JP2002504618A5 - - Google Patents
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- Publication number
- JP2002504618A5 JP2002504618A5 JP2000533505A JP2000533505A JP2002504618A5 JP 2002504618 A5 JP2002504618 A5 JP 2002504618A5 JP 2000533505 A JP2000533505 A JP 2000533505A JP 2000533505 A JP2000533505 A JP 2000533505A JP 2002504618 A5 JP2002504618 A5 JP 2002504618A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- group
- formula
- compound
- compounds
- 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 description 28
- 150000001875 compounds Chemical class 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000003884 phenylalkyl group Chemical group 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 125000004434 sulfur atom Chemical group 0.000 description 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 3
- 150000001335 aliphatic alkanes Chemical group 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 description 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- UYCICMIUKYEYEU-ZHACJKMWSA-N 3-[(e)-dodec-2-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCC\C=C\CC1CC(=O)OC1=O UYCICMIUKYEYEU-ZHACJKMWSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000005020 hydroxyalkenyl group Chemical group 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH44998 | 1998-02-25 | ||
| CH449/98 | 1998-02-25 | ||
| PCT/EP1999/001000 WO1999043762A1 (en) | 1998-02-25 | 1999-02-16 | Liquid polyfunctional additives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002504618A JP2002504618A (ja) | 2002-02-12 |
| JP2002504618A5 true JP2002504618A5 (enExample) | 2006-03-09 |
| JP4355986B2 JP4355986B2 (ja) | 2009-11-04 |
Family
ID=4187292
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000533505A Expired - Fee Related JP4355986B2 (ja) | 1998-02-25 | 1999-02-16 | 液体多機能性添加剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6448208B1 (enExample) |
| EP (1) | EP1060225B1 (enExample) |
| JP (1) | JP4355986B2 (enExample) |
| KR (1) | KR100596075B1 (enExample) |
| AU (1) | AU2834499A (enExample) |
| DE (1) | DE69927486T2 (enExample) |
| WO (1) | WO1999043762A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2368848B (en) * | 2000-09-21 | 2002-11-27 | Ciba Sc Holding Ag | Lubricants with 5-tert.-butyl-hydroxy-3-methylphenyl substituted fatty acid esters |
| JP3732773B2 (ja) * | 2001-08-08 | 2006-01-11 | ショーワ株式会社 | 熱媒体組成物 |
| ATE367382T1 (de) * | 2003-12-25 | 2007-08-15 | Council Scient Ind Res | Antiozonant funktionalisierte benzotriazole uv absorber und ihre herstellungsverfahren |
| US7329772B2 (en) * | 2004-04-29 | 2008-02-12 | Crompton Corporation | Method for the preparation of a hydroxyalkyl hindered phenolic antioxidant |
| WO2007077165A1 (en) * | 2006-01-04 | 2007-07-12 | Ciba Holding Inc. | Stabilized biodiesel fuel compositions |
| DE102007005863B4 (de) * | 2007-02-06 | 2009-12-24 | Sprügel, Friedrich A. | Additiv für Flüssiggas-Treibstoffe und seine Verwendung |
| DE102007027371A1 (de) * | 2007-06-11 | 2008-12-18 | Cognis Oleochemicals Gmbh | Verfahren zur Herstellung einer Verbindung aufweisend mindestens eine Ester-Gruppe |
| WO2009010441A2 (de) * | 2007-07-16 | 2009-01-22 | Basf Se | Synergistische mischung |
| EP2215156B1 (de) | 2007-11-28 | 2013-01-09 | Basf Se | Flüssige stabilisatormischung |
| US7897552B2 (en) * | 2007-11-30 | 2011-03-01 | Afton Chemical Corporation | Additives and lubricant formulations for improved antioxidant properties |
| US8377856B2 (en) | 2009-05-14 | 2013-02-19 | Afton Chemical Corporation | Extended drain diesel lubricant formulations |
| US20100292112A1 (en) * | 2009-05-14 | 2010-11-18 | Afton Chemical Corporation | Extended drain diesel lubricant formulations |
| KR101102577B1 (ko) * | 2010-04-21 | 2012-01-03 | 주식회사 비씨엠케이 | 커넥터 |
| US8343901B2 (en) | 2010-10-12 | 2013-01-01 | Chevron Oronite Company Llc | Lubricating composition containing multifunctional hydroxylated amine salt of a hindered phenolic acid |
| FR2980799B1 (fr) * | 2011-09-29 | 2013-10-04 | Total Raffinage Marketing | Composition lubrifiante pour moteur marin |
| CN104884584B (zh) * | 2012-12-21 | 2017-03-08 | 国际壳牌研究有限公司 | 含有有机遮光化合物的液体柴油燃料组合物 |
| JP6548640B2 (ja) * | 2013-10-24 | 2019-07-24 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイＳｈｅｌｌ Ｉｎｔｅｒｎａｔｉｏｎａｌｅ Ｒｅｓｅａｒｃｈ Ｍａａｔｓｃｈａｐｐｉｊ Ｂｅｓｌｏｔｅｎ Ｖｅｎｎｏｏｔｓｈａｐ | 液体燃料組成物 |
| EP2949732B1 (en) * | 2014-05-28 | 2018-06-20 | Shell International Research Maatschappij B.V. | Use of an oxanilide compound in a diesel fuel composition for the purpose of modifying the ignition delay and/or the burn period |
| WO2025109156A1 (en) * | 2023-11-24 | 2025-05-30 | Totalenergies Onetech | Use of glycerol ester as antiwear agent |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3839278A (en) | 1971-07-01 | 1974-10-01 | Ciba Geigy Corp | 3,5-dialkyl-4-hydroxyphenylalkanoic acid esters antioxidants |
| US4132702A (en) | 1974-03-27 | 1979-01-02 | Ciba-Geigy Corporation | Phenol esters and amides and polymers stabilized therewith |
| US4093587A (en) | 1974-07-23 | 1978-06-06 | Ciba-Geigy Corporation | Trisubstituted hydroxyphenylalkanoic acid ester and amide stabilized compositions |
| US4032562A (en) | 1974-11-05 | 1977-06-28 | Ciba-Geigy Corporation | 3,5-dialkyl-4-hydroxyphenylalkanoic acid esters of polyalkylene glycols |
| US4058502A (en) | 1974-12-12 | 1977-11-15 | Ciba-Geigy Corporation | Stabilized compositions containing hindered hydroxyalkanoates |
| US4101550A (en) * | 1976-05-03 | 1978-07-18 | Ciba-Geigy Corporation | Bis-piperazides of trisubstituted hydroxyphenylalkanoic acids |
| US5155244A (en) * | 1990-02-28 | 1992-10-13 | Karlshamns Ab | Preparation of antioxidant glyceride derivatives utilizing esterification |
| ES2101994T3 (es) * | 1992-04-08 | 1997-07-16 | Ciba Geigy Ag | Antioxidantes liquidos como estabilizadores. |
| ATE184310T1 (de) * | 1992-06-03 | 1999-09-15 | Henkel Corp | Polyol/ester-gemisch als schmiermittel für wärmeträgerflüssigkeiten in kälteanlagen |
| TW327185B (en) * | 1993-09-20 | 1998-02-21 | Ciba Sc Holding Ag | Liquid antioxidants |
| ES2248887T3 (es) * | 1997-02-03 | 2006-03-16 | Ciba Specialty Chemicals Holding Inc. | Aditivos liquidos polifuncionales para mejorar la lubricidad de carburantes. |
| GB2325239B (en) * | 1997-05-13 | 2001-08-08 | Ciba Sc Holding Ag | Liquid polyfunctional additives |
| GB2325472B (en) * | 1997-05-20 | 2001-06-06 | Ciba Sc Holding Ag | Liquid multifunctional additives |
| US6046263A (en) | 1997-05-26 | 2000-04-04 | Ciba Specialty Chemicals Corporation | Liquid antioxidants as stabilizers |
| BE1014162A3 (fr) * | 1997-05-26 | 2003-06-03 | Ciba Sc Holding Ag | Produits stabilisants, compositions et concentres les contenant, et leur procede d'utilisation. |
-
1999
- 1999-02-16 DE DE69927486T patent/DE69927486T2/de not_active Expired - Lifetime
- 1999-02-16 EP EP99908911A patent/EP1060225B1/en not_active Expired - Lifetime
- 1999-02-16 US US09/622,707 patent/US6448208B1/en not_active Expired - Fee Related
- 1999-02-16 AU AU28344/99A patent/AU2834499A/en not_active Abandoned
- 1999-02-16 KR KR20007009464A patent/KR100596075B1/ko not_active Expired - Fee Related
- 1999-02-16 WO PCT/EP1999/001000 patent/WO1999043762A1/en not_active Ceased
- 1999-02-16 JP JP2000533505A patent/JP4355986B2/ja not_active Expired - Fee Related
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