JP2002518488A5 - - Google Patents
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- Publication number
- JP2002518488A5 JP2002518488A5 JP2000555880A JP2000555880A JP2002518488A5 JP 2002518488 A5 JP2002518488 A5 JP 2002518488A5 JP 2000555880 A JP2000555880 A JP 2000555880A JP 2000555880 A JP2000555880 A JP 2000555880A JP 2002518488 A5 JP2002518488 A5 JP 2002518488A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrocarbyl
- functional
- alkyl
- formula
- coo
- 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.)
- Withdrawn
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- 125000001183 hydrocarbyl group Chemical group 0.000 description 150
- 125000000217 alkyl group Chemical group 0.000 description 23
- 229910052739 hydrogen Inorganic materials 0.000 description 20
- 239000001257 hydrogen Substances 0.000 description 20
- 150000001875 compounds Chemical class 0.000 description 13
- 150000002431 hydrogen Chemical class 0.000 description 13
- 230000005855 radiation Effects 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 125000002947 alkylene group Chemical group 0.000 description 10
- 229910052736 halogen Inorganic materials 0.000 description 9
- 150000002367 halogens Chemical class 0.000 description 9
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical group C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 description 6
- 125000004957 naphthylene group Chemical group 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 125000004430 oxygen atom Chemical group O* 0.000 description 5
- 125000006834 (C4-C20) alkylene group Chemical group 0.000 description 4
- 125000004450 alkenylene group Chemical group 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- -1 glycidyloxy Chemical group 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- SVSARCCKBMZNMR-UHFFFAOYSA-N [1-[2-[methyl-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethyl]amino]ethyl]pyridin-4-ylidene]methyl-oxoazanium;dichloride Chemical compound [Cl-].[Cl-].C1=CC(=C[NH+]=O)C=CN1CCN(C)CCN1C=CC(=C[NH+]=O)C=C1 SVSARCCKBMZNMR-UHFFFAOYSA-N 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 125000006839 xylylene group Chemical group 0.000 description 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9024798P | 1998-06-22 | 1998-06-22 | |
| US60/090,247 | 1998-06-22 | ||
| PCT/US1999/013825 WO1999067226A1 (en) | 1998-06-22 | 1999-06-18 | Non-yellowing para-tertiary-alkyl phenyl substituted triazine and pyrimidine ultraviolet light absorbers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002518488A JP2002518488A (ja) | 2002-06-25 |
| JP2002518488A5 true JP2002518488A5 (https=) | 2006-08-03 |
Family
ID=22221957
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000555880A Withdrawn JP2002518488A (ja) | 1998-06-22 | 1999-06-18 | 黄変しない、パラ第三級アルキルフェニル置換トリアジン及びピリミジン紫外線吸収剤 |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1089984B1 (https=) |
| JP (1) | JP2002518488A (https=) |
| KR (1) | KR20010053057A (https=) |
| CN (1) | CN1203065C (https=) |
| AT (1) | ATE280762T1 (https=) |
| AU (1) | AU755175B2 (https=) |
| BR (1) | BR9911401A (https=) |
| CA (1) | CA2335580A1 (https=) |
| DE (1) | DE69921478T2 (https=) |
| IL (1) | IL140448A0 (https=) |
| TW (1) | TW502027B (https=) |
| WO (1) | WO1999067226A1 (https=) |
| ZA (1) | ZA200006088B (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4557335B2 (ja) * | 1999-08-17 | 2010-10-06 | 株式会社資生堂 | 水溶性紫外線吸収剤及びこれを含有する紫外線吸収性組成物、皮膚外用剤 |
| JP2003532752A (ja) * | 2000-04-13 | 2003-11-05 | スリーエム イノベイティブ プロパティズ カンパニー | 光安定性の製品 |
| US6800757B2 (en) * | 2001-09-27 | 2004-10-05 | Cytec Technology Corp. | Red-shifted triazine ultravioletlight absorbers |
| US6855269B2 (en) | 2001-11-09 | 2005-02-15 | Cytec Technology Corp. | Phenyl ether-substituted hydroxyphenyl triazine ultraviolet light absorbers |
| WO2006115015A1 (ja) * | 2005-04-18 | 2006-11-02 | Konica Minolta Opto, Inc. | セルロースエステルフィルム及びその製造方法、光学フィルム、偏光板及び液晶表示装置 |
| JP2010287310A (ja) * | 2007-10-12 | 2010-12-24 | Asahi Glass Co Ltd | 光学フィルタ |
| ES2463674T3 (es) | 2009-01-19 | 2014-05-28 | Basf Se | Pigmentos negros orgánicos y su preparación |
| JP5600631B2 (ja) * | 2011-03-31 | 2014-10-01 | 富士フイルム株式会社 | 光学フィルムとその製造方法、偏光板および液晶表示装置 |
| WO2012170173A1 (en) * | 2011-06-09 | 2012-12-13 | Angus Chemical Company | Composition and method for removing excess formaldehyde |
| WO2013043987A1 (en) | 2011-09-21 | 2013-03-28 | Donaldson Company, Inc. | Fine fibers made from polymer crosslinked with resinous aldehyde composition |
| KR102139254B1 (ko) | 2013-03-09 | 2020-07-29 | 도널드선 컴파니 인코포레이티드 | 반응성 첨가제로부터 제조된 미세 섬유 |
| KR101710186B1 (ko) * | 2016-09-01 | 2017-03-10 | (주)에이씨티 | 6-아미노헥사노산 유도체 및 그 유도체를 함유하는 광반응성 화장료 조성물 |
| JP7673384B2 (ja) * | 2020-11-13 | 2025-05-09 | ａｒｔｉｅｎｃｅ株式会社 | 樹脂組成物、および成形体 |
| KR102563288B1 (ko) * | 2020-08-12 | 2023-08-02 | 삼성에스디아이 주식회사 | 레지스트 하층막용 조성물 및 이를 이용한 패턴형성방법 |
| CN112641651A (zh) * | 2020-12-29 | 2021-04-13 | 宁波市江北区伊人宝贸易有限公司 | 一种美白抗皱化妆品的制备方法 |
| CN120867094A (zh) * | 2025-09-26 | 2025-10-31 | 苏州大学 | 一种丝绸修复加固方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE639330A (https=) * | 1962-10-30 | |||
| CH484695A (de) * | 1962-10-30 | 1970-01-31 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Ultraviolettschutzmittel ausserhalb der Textilindustrie |
| CH480090A (de) * | 1962-10-30 | 1969-10-31 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Ultraviolettschutzmittel ausserhalb der Textilindustrie |
| NL130993C (https=) * | 1963-02-07 | |||
| CH469053A (de) * | 1963-07-26 | 1969-02-28 | Ciba Geigy | Verwendung von neuen Hydroxyphenyl-1,3,5-triazinen als Schutzmittel gegen Ultraviolettstrahlung für nichttextile organische Materialien |
| CH473818A (de) * | 1964-03-18 | 1969-06-15 | Ciba Geigy | Verfahren zur Herstellung von neuen Hydroxyphenyl-1,3,5-triazinen und deren Verwendung |
| US3660404A (en) * | 1969-02-24 | 1972-05-02 | Du Pont | U.v.-absorbing ortho-hydroxyphenyl substituted bipyrimidyls |
| EP0434619B1 (de) * | 1989-12-21 | 1995-09-06 | Ciba SC Holding AG | Verfahren zum Einbau von O-Hydroxyphenyl-S-triazinen in organische Polymere |
-
1999
- 1999-06-18 BR BR9911401-1A patent/BR9911401A/pt not_active IP Right Cessation
- 1999-06-18 WO PCT/US1999/013825 patent/WO1999067226A1/en not_active Ceased
- 1999-06-18 CN CNB998075329A patent/CN1203065C/zh not_active Expired - Fee Related
- 1999-06-18 CA CA002335580A patent/CA2335580A1/en not_active Abandoned
- 1999-06-18 JP JP2000555880A patent/JP2002518488A/ja not_active Withdrawn
- 1999-06-18 EP EP99928797A patent/EP1089984B1/en not_active Expired - Lifetime
- 1999-06-18 DE DE69921478T patent/DE69921478T2/de not_active Expired - Fee Related
- 1999-06-18 IL IL14044899A patent/IL140448A0/xx unknown
- 1999-06-18 AT AT99928797T patent/ATE280762T1/de not_active IP Right Cessation
- 1999-06-18 AU AU45783/99A patent/AU755175B2/en not_active Ceased
- 1999-06-18 KR KR1020007014519A patent/KR20010053057A/ko not_active Abandoned
- 1999-06-22 TW TW088110460A patent/TW502027B/zh not_active IP Right Cessation
-
2000
- 2000-10-27 ZA ZA200006088A patent/ZA200006088B/xx unknown
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