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Key Documents

W255408

Sigma-Aldrich

1-Hexadecanol

≥99%

Synonym(s):

Cetyl alcohol, Palmityl alcohol

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About This Item

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

biological source

synthetic

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

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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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
T Yoshida et al.
International journal of pharmaceutics, 365(1-2), 81-88 (2008-09-16)
Salting-out effects were utilized for developing a multiparticulate system balancing numbness masking and high bioavailability. A "salting-out taste-masking system" consisting of a drug core containing acetaminophen as a model drug, a salting-out layer containing sodium carbonate (Na(2)CO(3)) and hydroxypropylmethylcellulose (HPMC)
James L Hargrove et al.
Experimental biology and medicine (Maywood, N.J.), 229(3), 215-226 (2004-02-28)
Very long chain fatty alcohols obtained from plant waxes and beeswax have been reported to lower plasma cholesterol in humans. This review discusses nutritional or regulatory effects produced by wax esters or aliphatic acids and alcohols found in unrefined cereal
Laurent Perge et al.
International journal of pharmaceutics, 422(1-2), 59-67 (2011-10-27)
A hot melt dispersion method was used to prepare new sustained release ibuprofen composite microparticles of a solid lipid at ambient temperature, cetyl alcohol. The dispersion of colloidal silicon dioxide nanoparticles (hydrophilic Aerosil 200 or hydrophobic Aerosil R974) either in

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