JPS62290463A - Transparewnt gel like aroma composition - Google Patents
Transparewnt gel like aroma compositionInfo
- Publication number
- JPS62290463A JPS62290463A JP61133428A JP13342886A JPS62290463A JP S62290463 A JPS62290463 A JP S62290463A JP 61133428 A JP61133428 A JP 61133428A JP 13342886 A JP13342886 A JP 13342886A JP S62290463 A JPS62290463 A JP S62290463A
- Authority
- JP
- Japan
- Prior art keywords
- gel
- weight
- fragrance
- amount
- composition
- 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 description 35
- 239000003205 fragrance Substances 0.000 claims description 44
- 150000002430 hydrocarbons Chemical class 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims description 14
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 claims description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- 150000002334 glycols Chemical class 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 6
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 235000005979 Citrus limon Nutrition 0.000 description 4
- 244000131522 Citrus pyriformis Species 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 241000220317 Rosa Species 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 3
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 3
- 235000011613 Pinus brutia Nutrition 0.000 description 3
- 241000018646 Pinus brutia Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 3
- 235000000484 citronellol Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 229940067107 phenylethyl alcohol Drugs 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-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
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 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
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-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
- 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
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 235000019502 Orange oil Nutrition 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- 229940113087 geraniol Drugs 0.000 description 2
- AVIYEYCFMVPYST-UHFFFAOYSA-N hexane-1,3-diol Chemical compound CCCC(O)CCO AVIYEYCFMVPYST-UHFFFAOYSA-N 0.000 description 2
- 239000000077 insect repellent Substances 0.000 description 2
- 229930007744 linalool Natural products 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
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000010502 orange oil Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229940116411 terpineol Drugs 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 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
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
- -1 1.5-bentanediol Chemical compound 0.000 description 1
- JLWMMYZWEHHTFF-UHFFFAOYSA-N 2-[6-(3-carbamimidoylphenoxy)-4-[di(propan-2-yl)amino]-3,5-difluoropyridin-2-yl]oxy-5-(2-methylpropylcarbamoyl)benzoic acid Chemical compound OC(=O)C1=CC(C(=O)NCC(C)C)=CC=C1OC1=NC(OC=2C=C(C=CC=2)C(N)=N)=C(F)C(N(C(C)C)C(C)C)=C1F JLWMMYZWEHHTFF-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- 239000001293 FEMA 3089 Substances 0.000 description 1
- 241001632576 Hyacinthus Species 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 235000010254 Jasminum officinale Nutrition 0.000 description 1
- 240000005385 Jasminum sambac Species 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- DYUQAZSOFZSPHD-UHFFFAOYSA-N Phenylpropyl alcohol Natural products CCC(O)C1=CC=CC=C1 DYUQAZSOFZSPHD-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 239000010642 eucalyptus oil Substances 0.000 description 1
- 229940044949 eucalyptus oil Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- 239000010648 geranium oil Substances 0.000 description 1
- 235000019717 geranium oil Nutrition 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000010501 lemon oil Substances 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
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- FHJRFIYKPIXQNQ-UHFFFAOYSA-N n,n-diethyloctanamide Chemical compound CCCCCCCC(=O)N(CC)CC FHJRFIYKPIXQNQ-UHFFFAOYSA-N 0.000 description 1
- PREAZHGTUOIWRL-UHFFFAOYSA-N n-phenyl-n-propylacetamide Chemical compound CCCN(C(C)=O)C1=CC=CC=C1 PREAZHGTUOIWRL-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- WYNVIVRXHYGNRT-UHFFFAOYSA-N octane-3,5-diol Chemical compound CCCC(O)CC(O)CC WYNVIVRXHYGNRT-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229960005323 phenoxyethanol 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
- 239000010665 pine oil Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 3、発明の詳細な説明 く技術分野〉 本発明は透明ゲル状芳香剤組成物に関する。[Detailed description of the invention] 3. Detailed description of the invention Technical fields> The present invention relates to transparent gel fragrance compositions.
く従来の技術および発明が解決しようとする問題点〉
従来、炭化水素化合物のゲル化剤としてステアリン酸ナ
トリウムを使用する場合、水量の水のほかにアルコール
類またはグリコール類を使用することは知られていた。Prior Art and Problems to be Solved by the Invention Conventionally, when sodium stearate is used as a gelling agent for hydrocarbon compounds, it has not been known to use alcohols or glycols in addition to water. was.
例えば特開昭60−53148号、特開昭55−754
93号、特公昭61−8696号、特公昭57−168
18号、特開昭57−125752号各公報等によりジ
エチレングリコール、ジプロピレングリコール、エタノ
ール、3−メヂルー3−メトキシブタノール、セロソル
ブ、メチルカルピトール
リコール、プロピレングリコール、グリセリン、ポリエ
チレングリコール、ヘキシレングリコール、1、6−ヘ
キサンジオール、1.5−ベンタンジオール、2.2−
ジメチル−1.3ープロパンジオールなどが開示されて
いる。For example, JP-A-60-53148, JP-A-55-754
No. 93, Special Publication No. 61-8696, Special Publication No. 57-168
No. 18, JP-A No. 57-125752, diethylene glycol, dipropylene glycol, ethanol, 3-medylene-3-methoxybutanol, cellosolve, methylcarpitol recall, propylene glycol, glycerin, polyethylene glycol, hexylene glycol, 1 , 6-hexanediol, 1.5-bentanediol, 2.2-
Dimethyl-1,3-propanediol and the like are disclosed.
しかしながら上記の従来開示されたアルコール類または
グリコール類の使用では、得られた芳香剤組成物は透明
性を有しないか、あるいは初明は半透明でも経時的に完
全に不透明となり透明美観性を考慮するとき、難点のあ
るものであった。However, when using the alcohols or glycols disclosed above, the resulting fragrance composition does not have transparency, or even though it is initially translucent, it becomes completely opaque over time, making it difficult to consider the aesthetics of transparency. There were some difficulties when doing so.
一方特開昭60−85756号公報によりベンジルアル
コール、メチルベンジルアルコール、フェニルエチルア
ルコール、フェニルプロピルアルコール、フェノキシエ
タノールよりなる群より選ばれた少くとも1種を使用す
る透明固型芳香剤が開示されている。しかしこれを実施
するためには、上記芳香族1価アルコールの使用量が炭
化水素化合物、芳香族11ffJアルコール、ステアリ
ン酸ナトリウムおよび水の合計重量に基いて約10〜約
90重量%という大なる量が必要であり、このとき芳香
族1価アルコールは炭化水素化合物、芳香成分などが揮
散したのら残留成分として残るためゲルの残査足が多く
なり芳香剤使用終了時期が判別しに(くなるという避け
られない問題点が存在した。ざらに上記芳香族1価アル
コールの使用によっては、IFfられた芳香剤組成物は
約60°C程度の高温においたときに融解現色がおきや
すくなり、著しい場合には、完全に液状態にまで変化し
ゲルが破壊されてしまうなどの問題点を有していた。On the other hand, JP-A-60-85756 discloses a transparent solid fragrance using at least one selected from the group consisting of benzyl alcohol, methylbenzyl alcohol, phenylethyl alcohol, phenylpropyl alcohol, and phenoxyethanol. . However, in order to accomplish this, the amount of the aromatic monohydric alcohol used must be large, from about 10 to about 90% by weight, based on the total weight of the hydrocarbon compound, aromatic 11ffJ alcohol, sodium stearate, and water. At this time, the aromatic monohydric alcohol remains as a residual component after the hydrocarbon compounds and aromatic components are volatilized, so there is a large amount of gel residue, which makes it difficult to determine when the fragrance is used. However, depending on the use of the above-mentioned aromatic monohydric alcohol, the IFf fragrance composition tends to melt and develop color when placed at a high temperature of about 60°C. In severe cases, the gel completely changes to a liquid state and the gel is destroyed.
〈発明の目的〉
本発明は前記従来技術の欠点のないゲル状芳香剤組成物
、叩ら透明美観性を有し比較的高温においても形状及定
性が高くざらに揮散後のゲル残百量が少い、したがって
芳香剤使用終了時期が明瞭な透明ゲル状芳香剤組成物を
提供することを目的とする。<Object of the Invention> The present invention provides a gel-like fragrance composition that does not have the drawbacks of the prior art, has a transparent aesthetic appearance when beaten, has high shape and consistency even at relatively high temperatures, and has a low gel residual amount after being roughly volatilized. It is an object of the present invention to provide a transparent gel-like fragrance composition in which the amount of use of the fragrance is clear, and therefore the end of use of the fragrance is clear.
〈発明の、構成〉
本発明者らは前記目的を連成するために鋭息ω1究の結
果、炭化水素化合物のゲル化剤としてステアリン酸ナト
リウムを使用する場合、少但の水のほかにグリコール類
として2−エチル−1,3−ヘキサンジオールを使用す
ることによって従来技術の諸問題が一挙に解決されるこ
とをはじめて児出し本発明を完成した。<Structure of the Invention> In order to couple the above objects, the present inventors conducted intensive ω1 research and found that when using sodium stearate as a gelling agent for hydrocarbon compounds, in addition to a small amount of water, glycol The present invention was completed when the problems of the prior art were solved all at once by using 2-ethyl-1,3-hexanediol as a compound.
すなわち本発明は炭化水素化合物、グリコール類、ステ
アリン酸ナトリウムおよび水から主として成る組成物の
加熱溶解後冷却して得られるゲル状芳香剤組成物におい
て該グリコールが2−エチル−1,3−ヘキサンジオー
ルであることを特徴とする透明ゲル状芳香剤組成物を提
供するものである。That is, the present invention provides a gel-like fragrance composition obtained by heating and dissolving a composition mainly consisting of a hydrocarbon compound, glycols, sodium stearate, and water, and then cooling the composition, in which the glycol is 2-ethyl-1,3-hexanediol. The present invention provides a transparent gel-like fragrance composition characterized by the following.
本発明の透明ゲル状芳香剤組成物は炭化水素化合物、2
−エチル−1,3−ヘキサンジオール、ステアリン酸ナ
トリウムおよび水などを主とする成分を例えば約70’
C〜約90℃程度に混合加熱溶解してのち、至温に放冷
または強制的に冷却して1に造することができる。この
とき炭化水素化合物そのものを芳香成分として利用する
ことが出来るがざらに他の芳香成分として種々の合成香
料、天然香′I;!、および調合香料などを配合するこ
とができる。The transparent gel fragrance composition of the present invention comprises a hydrocarbon compound, 2
- Ethyl-1,3-hexanediol, sodium stearate, water, etc.
1 can be produced by mixing, heating and melting the mixture at a temperature of about 90° C. and then letting it cool or forcibly cooling it to the lowest temperature. At this time, the hydrocarbon compound itself can be used as the aromatic component, but various synthetic fragrances and natural fragrances can also be used as other aromatic components. , mixed fragrances, etc. can be blended.
この場合には上記の混合7JO熱溶解液の温度を約65
°C〜約80″C程度に低下させたのち芳香成分を加え
て均一に混合し冷却させて製造することがのぞましい。In this case, the temperature of the above-mentioned mixed 7JO hot solution should be set to about 65%.
Preferably, the temperature is lowered to about 80''C, then the aromatic component is added, mixed uniformly, and cooled.
本発明の組成物において用いられる2−エチル−1,3
−ヘキサンジオールの使用量は炭化水素化合物2−エチ
ル−1,3−ヘキサンジオール、ステアリン酸ナトリウ
ムおよび水の合計g間に基いて約2〜約70重量%であ
る。2-ethyl-1,3 used in the composition of the invention
- The amount of hexanediol used is from about 2 to about 70% by weight, based on the total grams of hydrocarbon compound 2-ethyl-1,3-hexanediol, sodium stearate and water.
約2重り%以下のときはゲルは透明にならない。When the amount is less than about 2% by weight, the gel does not become transparent.
また約70重量%以上でも透明性に難点が生じるので上
記例示範囲で適宜選択される。好ましくは約2〜約50
重量%を例示することができる。Further, if the amount is about 70% by weight or more, there will be a problem in transparency, so the amount should be appropriately selected within the above-mentioned range. Preferably about 2 to about 50
Weight % can be given as an example.
本発明の組成物に6いて用いられる炭化水素化合物とし
て揮発性テンベル系炭化水素および/またはイソパラフ
ィン系炭化水素を例示することが出来る。揮発性テンベ
ル系炭化水素としてはd−リモネン、α−ピネン、β−
ピネンならびにこれらの化合物の1種以上を主成分とす
る天然精油、たとえばレモン油、オレンジ油、テレピン
油などが挙げられる。イソパラフィン系炭化水素として
は主成分の沸点が150〜270’Cのもの、たとえば
IPソルベント1620.2028 <出光石油化学株
式会社製)を例示することができる。揮発性テンベル系
炭化水素とイソパラフィン系炭化水素は、各々甲独もし
くは両省任意の割合を混合し使用することができる。炭
化水素化合物の使用量は炭化水素化合物、2−エチル−
1,3−ヘキサンジオール、ステアリン酸ナトリウムお
よび水の合計重量に基いてたとえば約15〜約96.5
重量%の範囲を例示することができる。炭化水素化合物
の量が少なすぎるときは透明とならないし、また多すぎ
る場合にも透明とならない。好ましくは約15〜約95
弔最%を例示できる。Examples of the hydrocarbon compound used in the composition of the present invention include volatile tenbel hydrocarbons and/or isoparaffin hydrocarbons. Volatile tenbel hydrocarbons include d-limonene, α-pinene, and β-
Examples include natural essential oils containing pinene and one or more of these compounds as main components, such as lemon oil, orange oil, and turpentine oil. Examples of isoparaffinic hydrocarbons include those whose main component has a boiling point of 150 to 270'C, such as IP Solvent 1620.2028 (manufactured by Idemitsu Petrochemical Co., Ltd.). The volatile tenbel hydrocarbons and isoparaffin hydrocarbons can be used by mixing them in any proportions. The amount of hydrocarbon compound used is hydrocarbon compound, 2-ethyl-
For example, from about 15 to about 96.5, based on the combined weight of 1,3-hexanediol, sodium stearate, and water.
A range of weight % can be exemplified. If the amount of hydrocarbon compound is too small, it will not be transparent, and if it is too large, it will not be transparent. Preferably about 15 to about 95
I can give an example of the highest percentage.
本発明の組成物において用いられるステアリン酸ナトリ
ウムは特別に高純度のものは必要ではなく容易に入手す
ることのできる工業製品を使用できる。ステアリン酸ナ
トリウムの使用量は炭化水素化合物、2−エチル−1,
3−ヘキサンジオール、ステアリン酸ナトリウムおよび
水の合計重量に暴いて、たとえば約1〜約10重量%を
挙げることが出来る。ステアリン酸ナトリウムの使用量
が少なすぎる場合には適当な硬さをもつゲルが得られず
、10mm%以上となると溶解しずらくなり好ましくな
い。好ましくは約2〜約8重最%の範囲を例示できる。The sodium stearate used in the composition of the present invention does not need to be of particularly high purity, and easily available industrial products can be used. The amount of sodium stearate used is hydrocarbon compound, 2-ethyl-1,
For example, from about 1 to about 10% by weight, based on the total weight of 3-hexanediol, sodium stearate and water. If the amount of sodium stearate used is too small, a gel with appropriate hardness cannot be obtained, and if it exceeds 10 mm%, it becomes difficult to dissolve, which is not preferable. A preferred range is about 2% to about 8%.
本発明において用いられる水の使用量は炭化水素化合物
、2−エチル−1,3−ヘキサンジオール、ステアリン
酸ナトリウムおよび水の合計重量に暴いて約0.1〜約
5重量%、好ましくは約0.5〜約4重邑%の範囲を挙
げることが出来る。The amount of water used in the present invention is about 0.1% to about 5% by weight, preferably about 0% by weight based on the total weight of the hydrocarbon compound, 2-ethyl-1,3-hexanediol, sodium stearate, and water. A range of .5 to about 4% can be mentioned.
水の使用量が少ないほど、ゲルの耐熱性は改良されるが
ステアリン酸ナトリウムが溶解しずら(なり透明性に難
点が生じる。水の使用量が多すぎる場合には水と他の梧
成成分との分離がおこることがあり好ましくない。した
がって上記の範囲で過賞選択して用いる。The smaller the amount of water used, the better the heat resistance of the gel will be, but the sodium stearate will not be dissolved (and the transparency will be compromised.If the amount of water used is too large, the heat resistance of the gel will be improved.) This is not preferable as separation may occur. Therefore, it is used in a selective manner within the above range.
本発明の透明ゲル状芳香剤組成物は炭化水素化合物、2
−エチル−1,3−ヘキサンジオール、ステアリン酸す
i−リウムおよび水のほかに芳香成分として合成香料、
天然香料、調合香料などを自白に選択して使用すること
ができる。たとえばレモン系、オレンジ系等の柑橘系香
料をはじめパイン系、ローズ系、ムゲット系、ジャスミ
ン系、ヒヤシンス系などの香料が挙げられる。調合香料
の処方例としては以下のようなものが挙げられる。The transparent gel fragrance composition of the present invention comprises a hydrocarbon compound, 2
- Ethyl-1,3-hexanediol, siliium stearate, and water as well as synthetic fragrances as aromatic ingredients;
Natural fragrances, mixed fragrances, etc. can be selected and used in the confession. Examples include citrus fragrances such as lemon and orange fragrances, pine fragrances, rose fragrances, muguette fragrances, jasmine fragrances, and hyacinth fragrances. Examples of prescriptions for mixed fragrances include the following:
レモン系調合香料
レモン27504 (小林香料株式会社製)レモンベー
ス 70.0重量部オレンジ油
20.Oα−ピネン
5.0ゲラニオール 2.0シ
トロネロール 1.0リナリルアセテ
ート 1.0シトラール
0.5ゲラニルアセテート 0.5
100.0重量部
パイン系調合香料
パインオイル3131 (小林香料株式会社製)パイン
ベース 48.0重量部じツキオイル
25.0パインニードル油
18.0ユーカリ油 7.
0シブレス油 2.0100.0
重量部
ローズ系調合香料
ローズ35575 (小林香料株式会社製)ローズベー
ス 50.0重量部フェニルエチルア
ルコール 30.0シトロネロール
3.0ゲラニオール 5.0テ
ルピネオール 5.0リナロール
3.0フェニルエチルフォルメー
ト2.0
ゼラニウム油 2.0100.0重
量部
ムゲット系調合香料
ムゲット565(小林香料株式会社製)ムゲットベース
40.0重量部フェニルエチルアルコ
ール 20.0リナロール 1
0.0テルピネオール 10.0へキ
シルシンナミックアルデヒド
10.0
シトロネロール 3.0ベンジルアセ
テート 7.0100.0重量部
芳香成分の使用りは適宜選択することができるが、透明
ゲル状芳香剤組成物に基いて約0.1〜約30重ω%の
範囲を例示することができる。過剰な使用端ではゲルの
形成が不良になることがありさらにコスト上昇の原因に
もなるので好ましくない。Lemon-based blended fragrance Lemon 27504 (manufactured by Kobayashi Fragrance Co., Ltd.) Lemon base 70.0 parts by weight Orange oil
20. Oα-pinene
5.0 Geraniol 2.0 Citronellol 1.0 Linalyl Acetate 1.0 Citral
0.5 Geranyl acetate 0.5
100.0 parts by weight Pine-based blended fragrance Pine Oil 3131 (manufactured by Kobayashi Fragrance Co., Ltd.) Pine Base 48.0 parts by weight Jitsuki oil 25.0 Pine needle oil
18.0 Eucalyptus oil 7.
0 Shibres oil 2.0100.0
Parts by weight Rose-based mixed fragrance Rose 35575 (manufactured by Kobayashi Perfume Co., Ltd.) Rose base 50.0 parts by weight Phenylethyl alcohol 30.0 Citronellol
3.0 Geraniol 5.0 Terpineol 5.0 Linalool
3.0 Phenylethyl formate 2.0 Geranium oil 2.0 100.0 parts by weight Mugette-based blended fragrance Mugette 565 (manufactured by Kobayashi Fragrance Co., Ltd.) Mugette base 40.0 parts by weight Phenylethyl alcohol 20.0 Linalool 1
0.0 terpineol 10.0 hexyl cinnamic aldehyde 10.0 citronellol 3.0 benzyl acetate 7.0 100.0 parts by weight The use of aroma components can be selected as appropriate, but in the transparent gel fragrance composition Based on this, a range of about 0.1 to about 30 weight ω% can be exemplified. Excessive use end is not preferable because it may result in poor gel formation and may also cause an increase in cost.
本発明の透明ゲル状芳香剤組成物は特徴成分である2−
エチル−1,3−ヘキサンジオールをΦ独使用できるこ
とは勿論であるが、その本質が失われない範囲内で坐位
の他の有機溶剤と組み合せて使用することは何等差しつ
かえない。例えばエタノールを組み合わせて使用するこ
とにより芳香成分の揮散性を改善することもできる。そ
の使用億は組成物の短離に基いて約1〜約10重但%を
挙げることができる。約10重量%をこえるとゲルの耐
熱性に悪影響を与えることがあるのでその使用に際して
は注意を要する。The transparent gel-like fragrance composition of the present invention has two characteristic components:
Of course, ethyl-1,3-hexanediol can be used alone, but there is no problem in using it in combination with other organic solvents as long as the essence is not lost. For example, the volatility of aroma components can also be improved by using ethanol in combination. The amount used may range from about 1% to about 10% by weight, depending on the composition composition. If it exceeds about 10% by weight, it may have an adverse effect on the heat resistance of the gel, so care must be taken when using it.
本発明の透明ゲル状芳香剤組成物は前記諸成分以外に更
にたとえば所望により酸化防止剤、色素、澗臭剤、害虫
忌避剤、防腐殺菌剤、防虫殺虫剤、増粘剤等の目的に使
用しつる各種のものを使用することが出来る。使用する
量はそれぞれ目的を達成するための量が適宜選択される
。以下にそれぞれを例示する。In addition to the above-mentioned components, the transparent gel fragrance composition of the present invention can also be used as an antioxidant, pigment, odor agent, insect repellent, antiseptic bactericide, insect repellent, thickener, etc., if desired. You can use various types of vines. The amount to be used is appropriately selected to achieve the purpose. Examples of each are shown below.
酸化防止剤; 8l−IT、BHA、d!−α−トコフ
ェロール、没食子酸プロピルなど。Antioxidant; 8l-IT, BHA, d! -α-tocopherol, propyl gallate, etc.
色素;赤色501号、青色403号、黄色204@。Pigments: Red No. 501, Blue No. 403, Yellow 204@.
澗臭剤;ラウリルメタアクリレート、オクヂルクロトネ
ート、植物抽出物など。Deodorants: lauryl methacrylate, ocdyl crotonate, plant extracts, etc.
害虫忌避剤:N、N−ジエヂルーm−トルアミドカプリ
ル酸ジエチルアミド、N−プロピルアセトアニリドなど
。Pest repellents: N,N-diezyru-m-toluamide caprylic acid diethylamide, N-propylacetanilide, etc.
防腐殺菌剤;パラクロロメタキシレノール女息香酸、パ
ラオキシ安息香酸エステルなど。Preservatives and disinfectants; parachloromethaxylenol female zoic acid, paraoxybenzoic acid ester, etc.
防虫殺虫剤;パラジクロロベンゼン、ショウノウ、ナフ
タリンなど。Insecticides; paradichlorobenzene, camphor, naphthalene, etc.
増粘剤;エチルセルロース、ヒドロギシプロピルセルロ
ースなど。Thickener; ethyl cellulose, hydroxypropyl cellulose, etc.
本発明によれば透明ゲル状芳香剤組成物が得られるので
透明ゲル体中に各種の装飾体、例えば模造の花、魚、動
物、草木、果実およびスパンコール、A−ロラフィルム
などを装入することによって透明ゲル状芳香剤組成物の
観賞性や装飾性を一段と高めることも可能である。According to the present invention, a transparent gel-like fragrance composition is obtained, and various decorations, such as imitation flowers, fish, animals, plants, fruits, sequins, A-Lola film, etc., are charged into the transparent gel body. By doing so, it is also possible to further enhance the ornamental properties and decorative properties of the transparent gel-like fragrance composition.
〈実施例及び比較例〉
以下に実施例及び比較例を挙げて本発明を更に詳細に説
明する。<Examples and Comparative Examples> The present invention will be described in more detail below with reference to Examples and Comparative Examples.
実施例1〜4及び比較例1〜5
下記の第1表及び第2表に示す実施例及び比較(911
のゲル状芳香剤組成物を調整した。Examples 1 to 4 and Comparative Examples 1 to 5 Examples and comparisons (911
A gel fragrance composition was prepared.
第1表
第2表
次に上記で得た各ゲル状芳香剤組成物について透明性、
耐熱性の各々のテストを行った。試験法を下記に示す。Table 1 Table 2 Next, for each gel fragrance composition obtained above, the transparency,
Each test for heat resistance was conducted. The test method is shown below.
透明性テスト;水質試験法の十字標識板による透視度法
により行った。評(11jl準は10crn以上のとき
を透明、10〜1 cmのときを半透明、1 cm未満
のときを不透明と表わした。Transparency test: Conducted by the transparency method using a water quality test method using a cross sign board. Evaluation (11jl standards): Transparent when it is 10 crn or more, translucent when it is 10 to 1 cm, and opaque when it is less than 1 cm.
耐熱性テスト;密閉条件下のゲル状芳香剤組成物を60
℃の恒温槽に3時間放置したのち融解し液状態になった
重量を測定し、恒温槽に入れる前のゲル状芳香剤組成物
の重量を基として百分率で表わした。Heat resistance test: Gel fragrance composition under sealed conditions
After being left in a thermostatic bath at 0.degree. C. for 3 hours, the weight of the melted and liquid state was measured and expressed as a percentage based on the weight of the gel fragrance composition before being placed in the thermostatic bath.
試験結果を第3表に示す。The test results are shown in Table 3.
第3表
更に実施例1,2及び比較例1,4の各組成物について
揮散性テストを行った。試験法は下記のとうりでおる。Table 3 Furthermore, a volatility test was conducted on each of the compositions of Examples 1 and 2 and Comparative Examples 1 and 4. The test method is as follows.
揮散性テスト:約25℃(60%RH>の風通しの良い
至内に50日間放置し各々の組成物の残査重量を測定し
試験前の組成物の重量を基として百分率で表わした。Volatility test: The residual weight of each composition was measured after being left in a well-ventilated room at about 25° C. (60% RH) for 50 days, and expressed as a percentage based on the weight of the composition before the test.
試験結果を第4表に示す。The test results are shown in Table 4.
第4表
〈発明の効果〉
本発明によれば、透明美観性を有し、比較的高温におい
ても形状安定性が高く、更に揮発後のゲルの残査量が少
く、従って芳香剤使用終了時期が明瞭な透明ゲル状芳香
剤組成物が得られる。Table 4 <Effects of the Invention> According to the present invention, the present invention has a transparent aesthetic appearance, has high shape stability even at relatively high temperatures, and has a small amount of residual gel after volatilization. A transparent gel-like fragrance composition with clear characteristics is obtained.
Claims (2)
トリウムおよび水から主として成る 組成物の加熱溶解後冷却して得られるゲル 状芳香剤組成物において該グリコールが 2−エチル−1,3−ヘキサンジオールで あることを特徴とする透明ゲル状芳香剤組 成物。(1) In a gel-like fragrance composition obtained by heating and dissolving a composition mainly consisting of a hydrocarbon compound, glycols, sodium stearate, and water and cooling it, the glycol is 2-ethyl-1,3-hexanediol. A transparent gel-like fragrance composition characterized by the following.
炭化水素化合物、該2−エチル− 1,3−ヘキサンジオール、該ステアリン 酸ナトリウムおよび水の合計重量に基いて、約2〜約7
0重量%である特許請求の範囲 第1項記載の透明ゲル状芳香剤組成物。(2) the amount of 2-ethyl-1,3-hexanediol is from about 2 to about 7
The transparent gel fragrance composition according to claim 1, which has a content of 0% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61133428A JPS62290463A (en) | 1986-06-09 | 1986-06-09 | Transparewnt gel like aroma composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61133428A JPS62290463A (en) | 1986-06-09 | 1986-06-09 | Transparewnt gel like aroma composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62290463A true JPS62290463A (en) | 1987-12-17 |
Family
ID=15104539
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61133428A Pending JPS62290463A (en) | 1986-06-09 | 1986-06-09 | Transparewnt gel like aroma composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62290463A (en) |
-
1986
- 1986-06-09 JP JP61133428A patent/JPS62290463A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20040031191A1 (en) | Protection of fragrance in a wax candle using an antioxidant | |
US8679469B2 (en) | Gel air freshener | |
US6573235B1 (en) | Use of hydrofluoroethers as agents for dissolving aromatic compounds to make compositions | |
JPS61206450A (en) | Aromatic composition | |
JPS62290463A (en) | Transparewnt gel like aroma composition | |
JP4224175B2 (en) | Transparent gel fragrance / deodorant composition | |
JPS6364986B2 (en) | ||
JP2004105519A (en) | Gelled aromatic/deodorant composition | |
JP6283342B2 (en) | Oil-in-water gel composition and method for improving malodor removal of oil-in-water gel composition | |
JP4791143B2 (en) | Transparent gelling agent composition, transparent gel and method for producing transparent gel | |
JP3803141B2 (en) | Transparent oily gel air freshener composition | |
JPS6232961A (en) | Gel like aromatic composition | |
JPH0235578B2 (en) | ||
JPH10226749A (en) | Water-base gel composition | |
JPS6053148A (en) | Gel like aaromatic composition | |
JPS5921608A (en) | Cosmetic | |
JP4480991B2 (en) | Oily gel drug | |
JPH0580229B2 (en) | ||
JPS6241661A (en) | Transparent hydrogel aromatic agent | |
JPH02127496A (en) | Solid fuel with corrosion-proofing performance | |
JP3831260B2 (en) | Transparent gel fragrance / deodorant composition | |
JPS5813507A (en) | Gelatinous aromatic composition | |
JPS6143107A (en) | Aromatic gel composition | |
JP2003290331A (en) | Gel aromatic/deodorizer composition | |
JP2003126233A (en) | Oily transparent gel-like aroma composition |