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258741

Sigma-Aldrich

1-Hexadecanol

ReagentPlus®, 99%

Synonym(s):

Cetyl alcohol, Palmityl alcohol

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About This Item

Linear Formula:
CH3(CH2)15OH
CAS Number:
36653-82-4
Molecular Weight:
242.44
Beilstein/REAXYS Number:
1748475
EC Number:
253-149-0
MDL number:
MFCD00004760
UNSPSC Code:
12352100
PubChem Substance ID:
24855657
NACRES:
NA.22
grade:
reagent
assay:
99%
bp:
179-181 °C/10 mmHg (lit.)
vapor pressure:
<0.01 mmHg ( 43 °C)

grade

reagent

Quality Level

200

vapor density

8.34 (vs air)

vapor pressure

<0.01 mmHg ( 43 °C)

product line

ReagentPlus®

assay

99%

form

solid

autoignition temp.

483 °F

expl. lim.

8 %

dilution

(for general lab use)

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.)

functional group

hydroxyl

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG6217
BCCD8135
BCCB8142
BCBX9911
BCBV5058

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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
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)
S Karen Gomez et al.
BMC plant biology, 9, 10-10 (2009-01-24)
Most vascular flowering plants have the capacity to form symbiotic associations with arbuscular mycorrhizal (AM) fungi. The symbiosis develops in the roots where AM fungi colonize the root cortex and form arbuscules within the cortical cells. Arbuscules are enveloped in
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
Toru Uyama et al.
The Journal of biological chemistry, 290(28), 17520-17534 (2015-05-29)
Phospholipase A/acyltransferase (PLA/AT)-3 (also known as H-rev107 or AdPLA) was originally isolated as a tumor suppressor and was later shown to have phospholipase A1/A2 activity. We have also found that the overexpression of PLA/AT-3 in mammalian cells results in specific
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Global Trade Item Number

SKUGTIN
258741-1G4061826279342
258741-500G4061826062203
258741-100G4061826062142
258741-5G4061826062258

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