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Catalog Number:
33893
CAS Number:
14765-30-1
2-sec-Butylcyclohexanone
Grade:
meets FG specifications, KOSHER, FEMA 3261
Purity:
97 - 100% (GC)
Synonym(s):
2-(1-Methylpropyl)cyclohexanone
Hazmat
Documents
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Product Information
Synonyms
2-(1-Methylpropyl)cyclohexanone
CAS Number
14765-30-1
Purity
97 - 100% (GC)
Grade
meets FG specifications, KOSHER, FEMA 3261
Molecular Formula
C10H18O
Molecular Weight
0
MDL Number
MFCD00051454
PubChem ID
61771
Density
0.913
Appearance
Colorless to pale yellow liquid
Boiling Point
76 - 78 °C
Refractive Index
n20/D 1.457 - 1.461
Conditions
Store at 0 - 8 °C
General Information
Synonyms
2-(1-Methylpropyl)cyclohexanone
CAS Number
14765-30-1
Purity
97 - 100% (GC)
Grade
meets FG specifications, KOSHER, FEMA 3261
Molecular Formula
C10H18O
Molecular Weight
0
MDL Number
MFCD00051454
PubChem ID
61771
Density
0.913
Appearance
Colorless to pale yellow liquid
Boiling Point
76 - 78 °C
Refractive Index
n20/D 1.457 - 1.461
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-sec-Butylcyclohexanone is widely utilized in research focused on:

  • Solvent Applications: This compound serves as an effective solvent in various chemical reactions, particularly in organic synthesis, enhancing the solubility of reactants and improving reaction yields.
  • Fragrance Industry: It is used in the formulation of fragrances and perfumes, providing a unique scent profile that is appealing in cosmetic products.
  • Flavoring Agent: In the food industry, it acts as a flavoring agent, contributing to the taste of certain food products, making them more palatable.
  • Intermediate in Synthesis: This chemical is a valuable intermediate in the production of other chemical compounds, enabling the development of pharmaceuticals and agrochemicals.
  • Research and Development: It is often employed in laboratories for various research applications, including studies on reaction mechanisms and the development of new synthetic pathways.

Citations