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Merck

258741

Sigma-Aldrich

1-Hexadecanol

ReagentPlus®, 99%

Sinónimos:

Cetyl alcohol, Palmityl alcohol

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About This Item

Fórmula lineal:
CH3(CH2)15OH
Número de CAS:
Peso molecular:
242.44
Beilstein/REAXYS Number:
1748475
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

8.34 (vs air)

Quality Level

vapor pressure

<0.01 mmHg ( 43 °C)

product line

ReagentPlus®

assay

99%

form

solid

autoignition temp.

483 °F

expl. lim.

8 %

bp

179-181 °C/10 mmHg (lit.)

mp

48-50 °C (lit.)

solubility

ethanol: soluble 100 mL/mL, clear to very slightly hazy, colorless

density

0.818 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCO

InChI

1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3

InChI key

BXWNKGSJHAJOGX-UHFFFAOYSA-N

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General description

1-Hexadecanol is a fatty alcohol used in surfactants, lubricants, detergents, pharmaceuticals and cosmetics.

Application

1-Hexadecanol has been used in preparation of:
  • (±)-2-methoxyheptadecanoic acid (fatty acid)
  • high-chain fatty acid esters of 1-hexadecanol, novel organic phase change material for thermal energy storage
  • hexadecane (alkane) in the presence of membrane fraction of Vibrio furnissii M1

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Los clientes también vieron

Metabolic engineering of Saccharomyces cerevisiae to produce 1-hexadecanol from xylose
Guo, et al.
Microbial cell factories, 15, 1-11 (2016)
Néstor M Carballeira et al.
Pure and applied chemistry. Chimie pure et appliquee, 84(9), 1867-1875 (2012-11-03)
The fatty acids (±)-2-methoxy-6Z-heptadecenoic acid (1), (±)-2-methoxy-6-heptadecynoic acid (2) and (±)-2-methoxyheptadecanoic acid (3) were synthesized and their inhibitory activity against the Leishmania DNA topoisomerase IB enzyme (LdTopIB) determined. Acids 1 and 2 were synthesized from 4-bromo-1-pentanol, the former in ten
Metabolic engineering of Saccharomyces cerevisiae to improve 1-hexadecanol production
Feng, et al.
Metabolic engineering, 27, 10-19 (2015)
High-chain fatty acid esters of 1-hexadecanol for low temperature thermal energy storage with phase change materials.
Aydin AA and Aydin A.
Solar Energy Mat. and Solar Cells, 96, 93-100 (2012)
Myong-Ok Park
Journal of bacteriology, 187(4), 1426-1429 (2005-02-03)
Alkane biosynthesis in the bacterium Vibrio furnissii M1 involves the synthesis of long-chain alkanes via 1-alcohol. Evidence for this novel pathway are the following. (i) Both even- and odd-carbon-number n-alkanes were produced from glucose, while only even-carbon-number fatty acids were

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