JP2005516045A - オリゴエステルを含む添加剤および生成物 - Google Patents
オリゴエステルを含む添加剤および生成物 Download PDFInfo
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- JP2005516045A JP2005516045A JP2003563486A JP2003563486A JP2005516045A JP 2005516045 A JP2005516045 A JP 2005516045A JP 2003563486 A JP2003563486 A JP 2003563486A JP 2003563486 A JP2003563486 A JP 2003563486A JP 2005516045 A JP2005516045 A JP 2005516045A
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- Prior art keywords
- oligoester
- fragment
- groups
- diol
- acid
- 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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- 229920002601 oligoester Polymers 0.000 title claims abstract description 361
- 239000000654 additive Substances 0.000 title claims abstract description 57
- 239000000203 mixture Substances 0.000 claims abstract description 215
- 239000002537 cosmetic Substances 0.000 claims abstract description 47
- 239000002453 shampoo Substances 0.000 claims abstract description 24
- 239000003814 drug Substances 0.000 claims abstract description 18
- -1 siloxanes Chemical class 0.000 claims description 113
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 108
- 150000002009 diols Chemical group 0.000 claims description 106
- 150000001875 compounds Chemical class 0.000 claims description 91
- 229910052757 nitrogen Inorganic materials 0.000 claims description 90
- 239000012634 fragment Substances 0.000 claims description 65
- 239000002253 acid Substances 0.000 claims description 64
- 125000000217 alkyl group Chemical group 0.000 claims description 51
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 50
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 46
- 125000003545 alkoxy group Chemical group 0.000 claims description 46
- 125000004432 carbon atom Chemical group C* 0.000 claims description 46
- 229910052739 hydrogen Inorganic materials 0.000 claims description 45
- 239000001257 hydrogen Substances 0.000 claims description 44
- 230000000996 additive effect Effects 0.000 claims description 42
- 230000000694 effects Effects 0.000 claims description 37
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 36
- 239000002904 solvent Substances 0.000 claims description 36
- 239000004615 ingredient Substances 0.000 claims description 33
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 33
- 150000002148 esters Chemical class 0.000 claims description 28
- 230000000475 sunscreen effect Effects 0.000 claims description 26
- 239000000516 sunscreening agent Substances 0.000 claims description 26
- 150000001412 amines Chemical class 0.000 claims description 23
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- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 21
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- 229930195729 fatty acid Natural products 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 150000004665 fatty acids Chemical class 0.000 claims description 19
- 239000001361 adipic acid Substances 0.000 claims description 18
- 235000011037 adipic acid Nutrition 0.000 claims description 18
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 17
- 239000004094 surface-active agent Substances 0.000 claims description 17
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 16
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 claims description 15
- 125000002947 alkylene group Chemical group 0.000 claims description 15
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 claims description 14
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- 229940114069 12-hydroxystearate Drugs 0.000 claims description 12
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- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims description 12
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 12
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- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 9
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- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 claims description 8
- WYWZRNAHINYAEF-UHFFFAOYSA-N Padimate O Chemical compound CCCCC(CC)COC(=O)C1=CC=C(N(C)C)C=C1 WYWZRNAHINYAEF-UHFFFAOYSA-N 0.000 claims description 8
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- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical group C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 claims description 8
- WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 claims description 8
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- 239000000049 pigment Substances 0.000 claims description 8
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- MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 claims description 7
- WSSJONWNBBTCMG-UHFFFAOYSA-N 2-hydroxybenzoic acid (3,3,5-trimethylcyclohexyl) ester Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C1=CC=CC=C1O WSSJONWNBBTCMG-UHFFFAOYSA-N 0.000 claims description 7
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 7
- XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 claims description 7
- 229960005193 avobenzone Drugs 0.000 claims description 7
- 229940111759 benzophenone-2 Drugs 0.000 claims description 7
- WXNRYSGJLQFHBR-UHFFFAOYSA-N bis(2,4-dihydroxyphenyl)methanone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O WXNRYSGJLQFHBR-UHFFFAOYSA-N 0.000 claims description 7
- SODJJEXAWOSSON-UHFFFAOYSA-N bis(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O SODJJEXAWOSSON-UHFFFAOYSA-N 0.000 claims description 7
- 210000004899 c-terminal region Anatomy 0.000 claims description 7
- 239000003599 detergent Substances 0.000 claims description 7
- CBZHHQOZZQEZNJ-UHFFFAOYSA-N ethyl 4-[bis(2-hydroxypropyl)amino]benzoate Chemical compound CCOC(=O)C1=CC=C(N(CC(C)O)CC(C)O)C=C1 CBZHHQOZZQEZNJ-UHFFFAOYSA-N 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 229960000601 octocrylene Drugs 0.000 claims description 7
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 7
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 claims description 7
- 229960000368 sulisobenzone Drugs 0.000 claims description 7
- HEOCBCNFKCOKBX-RELGSGGGSA-N (1s,2e,4r)-4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical compound C1=CC(C)=CC=C1\C=C/1C(=O)[C@]2(C)CC[C@H]\1C2(C)C HEOCBCNFKCOKBX-RELGSGGGSA-N 0.000 claims description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- 125000005157 alkyl carboxy group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- 150000001924 cycloalkanes Chemical class 0.000 claims description 6
- UVCJGUGAGLDPAA-UHFFFAOYSA-N ensulizole Chemical compound N1C2=CC(S(=O)(=O)O)=CC=C2N=C1C1=CC=CC=C1 UVCJGUGAGLDPAA-UHFFFAOYSA-N 0.000 claims description 6
- 239000003205 fragrance Substances 0.000 claims description 6
- 229960004881 homosalate Drugs 0.000 claims description 6
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 claims description 6
- 239000003921 oil Substances 0.000 claims description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000002562 thickening agent Substances 0.000 claims description 6
- AMOKUAKXKXBFIW-WJDWOHSUSA-N 9-[(z)-non-3-enyl]-10-octylnonadecanedioic acid Chemical compound OC(=O)CCCCCCCCC(CCCCCCCC)C(CCCCCCCC(O)=O)CC\C=C/CCCCC AMOKUAKXKXBFIW-WJDWOHSUSA-N 0.000 claims description 5
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- 150000001298 alcohols Chemical class 0.000 claims description 5
- 239000010408 film Substances 0.000 claims description 5
- 150000002334 glycols Chemical class 0.000 claims description 5
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 5
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- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical class OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 claims description 4
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
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- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
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| EP1590009B1 (en) * | 2002-10-22 | 2012-06-06 | Allegiance Corporation | Coating composition for skin-contacting surface of elastomeric articles and articles containing the same |
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| US9012379B2 (en) * | 2013-03-05 | 2015-04-21 | Halliburton Energy Services, Inc. | Alkyl polyglycoside derivative as biodegradable spacer surfactant |
| US9744116B2 (en) | 2013-09-18 | 2017-08-29 | L'oreal | High color intensity and easily removable mascara |
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-
2003
- 2003-01-31 JP JP2003563486A patent/JP2005516045A/ja not_active Withdrawn
- 2003-01-31 AU AU2003212874A patent/AU2003212874A1/en not_active Abandoned
- 2003-01-31 CN CNA038053519A patent/CN1638718A/zh active Pending
- 2003-01-31 WO PCT/US2003/002898 patent/WO2003063790A2/en not_active Ceased
- 2003-01-31 EP EP03708916.6A patent/EP1469813B1/en not_active Expired - Lifetime
- 2003-01-31 US US10/356,208 patent/US7611725B2/en not_active Expired - Lifetime
-
2009
- 2009-09-22 US US12/586,442 patent/US8414906B2/en not_active Expired - Fee Related
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2010
- 2010-02-15 JP JP2010030168A patent/JP2010174014A/ja not_active Withdrawn
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2014
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2016
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2018
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013069690A1 (ja) * | 2011-11-07 | 2013-05-16 | 日清オイリオグループ株式会社 | 洗浄料用組成物及び洗浄料 |
| KR20140091517A (ko) * | 2011-11-07 | 2014-07-21 | 닛신 오일리오그룹 가부시키가이샤 | 세정료용 조성물 및 세정료 |
| JPWO2013069690A1 (ja) * | 2011-11-07 | 2015-04-02 | 日清オイリオグループ株式会社 | 洗浄料用組成物及び洗浄料 |
| US9428715B2 (en) | 2011-11-07 | 2016-08-30 | The Nisshin Oillio Group, Ltd. | Composition for cleansing agent and cleansing agent |
| KR101940846B1 (ko) | 2011-11-07 | 2019-01-21 | 닛신 오일리오그룹 가부시키가이샤 | 세정료용 조성물 및 세정료 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2015057389A (ja) | 2015-03-26 |
| AU2003212874A1 (en) | 2003-09-02 |
| JP6697030B2 (ja) | 2020-05-20 |
| US7611725B2 (en) | 2009-11-03 |
| US20030199593A1 (en) | 2003-10-23 |
| WO2003063790A2 (en) | 2003-08-07 |
| JP2018165267A (ja) | 2018-10-25 |
| EP1469813A2 (en) | 2004-10-27 |
| WO2003063790A3 (en) | 2003-12-04 |
| EP1469813A4 (en) | 2008-08-27 |
| JP6449834B2 (ja) | 2019-01-09 |
| JP2010174014A (ja) | 2010-08-12 |
| EP1469813B1 (en) | 2016-12-21 |
| CN1638718A (zh) | 2005-07-13 |
| US20100035999A1 (en) | 2010-02-11 |
| US8414906B2 (en) | 2013-04-09 |
| JP2017043629A (ja) | 2017-03-02 |
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