JP5128819B2 - 活性成分の放出用環状シロキサン組成物 - Google Patents
活性成分の放出用環状シロキサン組成物 Download PDFInfo
- Publication number
- JP5128819B2 JP5128819B2 JP2006545697A JP2006545697A JP5128819B2 JP 5128819 B2 JP5128819 B2 JP 5128819B2 JP 2006545697 A JP2006545697 A JP 2006545697A JP 2006545697 A JP2006545697 A JP 2006545697A JP 5128819 B2 JP5128819 B2 JP 5128819B2
- Authority
- JP
- Japan
- Prior art keywords
- acetate
- methyl
- ethyl
- butyrate
- propionate
- 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 - Fee Related
Links
- -1 Cyclic siloxane Chemical class 0.000 title claims description 118
- 239000000203 mixture Substances 0.000 title claims description 40
- 239000004480 active ingredient Substances 0.000 title description 19
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 37
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 150000002430 hydrocarbons Chemical group 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 24
- 229940022663 acetate Drugs 0.000 claims description 21
- 239000003205 fragrance Substances 0.000 claims description 21
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 19
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 17
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 239000001301 oxygen Substances 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 15
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 229910052698 phosphorus Inorganic materials 0.000 claims description 14
- 239000011574 phosphorus Substances 0.000 claims description 14
- 229910052717 sulfur Inorganic materials 0.000 claims description 14
- 239000011593 sulfur Substances 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 claims description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims description 12
- 150000002085 enols Chemical class 0.000 claims description 12
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims description 12
- RGFNRWTWDWVHDD-UHFFFAOYSA-N sec-butyl ester of butyric acid Natural products CCCC(=O)OCC(C)C RGFNRWTWDWVHDD-UHFFFAOYSA-N 0.000 claims description 11
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims description 10
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 claims description 9
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 9
- YGCZTXZTJXYWCO-UHFFFAOYSA-N 3-phenylpropanal Chemical compound O=CCCC1=CC=CC=C1 YGCZTXZTJXYWCO-UHFFFAOYSA-N 0.000 claims description 9
- MSHFRERJPWKJFX-UHFFFAOYSA-N 4-Methoxybenzyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 9
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 9
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 claims description 9
- IFYYFLINQYPWGJ-UHFFFAOYSA-N gamma-decalactone Chemical compound CCCCCCC1CCC(=O)O1 IFYYFLINQYPWGJ-UHFFFAOYSA-N 0.000 claims description 9
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 claims description 9
- ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 claims description 9
- FLUWAIIVLCVEKF-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl acetate Chemical compound CC(=O)OC(C)(C)CC1=CC=CC=C1 FLUWAIIVLCVEKF-UHFFFAOYSA-N 0.000 claims description 8
- PVYFCGRBIREQLL-UHFFFAOYSA-N 2-Methylbutyl 2-methylbutanoate Chemical compound CCC(C)COC(=O)C(C)CC PVYFCGRBIREQLL-UHFFFAOYSA-N 0.000 claims description 8
- CRBJBYGJVIBWIY-UHFFFAOYSA-N 2-isopropylphenol Chemical compound CC(C)C1=CC=CC=C1O CRBJBYGJVIBWIY-UHFFFAOYSA-N 0.000 claims description 8
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 claims description 8
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 8
- PWLNAUNEAKQYLH-UHFFFAOYSA-N Octyl butanoate Chemical compound CCCCCCCCOC(=O)CCC PWLNAUNEAKQYLH-UHFFFAOYSA-N 0.000 claims description 8
- 235000000484 citronellol Nutrition 0.000 claims description 8
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 8
- PQLMXFQTAMDXIZ-UHFFFAOYSA-N isoamyl butyrate Chemical compound CCCC(=O)OCCC(C)C PQLMXFQTAMDXIZ-UHFFFAOYSA-N 0.000 claims description 8
- GYCKQBWUSACYIF-UHFFFAOYSA-N Ethyl salicylate Chemical compound CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 claims description 7
- JSLCOZYBKYHZNL-UHFFFAOYSA-N butylisobutyrate Chemical compound CCCCOC(=O)C(C)C JSLCOZYBKYHZNL-UHFFFAOYSA-N 0.000 claims description 7
- 238000004140 cleaning Methods 0.000 claims description 7
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims description 7
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 claims description 7
- OHEFFKYYKJVVOX-UHFFFAOYSA-N sulcatol Chemical compound CC(O)CCC=C(C)C OHEFFKYYKJVVOX-UHFFFAOYSA-N 0.000 claims description 7
- 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 6
- XHXUANMFYXWVNG-ADEWGFFLSA-N (-)-Menthyl acetate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(C)=O XHXUANMFYXWVNG-ADEWGFFLSA-N 0.000 claims description 6
- CIXAYNMKFFQEFU-UHFFFAOYSA-N (4-Methylphenyl)acetaldehyde Chemical compound CC1=CC=C(CC=O)C=C1 CIXAYNMKFFQEFU-UHFFFAOYSA-N 0.000 claims description 6
- RXBQNMWIQKOSCS-UHFFFAOYSA-N (7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)methanol Chemical compound C1C2C(C)(C)C1CC=C2CO RXBQNMWIQKOSCS-UHFFFAOYSA-N 0.000 claims description 6
- HRHOWZHRCRZVCU-AATRIKPKSA-N (E)-hex-2-enyl acetate Chemical compound CCC\C=C\COC(C)=O HRHOWZHRCRZVCU-AATRIKPKSA-N 0.000 claims description 6
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims description 6
- ZPVOLGVTNLDBFI-UHFFFAOYSA-N (±)-2,2,6-trimethylcyclohexanone Chemical compound CC1CCCC(C)(C)C1=O ZPVOLGVTNLDBFI-UHFFFAOYSA-N 0.000 claims description 6
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 claims description 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims description 6
- KLTVSWGXIAYTHO-UHFFFAOYSA-N 1-Octen-3-one Chemical compound CCCCCC(=O)C=C KLTVSWGXIAYTHO-UHFFFAOYSA-N 0.000 claims description 6
- DOJDQRFOTHOBEK-UHFFFAOYSA-N 1-Octen-3-yl acetate Chemical compound CCCCCC(C=C)OC(C)=O DOJDQRFOTHOBEK-UHFFFAOYSA-N 0.000 claims description 6
- QUMXDOLUJCHOAY-UHFFFAOYSA-N 1-Phenylethyl acetate Chemical compound CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 claims description 6
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 claims description 6
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 claims description 6
- BVQVLAIMHVDZEL-UHFFFAOYSA-N 1-phenyl-1,2-propanedione Chemical compound CC(=O)C(=O)C1=CC=CC=C1 BVQVLAIMHVDZEL-UHFFFAOYSA-N 0.000 claims description 6
- FJPGAMCQJNLTJC-UHFFFAOYSA-N 2,3-Heptanedione Chemical compound CCCCC(=O)C(C)=O FJPGAMCQJNLTJC-UHFFFAOYSA-N 0.000 claims description 6
- NKTOLZVEWDHZMU-UHFFFAOYSA-N 2,5-xylenol Chemical compound CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 claims description 6
- ZFBNNSOJNZBLLS-UHFFFAOYSA-N 2,6-Dimethoxy-4-methylphenol Chemical compound COC1=CC(C)=CC(OC)=C1O ZFBNNSOJNZBLLS-UHFFFAOYSA-N 0.000 claims description 6
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 claims description 6
- KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical compound COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 claims description 6
- FZOZFDAMVVEZSJ-UHFFFAOYSA-N 2-Acetyl-4,5-dihydrothiazole Chemical compound CC(=O)C1=NCCS1 FZOZFDAMVVEZSJ-UHFFFAOYSA-N 0.000 claims description 6
- PETRWTHZSKVLRE-UHFFFAOYSA-N 2-Methoxy-4-methylphenol Chemical compound COC1=CC(C)=CC=C1O PETRWTHZSKVLRE-UHFFFAOYSA-N 0.000 claims description 6
- FTZILAQGHINQQR-UHFFFAOYSA-N 2-Methylpentanal Chemical compound CCCC(C)C=O FTZILAQGHINQQR-UHFFFAOYSA-N 0.000 claims description 6
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 claims description 6
- FZXRXKLUIMKDEL-UHFFFAOYSA-N 2-Methylpropyl propanoate Chemical compound CCC(=O)OCC(C)C FZXRXKLUIMKDEL-UHFFFAOYSA-N 0.000 claims description 6
- CJPNOLIZCWDHJK-UHFFFAOYSA-N 2-Pentadecanone Chemical compound CCCCCCCCCCCCCC(C)=O CJPNOLIZCWDHJK-UHFFFAOYSA-N 0.000 claims description 6
- CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 claims description 6
- CFAKWWQIUFSQFU-UHFFFAOYSA-N 2-hydroxy-3-methylcyclopent-2-en-1-one Chemical compound CC1=C(O)C(=O)CC1 CFAKWWQIUFSQFU-UHFFFAOYSA-N 0.000 claims description 6
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 claims description 6
- BYGQBDHUGHBGMD-UHFFFAOYSA-N 2-methylbutanal Chemical compound CCC(C)C=O BYGQBDHUGHBGMD-UHFFFAOYSA-N 0.000 claims description 6
- NGDNVOAEIVQRFH-UHFFFAOYSA-N 2-nonanol Chemical compound CCCCCCCC(C)O NGDNVOAEIVQRFH-UHFFFAOYSA-N 0.000 claims description 6
- KVFQMAZOBTXCAZ-UHFFFAOYSA-N 3,4-Hexanedione Chemical compound CCC(=O)C(=O)CC KVFQMAZOBTXCAZ-UHFFFAOYSA-N 0.000 claims description 6
- WGAVDEVFJDQIMZ-UHFFFAOYSA-N 3,4-dimethyl-1,2-cyclopentanedione Chemical compound CC1CC(=O)C(=O)C1C WGAVDEVFJDQIMZ-UHFFFAOYSA-N 0.000 claims description 6
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 claims description 6
- TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-UHFFFAOYSA-N 0.000 claims description 6
- IITQJMYAYSNIMI-UHFFFAOYSA-N 3-Methyl-2-cyclohexen-1-one Chemical compound CC1=CC(=O)CCC1 IITQJMYAYSNIMI-UHFFFAOYSA-N 0.000 claims description 6
- CHCCBPDEADMNCI-UHFFFAOYSA-N 3-Methyl-2-cyclopenten-1-one Chemical compound CC1=CC(=O)CC1 CHCCBPDEADMNCI-UHFFFAOYSA-N 0.000 claims description 6
- XJLDYKIEURAVBW-UHFFFAOYSA-N 3-decanone Chemical compound CCCCCCCC(=O)CC XJLDYKIEURAVBW-UHFFFAOYSA-N 0.000 claims description 6
- XPCTZQVDEJYUGT-UHFFFAOYSA-N 3-hydroxy-2-methyl-4-pyrone Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 claims description 6
- HNVRRHSXBLFLIG-UHFFFAOYSA-N 3-hydroxy-3-methylbut-1-ene Chemical compound CC(C)(O)C=C HNVRRHSXBLFLIG-UHFFFAOYSA-N 0.000 claims description 6
- JDXJKLGWPNXSHL-UHFFFAOYSA-N 3-methyl-1,2-cyclohexanedione Chemical compound CC1CCCC(=O)C1=O JDXJKLGWPNXSHL-UHFFFAOYSA-N 0.000 claims description 6
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-methyl-2-butanol Chemical compound CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 claims description 6
- YGHRJJRRZDOVPD-UHFFFAOYSA-N 3-methylbutanal Chemical compound CC(C)CC=O YGHRJJRRZDOVPD-UHFFFAOYSA-N 0.000 claims description 6
- XKWSWANXMRXDES-UHFFFAOYSA-N 3-methylbutyl octanoate Chemical compound CCCCCCCC(=O)OCCC(C)C XKWSWANXMRXDES-UHFFFAOYSA-N 0.000 claims description 6
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 claims description 6
- VLJSLTNSFSOYQR-UHFFFAOYSA-N 3-propan-2-ylphenol Chemical compound CC(C)C1=CC=CC(O)=C1 VLJSLTNSFSOYQR-UHFFFAOYSA-N 0.000 claims description 6
- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 claims description 6
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 6
- CWRKZMLUDFBPAO-SREVYHEPSA-N 4-Decenal Chemical compound CCCCC\C=C/CCC=O CWRKZMLUDFBPAO-SREVYHEPSA-N 0.000 claims description 6
- HFNGYHHRRMSKEU-UHFFFAOYSA-N 4-Methoxybenzyl acetate Chemical compound COC1=CC=C(COC(C)=O)C=C1 HFNGYHHRRMSKEU-UHFFFAOYSA-N 0.000 claims description 6
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 claims description 6
- FUGYGGDSWSUORM-UHFFFAOYSA-N 4-hydroxystyrene Chemical compound OC1=CC=C(C=C)C=C1 FUGYGGDSWSUORM-UHFFFAOYSA-N 0.000 claims description 6
- OIGWAXDAPKFNCQ-UHFFFAOYSA-N 4-isopropylbenzyl alcohol Chemical compound CC(C)C1=CC=C(CO)C=C1 OIGWAXDAPKFNCQ-UHFFFAOYSA-N 0.000 claims description 6
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 claims description 6
- PXRBWNLUQYZAAX-UHFFFAOYSA-N 6-Butyltetrahydro-2H-pyran-2-one Chemical compound CCCCC1CCCC(=O)O1 PXRBWNLUQYZAAX-UHFFFAOYSA-N 0.000 claims description 6
- GHBSPIPJMLAMEP-UHFFFAOYSA-N 6-pentyloxan-2-one Chemical compound CCCCCC1CCCC(=O)O1 GHBSPIPJMLAMEP-UHFFFAOYSA-N 0.000 claims description 6
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 claims description 6
- SCCDQYPEOIRVGX-UHFFFAOYSA-N Acetyleugenol Chemical compound COC1=CC(CC=C)=CC=C1OC(C)=O SCCDQYPEOIRVGX-UHFFFAOYSA-N 0.000 claims description 6
- HVJKZICIMIWFCP-UHFFFAOYSA-N Benzyl 3-methylbutanoate Chemical compound CC(C)CC(=O)OCC1=CC=CC=C1 HVJKZICIMIWFCP-UHFFFAOYSA-N 0.000 claims description 6
- YPQSPODHFDGVAC-UHFFFAOYSA-N Butyl heptanoate Chemical compound CCCCCCC(=O)OCCCC YPQSPODHFDGVAC-UHFFFAOYSA-N 0.000 claims description 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 6
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims description 6
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 6
- NUPSHWCALHZGOV-UHFFFAOYSA-N Decyl acetate Chemical compound CCCCCCCCCCOC(C)=O NUPSHWCALHZGOV-UHFFFAOYSA-N 0.000 claims description 6
- VLSVVMPLPMNWBH-UHFFFAOYSA-N Dihydro-5-propyl-2(3H)-furanone Chemical compound CCCC1CCC(=O)O1 VLSVVMPLPMNWBH-UHFFFAOYSA-N 0.000 claims description 6
- BHJHPYFAYGAPLS-UHFFFAOYSA-N Guaicyl acetate Chemical compound COC1=CC=CC=C1OC(C)=O BHJHPYFAYGAPLS-UHFFFAOYSA-N 0.000 claims description 6
- RZKSECIXORKHQS-UHFFFAOYSA-N Heptan-3-ol Chemical compound CCCCC(O)CC RZKSECIXORKHQS-UHFFFAOYSA-N 0.000 claims description 6
- RFDUMBPGZUIKOG-UHFFFAOYSA-N Heptyl 2-methylpropanoate Chemical compound CCCCCCCOC(=O)C(C)C RFDUMBPGZUIKOG-UHFFFAOYSA-N 0.000 claims description 6
- CYHBDKTZDLSRMY-UHFFFAOYSA-N Hexyl 2-methylpropanoate Chemical compound CCCCCCOC(=O)C(C)C CYHBDKTZDLSRMY-UHFFFAOYSA-N 0.000 claims description 6
- RSDDTPVXLMVLQE-UHFFFAOYSA-N Hexyl 3-methylbutanoate Chemical compound CCCCCCOC(=O)CC(C)C RSDDTPVXLMVLQE-UHFFFAOYSA-N 0.000 claims description 6
- XXIKYCPRDXIMQM-UHFFFAOYSA-N Isopentenyl acetate Chemical compound CC(C)=CCOC(C)=O XXIKYCPRDXIMQM-UHFFFAOYSA-N 0.000 claims description 6
- FFOPEPMHKILNIT-UHFFFAOYSA-N Isopropyl butyrate Chemical compound CCCC(=O)OC(C)C FFOPEPMHKILNIT-UHFFFAOYSA-N 0.000 claims description 6
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 claims description 6
- FHLGUOHLUFIAAA-UHFFFAOYSA-N Linalyl butyrate Chemical compound CCCC(=O)OC(C)(C=C)CCC=C(C)C FHLGUOHLUFIAAA-UHFFFAOYSA-N 0.000 claims description 6
- OCWLYWIFNDCWRZ-UHFFFAOYSA-N Methyl (S)-2-Methylbutanoate Chemical compound CCC(C)C(=O)OC OCWLYWIFNDCWRZ-UHFFFAOYSA-N 0.000 claims description 6
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
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- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
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- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
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- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
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- OBAJXDYVZBHCGT-UHFFFAOYSA-N tris(pentafluorophenyl)borane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1B(C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F OBAJXDYVZBHCGT-UHFFFAOYSA-N 0.000 description 1
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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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A61K8/585—Organosilicon compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- 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
- C07F7/21—Cyclic compounds having at least one ring containing silicon, but no carbon in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/02—Polysilicates
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/162—Organic compounds containing Si
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/507—Compounds releasing perfumes by thermal or chemical activation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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Description
式中、MはB、Al、Ga、In又はTlであり、R9は同一又は異なる炭素原子数6〜14の一価芳香族炭化水素基であって、1以上の−CF3、−NO2若しくは−CNのような電子求引性の元素若しくは基又は2個以上のハロゲン原子を有する一価芳香剤族炭化水素基をを表し、Xはハロゲン原子であり、sは1、2、又は3であり、tは0、1又は2である。但し、s+t=3である。さらに好ましくは、ルイス酸は次式(VI)で表される。
式中、R10は同一又は異なる炭素原子数6〜14の一価芳香族炭化水素基であって、1以上の−CF3、−NO2若しくは−CNのような電子求引性の元素若しくは基又は2個以上のハロゲン原子を有する一価芳香剤族炭化水素基をを表し、Xはハロゲン原子であり、sは1、2、又は3であり、tは0、1又は2であるが、但し、s+t=3である。最も好ましくは、B(C6F5)3である。
実施例1
シトロネロール(5.89g、0.038mol)と環状水素化シリコーン混合物(2.0g、0.033mol)を一緒に加え、混合し、カリウムシラノラート−官能化シリコーン(0.02g、0.015mmol)で処理した。15min撹拌した後、溶液を60℃に18h加熱した。80℃/6mmHgで1hの真空ストリッピングにより揮発性成分を除去して生成物(6.5g、91%)を得た。
環状水素化シリコーンの混合物(6.50g、0.108mol水素化物)を丸底フラスコに仕込んだ。シトロネロール(18.58g、0.119mol)とジビニルテトラメチルシロキサン中Pt(0)の10.9%溶液(28.9mg溶液、126ppmPt)とを混和し、45minかけて滴下して水素化物に加えた。ガスの発生が観察された。次に、フラスコを70℃に68h加熱した後、70℃/2mmHgで3hの真空ストリッピングにより薄茶色の溶液から揮発性成分を除去して22.77gの生成物(98%)を得た。
環状水素化シリコーンの混合物(7.75g、0.129mol水素化物)を丸底フラスコに仕込み、70℃に加熱した。フェネチルアルコール(17.32g、0.142mol)とジビニルテトラメチルシロキサン中Pt(0)の10.9%溶液(6.7mg溶液、29ppmPt)を混和し、2hかけて水素化物に滴下して加えた。ガスの発生が観察された。浅黄色の溶液を70℃で5.5d撹拌した後、80℃/1mmHgで4hの真空ストリッピングにより溶液から揮発性成分を除去して23.14gの生成物(99.5%)を得た。
丸底フラスコで、トリス(ペンタフルオロフェニル)ボラン(42.7mg、83.4μmol)をオイゲノール(15.04g、0.092mol)に溶解して山吹色の溶液を得た。環状水素化シリコーンの混合物(5g、0.083mol水素化物)を滴下して加えたところ、溶液が曇った。添加は7minで完了し、乳白色の混合物が得られた。30minの撹拌後、ガスの発生が観察され、混合物は透明になって浅黄色の溶液が得られ、これを周囲温度で合計14.5h撹拌した。70℃/0.1mmHgの真空下で5h揮発性成分を除去した。混合物をろ過して、17.89の浅黄色の液体(97%)を得た。
丸底フラスコで、2−イソプロピルフェノール(13.94g、0.102mol)とトリス(ペンタフルオロフェニルボラン)(0.052g、101μmol)を15min撹拌して、薄い黄緑色の溶液を得た。環状水素化シリコーンの混合物(6.23g、0.102mol水素化物)を1hかけて滴下して加えた。添加中水素ガスの発生が観察された。この溶液を周囲温度で40min、その後50℃で2.5h撹拌した。70℃(3mmHg)の真空下で1.5h揮発性成分を除去して、16.5g(82.5%)を得た。
丸底フラスコで、フェネチルアルコール(6.74g、0.055mol)とエタノール中(nBu2S)3RhCl3の1.36%Rh溶液(42mg溶液、100ppmRh)を周囲温度で一緒に撹拌した。環状水素化シリコーンの混合物(3.37g、0.055mol水素化物)を75minかけて滴下して加え、さらに75min撹拌した。この溶液を70℃に加熱したところ、ガスの発生が観察された。70℃で18.5h撹拌した後、溶液は深い灰緑色であった。フラスコを周囲温度まで冷却し、70℃/1.2mmHgの真空下で1.5h揮発性成分を除去した。生成物をろ過して7.65gの生成物(76.5%)を得た。
丸底フラスコで、シトロネロール(7.26g、0.046mol)とエタノール中(nBu2S)3RhCl3の1.36%Rh溶液(35mg溶液、100ppmRh)を周囲温度で一緒に撹拌した。環状水素化シリコーンの混合物(2.83g、0.046mol水素化物)を55minかけて滴下して加えた。溶液を70℃に加熱した。数分以内にガスの発生が観察された。70℃で40h撹拌した後、フラスコを周囲温度まで冷却し、70℃/1〜2mmHgの真空下で1h揮発性成分を除去した。生成物をろ過して7.85gの深い灰色流体(78.5%)を得た。
丸底フラスコで、アセトフェノン(6.74g、0.056mol)と4.3%KOH−等価カリウムシラノラート−官能性シリコーン(0.073g、56μmol)を周囲温度で15mLのトルエンに溶解した。純粋な環状水素化シリコーン1,3,5,7−テトラメチルシクロテトラシロキサン(3.37g、0.056mol水素化物)を30minかけて滴下して加えた。ガスの発生が観察された。添加後、溶液を周囲温度で2h撹拌した。次に、この溶液を70℃に加熱し、2h撹拌した。70℃/5mmHgで1.5h揮発性成分を除去した。生成物をろ過して8.30gの薄いオレンジ色の流体(83%)を得た。
丸底フラスコで、ヘキサナール(6.33g、0.063mol)、トルエン(15g)、トリエチルアミン(0.012g、0.126mmol)、及びジビニルテトラメチルシロキサン中Pt(0)の10.9%溶液(17mg溶液、150ppmPt)を周囲温度で10min撹拌した。純粋な環状水素化シリコーン1,3,5,7−テトラメチルシクロテトラシロキサンを15minかけて滴下して加えた。ガスの発生が観察され、混合物を70℃に加熱し24h保持した後、さらにジビニルテトラメチルシロキサン中Pt(0)の10.9%溶液(17mg溶液添加、300ppm合計Pt)を加えた。この混合物をさらに12h70℃で撹拌した後、70℃/3mmHgで1.5hストリッピングして8.3gのえび茶色の流体(83%)を得た。
加水分解の一般的な手順は次の通り。
Claims (21)
- 以下の式のシロキサンからなるシロキサンの群から選択されるシロキサン。
- 前記シロキサンがアルコールを放出する、請求項2記載のシロキサン。
- 以下の式のシロキサンからなるシロキサンの群から選択されるシロキサン。
- 前記シロキサンがカルボニル化合物を放出する、請求項2記載のシロキサン。
- 以下の式のシロキサンからなるシロキサンの群から選択されるシロキサン。
- 前記シロキサンがアルコールを放出する、請求項7記載のシロキサン。
- 次式を有するシロキサン。
- 前記シロキサンがカルボニル化合物を放出する、請求項7記載のシロキサン。
- 次式を有するシロキサン。
- 酸素原子に結合するFragが、前記酸素原子がOH基に変換されたうえで前記シロキサンから脱離した、請求項1のシロキサンの加水分解物。
- 請求項1記載のシロキサンを含んでなる香料組成物。
- 請求項2記載のシロキサンを含んでなる香料組成物。
- 請求項3記載のシロキサンを含んでなる香料組成物。
- 請求項5記載のシロキサンを含んでなる香料組成物。
- 請求項7記載のシロキサンを含んでなる香料組成物。
- 請求項8記載のシロキサンを含んでなる香料組成物。
- 請求項10記載のシロキサンを含んでなる香料組成物。
- 請求項1記載のシロキサンを含んでなるパーソナルケア製品、クリーニング製品、香料製品、家庭用製品、洗剤、濯ぎ用添加剤、自動車用材料、織物、成形材料、又はプラスチック製品。
- 請求項1記載のシロキサンからなる香料組成物。
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US10/742,415 | 2003-12-19 | ||
US10/742,415 US7576170B2 (en) | 2003-12-19 | 2003-12-19 | Cyclic siloxane compositions for the release of active ingredients |
PCT/US2004/040157 WO2005066186A2 (en) | 2003-12-19 | 2004-12-01 | Cyclic siloxane compositions for the release of active ingredients |
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Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101218282B (zh) * | 2005-07-18 | 2012-03-28 | 陶氏康宁公司 | 醛官能的硅氧烷 |
US7767754B2 (en) * | 2005-11-08 | 2010-08-03 | Momentive Performance Materials Inc. | Silicone composition and process of making same |
US7479522B2 (en) | 2005-11-09 | 2009-01-20 | Momentive Performance Materials Inc. | Silicone elastomer composition |
DE102007012910A1 (de) * | 2007-03-19 | 2008-09-25 | Momentive Performance Materials Gmbh | Mit Duftstoffen modifizierte, verzweigte Polyorganosiloxane |
US7897558B1 (en) | 2009-12-16 | 2011-03-01 | The United States Of America As Represented By The Secretary Of The Navy | Siloxane solvent compositions |
JP5253608B2 (ja) * | 2011-07-26 | 2013-07-31 | 花王株式会社 | 香料放出剤 |
KR101774896B1 (ko) * | 2012-06-15 | 2017-09-05 | 다이니혼 죠츄기쿠 가부시키가이샤 | 비상 해충 기피 제품, 및 비상 해충 기피 방법 |
EP3010555B1 (en) * | 2013-06-19 | 2020-07-15 | The Procter and Gamble Company | Absorbent article comprising complexed or encapsulated reactive compounds |
DE102015004437A1 (de) * | 2015-04-02 | 2016-10-06 | BAM Bundesanstalt für Materialforschung und -prüfung | Fluoreszierendes Siloxanelastomer, Verfahren zu dessen Herstellung und die Verwendung |
US9920280B2 (en) | 2016-02-25 | 2018-03-20 | The United States Of America, As Represented By The Secretary Of The Navy | Non-aqueous siloxane solvent compositions for cleaning a metal or plastic surface |
CN107432497B (zh) * | 2016-05-25 | 2021-01-19 | 浙江中烟工业有限责任公司 | 一种适用于加热非燃烧型烟草制品的功能香精 |
CN111108232A (zh) * | 2017-09-19 | 2020-05-05 | 应用材料公司 | 用于在二氧化硅上选择性沉积电介质的方法 |
DE102017123282A1 (de) | 2017-10-06 | 2019-04-11 | Henkel Ag & Co. Kgaa | Hydrolyselabile Silylenolether von Riechstoffketonen oder -aldehyden |
DE102017124612A1 (de) | 2017-10-20 | 2019-04-25 | Henkel Ag & Co. Kgaa | Hydrolyselabile Dienolsilylether von Riechstoffketonen oder -aldehyden |
DE102017127776A1 (de) | 2017-11-24 | 2019-05-29 | Henkel Ag & Co. Kgaa | Hydrolyselabile Heterocyclen von Riechstoffketonen oder -aldehyden |
CN114907143B (zh) * | 2022-04-13 | 2023-05-05 | 宁波信远炭材料有限公司 | 一种表面陶瓷膜膨胀石墨材料及其制备方法 |
Family Cites Families (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US558715A (en) * | 1896-04-21 | Measure | ||
GB971309A (en) | 1961-04-28 | 1964-09-30 | Ici Ltd | New siloxanes |
US3215719A (en) * | 1961-09-01 | 1965-11-02 | Dan River Mills Inc | Silicate esters of essential alcohols |
US3271305A (en) * | 1961-09-01 | 1966-09-06 | Dan River Mills Inc | Textile treatments and treated textiles |
US3220972A (en) | 1962-07-02 | 1965-11-30 | Gen Electric | Organosilicon process using a chloroplatinic acid reaction product as the catalyst |
US3159601A (en) | 1962-07-02 | 1964-12-01 | Gen Electric | Platinum-olefin complex catalyzed addition of hydrogen- and alkenyl-substituted siloxanes |
US3159662A (en) | 1962-07-02 | 1964-12-01 | Gen Electric | Addition reaction |
US3814730A (en) | 1970-08-06 | 1974-06-04 | Gen Electric | Platinum complexes of unsaturated siloxanes and platinum containing organopolysiloxanes |
US3715334A (en) | 1970-11-27 | 1973-02-06 | Gen Electric | Platinum-vinylsiloxanes |
US3775452A (en) | 1971-04-28 | 1973-11-27 | Gen Electric | Platinum complexes of unsaturated siloxanes and platinum containing organopolysiloxanes |
IT1209302B (it) | 1979-02-01 | 1989-07-16 | Dow Corning Ltd | Composizione saponificante contenente composti al silicio quali ingredienti profumati di lunga durata |
NL8000387A (nl) | 1979-02-01 | 1980-08-05 | Dow Corning | Preparaat met anti-transpiratie- en/of deodorant- eigenschappen. |
US4500725A (en) * | 1981-07-30 | 1985-02-19 | Chisso Corporation | Silane derivative and fragrant article |
US4445641A (en) * | 1982-01-08 | 1984-05-01 | Bend Research, Inc. | Controlled-release dispenser |
JPS58208211A (ja) * | 1982-05-28 | 1983-12-03 | Chisso Corp | 徐分解性香料を使用した芳香剤 |
DE3237928A1 (de) | 1982-10-13 | 1984-04-19 | Karl Meinig KG, 7201 Rietheim-Weilheim | Vorrichtung zum anformen von flanschen an luftkanalwandungen |
CA1306192C (en) | 1986-12-17 | 1992-08-11 | Andrew Hamilton Ward | Medicament containing a silicon derivative of menthol |
EP0281034A3 (en) * | 1987-02-26 | 1990-09-19 | Tohru Yamamoto | An aromatic composition and a method for the production of the same |
US4842761A (en) | 1988-03-23 | 1989-06-27 | International Flavors & Fragrances, Inc. | Compositions and methods for controlled release of fragrance-bearing substances |
US4908208A (en) * | 1988-04-22 | 1990-03-13 | Dow Corning Corporation | Matrix for release of active ingredients |
US5008115A (en) * | 1988-04-22 | 1991-04-16 | Dow Corning Corporation | Matrix for release of active ingredients |
FR2643572A1 (fr) * | 1988-12-22 | 1990-08-31 | Rhone Poulenc Chimie | Procede d'encapsulation de particules par pelliculage au moyen d'un copolymere silicone thermoplastique |
US5049182A (en) * | 1989-02-03 | 1991-09-17 | Ici Americas Inc. | Single-package agricultural formulations combining immediate and time-delayed delivery |
US5071704A (en) * | 1990-06-13 | 1991-12-10 | Fischel Ghodsian Fariba | Device for controlled release of vapors and scents |
GB9021061D0 (en) * | 1990-09-27 | 1990-11-07 | Unilever Plc | Encapsulating method and products containing encapsulated material |
US5387411A (en) * | 1990-10-05 | 1995-02-07 | Dow Corning Corporation | Antiperspirant containing a hydrophobic macroporous polymer as the suspending agent |
US5234689A (en) * | 1990-11-08 | 1993-08-10 | La Parfumerie, Inc. | Multi-purpose fragrance composition |
US5176903A (en) * | 1990-12-13 | 1993-01-05 | Revlon Consumer Products Corporation | Antiperspirant/deodorant containing microcapsules |
US5139864A (en) * | 1991-11-11 | 1992-08-18 | International Flavors & Fragrances Inc. | Multi-layer, multi-functional volatilizable substance delivery articles |
US5213409A (en) * | 1991-11-18 | 1993-05-25 | Fisher David B | Decorative light grid |
ES2091591T3 (es) * | 1991-12-20 | 1996-11-01 | Procter & Gamble | Un procedimiento para preparar una composicion de capsulas de perfume. |
US5372806A (en) * | 1992-01-03 | 1994-12-13 | Soft And Shine | Grooming composition |
US5160494A (en) * | 1992-04-14 | 1992-11-03 | Dow Corning Corporation | Alkylmethylsiloxane containing perfume compositions |
US5378468A (en) * | 1992-09-22 | 1995-01-03 | The Mennen Company | Composition containing body activated fragrance for contacting the skin and method of use |
US5447893A (en) * | 1994-08-01 | 1995-09-05 | Dow Corning Corporation | Preparation of high density titanium carbide ceramics with preceramic polymer binders |
US5525588A (en) * | 1994-09-14 | 1996-06-11 | Elzabeth Arden Co. | Cosmetic composition |
US5449512A (en) * | 1994-08-24 | 1995-09-12 | The Procter & Gamble Company | Anhydrous after shave lotions |
FR2727114B1 (fr) * | 1994-11-17 | 1996-12-27 | Oreal | Nouveaux filtres solaires, compositions cosmetiques photoprotectrices les contenant et utilisations |
US5490982A (en) * | 1995-02-01 | 1996-02-13 | Elizabeth Arden Company, Division Of Conopco, Inc. | Cosmetic composition |
CH689622A5 (fr) | 1995-03-15 | 1999-07-15 | Firmenich & Cie | Polysiloxanes nouveaux, leur utilisation en parfumerie et procédé pour leur préparation. |
EP0778506A1 (en) * | 1995-12-05 | 1997-06-11 | Brother Kogyo Kabushiki Kaisha | Electrophotographic type image forming device and developing roller for use in the device |
WO1998015192A1 (en) | 1996-10-09 | 1998-04-16 | Givaudan-Roure (International) S.A. | Process for preparing beads as food additive |
WO1998015191A1 (en) * | 1996-10-09 | 1998-04-16 | Givaudan-Roure (International) S.A. | Process for preparing beads as food or tobacco additive |
CA2236189A1 (en) * | 1997-05-15 | 1998-11-15 | Givaudan-Roure (International) Sa | Fragrance precursor compounds |
EP0878497A3 (en) | 1997-05-15 | 1999-12-15 | Givaudan-Roure (International) S.A. | Fragrance precursor compounds |
JPH1147581A (ja) | 1997-07-30 | 1999-02-23 | Takasago Internatl Corp | 徐放性カプセル及びその製造方法 |
US6042792A (en) * | 1997-09-18 | 2000-03-28 | International Flavors & Fragrances Inc. | Apparatus for preparing a solid phase microparticulate composition |
US5847179A (en) * | 1997-10-02 | 1998-12-08 | Pcr, Inc. | High purity alkoxytrimethylsilane fluids |
JPH11106629A (ja) * | 1997-10-03 | 1999-04-20 | Takasago Internatl Corp | 香料含有徐放性生分解性樹脂組成物 |
US6624136B2 (en) * | 1998-02-02 | 2003-09-23 | Rhodia Chimie | Water-dispersible granules comprising a fragrance in a water-soluble or water-dispersible matrix, and process for their preparation |
US6143309A (en) * | 1998-03-12 | 2000-11-07 | Archimica (Florida), Inc. | Delivery of hydroxy carboxylic acids |
US6213409B1 (en) | 1998-03-19 | 2001-04-10 | International Flavors & Fragances Inc. | Time release fragrance sachet, method of using same and method of fabricating same |
US6046156A (en) * | 1998-08-28 | 2000-04-04 | General Electric Company | Fragrance releasing olefinic silanes |
US6083901A (en) | 1998-08-28 | 2000-07-04 | General Electric Company | Emulsions of fragrance releasing silicon compounds |
US6054547A (en) * | 1998-08-28 | 2000-04-25 | General Electric Company | Fragrance releasing non-volatile polymeric-siloxanes |
US6075111A (en) * | 1998-08-28 | 2000-06-13 | General Electric Company | Fragrance releasing non-volatile polymeric siloxanes |
US6063365A (en) * | 1998-09-10 | 2000-05-16 | International Flavors & Fragrances Inc. | Application of film forming technology to fragrance control release systems; and resultant fragrance control release systems |
JP2002526565A (ja) | 1998-09-18 | 2002-08-20 | ハーマン・ウント・ライマー・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 特定の放出挙動を有するカプセルに包まれた香料及び/又は芳香剤 |
WO2000024435A1 (en) * | 1998-10-22 | 2000-05-04 | Firmenich S.A. | Gel type vapor release device |
US20020004033A1 (en) | 1999-04-22 | 2002-01-10 | Dirk Sorgenfrey | Emulsion type vapor generator |
TW449519B (en) * | 1999-05-31 | 2001-08-11 | Hitachi Ltd | A manufacturing method of a structure body |
EP1061124A1 (en) | 1999-06-15 | 2000-12-20 | Givaudan SA | Method for preparing fragrance products |
FR2794980B1 (fr) | 1999-06-18 | 2001-09-07 | V Man Fils Ets | Article pour la liberation controlee et sensiblement reguliere d'une substance organique volatile |
US6500444B1 (en) | 1999-12-21 | 2002-12-31 | International Flavors & Fragrances Inc. | Continuously fragrance-emitting dry or wet wipe fabric article and method for preparing same |
US6200949B1 (en) * | 1999-12-21 | 2001-03-13 | International Flavors And Fragrances Inc. | Process for forming solid phase controllably releasable fragrance-containing consumable articles |
AU7247000A (en) | 2000-01-11 | 2001-07-19 | Givaudan Sa | Composite materials |
EP1116515A3 (en) | 2000-01-11 | 2002-08-21 | Givaudan SA | Encapsulated liquid |
DE10012199A1 (de) | 2000-03-13 | 2001-09-20 | Haarmann & Reimer Gmbh | Eingekapselte Substanzen mit kontrollierter Freisetzung |
WO2001073188A1 (en) | 2000-03-27 | 2001-10-04 | Givaudan Sa | Disposable cleaning cloth |
EP1146057A1 (en) | 2000-04-15 | 2001-10-17 | Givaudan SA | Polymeric nanoparticles including olfactive molecules |
JP3970540B2 (ja) | 2000-05-30 | 2007-09-05 | 高砂香料工業株式会社 | コーティング剤およびコーティング粉末 |
EP1167362B1 (en) | 2000-06-19 | 2005-05-25 | Givaudan SA | Fragance precursors |
SE518782C2 (sv) | 2000-07-19 | 2002-11-19 | Akzo Nobel Nv | Användning av en alkylhydroxialkylcellulosa för att förbättra glans och tryckbarhet samt en vattenhaltig bestrykningskomposition |
EP1178107A3 (en) | 2000-07-24 | 2002-03-27 | Givaudan SA | Process for refreshing and de-wrinkling fabrics |
US6309715B1 (en) * | 2000-08-02 | 2001-10-30 | International Flavors & Fragrances Inc. | Decorative materials encased in a polymer with fragrance releasing characteristics |
EP1208754A1 (en) | 2000-11-21 | 2002-05-29 | Givaudan SA | Particulate material |
US6482912B2 (en) | 2001-01-29 | 2002-11-19 | Ndsu Research Foundation | Method of preparing aminofunctional alkoxy polysiloxanes |
US6932982B2 (en) | 2001-02-16 | 2005-08-23 | Firmenich Sa | Encapsulated flavor and/or fragrance composition |
AU2002249265A1 (en) | 2001-03-23 | 2002-10-08 | Symrise Gmbh & Co. Kg | Use of solid particles for thermally extracting perfume oils and/or aromas |
US20030004072A1 (en) | 2001-04-10 | 2003-01-02 | The Procter & Gamble Company | Photo-activated pro-fragrances |
JP3553521B2 (ja) | 2001-04-26 | 2004-08-11 | 高砂香料工業株式会社 | コーティング剤及びコーティング粉末 |
US6723359B2 (en) | 2001-10-18 | 2004-04-20 | Firmenich Sa | Spray-dried compositions and method for their preparation |
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2003
- 2003-12-19 US US10/742,415 patent/US7576170B2/en not_active Expired - Fee Related
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2004
- 2004-12-01 CN CN2013100965861A patent/CN103319521A/zh active Pending
- 2004-12-01 KR KR1020067011934A patent/KR101248700B1/ko not_active IP Right Cessation
- 2004-12-01 CA CA002548996A patent/CA2548996A1/en not_active Abandoned
- 2004-12-01 EP EP10011306A patent/EP2281545A1/en not_active Withdrawn
- 2004-12-01 BR BRPI0416716-3A patent/BRPI0416716A/pt not_active Application Discontinuation
- 2004-12-01 MX MXPA06006842A patent/MXPA06006842A/es active IP Right Grant
- 2004-12-01 WO PCT/US2004/040157 patent/WO2005066186A2/en not_active Application Discontinuation
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- 2004-12-01 JP JP2006545697A patent/JP5128819B2/ja not_active Expired - Fee Related
- 2004-12-10 CN CNA2004800379826A patent/CN1893910A/zh active Pending
- 2004-12-10 KR KR1020137000070A patent/KR20130018975A/ko not_active Application Discontinuation
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Also Published As
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HK1098159A1 (en) | 2007-07-13 |
WO2005066186A2 (en) | 2005-07-21 |
US7576170B2 (en) | 2009-08-18 |
US20050136022A1 (en) | 2005-06-23 |
MXPA06006842A (es) | 2006-08-23 |
EP1716159A2 (en) | 2006-11-02 |
KR20130018975A (ko) | 2013-02-25 |
WO2005066186A3 (en) | 2005-08-25 |
EP1716159B1 (en) | 2011-07-13 |
CA2548996A1 (en) | 2005-07-21 |
CN1893910A (zh) | 2007-01-10 |
KR101248700B1 (ko) | 2013-03-29 |
CN103319521A (zh) | 2013-09-25 |
BRPI0416716A (pt) | 2007-01-16 |
EP2281545A1 (en) | 2011-02-09 |
KR20070003792A (ko) | 2007-01-05 |
WO2005066186A8 (en) | 2006-08-17 |
JP2007514784A (ja) | 2007-06-07 |
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