412228
1-Pentadecanol
99%
Synonym(s):
Pentadecyl alcohol
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About This Item
Linear Formula:
CH3(CH2)14OH
CAS Number:
Molecular Weight:
228.41
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-107-9
Beilstein/REAXYS Number:
1700695
MDL number:
Product Name
1-Pentadecanol, 99%
InChI key
REIUXOLGHVXAEO-UHFFFAOYSA-N
InChI
1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3
SMILES string
CCCCCCCCCCCCCCCO
assay
99%
bp
269-271 °C
mp
41-44 °C (lit.)
Quality Level
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Application
1-Pentadecanol may be employed as starting reagent for the asymmetric synthesis of jaspine B.
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.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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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)
A novel stereoselective synthesis of pachastrissamine (jaspine B) starting from 1-pentadecanol.
Venkatesan K and Sreenivasan KV.
Tetrahedron Asymmetry, 19(2), 209-215 (2008)
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
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
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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.
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