JP2009522421A5 - - Google Patents
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- JP2009522421A5 JP2009522421A5 JP2008548982A JP2008548982A JP2009522421A5 JP 2009522421 A5 JP2009522421 A5 JP 2009522421A5 JP 2008548982 A JP2008548982 A JP 2008548982A JP 2008548982 A JP2008548982 A JP 2008548982A JP 2009522421 A5 JP2009522421 A5 JP 2009522421A5
- 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.)
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- 125000004432 carbon atom Chemical group C* 0.000 claims 100
- 125000000217 alkyl group Chemical group 0.000 claims 30
- -1 5,6,7,8-tetrahydro- 2-naphthyl group Chemical group 0.000 claims 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 14
- 125000004430 oxygen atom Chemical group O* 0.000 claims 14
- 229910052717 sulfur Inorganic materials 0.000 claims 12
- 125000004434 sulfur atom Chemical group 0.000 claims 12
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 11
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 7
- 150000001721 carbon Chemical group 0.000 claims 6
- 125000002252 acyl group Chemical group 0.000 claims 5
- 125000004414 alkyl thio group Chemical group 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 125000004423 acyloxy group Chemical group 0.000 claims 4
- 150000001412 amines Chemical class 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
- 150000002148 esters Chemical class 0.000 claims 4
- 125000003884 phenylalkyl group Chemical group 0.000 claims 4
- 125000001544 thienyl group Chemical group 0.000 claims 4
- 125000003277 amino group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 150000005846 sugar alcohols Polymers 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
- 239000000654 additive Substances 0.000 claims 2
- 125000005236 alkanoylamino 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
- 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
- 125000004429 atom Chemical group 0.000 claims 2
- 125000005605 benzo group Chemical group 0.000 claims 2
- 239000003225 biodiesel Substances 0.000 claims 2
- 125000006267 biphenyl group Chemical group 0.000 claims 2
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 239000004611 light stabiliser Substances 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000004957 naphthylene group Chemical group 0.000 claims 2
- 125000005561 phenanthryl group Chemical group 0.000 claims 2
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 239000003381 stabilizer Substances 0.000 claims 2
- QLMGIWHWWWXXME-UHFFFAOYSA-N 2-(3,5-ditert-butyl-4-hydroxyphenyl)acetic acid Chemical compound CC(C)(C)C1=CC(CC(O)=O)=CC(C(C)(C)C)=C1O QLMGIWHWWWXXME-UHFFFAOYSA-N 0.000 claims 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 claims 1
- FLZYQMOKBVFXJS-UHFFFAOYSA-N 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoic acid Chemical compound CC1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O FLZYQMOKBVFXJS-UHFFFAOYSA-N 0.000 claims 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 claims 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 claims 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 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
- 125000003342 alkenyl group Chemical group 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
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- OGBVRMYSNSKIEF-UHFFFAOYSA-L benzyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)CC1=CC=CC=C1 OGBVRMYSNSKIEF-UHFFFAOYSA-L 0.000 claims 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 claims 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 claims 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 claims 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 claims 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 1
- 125000002837 carbocyclic 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
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims 1
- 125000002993 cycloalkylene group Chemical group 0.000 claims 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims 1
- 125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 claims 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical group C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims 1
- 125000003838 furazanyl group Chemical group 0.000 claims 1
- 230000009931 harmful effect Effects 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 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
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 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
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 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
- 239000002530 phenolic antioxidant Substances 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 group [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
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims 1
- 235000019260 propionic acid Nutrition 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
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 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
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims 1
- 235000010384 tocopherol Nutrition 0.000 claims 1
- 229960001295 tocopherol Drugs 0.000 claims 1
- 229930003799 tocopherol Natural products 0.000 claims 1
- 239000011732 tocopherol Substances 0.000 claims 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 claims 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75609006P | 2006-01-04 | 2006-01-04 | |
| PCT/EP2006/070139 WO2007077165A1 (en) | 2006-01-04 | 2006-12-22 | Stabilized biodiesel fuel compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009522421A JP2009522421A (ja) | 2009-06-11 |
| JP2009522421A5 true JP2009522421A5 (enExample) | 2010-02-18 |
Family
ID=37964370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008548982A Pending JP2009522421A (ja) | 2006-01-04 | 2006-12-22 | 安定化されたバイオディーゼル燃料組成物 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20070151143A1 (enExample) |
| EP (1) | EP1969097A1 (enExample) |
| JP (1) | JP2009522421A (enExample) |
| KR (1) | KR20080089386A (enExample) |
| CN (1) | CN101351531A (enExample) |
| AU (1) | AU2006334370A1 (enExample) |
| BR (1) | BRPI0620902A2 (enExample) |
| CA (1) | CA2646216A1 (enExample) |
| MX (1) | MX2008008745A (enExample) |
| TW (1) | TW200745323A (enExample) |
| WO (1) | WO2007077165A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20080040640A (ko) * | 2005-07-07 | 2008-05-08 | 시바 스폐셜티 케미칼스 홀딩 인코포레이티드 | 포스포네이트의 존재 하에서 폴리아미드의 제조방법 |
| CN101535451A (zh) * | 2006-07-11 | 2009-09-16 | 英诺斯派克燃料专业有限责任公司 | 石油和可再生燃料混合物的稳定剂组合物 |
| US8430936B2 (en) | 2007-11-30 | 2013-04-30 | Baker Hughes Incorporated | Stabilization of fatty oils and esters with alkyl phenol amine aldehyde condensates |
| EP2342311B1 (en) * | 2008-09-17 | 2016-03-09 | ExxonMobil Research and Engineering Company | Method for improving the oxidation stability of biodiesel as measured by the rancimat test |
| EP2174554A3 (en) * | 2008-10-09 | 2011-01-12 | Infineum International Limited | Improving the oxidation stability of oils of vegetable or animal origin |
| US20100107474A1 (en) * | 2008-10-31 | 2010-05-06 | Mahesh Talwar | Apparatus and method for Rapid Biodiesel Fuel Production |
| US20110016772A1 (en) * | 2009-07-24 | 2011-01-27 | Mahesh Talwar | Acid Esterification Through Nano Reactor |
| US8680029B2 (en) * | 2009-10-02 | 2014-03-25 | Exxonmobil Research And Engineering Company | Lubricating oil compositions for biodiesel fueled engines |
| US8367593B2 (en) * | 2009-10-02 | 2013-02-05 | Exxonmobil Research And Engineering Company | Method for improving the resistance to one or more of corrosion, oxidation, sludge and deposit formation of lubricating oil compositions for biodiesel fueled engines |
| JP5756972B2 (ja) | 2010-02-24 | 2015-07-29 | 国立研究開発法人産業技術総合研究所 | バイオディーゼル燃料の製造方法及びバイオディーゼル燃料組成物 |
| JP5921667B2 (ja) * | 2011-03-25 | 2016-05-24 | エボニック オイル アディティヴス ゲゼルシャフト ミット ベシュレンクテル ハフツングＥｖｏｎｉｋ Ｏｉｌ Ａｄｄｉｔｉｖｅｓ ＧｍｂＨ | 燃料油の酸化安定性を向上させるための組成物 |
| US20130104447A1 (en) | 2011-10-28 | 2013-05-02 | Exxonmobil Research And Engineering Company | Dye-stable biofuel blend compositions |
| EP2816097A1 (en) | 2013-06-18 | 2014-12-24 | Shell Internationale Research Maatschappij B.V. | Lubricating oil composition |
| JP6229791B2 (ja) | 2014-03-03 | 2017-11-15 | 国立研究開発法人産業技術総合研究所 | バイオディーゼル燃料の水素化処理方法 |
| CN105985865B (zh) * | 2015-02-02 | 2019-07-05 | 中国石油天然气股份有限公司 | 一种非食用动植物油的储存方法 |
| WO2016156328A1 (en) | 2015-03-31 | 2016-10-06 | Shell Internationale Research Maatschappij B.V. | Use of a lubricating composition comprising a hindered amine light stabilizer for improved piston cleanliness in an internal combustion engine |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4191682A (en) * | 1976-06-28 | 1980-03-04 | Ciba-Geigy Corporation | Hindered piperidine carboxylic acids, metal salts thereof and stabilized compositions |
| US5185448A (en) * | 1991-05-07 | 1993-02-09 | Ciba-Geigy Corporation | Substituted 1-oxy-4-acyloxypiperidine and 1-oxy-4-acylaminopiperidine stabilizers |
| CH686306A5 (de) * | 1993-09-17 | 1996-02-29 | Ciba Geigy Ag | 3-Aryl-benzofuranone als Stabilisatoren. |
| DE19756276A1 (de) * | 1997-12-18 | 1999-06-24 | Basf Ag | Verwendung von durch sterisch gehinderte Amine oder deren N-Hydroxy- oder N-Oxylderivate stabilisierten Ethylenhomo- und -copolymeren zur Herstellung von Kunststoffkörpern und Bauteilen für die Lagerung und den Transport von Pflanzenölestern |
| KR100596075B1 (ko) * | 1998-02-25 | 2006-07-03 | 시바 스폐셜티 케미칼스 홀딩 인코포레이티드 | 액체 다관능성 첨가제 |
| EP1263860A1 (en) * | 2000-02-14 | 2002-12-11 | Ciba SC Holding AG | New 3-arylbenzofuranones with electron-withdrawing substituents as stabilizers |
| US20060201056A1 (en) * | 2000-04-14 | 2006-09-14 | Oryxe Energy International, Inc. | Biodiesel fuel additive |
| US20050160662A1 (en) * | 2002-06-11 | 2005-07-28 | Oryxe Energy International, Inc. | Method and composition for using stabilized beta-carotene as cetane improver in hydrocarbonaceous diesel fuels |
| ES2308038T3 (es) * | 2002-11-13 | 2008-12-01 | Lanxess Deutschland Gmbh | Uso de 2,6-di-terc-butil-p-cresol para el aumento de la estabilidad al almacenamiento de biodiesel. |
| WO2004055141A2 (en) * | 2002-12-18 | 2004-07-01 | Ciba Specialty Chemicals Holding Inc. | Antioxidant for fats, oils and food |
| JP4648618B2 (ja) * | 2003-09-16 | 2011-03-09 | Ｊｘ日鉱日石エネルギー株式会社 | 軽油組成物 |
| JP2007016089A (ja) * | 2005-07-06 | 2007-01-25 | Nissan Motor Co Ltd | バイオディーゼル燃料組成物及びその使用方法 |
-
2006
- 2006-12-22 MX MX2008008745A patent/MX2008008745A/es unknown
- 2006-12-22 BR BRPI0620902-5A patent/BRPI0620902A2/pt not_active IP Right Cessation
- 2006-12-22 AU AU2006334370A patent/AU2006334370A1/en not_active Abandoned
- 2006-12-22 CA CA002646216A patent/CA2646216A1/en not_active Abandoned
- 2006-12-22 KR KR1020087016560A patent/KR20080089386A/ko not_active Withdrawn
- 2006-12-22 CN CNA2006800503485A patent/CN101351531A/zh active Pending
- 2006-12-22 EP EP06830796A patent/EP1969097A1/en not_active Withdrawn
- 2006-12-22 JP JP2008548982A patent/JP2009522421A/ja active Pending
- 2006-12-22 WO PCT/EP2006/070139 patent/WO2007077165A1/en not_active Ceased
-
2007
- 2007-01-02 US US11/648,329 patent/US20070151143A1/en not_active Abandoned
- 2007-01-02 TW TW096100006A patent/TW200745323A/zh unknown
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