JP2018108192A - 芳香剤組成物 - Google Patents
芳香剤組成物 Download PDFInfo
- Publication number
- JP2018108192A JP2018108192A JP2016257037A JP2016257037A JP2018108192A JP 2018108192 A JP2018108192 A JP 2018108192A JP 2016257037 A JP2016257037 A JP 2016257037A JP 2016257037 A JP2016257037 A JP 2016257037A JP 2018108192 A JP2018108192 A JP 2018108192A
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- Prior art keywords
- group
- component
- fragrance
- fragrance composition
- oil
- Prior art date
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- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 85
- 239000002304 perfume Substances 0.000 title abstract description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 45
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 41
- 239000001000 anthraquinone dye Substances 0.000 claims abstract description 25
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 22
- 239000000796 flavoring agent Substances 0.000 claims abstract description 11
- 235000019634 flavors Nutrition 0.000 claims abstract description 11
- 125000001743 benzylic group Chemical group 0.000 claims abstract description 5
- 239000003205 fragrance Substances 0.000 claims description 138
- -1 lyial Chemical compound 0.000 claims description 54
- 150000001875 compounds Chemical class 0.000 claims description 19
- 125000003277 amino group Chemical group 0.000 claims description 16
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 claims description 10
- 125000003282 alkyl amino group Chemical group 0.000 claims description 10
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims description 10
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 claims description 10
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims description 9
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 9
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 8
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims description 8
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- 239000005977 Ethylene Substances 0.000 claims description 5
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- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
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- 238000005562 fading Methods 0.000 abstract description 29
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- 238000000034 method Methods 0.000 abstract description 6
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 17
- 239000000049 pigment Substances 0.000 description 17
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 16
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- 125000000217 alkyl group Chemical group 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
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- 241000402754 Erythranthe moschata Species 0.000 description 4
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- 238000002360 preparation method Methods 0.000 description 4
- 150000003141 primary amines Chemical class 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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- 150000001241 acetals Chemical class 0.000 description 3
- 239000002386 air freshener Substances 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000012360 testing method Methods 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
- ZCHHRLHTBGRGOT-SNAWJCMRSA-N (E)-hex-2-en-1-ol Chemical compound CCC\C=C\CO ZCHHRLHTBGRGOT-SNAWJCMRSA-N 0.000 description 2
- LOKPJYNMYCVCRM-UHFFFAOYSA-N 16-Hexadecanolide Chemical compound O=C1CCCCCCCCCCCCCCCO1 LOKPJYNMYCVCRM-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- ZJPKYCLAROITRY-UHFFFAOYSA-N 3-(1-ethoxyethoxy)-3,7-dimethylocta-1,6-diene Chemical compound CCOC(C)OC(C)(C=C)CCC=C(C)C ZJPKYCLAROITRY-UHFFFAOYSA-N 0.000 description 2
- XPCTZQVDEJYUGT-UHFFFAOYSA-N 3-hydroxy-2-methyl-4-pyrone Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
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- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
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- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
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- 229960002903 benzyl benzoate Drugs 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 2
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- 238000013461 design Methods 0.000 description 2
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- 238000005516 engineering process Methods 0.000 description 2
- HCRBXQFHJMCTLF-ZCFIWIBFSA-N ethyl (2r)-2-methylbutanoate Chemical compound CCOC(=O)[C@H](C)CC HCRBXQFHJMCTLF-ZCFIWIBFSA-N 0.000 description 2
- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 2
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Landscapes
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Abstract
Description
項1.(A)窒素原子を有するアントラキノン系色素成分、及び(B)ヘテロ原子が単結合したベンジル位を有する香料成分を含有し、前記(A)成分1モル当たり、前記(B)成分が1〜600モル含まれることを特徴とする、芳香剤組成物。
項2.前記(A)成分が、窒素原子を1つ又は2つ有する、項1に記載の芳香剤組成物。
項3.前記(A)成分において、窒素原子が1級アミン又は2級アミンの形態で存在する、項1又は2に記載の芳香剤組成物。
項4.前記(B)成分が、下記一般式(AO)に示す化合物である、項1〜3のいずれかに記載の芳香剤組成物。
項7.更に、ベンジルアセテート、リナロール、リナリルアセテート、リリアール、ガラクソリド、エチレンブラシレート、サイクロペンタデカノライド、サイクロペンタデセノライド、及び5−シクロヘキサデセン−1−オンよりなる群から選択される少なくとも1種の香料成分を含む、項1〜6のいずれかに記載の芳香剤組成物。
項8.更に、1価アルコール、多価アルコール、イソパラフィン、及びグリコールエーテルよりなる群から選択される少なくとも1種の有機溶剤を含む、項1〜7のいずれかに記載の芳香剤組成物。
本発明の芳香剤組成物では、1分子当たり窒素原子を少なくとも1つ有するアントラキノン系色素成分が含まれる。前記アントラキノン系色素成分は、1分子当たり窒素原子を1つ又は2つ有することが好ましい。
本発明の芳香剤組成物では、ヘテロ原子が単結合したベンジル位を有する香料成分が含まれる。前記ヘテロ原子が単結合したベンジル位を有する香料成分とは、ヘテロ原子が単結合したベンジル位を有する構造を有し、揮発して香気を呈する化合物である。なお、本発明において、(B)成分には、ベンジル位にヘテロ原子が単結合したものであっても、当該ベンジル位に更にヘテロ原子が二重結合した構造を有する香料成分は含まれない。
本発明の芳香剤組成物において、(A)成分と(B)成分の比率は、(A)成分1モル当たり、(B)成分が1〜600モルを満たすように設定される。このような比率を満たすことによって、(A)成分と(B)成分が共存しても、(A)成分の光暴露による退色を抑制することが可能になる。
本発明の芳香剤組成物は、所望の香気を呈するように調香するために、必要に応じて、(B)成分以外の香料成分が含まれていてもよい。このような香料成分の種類については、特に制限されないが、例えば、炭化水素系香料成分、エーテル系香料成分、エステル系香料成分、アルコール系香料成分、ケトン系香料成分、ラクトン系香料成分、アセタール系香料成分、ムスク系香料成分、ニトリル系香料成分、精油等が挙げられる。
本発明の芳香剤組成物は、(A)成分及び(B)成分を溶解又は分散させるための有機溶剤が含まれる。
更に、本発明の芳香剤組成物には、前述する成分の他に、必要に応じて、増粘剤、酸化防止剤、紫外線吸収剤、溶解剤、pH調整剤、(A)成分以外の着色剤、消臭剤、キレート剤等が含まれていてもよい。
本発明の芳香剤組成物の形態については、特に制限されず、例えば、液状、ゲル状が挙げられる。本発明の芳香剤組成物の形態として、好ましくは液状である。
1.芳香剤組成物の調製
表1に示す各色素成分及び表2に示す組成の香料組成物を用いて、表3に示す組成の芳香剤組成物を調製した。なお、表3において、香料組成物4を用いた場合のみ、イソパラフィン系溶剤の代わりに99度合成エタノールを用いて同様に調製した。
1.芳香剤組成物の調製
表8に示す組成の芳香剤組成物を調製した。
各芳香剤組成物をガラス製の透明容器に充填して密封し、昼間には太陽光が当たる室内に4週間保存した。保存1週間後及び4週間後に、各芳香剤組成物の色調を目視により観察し、保存前後の色調変化を評価した。得られた結果を表9に示す。単一香料成分を使用した結果からは、窒素原子を有するアントラキノン系色素成分は、エステル系香料成分、芳香族アルコール系香料成分がいずれも、ヘテロ原子が単結合したベンジル位を有する香料成分である場合に、これらと共存させると、光暴露環境下での保存後に退色して色調が変化していた(表9参照)。一方、エステル系香料成分、又は芳香族アルコール系香料成分であっても、ヘテロ原子が単結合したベンジル位を有する香料成分でない場合は、窒素原子を有するアントラキノン系色素成分と共存しても、光暴露環境下での保存後の色調変化の問題はさほど生じなかった。また、ベンジル位にヘテロ原子が単結合したものであっても、当該ベンジル位に更にヘテロ原子が二重結合した構造を有する香料成分は、窒素原子を有するアントラキノン系色素成分と共存しても、光暴露環境下での保存後の色調変化の問題は生じなかった。以上の結果から、窒素原子を有するアントラキノン系色素成分は、ヘテロ原子が単結合したベンジル位を有する香料成分と共存させると、当該ベンジル位に更にヘテロ原子が二重結合した構造を有さない場合は、光暴露環境下での保存後に退色して色調の変化が生じることが確認された。
1.芳香剤組成物の調製
表10、11に示す組成の芳香剤組成物を調製した。
各芳香剤組成物をガラス製の透明容器に充填して密封し、昼間には太陽光が当たる室内に4週間保存した。保存1週間後、2週間後及び4週間後に、各芳香剤組成物の色調を目視により観察し、保存前後の色調変化を評価した。得られた結果を表12〜27に示す。
Claims (8)
- (A)窒素原子を有するアントラキノン系色素成分、及び(B)ヘテロ原子が単結合したベンジル位を有する香料成分を含有し、
前記(A)成分1モル当たり、前記(B)成分が1〜600モル含まれることを特徴とする、芳香剤組成物。 - 前記(A)成分が、窒素原子を1つ又は2つ有する、請求項1に記載の芳香剤組成物。
- 前記(A)成分において、窒素原子が1級アミン又は2級アミンの形態で存在する、請求項1又は2に記載の芳香剤組成物。
- 前記一般式(A1)において、Ra1及び/又はRa4が、アミノ基、C1〜4アルキルフェニルアミノ基、C1〜4アルコキシフェニルアミノ基、フェニルアミノ基、又はC1〜4アルキルアミノ基である、請求項5に記載の芳香剤組成物。
- 更に、ベンジルアセテート、リナロール、リナリルアセテート、リリアール、ガラクソリド、エチレンブラシレート、サイクロペンタデカノライド、サイクロペンタデセノライド、及び5―シクロヘキサデセン−1−オンよりなる群から選択される少なくとも1種の香料成分を含む、請求項1〜6のいずれかに記載の芳香剤組成物。
- 更に、1価アルコール、多価アルコール、イソパラフィン、及びグリコールエーテルよりなる群から選択される少なくとも1種の有機溶剤を含む、請求項1〜7のいずれかに記載の芳香剤組成物。
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