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Atomfair Methyl 4-methoxybutanoate C6H12O3

Description Methyl 4-methoxybutanoate (CAS No. 29006-01-7) is a high-purity ester compound with the molecular formula C6H12O3. This versatile chemical is widely used in organic synthesis, pharmaceutical research, and specialty chemical applications. Its clear liquid form and defined molecular structure (IUPAC name: methyl 4-methoxybutanoate) make it ideal for controlled reactions and as a building block for complex molecules. Our product is rigorously tested for purity and consistency, ensuring reliable performance in your laboratory workflows. Suitable for use as a solvent, intermediate, or reagent in advanced chemical processes.

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Description

Description

Methyl 4-methoxybutanoate (CAS No. 29006-01-7) is a high-purity ester compound with the molecular formula C6H12O3. This versatile chemical is widely used in organic synthesis, pharmaceutical research, and specialty chemical applications. Its clear liquid form and defined molecular structure (IUPAC name: methyl 4-methoxybutanoate) make it ideal for controlled reactions and as a building block for complex molecules. Our product is rigorously tested for purity and consistency, ensuring reliable performance in your laboratory workflows. Suitable for use as a solvent, intermediate, or reagent in advanced chemical processes.

  • CAS No: 29006-01-7
  • Molecular Formula: C6H12O3
  • Molecular Weight: 132.16
  • Exact Mass: 132.078644241
  • Monoisotopic Mass: 132.078644241
  • IUPAC Name: methyl 4-methoxybutanoate
  • SMILES: COCCCC(=O)OC
  • Synonyms: Methyl 4-methoxybutanoate, 29006-01-7, Methyl 4-methoxybutyrate, Butanoic acid, 4-methoxy-, methyl ester, Butyric acid, 4-methoxy-, methyl ester

Application

Methyl 4-methoxybutanoate serves as a valuable intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its ester and ether functional groups make it suitable for use in flavor and fragrance formulations. Researchers also employ it as a solvent or co-solvent in specialized reactions requiring controlled polarity.

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