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Atomfair Sulfuric acid, dibutyl ester C8H18O4S
Description Sulfuric acid, dibutyl ester (Dibutyl sulfate) is a high-purity organic sulfate ester with the molecular formula C8H18O4S (CAS No. 625-22-9 ). This colorless to pale yellow liquid is widely utilized in synthetic organic chemistry and industrial applications due to its role as an alkylating agent and intermediate. With a boiling point of approximately 280-290??C and a density of 1.06 g/cm3, it is soluble in common organic solvents but reacts vigorously with water. Our product is rigorously tested for purity ( ??98% by GC) and is supplied in amber glass bottles or specialized chemical-resistant containers to ensure stability. Ideal for…
Description
Description
Sulfuric acid, dibutyl ester (Dibutyl sulfate) is a high-purity organic sulfate ester with the molecular formula C8H18O4S (CAS No. 625-22-9). This colorless to pale yellow liquid is widely utilized in synthetic organic chemistry and industrial applications due to its role as an alkylating agent and intermediate. With a boiling point of approximately 280-290??C and a density of 1.06 g/cm3, it is soluble in common organic solvents but reacts vigorously with water. Our product is rigorously tested for purity (??98% by GC) and is supplied in amber glass bottles or specialized chemical-resistant containers to ensure stability. Ideal for laboratory-scale reactions and process optimization, this compound requires handling under inert conditions due to its moisture sensitivity. Store in a cool, dry place with proper ventilation.
- CAS No: 625-22-9
- Molecular Formula: C8H18O4S
- Molecular Weight: 210.29
- Exact Mass: 210.09258022
- Monoisotopic Mass: 210.09258022
- IUPAC Name: dibutyl sulfate
- SMILES: CCCCOS(=O)(=O)OCCCC
- Synonyms: Dibutyl sulfate, 625-22-9, Dibutylsulfate, Di-n-butyl sulphate, SULFURIC ACID, DIBUTYL ESTER
Application
Dibutyl sulfate is primarily employed as an alkylating agent in the synthesis of specialty chemicals and pharmaceuticals. It serves as a key intermediate in the production of surfactants and ester derivatives. Researchers also utilize it in polymer modification and catalysis studies. Its reactivity makes it valuable for quaternary ammonium compound synthesis.
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