 wherein the vehicle is a lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms. 7
6. The composition of claim 5 wherein the sun-screening agent is selected from the group consisting of the esters of p-aminobenzoic acid, p-(lower-alkyl-substituted) aminobenz-oic acid, salicylic acid and p-aminosalicylic acid.
7. The composition of claim 6 wherein the propellant comprises a halogenated lower alkane.
8. The composition of claim 5 wherein the sun-screening agent is homomenthyl salicylate.
9. An aerosol composition consisting essentially of a halogenated lower alkane propellant and sun-screeningfilm-forming active ingredients consisting essentially of homomenthyl salicylate, a mono-lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms, and a polysiloxane fluid, wherein said homo- References Cited in the file of this patent UNITED STATES PATENTS 2,257,106 Christiansen Sept. 30, 1941 2,446,272 Farris Aug. 3, 1948 2,639,213 Barth May 19, 1953 FOREIGN PATENTS 84,595 Argentina May 22, 1947 OTHER REFERENCES Soap and Sanitary Chem., Sept. 1953, pp. 142, 143, 145, 147, 153 and 155.
E. G. Tajkowski et al.: Proc. of the Sci. Sec. of Toilet Goods Asso., No. 20, Dec. 1953, pp. 1-7.
E. N. Cooper: Chem. Ind., Dec. 1948, pp. 970, 972 and 1058.
G. S. Pears: Perf. and Ess. Oil Rec., Mar. 1953, pp. 84-90, 101.
Claims (1)
1. AN AEROSOL COMPOSITION CONSISTING ESSENTIALLY OF: A SUN-SCREENING AGENT; A PROPELLANT; AND WATER-REPELLENT, FILM-FORMING LIQUID ESTER VEHICLE OF HIGH FLASH POINT, SAID ESTER HAVING AN ACID MOIETY SELETED FROM THE GROUP CONSISTING OF HIGHER ALKONIC ACIDS, HIGHER ALKENOIC ACIDS AND HIGHER ALKANEODIC ACIDS, SAID ACIDS HAVING NOT MORE THAN 18 CARBON ATOMS, AND AN ALCOHOL MOIETY SELECTED FROM THE GROUP CONSISTING OF SATURATED, UNSUBSTITUTED LOWER ALIPHATIC MONOHYDRIC ALCOHOLS, LOWER ALKYLENE GLYCOLS OF LOW MOLECULAR WEIGHT, SORBITOL AND MANNITOL.
Priority Applications (1)
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US510050A US2853423A (en) | 1955-05-20 | 1955-05-20 | Aerosol sun-screening composition |
Applications Claiming Priority (1)
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US510050A US2853423A (en) | 1955-05-20 | 1955-05-20 | Aerosol sun-screening composition |
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US2853423A true US2853423A (en) | 1958-09-23 |
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Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3081232A (en) * | 1960-12-27 | 1963-03-12 | Warner Lambert Pharmaceutical | Iodine preparation and method of disinfecting the skin |
US3175950A (en) * | 1960-07-22 | 1965-03-30 | Armour Pharmaceutrical Company | Sunscreening preparations |
US3275520A (en) * | 1962-05-29 | 1966-09-27 | Gen Aniline & Film Corp | Methods for protecting the skin against actinic radiations |
US3403207A (en) * | 1966-11-14 | 1968-09-24 | Saul I. Kreps | Method of and composition for screening erythema inducing ultraviolet bands |
US3479428A (en) * | 1963-07-12 | 1969-11-18 | Boots Pure Drug Co Ltd | Sunscreen composition and method of using the same |
US4001391A (en) * | 1969-04-18 | 1977-01-04 | Plough, Inc. | Means for depositing aerosol sprays in buttery form |
US4036951A (en) * | 1973-03-12 | 1977-07-19 | Synergistics, Inc. | Ultra-violet filtration with certain aminosalicylic acid esters |
US4069309A (en) * | 1972-09-19 | 1978-01-17 | Avon Products, Inc. | Cationic skin substantive sunscreen composition and method |
US4107290A (en) * | 1972-06-29 | 1978-08-15 | L'oreal | Anti-solar polymers, method of making the same and cosmetic compositions containing the same |
FR2385685A1 (en) * | 1977-04-01 | 1978-10-27 | Mundipharma Ag | PROCESS FOR OBTAINING CERTAIN ESTERS OF AN AMINO-SALICYLIC ACID AND THEIR APPLICATION TO THE FILTRATION OF ULTRAVIOLET RAYS |
US4217344A (en) * | 1976-06-23 | 1980-08-12 | L'oreal | Compositions containing aqueous dispersions of lipid spheres |
US4793990A (en) * | 1980-04-02 | 1988-12-27 | L'oreal | Use of coffee bean oil as a sun filter |
US4940574A (en) * | 1988-12-22 | 1990-07-10 | Plough, Inc. | Non-aqueous high SPF sunscreen oils |
US5268166A (en) * | 1991-07-15 | 1993-12-07 | Elizabeth Arden Company, Division Of Conopco, Inc. | Cosmetic application system |
WO1994000104A1 (en) * | 1992-06-25 | 1994-01-06 | Stewart Ernest G | Water resistant sunscreen protection and insect repellent compound |
WO1995019161A1 (en) * | 1993-11-18 | 1995-07-20 | Stewart Ernest G | Improved water resistant sunscreen protection and insect repellent compound |
US5447715A (en) * | 1987-04-01 | 1995-09-05 | Scholl Inc. | Non-aqueous suncare compositions having high SPF values |
US5756075A (en) * | 1992-08-24 | 1998-05-26 | Schering-Plough Healthcare Products, Inc. | Apparatus and method for sunless tanning |
US5916541A (en) * | 1992-06-25 | 1999-06-29 | Stewart; Ernest G. | Water resistant sunscreen and insect repellent composition |
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US2446272A (en) * | 1941-12-15 | 1948-08-03 | Lockheed Aircraft Corp | Fire extinguisher fluid |
US2639213A (en) * | 1950-03-21 | 1953-05-19 | Price Driscoll Corp | Mold parting surface and method of application |
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US2257106A (en) * | 1938-02-26 | 1941-09-30 | Squibb & Sons Inc | Dermal lotion |
US2446272A (en) * | 1941-12-15 | 1948-08-03 | Lockheed Aircraft Corp | Fire extinguisher fluid |
US2639213A (en) * | 1950-03-21 | 1953-05-19 | Price Driscoll Corp | Mold parting surface and method of application |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3175950A (en) * | 1960-07-22 | 1965-03-30 | Armour Pharmaceutrical Company | Sunscreening preparations |
US3081232A (en) * | 1960-12-27 | 1963-03-12 | Warner Lambert Pharmaceutical | Iodine preparation and method of disinfecting the skin |
US3275520A (en) * | 1962-05-29 | 1966-09-27 | Gen Aniline & Film Corp | Methods for protecting the skin against actinic radiations |
US3479428A (en) * | 1963-07-12 | 1969-11-18 | Boots Pure Drug Co Ltd | Sunscreen composition and method of using the same |
US3403207A (en) * | 1966-11-14 | 1968-09-24 | Saul I. Kreps | Method of and composition for screening erythema inducing ultraviolet bands |
US4001391A (en) * | 1969-04-18 | 1977-01-04 | Plough, Inc. | Means for depositing aerosol sprays in buttery form |
US4107290A (en) * | 1972-06-29 | 1978-08-15 | L'oreal | Anti-solar polymers, method of making the same and cosmetic compositions containing the same |
US4069309A (en) * | 1972-09-19 | 1978-01-17 | Avon Products, Inc. | Cationic skin substantive sunscreen composition and method |
US4036951A (en) * | 1973-03-12 | 1977-07-19 | Synergistics, Inc. | Ultra-violet filtration with certain aminosalicylic acid esters |
US4217344A (en) * | 1976-06-23 | 1980-08-12 | L'oreal | Compositions containing aqueous dispersions of lipid spheres |
FR2385685A1 (en) * | 1977-04-01 | 1978-10-27 | Mundipharma Ag | PROCESS FOR OBTAINING CERTAIN ESTERS OF AN AMINO-SALICYLIC ACID AND THEIR APPLICATION TO THE FILTRATION OF ULTRAVIOLET RAYS |
US4793990A (en) * | 1980-04-02 | 1988-12-27 | L'oreal | Use of coffee bean oil as a sun filter |
US5447715A (en) * | 1987-04-01 | 1995-09-05 | Scholl Inc. | Non-aqueous suncare compositions having high SPF values |
US4940574A (en) * | 1988-12-22 | 1990-07-10 | Plough, Inc. | Non-aqueous high SPF sunscreen oils |
US5268166A (en) * | 1991-07-15 | 1993-12-07 | Elizabeth Arden Company, Division Of Conopco, Inc. | Cosmetic application system |
WO1994000104A1 (en) * | 1992-06-25 | 1994-01-06 | Stewart Ernest G | Water resistant sunscreen protection and insect repellent compound |
US5518712A (en) * | 1992-06-25 | 1996-05-21 | Stewart; Ernest | Water resistant sunscreen protection and insect repellent compound |
US5916541A (en) * | 1992-06-25 | 1999-06-29 | Stewart; Ernest G. | Water resistant sunscreen and insect repellent composition |
US5756075A (en) * | 1992-08-24 | 1998-05-26 | Schering-Plough Healthcare Products, Inc. | Apparatus and method for sunless tanning |
WO1995019161A1 (en) * | 1993-11-18 | 1995-07-20 | Stewart Ernest G | Improved water resistant sunscreen protection and insect repellent compound |
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