Atomfair tert-Butyl acetate C6H12O2

Description tert-Butyl acetate (CAS No. 13211-32-0) is a high-purity ester with the molecular formula C6H12O2, widely utilized in organic synthesis and industrial applications. This colorless liquid exhibits a characteristic ester-like odor and is highly soluble in common organic solvents, making it an excellent choice for reactions requiring a non-polar, aprotic medium. With its IUPAC name tert-butyl acetate , this compound is rigorously tested to meet the highest standards of purity and consistency, ensuring reliable performance in research and manufacturing processes. tert-Butyl acetate is packaged under inert conditions to maintain stability and is available in various quantities to suit laboratory and…

Description

Description

tert-Butyl acetate (CAS No. 13211-32-0) is a high-purity ester with the molecular formula C6H12O2, widely utilized in organic synthesis and industrial applications. This colorless liquid exhibits a characteristic ester-like odor and is highly soluble in common organic solvents, making it an excellent choice for reactions requiring a non-polar, aprotic medium. With its IUPAC name tert-butyl acetate, this compound is rigorously tested to meet the highest standards of purity and consistency, ensuring reliable performance in research and manufacturing processes. tert-Butyl acetate is packaged under inert conditions to maintain stability and is available in various quantities to suit laboratory and bulk-scale needs.

  • CAS No: 13211-32-0
  • Molecular Formula: C6H12O2
  • Molecular Weight: 116.16
  • Exact Mass: 116.083729621
  • Monoisotopic Mass: 116.083729621
  • IUPAC Name: tert-butyl acetate
  • SMILES: CC(=O)OC(C)(C)C
  • Synonyms: TERT-BUTYL ACETATE, t-Butyl acetate, tert-Butyl ethanoate, Acetic acid, 1,1-dimethylethyl ester, Acetic acid, tert-butyl ester

Application

tert-Butyl acetate is commonly employed as a solvent in coatings, adhesives, and specialty chemical formulations due to its favorable evaporation rate and compatibility with resins. It serves as a versatile reagent in organic synthesis, particularly for protecting group strategies and esterification reactions. Researchers also utilize it as a reaction medium in catalytic processes where its low nucleophilicity is advantageous.

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