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Atomfair 3-Buten-1-ol C4H8O

Description 3-Buten-1-ol (CAS No. 627-27-0) is a versatile unsaturated alcohol with the molecular formula C4H8O , commonly referred to by its IUPAC name but-3-en-1-ol . This clear, colorless liquid is characterized by its reactive terminal double bond and primary hydroxyl group, making it a valuable intermediate in organic synthesis and industrial applications. With a molecular weight of 72.11 g/mol and a boiling point of approximately 114-116??C, it is soluble in water and most organic solvents. Ideal for researchers and scientists, our high-purity grade (??98%) is rigorously tested via GC analysis to ensure consistency for use in pharmaceuticals, fragrances, and polymer…

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Description

Description

3-Buten-1-ol (CAS No. 627-27-0) is a versatile unsaturated alcohol with the molecular formula C4H8O, commonly referred to by its IUPAC name but-3-en-1-ol. This clear, colorless liquid is characterized by its reactive terminal double bond and primary hydroxyl group, making it a valuable intermediate in organic synthesis and industrial applications. With a molecular weight of 72.11 g/mol and a boiling point of approximately 114-116??C, it is soluble in water and most organic solvents. Ideal for researchers and scientists, our high-purity grade (??98%) is rigorously tested via GC analysis to ensure consistency for use in pharmaceuticals, fragrances, and polymer chemistry. Packaged under inert gas to prevent oxidation, it is available in various quantities with customizable bulk options.

  • CAS No: 627-27-0
  • Molecular Formula: C4H8O
  • Molecular Weight: 72.11
  • Exact Mass: 72.057514874
  • Monoisotopic Mass: 72.057514874
  • IUPAC Name: but-3-en-1-ol
  • SMILES: C=CCCO
  • Synonyms: 3-Buten-1-ol, 627-27-0, but-3-en-1-ol, Allylcarbinol, 3-Butenyl alcohol

Application

3-Buten-1-ol serves as a key precursor in the synthesis of flavor and fragrance compounds, leveraging its allylic alcohol functionality. It is widely employed in polymer science as a monomer or crosslinking agent due to its reactive double bond. Additionally, it finds use in pharmaceutical intermediates and agrochemical production, where its bifunctional reactivity enables diverse derivatization pathways.

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