JP2000109489A5 - - Google Patents
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- JP2000109489A5 JP2000109489A5 JP1999240689A JP24068999A JP2000109489A5 JP 2000109489 A5 JP2000109489 A5 JP 2000109489A5 JP 1999240689 A JP1999240689 A JP 1999240689A JP 24068999 A JP24068999 A JP 24068999A JP 2000109489 A5 JP2000109489 A5 JP 2000109489A5
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- JP
- Japan
- Prior art keywords
- alcohol
- cis
- trans
- silicon compound
- salicylate
- 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.)
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- 150000003377 silicon compounds Chemical class 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- GLZPCOQZEFWAFX-JXMROGBWSA-N β-Geraniol Chemical compound CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 3
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 2
- -1 -Pentanol Chemical compound 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N 1-Decanol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N 1-Hexanol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 2
- JYVLIDXNZAXMDK-UHFFFAOYSA-N 2-Pentanol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
- NMRPBPVERJPACX-QMMMGPOBSA-N 3-Octanol Natural products CCCCC[C@@H](O)CC NMRPBPVERJPACX-QMMMGPOBSA-N 0.000 description 2
- RECUKUPTGUEGMW-UHFFFAOYSA-N Carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 description 2
- OOCCDEMITAIZTP-QPJJXVBHSA-N Cinnamyl alcohol Natural products OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N Eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N Methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- KCDXJAYRVLXPFO-UHFFFAOYSA-N Syringaldehyde Chemical compound COC1=CC(C=O)=CC(OC)=C1O KCDXJAYRVLXPFO-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atoms Chemical group 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- ZYTMANIQRDEHIO-KXUCPTDWSA-N isopulegol Chemical compound C[C@@H]1CC[C@@H](C(C)=C)[C@H](O)C1 ZYTMANIQRDEHIO-KXUCPTDWSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N n-pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- 239000001871 (1R,2R,5S)-5-methyl-2-prop-1-en-2-ylcyclohexan-1-ol Substances 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- NSSALFVIQPAIQK-BQYQJAHWSA-N (E)-non-2-en-1-ol Chemical compound CCCCCC\C=C\CO NSSALFVIQPAIQK-BQYQJAHWSA-N 0.000 description 1
- AYQPVPFZWIQERS-VOTSOKGWSA-N (E)-oct-2-en-1-ol Chemical compound CCCCC\C=C\CO AYQPVPFZWIQERS-VOTSOKGWSA-N 0.000 description 1
- WUOACPNHFRMFPN-VIFPVBQESA-N (R)-(+)-α-terpineol Chemical compound CC1=CC[C@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-VIFPVBQESA-N 0.000 description 1
- RNLHVODSMDJCBR-VURMDHGXSA-N (Z)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol Chemical compound CC(O)C(C)\C=C/C1CC=C(C)C1(C)C RNLHVODSMDJCBR-VURMDHGXSA-N 0.000 description 1
- XJHRZBIBSSVCEL-ARJAWSKDSA-N (Z)-non-6-en-1-ol Chemical compound CC\C=C/CCCCCO XJHRZBIBSSVCEL-ARJAWSKDSA-N 0.000 description 1
- YDXQPTHHAPCTPP-WAYWQWQTSA-N (Z)-oct-3-en-1-ol Chemical compound CCCC\C=C/CCO YDXQPTHHAPCTPP-WAYWQWQTSA-N 0.000 description 1
- 239000005968 1-Decanol Substances 0.000 description 1
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-Heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 1
- ZWRUINPWMLAQRD-UHFFFAOYSA-N 1-Nonanol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
- HGDVHRITTGWMJK-UHFFFAOYSA-N 2,6-dimethylheptan-2-ol Chemical compound CC(C)CCCC(C)(C)O HGDVHRITTGWMJK-UHFFFAOYSA-N 0.000 description 1
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-Methyl-1-butanol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 1
- PFNHSEQQEPMLNI-UHFFFAOYSA-N 2-Methyl-1-pentanol Chemical compound CCCC(C)CO PFNHSEQQEPMLNI-UHFFFAOYSA-N 0.000 description 1
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-Phenylethanol Natural products OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 1
- YNMSDIQQNIRGDP-UHFFFAOYSA-N 2-phenylethyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OCCC1=CC=CC=C1 YNMSDIQQNIRGDP-UHFFFAOYSA-N 0.000 description 1
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 description 1
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-phenylpropan-1-ol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 1
- MSHFRERJPWKJFX-UHFFFAOYSA-N Anisyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 description 1
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 1
- WCASXYBKJHWFMY-NSCUHMNNSA-N Crotyl alcohol Chemical compound C\C=C\CO WCASXYBKJHWFMY-NSCUHMNNSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N Dodecanol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- GYCKQBWUSACYIF-UHFFFAOYSA-N Ethyl salicylate Chemical compound CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 description 1
- CBOQJANXLMLOSS-UHFFFAOYSA-N Ethylvanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 229960002217 Eugenol Drugs 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- 229960004873 LEVOMENTHOL Drugs 0.000 description 1
- 229940041616 Menthol Drugs 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N Oleyl alcohol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N Phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- 229960005323 Phenoxyethanol Drugs 0.000 description 1
- ASUAYTHWZCLXAN-UHFFFAOYSA-N Prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 description 1
- NJGBTKGETPDVIK-UHFFFAOYSA-N Raspberry ketone Chemical compound CC(=O)CCC1=CC=C(O)C=C1 NJGBTKGETPDVIK-UHFFFAOYSA-N 0.000 description 1
- MGSRCZKZVOBKFT-UHFFFAOYSA-N Thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- WUOACPNHFRMFPN-SECBINFHSA-N alpha-Terpineol Natural products CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 1
- 229940088601 alpha-terpineol Drugs 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 235000007746 carvacrol Nutrition 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 229930004021 citronellol Natural products 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229940005667 ethyl salicylate Drugs 0.000 description 1
- 229940073505 ethyl vanillin Drugs 0.000 description 1
- 229930008393 geraniol Natural products 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- 229940095045 isopulegol Drugs 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- 229930007823 thymol Natural products 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
Description
【特許請求の範囲】
【請求項1】 次式のケイ素化合物。
(R1O)a(R2O)b(R3O)c(R4)d(R5)eSiR6
式中、R1、R2及びR3は3−メチル−5−(2,2,3−トリメチル−3−シクロペンテン−1−イル)−4−ペンテン−2−オール、2−メチルブタノール、3−ペンタノール、n−ペンタノール、2−ペンタノール、n−ヘキサノール、2−メチルペンタノール、1−デカノール、サンデラ、ノナジル、ジメトール、チモール、1−ヘプタノール、メントール、オイゲノール、バニラン、o−バニラン、4−(p−ヒドロキシフェニル)−2−ブタノン、シリンガアルデヒド、プレノール、cis−3−ヘキサノール、trans−3−ヘキサノール、cis−4−ヘプテノール、trans−2−オクテノール、trans−2−cis−6−ノナジエノール、ゲラニオール、ネロール、シトロネロール、クロチルアルコール、オレイルアルコール、リナロール、α−テルピネオール、β−フェネチルアルコール、シンナミルアルコール、ベンジルアルコール、α−メチルベンジルアルコール、ノニルアルコール、1−オクタノール、3−オクタノール、サリチル酸フェネチル、ヒドロシンナミルアルコール、cis−6−ノネン−1−オール、trans−2−ノネン−1−オール、サリチル酸メチル、cis−3−オクテノール、アニシルアルコール、カルバクロール、ジヒドロカルベオール、サリチル酸ベンジル、テトラヒドロゲラニオール、サリチル酸エチル、エチルバニリン、イソオイゲノール、イソプレゴール、ラウリルアルコール、テトラヒドロリナロール及び2−フェノキシエタノールからなる香気性アルコールの群から誘導され、R4及びR5は炭素原子数1〜40の一価炭化水素基からなる群から選択され、R6はオレフィン性又はアセチレン性末端部分を含む原子数2〜40の一価不飽和炭化水素基であり、符号aは1〜2の範囲の値を有し、符号b、c、d及びeはa+b+c+d+e=3であることを条件として0〜2の範囲の値を有する。
【請求項2】 aが2の値を有する、請求項1記載のケイ素化合物。
【請求項3】 請求項1又は請求項2記載のケイ素化合物を含んでなる組成物。
【請求項4】 請求項1又は請求項2記載のケイ素化合物を含んでなる化粧品組成物。
【請求項1】 次式のケイ素化合物。
(R1O)a(R2O)b(R3O)c(R4)d(R5)eSiR6
式中、R1、R2及びR3は3−メチル−5−(2,2,3−トリメチル−3−シクロペンテン−1−イル)−4−ペンテン−2−オール、2−メチルブタノール、3−ペンタノール、n−ペンタノール、2−ペンタノール、n−ヘキサノール、2−メチルペンタノール、1−デカノール、サンデラ、ノナジル、ジメトール、チモール、1−ヘプタノール、メントール、オイゲノール、バニラン、o−バニラン、4−(p−ヒドロキシフェニル)−2−ブタノン、シリンガアルデヒド、プレノール、cis−3−ヘキサノール、trans−3−ヘキサノール、cis−4−ヘプテノール、trans−2−オクテノール、trans−2−cis−6−ノナジエノール、ゲラニオール、ネロール、シトロネロール、クロチルアルコール、オレイルアルコール、リナロール、α−テルピネオール、β−フェネチルアルコール、シンナミルアルコール、ベンジルアルコール、α−メチルベンジルアルコール、ノニルアルコール、1−オクタノール、3−オクタノール、サリチル酸フェネチル、ヒドロシンナミルアルコール、cis−6−ノネン−1−オール、trans−2−ノネン−1−オール、サリチル酸メチル、cis−3−オクテノール、アニシルアルコール、カルバクロール、ジヒドロカルベオール、サリチル酸ベンジル、テトラヒドロゲラニオール、サリチル酸エチル、エチルバニリン、イソオイゲノール、イソプレゴール、ラウリルアルコール、テトラヒドロリナロール及び2−フェノキシエタノールからなる香気性アルコールの群から誘導され、R4及びR5は炭素原子数1〜40の一価炭化水素基からなる群から選択され、R6はオレフィン性又はアセチレン性末端部分を含む原子数2〜40の一価不飽和炭化水素基であり、符号aは1〜2の範囲の値を有し、符号b、c、d及びeはa+b+c+d+e=3であることを条件として0〜2の範囲の値を有する。
【請求項2】 aが2の値を有する、請求項1記載のケイ素化合物。
【請求項3】 請求項1又は請求項2記載のケイ素化合物を含んでなる組成物。
【請求項4】 請求項1又は請求項2記載のケイ素化合物を含んでなる化粧品組成物。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/143136 | 1998-08-28 | ||
US09/143,136 US6046156A (en) | 1998-08-28 | 1998-08-28 | Fragrance releasing olefinic silanes |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2000109489A JP2000109489A (ja) | 2000-04-18 |
JP2000109489A5 true JP2000109489A5 (ja) | 2006-10-05 |
JP4562224B2 JP4562224B2 (ja) | 2010-10-13 |
Family
ID=22502753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24068999A Expired - Fee Related JP4562224B2 (ja) | 1998-08-28 | 1999-08-27 | 香気放出性オレフィン性シラン |
Country Status (4)
Country | Link |
---|---|
US (2) | US6046156A (ja) |
EP (1) | EP0982313B1 (ja) |
JP (1) | JP4562224B2 (ja) |
DE (1) | DE69929659T2 (ja) |
Families Citing this family (45)
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US6075111A (en) * | 1998-08-28 | 2000-06-13 | General Electric Company | Fragrance releasing non-volatile polymeric siloxanes |
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US6949587B1 (en) * | 1999-08-06 | 2005-09-27 | Ecosmart Technologies, Inc. | Pesticidal compositions containing plant essential oils against beetles |
US6531540B1 (en) | 2001-05-16 | 2003-03-11 | General Electric Company | Polyether siloxane copolymer network compositions |
US6538061B2 (en) * | 2001-05-16 | 2003-03-25 | General Electric Company | Cosmetic compositions using polyether siloxane copolymer network compositions |
US7241835B2 (en) * | 2001-05-16 | 2007-07-10 | General Electric Company | Cosmetic compositions comprising silicone gels |
US20030203978A1 (en) * | 2001-05-16 | 2003-10-30 | O'brien Michael Joseph | Cosmetic compositions comprising silicone gels comprising entrapped, occluded or encapsulated pigments |
US20030095935A1 (en) * | 2001-11-16 | 2003-05-22 | General Electric Company | Transfer resistant cosmetic compositions comprising silicone gels |
DE10338070A1 (de) * | 2003-08-19 | 2005-03-17 | Henkel Kgaa | Auf Substratoberflächen aufziehende Mittel |
US20050164063A1 (en) * | 2003-10-20 | 2005-07-28 | Fuji Photo Film Co., Ltd. | Compound, and solid electrolyte, proton conductor, membrane electrode assembly and fuel cell comprising the compound |
US7579495B2 (en) * | 2003-12-19 | 2009-08-25 | Momentive Performance Materials Inc. | Active-releasing cyclic siloxanes |
US7576170B2 (en) | 2003-12-19 | 2009-08-18 | Momentive Performance Materials | Cyclic siloxane compositions for the release of active ingredients |
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US20090171108A1 (en) * | 2007-12-26 | 2009-07-02 | Momentive Performance Materials Inc. | Mixtures comprising hydrolysis resistant organomodified disiloxane ionic surfactants |
US20090173912A1 (en) * | 2007-12-26 | 2009-07-09 | Momentive Performance Materials Inc. | Mixtures of hydrolysis resistant organomodified trisiloxane ionic surfactants |
US20090176893A1 (en) * | 2007-12-26 | 2009-07-09 | Momentive Performance Materials Inc. | Hydrolysis resistant organomodified trisiloxane ionic surfactants |
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JP5133092B2 (ja) * | 2008-03-06 | 2013-01-30 | 花王株式会社 | 機能性物質放出剤 |
CN102438583A (zh) * | 2008-12-18 | 2012-05-02 | 莫门蒂夫性能材料股份有限公司 | 包含至少两种不同的环状的烷基硅氧烷的组合物及其使用 |
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-
1999
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- 1999-08-26 EP EP99306790A patent/EP0982313B1/en not_active Expired - Lifetime
- 1999-08-27 JP JP24068999A patent/JP4562224B2/ja not_active Expired - Fee Related
- 1999-08-30 US US09/385,319 patent/US6153578A/en not_active Expired - Lifetime
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