JPH04153299A - Perfume composition - Google Patents
Perfume compositionInfo
- Publication number
- JPH04153299A JPH04153299A JP27856490A JP27856490A JPH04153299A JP H04153299 A JPH04153299 A JP H04153299A JP 27856490 A JP27856490 A JP 27856490A JP 27856490 A JP27856490 A JP 27856490A JP H04153299 A JPH04153299 A JP H04153299A
- Authority
- JP
- Japan
- Prior art keywords
- fragrance
- jasmones
- damascones
- sesquiterpenes
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 19
- 239000002304 perfume Substances 0.000 title abstract description 12
- 229930004725 sesquiterpene Natural products 0.000 claims abstract description 9
- 150000004354 sesquiterpene derivatives Chemical class 0.000 claims abstract description 9
- 150000003216 pyrazines Chemical class 0.000 claims abstract description 8
- 239000003205 fragrance Substances 0.000 claims description 42
- ZFMSMUAANRJZFM-UHFFFAOYSA-N Estragole Chemical compound COC1=CC=C(CC=C)C=C1 ZFMSMUAANRJZFM-UHFFFAOYSA-N 0.000 abstract description 8
- 230000000694 effects Effects 0.000 abstract description 6
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 abstract description 6
- -1 2-methylpyrazine) Chemical class 0.000 abstract description 5
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 abstract description 4
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 abstract description 4
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 abstract description 4
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 abstract description 3
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 abstract description 3
- 229930007744 linalool Natural products 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 3
- XMLSXPIVAXONDL-PLNGDYQASA-N Jasmone Chemical compound CC\C=C/CC1=C(C)CCC1=O XMLSXPIVAXONDL-PLNGDYQASA-N 0.000 abstract description 2
- IVLCENBZDYVJPA-ARJAWSKDSA-N cis-Jasmone Natural products C\C=C/CC1=C(C)CCC1=O IVLCENBZDYVJPA-ARJAWSKDSA-N 0.000 abstract description 2
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 abstract description 2
- CAWHJQAVHZEVTJ-UHFFFAOYSA-N methylpyrazine Chemical compound CC1=CN=CC=N1 CAWHJQAVHZEVTJ-UHFFFAOYSA-N 0.000 abstract 2
- ZHHYXNZJDGDGPJ-BSWSSELBSA-N (2e,4e)-nona-2,4-dienal Chemical compound CCCC\C=C\C=C\C=O ZHHYXNZJDGDGPJ-BSWSSELBSA-N 0.000 abstract 1
- CRIGTVCBMUKRSL-FNORWQNLSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-enone Chemical compound C\C=C\C(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-FNORWQNLSA-N 0.000 abstract 1
- ZHHYXNZJDGDGPJ-UHFFFAOYSA-N 2,4-Nonadienal Natural products CCCCC=CC=CC=O ZHHYXNZJDGDGPJ-UHFFFAOYSA-N 0.000 abstract 1
- CRIGTVCBMUKRSL-UHFFFAOYSA-N alpha-Damascone Natural products CC=CC(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-UHFFFAOYSA-N 0.000 abstract 1
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 description 2
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- 239000001500 (2R)-6-methyl-2-[(1R)-4-methyl-1-cyclohex-3-enyl]hept-5-en-2-ol Substances 0.000 description 2
- JGBBQKAJVHEQJM-FNORWQNLSA-N (e)-1-(2,6,6-trimethylcyclohexa-2,4-dien-1-yl)but-2-en-1-one Chemical compound C\C=C\C(=O)C1C(C)=CC=CC1(C)C JGBBQKAJVHEQJM-FNORWQNLSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 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
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- RGZSQWQPBWRIAQ-LSDHHAIUSA-N alpha-Bisabolol Natural products CC(C)=CCC[C@@](C)(O)[C@@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-LSDHHAIUSA-N 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- WTWBUQJHJGUZCY-UHFFFAOYSA-N cuminaldehyde Chemical compound CC(C)C1=CC=C(C=O)C=C1 WTWBUQJHJGUZCY-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
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 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
- MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- RUMOYJJNUMEFDD-UHFFFAOYSA-N perillyl aldehyde Chemical compound CC(=C)C1CCC(C=O)=CC1 RUMOYJJNUMEFDD-UHFFFAOYSA-N 0.000 description 2
- 229940067107 phenylethyl alcohol Drugs 0.000 description 2
- YHBUQBJHSRGZNF-UHFFFAOYSA-N trans-α-Bisabolene Chemical compound CC(C)=CCC=C(C)C1CCC(C)=CC1 YHBUQBJHSRGZNF-UHFFFAOYSA-N 0.000 description 2
- NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 description 1
- WTOYNNBCKUYIKC-JMSVASOKSA-N (+)-nootkatone Chemical compound C1C[C@@H](C(C)=C)C[C@@]2(C)[C@H](C)CC(=O)C=C21 WTOYNNBCKUYIKC-JMSVASOKSA-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
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 1
- ZPSJGADGUYYRKE-UHFFFAOYSA-N 2H-pyran-2-one Chemical class O=C1C=CC=CO1 ZPSJGADGUYYRKE-UHFFFAOYSA-N 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- BGTBFNDXYDYBEY-FNORWQNLSA-N 4-(2,6,6-Trimethylcyclohex-1-enyl)but-2-en-4-one Chemical compound C\C=C\C(=O)C1=C(C)CCCC1(C)C BGTBFNDXYDYBEY-FNORWQNLSA-N 0.000 description 1
- MSHFRERJPWKJFX-UHFFFAOYSA-N 4-Methoxybenzyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 235000019499 Citrus oil Nutrition 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 1
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 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
- YHBUQBJHSRGZNF-HNNXBMFYSA-N alpha-bisabolene Natural products CC(C)=CCC=C(C)[C@@H]1CCC(C)=CC1 YHBUQBJHSRGZNF-HNNXBMFYSA-N 0.000 description 1
- UZFLPKAIBPNNCA-BQYQJAHWSA-N alpha-ionone Chemical compound CC(=O)\C=C\C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-BQYQJAHWSA-N 0.000 description 1
- UZFLPKAIBPNNCA-UHFFFAOYSA-N alpha-ionone Natural products CC(=O)C=CC1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-UHFFFAOYSA-N 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- POIARNZEYGURDG-FNORWQNLSA-N beta-damascenone Chemical compound C\C=C\C(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-FNORWQNLSA-N 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 229930006739 camphene Natural products 0.000 description 1
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 239000010628 chamomile oil Substances 0.000 description 1
- 235000019480 chamomile oil Nutrition 0.000 description 1
- CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 239000001524 citrus aurantium oil Substances 0.000 description 1
- 239000010500 citrus oil Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- WTOYNNBCKUYIKC-UHFFFAOYSA-N dl-nootkatone Natural products C1CC(C(C)=C)CC2(C)C(C)CC(=O)C=C21 WTOYNNBCKUYIKC-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 239000010651 grapefruit oil Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229940117955 isoamyl acetate Drugs 0.000 description 1
- 239000010656 jasmine oil Substances 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- 239000010501 lemon oil Substances 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229930007503 menthone Natural products 0.000 description 1
- GEWDNTWNSAZUDX-UHFFFAOYSA-N methyl 7-epi-jasmonate Natural products CCC=CCC1C(CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-UHFFFAOYSA-N 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- CCRCUPLGCSFEDV-BQYQJAHWSA-N methyl trans-cinnamate Chemical compound COC(=O)\C=C\C1=CC=CC=C1 CCRCUPLGCSFEDV-BQYQJAHWSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 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 1
- 229930007850 β-damascenone Natural products 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
【発明の詳細な説明】
（産業上の利用分野〕
本発明は、自然感やハーブ感が付与された香料組成物に
関するものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a fragrance composition imparted with a natural or herbal feel.
〔従来の技術及び発明が解決しようとする課題〕従来、
香料基剤に自然感やハーブ惑を付与する方法としては、
直接、天然ハーブ系香料を添加する方法が知られている
が、この方法では、付与したいハーブ感以外に別の香調
を同時に付与してしまうため、目的にあったハーブ感の
みを付与することは困難であった。また、文献等に記載
（報告）されている天然精油等の分析データからはこれ
らの問題を解決するのに有益な情報は得られない。[Problems to be solved by conventional techniques and inventions] Conventionally,
As a method of imparting a natural or herbal feel to a fragrance base,
A method of directly adding natural herbal fragrances is known, but this method simultaneously imparts a different aroma tone in addition to the desired herbal flavor, so it is difficult to impart only the desired herbal flavor. was difficult. In addition, useful information for solving these problems cannot be obtained from analysis data of natural essential oils etc. described (reported) in literature and the like.
従って、本発明の目的は、自然感やハーブ怒の付与効果
が顕著な香料組成物を提供することにある。Therefore, an object of the present invention is to provide a fragrance composition that has a remarkable effect of imparting a natural feel and herbal aroma.
本発明者らは、種々検討した結果、香料基剤に、特定の
５つの香料群の内の２群以上からそれぞれ１以上選択さ
れた計２以上の香料を添加することにより、上記目的が
達成されることを知見した。As a result of various studies, the present inventors have found that the above objective can be achieved by adding a total of two or more fragrances selected from two or more groups of five specific fragrance groups to a fragrance base. I found out that this happens.
本発明は、上記知見に基づいてなされたもので、香料基
剤に、ピラノン類、ジェナール類、ダマスコン類、セス
キテルペン類及びジャスモン類の５つの香料群の内の２
群以上から選択された２以上の香料を添加してなる香料
組成物を提供するものである。The present invention was made based on the above findings, and includes two of the five fragrance groups, pyranones, genards, damascones, sesquiterpenes, and jasmones, as a fragrance base.
The present invention provides a fragrance composition containing two or more fragrances selected from at least one group.
以下、本発明の香料組成物について詳述する。Hereinafter, the fragrance composition of the present invention will be explained in detail.
本発明で用いられる５つの香料群のそれぞれに含まれる
香料としては、例えば、それぞれ下記に示すものが挙げ
られる。Examples of fragrances included in each of the five fragrance groups used in the present invention include those shown below.
ピラジン類 −２−メチルピラジン、２−メチノ１３〜
メトキンピラジン、２−イソプロピノ１−３−メトキン
ピラノン、２−（１−メ千）１プロピル）−３−メトキ
ンピラジン等。Pyrazines -2-methylpyrazine, 2-methino 13~
methquinpyrazine, 2-isopropino-1-3-methquinpyranone, 2-(1-methoxy)1propyl)-3-methquinpyrazine, and the like.
ジェナール類 ２．４−ノナジェナール、２ 〔−ノナ
ジェナール、２，４−オクタジェナール、２．４−デカ
ジェナール等。Jenals 2.4-nonajenal, 2 [-nonajenal, 2,4-octagenal, 2.4-decajenal, etc.
ダマスコン類 アルファーダマセノン、ヘータダマスコ
ン、ヘーターダマセノン、アルファーダマセノン等。Damascones Alpha damascenone, heta damascone, heta damascenone, alpha damascenone, etc.
セスキテルペン類 アルファービサボレン、ネロリドー
ル、アルファービサボロール等。Sesquiterpenes: alpha-bisabolene, nerolidol, alpha-bisabolol, etc.
ジャスモン類−メチルジャスモネート、メチルユピジャ
スモネート、シス−ジャスモン等。Jasmones - methyl jasmonate, methylupijasmonate, cis-jasmonate, etc.
本発明は、上記５つの香料群の内の２群以上刃らそれぞ
れ１以上（計２以上）の香料、好ましくは５群全てから
それぞれ１以上（計５以上）の香料を選択使用する。The present invention selects and uses one or more fragrances from each of two or more groups (total of 2 or more) among the five fragrance groups, preferably one or more fragrances from each of all five groups (total of 5 or more).
これらの香料の使用量は、組成物中、ピラジン類の場合
０．０００１〜０．００１重量％、ジェナール類の場合
０．０００１〜Ｏ，ＯＯ２重量％、ダマスコン類の場合
０．００１〜０．１重量％、セスキテルペン類の場合０
．１〜１重量％、及びジャスモン類の場合０．０１〜１
重量％であるのがそれぞれ好ましく、また選択使用され
る２以上の香料の使用量の合計量は、香料の種類の違い
によっても異なるが、組成物中０． ＯＯＯ１〜２重量
％となるようにするのが好ましい。The amount of these fragrances to be used in the composition is 0.0001 to 0.001% by weight for pyrazines, 0.0001 to 0.02% by weight for genards, and 0.001 to 0.00% for damascones. 1% by weight, 0 for sesquiterpenes
．． 1 to 1% by weight, and 0.01 to 1 in the case of jasmones
The total amount of the two or more selected fragrances varies depending on the type of fragrance, but it is preferably 0.0% by weight in the composition. It is preferable that OOO be 1 to 2% by weight.
また、本発明における香料基剤としては、特に制限され
るものではなく、天然香料及び合成香料等から用途に応
して適宜選択される１種又は２種以上の組合せが用いら
れる。Further, the fragrance base in the present invention is not particularly limited, and one type or a combination of two or more types can be used, which are appropriately selected from natural fragrances, synthetic fragrances, etc. depending on the purpose.
上記天然香料としては、レモン油、グレープフルーツ油
、ベルガモツト油、パイン油、カモミル油、ジャスミン
油、スペアミント油、ペパーミント油、バンカ油、ラベ
ンダー油、ローズ油、ネロリ油、シトロ２う油等が挙げ
られる。Examples of the above natural fragrances include lemon oil, grapefruit oil, bergamot oil, pine oil, chamomile oil, jasmine oil, spearmint oil, peppermint oil, banca oil, lavender oil, rose oil, neroli oil, citrus oil, and the like. .
上記合成香料としては、リモネン、α−ピネン、カンフ
エン、カンファー、テルピノーレン、ミルセン、オンメ
ン等の炭化水素類；リナロール、ゲラニオール、シトロ
ネロール、Ｐ−メントール、ヘンンルアルコール、フェ
ニルエチルアルコールアニスアルコール、エストラゴー
ル、シンナミックアルコール、オイゲノール、テルピネ
オール等のアルコール類りｎ−オクチルアルデヒド、ノ
トラール、ントロ不う−ル、ペリラアルデヒド、クミン
アルデヒド、シクラメンアルデヒド等のアルデヒド類；
メチルヘブチノン、メチル−〇−アミルケトン、Ｐ−カ
ルボン、メントン、アセトフェノン、α−ヨノン、ヌー
トカトン等のケ１ン類；酢酸イソアミル、酢酸ゲラニル
、酢酸リナリル、酢酸チルビニル、酢酸ジヒドロチルビ
ニル、安に、香酸メチル、桂皮酸メチル、サリチル酸メ
チル等のエステル頻；安息香酸、酪酸、イソ吉草酸、ゲ
ラニル酸等の酸類；ソ茅オール等のオキノド類、及びク
マリン等のラクトン類、アセタール類、含窒素化合物等
が挙げられる。The synthetic fragrances mentioned above include hydrocarbons such as limonene, α-pinene, camphene, camphor, terpinolene, myrcene, and ommen; linalool, geraniol, citronellol, P-menthol, hemyl alcohol, phenylethyl alcohol, anis alcohol, estragol, Alcohols such as cinnamic alcohol, eugenol, and terpineol; aldehydes such as n-octylaldehyde, notral, thorol, perillaldehyde, cuminaldehyde, and cyclamenaldehyde;
Keynes such as methylhebutynone, methyl-〇-amylketone, P-carvone, menthone, acetophenone, α-ionone, and nootkatone; isoamyl acetate, geranyl acetate, linalyl acetate, tilvinyl acetate, dihydrothylvinyl acetate, albinol, aromatic acid Frequent esters such as methyl, methyl cinnamate, and methyl salicylate; acids such as benzoic acid, butyric acid, isovaleric acid, and geranilic acid; oquinodos such as sokyol, lactones such as coumarin, acetals, nitrogen-containing compounds, etc. can be mentioned.
本発明は、上記香料基剤の中でも、特に、主成分がリナ
ロール又はエストラゴールである香料基剤に適用した場
合に、その効果が顕著に認められ〔実施例〕
以下に実施例を挙げ、
する。Among the above fragrance bases, the present invention is particularly effective when applied to a fragrance base whose main ingredient is linalool or estragole [Examples] Examples are given below, and .
実施例１
下記配合により、
香料基剤Ａの配合
エストラゴール ５００
リ す ロ − ル ３
６０カ ン フ ァ −５，０
ソ ト ラ − ル −
２．０１．８−ン不オール ４０
ゲラニオール ３．０
酢酸ゲラニル − １５
本発明を更に詳しく説明
香＃４基剤Ａを調製した。Example 1 Combination of fragrance base A according to the following formulation Estragol 500 Lis Roll 3
60 conference -5,0 sotra rule -
2.01.8-Nonol 40 Geraniol 3.0 Geranyl Acetate - 15 Further Detailed Description of the Invention Fragrance #4 Base A was prepared.
９５５重量部
この香料基剤Ａに対し、ピラジン類がら２−イソプロピ
ル−３−メトキノピラジン、ジェナール類から２．６−
ノナジェナール、ダマスコン類がらヘーターダマセノン
、セスキテルペン類がらアルファービサボロール、及び
ジャスモン類からメチルジャスモ不一トをそれぞれ選択
し、下記第１表に示す配合により、香料組成物（本発明
品１〜４及び比較品１〜５）をそれぞれ調製した。955 parts by weight of this fragrance base A, 2-isopropyl-3-methoquinopyrazine from pyrazines, 2.6-
Nonagenal, heterdamascenone from damascones, alpha-bisabolol from sesquiterpenes, and methyl jasmonite from jasmones were selected, and perfume compositions (products of the present invention 1 to 1) were prepared according to the formulations shown in Table 1 below. 4 and comparative products 1 to 5) were prepared, respectively.
これらの香料組成物それぞれについて、専門ノ々ネリス
トにより、自然感の評価を下記基準により行った。その
評価結果を下記第１表に示す。下記第１表に示す結果か
ら、２群以上から選択された２以上の香料が添加された
本発明品は、何れも、優れた自然感を有し、特に上記５
つの香料全てが添加されたもの（本発明品４）が最も優
れた効果を有していることが判る。Each of these perfume compositions was evaluated for natural feel by a specialist expert according to the following criteria. The evaluation results are shown in Table 1 below. From the results shown in Table 1 below, all of the products of the present invention to which two or more fragrances selected from two or more groups were added had an excellent natural feel, and especially the above-mentioned 5.
It can be seen that the product to which all three fragrances were added (invention product 4) had the most excellent effect.
基剤と比較して ◎；極めて優れた自然感を有する。 compared to base ◎; Has an extremely excellent natural feel.
○；優れた自然感を有する。○: Excellent natural feel.
△；自然感をやや有する。Δ: Slightly natural feel.
×；基剤と同等。×; Equivalent to base material.
ン 〈口 （ｌｉ’ｌｉ と） 実施例２ 下記配合により、香料基剤Ｂを調製した。hmm <mouth (with li’li) Example 2 Perfume base B was prepared using the following formulation.
・香料基剤Ｂの配合
！ −メ ン ト − ル
６００１８−ノネオール １２０
リ モ 不 ン
４０酢酸ジヒドロチルビニル ５０
フエニルエチルアルコール １０
り マ リ ン −−−３
カ ン フ ァ −−２リ す
ロ −ル −５０ノンナミノクアルコ
ール １０
酢酸チルビニル −２０
α−テルピ矛オール −−−−１０
９１５重量部
この香料基剤Ｂに対し、ピラジン類から２（１−メチル
プロピル）−３−メトキシピラジン、ジェナール類から
２，６−ノナジェナール、ダマスコン類カらヘーターダ
マセノン、セスキテルペン類からネロリドール、及びジ
ャスモン類からシス−ジャスモンをそれぞれ選択し、下
記第２表に示す配合により、香料組成物（本発明品５〜
８）をそれぞれ調製した。・Contains fragrance base B! - Mentor
60018-Noneol 120
40 Dihydrothyl vinyl acetate 50 Phenylethyl alcohol 10 Marine ---3
Conference--2
Roll -50 Nonnaminok alcohol 10 Tivinyl acetate -20 α-Terpine alcohol ----10 915 parts by weight For this fragrance base B, from pyrazines, 2(1-methylpropyl)-3-methoxypyrazine , 2,6-nonajenal from the genals, nerolidol from the damascones, nerolidol from the sesquiterpenes, and cis-jasmone from the jasmones, and according to the formulation shown in Table 2 below, a fragrance composition was prepared. (Products of the present invention 5~
8) were prepared respectively.
これらの香料組成物それぞれについて、実施例１と同様
の評価を行った。その評価結果を下記第２表に示す。下
記第２表に示す結果から、実施例１の結果と同様に、本
発明品は、何れも、優れた自然感を有し、特に上記５つ
の香料全てが添加されたもの（本発明品８）が最も優れ
た効果を有し第
表
〔発明の効果〕
本発明の香料組成物は、
自然感やハーブ感の付
与効果が顕著なものである。The same evaluation as in Example 1 was performed for each of these fragrance compositions. The evaluation results are shown in Table 2 below. From the results shown in Table 2 below, similar to the results of Example 1, all of the products of the present invention have an excellent natural feel, especially those to which all the above five fragrances are added (Product 8 of the present invention). ) had the most excellent effect, as shown in Table 1 [Effects of the Invention] The fragrance composition of the present invention has a remarkable effect of imparting a natural feel and a herbal feel.
特 許 出 願 人 花 王 株 式Special permission Out wish Man flower king KK formula
Claims (1)
、セスキテルペン類及びジャスモン類の５つの香料群の
内の２群以上から選択された２以上の香料を添加してな
る香料組成物。A fragrance composition comprising a fragrance base and two or more fragrances selected from two or more of the five fragrance groups of pyrazines, dienals, damascones, sesquiterpenes, and jasmones.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27856490A JPH04153299A (en) | 1990-10-17 | 1990-10-17 | Perfume composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27856490A JPH04153299A (en) | 1990-10-17 | 1990-10-17 | Perfume composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04153299A true JPH04153299A (en) | 1992-05-26 |
Family
ID=17599025
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27856490A Pending JPH04153299A (en) | 1990-10-17 | 1990-10-17 | Perfume composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04153299A (en) |
-
1990
- 1990-10-17 JP JP27856490A patent/JPH04153299A/en active Pending
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