N-Hexaldehyde
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  • N-Hexaldehyde

N-Hexaldehyde

Our factory produces high-purity isophthaloyl chloride that meets polymerization-grade requirements. It can be used as a monomer for polyamides, polyesters, polyarylates, polyaramids, liquid crystal polymers, and aramid 1313 (Nomax), and also as a modifier for high polymers and an intermediate in the pesticide and pharmaceutical industries.

CAS: 66-25-1
Molecular Formula: C 6H12O
Molecular Weight: 100.16
  • Product Description
    • Commodity name: N-Hexaldehyde
    • CAS: 66-25-1

    Our factory produces high-purity isophthaloyl chloride that meets polymerization-grade requirements. It can be used as a monomer for polyamides, polyesters, polyarylates, polyaramids, liquid crystal polymers, and aramid 1313 (Nomax), and also as a modifier for high polymers and an intermediate in the pesticide and pharmaceutical industries. </br><link href="https://m2cdn.fastindexs.com/npmanager/static/lib/ckeditor5/preview.css?v=1.3.044" rel="stylesheet" /><hr /> CAS: 66-25-1 </br> Molecular Formula: C <sub>6</sub>H<sub>12</sub>O</br> Molecular Weight: 100.16

    Product Name  ( Product name ) : Hexanal  ( Caproaldehyde )

    Structural Formula   (Structure):

    Molecular Formula   (Molecular Formula): C 6 H 12 

    Molecular Weight   (Molecular Weight): 100.16

    CAS Registry Number   (Number):   66-25-1

    HexanalMolecular FormulaC 6 H 12 OMolecular Weight (g/mol)100.16
    Physical PropertiesAppearance and OdorColorless transparent liquid with a pungent odor
    Boiling Point (°C)128-131Melting Point (°C)-56.3
    Density (g/cm3)0.813-0.818 (20℃)Flash Point (°C)32
    Saturation Vapor Pressure (KPa)1.33 (20℃)Explosion Limits1.1%-7.3%
    SolubilitySlightly soluble in water (1.2g/L), soluble in benzene and acetone, readily soluble in ethanol and ether.
    Chemical PropertiesOxidation Reaction: Easily oxidized to caproic acid by air; needs to be stored away from light
    Reduction Reaction: Catalytic hydrogenation to produce hexanol
    Nucleophilic Addition Reaction: Forms acetal with alcohol under acid catalysis
    Condensation Reaction: Undergoes aldol condensation under alkaline catalysis

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