412228
1-Pentadecanol
99%
Synonym(s):
Pentadecyl alcohol
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
CH3(CH2)14OH
CAS Number:
Molecular Weight:
228.41
Beilstein:
1700695
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99%
bp
269-271 °C
mp
41-44 °C (lit.)
SMILES string
CCCCCCCCCCCCCCCO
InChI
1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3
InChI key
REIUXOLGHVXAEO-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
1-Pentadecanol is a linear alcohol. Vapor-phase composition of 1-pentadecanol in supercritical carbon dioxide at 323.15K has been evaluated by a flow-type apparatus. Molar heat capacities of 1-pentadecanol has been evaluated between 300K and 370K.
Application
1-Pentadecanol may be employed as starting reagent for the asymmetric synthesis of jaspine B.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
233.6 °F - closed cup
Flash Point(C)
112 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
A novel stereoselective synthesis of pachastrissamine (jaspine B) starting from 1-pentadecanol.
Venkatesan K and Sreenivasan KV.
Tetrahedron Asymmetry, 19(2), 209-215 (2008)
Solubilities of 1-nonanol, 1-undecanol, 1-tridecanol, and 1-pentadecanol in supercritical carbon dioxide at T= 323.15 K.
Artal M, et al
Journal of Chemical and Engineering Data, 43(6), 983-985 (1998)
Qianqian Gao et al.
Biotechnology for biofuels, 5(1), 17-17 (2012-03-22)
Direct conversion of solar energy and carbon dioxide to drop in fuel molecules in a single biological system can be achieved from fatty acid-based biofuels such as fatty alcohols and alkanes. These molecules have similar properties to fossil fuels but
Hajime Ono et al.
Bioscience, biotechnology, and biochemistry, 84(1), 25-30 (2019-09-14)
The Japanese orange fly, Bactrocera tsuneonis, infests various citrus crops. While male pheromone components accumulated in the rectal glands are well characterized for Bactrocera, but information regarding the chemical factors involved in the life cycles of B. tsuneonis remains scarce.
Kalpana Shanmugarajah et al.
Scientific reports, 9(1), 11381-11381 (2019-08-08)
Diffusion barriers enable plant survival under fluctuating environmental conditions. They control internal water potential and protect against biotic or abiotic stress factors. How these protective molecules are deposited to the extracellular environment is poorly understood. We here examined the role
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service