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

Description

Dibutyl succinate is a diester compound characterized by its mobile liquid nature and solubility in alcohol, benzene, and ether. It has a melting point of -29°C and a boiling point of 274.5°C, with a flash point of 275°F. Dibutyl succinate is particularly useful in various applications across different industries due to its unique chemical properties.

Uses

Used in Proteomics Research:
Dibutyl succinate is utilized as a diester compound in proteomics research, contributing to the study of proteins and their functions within biological systems. Its chemical properties make it a valuable tool for researchers in this field.
Used in Agriculture:
Dibutyl succinate serves as an effective agent against biting flies of cattle, household ants, and roaches. Its application in agriculture helps to protect livestock and maintain a healthy living environment for both humans and animals by controlling these pests.

Upstream product

• 1809-19-4 dibutyl hydrogen phosphite 
• 110-15-6 succinic acid 
• 5150-93-6 succinic anhydride monobutyl ester 
• 71-36-3 butan-1-ol 
• 109-65-9 1-bromo-butane 
• 543-20-4 succinoyl dichloride 
• 201230-82-2 carbon monoxide 
• 74-86-2 acetylene 
• 2226-88-2 diammonium succinate 
• 2922-54-5 sodium hydrogen succinate 
• 134101-64-7 3-(2-butoxycarbonyl-ethyl)-2,4-pentanedione 
• 5259-72-3 cyclo-octa-1,5-diene 
• 1490-25-1 succinic acid monomethylester chloride 
• 106-98-9 1-butylene 

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.

Synthesis of Esters from Stable and Convenient Sulfoxonium Precursors under Catalyst- And Additive-Free Conditions

A convenient and efficient procedure for the construction of esters from stable sulfoxonium ylides and alcohols has been developed. This protocol presents a broad substrate scope and good yields of the desired esters can be isolated. Notably, no catalyst, oxidant, base or any other additive is required.