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Catalog Number:
33778
CAS Number:
123-68-2
Allyl hexanoate
Grade:
Natural, meets FG specifications, Kosher, FEMA 2
Purity:
98 - 100% (GC)
Synonym(s):
2-Propenyl hexanoate, Allyl caproate
Hazmat
Documents
$36.65 /25G
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Product Information
Synonyms
2-Propenyl hexanoate, Allyl caproate
CAS Number
123-68-2
Purity
98 - 100% (GC)
Grade
Natural, meets FG specifications, Kosher, FEMA 2
Molecular Formula
C9H16O2
Molecular Weight
0
MDL Number
MFCD00038339
PubChem ID
31266
Density
0.887 g/mL at 25 °C
Appearance
Clear colorless liquid
Boiling Point
185 - 188 °C
Refractive Index
n20/D 1.422 - 1.426
Conditions
Store at 0-8 °C
General Information
Synonyms
2-Propenyl hexanoate, Allyl caproate
CAS Number
123-68-2
Purity
98 - 100% (GC)
Grade
Natural, meets FG specifications, Kosher, FEMA 2
Molecular Formula
C9H16O2
Molecular Weight
0
MDL Number
MFCD00038339
PubChem ID
31266
Density
0.887 g/mL at 25 °C
Appearance
Clear colorless liquid
Boiling Point
185 - 188 °C
Refractive Index
n20/D 1.422 - 1.426
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Allyl hexanoate is widely utilized in research focused on:

  • Flavoring and Fragrance Industry: This compound is commonly used as a flavoring agent in food products and beverages, providing a fruity aroma that enhances sensory appeal.
  • Cosmetic Formulations: In cosmetics, it serves as a fragrance component, contributing to the scent profile of perfumes and personal care products, making them more appealing to consumers.
  • Polymer Chemistry: Allyl hexanoate is employed in the synthesis of specialty polymers and resins, offering flexibility and improved thermal stability compared to other similar compounds.
  • Agricultural Applications: It can be used as an intermediate in the production of agrochemicals, helping to develop effective pest control agents while being less toxic to non-target organisms.
  • Research and Development: In laboratories, it is utilized as a reagent in organic synthesis, facilitating the creation of complex molecules in medicinal chemistry and materials science.

Citations