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Merck

W255408

Sigma-Aldrich

1-Hexadecanol

≥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
FEMA Number:
2554
Beilstein/REAXYS Number:
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

Quality Level

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

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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Visite la Librería de documentos

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
Luca Lo Piccolo et al.
Applied and environmental microbiology, 77(4), 1204-1213 (2010-12-25)
Enzymes involved in oxidation of long-chain n-alkanes are still not well known, especially those in gram-positive bacteria. This work describes the alkane degradation system of the n-alkane degrader actinobacterium Gordonia sp. strain SoCg, which is able to grow on n-alkanes
Dhanalakshmi S Anbukumar et al.
Journal of lipid research, 51(5), 1085-1092 (2009-12-19)
Neutrophils are important in the host response against invading pathogens. One chemical defense mechanism employed by neutrophils involves the production of myeloperoxidase (MPO)-derived HOCl. 2-Chlorohexadecanal (2-ClHDA) is a naturally occurring lipid product of HOCl targeting the vinyl ether bond of

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