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Catalog Number:
39018
CAS Number:
7367-81-9
Trans -2-octenoato de metilo
Purity:
≥ 95% (GC)
Synonym(s):
éster metílico del ácido trans-2-octenoico
Documents
$35.00 /5 ml
Tamaño
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Product Information

Conservar bajo gas inerte.

Synonyms
éster metílico del ácido trans-2-octenoico
CAS Number
7367-81-9
Purity
≥ 95% (GC)
Molecular Formula
C9H16O2
Molecular Weight
156.23
MDL Number
MFCD00036620
PubChem ID
61313
Density
0.910 (Literatura)
Appearance
Líquido incoloro a amarillo.
Boiling Point
61 °C
Refractive Index
n20/D 1.430-1.450
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
éster metílico del ácido trans-2-octenoico
CAS Number
7367-81-9
Purity
≥ 95% (GC)
Molecular Formula
C9H16O2
Molecular Weight
156.23
MDL Number
MFCD00036620
PubChem ID
61313
Density
0.910 (Literatura)
Appearance
Líquido incoloro a amarillo.
Boiling Point
61 °C
Refractive Index
n20/D 1.430-1.450
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Methyl trans-2-octenoate is widely utilized in research focused on

  • Flavor and Fragrance Industry: This compound is used as a flavoring agent in food products and as a fragrance component in perfumes, providing a fruity aroma that enhances sensory experiences.
  • Cosmetic Formulations: It serves as an ingredient in cosmetic products, contributing to the scent and enhancing the texture of creams and lotions, making them more appealing to consumers.
  • Chemical Synthesis: Methyl trans-2-octenoate is a valuable intermediate in organic synthesis, allowing researchers to create various complex molecules for pharmaceuticals and agrochemicals.
  • Polymer Production: This compound can be used in the production of specialty polymers, offering unique properties such as flexibility and durability, which are essential in manufacturing high-performance materials.
  • Research Applications: In academic and industrial research, it is utilized in studies related to reaction mechanisms and the development of new synthetic pathways, aiding in the advancement of organic chemistry.

Citas