JP5681751B2 - 香料組成物 - Google Patents
香料組成物 Download PDFInfo
- Publication number
- JP5681751B2 JP5681751B2 JP2013111115A JP2013111115A JP5681751B2 JP 5681751 B2 JP5681751 B2 JP 5681751B2 JP 2013111115 A JP2013111115 A JP 2013111115A JP 2013111115 A JP2013111115 A JP 2013111115A JP 5681751 B2 JP5681751 B2 JP 5681751B2
- Authority
- JP
- Japan
- Prior art keywords
- fragrance
- pentylcyclopentanone
- oxime
- composition
- trade name
- 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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- 239000000203 mixture Substances 0.000 title claims description 234
- 239000003205 fragrance Substances 0.000 title claims description 228
- AIQPASUJNNATHD-UHFFFAOYSA-N N-(2-pentylcyclopentylidene)hydroxylamine Chemical compound CCCCCC1CCCC1=NO AIQPASUJNNATHD-UHFFFAOYSA-N 0.000 claims description 100
- 238000004140 cleaning Methods 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 38
- 238000004519 manufacturing process Methods 0.000 claims description 35
- VNWOJVJCRAHBJJ-UHFFFAOYSA-N 2-pentylcyclopentan-1-one Chemical compound CCCCCC1CCCC1=O VNWOJVJCRAHBJJ-UHFFFAOYSA-N 0.000 claims description 33
- -1 nitrogen-containing compound Chemical class 0.000 claims description 33
- 239000002304 perfume Substances 0.000 claims description 28
- 239000002537 cosmetic Substances 0.000 claims description 24
- 239000000835 fiber Substances 0.000 claims description 23
- 238000002156 mixing Methods 0.000 claims description 22
- 239000003921 oil Substances 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 19
- 239000000796 flavoring agent Substances 0.000 claims description 15
- 235000019634 flavors Nutrition 0.000 claims description 15
- 238000006146 oximation reaction Methods 0.000 claims description 14
- 150000001299 aldehydes Chemical class 0.000 claims description 11
- 150000001298 alcohols Chemical class 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 8
- 150000002576 ketones Chemical class 0.000 claims description 8
- 150000002923 oximes Chemical class 0.000 claims description 7
- 241000207199 Citrus Species 0.000 claims description 6
- 239000002262 Schiff base Substances 0.000 claims description 6
- 150000004753 Schiff bases Chemical class 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 150000001241 acetals Chemical class 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 235000020971 citrus fruits Nutrition 0.000 claims description 6
- 150000002170 ethers Chemical class 0.000 claims description 6
- 239000000284 extract Substances 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 150000002596 lactones Chemical class 0.000 claims description 6
- 150000002825 nitriles Chemical class 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 239000000341 volatile oil Substances 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 5
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 5
- 235000012907 honey Nutrition 0.000 claims description 5
- 239000010985 leather Substances 0.000 claims description 5
- 150000002989 phenols Chemical class 0.000 claims description 5
- 230000000052 comparative effect Effects 0.000 description 39
- 238000011156 evaluation Methods 0.000 description 24
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 21
- 239000000047 product Substances 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 20
- 230000002708 enhancing effect Effects 0.000 description 18
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- 239000000463 material Substances 0.000 description 11
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 10
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
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- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 7
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- 239000012043 crude product Substances 0.000 description 6
- 230000001965 increasing effect Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 5
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- 235000007769 Vetiveria zizanioides Nutrition 0.000 description 5
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- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
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- 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 5
- ZCHHRLHTBGRGOT-SNAWJCMRSA-N (E)-hex-2-en-1-ol Chemical compound CCC\C=C\CO ZCHHRLHTBGRGOT-SNAWJCMRSA-N 0.000 description 4
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 4
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- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 4
- FPCCDPXRNNVUOM-UHFFFAOYSA-N Hydroxycitronellol Chemical compound OCCC(C)CCCC(C)(C)O FPCCDPXRNNVUOM-UHFFFAOYSA-N 0.000 description 4
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- AKGGYBADQZYZPD-UHFFFAOYSA-N benzylacetone Chemical compound CC(=O)CCC1=CC=CC=C1 AKGGYBADQZYZPD-UHFFFAOYSA-N 0.000 description 4
- RADAAKRXEPVXBU-UHFFFAOYSA-N buccoxime Chemical compound C1CCC2(C)CCC1(C)C2=NO RADAAKRXEPVXBU-UHFFFAOYSA-N 0.000 description 4
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 229910017053 inorganic salt Inorganic materials 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 4
- CZCBTSFUTPZVKJ-UHFFFAOYSA-N rose oxide Chemical compound CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 4
- KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 description 3
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 3
- XVOKPNRYHDZDMX-UHFFFAOYSA-N 1-(4-ethyl-2-bicyclo[2.2.1]heptanyl)cyclohexan-1-ol Chemical compound C1C(CC)(C2)CCC1C2C1(O)CCCCC1 XVOKPNRYHDZDMX-UHFFFAOYSA-N 0.000 description 3
- JTHVYOIHZNYRCC-UHFFFAOYSA-N 2-hexylcyclopentan-1-one Chemical compound CCCCCCC1CCCC1=O JTHVYOIHZNYRCC-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 235000010254 Jasminum officinale Nutrition 0.000 description 3
- 240000005385 Jasminum sambac Species 0.000 description 3
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- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 3
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- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 3
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- 238000004445 quantitative analysis Methods 0.000 description 3
- 238000010183 spectrum analysis Methods 0.000 description 3
- 235000007586 terpenes Nutrition 0.000 description 3
- 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 3
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- GEWDNTWNSAZUDX-WQMVXFAESA-N (-)-methyl jasmonate Chemical compound CC\C=C/C[C@@H]1[C@@H](CC(=O)OC)CCC1=O GEWDNTWNSAZUDX-WQMVXFAESA-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
- DMXUBGVVJLVCPB-UHFFFAOYSA-N (2,4,6-trimethylcyclohex-3-en-1-yl)methanol Chemical compound CC1CC(C)=CC(C)C1CO DMXUBGVVJLVCPB-UHFFFAOYSA-N 0.000 description 2
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- ZHWLEUGSDGROJS-UHFFFAOYSA-N (2-tert-butylcyclohexyl) ethyl carbonate Chemical compound CCOC(=O)OC1CCCCC1C(C)(C)C ZHWLEUGSDGROJS-UHFFFAOYSA-N 0.000 description 2
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- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- WCTNXGFHEZQHDR-UHFFFAOYSA-N valencene Natural products C1CC(C)(C)C2(C)CC(C(=C)C)CCC2=C1 WCTNXGFHEZQHDR-UHFFFAOYSA-N 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
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- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
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- 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
- C11D3/26—Organic compounds containing nitrogen
-
- 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
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Fats And Perfumes (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Description
また、非特許文献2には、シクロペンタン環構造を有する2−ペンチルシクロペンタノンオキシムを経由する新規なアルカロイドの合成方法が記載されているが、2−ペンチルシクロペンタノンオキシムの香気に関する記載はない。
本発明の香料組成物は、2−n−ペンチルシクロペンタノンオキシムを含有する。
本発明の2−n−ペンチルシクロペンタノンオキシムを含有する香料組成物は、グリーンフローラル及びフルーティ様香気を有し、残香性に優れる調合香料として、各種製品の賦香成分として使用することができる。従って、本発明は、2−n−ペンチルシクロペンタノンオキシムを賦香成分として使用する方法、好ましくは、2−n−ペンチルシクロペンタノンオキシムを香料組成物、洗浄剤組成物、繊維処理組成物又は化粧料の賦香成分として使用する方法である。当該化合物の具体的な使用方法としては、単独で又は他の成分と組み合わせて、石鹸、化粧料、洗剤、柔軟剤、スプレー製品、芳香剤、香水、入浴剤等のトイレタリー製品のベースに含有させることができる。
身体用洗浄剤組成物の例としては、皮膚用洗浄剤組成物、毛髪用洗浄剤組成物が挙げられ、皮膚用洗浄剤組成物が好ましい。
硬質表面用洗浄剤組成物の例としては、多用途洗浄剤(All purpose Cleaner)、食器用洗浄剤組成物が挙げられる。
本発明の繊維処理組成物としては、柔軟剤組成物が好ましい。
本発明の化粧料としては、香水が好ましい。
本発明において用いられる2−n−ペンチルシクロペンタノンオキシムは、一般的な有機化学反応を用いて合成することができ、その製造方法に制限はない。2−n−ペンチルシクロペンタノンオキシムを製造する方法としては、2−n−ペンチルシクロペンタノンをオキシム化する工程により、製造することが好ましい。
本工程における好適な方法としては、2−n−ペンチルシクロペンタノンとヒドロキシルアミンを混合する方法が好ましく、具体的には2−n−ペンチルシクロペンタノンにヒドロキシルアミン水溶液を滴下する方法、ヒドロキシルアミン水溶液に2−n−ペンチルシクロペンタノンを滴下する方法、2−n−ペンチルシクロペンタノンとヒドロキシルアミンの無機酸塩の水溶液を混合したところに、塩基を滴下する方法が挙げられ、なかでも、2−n−ペンチルシクロペンタノンとヒドロキシルアミンの無機酸塩の水溶液を混合したところに、塩基を滴下する方法が好ましい。この方法によれば、塩基を滴下することで、反応系内で遊離ヒドロキシルアミンを発生させることができ、その結果、副反応を抑制し、反応を安全に行うことができる。
用いる溶媒の量としては、徐熱と反応の進行に伴う反応液の粘度上昇を抑制する観点から、ヒドロキシルアミン又はその無機酸塩を用いる場合、ヒドロキシルアミン又はその無機酸塩に対して、0.5〜10質量倍が好ましく、1〜5質量倍がより好ましく、2〜4質量倍が更に好ましい。また、用いる溶媒の量としては、徐熱と反応の進行に伴う反応液の粘度上昇を抑制する観点から、2−n−ペンチルシクロペンタノンに対しては、0.1〜5質量倍が好ましく、0.5〜3質量倍がより好ましく、1〜2質量倍が更に好ましい。
〔転化率および反応収率〕
以下の製造例に示した転化率および反応収率は、内部標準法ガスクロマトグラフィー(GC)定量分析によって求めた。
<ガスクロマトグラフィーの装置及び分析条件>
GC装置:HEWLWTT PACKARD社製、型式:HP6850
カラム:J&W社製、DB−1(内径0.25mm、長さ30m、膜厚0.25μm)
キャリアガス:He、1.5mL/min
注入条件:280℃、スプリット比1/100
検出条件:FID方式、280℃
カラム温度条件:100℃→10℃/分昇温→300℃10分間保持
内部標準化合物:n−ウンデカン
以下の製造例で得られた各化合物は、核磁気共鳴スペクトル(Varian社製、型式:Mercury 400)(1H−NMR、13C−NMR)およびフーリエ変換赤外分光光度計(堀場製作所社製、型式:FT−710)のスペクトル分析により同定した。測定条件等は各測定結果に記載した。
調香・香料評価業務の経験が5年以上10年未満の熟練者1名、および25年以上の熟練者2名により、におい紙法により香調と強度を判定した。におい紙(幅6mm長さ150mmの香料試験紙)の先端約5mmを、試料に浸漬し、評価した。
匂い強度は、無臭を0、きわめて強いものを5とする相対評価で表した。
上記におい紙法と同様にして、試料に浸漬してから、25℃、無風、5m3の室内に放置し、6時間毎に評価して、主香気のにおい強度が0となった時間を示した。時間が大きいものほど、残香性に優れる。
評価は、調香・香料評価業務の経験が5年以上10年未満の熟練者1名、および25年以上の熟練者2名により、瓶口香気の香調を判定した。
(1)1H−NMR(CDCl3、400MHz);δ(ppm):0.88(3H、t、J=6.8Hz)、1.22−1.42(8H、m)、1.51−1.66(1H、m)、1.66−1.76(1H、m)、1.76−1.90(1H、m)、1.94−2.02(1H、m)、2.32−2.50(2H、m)、2.55−2.63(1H、m)、9.29(1H、S)。
(2)13C−NMR(CDCl3、100MHz);δ(ppm):14.5、22.9、23.0、27.7、27.8、32.1、32.3、32.6、43.6、169.3。
(3)FT−IR(neat);cm-1:725、846、919、954、1197、1376、1421、1461、1677、2856、2925、2954,3257(br)。
(4)香気:(主香気)グリーン−フローラル(マグノリア)(副香気)フルーティ。
(5)匂い強度:3。
1Lセパラブルフラスコに、ヒドロキシルアミン硫酸塩138g(0.83モル、ヒドロキシルアミン換算でケトンに対し1.30モル倍)、イオン交換水406g、イソプロピルアルコール129g、アミルシクロペンタノン198g(2−n−ペンチルシクロペンタノン、Firmenich社製Delphone、1.28モル)、を順に加え、窒素雰囲気下で撹拌しながら45℃に加熱した。反応温度を45〜55℃に保ちながら33質量%水酸化ナトリウム水溶液185g(1.53モル、ヒドロキシルアミン硫酸塩に対し1.84モル倍)を1時間かけて滴下した。滴下終了後、50℃で4.5時間加熱撹拌を続けた。反応終了後、水層を1モル/L硫酸水溶液で中和後、酢酸エチル300gを加え、抽出した。静置分層で水層を抜き出し、飽和食塩水で水洗し、有機層を硫酸ナトリウムで乾燥、ろ過後、溶媒を減圧留去し、無色粘稠液体の粗生成物220gを得た。粗生成物のガスクロマトグラフィー定量分析の結果、アミルシクロペンタノンの転化率は99.8%、2−n−ペンチルシクロペンタノンオキシムの純分は211g(1.24モル)、純度は95.5%、粗収率は96.8%であった。
アミルシクロペンタノンに変えて、2−n−ヘキシルシクロペンタノンを用いた以外は、製造例1と同様にして、2−n−ヘキシルシクロペンタノンオキシムを得た。
(1)1H−NMR(CDCl3、400MHz);δ(ppm):0.88(3H、t、J=6.8Hz)、1.22−1.42(10H、m)、1.52−1.66(1H、m)、1.66−1.77(1H、m)、1.77−1.92(1H、m)、1.94−2.02(1H、m)、2.31−2.52(2H、m)、2.54−2.63(1H、m)、9.02(1H、S)。
(2)13C−NMR(CDCl3、100MHz);δ(ppm):14.6、22.9、23.1、27.7、28.0、29.8、32.1、32.2、32.6、43.6、169.4。
(3)FT−IR(neat);cm-1:723、919、960、1207、1376、1421、1455、1670、2856、2925、2954,3276(br)。
アミルシクロペンタノンに変えて、2−n−ヘプチルシクロペンタノンを用いた以外は、製造例1と同様にして、2−n−ヘプチルシクロペンタノンオキシムを得た。
(1)1H−NMR(CDCl3、400MHz);δ(ppm):0.88(3H、t、J=6.8Hz)、1.20−1.42(12H、m)、1.52−1.66(1H、m)、1.66−1.77(1H、m)、1.77−1.92(1H、m)、1.94−2.02(1H、m)、2.31−2.52(2H、m)、2.54−2.63(1H、m)、8.99(1H、S)。
(2)13C−NMR(CDCl3、100MHz);δ(ppm):14.6、23.0、23.1、27.7、28.1、29.7、30.1、32.1、32.3、32.7、43.6、169.4。
(3)FT−IR(neat);cm-1:723、919、964、1205、1376、1421、1455、1673、2854、2921、2954,3286(br)。
製造例1で得られた化合物をジプロピレングリコールに90質量%の濃度で溶解し、実施例1の香料組成物を調製した後、前記香気評価方法により、香気評価を行った。製造例1で得られた化合物の代わりに、製造例3で得られた化合物、製造例4で得られた化合物または、アミルシクロペンタノン(Fimenich社製 Delphone)を用いて実施例1と同様に行い、比較例1、比較例2または比較例3の組成物を得た。得られた比較例1、比較例2および比較例3の組成物について、実施例1の組成物と同様、香気評価を行った。得られた結果を表1に示す。
製造例1で得られた2−n−ペンチルシクロペンタノンオキシムを用いて、表2に記載の配合組成になるように、香料を調合し、実施例2及び比較例4、5、6のフルーティ(ピーチ)調の香料組成物をそれぞれ調製した。
2)IFF社商品名、2,4−ジメチル−3−シクロヘキサン−1−カルボキシアルデヒド
3)花王商品名、ジヒドロジャスモン酸メチル
4)花王商品名、(4−エチル−ビシクロ[2.2.1]ヘプト−2−イル)シクロヘキサノールおよび(2−エチル−ビシクロ[2.2.1]ヘプト−7−イル)シクロヘキサノールなどを含む異性体混合物
5)シムライズ社商品名、1,5−ジメチル−ビシクロ[3.2.1]オクタン−8−オンオキシム
表4に示す組成の未賦香の濃縮液体柔軟剤組成物に、実施例2及び比較例4、5、6で得られた香料組成物を1.0質量%となるように加え、実施例3及び比較例7、8、9の濃縮液体柔軟剤組成物をそれぞれ調製した。
2)Lonza社商品名:Lonzaserve SG
製造例1で得られた2−n−ペンチルシクロペンタノンオキシムを用いて、表6に記載の配合組成になるように、香料を調合し、実施例4及び比較例10のフローラル(オレンジフラワー)調の香料組成物をそれぞれ調製した。
表7に示す組成の未賦香の皮膚用洗浄剤組成物(ボディーウォッシュ)に対し、実施例4及び比較例10で得られた香料組成物を0.5質量%となるように加え、実施例5及び比較例11の皮膚用洗浄剤組成物(ボディーウォッシュ)をそれぞれ調製した。
2)花王商品名:Betadet HR
3)花王商品名:Amidet B−112
4)Lonza社商品名:Isocil PC
製造例1で得られた2−n−ペンチルシクロペンタノンオキシムを用いて、表8に記載の配合組成になるように、香料を調合し、実施例6及び比較例12のフローラル(マグノリア)調の香料組成物をそれぞれ調製した。
2)花王商品名、エトキシメチルシクロドデシルエーテル
3)ジボダン社商品名、4−メチル−2−(2−メチルプロピル)テトラヒドロ−2H−4−ピラノール
4)花王商品名、ジヒドロジャスモン酸メチル
5)IFF社商品名、2,4−ジメチル−3−シクロヘキサン−1−カルボキシアルデヒド
6)花王商品名、5−メチル−5−プロピル−2−(1−メチル−ブチル)−1,3−ジオキサン
表9に示す組成の未賦香の毛髪用洗浄剤に、実施例6及び比較例12で得られた香料組成物を0.5質量%となるように加え、実施例7及び比較例13の毛髪用洗浄剤組成物をそれぞれ調製した。
2)花王商品名:Betadet HR
3)花王商品名:Amidet B−112
4)Lonza社商品名:Isocil PC
製造例1で得られた2−n−ペンチルシクロペンタノンオキシムを用いて、表10に記載の配合組成になるように、香料を調合し、実施例8及び比較例14のウッディ(ベチバー)調の香料組成物をそれぞれ調製した。
2)シムライズ社商品名、4−メチル−4−フェニル−2−ペンタノン
エタノールに、実施例8及び比較例14で得られた香料組成物を10質量%となるように加え、実施例9及び比較例15の香水をそれぞれ調製した。
Claims (11)
- 2−n−ペンチルシクロペンタノンオキシムを含有する香料組成物。
- 2−n−ペンチルシクロペンタノンオキシム以外の香料を更に含有する請求項1に記載の香料組成物。
- 更に油剤を含有する、請求項1または2に記載の香料組成物。
- 前記2−n−ペンチルシクロペンタノンオキシム以外の香料が、炭化水素類、アルコール類、フェノール類、アルデヒド類、ケトン類、アセタール類、エーテル類、エステル類、カーボネート類、ラクトン類、オキシム類、ニトリル類、シッフ塩基類、アミド類、含窒素化合物、含硫黄化合物、天然精油および天然抽出物のうち1種以上を含有する、請求項2または3に記載の香料組成物。
- 前記2−n−ペンチルシクロペンタノンオキシム以外の香料が、シトラス調、フローラル調、フルーティ調、ハーバル調、スパイシー調、グリーン調、ウッディ調、バルサミック調、アルデハイディック調、ミンティ調、アロマティック調、アーシー調、モッシー調、ハニー調、レザー調、アニマリック調、アンバー調、およびムスキー調の各香調を有する香料のうち1種以上を含有する、請求項2〜4のいずれかに記載の香料組成物。
- 請求項1〜5のいずれかに記載の香料組成物を含有する洗浄剤組成物。
- 請求項1〜5のいずれかに記載の香料組成物を含有する繊維処理組成物。
- 請求項1〜5のいずれかに記載の香料組成物を含有する化粧料。
- 2−n−ペンチルシクロペンタノンオキシムを賦香成分として使用する方法。
- 2−n−ペンチルシクロペンタノンをオキシム化して2−n−ペンチルシクロペンタノンオキシムを得る工程、及び油剤及び/又は2−n−ペンチルシクロペンタノンオキシム以外の香料を混合する工程を有する、2−n−ペンチルシクロペンタノンオキシムを含有する香料組成物の製造方法。
- オキシム化反応に溶媒を用いる請求項10に記載の2−n−ペンチルシクロペンタノンオキシムを含有する香料組成物の製造方法。
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JP2013111115A JP5681751B2 (ja) | 2013-05-27 | 2013-05-27 | 香料組成物 |
EP14729733.7A EP3004303B1 (en) | 2013-05-27 | 2014-05-20 | Fragrance composition |
CN201480030682.9A CN105264057B (zh) | 2013-05-27 | 2014-05-20 | 香料组合物 |
PCT/JP2014/002654 WO2014192250A1 (en) | 2013-05-27 | 2014-05-20 | Fragrance composition |
US14/894,448 US9506012B2 (en) | 2013-05-27 | 2014-05-20 | Fragrance composition |
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