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Malonic acid

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Products Intro: CAS:141-82-2
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Purity:98% HPLC Package:10G,100G,1KG,25KG

Malonic acid manufacturers

  • Malonic acid
  • $1.00 / 1KG
  • 2022-02-25
  • CAS:141-82-2
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20tons
  • Malonic acid
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  • 2022-02-25
  • CAS:141-82-2
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 5000mt

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  • Nov 28,2019
Malonic acid Basic information
Dibasic acid Uses Preparation Chemical Properties Uses Production method
Product Name:Malonic acid
Synonyms:MALONIC ACID, 99%MALONIC ACID, 99%MALONIC ACID, 99%MALONIC ACID, 99%;Valproic Acid Impurity 2 (Malonic Acid);Malonic acid 141-82-2;141-82-2 Malonic acid 1,3-Propanedioic acid;Sodium Valproate Impurity 24;Malonic acid, AR,99.5%;Malonate, AR,99.5%;Malonic acid anhydrous, free-flowing, Redi-Dri(TM), ReagentPlus(R), 99%
Product Categories:Acids;Electronic Chemicals;Materials Science;Micro &;Micro/NanoElectronics;Nanoelectronics;Intermediates;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;alpha,omega-Alkanedicarboxylic Acids;alpha,omega-Bifunctional Alkanes;Monofunctional & alpha,omega-Bifunctional Alkanes;New Products for Materials Research and Engineering
Mol File:141-82-2.mol
Malonic acid Structure
Malonic acid Chemical Properties
Melting point 132-135 °C (dec.) (lit.)
Boiling point 140℃(分解)
density 1.619 g/cm3 at 25 °C
refractive index 1.4780
Fp 157°C
storage temp. Sealed in dry,Room Temperature
solubility 1 M NaOH: soluble100mg/mL, clear to slightly hazy, colorless to faintly yellow
pka2.83(at 25℃)
form Liquid
color White
PH3.17(1 mM solution);2.5(10 mM solution);1.94(100 mM solution)
Water Solubility 1400 g/L (20 ºC)
Merck 14,5710
BRN 1751370
Stability:Stable. Incompatible with oxidizing agents, reducing agents, bases.
CAS DataBase Reference141-82-2(CAS DataBase Reference)
NIST Chemistry ReferenceMalonic acid(141-82-2)
EPA Substance Registry SystemPropanedioic acid (141-82-2)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/22-41-36/37/38-22
Safety Statements 26-36/39-37/39-36
WGK Germany 1
RTECS OO0175000
PackingGroup III
HS Code 29171910
Hazardous Substances Data141-82-2(Hazardous Substances Data)
MSDS Information
1,3-Propanedioic acid English
SigmaAldrich English
ACROS English
ALFA English
Malonic acid Usage And Synthesis
Dibasic acidMalonic acid is also known as methane dicarboxylic acid, carrot acid, malic acid reduction, beet acid. There are three kinds of crystal forms, of which two are triclinic, and one is monoclinic. That crystallized from ethanol is white triclinic crystals. Its relative molecular mass is 104.06. The relative density is 1.631 (15 ℃). Melting point is 135.6℃. It decomposes to acetic acid and carbon dioxide at 140℃. It does not decompose at 1.067×103~1.333×103Pa vacuum, but directly sublimates. It is not soluble in benzene. It is soluble in water, and the solubility is respectively 61.1 (0 ℃), 73.5 (20 ℃), 92.6 (50 ℃) in water, and 57 (20 ℃)in ethanol, 5.7 (20 ℃) in diethyl ether. It is slightly soluble in pyridine. It can decompose to formic acid and carbon dioxide in case of potassium permanganate. Malonic acid is dibasic acid. It has a typical reactive of dibasic acids, such as that its methylene is active, and it can be an addition, alkylation, amination, halogenation reaction; its two carboxyl groups are very close and they can be dehydrated; esterification with alcohol; decarboxylation by heating; condensation with carbonyl compounds; addition with compounds that containing active double bonds. Hydroxyl in two carboxyl groups of malonic acid were all replaced by ethoxy (see substitution reaction) to produce diethyl malonate. Diethyl malonate is important raw materials in organic synthesis for dyes and drugs synthesis. Because its molecules containing active methylene, which can react with sodium alcohol to generate sodium malonate. Then sodium malonate reacts with a variety of lively halides to generate substituted malonate. Malonate can prepare various monocarboxylic acids, dicarboxylic acids, keto acids and other compounds by hydrolysis reaction to lose carboxyl. As substituted malonate reacts with urea to prepare a commonly used hypnotic barbiturates.
Since that malonic acid generates carbon dioxide and water after heated without pollution problems, it can be directly used as aluminum surface treatment agent; it is also the raw material in the production of pesticides fungicides Fujione, herbicides Alloxydim; malonic acid is used to prepare diuretic sulfinpyrazone medicine, anti-inflammatory drug phenylbutazone paraben, sedatives bromomethyl Jacinto goods in pharmaceutical industries. In addition, malonic acid and its esters are widely used as pharmaceutical intermediates, such as preparing barbiturates, vitamins B1 and B6, etc. Esters of malonic acid are commonly used in organic synthesis. It also can be used as binding agent, perfum, resin additive, electroplating polishing agent, welding flux and so on.
The above information is edited by the chemicalbook of Ge Qian.
UsesMalonic acid, also known as Propanedioic acid, Methane dicarbonic acid or Carboxyacetic acid, is an organic acid. Mainly used in perfumes, pharmaceutical intermediates, adhesives, resin additives, electroplating polishing agents, etc. Used in the pharmaceutical industry to produce barbituric acid, vitamin B1, vitamin B2, vitamin B6, etc. In agriculture, malonic acid is an intermediate of the fungicide rice pestin and an intermediate of the plant growth regulator indyl ester. In addition, it can also be used in the production of adhesives and resin additives, and can also be used as a surface treatment agent for leather and aluminum products.
PreparationChloroacetic acid is used as raw material in Laboratories. It is neutralized by NaOH or Na2CO3 to generate chloroacetic acid sodium salt. The sodium salt reacts with KCN (or NaCN) to yield α-cyano sodium acetate. And then malonic acid can be prepared after alkaline hydrolysis, calcium replacement and acidification. Chemical reaction equation is as follows:
Chemical PropertiesWhite crystals. It dissolves easily in water. And it is soluble in alcohol, ether and pyridine.
Uses1. It mainly can be used as pharmaceutical intermediates. It also can be used as perfumery, adhesives, resin additives, electroplating polishing agent and so on.
2. It can be used as complexing agent. It also can be used to prepare barbituric salt.
3. Malonic acid is the intermediate of fungicides isoprothiolane. It is also the intermediate of plant growth regulator ethychlozate.
4. Malonic acid and its esters is mainly used as perfumery, adhesives, resin additives, pharmaceutical intermediates, electroplating, polishing agent, explosion control agents, heat welding fluxing additives and the like. In the pharmaceutical industry, it can be used to produce phenobarbital, barbiturates, vitamin B1, vitamin B2, vitamin B6, phenylbutazone, amino acids and so on. Malonic acid can be used as the aluminum surface treatment agent since that malonic acid generates carbon dioxide and water after heated without pollution problems. At this point, it has a great advantage when compared with acidic treating agent like formic acid in the past.
5. It can be used as complexing agent in the determination of beryllium, copper, calibration standard alkaline solution, biochemical studies, organic synthesis, preparing barbiturates, gas chromatography analysis of the standard.
Production methodThe preparation method is that firstly sodium carbonate aqueous solution is added chloroacetic acid in the reaction vessel to get sodium chloroacetate aqueous solution. And then 30% sodium cyanide solution is slowly dripped at a predetermined temperature to generate sodium cyanide. After the reaction of cyanide finishes, sodium hydroxide is added to hydrolyze under heating in order to form sodium malonate solution. After the solution is concentrated, added dropwise to generate malonic acid, filtered and dried, then the product is obtained.
DescriptionMalonic acid (IUPAC systematic name: propanedioic acid) is a dicarboxylic acid with structure CH2(COOH)2. The ionized form of malonic acid, as well as its esters and salts, are known as malonates. For example, diethyl malonate is malonic acid's diethyl ester. The name originates from the Greek word (malon) meaning 'apple'.
Chemical PropertiesCrystalline
UsesMalonic acid is used as an intermediate in the manufacture of barbiturates and other pharmaceuticals.
UsesMalonic acid is used as building block in chemical synthesis, specifically to introduce the molecular group -CH2-COOH. Product Data Sheet
UsesMalonic acid is acts as a building block in organic synthesis. It is also useful as a precursor for polyesters and alkyd resins, which is used in coating applications, thereby protecting against UV light, corrosion and oxidation. It acts as a cross linker in the coating industry and surgical adhesive. It finds application in the production of specialty chemicals, flavors and fragrances, polymer cross linkers and pharmaceuticals.
PreparationA classical preparation of malonic acid starts from chloroacetic acid :
Sodium carbonate generates the sodium salt, which is then reacted with sodium cyanide to provide the cyano acetic acid salt via a nucleophilic substitution. The nitrile group can be hydrolyzed with sodium hydroxide to sodium malonate, and acidification affords malonic acid.
DefinitionChEBI: An alpha,omega-dicarboxylic acid in which the two carboxy groups are separated by a single methylene group.
ReactionsIn a well - known reaction, malonic acid condenses with urea to form barbituric acid. Malonic acid is also frequently used as an enolate in Knoevenagel condensations or condensed with acetone to form Meldrum's acid. The esters of malonic acid are also used as a - CH2COOH synthon in the malonic ester synthesis.
General DescriptionWhite crystals or crystalline powder. Sublimes in vacuum.
Air & Water ReactionsWater soluble.
Reactivity ProfileMalonic 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 Malonic acid 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 Malonic acid is incompatible with strong oxidizers. Malonic acid is also incompatible with bases and reducing agents.
HazardStrong irritant.
Fire HazardFlash point data for Malonic acid are not available; however, Malonic acid is probably combustible.
Biotechnological ApplicationsThe calcium salt of malonic acid occurs in high concentrations in beetroot. It exists in its normal state as white crystals. Malonic acid is the classic example of a competitive inhibitor: It acts against succinate dehydrogenase (complex II) in the respiratory electron transport chain.
Purification MethodsCrystallise malonic acid from *benzene/diethyl ether (1:1) containing 5% of pet ether (b 60-80o), wash with diethyl ether, then recrystallise it from H2O or acetone. Dry it under vacuum over conc H2SO4. [Beilstein 2 IV 1874.]
Tag:Malonic acid(141-82-2) Related Product Information
Malonic acid chloride,Malonic acid dichloride Di-tert-Butyl malonate 2,2-Dimethyl-1,3-dioxane-4,6-dione Diethyl dipropylmalonate 2-Propylvaleric acid methyl ester PROPYLMALONIC ACID 2-Acetyl-2-propylvaleric acid methyl ester 2,2-Dipropylmalonic acid DIETHYL DIALLYLMALONATE ETHYL N-PROPYL ETHER 1-Chloropropane Diethyl malonate Propionic acid TERT-BUTYL ETHYL MALONATE Ethyl hydrogen malonate Potassium 3-methoxy-3-oxopropanoate MONOMETHYL MALONATE 3-tert-Butoxy-3-oxopropanoic acid