SK83297A3 - Agents on dimeticone derivatives base delivering odour and acting as cooling and antimicrobial agent silicone compositions - Google Patents
Agents on dimeticone derivatives base delivering odour and acting as cooling and antimicrobial agent silicone compositions Download PDFInfo
- Publication number
- SK83297A3 SK83297A3 SK832-97A SK83297A SK83297A3 SK 83297 A3 SK83297 A3 SK 83297A3 SK 83297 A SK83297 A SK 83297A SK 83297 A3 SK83297 A3 SK 83297A3
- Authority
- SK
- Slovakia
- Prior art keywords
- oil
- acetate
- alkyl
- acid
- alkoxy
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 80
- 239000002826 coolant Substances 0.000 title claims abstract description 14
- 238000001816 cooling Methods 0.000 title claims description 9
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical class C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 title claims description 8
- 239000003795 chemical substances by application Substances 0.000 title description 19
- 239000004599 antimicrobial Substances 0.000 title description 14
- 229920001296 polysiloxane Polymers 0.000 title description 9
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 28
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims abstract description 27
- 239000002304 perfume Substances 0.000 claims abstract description 27
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 26
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 19
- 229940008099 dimethicone Drugs 0.000 claims abstract description 12
- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 12
- 239000000796 flavoring agent Substances 0.000 claims abstract description 12
- 235000019634 flavors Nutrition 0.000 claims abstract description 12
- 125000002252 acyl group Chemical group 0.000 claims abstract description 11
- 230000000845 anti-microbial effect Effects 0.000 claims abstract description 10
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 125000006353 oxyethylene group Chemical group 0.000 claims abstract description 6
- -1 4- (4-hydroxy-4-methylpentyl) -3cyclohexenecarboxylic acid aldehyde Chemical class 0.000 claims description 29
- 229920000570 polyether Polymers 0.000 claims description 27
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 26
- 239000000126 substance Substances 0.000 claims description 16
- 229940124447 delivery agent Drugs 0.000 claims description 11
- 239000000341 volatile oil Substances 0.000 claims description 9
- 241000402754 Erythranthe moschata Species 0.000 claims description 8
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 6
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims description 6
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- 229940022663 acetate Drugs 0.000 claims description 5
- 150000002825 nitriles Chemical class 0.000 claims description 5
- 239000003921 oil Substances 0.000 claims description 5
- 235000019198 oils Nutrition 0.000 claims description 5
- 239000010678 thyme oil Substances 0.000 claims description 5
- UWKAYLJWKGQEPM-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl acetate Chemical compound CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 claims description 4
- ZISGOYMWXFOWAM-UHFFFAOYSA-N 3-methyl-2-pentylcyclopentan-1-one Chemical compound CCCCCC1C(C)CCC1=O ZISGOYMWXFOWAM-UHFFFAOYSA-N 0.000 claims description 4
- INIOTLARNNSXAE-UHFFFAOYSA-N 4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1h-azulen-6-ol Chemical compound CC1CC(O)C=C(C)C2CC(=C(C)C)CC12 INIOTLARNNSXAE-UHFFFAOYSA-N 0.000 claims description 4
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 claims description 4
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 4
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims description 4
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 claims description 4
- 229940085262 cetyl dimethicone Drugs 0.000 claims description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 4
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 claims description 4
- 229940041616 menthol Drugs 0.000 claims description 4
- 235000019501 Lemon oil Nutrition 0.000 claims description 3
- HIGQPQRQIQDZMP-DHZHZOJOSA-N Neryl acetate Natural products CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 claims description 3
- 239000010501 lemon oil Substances 0.000 claims description 3
- VHVRYMDFTKNLFA-UHFFFAOYSA-N (2-methyl-6-methylideneoctan-2-yl) acetate Chemical compound CCC(=C)CCCC(C)(C)OC(C)=O VHVRYMDFTKNLFA-UHFFFAOYSA-N 0.000 claims description 2
- 239000001716 (4-methyl-1-propan-2-yl-1-cyclohex-2-enyl) acetate Substances 0.000 claims description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 2
- 239000001875 1-phenylethyl acetate Substances 0.000 claims description 2
- FYERTDTXGGOMGT-UHFFFAOYSA-N 2,2-diethoxyethylbenzene Chemical compound CCOC(OCC)CC1=CC=CC=C1 FYERTDTXGGOMGT-UHFFFAOYSA-N 0.000 claims description 2
- WNJSKZBEWNVKGU-UHFFFAOYSA-N 2,2-dimethoxyethylbenzene Chemical compound COC(OC)CC1=CC=CC=C1 WNJSKZBEWNVKGU-UHFFFAOYSA-N 0.000 claims description 2
- WRFXXJKURVTLSY-UHFFFAOYSA-N 2,6-dimethyloctan-2-ol Chemical compound CCC(C)CCCC(C)(C)O WRFXXJKURVTLSY-UHFFFAOYSA-N 0.000 claims description 2
- PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 claims description 2
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 claims description 2
- RQRYGVZUUYYXGA-UHFFFAOYSA-N 2-methyl-3-(4-propan-2-ylphenyl)propan-1-ol Chemical compound OCC(C)CC1=CC=C(C(C)C)C=C1 RQRYGVZUUYYXGA-UHFFFAOYSA-N 0.000 claims description 2
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims description 2
- SJMDLCVBSNYMMJ-UHFFFAOYSA-N 3-(4-tert-butylphenyl)-2-methylpropan-1-ol Chemical compound OCC(C)CC1=CC=C(C(C)(C)C)C=C1 SJMDLCVBSNYMMJ-UHFFFAOYSA-N 0.000 claims description 2
- QFIGRGCEUZQJNG-UHFFFAOYSA-N 3-(4-tert-butylphenyl)propan-1-ol Chemical compound CC(C)(C)C1=CC=C(CCCO)C=C1 QFIGRGCEUZQJNG-UHFFFAOYSA-N 0.000 claims description 2
- HTLBMZKXJYNJSK-UHFFFAOYSA-N 3-naphthalen-2-yl-1,2-oxazol-5-amine Chemical compound O1C(N)=CC(C=2C=C3C=CC=CC3=CC=2)=N1 HTLBMZKXJYNJSK-UHFFFAOYSA-N 0.000 claims description 2
- PBGWNXWNCSSXCO-UHFFFAOYSA-N Caprylsaeure-hexenylester Natural products CCCCCCCC(=O)OCCCCCC PBGWNXWNCSSXCO-UHFFFAOYSA-N 0.000 claims description 2
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 claims description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 2
- 241000723346 Cinnamomum camphora Species 0.000 claims description 2
- 235000014493 Crataegus Nutrition 0.000 claims description 2
- 241001092040 Crataegus Species 0.000 claims description 2
- 239000005770 Eugenol Substances 0.000 claims description 2
- 244000147568 Laurus nobilis Species 0.000 claims description 2
- 235000017858 Laurus nobilis Nutrition 0.000 claims description 2
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 claims description 2
- 235000019502 Orange oil Nutrition 0.000 claims description 2
- 235000011203 Origanum Nutrition 0.000 claims description 2
- 240000000783 Origanum majorana Species 0.000 claims description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 claims description 2
- 235000005212 Terminalia tomentosa Nutrition 0.000 claims description 2
- NUPSHWCALHZGOV-UHFFFAOYSA-N acetic acid n-decyl ester Natural products CCCCCCCCCCOC(C)=O NUPSHWCALHZGOV-UHFFFAOYSA-N 0.000 claims description 2
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 claims description 2
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 claims description 2
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 claims description 2
- 239000010617 anise oil Substances 0.000 claims description 2
- 229940007550 benzyl acetate Drugs 0.000 claims description 2
- 229960002903 benzyl benzoate Drugs 0.000 claims description 2
- 229960000846 camphor Drugs 0.000 claims description 2
- 229930008380 camphor Natural products 0.000 claims description 2
- 229940119201 cedar leaf oil Drugs 0.000 claims description 2
- 235000013985 cinnamic acid Nutrition 0.000 claims description 2
- 229930016911 cinnamic acid Natural products 0.000 claims description 2
- 239000010634 clove oil Substances 0.000 claims description 2
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 claims description 2
- XSNQECSCDATQEL-UHFFFAOYSA-N dihydromyrcenol Chemical compound C=CC(C)CCCC(C)(C)O XSNQECSCDATQEL-UHFFFAOYSA-N 0.000 claims description 2
- 229930008394 dihydromyrcenol Natural products 0.000 claims description 2
- 229960002217 eugenol Drugs 0.000 claims description 2
- HEBMCVBCEDMUOF-UHFFFAOYSA-N isochromane Chemical compound C1=CC=C2COCCC2=C1 HEBMCVBCEDMUOF-UHFFFAOYSA-N 0.000 claims description 2
- HMRWHLXCRJQBMQ-BQELKBSMSA-N isolongifolane Chemical compound C1CCC(C)(C)[C@@]2(C3)C1C(C)(C)[C@H]3CC2 HMRWHLXCRJQBMQ-BQELKBSMSA-N 0.000 claims description 2
- 229930002169 isolongifolane Natural products 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 claims description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 claims description 2
- 239000008164 mustard oil Substances 0.000 claims description 2
- NCDCLPBOMHPFCV-UHFFFAOYSA-N n-hexyl n-hexanoate Natural products CCCCCCOC(=O)CCCCC NCDCLPBOMHPFCV-UHFFFAOYSA-N 0.000 claims description 2
- 239000010502 orange oil Substances 0.000 claims description 2
- 239000010661 oregano oil Substances 0.000 claims description 2
- 229940111617 oregano oil Drugs 0.000 claims description 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 claims description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 2
- MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 claims description 2
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 claims description 2
- 239000001327 prunus amygdalus amara l. extract Substances 0.000 claims description 2
- 239000010670 sage oil Substances 0.000 claims description 2
- 229940116411 terpineol Drugs 0.000 claims description 2
- 239000001789 thuja occidentalis l. leaf oil Substances 0.000 claims description 2
- 239000009637 wintergreen oil Substances 0.000 claims description 2
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 claims 2
- 239000010665 pine oil Substances 0.000 claims 2
- MJTPMXWJHPOWGH-UHFFFAOYSA-N 2-Phenoxyethyl isobutyrate Chemical compound CC(C)C(=O)OCCOC1=CC=CC=C1 MJTPMXWJHPOWGH-UHFFFAOYSA-N 0.000 claims 1
- KSXHXCWTPJPLAT-UHFFFAOYSA-N 3-[3-(trifluoromethyl)phenyl]benzaldehyde Chemical compound FC(F)(F)C1=CC=CC(C=2C=C(C=O)C=CC=2)=C1 KSXHXCWTPJPLAT-UHFFFAOYSA-N 0.000 claims 1
- 235000005979 Citrus limon Nutrition 0.000 claims 1
- 244000131522 Citrus pyriformis Species 0.000 claims 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-UHFFFAOYSA-N 0.000 claims 1
- XRHCAGNSDHCHFJ-UHFFFAOYSA-N Ethylene brassylate Chemical compound O=C1CCCCCCCCCCCC(=O)OCCO1 XRHCAGNSDHCHFJ-UHFFFAOYSA-N 0.000 claims 1
- 239000005792 Geraniol Substances 0.000 claims 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims 1
- 235000004263 Ocotea pretiosa Nutrition 0.000 claims 1
- OIZXRZCQJDXPFO-UHFFFAOYSA-N Octadecyl acetate Chemical compound CCCCCCCCCCCCCCCCCCOC(C)=O OIZXRZCQJDXPFO-UHFFFAOYSA-N 0.000 claims 1
- 244000009660 Sassafras variifolium Species 0.000 claims 1
- JKRWZLOCPLZZEI-UHFFFAOYSA-N alpha-Trichloromethylbenzyl acetate Chemical compound CC(=O)OC(C(Cl)(Cl)Cl)C1=CC=CC=C1 JKRWZLOCPLZZEI-UHFFFAOYSA-N 0.000 claims 1
- 229940062909 amyl salicylate Drugs 0.000 claims 1
- 239000010630 cinnamon oil Substances 0.000 claims 1
- NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 claims 1
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- 150000007931 macrolactones Chemical class 0.000 claims 1
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- 125000000963 oxybis(methylene) group Chemical group [H]C([H])(*)OC([H])([H])* 0.000 claims 1
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- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
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- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
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Classifications
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- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
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- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/70—Fixation, conservation, or encapsulation of flavouring agents
- A23L27/74—Fixation, conservation, or encapsulation of flavouring agents with a synthetic polymer matrix or excipient, e.g. vinylic, acrylic polymers
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
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- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
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- A—HUMAN NECESSITIES
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
- A61Q11/02—Preparations for deodorising, bleaching or disinfecting dentures
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0838—Compounds with one or more Si-O-Si sequences
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- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
- A61K2800/244—Endothermic; Cooling; Cooling sensation
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Birds (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fats And Perfumes (AREA)
- Glass Compositions (AREA)
- Endoscopes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9425928.0A GB9425928D0 (en) | 1994-12-22 | 1994-12-22 | Silicone compositions |
| PCT/US1995/016675 WO1996019119A1 (en) | 1994-12-22 | 1995-12-13 | Silicone compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK83297A3 true SK83297A3 (en) | 1998-01-14 |
Family
ID=10766382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK832-97A SK83297A3 (en) | 1994-12-22 | 1995-12-13 | Agents on dimeticone derivatives base delivering odour and acting as cooling and antimicrobial agent silicone compositions |
Country Status (21)
| Country | Link |
|---|---|
| EP (1) | EP0792110B1 (de) |
| JP (1) | JPH10512854A (de) |
| KR (1) | KR100225666B1 (de) |
| CN (1) | CN1090918C (de) |
| AT (1) | ATE217761T1 (de) |
| AU (1) | AU688193B2 (de) |
| BR (1) | BR9510477A (de) |
| CA (1) | CA2206463C (de) |
| CZ (1) | CZ190997A3 (de) |
| DE (1) | DE69526798T2 (de) |
| DK (1) | DK0792110T3 (de) |
| ES (1) | ES2173990T3 (de) |
| GB (1) | GB9425928D0 (de) |
| HU (1) | HUT77710A (de) |
| MX (1) | MX9704666A (de) |
| NZ (1) | NZ300505A (de) |
| PL (1) | PL320863A1 (de) |
| PT (1) | PT792110E (de) |
| SK (1) | SK83297A3 (de) |
| TR (1) | TR199501648A2 (de) |
| WO (1) | WO1996019119A1 (de) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19650102A1 (de) * | 1996-12-03 | 1998-06-04 | Basf Ag | Verwendung von Bis(dicarbonsäure)diaminoalkylen-Derivaten als biologisch abbaubare Komplexbildner für Erdalkali- und Schwermetallionen |
| CA2236189A1 (en) | 1997-05-15 | 1998-11-15 | Givaudan-Roure (International) Sa | Fragrance precursor compounds |
| NZ506250A (en) * | 1998-02-13 | 2003-10-31 | Britesmile Inc | Light-activated tooth whitening composition containing a whitening compound and a carrier |
| JP4783491B2 (ja) * | 2000-04-17 | 2011-09-28 | 東レ・ダウコーニング株式会社 | オルガノポリシロキサン系組成物およびその製造方法 |
| JP4768902B2 (ja) * | 2000-04-17 | 2011-09-07 | 東レ・ダウコーニング株式会社 | オルガノポリシロキサン組成物およびその製造方法 |
| JP4783490B2 (ja) * | 2000-04-17 | 2011-09-28 | 東レ・ダウコーニング株式会社 | オルガノポリシロキサン組成物およびその製造方法 |
| EP1181866A1 (de) * | 2000-08-14 | 2002-02-27 | Givaudan SA | Antibakterielle Zusammensetzung enthaltend Sandela |
| EP1184030A1 (de) * | 2000-08-14 | 2002-03-06 | Givaudan SA | Antibakterielle Zusammensetzung enthaltend Trimethylnorbornanylcyclohexanolderivate |
| US6524494B2 (en) | 2001-02-02 | 2003-02-25 | Givaudan Sa | Compositions to enhance fabric freshness and appearance |
| GB0207647D0 (en) * | 2002-04-03 | 2002-05-15 | Dow Corning | Emulsions |
| GB0306995D0 (en) * | 2003-03-27 | 2003-04-30 | Dow Corning | Fragrance compositions |
| US20060167117A1 (en) | 2003-03-27 | 2006-07-27 | Leaym Tine M | Controlled release compositions |
| BRPI0613324A2 (pt) * | 2005-05-31 | 2011-01-04 | Takasago Internat Corp U S A | composição de aquecimento, composição de resfriamento, kit compreendendo um creme ou gel de massagem esportiva, kit compreendendo um gel ou creme de barbear, kit compreendendo um produto de cuidado pessoal, método para aliviar músculos doloridos, método para preparar uma loção, creme ou spray analgésico tópico ou remédio tópico e método para aumentar o efeito de um material sensibilizador |
| US9040031B2 (en) | 2010-07-08 | 2015-05-26 | Conopco, Inc. | Hair care composition |
| WO2012150259A1 (en) | 2011-05-04 | 2012-11-08 | Unilever Plc | Composition |
| WO2012150260A1 (en) | 2011-05-04 | 2012-11-08 | Unilever Plc | Hair care composition comprising hydrophobically-modified anionic polymer and a methylcellulose |
| GB202100945D0 (en) * | 2021-01-25 | 2021-03-10 | Brightcure Ltd | A composition useful for treating bacterial infections |
| CN113024818B (zh) * | 2021-03-01 | 2022-07-08 | 浙江润禾有机硅新材料有限公司 | 一种高纯度低副产的聚醚改性硅氧烷的制备方法 |
| CN115612109B (zh) * | 2022-11-08 | 2023-08-08 | 江苏美思德化学股份有限公司 | 有机硅共聚物、其制备方法及其应用、软质泡沫稳定剂和软质聚氨酯泡沫 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3723491A (en) * | 1971-01-25 | 1973-03-27 | Goldschmidt Ag Th | Polysiloxane-polyalkyleneglycol block copolymers suitable as foam stabilizers in the manufacture of polyurethane foams |
| US4157384A (en) * | 1972-01-28 | 1979-06-05 | Wilkinson Sword Limited | Compositions having a physiological cooling effect |
| US4136250A (en) * | 1977-07-20 | 1979-01-23 | Ciba-Geigy Corporation | Polysiloxane hydrogels |
| US4725575A (en) * | 1986-12-10 | 1988-02-16 | Union Camp Corporation | Silicone rubber dispensers of volatile organic liquids |
| FR2693466B1 (fr) * | 1992-07-09 | 1994-09-16 | Oreal | Composition cosmétique sous forme d'émulsion triple eau/huile de silicone/eau gélifiée. |
| EP0596304B1 (de) * | 1992-10-31 | 1998-04-01 | Th. Goldschmidt AG | Kosmetische oder pharmazeutische Zubereitungen |
| FR2701845B1 (fr) * | 1993-02-23 | 1995-04-07 | Oreal | Emulsion eau-dans-huile à usage cosmétique ou pharmaceutique. |
| DE69433131T2 (de) * | 1993-02-26 | 2004-07-08 | Estee Lauder Inc. | Titandioxiddispersionen, kosmetische präparate und verfahren für ihre verwendung |
| FR2718022B1 (fr) * | 1994-04-01 | 1996-04-26 | Roussel Uclaf | Compositions cosmétiques ou dermatologiques et leur préparation. |
| US5589177A (en) * | 1994-12-06 | 1996-12-31 | Helene Curtis, Inc. | Rinse-off water-in-oil-in-water compositions |
-
1994
- 1994-12-22 GB GBGB9425928.0A patent/GB9425928D0/en active Pending
-
1995
- 1995-12-13 AT AT95943929T patent/ATE217761T1/de active
- 1995-12-13 MX MX9704666A patent/MX9704666A/es not_active IP Right Cessation
- 1995-12-13 JP JP8519994A patent/JPH10512854A/ja active Pending
- 1995-12-13 HU HU9800735A patent/HUT77710A/hu unknown
- 1995-12-13 CA CA002206463A patent/CA2206463C/en not_active Expired - Fee Related
- 1995-12-13 ES ES95943929T patent/ES2173990T3/es not_active Expired - Lifetime
- 1995-12-13 PL PL95320863A patent/PL320863A1/xx unknown
- 1995-12-13 KR KR1019970704211A patent/KR100225666B1/ko not_active IP Right Cessation
- 1995-12-13 WO PCT/US1995/016675 patent/WO1996019119A1/en active IP Right Grant
- 1995-12-13 NZ NZ300505A patent/NZ300505A/xx not_active IP Right Cessation
- 1995-12-13 BR BR9510477A patent/BR9510477A/pt not_active IP Right Cessation
- 1995-12-13 EP EP95943929A patent/EP0792110B1/de not_active Expired - Lifetime
- 1995-12-13 CN CN95196845A patent/CN1090918C/zh not_active Expired - Fee Related
- 1995-12-13 AU AU45268/96A patent/AU688193B2/en not_active Ceased
- 1995-12-13 SK SK832-97A patent/SK83297A3/sk unknown
- 1995-12-13 CZ CZ971909A patent/CZ190997A3/cs unknown
- 1995-12-13 PT PT95943929T patent/PT792110E/pt unknown
- 1995-12-13 DE DE69526798T patent/DE69526798T2/de not_active Expired - Lifetime
- 1995-12-13 DK DK95943929T patent/DK0792110T3/da active
- 1995-12-22 TR TR95/01648A patent/TR199501648A2/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT77710A (hu) | 1998-07-28 |
| BR9510477A (pt) | 1998-06-02 |
| MX9704666A (es) | 1997-09-30 |
| EP0792110A1 (de) | 1997-09-03 |
| PL320863A1 (en) | 1997-11-10 |
| ATE217761T1 (de) | 2002-06-15 |
| AU4526896A (en) | 1996-07-10 |
| CA2206463A1 (en) | 1996-06-27 |
| DE69526798T2 (de) | 2003-02-06 |
| NZ300505A (en) | 1999-07-29 |
| GB9425928D0 (en) | 1995-02-22 |
| AU688193B2 (en) | 1998-03-05 |
| DE69526798D1 (de) | 2002-06-27 |
| ES2173990T3 (es) | 2002-11-01 |
| TR199501648A2 (tr) | 1996-07-21 |
| CZ190997A3 (en) | 1997-11-12 |
| JPH10512854A (ja) | 1998-12-08 |
| EP0792110A4 (de) | 1998-04-01 |
| CN1090918C (zh) | 2002-09-18 |
| WO1996019119A1 (en) | 1996-06-27 |
| CN1170340A (zh) | 1998-01-14 |
| CA2206463C (en) | 2000-10-03 |
| EP0792110B1 (de) | 2002-05-22 |
| DK0792110T3 (da) | 2002-06-17 |
| KR100225666B1 (ko) | 1999-10-15 |
| PT792110E (pt) | 2002-10-31 |
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