JP7001344B2 - 芳香剤組成物 - Google Patents
芳香剤組成物 Download PDFInfo
- Publication number
- JP7001344B2 JP7001344B2 JP2016257038A JP2016257038A JP7001344B2 JP 7001344 B2 JP7001344 B2 JP 7001344B2 JP 2016257038 A JP2016257038 A JP 2016257038A JP 2016257038 A JP2016257038 A JP 2016257038A JP 7001344 B2 JP7001344 B2 JP 7001344B2
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- JP
- Japan
- Prior art keywords
- component
- group
- fragrance
- aldehyde
- carbon atoms
- 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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- 239000003205 fragrance Substances 0.000 title claims description 153
- 239000000203 mixture Substances 0.000 title claims description 84
- -1 aliphatic aldehyde Chemical class 0.000 claims description 40
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 20
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 16
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 239000000049 pigment Substances 0.000 claims description 11
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims description 10
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims description 10
- AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 claims description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 7
- 239000003960 organic solvent Substances 0.000 claims description 7
- 239000005792 Geraniol Substances 0.000 claims description 6
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 229940113087 geraniol Drugs 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims description 5
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 claims description 5
- 239000001875 1-phenylethyl acetate Substances 0.000 claims description 5
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims description 5
- HTLBMZKXJYNJSK-UHFFFAOYSA-N 3-naphthalen-2-yl-1,2-oxazol-5-amine Chemical compound O1C(N)=CC(C=2C=C3C=CC=CC3=CC=2)=N1 HTLBMZKXJYNJSK-UHFFFAOYSA-N 0.000 claims description 5
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims description 5
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims description 5
- 235000000484 citronellol Nutrition 0.000 claims description 5
- ONKNPOPIGWHAQC-UHFFFAOYSA-N galaxolide Chemical compound C1OCC(C)C2=C1C=C1C(C)(C)C(C)C(C)(C)C1=C2 ONKNPOPIGWHAQC-UHFFFAOYSA-N 0.000 claims description 5
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- HLCSDJLATUNSSI-JXMROGBWSA-N (2e)-3,7-dimethylocta-2,6-dienenitrile Chemical compound CC(C)=CCC\C(C)=C\C#N HLCSDJLATUNSSI-JXMROGBWSA-N 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 125000005907 alkyl ester group Chemical group 0.000 claims description 3
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 3
- IEZPIUQRQRWIFE-UHFFFAOYSA-N 2,4,6-trimethyl-4-phenyl-1,3-dioxane Chemical compound O1C(C)OC(C)CC1(C)C1=CC=CC=C1 IEZPIUQRQRWIFE-UHFFFAOYSA-N 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 3
- 150000001450 anions Chemical class 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 description 23
- 238000005562 fading Methods 0.000 description 21
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- 239000007788 liquid Substances 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 6
- 150000003934 aromatic aldehydes Chemical class 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 5
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- 150000002825 nitriles Chemical class 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 239000000341 volatile oil Substances 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
- MBDOYVRWFFCFHM-SNAWJCMRSA-N (2E)-hexenal Chemical compound CCC\C=C\C=O MBDOYVRWFFCFHM-SNAWJCMRSA-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
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-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
- 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
- CWRKZMLUDFBPAO-SREVYHEPSA-N 4-Decenal Chemical compound CCCCC\C=C/CCC=O CWRKZMLUDFBPAO-SREVYHEPSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 2
- 241001672694 Citrus reticulata Species 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000402754 Erythranthe moschata Species 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
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 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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- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
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- JOZKFWLRHCDGJA-UHFFFAOYSA-N citronellol acetate Chemical compound CC(=O)OCCC(C)CCC=C(C)C JOZKFWLRHCDGJA-UHFFFAOYSA-N 0.000 description 2
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- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical group CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
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- 229930195733 hydrocarbon Natural products 0.000 description 2
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- 239000004615 ingredient Substances 0.000 description 2
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- 150000002576 ketones Chemical class 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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- 235000019719 rose oil Nutrition 0.000 description 2
- CZCBTSFUTPZVKJ-UHFFFAOYSA-N rose oxide Chemical compound CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 description 2
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- 239000001112 (2E)-1,1-diethoxy-3,7-dimethylocta-2,6-diene Substances 0.000 description 1
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- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
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- Fats And Perfumes (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Description
項1. (A)窒素原子を有するキサンテン系色素成分、及び(B)アルデヒド系香料成分を含有し、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)成分がローダミン系色素である、項1に記載の芳香剤組成物。
項3. 前記(B)成分が脂肪族アルデヒド系香料である、項1又は2に記載の芳香剤組成物。
項4. 前記(A)成分が、下記一般式(A1)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5. 前記一般式(A1)において、Ra2、Ra3、Ra12、及びRa13が、C1~4アルキルエステル基である、項4に記載の芳香剤組成物。
項6. 更に、ヘキサノール、ヘキシルアセテート、ダイナスコン、ゲラニルニトリル、スチラリルアセテート、4-フェニル-2,4,6-トリメチル-1,3-ジオキサン、オキサン、ガラクソリド、クマリン、ゲラニオール、シトロネロール、及びメチルイオノンガンマ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1~5のいずれかに記載の芳香剤組成物。
項7. 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1~6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は、窒素原子を有するキサンテン系色素成分を含む。キサンテン系色素成分は、キサンテン骨格を有する化合物である。
本発明の芳香剤組成物では、アルデヒド系香料成分が含まれる。アルデヒド系香料成分とは、ホルミル基(-CHO)を有し、揮発して香気を呈する化合物である。
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。
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1週間保存した。保存1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4に示す。
1.芳香剤組成物の調製
表6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7に示す。単一香料成分を使用した結果からも、前記試験例1の場合と同様に、窒素原子を有するキサンテン系色素成分と、アルデヒド系香料成分を共存させると、光暴露環境下での保存後に退色して色調変化が生じることが確認された。なお、アルデヒド系香料成分以外の香料成分を使用した場合には、窒素原子を有するキサンテ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。
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、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9~12に示す。
Claims (7)
- 空間に香気を付与するために使用される芳香剤組成物であって、
(A)窒素原子を有するキサンテン系色素成分、及び(B)アルデヒド系香料成分を含有し、
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(但し、下記一般式(1)で示される含窒素界面活性剤を含む場合を除く)。
- 前記(A)成分がローダミン系色素である、請求項1に記載の芳香剤組成物。
- 前記(B)成分が脂肪族アルデヒド系香料である、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、Ra2、Ra3、Ra12、及びRa13が、C1~4アルキル基である、請求項4に記載の芳香剤組成物。
- 更に、ヘキサノール、ヘキシルアセテート、ダイナスコン、ゲラニルニトリル、スチラリルアセテート、4-フェニル-2,4,6-トリメチル-1,3-ジオキサン、オキサン、ガラクソリド、クマリン、ゲラニオール、シトロネロール、及びメチルイオノンガンマ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1~5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1~6のいずれかに記載の芳香剤組成物。
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JP2003205024A (ja) | 2002-01-16 | 2003-07-22 | T Hasegawa Co Ltd | 透明ゲル状芳香・消臭剤組成物の製造方法 |
JP2005080792A (ja) | 2003-09-05 | 2005-03-31 | Kao Corp | 透明油性ゲル状芳香消臭剤組成物 |
JP2008302079A (ja) | 2007-06-08 | 2008-12-18 | T Hasegawa Co Ltd | 液体芳香剤 |
WO2009107813A1 (ja) | 2008-02-27 | 2009-09-03 | 小林製薬株式会社 | 開閉可能な収納空間用の芳香剤組成物 |
JP2009286938A (ja) | 2008-05-30 | 2009-12-10 | Kao Corp | 水性液体洗浄剤組成物 |
JP2010284511A (ja) | 2009-05-15 | 2010-12-24 | Kao Corp | ゲル状消臭芳香剤 |
US20110146001A1 (en) | 2009-12-17 | 2011-06-23 | Ricky Ah-Man Woo | Laundry Detergent Composition Having A Malodor Control Component And Methods Of Laundering Fabrics |
JP2012158559A (ja) | 2011-02-01 | 2012-08-23 | Lion Corp | ベルベリン含有歯磨剤組成物及びその安定化方法 |
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Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2003205024A (ja) | 2002-01-16 | 2003-07-22 | T Hasegawa Co Ltd | 透明ゲル状芳香・消臭剤組成物の製造方法 |
JP2005080792A (ja) | 2003-09-05 | 2005-03-31 | Kao Corp | 透明油性ゲル状芳香消臭剤組成物 |
JP2008302079A (ja) | 2007-06-08 | 2008-12-18 | T Hasegawa Co Ltd | 液体芳香剤 |
WO2009107813A1 (ja) | 2008-02-27 | 2009-09-03 | 小林製薬株式会社 | 開閉可能な収納空間用の芳香剤組成物 |
JP2009286938A (ja) | 2008-05-30 | 2009-12-10 | Kao Corp | 水性液体洗浄剤組成物 |
JP2010284511A (ja) | 2009-05-15 | 2010-12-24 | Kao Corp | ゲル状消臭芳香剤 |
US20110146001A1 (en) | 2009-12-17 | 2011-06-23 | Ricky Ah-Man Woo | Laundry Detergent Composition Having A Malodor Control Component And Methods Of Laundering Fabrics |
JP2012158559A (ja) | 2011-02-01 | 2012-08-23 | Lion Corp | ベルベリン含有歯磨剤組成物及びその安定化方法 |
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