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3-TRIDECANONE(CAS#1534-26-5)

Chemical Property:

1534-26-5 - Physico-chemical Properties

Molecular Formula C13H26O
Molar Mass 198.34
Density 0.8275 (estimate)
Melting Point 31°C
Boling Point 260.68°C (estimate)
Flash Point 26 °C
Refractive Index 1.4365 (estimate)

Product Detail

Product Tags

1534-26-5‌ is ‌3-Tridecanone‌, an organic ketone compound widely used in fragrance, flavor, and scientific research.

Safety & Storage

  • ‌GHS Pictogram‌: GHS07 (Warning)
  • ‌Hazard Statements‌:
    • H315: Causes skin irritation
    • H319: Causes serious eye irritation
    • H335: May cause respiratory irritation
  • ‌Personal Protection‌: It is recommended to wear ‌protective goggles and gloves‌, and avoid inhalation of vapors or skin contact
  • ‌Storage Conditions‌: Store in a ‌light-resistant, sealed container under inert atmosphere at room temperature‌ to prevent oxidation
  • ‌WGK Germany‌: ‌3‌ (Severe hazard to aquatic environment)

Uses & Applications

  1. ‌Fragrance & Flavor‌:
    • Used in blending ‌floral and fruity fragrance types‌, such as violet, cucumber, and watermelon notes, enhancing naturalness and complexity
    • Due to its stable molecular structure, it can serve as a ‌fragrance fixative‌
  2. ‌Food Additive‌:
    • Listed as ‌FEMA GRAS‌ (Generally Recognized as Safe), approved for use as a flavoring agent
    • Recommended usage levels:
      • Soft drinks, cold beverages: ‌0.15 mg/kg‌
      • Candies, baked goods: ‌0.20 mg/kg‌
      • Puddings, meat products, soups: ‌0.15 mg/kg‌
  3. ‌Scientific Research & Biochemical Reagent‌:
    • Serves as a ‌biochemical reagent‌ for olfactory receptor function studies and insect behavioral experiments (e.g., repellent activity research)
    • Used as a ‌standard or reference substance‌ in life science research
  4. ‌Industrial Raw Material‌:
    • Used to synthesize ‌ester derivatives‌, such as trans-2-nonenyl acetate, for further fragrance formulation
    • Acts as an organic synthesis intermediate in constructing complex molecules

Synthesis Method

Prepared by reacting ‌1-bromo-2-nonen‌ with ‌acetic anhydride‌ in acetic acid to form an acetate ester, followed by ‌hydrolysis‌. Purification is achieved through ‌vacuum distillation‌ or ‌column chromatography‌.

⚠️ ‌Note‌: This product is a chemical substance, ‌not for direct consumption or medicinal use‌. For industrial, research, or flavor formulation purposes only. Purchase requires appropriate qualifications.


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