
物理性质
- 熔点132-135 °C (分解) (文献)
- 沸点140°C(decomposition)
- 闪点157°C
- 密度1.619 g/cm3 at 25 °C
- pKa:2.83(at 25°C)
- PSA:74.6
- LogP:-0.81
- 折射率1.478
- 蒸汽压2.7X10-6 mm Hg at 23 °C
- 溶解性1MNaOH:soluble100mg/mL,清澈至微混浊,无色至淡黄色
- 敏感性MALONIC ACID is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in it to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions This chemical is incompatible with strong oxidizers. It is also incompatible with bases and reducing agents. (NTP, 1992)
- 外观形态Crystalline
- 储存条件1. 密封保存. 2. 使用编织袋内衬塑料薄膜包装,每包净重25公斤,并按照一般化学品的规定进行储运.
- 产品应用用于生产巴比妥酸盐和其他药物等.
- 性质描述白色结晶.熔点135.6°C(少量升华),沸点140°C(分解),相对密度1.619(16/4°C).1g该品可溶于0.65ml水;2ml乙醇;1.1ml甲醇;3ml丙醇;13ml乙醚;7ml吡啶.在真空中升华.脱水后生成丙二酸酐,脱羧生成乙酸.
欧盟法规
REACH注册ECHA物质ECHA物质C&L通报REACH预注册上下游产品
BARBITURIC ACID mucobromic acid propene carbon suboxide2-((Z)-3-Phenyl-allylidene)-malonic acid 5-phenyl-2,4-pentadienoic acid 2,3-(methylenedioxy)cinnamic acid (2E)-3-(2,4,6-trimethylphenyl)propenoic acid合成工艺路线路线简述
- 9005-53-2 = 141-82-2 + 110-17-8 + 6915-15-7 + 87-69-4
反应条件:1.1R:H2So4,R:H2O2
标题:Electrochemical Conversion Of Lignin To Short-Chain Carboxylic Acids
作者:By Sun,Shirong Et Al
参考文献:Green Chemistry 日期:2023 卷标:25(8) 页码:3127-3136]
9004-34-6 = 141-82-2 + 110-17-8
反应条件:1.1R:R:O2,S:H2O,175°C,30 Bar
标题:Lignin Alkaline Oxidation Using Reversibly-Soluble Bases
作者:By Kruger,Jacob S. Et Al
参考文献:Green Chemistry 日期:2022 卷标:24(22) 页码:8733-8741]
8068-05-1 = 141-82-2 + 6915-15-7 + 80-69-3 + 90-05-1 + 121-34-6 + 99-96-7
反应条件:1.1R:Naoh,C:Tio2,C:Cuo,Rt,20 Bar; Rt -> 150°C
标题:Potential Of Catalytic Oxidation Of Kraft Black Liquor For The Production Of Biosourced Compounds
作者:By Vilcocq,Lea Et Al
参考文献:Chemrxiv 日期:2023 卷标:From Chemrxiv 页码:1-14]
9005-53-2 = 141-82-2 + 6915-15-7
反应条件:1.1R:Naoh,R:O2,C:Cucl,S:H2O,60 Min,160°C,5 Bar2.1R:Naoh,R:O2,C:Cucl,S:H2O,30 Min,160°C,5 Bar3.1R:Naoh,R:O2,C:Cucl,S:H2O,30 Min,160°C,5 Bar
标题:Catalytic Oxidation Of Native Lignin To Phenolic Monomers: Insight Into Aldehydes Formation And Stabilization
作者:By Hu,Yuzhen Et Al
参考文献:Catalysis Communications 日期:2022 卷标:172 页码:106532]
= 141-82-2 + 6915-15-7 + 923-42-2 + 99-14-9
反应条件:1.1 Solvents: Water
标题:The Possible Role Of Hydrothermal Vents In Chemical Evolution: Succinic Acid Radiolysis And Thermolysis
作者:Cruz-Castaneda,J.; Colin-Garcia,M.; Negron-Mendoza,A.
参考文献:Aip Conference Proceedings 日期:2014 卷标:1607(1) 页码:104-110]
= 141-82-2 + 617-45-8 + 6915-15-7 + 80-69-3 + 66-22-8 + 2577-38-0 + 134434-28-9 + 1068-84-4 + 496-76-4 + 57-13-6
反应条件:1.1 Reagents: Ammonium Chloride Solvents: Water; 3 - 30 D,38 °C1.2 Reagents: Hydrochloric Acid Solvents: Water; 24 H,110 °C
标题:New Insights Into The Characterization Of 'Insoluble Black Hcn Polymers'
作者:Ruiz-Bermejo,Marta; De La Fuente,Jose L.; Rogero,Celia; Menor-Salvan,Cesar; Osuna-Esteban,Susana; Et Al
参考文献:Chemistry & Biodiversity 日期:2012 卷标:9(1) 页码:25-40
丙二酸二乙酯置于sodium Hydroxide体系中,用 甲醇,二氯甲烷 用作溶剂,化学反应 0.58H,反应生成丙二酸
参考文献:酯碱水解的简单方法
标题:酯碱水解的简单方法
摘要:通过使用二氯甲烷/甲醇(9:1)作用作溶剂,已经开发出一种非常温和,快速的方法,可在非水条件下有效地进行酯的碱性水解.该方法可在室温下几分钟内方便地由相应的酯和氢氧化钠提供羧酸和醇.提出了合理的反应机理.
Doi:10.1016/j.Tetlet.2007.09.074
海关参考信息
- 2905121000-正丙醇
2905399001-1,3-丙二醇
2912110000-甲醛
2912120000-乙醛 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-11667658-B2
优先权日:2021-06-30
标 题:Chemical synthesis of the organoarsenical antibiotic arsinothricin
发明人:ROSEN BARRY P; YOSHINAGA MASAFUMI; WNUK STANISLAW F; HOWLADER MD ABU HASAN; SUZOL SK MD SAZZAD HOSSAIN
权利人:ROSEN BARRY P; YOSHINAGA MASAFUMI; WNUK STANISLAW F; HOWLADER MD ABU HASAN; SUZOL SK MD SAZZAD HOSSAIN; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES
摘要:The subject invention provides methods for the chemical synthesis of racemic arsinothricin (D,L-AST), the novel organoarsenical antibiotic. One is by condensation of the 2-chloroethyl(methyl)arsinic acid with acetamidomalonate, and the second involves reduction of the N-acetyl-protected derivative of hydroxyarsinothricin (AST-OH) and subsequent methylation of the resulting sodium salt of trivalent arsenic intermediate with methyl iodide. The enzyme AST N-acetyltransferase (ArsN1) was utilized to purify L-AST from racemic AST. This expedient chemical synthesis of AST provides a source of this novel antibiotic for future drug development.
专利号:WO-2013138200-A1
优先权日:2012-03-13
标 题 :Green chemistry synthesis of the malaria drug amodiaquine and analogs thereof
发明人:FORTUNAK JOSEPH MARIAN; KULKARNI AMOL ANANT; KING CHRISTOPHER
权利人:UNIV HOWARD
摘要:Methods are provided for a green chemistry one-pot synthesis of amodiaquine and amodiaquine analogs. The methods have a lower environmental impact, lower investment cost, reduced amounts of byproducts and impurities, and a shorter synthesis time, compared to current conventional synthesis methods. The methods reduce the total number of steps in the synthesis from four to five down to two, thereby simplifying production; and allow a reduced number of solvents and reagents to be used in production, thereby reducing the waste generated in the synthesis. The methods can reduce the waste to about 3-5 kilograms of waste generated per kilogram of product produced; and surprisingly improve the overall yield from 60-65% to greater than 90% as compared to the current conventional synthesis methods for amodiaquine and its analogs.
专利号:US-8822702-B2
优先权日:2002-12-20
标 题 :Synthesis of amines and intermediates for the synthesis thereof
发明人:BERENS ULRICH; DOSENBACH OLIVER; SPRENGER DANIEL
权利人:BERENS ULRICH; DOSENBACH OLIVER; SPRENGER DANIEL; BASF SE
摘要:The invention relates in a first embodiment to a method for the manufacture of esters of the formula I, n nor especially of amides of the formula II,n n nwherein the symbols have the meanings given in the specification, as well as other intermediates and compounds useful in the synthesis of tryptamines and other substances mentioned in the title. The synthesis methods and intermediates are useful in the synthesis of pharmaceuticals.
专利号:US-6013829-A
优先权日:1996-02-05
标 题 :Process for the asymmetric synthesis of S-acyl derivatives of 2-mercaptomethyl -3- phenyl propanoic acid, application to the synthesis of N-(mercaptoacyl) amino acid derivatives
发明人:DANVY DENIS; MONTEIL THIERRY; DUHAMEL PIERRE; DUHAMEL LUCETTE; LECOMTE JEANNE-MARIE; SCHWARTZ JEAN-CHARLES; NOEL-LEFEBVRE NADINE; GROS CLAUDE; PLAQUEVENT JEAN-CHRISTOPHE
权利人:BIOPROJET SOC CIV
摘要:PCT No. PCT/FR97/00218 Sec. 371 Date Nov. 26, 1997 Sec. 102(e) Date Nov. 26, 1997 PCT Filed Feb. 4, 1997 PCT Pub. No. WO97/29086 PCT Pub. Date Aug. 14, 1997Process for the asymmetric synthesis of S-acyl derivatives of 2-mercaptomethyl-3-phenylpropanoic acid of formula (I): characterized in that it comprises the steps consisting in: a) preparing the diol (VI) by reduction of a malonic ester (V) in the presence of a hydride; b) preparing the monoacetates (VII R) or (VII S) respectively; c) subjecting these monoacetates to an oxidation in order to form the acids (IX S) or (IX R); d) saponifying the compounds (IX S) or (IX R) in order to form the hydroxy acids (X S) or (X R); e) thioacylating the hydroxy acids (X S) or (X R) with a mercapto acid R1SH (XI), according to a Mitsunobu-type reaction, in order to lead to the desired acids (I R) (I S) respectively and application to the synthesis of N-(mercaptoacyl)amino acid derivatives (II).
专利号:US-7928223-B2
优先权日:2008-06-20
标题:Process for the synthesis of 7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one, and application in the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid
发明人:LERESTIF JEAN-MICHEL; LECOUVE JEAN-PIERRE; BRIGOT DANIEL
权利人:SERVIER LAB
摘要:Process for the synthesis of the compound of formula (I): n n n n n n n n n n Application in the synthesis of ivabradine, addition salts thereof with a pharmaceutically acceptable acid and hydrates thereof.
专利号:US-3836544-A
优先权日:1972-04-25
标 题:Synthesis of zearalanes ii and related compounds and intermediates useful in the syntheses thereof
发明人:URRY W; MULLENBACH G
权利人:COMMERCIAL SOLVENTS CORP
摘要:THIS INVENTION PROVIDES A NEW SYNTHESIS FOR NORZEARALANE II AND RELATED COMPOUNDS WHICH RELATED COMPOUNDS AND NORZEARALANE II ARE REPRESENTED BY THE FORMULA 1,5-DI(HO-),2,3-(-CO-O-CH2-(CH2)X-)-BENZENE WHERE X IS AN INTEGER HAVING A VALUE FROM 1 TO 13 INCLUSIVE. THE ANABOLIC AGENT NORZEARALANE II, IN WHICH X=9 IN THEFOREGOING FORMULA, IS PREPARED BY A TOTAL CHEMICAL SYNTHESIS INVOLVING THE REACTION OF 10-UNDECENAL WITH MALONIC ACID TO PRODUCE TRANS-2,12-TRIDECADIENOIC ACID; TREATING THE ACID SO FORMED WITH DIAZOMSTHANE TO YIELD METHYL TRANS-2,12-TRIDECADIENOATE; REACTING THE METHYL ESTER WITH ETHYL ACETOACETATE AND SODIUM ETHOXIDE TO FORM THE SODIUM SALT OF ETHYL 6-(9-DECENYL)-B-DIHYDRORESORCYLATE; BROMINATING THE DIHYDRORESORCYLATE TO PREPARE ETHYL 3-BROMO- 6 - (9-DECENYL)-B-DIHYDRORESOCRYLATE; DE-HYDROBROMINATING THE FOREGOING BROMO DERIVATIVE TO GIVE ETHYL 6-(9-DECENYL)-B-RESORCYLATE; REACTING THE RESORCYLATE ESTER WITH BENZYL CHLORIDE TO PRODUCE ETHYL 6-(9-DECENYL)-BRESORCYLATE DIBENZYL ETHER; SUBJECTING THE BENZYLATED ESTER TO THE ACTION OF DIBORANE, WATER AND HYDROGEN PEROXIDE TO FORM ETHYL 2,4-BIS (BENZYLOXY)-6-(10-HYDROXYDECYL)BENZOATE; TREATING THE FOREGOING BENZOATE WITH SODIUM ETHOXIDE TO PREPARE NORZEARALANE II DIBENZYL ETHER, ONE ALSO TO PREPARE AS A BY-PRODUCT THE DIMERIC DILACTONE OF 2,4-BIS(BENZYLOXY)-6-(10-HYDROXYDECYL)-BENZOIC ACID; HYDROGENATING NORZEARALANE II DIBENZYL ETHER TO FORM NORZEARALANE II. IN GENERAL, A HOMOLOGUE OF NORZEARALANE II AND/OR OF THE CORRESPONDING DIMERIC DILACTONE IS PREPARED BY SUBSTITUTING FOOR 10-UNDECENAL IN THE FOREGOING SEQUENCE OF REACTIONS AN UNSATURATED ALDEHYDE HAVING THE FORMULA CH2=CH-(CH2)X-1-CHO WHERE X IS AN INTEGER WHICH MAY HAVE THE VALUE 1,2,3,4, 5, 6, 7, 8, 9, 10, 11, 12 OR 13 SPECIFICALLY ZEARALANE II (WHERE X=10) IS PREPARED STARTING WITH 11-DODECENAL AND THE DIMERIC DILACTONE FROM 6-(5-HYDROXYPENTYL-B-RESORCYCLIC ACID DIBENZYL ETHER IS PREPARED WHEN THE STARTING ALDEHYDE IS 5-HEXENAL (WHERE X= 4) THE INVENTION ALSO COVERS PHYSIOLOGICALLY ACTIVE COMPOUNDS RELATED TO THE ZEARALANES II AND KNOW AS DIMERIC DILACTONES HAVING THE FORMULA, 1,5-DI(RO-),2,3-(-CO-O-CH2-(CH2)X-(3,5-DI(RO-)-1,6-PHENYL ENE)-CO-O-CH2-(CH2)X-)-BENZENE X IS AN INTEGER WHICH MAY HAVE THE VALUE 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 OR 13 AND WHERE R IS EITHE HYDROGEN OR A BENZYL RADICAL (C6H5CH2-). MORE PARTICULARLY, THIS INVENTION RELATES TO NOVEL INTERMEDIATES PRODUCED IN THE SYNTHESIS OF THE ABOVE COMPOUNDS AND TO PROCESSES FOR MAKING THESE INTERMEDIATES.