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Merck

W283215

Sigma-Aldrich

Palmitic acid

natural, 98%, FG

Sinónimos:

1-Pentadecanecarboxylic acid, C16:0, Cetylic acid, Hexadecanoic acid, NSC 5030, PamOH

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About This Item

Fórmula lineal:
CH3(CH2)14COOH
Número de CAS:
Peso molecular:
256.42
FEMA Number:
2832
Beilstein/REAXYS Number:
607489
EC Number:
Council of Europe no.:
14
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
8.014
NACRES:
NA.21

grade

FG
Fragrance grade
Halal
Kosher
natural

Quality Level

agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 172.210
FDA 21 CFR 172.860
FDA 21 CFR 173.340

vapor pressure

10 mmHg ( 210 °C)

assay

98%

form

crystals or chunks

bp

271.5 °C/100 mmHg (lit.)

mp

61-62.5 °C (lit.)

solubility

water: 0.00005 g/L at 20 °C

density

0.852 g/mL at 25 °C (lit.)

cation traces

As: ≤3 ppm
Cd: ≤1 ppm
Hg: ≤1 ppm
Pb: ≤10 ppm

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

faint; fatty

SMILES string

CCCCCCCCCCCCCCCC(O)=O

InChI

1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)

InChI key

IPCSVZSSVZVIGE-UHFFFAOYSA-N

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General description

Palmitic acid is the main constituent of human milk fatty acids. It is also found in sea weeds and air-dried fruit of Cornus officinalis.

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

235.4 °F

flash_point_c

113 °C


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Evidence that palmitic acid is absorbed assn-2 monoacylglycerol from human milk by breast-fed infants.
Innis SM, et al.
Lipids, 29(8), 541-545 (1994)
Distribution of an enzyme system producing seaweed flavor: conversion of fatty acids to long-chain aldehydes in seaweeds.
Kajiwara T, et al.
Journal of Applied Phycology, 5(2), 225-230 (1993)
Volatile flavor components of corni fructus (Cornus officinalis Sieb. Et Zucc.).
Miyazawa M & Kameoka H.
Agricultural and Biological Chemistry, 53(12), 3337-3340 (1989)
Andrea Felser et al.
Toxicology, 323, 1-9 (2014-06-03)
Dronedarone is an amiodarone-like antiarrhythmic drug associated with severe liver injury. Since dronedarone inhibits mitochondrial respiration and β-oxidation in vitro, mitochondrial toxicity may also explain dronedarone-associated hepatotoxicity in vivo. We therefore studied hepatotoxicity of dronedarone (200mg/kg/day for 2 weeks or
Sabeera Bonala et al.
Molecular endocrinology (Baltimore, Md.), 27(9), 1518-1535 (2013-08-10)
Obesity is associated with insulin resistance and abnormal peripheral tissue glucose uptake. However, the mechanisms that interfere with insulin signaling and glucose uptake in human skeletal muscle during obesity are not fully characterized. Using microarray, we have identified that the

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