JP2006510362A5 - - Google Patents
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- Publication number
- JP2006510362A5 JP2006510362A5 JP2004560500A JP2004560500A JP2006510362A5 JP 2006510362 A5 JP2006510362 A5 JP 2006510362A5 JP 2004560500 A JP2004560500 A JP 2004560500A JP 2004560500 A JP2004560500 A JP 2004560500A JP 2006510362 A5 JP2006510362 A5 JP 2006510362A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl
- substituted
- atom
- 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.)
- Granted
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- 125000004432 carbon atom Chemical group C* 0.000 claims 136
- 125000000217 alkyl group Chemical group 0.000 claims 55
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 19
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims 13
- 125000004430 oxygen atom Chemical group O* 0.000 claims 13
- 229910052717 sulfur Inorganic materials 0.000 claims 12
- 125000004434 sulfur atom Chemical group 0.000 claims 12
- 125000003545 alkoxy group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- -1 hydroxy- Chemical class 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000002252 acyl group Chemical group 0.000 claims 5
- 125000002877 alkyl aryl group Chemical group 0.000 claims 5
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 5
- 125000004414 alkyl thio group Chemical group 0.000 claims 5
- 125000003277 amino group Chemical group 0.000 claims 5
- 125000003118 aryl group Chemical group 0.000 claims 5
- 150000001721 carbon Chemical group 0.000 claims 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 4
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 125000003884 phenylalkyl group Chemical group 0.000 claims 4
- 125000001544 thienyl group Chemical group 0.000 claims 4
- 125000004423 acyloxy group Chemical group 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 125000005605 benzo group Chemical group 0.000 claims 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 3
- 239000000126 substance Substances 0.000 claims 3
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 2
- 125000005236 alkanoylamino group Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims 2
- 239000003963 antioxidant agent Substances 0.000 claims 2
- 125000006267 biphenyl group Chemical group 0.000 claims 2
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims 2
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 2
- 235000013305 food Nutrition 0.000 claims 2
- 150000002443 hydroxylamines Chemical class 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000004957 naphthylene group Chemical group 0.000 claims 2
- 239000011368 organic material Substances 0.000 claims 2
- 238000010525 oxidative degradation reaction Methods 0.000 claims 2
- 125000005561 phenanthryl group Chemical group 0.000 claims 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 239000003760 tallow Substances 0.000 claims 2
- CWGBFIRHYJNILV-UHFFFAOYSA-N (1,4-diphenyl-1,2,4-triazol-4-ium-3-yl)-phenylazanide Chemical compound C=1C=CC=CC=1[N-]C1=NN(C=2C=CC=CC=2)C=[N+]1C1=CC=CC=C1 CWGBFIRHYJNILV-UHFFFAOYSA-N 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical compound C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims 1
- 101100011369 Caenorhabditis elegans egl-26 gene Proteins 0.000 claims 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000003302 alkenyloxy group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 125000001118 alkylidene group Chemical group 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- GRKUXCWELVWVMZ-UHFFFAOYSA-N amino acetate Chemical compound CC(=O)ON GRKUXCWELVWVMZ-UHFFFAOYSA-N 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 150000001602 bicycloalkyls Chemical group 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000004230 chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 claims 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims 1
- 125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 239000010685 fatty oil Substances 0.000 claims 1
- 239000002778 food additive Substances 0.000 claims 1
- 235000013373 food additive Nutrition 0.000 claims 1
- 235000019261 food antioxidant Nutrition 0.000 claims 1
- 125000003838 furazanyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims 1
- 125000005956 isoquinolyl group Chemical group 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- UBINNYMQZVKNFF-UHFFFAOYSA-N n-benzyl-1-phenylmethanimine oxide Chemical compound C=1C=CC=CC=1C=[N+]([O-])CC1=CC=CC=C1 UBINNYMQZVKNFF-UHFFFAOYSA-N 0.000 claims 1
- LRUUZFQPCUFYPV-UHFFFAOYSA-N n-dodecyldodecan-1-imine oxide Chemical compound CCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCC LRUUZFQPCUFYPV-UHFFFAOYSA-N 0.000 claims 1
- GBMIPYGHTZRCRH-UHFFFAOYSA-N n-ethylethanimine oxide Chemical compound CC[N+]([O-])=CC GBMIPYGHTZRCRH-UHFFFAOYSA-N 0.000 claims 1
- DBCWENWKZARTGU-UHFFFAOYSA-N n-heptadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCCC DBCWENWKZARTGU-UHFFFAOYSA-N 0.000 claims 1
- GCDJFNYVSDFWDB-UHFFFAOYSA-N n-hexadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC GCDJFNYVSDFWDB-UHFFFAOYSA-N 0.000 claims 1
- FHAFFFSIDLDWQA-UHFFFAOYSA-N n-hexadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCC FHAFFFSIDLDWQA-UHFFFAOYSA-N 0.000 claims 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 claims 1
- MGQWDTODAGEVEG-UHFFFAOYSA-N n-methyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+](C)[O-] MGQWDTODAGEVEG-UHFFFAOYSA-N 0.000 claims 1
- FBJWIRNTQZKOLG-UHFFFAOYSA-N n-octadecyl-n-prop-2-enoxyoctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(OCC=C)CCCCCCCCCCCCCCCCCC FBJWIRNTQZKOLG-UHFFFAOYSA-N 0.000 claims 1
- ZXGDIORKSOYRMQ-UHFFFAOYSA-N n-octadecylheptadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCC ZXGDIORKSOYRMQ-UHFFFAOYSA-N 0.000 claims 1
- MCMMSXFAWOGWQE-UHFFFAOYSA-N n-octadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC MCMMSXFAWOGWQE-UHFFFAOYSA-N 0.000 claims 1
- HORBOHJHQGXXOR-UHFFFAOYSA-N n-octadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCCC HORBOHJHQGXXOR-UHFFFAOYSA-N 0.000 claims 1
- QXJGVICBAANVMZ-UHFFFAOYSA-N n-octyloctan-1-imine oxide Chemical compound CCCCCCCC[N+]([O-])=CCCCCCCC QXJGVICBAANVMZ-UHFFFAOYSA-N 0.000 claims 1
- SLYJXPKHTZCZOG-UHFFFAOYSA-N n-tetradecyltetradecan-1-imine oxide Chemical compound CCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCC SLYJXPKHTZCZOG-UHFFFAOYSA-N 0.000 claims 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000005327 perimidinyl group Chemical group N1C(=NC2=CC=CC3=CC=CC1=C23)* 0.000 claims 1
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 claims 1
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 claims 1
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 claims 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 claims 1
- 125000005954 phenoxathiinyl group Chemical group 0.000 claims 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 claims 1
- 125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
- 125000002071 phenylalkoxy group Chemical group 0.000 claims 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 1
- 125000005493 quinolyl group Chemical group 0.000 claims 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 239000000375 suspending agent Substances 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- 125000005270 trialkylamine group Chemical group 0.000 claims 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 claims 1
- 125000004933 β-carbolinyl group Chemical group C1(=NC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 1
- 0 *C(*)(*)*C(*)(c1c(*)c(*)c(*)c(*)c1O1)C1=O Chemical compound *C(*)(*)*C(*)(c1c(*)c(*)c(*)c(*)c1O1)C1=O 0.000 description 3
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43471502P | 2002-12-18 | 2002-12-18 | |
| PCT/EP2003/050954 WO2004055141A2 (en) | 2002-12-18 | 2003-12-08 | Antioxidant for fats, oils and food |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006510362A JP2006510362A (ja) | 2006-03-30 |
| JP2006510362A5 true JP2006510362A5 (https=) | 2007-01-18 |
| JP4484712B2 JP4484712B2 (ja) | 2010-06-16 |
Family
ID=32595300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004560500A Expired - Fee Related JP4484712B2 (ja) | 2002-12-18 | 2003-12-08 | 脂肪、油及び食品のための抗酸化剤 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US20060051478A1 (https=) |
| EP (1) | EP1571928A2 (https=) |
| JP (1) | JP4484712B2 (https=) |
| KR (1) | KR20050089968A (https=) |
| CN (1) | CN1726026B (https=) |
| AU (1) | AU2003302176A1 (https=) |
| BR (1) | BR0317474A (https=) |
| MX (1) | MXPA05006544A (https=) |
| WO (1) | WO2004055141A2 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5384791B2 (ja) | 2003-11-03 | 2014-01-08 | チバ ホールディング インコーポレーテッド | 安定化されたボディケア製品、家庭用製品、生地及び繊維 |
| WO2005070913A1 (en) * | 2004-01-22 | 2005-08-04 | University Of Ottawa | Thermally modulated antioxidants |
| KR100641506B1 (ko) * | 2004-09-17 | 2006-11-01 | 동부일렉트로닉스 주식회사 | 반도체 소자 세정 방법 |
| KR100639969B1 (ko) * | 2004-12-02 | 2006-11-01 | 한국전자통신연구원 | 이상 트래픽 제어 장치 및 그 제어 방법 |
| CA2646216A1 (en) * | 2006-01-04 | 2007-07-12 | Ciba Holding Inc. | Stabilized biodiesel fuel compositions |
| CN102603719B (zh) * | 2011-01-25 | 2015-12-16 | 北京贵千金医药科技有限公司 | 化合物2-糠醇-(5’→11)-1,3-环戊二烯并[5,4-c]-1H-噌啉及其作为抗氧化剂在食品、化妆品或药品中的应用 |
| JP6241702B2 (ja) * | 2012-09-14 | 2017-12-06 | 国立大学法人九州大学 | メカノクロミック材料 |
| KR101792548B1 (ko) * | 2014-12-22 | 2017-11-03 | 주식회사농심 | 수중유적형 나노항산화제의 제조 방법 및 이를 이용한 가공식품의 유통기한 향상방법 |
| CN109642177B (zh) * | 2016-09-20 | 2022-01-04 | 朗盛解决方案美国公司 | 烷基化3-羟基二苯胺抗氧化剂 |
| CN120290045B (zh) * | 2025-06-13 | 2025-09-12 | 三宝科技(湖州)有限公司 | 一种生物质环保色浆及其制备方法和应用 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2654722A (en) * | 1950-09-16 | 1953-10-06 | Standard Oil Dev Co | Stabilized solid organic compositions containing acyl-p-aminophenols |
| US2768084A (en) * | 1952-06-25 | 1956-10-23 | Griffith Laboratories | Oil soluble synergistic antioxidant |
| GB1174051A (en) * | 1965-11-30 | 1969-12-10 | Beecham Group Ltd | Aminophenol Derivatives and Analgesic and Antipyretic Compositions |
| US3778464A (en) * | 1972-10-10 | 1973-12-11 | P Klemchuk | Substituted hydroxylamine anti-oxidants |
| US4038434A (en) * | 1976-03-12 | 1977-07-26 | Howard Hall & Company | Antioxidant stabilized edible compositions |
| US4094999A (en) * | 1977-08-08 | 1978-06-13 | Borg-Warner Corporation | Antioxidant for foods |
| HU182010B (en) * | 1979-02-21 | 1983-12-28 | Chinoin Gyogyszer Es Vegyeszet | Novel 2,2-dimethyl-1,2-dihydro-quinoline derivatives having anti-oxidant activity |
| US4925681A (en) * | 1983-12-15 | 1990-05-15 | Nestec S.A. | Process for inhibiting lipid oxidation in food and composition thereby |
| US4876300A (en) * | 1987-12-30 | 1989-10-24 | Ciba-Geigy Corporation | Polyolefin compositions stabilized with long chain N,N-dialkylhydroxylamines |
| KR910004884B1 (ko) * | 1989-02-01 | 1991-07-15 | 한국식품개발연구원 | 유지류의 산화억제방법 |
| EP0692934A4 (en) * | 1993-04-01 | 1997-11-26 | Kalamazoo Holdings Inc | FAT-SOLUBLE ANTIOXIDANT SOLUTIONS WITH GREEN TEA CATECHIN |
| CH686306A5 (de) * | 1993-09-17 | 1996-02-29 | Ciba Geigy Ag | 3-Aryl-benzofuranone als Stabilisatoren. |
| US5922794A (en) * | 1997-03-26 | 1999-07-13 | General Electric Company | Compositions stabilized with tertiary amine oxides |
-
2003
- 2003-12-08 US US10/538,891 patent/US20060051478A1/en not_active Abandoned
- 2003-12-08 JP JP2004560500A patent/JP4484712B2/ja not_active Expired - Fee Related
- 2003-12-08 BR BR0317474-3A patent/BR0317474A/pt not_active IP Right Cessation
- 2003-12-08 KR KR1020057010902A patent/KR20050089968A/ko not_active Ceased
- 2003-12-08 CN CN2003801064960A patent/CN1726026B/zh not_active Expired - Fee Related
- 2003-12-08 MX MXPA05006544A patent/MXPA05006544A/es not_active Application Discontinuation
- 2003-12-08 WO PCT/EP2003/050954 patent/WO2004055141A2/en not_active Ceased
- 2003-12-08 AU AU2003302176A patent/AU2003302176A1/en not_active Abandoned
- 2003-12-08 EP EP03809982A patent/EP1571928A2/en not_active Withdrawn
-
2008
- 2008-07-30 US US12/221,005 patent/US20080286430A1/en not_active Abandoned
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