1457-39-2

Basic information

• Product Name: 2-BUTYLSUCCINIC ACID
• Synonyms: 2-BUTYLSUCCINIC ACID;n-butylsuccinic acid
• CAS NO: 1457-39-2
• Molecular Formula: C₈H₁₄O₄
• Molecular Weight: 174.19
• Mol File: 1457-39-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 81 °C
• Boiling Point: 281.3±13.0 °C(Predicted)
• Appearance: /
• Density: 1.159±0.06 g/cm3(Predicted)
• PKA: 4.56±0.19(Predicted)
• CAS DataBase Reference: 2-BUTYLSUCCINIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BUTYLSUCCINIC ACID(1457-39-2)
• EPA Substance Registry System: 2-BUTYLSUCCINIC ACID(1457-39-2)

Safety Data

• Hazardous Substances Data: 1457-39-2(Hazardous Substances Data)

Upstream product

• 5653-96-3 (+/-)-but-2t-enyl-succinic acid 
• 693-03-8 n-butyl magnesium bromide 
• 50485-76-2 hexa-2t,4t-dienoic acid sec-butyl ester 
• 14447-12-2 di-sec-butyl maleate 
• 79-08-3 bromoacetic acid 
• 142-62-1 hexanoic acid 
• 25236-78-6 2-n-Butyl-4,4,4-trichlorbutyramid 
• 42858-60-6 3,5-cyclohexanedione-1-carboxylic acid 
• 133-08-4 diethyl butylmalonate 
• 308349-48-6 3-(tert-butoxycarbonyl)heptanoic acid 
• 105-39-5 chloroacetic acid ethyl ester 
• 996-82-7 sodium diethylmalonate 
• 135386-87-7 5-hydroxy-4-butyl-4,5-dihydro-3H-furan-2-one 
• 110-62-3 pentanal 

Downstream Products

• 2035-76-9 3-butyldihydrofuran-2,5-dione 
• 34722-01-5 3-butylthiophene 
• 101434-34-8 2-Butyl-bernsteinsaeure-dibutylester 
• 4136-86-1 dimethyl 2-butylsuccinate 

Relevant articles and documents

Synthesis of monosubstituted succinic acids from tert-butylsuccinate

We report the preparation and alkylation of the dianion of t-butylsuccinate. This alkylation reaction has proven to be a useful method for the preparation of monosubstituted succinic acids and anhydrides.

Inhibition of Liver Alcohol Dehydrogenase and Ethanol Metabolism by 3-Substituted Thiolane 1-Oxides

3-Substituted thiolane oxides (methyl, n-butyl, n-hexyl, and phenyl) were prepared and tested as inhibitors of horse, monkey, and rat liver alcohol dehydrogenases and of ethanol metabolism in rats.These compounds inhibit alcohol oxidation in an uncompetit

Polymers of sulfonic acid monomers

The present invention is concerned with novel monomers containing sulfonic acid groups or salts thereof and polymers thereof which are useful for many purposes, such as antistatic agents for textiles and other shaped articles formed of hydrophilic materials. They are useful for making copolymers that are particularly valuable in coating compositions, especially in the form of aqueous latices or organic solvent solutions thereof. Examples of the monomers are of the formula STR1 wherein R is hydrogen or lower (C1 -C4)alkyl, such as methyl, A is an alkylene group having 2 to 10 carbon atoms, at least 2 of which extend in one chain between the oxygen atoms, and X is an aromatic nucleus or an alkyl group, substituted by a sulfonic acid group and optionally one or more groups selected from sulfonic acid, carboxylic acid, and lower alkyl, such as methyl, ethyl, propyl, or butyl.