141-03-7

Basic information

• Product Name: Dibutyl succinate
• Synonyms: Butyl succinate;butanedioic acid dibutyl ester;DI-N-BUTYL SUCCINATE;DIBUTYL SUCCINATE;TABATREX(R);TABUTREX;SUCCINIC ACID DIBUTYL ESTER;SUCCINIC ACID DI-N-BUTYL ESTER
• CAS NO: 141-03-7
• Molecular Formula: C₁₂H₂₂O₄
• Molecular Weight: 230.3
• EINECS: 205-449-8
• Mol File: 141-03-7.mol
• Article Data: 34

Chemical Properties

• Melting Point: -29℃
• Boiling Point: 274 °C
• Flash Point: 144 °C
• Appearance: White crystalline powder
• Density: 0,98 g/cm3
• Vapor Pressure: 0.00546mmHg at 25°C
• Refractive Index: nD20 1.4299
• Water Solubility: 229.9mg/L(temperature not stated)
• CAS DataBase Reference: Dibutyl succinate(CAS DataBase Reference)
• NIST Chemistry Reference: Dibutyl succinate(141-03-7)
• EPA Substance Registry System: Dibutyl succinate(141-03-7)

Safety Data

• Hazard Codes: N
• Statements: 51/53
• Safety Statements: 61
• RIDADR: UN 3082
• WGK Germany: 2
• RTECS: WM6250000
• Hazardous Substances Data: 141-03-7(Hazardous Substances Data)

Usage

Chemical Properties

It is a mobile liquid that is soluble in alcohol, benzene, and ether, but insoluble in water. Its melting and boiling points are -29 and 274.5°C, respectively. The flash point is 275°F.

Uses

Different sources of media describe the Uses of 141-03-7 differently. You can refer to the following data:
1. Dibutyl succinate is a diester compound for proteomics research.
2. Dibutyl succinate especially against biting flies of cattle, household ants and roaches.

Upstream product

• 5150-93-6 succinic anhydride monobutyl ester 
• 110-15-6 succinic acid 
• 71-36-3 butan-1-ol 
• 543-20-4 succinoyl dichloride 
• 2226-88-2 diammonium succinate 
• 2922-54-5 sodium hydrogen succinate 
• 109-65-9 1-bromo-butane 
• 5259-72-3 cyclo-octa-1,5-diene 
• 1490-25-1 succinic acid monomethylester chloride 
• 2052-15-5 butyl levulinate 
• 105-75-9 dibutyl fumarate 
• 105-76-0 Dibutyl maleate 
• 1280724-97-1 2-(cyclohexanecarbonyl)butanedioic acid 1,4-dibutyl ester 
• 82807-35-0 2-butenedioic acid dibutyl ester 

Downstream Products

• 1160-32-3 2,5-dibutylformate 1,4-cyclohexanedione 
• 109-99-9 tetrahydrofuran 
• 110-63-4 Butane-1,4-diol 
• 142-96-1 dibutyl ether 
• 71-36-3 butan-1-ol 
• 88949-34-2 3,6-bis(furan-2-yl)-2,5-dihydropyrrolo[3,4-c]pyrrolo-1,4-dione 
• 96-48-0 4-butanolide 
• 71-23-8 propan-1-ol 

Relevant articles and documents

CARBALKOXYLATION OF ACETYLENE IN SOLUTIONS OF MOLYBDENUM AND TUNGSTEN COMPLEXES

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Biobased compositions

A composition comprised of a component selected from the group consisting of a biobased bis-alkyl succinate and a biobased bis-alkyl sebacate, each derived, for example, from the esterification of biobased diacid such as succinic acid or sebacic acid, and a biobased alcohol and a biobased polyester.

Exceptionally active and reusable nanobiocatalyst comprising lipase non-covalently immobilized on multi-wall carbon nanotubes for the synthesis of diester plasticizers

A new method for the synthesis of dicarboxylic acid esters in the presence of a new heterogeneous nanobiocatalyst consisting of Candida antarctica lipase B immobilized on multi-walled carbon nanotubes (MWCNTs) has been developed. Selection and characterization of the support for Candida antarctica lipase B (CALB) was initially performed. Pristine and modified MWCNTs of different geometries, morphologies and surface/core modifications were tested as a lipase carrier and determining that the CheapTubes MWCNTs nanobiocatalyst with a 15.7 wt.% CALB loading was the most active nanobiocatalyst. The model reaction of succinic acid with n-butanol was carried out with a 4-molar excess of alcohol and 150 mg of nanobiocatalyst per 1 mmol of succinic acid at 45 °C in cyclohexane. The di-n-butyl succinate was obtained with 95% yield after 3 h. The activities of the new nanobiocatalysts were compared with the benchmark Novozyme-435 and other acidic catalysts. Recycling studies demonstrated the possibility of utilizing the most active MWCNTs-lipase biocatalyst six times without any significant loss of activity. The main advantage of this study is the superior activity of the new nanobiocatalyst, which resulted in a significant reduction of reaction times as compared to those reported in the literature.