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    4501-58-0

    Catalog No. EBD1757

    CAS 4501-58-0

    Name Campholenic aldehyde

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    Basic Information

    Synonyms: CampholenicAldehyde Aromavert 2,2,3-trimethyl-1-acetaldehyde-3-cyclopentene AlphaCampholenicAldehyde 1-(2,2,3-trimethylcyclopent-3-en-1-yl)ethanone [(1R)-2,2,3-trimethylcyclopent-3-en-1-yl]acetaldehyde 2,2,3-Trimethylcyclopent-3-en-1-yl-acetaldehyde Trimethylcyclopentenylacetaldehyde

    Molecular Formula: C10H16O

    Molecular Weight: 152.24

    Categories: Materials Chemistry > Optoelectronic and Organic Semiconductor Materials > Dye Precursors Synthetic Chemistry > Organic Building Blocks > Aldehydes and Ketones

    Product Description:
    Campholenic aldehyde is a monoterpenoid aldehyde derived from α-pinene. It is a colorless to pale yellow liquid with a characteristic woody, amber-like odor. Its structure features a cyclopentane ring fused to a cyclohexane ring, with an aldehyde group and an exocyclic double bond, making it a versatile chiral building block. The primary industrial application of campholenic aldehyde is as a key intermediate in the synthesis of high-value fragrance ingredients. It is most notably used in the production of Sandalore® (2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol), a widely used sandalwood odorant in perfumery and cosmetic formulations. Its rigid, chiral structure also makes it a valuable starting material for the synthesis of other specialty chemicals, including certain dyes and functional materials that require specific steric and electronic properties. As a fragrance intermediate and a chiral synthon, campholenic aldehyde is handled as a chemical substance requiring standard safety precautions. It should be stored in a cool, well-ventilated area away from strong oxidizers.
    Physical Properties

    Boiling Point: 201.8 °C at 760 mmHg

    Flash Point: 70.6 °C

    Density: 0.878 g/cm3

    mg g kg ml l t