GB1103145A - Process for the preparation of organic esters - Google Patents
Process for the preparation of organic estersInfo
- Publication number
- GB1103145A GB1103145A GB23339/65A GB2333965A GB1103145A GB 1103145 A GB1103145 A GB 1103145A GB 23339/65 A GB23339/65 A GB 23339/65A GB 2333965 A GB2333965 A GB 2333965A GB 1103145 A GB1103145 A GB 1103145A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tert
- butyl
- hydroxyphenyl
- carbon atoms
- residue
- 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title abstract 3
- 150000002895 organic esters Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 18
- 150000002148 esters Chemical class 0.000 abstract 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 7
- -1 polyethylene Polymers 0.000 abstract 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 5
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 abstract 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- 239000007858 starting material Substances 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 150000002894 organic compounds Chemical class 0.000 abstract 3
- 239000003381 stabilizer Substances 0.000 abstract 3
- 150000003568 thioethers Chemical group 0.000 abstract 3
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 3
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
- 125000002723 alicyclic group Chemical group 0.000 abstract 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 abstract 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 abstract 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 abstract 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 abstract 2
- 230000000087 stabilizing effect Effects 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- YAXKTBLXMTYWDQ-UHFFFAOYSA-N 1,2,3-butanetriol Chemical compound CC(O)C(O)CO YAXKTBLXMTYWDQ-UHFFFAOYSA-N 0.000 abstract 1
- 229940031723 1,2-octanediol Drugs 0.000 abstract 1
- TZLNEJKFOLYZRP-UHFFFAOYSA-N 1-(2-octylsulfanylethylsulfanyl)ethanol Chemical compound C(CCCCCCC)SCCSC(C)O TZLNEJKFOLYZRP-UHFFFAOYSA-N 0.000 abstract 1
- KKLFAZSAQYFWPV-UHFFFAOYSA-N 1-dodecylsulfanylpropan-1-ol Chemical compound CCCCCCCCCCCCSC(O)CC KKLFAZSAQYFWPV-UHFFFAOYSA-N 0.000 abstract 1
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 abstract 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004698 Polyethylene Substances 0.000 abstract 1
- 239000004743 Polypropylene Substances 0.000 abstract 1
- 239000004793 Polystyrene Substances 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 abstract 1
- 150000004678 hydrides Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 abstract 1
- 229960000367 inositol Drugs 0.000 abstract 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 239000010687 lubricating oil Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229940017219 methyl propionate Drugs 0.000 abstract 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 229920000573 polyethylene Polymers 0.000 abstract 1
- 229920001155 polypropylene Polymers 0.000 abstract 1
- 229920002223 polystyrene Polymers 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 1
- 239000004108 vegetable carbon Substances 0.000 abstract 1
- 235000013311 vegetables Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/084—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37208364A | 1964-06-02 | 1964-06-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1103145A true GB1103145A (en) | 1968-02-14 |
Family
ID=23466654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23339/65A Expired GB1103145A (en) | 1964-06-02 | 1965-06-01 | Process for the preparation of organic esters |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT253491B (enrdf_load_stackoverflow) |
| BE (1) | BE664811A (enrdf_load_stackoverflow) |
| CH (1) | CH454171A (enrdf_load_stackoverflow) |
| ES (1) | ES313657A1 (enrdf_load_stackoverflow) |
| FR (1) | FR1436393A (enrdf_load_stackoverflow) |
| GB (1) | GB1103145A (enrdf_load_stackoverflow) |
| NL (1) | NL6506933A (enrdf_load_stackoverflow) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0255743A1 (en) * | 1986-07-25 | 1988-02-10 | ENICHEM SYNTHESIS S.p.A. | Tetrakis[3-(3,5-di-tert.buthyl-4-hydroxyphenyl)propionyl-oxymethyl]methane with amorphous structure, process for its preparation and its use as a stabilizer |
| EP0358157A1 (en) * | 1988-09-07 | 1990-03-14 | Yoshitomi Pharmaceutical Industries, Ltd. | Individual alpha-form particle crystals of tetrakis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionyl-oxymethyl]methane and process for its production |
| EP0573393A1 (en) * | 1992-06-04 | 1993-12-08 | Ciba-Geigy Ag | Perfluoroalkyl substituted hydroxyphenylalkanoic ester antioxidants |
| US6878843B2 (en) | 2000-06-23 | 2005-04-12 | Ciba Specialty Chemicals Corp. | Method for preparing hydroxyphenyl carboxylic acid esters |
| CN103193635A (zh) * | 2013-04-08 | 2013-07-10 | 南通惠康国际企业有限公司 | 一种抗氧剂二[3-(3,5-二叔丁基-4-羟基苯基)]丙酸丁二醇酯的制备方法 |
| WO2019096868A1 (de) * | 2017-11-17 | 2019-05-23 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verbindungen mit stabilisierender wirkung, verfahren zu deren herstellung, zusammensetzung enthaltend diese stabilisierenden verbindungen, verfahren zur stabilisierung einer organischen komponente sowie verwendung von stabilisierenden verbindungen |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH585178A5 (enrdf_load_stackoverflow) * | 1972-12-27 | 1977-02-28 | Ciba Geigy Ag | |
| US3984460A (en) * | 1973-09-25 | 1976-10-05 | Ciba-Geigy Corporation | Esters of trisubstituted hydroxyphenylalkanoic acids |
| JPS50147711A (enrdf_load_stackoverflow) | 1974-05-17 | 1975-11-27 | ||
| US3956361A (en) | 1974-05-23 | 1976-05-11 | Ciba-Geigy Corporation | Hindered phenolic derivatives of norbornane thioalcohols |
| US4093587A (en) * | 1974-07-23 | 1978-06-06 | Ciba-Geigy Corporation | Trisubstituted hydroxyphenylalkanoic acid ester and amide stabilized compositions |
| US4001299A (en) * | 1974-12-12 | 1977-01-04 | Ciba-Geigy Corporation | Hindered hydroxyphenylalkanoates of substituted isopropanols |
| US3954839A (en) * | 1974-12-12 | 1976-05-04 | Ciba-Geigy Corporation | Hindered hydroxyphenylalkanoates of thioether isopropanols |
| US3987086A (en) * | 1974-12-12 | 1976-10-19 | Ciba-Geigy Corporation | Hindered hydroxyphenylalkanoates of substituted vicinal glycols |
-
1965
- 1965-05-25 CH CH732265A patent/CH454171A/de unknown
- 1965-06-01 GB GB23339/65A patent/GB1103145A/en not_active Expired
- 1965-06-01 NL NL6506933A patent/NL6506933A/xx unknown
- 1965-06-01 ES ES0313657A patent/ES313657A1/es not_active Expired
- 1965-06-01 AT AT497565A patent/AT253491B/de active
- 1965-06-02 BE BE664811D patent/BE664811A/xx unknown
- 1965-06-02 FR FR19216A patent/FR1436393A/fr not_active Expired
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0255743A1 (en) * | 1986-07-25 | 1988-02-10 | ENICHEM SYNTHESIS S.p.A. | Tetrakis[3-(3,5-di-tert.buthyl-4-hydroxyphenyl)propionyl-oxymethyl]methane with amorphous structure, process for its preparation and its use as a stabilizer |
| EP0358157A1 (en) * | 1988-09-07 | 1990-03-14 | Yoshitomi Pharmaceutical Industries, Ltd. | Individual alpha-form particle crystals of tetrakis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionyl-oxymethyl]methane and process for its production |
| US5089655A (en) * | 1988-09-07 | 1992-02-18 | Yoshitomi Pharmaceutical Industries, Ltd. | Individual α-form particle crystals of tetrakis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionyloxymethyl]methane and process for its production |
| EP0573393A1 (en) * | 1992-06-04 | 1993-12-08 | Ciba-Geigy Ag | Perfluoroalkyl substituted hydroxyphenylalkanoic ester antioxidants |
| US5310773A (en) * | 1992-06-04 | 1994-05-10 | Ciba-Geigy Corporation | Perfluoroalkyl substituted hydroxyphenylalkanoic ester antioxidants and stabilized compositions |
| US6878843B2 (en) | 2000-06-23 | 2005-04-12 | Ciba Specialty Chemicals Corp. | Method for preparing hydroxyphenyl carboxylic acid esters |
| CN103193635A (zh) * | 2013-04-08 | 2013-07-10 | 南通惠康国际企业有限公司 | 一种抗氧剂二[3-(3,5-二叔丁基-4-羟基苯基)]丙酸丁二醇酯的制备方法 |
| CN103193635B (zh) * | 2013-04-08 | 2015-06-03 | 南通大学 | 一种抗氧剂二[3-(3,5-二叔丁基-4-羟基苯基)]丙酸丁二醇酯的制备方法 |
| WO2019096868A1 (de) * | 2017-11-17 | 2019-05-23 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verbindungen mit stabilisierender wirkung, verfahren zu deren herstellung, zusammensetzung enthaltend diese stabilisierenden verbindungen, verfahren zur stabilisierung einer organischen komponente sowie verwendung von stabilisierenden verbindungen |
| CN111556864A (zh) * | 2017-11-17 | 2020-08-18 | 弗劳恩霍弗应用研究促进协会 | 具有稳定作用的化合物，该化合物的制备方法，含有该稳定化化合物的组合物，使有机成分稳定的方法以及稳定化化合物的用途 |
| JP2021503456A (ja) * | 2017-11-17 | 2021-02-12 | フラウンホーファー−ゲゼルシャフト ツゥア フェアデルング デア アンゲヴァンドテン フォァシュング エー．ファウ． | 安定化効果を有する化合物、当該化合物の製造方法、当該該安定化化合物を含む組成物、有機成分の安定化方法、及び安定化化合物の使用 |
| CN111556864B (zh) * | 2017-11-17 | 2022-07-08 | 弗劳恩霍弗应用研究促进协会 | 具有稳定作用的化合物，其制备方法和用途，含有其的组合物以及使有机成分稳定的方法 |
| US11407720B2 (en) | 2017-11-17 | 2022-08-09 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Compounds having a stabilizing effect, method for producing said compounds, composition containing said stabilizing compounds, and uses of the compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| ES313657A1 (es) | 1966-02-16 |
| BE664811A (enrdf_load_stackoverflow) | 1965-12-02 |
| AT253491B (de) | 1967-04-10 |
| NL6506933A (enrdf_load_stackoverflow) | 1965-12-03 |
| FR1436393A (fr) | 1966-04-22 |
| CH454171A (de) | 1968-04-15 |
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