JPS6111996B2 - - Google Patents
Info
- Publication number
- JPS6111996B2 JPS6111996B2 JP58130553A JP13055383A JPS6111996B2 JP S6111996 B2 JPS6111996 B2 JP S6111996B2 JP 58130553 A JP58130553 A JP 58130553A JP 13055383 A JP13055383 A JP 13055383A JP S6111996 B2 JPS6111996 B2 JP S6111996B2
- Authority
- JP
- Japan
- Prior art keywords
- fragrance
- group
- enzyme
- acetate
- fragrances
- 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
Links
- 239000003205 fragrance Substances 0.000 claims description 54
- 102000004190 Enzymes Human genes 0.000 claims description 46
- 108090000790 Enzymes Proteins 0.000 claims description 46
- -1 monoterpene alcohols Chemical class 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 18
- 239000007844 bleaching agent Substances 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 150000002978 peroxides Chemical class 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 229930003658 monoterpene Natural products 0.000 claims description 6
- 235000002577 monoterpenes Nutrition 0.000 claims description 6
- 229930004725 sesquiterpene Natural products 0.000 claims description 5
- 150000003934 aromatic aldehydes Chemical class 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims 1
- 229940088598 enzyme Drugs 0.000 description 44
- 235000019645 odor Nutrition 0.000 description 19
- 230000000873 masking effect Effects 0.000 description 12
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 6
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 4
- 108010056079 Subtilisins Proteins 0.000 description 4
- 102000005158 Subtilisins Human genes 0.000 description 4
- 229940022663 acetate Drugs 0.000 description 4
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 4
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 4
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 229940095672 calcium sulfate Drugs 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 3
- 229940045872 sodium percarbonate Drugs 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- 239000001306 (7E,9E,11E,13E)-pentadeca-7,9,11,13-tetraen-1-ol Substances 0.000 description 2
- 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
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 2
- IKDIJXDZEYHZSD-UHFFFAOYSA-N 2-phenylethyl formate Chemical compound O=COCCC1=CC=CC=C1 IKDIJXDZEYHZSD-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N Benzylformate Chemical compound O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000005792 Geraniol Substances 0.000 description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
- BTJXBZZBBNNTOV-UHFFFAOYSA-N Linalyl benzoate Chemical compound CC(C)=CCCC(C)(C=C)OC(=O)C1=CC=CC=C1 BTJXBZZBBNNTOV-UHFFFAOYSA-N 0.000 description 2
- 102000035195 Peptidases Human genes 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 2
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 2
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 2
- 229940088601 alpha-terpineol Drugs 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 229940007550 benzyl acetate Drugs 0.000 description 2
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 2
- SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 description 2
- 229940026455 cedrol Drugs 0.000 description 2
- PCROEXHGMUJCDB-UHFFFAOYSA-N cedrol Natural products CC1CCC2C(C)(C)C3CC(C)(O)CC12C3 PCROEXHGMUJCDB-UHFFFAOYSA-N 0.000 description 2
- 235000000484 citronellol Nutrition 0.000 description 2
- JOZKFWLRHCDGJA-UHFFFAOYSA-N citronellol acetate Chemical compound CC(=O)OCCC(C)CCC=C(C)C JOZKFWLRHCDGJA-UHFFFAOYSA-N 0.000 description 2
- 229940019836 cyclamen aldehyde Drugs 0.000 description 2
- 230000009849 deactivation Effects 0.000 description 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
- 230000002255 enzymatic effect Effects 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 2
- 229940113087 geraniol Drugs 0.000 description 2
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- SVURIXNDRWRAFU-UHFFFAOYSA-N juniperanol Natural products C1C23C(C)CCC3C(C)(C)C1C(O)(C)CC2 SVURIXNDRWRAFU-UHFFFAOYSA-N 0.000 description 2
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 2
- 235000001510 limonene Nutrition 0.000 description 2
- 229940087305 limonene Drugs 0.000 description 2
- 229930007744 linalool Natural products 0.000 description 2
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- OSORMYZMWHVFOZ-UHFFFAOYSA-N phenethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCC1=CC=CC=C1 OSORMYZMWHVFOZ-UHFFFAOYSA-N 0.000 description 2
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 2
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 1
- QQLIGMASAVJVON-UHFFFAOYSA-N 1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=CC2=C1 QQLIGMASAVJVON-UHFFFAOYSA-N 0.000 description 1
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- VVUMWAHNKOLVSN-UHFFFAOYSA-N 2-(4-ethoxyanilino)-n-propylpropanamide Chemical compound CCCNC(=O)C(C)NC1=CC=C(OCC)C=C1 VVUMWAHNKOLVSN-UHFFFAOYSA-N 0.000 description 1
- RJASFPFZACBKBE-UHFFFAOYSA-N 2-Methylpropyl phenylacetate Chemical compound CC(C)COC(=O)CC1=CC=CC=C1 RJASFPFZACBKBE-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- BDCFWIDZNLCTMF-UHFFFAOYSA-N 2-phenylpropan-2-ol Chemical compound CC(C)(O)C1=CC=CC=C1 BDCFWIDZNLCTMF-UHFFFAOYSA-N 0.000 description 1
- DLHQZZUEERVIGQ-UHFFFAOYSA-N 3,7-dimethyl-3-octanol Chemical compound CCC(C)(O)CCCC(C)C DLHQZZUEERVIGQ-UHFFFAOYSA-N 0.000 description 1
- 239000001629 3,7-dimethylocta-2,6-dienyl benzoate Substances 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
- 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 description 1
- 108090000915 Aminopeptidases Proteins 0.000 description 1
- 102000004400 Aminopeptidases Human genes 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- CBOCVOKPQGJKKJ-UHFFFAOYSA-L Calcium formate Chemical class [Ca+2].[O-]C=O.[O-]C=O CBOCVOKPQGJKKJ-UHFFFAOYSA-L 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 108090000087 Carboxypeptidase B Proteins 0.000 description 1
- 102000003670 Carboxypeptidase B Human genes 0.000 description 1
- 108010080937 Carboxypeptidases A Proteins 0.000 description 1
- 102000000496 Carboxypeptidases A Human genes 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 108090000317 Chymotrypsin Proteins 0.000 description 1
- JOZKFWLRHCDGJA-LLVKDONJSA-N Citronellyl acetate Natural products CC(=O)OCC[C@H](C)CCC=C(C)C JOZKFWLRHCDGJA-LLVKDONJSA-N 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 241000402754 Erythranthe moschata Species 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 102000004157 Hydrolases Human genes 0.000 description 1
- 108090000604 Hydrolases Proteins 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- 102000003960 Ligases Human genes 0.000 description 1
- 108090000364 Ligases Proteins 0.000 description 1
- 102000004317 Lyases Human genes 0.000 description 1
- 108090000856 Lyases Proteins 0.000 description 1
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 1
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 description 1
- YDVXYTIIPGKIJP-UHFFFAOYSA-N O-Benzoyl-geraniol Natural products CC(C)=CCCC(C)=CCOC(=O)C1=CC=CC=C1 YDVXYTIIPGKIJP-UHFFFAOYSA-N 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 108090000526 Papain Proteins 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- 108010022999 Serine Proteases Proteins 0.000 description 1
- 102000012479 Serine Proteases Human genes 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 108090000787 Subtilisin Proteins 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 102000004357 Transferases Human genes 0.000 description 1
- 108090000992 Transferases Proteins 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229940095564 anhydrous calcium sulfate Drugs 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940095076 benzaldehyde Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 229940115397 bornyl acetate Drugs 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical class [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Chemical class 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229960003563 calcium carbonate Drugs 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 235000019255 calcium formate Nutrition 0.000 description 1
- 239000004281 calcium formate Chemical class 0.000 description 1
- 229940044172 calcium formate Drugs 0.000 description 1
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical class [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 1
- 235000010261 calcium sulphite Nutrition 0.000 description 1
- RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 description 1
- HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 description 1
- 235000007746 carvacrol Nutrition 0.000 description 1
- 229960002376 chymotrypsin Drugs 0.000 description 1
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
- 229960002424 collagenase Drugs 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- FQMZVFJYMPNUCT-UHFFFAOYSA-N geraniol formate Natural products CC(C)=CCCC(C)=CCOC=O FQMZVFJYMPNUCT-UHFFFAOYSA-N 0.000 description 1
- YDVXYTIIPGKIJP-QINSGFPZSA-N geranyl benzoate Chemical compound CC(C)=CCC\C(C)=C/COC(=O)C1=CC=CC=C1 YDVXYTIIPGKIJP-QINSGFPZSA-N 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229930002839 ionone Natural products 0.000 description 1
- 150000002499 ionone derivatives Chemical class 0.000 description 1
- WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 description 1
- 108010059345 keratinase Proteins 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940097364 magnesium acetate tetrahydrate Drugs 0.000 description 1
- 229940076230 magnesium sulfate monohydrate Drugs 0.000 description 1
- XKPKPGCRSHFTKM-UHFFFAOYSA-L magnesium;diacetate;tetrahydrate Chemical compound O.O.O.O.[Mg+2].CC([O-])=O.CC([O-])=O XKPKPGCRSHFTKM-UHFFFAOYSA-L 0.000 description 1
- LFCFXZHKDRJMNS-UHFFFAOYSA-L magnesium;sulfate;hydrate Chemical compound O.[Mg+2].[O-]S([O-])(=O)=O LFCFXZHKDRJMNS-UHFFFAOYSA-L 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 108010003855 mesentericopeptidase Proteins 0.000 description 1
- 229940095102 methyl benzoate Drugs 0.000 description 1
- BGEHHAVMRVXCGR-UHFFFAOYSA-N methylundecylketone Natural products CCCCCCCCCCCCC=O BGEHHAVMRVXCGR-UHFFFAOYSA-N 0.000 description 1
- 150000002773 monoterpene derivatives Chemical class 0.000 description 1
- NIOYUNMRJMEDGI-UHFFFAOYSA-N n-hexadecylaldehyde Natural products CCCCCCCCCCCCCCCC=O NIOYUNMRJMEDGI-UHFFFAOYSA-N 0.000 description 1
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229940038597 peroxide anti-acne preparations for topical use Drugs 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229940100595 phenylacetaldehyde Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000010378 sodium ascorbate Nutrition 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 229960005055 sodium ascorbate Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229960001322 trypsin Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Description
本発明は香気を有し使用感に優れた酵素含有漂
白剤組成物に関する。
過炭酸ナトリウムに代表される無機過酸化物を
主成分とする酵素系漂白剤は、次亜塩素酸のよう
な塩素系漂白剤に比べて、使用可能な繊維の多い
こと、色・柄物にも使用できること、塩素系漂白
剤特有の臭いがないことなどの優れた性質を有し
ており、広く用いられるようになつている。
しかし、酸素系漂白剤は衣類に付着した種々の
汚れに対する漂白効果が塩素系漂白剤に比べて劣
るために漂白効果の向上が試みられており、特に
落ちにくい蛋白、油脂、澱粉汚れに対しては、酵
素を酸素系漂白剤と併用して汚れを除去すること
が提案されている。
しかしながら、酵素には酵素臭という独特の異
臭があり、特に酵素を過酸化物の存在下で保存す
るときに異臭が著しくなるという問題が生じた。
そこで、香料を添加して酵素臭をマスキングする
と共に使用感を高めることが必要となるが、酵素
臭のマスキングは困難であり、しかも、香料が保
存中に酵素と作用して香りが変質したり、過酸化
物により分解してしまう問題があつた。
本発明はこのような酵素含有漂白剤組成物にお
ける問題点を解消するためになされたものであ
り、酵素臭のマスキング性に優れ、しかも、長期
保存によつても香気の質が変化しない香料系を含
む漂白剤組成物を提供することを目的とする。
すなわち、本発明の酵素含有漂白剤組成物は、
無機過酸化物、酵素および香料を含有する組成物
において、この香料として、以下のA群とB群と
の双方の香料を含み、しかも、フエノール系香料
および炭素数8〜14の脂肪族アルデヒド系香料の
合計含有量が3重量%以下の混合香料を用いるこ
とを特徴とする。
A 群
モノテルペンアルコール、セスキテルペンアル
コールおよび炭素数7〜10の芳香族アルコールの
群から選ばれる少なくとも1種の香料。
B 群
炭素数8〜17のギ酸エステルまたは酢酸エステ
ル、炭素数10〜15の炭化水素および炭素数7〜15
の芳香族アルデヒドの群から選ばれる少なくとも
1種の香料。
以下、本発明についてさらに詳細に説明する。
無機過酸化物の具体例としては、過酸化ナトリ
ウム、過硼酸ナトリウム、過硫酸ナトリウムなど
が例示され、この中でも過炭酸ナトリウムは低温
における漂白効果が優れている点で好ましい。無
機過酸化物の配合量は50〜99.8wt%が適当であ
り、好ましくは70〜95wt%である。
本発明の漂白剤組成物に配合される酵素として
は、水の付加、除去を促進する加水分解酵素、酸
化還元を促進する酸化還元酵素、基を1つの分子
から他の分子へ転移し汚れを変質させて除去を促
進する転移酵素、分子間の結合を切断し汚れを分
解して除去を促進するリガーゼ、リアーゼ、汚れ
を化学的に変質して除去を促進する酵素が適当で
あり、これらの中でも加水分解酵素が好ましく、
加水分解酵素の中でもプロテアーゼが特に好まし
い。プロテアーゼの具体例としては、セリンプロ
テアーゼ、ペプシン、トリプシン、キモトリプシ
ン、コラーゲナーゼ、ケラチナーゼ、エステラー
ゼ、スブチリシン、パパイン、カルボキシペプチ
ターゼAおよびB、アミノペプチターゼが挙げら
れ、これらの酵素は、たとえば以下の市販品とし
て入手することもできる。
アルカラーゼ:ノボ・インダストリー社
エスペラーゼ:ノボ・インダストリー社
ビロプラーゼ:長瀬産業(株)
マクサターゼ:ギスト・プロゲデス社
ALD−2:明治製菓(株)
スペラーゼ:フアイザー社
これらの酵素は単独であるいは併用して漂白剤
組政物に配合され、この配合量は0.01〜5重量%
が適当であり、好ましくは0.1〜3重量%であ
る。
本発明のA群の香料の具体例としては以下のも
のが例示され、この中でもモノテルペンアルコー
ルがマスキング性および安定性の点で好ましい。
(1) モノテルペンアルコール
リナロール、ゲラニオール、ネロール、シト
ロネロール、ジメチルオクタノール、ヒドロキ
シシトロネール、テトラヒドロリナロールなど
の鎖状テルペンアルコール、および、α−テル
ピネオール、l−メントール、ボルネオールな
どの環状テルペンアルコール。
(2) セスキテルペンアルコール
フアルネソール、ネロリドール、サンタロー
ル、セドロール、ベチベロール。
(3) C7〜10の芳香族アルコール
ベンジルアルコール、β−フエニルエチルア
ルコール、シンナミツクアルコール、ジメチル
ベンジルカルビノール、ジメチルフエニルカル
ビノール。
また、B群の香料の具体例としては以下のもの
が例示され、この中でも炭素数8〜17のギ酸エス
テルまたは酢酸エステルがマスキング性および安
定性の点で好ましい。
(1) C8〜17のギ酸または酢酸エステル
ギ酸ゲラニル、ギ酸ベンジル、ギ酸フエニル
エチル、酢酸シトロネリル、酢酸ゲラニル、酢
酸リナリル、酢酸ボルニル、酢酸テルピニル、
酢酸ベンジル、酢酸セドリル、酢酸−p−t−
ブチルシクロヘキシル。
(2) C10〜15の炭化水素
α−ピネン、β−ピネン、リモネン、テルピ
ノーレンなどのモノテルペン炭化水素、β−カ
リオレフレインなどのセスキテルペン炭化水
素。
(3) C7〜15の芳香族アルデヒド
ベンズアルデヒド、フエニルアセトアルデヒ
ド、シンナミツクアルデヒド、α−ヘキシルシ
ンナミツクアルデヒド、シクラメンアルデヒ
ド、リリーアルデヒド。
これらA群の香料とB群の香料は併用して組成
物に配され、重量比でA群/B群=9/1〜1/
9の割合で配合するのが適当であり、好ましくは
7/3〜3/7である。A群とB群の香料は合計
で0.01〜1wt%組成物中に配合するのが適当であ
り、好ましくは0.05〜0.5wt%である。
本発明では、配合される全香料中、フエノール
系香料および脂肪族アルデヒド系香料の合計含有
量が3wt%以下、好ましくは2wt%以下となるよ
うに、香料が配合される。この値が3wt%を越え
ると、マスキング効果および香気安定性のいずれ
もが低下する。フエノール系香料の具体例として
はチモール、カルバクロール、オイゲノール、イ
ソオイゲノールなどが例示され、また、脂肪族ア
ルデヒド系香料としてはn−オクチルアルデヒ
ド、n−ノニルアルデヒド、n−デシルアルデヒ
ド、n−ウンデシルアルデヒド、ウンデシレンア
ルデヒド、ドデシルアルデヒド、n−ヘキサデシ
ルアルデヒドなどが挙げられる。
さらに、上記以外の香料成分も必要により配合
することが可能であり、これらとしてはn−アク
チルアルコール、n−ラウリルアルコールなどの
脂肪族アルコール、ベンゾフエノン、ヨノン、メ
チルナフチルケトンなどのケトン、ムスク系香
料、安息香族メチル、安息香酸エチル、安息香酸
ゲラニル、安息香酸リナリル、安息香酸フエニル
エチル、フエニル酢酸イソブチルなどが挙げられ
る。
本発明の混合香料は、A群およびB群のそれぞ
れ1種を併用することによつても所期の効果を得
ることができるが、数種あるいは数十種の香料を
調合して目的とする芳香を発現せしめるのが一般
的である。
すでに説明したように酵素系漂白剤の汚れ除去
能の増進に酵素は有用であるが、一方において、
酵素系漂白剤に酵素を配合すると保存下に酵素が
失活して所期の効果が得られないという問題があ
る。そこで、保存安定剤を添加し酵素の失活を防
止して保存安定性を改善しうることが好ましい。
このような保存安定化剤として特に好ましいもの
は、特開昭59−129300号公報(特願昭58−3714
号)において本出願人が提案した結晶系が六方晶
系である無水硫酸カルシウム、硫酸カルシウム1/
2水塩、硫酸マグネシウム1水塩であり、少なく
ともこの1種を配合することにより酵素の失活を
有効に防止することができる。この他、無水硫酸
アルミニウム、無水塩化マグネシウム、無水クエ
ン酸ナトリウム、無水塩化カルシウム、無水硫酸
亜鉛も有効な安定化剤である。また、炭酸カルシ
ウム、ギ酸カルシウム、酢酸カルシウムの無水塩
または1水塩、亜硫酸カルシウム1/2水塩、酢酸
マグネシウム4水塩を用いることができる。これ
ら酵素の安定化剤の配合量は0.1〜20wt%が適当
であり、好ましくは0.5〜5wt%である。
また、酢酸ナトリウム、アスコルビン酸ナトリ
ウム、安息香酸ナトリウム、塩化亜塩を配合して
香気の安定性をさらに増加させることもできる。
さらに、本発明の組成物中には酵素の失活を促
進したり、無機過酸化物に悪影響を与えない範囲
で、陰イオン界面活性剤、非イオン界面活性剤、
顔料、螢光剤などの種々の添加剤を添加すること
ができる。
本発明の漂白剤組成物によれば、特定の香料系
を用いることにより、無機過酸化物あるいは酵素
のように活性の高い物質との共存下にあつても、
長期保存後によつて酵素臭のマスキング性が劣化
したり、香気の安定性が損なわれることがない。
実施例 1
次の処方でA群香料およびB群香料を調製し
た。
A群香料
モノテルペンアルコール
リナロール 20wt%
ゲラニオール 15wt%
シトロネロール 15wt%
テトラヒドロリナロール 5wt%
α−テルピネオール 15wt%
セスキテルペンアルコール
セドロール 5wt%
サンタロール 5wt%
C7〜10芳香族アルコール
β−フエニルエチルアルコール 20wt%
B群香料
C8〜17ギ酸または酢酸エステル
酢酸ゲラニル 5wt%
酢酸リナリル 15wt%
酢酸テルピニル 10wt%
酢酸ベンジル 25wt%
酢酸セドリル 5wt%
酢酸−p−t−ブチルシクロヘキシル 10wt%
C10〜15炭化水素
リモネン 10wt%
C7〜15芳香族アルデヒド
α−ヘキシルシンナミツクアルデヒド 10wt%
シクラメンアルデヒド 5wt%
リリーアルデヒド 5wt%
ついで、過炭酸ナトリウム93.7〜93.9wt%、酵
素(アルカラーゼ2.0T)1wt%および安定化剤と
しての硫酸カルシウム1/2水塩5wt%に対し、第
1表に示したA群香料、B群香料あるいはさらに
他の香料を配合した香料を0.1〜0.3wt%添加して
酵素含有漂白剤組成物を調製し、これら試料をポ
リ容器ボトルに密封保存し、45℃で30日間放置し
て保存したのち、酵素臭マスキング性および香気
安定性について評価した。
酵素臭マスキング性
◎:酵素臭が殆ど認められない
〇:酵素臭がわずかに認められる
△:酵素臭が認められる
×:酵素臭がかなり認められる
香気安定性
5:殆ど変化が認められない
4:わずかに変化が認められる
3:変化が認められる
2:変化がかなり認められる
1:変化が著しく認められる
The present invention relates to an enzyme-containing bleach composition that has an aroma and is comfortable to use. Enzyme-based bleaches whose main ingredients are inorganic peroxides, such as sodium percarbonate, can be used with more fibers than chlorine-based bleaches such as hypochlorous acid, and are more effective against colors and patterns. It has excellent properties such as ease of use and no odor typical of chlorine bleach, and has become widely used. However, oxygen bleach is less effective than chlorine bleach in bleaching various types of stains on clothing, so attempts have been made to improve its bleaching effect, especially on protein, oil, and starch stains that are difficult to remove. proposed the use of enzymes in conjunction with oxygen bleach to remove stains. However, enzymes have a unique odor called enzyme odor, and a problem has arisen in that the odor becomes particularly pronounced when enzymes are stored in the presence of peroxide.
Therefore, it is necessary to add fragrances to mask the enzyme odor and improve the usability, but masking the enzyme odor is difficult, and moreover, the fragrance may interact with enzymes during storage and the fragrance may deteriorate. There was a problem that it decomposed due to peroxide. The present invention has been made in order to solve these problems with enzyme-containing bleach compositions, and provides a fragrance system that has excellent enzyme odor masking properties and that does not change in aroma quality even after long-term storage. An object of the present invention is to provide a bleach composition containing the following. That is, the enzyme-containing bleach composition of the present invention is
In a composition containing an inorganic peroxide, an enzyme, and a fragrance, the fragrance includes both the following group A and B fragrances, and further includes a phenolic fragrance and an aliphatic aldehyde having 8 to 14 carbon atoms. It is characterized by using a mixed fragrance whose total content of fragrance is 3% by weight or less. Group A At least one fragrance selected from the group of monoterpene alcohols, sesquiterpene alcohols, and aromatic alcohols having 7 to 10 carbon atoms. Group B Formic acid ester or acetate ester having 8 to 17 carbon atoms, hydrocarbon having 10 to 15 carbon atoms, and 7 to 15 carbon atoms
At least one fragrance selected from the group of aromatic aldehydes. The present invention will be explained in more detail below. Specific examples of inorganic peroxides include sodium peroxide, sodium perborate, and sodium persulfate. Among these, sodium percarbonate is preferred because it has an excellent bleaching effect at low temperatures. The appropriate amount of inorganic peroxide is 50 to 99.8 wt%, preferably 70 to 95 wt%. Enzymes to be incorporated into the bleach composition of the present invention include hydrolytic enzymes that promote the addition and removal of water, oxidoreductases that promote redox, and enzymes that transfer groups from one molecule to another to remove stains. Transferases that promote denaturation and removal, ligases and lyases that cleave intermolecular bonds and decompose dirt to promote removal, and enzymes that chemically denature dirt and promote removal are suitable. Among them, hydrolytic enzymes are preferred;
Among hydrolases, proteases are particularly preferred. Specific examples of proteases include serine protease, pepsin, trypsin, chymotrypsin, collagenase, keratinase, esterase, subtilisin, papain, carboxypeptidase A and B, and aminopeptidase. It is also available as a product. Alcalase: Novo Industries Co., Ltd. Esperase: Novo Industries Co., Ltd. Viroplase: Nagase Sangyo Co., Ltd. Maxatase: Gist Progedes Co., Ltd. ALD-2: Meiji Seika Co., Ltd. Sperase: Phaizer Co., Ltd. These enzymes are used alone or in combination as bleaching agents. It is blended into the composition, and the blending amount is 0.01 to 5% by weight.
is suitable, preferably 0.1 to 3% by weight. Specific examples of the fragrance of Group A of the present invention include the following, and among these, monoterpene alcohols are preferred in terms of masking properties and stability. (1) Monoterpene alcohols Chain terpene alcohols such as linalool, geraniol, nerol, citronellol, dimethyloctanol, hydroxycitronel, and tetrahydrolinalol, and cyclic terpene alcohols such as α-terpineol, l-menthol, and borneol. (2) Sesquiterpene alcohols fulnesol, nerolidol, santalol, cedrol, vetiverol. (3) C7-10 aromatic alcohol benzyl alcohol, β-phenylethyl alcohol, cinnamic alcohol, dimethylbenzylcarbinol, dimethylphenylcarbinol. Moreover, the following are illustrated as a specific example of the fragrance|flavor of the B group, Among these, formic acid ester or acetate ester of carbon number 8-17 is preferable from the point of masking property and stability. (1) C8-17 formic acid or acetate geranyl formate, benzyl formate, phenylethyl formate, citronellyl acetate, geranyl acetate, linalyl acetate, bornyl acetate, terpinyl acetate,
Benzyl acetate, cedryl acetate, acetic acid-pt-
Butylcyclohexyl. (2) C10-15 hydrocarbons Monoterpene hydrocarbons such as α-pinene, β-pinene, limonene, and terpinolene, and sesquiterpene hydrocarbons such as β-caryorefrein. (3) C7-15 aromatic aldehyde benzaldehyde, phenyl acetaldehyde, cinnamic aldehyde, α-hexyl cinnamic aldehyde, cyclamen aldehyde, lily aldehyde. These fragrances of group A and fragrances of group B are used together in a composition, and the weight ratio of group A/group B = 9/1 to 1/
It is appropriate to mix them in a ratio of 9/9, preferably 7/3 to 3/7. It is appropriate that the fragrances of Group A and Group B be incorporated in the composition in a total amount of 0.01 to 1 wt%, preferably 0.05 to 0.5 wt%. In the present invention, fragrances are blended such that the total content of phenolic fragrances and aliphatic aldehyde fragrances is 3wt% or less, preferably 2wt% or less of all fragrances to be blended. If this value exceeds 3 wt%, both the masking effect and the aroma stability will decrease. Specific examples of phenolic fragrances include thymol, carvacrol, eugenol, and isoeugenol, and examples of aliphatic aldehyde fragrances include n-octylaldehyde, n-nonylaldehyde, n-decylaldehyde, and n-undecyl. Examples include aldehyde, undecylene aldehyde, dodecyl aldehyde, and n-hexadecyl aldehyde. Furthermore, fragrance ingredients other than those mentioned above can be blended if necessary, and these include aliphatic alcohols such as n-actyl alcohol and n-lauryl alcohol, ketones such as benzophenone, ionone, and methylnaphthyl ketone, and musk-based fragrances. Examples include perfume, methyl benzoate, ethyl benzoate, geranyl benzoate, linalyl benzoate, phenylethyl benzoate, isobutyl phenyl acetate, and the like. The mixed fragrance of the present invention can obtain the desired effect by using one type of each of Group A and Group B together, but it is also possible to obtain the desired effect by blending several or dozens of types of fragrance. It is common to develop a fragrance. As already explained, enzymes are useful in enhancing the stain removal ability of enzymatic bleaches, but on the other hand,
When enzymes are added to enzymatic bleaches, there is a problem in that the enzymes become deactivated during storage and the desired effect cannot be obtained. Therefore, it is preferable to add a storage stabilizer to prevent enzyme deactivation and improve storage stability.
Particularly preferable storage stabilizers are those described in Japanese Patent Application Laid-Open No. 59-129300 (Japanese Patent Application No. 58-3714).
Anhydrous calcium sulfate, calcium sulfate 1/
dihydrate and magnesium sulfate monohydrate, and by blending at least one of these, deactivation of the enzyme can be effectively prevented. In addition, anhydrous aluminum sulfate, anhydrous magnesium chloride, anhydrous sodium citrate, anhydrous calcium chloride, and anhydrous zinc sulfate are also effective stabilizers. Further, anhydrous or monohydrate salts of calcium carbonate, calcium formate, calcium acetate, calcium sulfite 1/2 hydrate, and magnesium acetate tetrahydrate can be used. The appropriate amount of these enzyme stabilizers is 0.1 to 20 wt%, preferably 0.5 to 5 wt%. Additionally, sodium acetate, sodium ascorbate, sodium benzoate, and subsalt chloride may be added to further increase the stability of the aroma. Furthermore, in the composition of the present invention, anionic surfactants, nonionic surfactants,
Various additives such as pigments and fluorescent agents can be added. According to the bleach composition of the present invention, by using a specific fragrance system, even when coexisting with highly active substances such as inorganic peroxides or enzymes,
Enzyme odor masking properties do not deteriorate after long-term storage, and aroma stability does not deteriorate. Example 1 Group A fragrances and Group B fragrances were prepared using the following formulations. Group A fragrance Monoterpene alcohol Linalool 20wt% Geraniol 15wt% Citronellol 15wt% Tetrahydrolinalool 5wt% α-Terpineol 15wt% Sesquiterpene alcohol Cedrol 5wt% Santalol 5wt% C 7-10 aromatic alcohol β-Phenylethyl alcohol 20wt% B Group fragrance C 8-17 Formic acid or acetate ester Geranyl acetate 5wt% Linalyl acetate 15wt% Terpinyl acetate 10wt% Benzyl acetate 25wt% Cedryl acetate 5wt% pt-Butylcyclohexyl acetate 10wt% C 10-15 Hydrocarbon Limonene 10wt% C 7-15 Aromatic aldehyde α-hexyl cinnamic aldehyde 10wt% Cyclamenaldehyde 5wt% Lilyaldehyde 5wt% Then, sodium percarbonate 93.7-93.9wt%, enzyme (Alcalase 2.0T) 1wt% and calcium sulfate 1 as a stabilizer. An enzyme-containing bleach composition is prepared by adding 0.1 to 0.3 wt% of a fragrance containing a group A fragrance, a group B fragrance, or another fragrance shown in Table 1 to 5 wt% of /2 hydrate salt, These samples were stored in sealed plastic containers and stored at 45°C for 30 days, and then evaluated for enzyme odor masking ability and aroma stability. Enzyme odor masking property ◎: Enzyme odor is almost not observed ○: Enzyme odor is slightly observed △: Enzyme odor is observed ×: Enzyme odor is observed considerably Aroma stability 5: Almost no change is observed 4: Slight change observed 3: Change observed 2: Significant change observed 1: Significant change observed
【表】
参考例
過酸化ナトリウム93.8wt%、酵素(アルカラー
セ2.0T)1wt%および安定化剤としての硫酸カル
シウム1/2水塩5wt%に対し、第2表に示す各種
香料を0.2wt%添加して、酵素含有漂白剤組成物
を調製し、これら試料をポリ容器ボトルに密封保
存し、45℃で30日間放置して保存したのち、酵素
臭マスキング性および香気安定性を実施例1に準
じて評価した。その結果を第2表に示す。
第2表に示す結果から明らかな通り、A群また
はB群に属する香料は、必ずしも充分ではないも
のの、ある程度の酵素臭マスキング性と香気安定
性を具えているが、他の香料にはそうした効果を
ほとんど期待できない。[Table] Reference example: 0.2 wt% of various fragrances shown in Table 2 are added to 93.8 wt% of sodium peroxide, 1 wt% of enzyme (Alcalase 2.0T), and 5 wt% of calcium sulfate 1/2 hydrate as a stabilizer. An enzyme-containing bleach composition was prepared, and these samples were sealed and stored in a plastic container bottle and left to stand at 45°C for 30 days.The enzyme odor masking property and aroma stability were evaluated according to Example 1. It was evaluated. The results are shown in Table 2. As is clear from the results shown in Table 2, fragrances belonging to Group A or Group B have a certain degree of enzyme odor masking ability and aroma stability, although not necessarily sufficient, whereas other fragrances have such effects. can hardly be expected.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
実施例 2
過酸化ナトリウム93.8wt%、酵素(アルカラー
ゼ2.0T)1wt%および安定化剤としての硫酸カル
シウム1/2水塩5wt%に対し、A群香料およびB
群香料の組合わせを変えた混合香料を0.2wt%配
合して酵素含有漂白剤組成物を調製し、実施例1
と同様にして酵素臭マスキング性と香気安定性を
評価した。
また比較のため、A群同志およびB群同志の香
料を組合わせて上と同様な酵素含有漂白剤組成物
を調製し、それらの酵素臭マスキング性と香気安
定性についても評価した。結果を第3表に示す。
第3表に示す結果は、たとえ本発明でA群及び
B群に特定した香料を使用しても、その組合わせ
がA群同志またはB群同志である場合には、酵素
臭を充分にマスキングスることができず、A群と
B群を組合わせることによつて初めて所期の効果
が得られることを示している。[Table] Example 2 Group A fragrance and B
Example 1 An enzyme-containing bleach composition was prepared by blending 0.2 wt% of mixed fragrances with different combinations of group fragrances.
Enzyme odor masking properties and aroma stability were evaluated in the same manner as above. For comparison, enzyme-containing bleach compositions similar to those above were prepared by combining fragrances from group A and group B, and their enzyme odor masking properties and fragrance stability were also evaluated. The results are shown in Table 3. The results shown in Table 3 show that even if fragrances specified in Group A and Group B are used in the present invention, enzyme odors can be sufficiently masked if the combination is of Group A or Group B. This shows that the desired effect can only be obtained by combining Group A and Group B.
Claims (1)
白剤組成物において、香料として、 (A) モノテルペンアルコール、セスキテルペンア
ルコールおよび炭素数7〜10の芳香族アルコー
ルの群から選ばれる少なくとも1種の香料と (B) 炭素数8〜17のギ酸エステルまたは酢酸エス
テル、炭素数10〜15の炭化水素および炭素数7
〜15の芳香族アルデヒドの群から選ばれる少な
くとも1種の香料 とを含有し、かつ、フエノール系香料および炭素
数8〜14の脂肪族アルデヒド系香料の合計含有量
が香料中の3重量%以下である混合香料を用いる
ことを特徴とする酵素含有漂白剤組成物。[Scope of Claims] 1. In a bleach composition containing an inorganic peroxide, an enzyme, and a fragrance, as the fragrance, (A) from the group of monoterpene alcohols, sesquiterpene alcohols, and aromatic alcohols having 7 to 10 carbon atoms; At least one selected fragrance and (B) a formate or acetate having 8 to 17 carbon atoms, a hydrocarbon having 10 to 15 carbon atoms, and 7 carbon atoms.
at least one fragrance selected from the group of ~15 aromatic aldehydes, and the total content of the phenolic fragrance and the aliphatic aldehyde fragrance having 8 to 14 carbon atoms is 3% by weight or less in the fragrance. An enzyme-containing bleach composition characterized by using a mixed fragrance.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13055383A JPS6023498A (en) | 1983-07-18 | 1983-07-18 | Enzyme-containing bleaching agent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13055383A JPS6023498A (en) | 1983-07-18 | 1983-07-18 | Enzyme-containing bleaching agent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6023498A JPS6023498A (en) | 1985-02-06 |
JPS6111996B2 true JPS6111996B2 (en) | 1986-04-05 |
Family
ID=15037020
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13055383A Granted JPS6023498A (en) | 1983-07-18 | 1983-07-18 | Enzyme-containing bleaching agent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6023498A (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH068436B2 (en) * | 1985-09-20 | 1994-02-02 | ライオン株式会社 | Granular detergent composition |
JPS6315899A (en) * | 1986-07-07 | 1988-01-22 | 花王株式会社 | Detergent composition |
GB8921995D0 (en) * | 1989-09-29 | 1989-11-15 | Unilever Plc | Perfumed laundry detergents |
WO1996002625A1 (en) * | 1994-07-19 | 1996-02-01 | The Procter & Gamble Company | Perfumes for laundry and cleaning compositions |
EP0784091A1 (en) * | 1996-01-12 | 1997-07-16 | The Procter & Gamble Company | Stable perfumed bleaching composition |
JP3617613B2 (en) * | 1999-06-30 | 2005-02-09 | ライオン株式会社 | Liquid detergent composition |
EP1072673A3 (en) * | 1999-07-20 | 2001-03-21 | The Procter & Gamble Company | Perfume compositions |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5773100A (en) * | 1980-10-24 | 1982-05-07 | Kao Corp | Enzyme-containing bleaching agent composition |
JPS5821498A (en) * | 1981-07-30 | 1983-02-08 | ダスキンフランチヤイズ株式会社 | Bleaching agent composition and manufacture |
-
1983
- 1983-07-18 JP JP13055383A patent/JPS6023498A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5773100A (en) * | 1980-10-24 | 1982-05-07 | Kao Corp | Enzyme-containing bleaching agent composition |
JPS5821498A (en) * | 1981-07-30 | 1983-02-08 | ダスキンフランチヤイズ株式会社 | Bleaching agent composition and manufacture |
Also Published As
Publication number | Publication date |
---|---|
JPS6023498A (en) | 1985-02-06 |
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