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412228

Sigma-Aldrich

1-Pentadecanol

99%

Synonym(s):

Pentadecyl alcohol

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5 G
$141.00

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5 G
$141.00

About This Item

Linear Formula:
CH3(CH2)14OH
CAS Number:
629-76-5
Molecular Weight:
228.41
Beilstein/REAXYS Number:
1700695
EC Number:
211-107-9
MDL number:
MFCD00004759
UNSPSC Code:
12352100
PubChem Substance ID:
24865795
NACRES:
NA.22

$141.00

Available to ship onApril 29, 2025Details

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Quality Level

100

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

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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.[1] Molar heat capacities of 1-pentadecanol has been evaluated between 300K and 370K.[2]

Application

1-Pentadecanol may be employed as starting reagent for the asymmetric synthesis of jaspine B.[3]

Storage Class

11 - Combustible Solids

wgk_germany

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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Certificates of Analysis (COA)

Lot/Batch Number
0000418094
0000418094
0000323968
0000323968
SHBR0515

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Vasiliki Gkarane et al.
Food research international (Ottawa, Ont.), 115, 54-64 (2019-01-03)
Animal production factors can affect the sensory quality of lamb meat. The study investigated the effect of diet composition and duration of consumption on the proximate analysis, volatile profile and sensory quality of lamb meat. Ninety-nine male Texel × Scottish
Heat Capacities and Derived Thermodynamic Functions of 1-Dodecanol and 1-Tridecanol between 10 K and 370 K and Heat Capacities of 1-Pentadecanol and 1-Heptadecanol between 300 K and 380 K and Correlations for the Heat Capacity and the Entropy of Liquid n-Alcohols.
van Miltenburg JC, et al.
Journal of Chemical and Engineering Data, 48(1), 36-43 (2003)
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
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.
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