Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

W255408

Sigma-Aldrich

1-Hexadecanol

≥99%

Synonym(s):

Cetyl alcohol, Palmityl alcohol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3(CH2)15OH
CAS Number:
36653-82-4
Molecular Weight:
242.44
FEMA Number:
2554
Beilstein:
1748475
EC Number:
253-149-0
Council of Europe no.:
57
MDL number:
MFCD00004760
UNSPSC Code:
12164502
PubChem Substance ID:
24901140
Flavis number:
2.009
NACRES:
NA.21

biological source

synthetic

Quality Level

400

Agency

meets purity specifications of JECFA

reg. compliance

FDA 21 CFR 172.515

vapor density

8.34 (vs air)

vapor pressure

<0.01 mmHg ( 43 °C)

Assay

≥99%

autoignition temp.

483 °F

expl. lim.

8 %

bp

179-181 °C/10 mmHg (lit.)

mp

48-50 °C (lit.)

density

0.818 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

waxy

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

1-Hexadecanol is a free fatty acid alcohol generally used as an emulsifier, emollient, opacifier and surfactant in cosmetics formulations.

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Storage Class Code

11 - Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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
STBK3981
STBJ9017
STBK2816
STBK2138
STBK1621

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.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ash M
Handbook of Green Chemicals, 665-665 (2004)
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
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
N Dashti et al.
Chemosphere, 70(3), 475-479 (2007-08-07)
Bacteria and fungi in pristine and oily desert soil samples were counted on inorganic medium aliquots containing 0.5% hexadecane, hexadecanol, hexadecanal or hexadecanoic acid, as sole sources of carbon and energy. It was found that the carbon and energy source
Daniel Wehrung et al.
Colloids and surfaces. B, Biointerfaces, 94, 259-265 (2012-03-06)
The main objective of the study is to investigate the efficacy of Gelucire 44/14 (gelucire) in facilitating formation of cetyl alcohol (CA)-based nanoparticle (NP) and to assess the effects on key NP properties and functions. NPs from oil-in-water nanoemulsion precursors
View All Related Papers

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