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Merck

27734

Sigma-Aldrich

Palmitic acid

≥98% palmitic acid basis (GC)

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
Beilstein/REAXYS Number:
607489
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor pressure

10 mmHg ( 210 °C)

Quality Level

assay

≥98% palmitic acid basis (GC)

form

flakes
powder or crystals

technique(s)

gas chromatography (GC): suitable
thin layer chromatography (TLC): suitable

impurities

≤1% stearic acid (GC)

bp

271.5 °C/100 mmHg (lit.)

mp

61-62.5 °C (lit.)
62-65 °C

acid value

≤240

iodine value

≤0.5

saponification value

≤240

density

0.852 g/mL at 25 °C (lit.)

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

Gene Information

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General description

Palmiticacid (C16:0) is a saturated fatty acid commonly found in various naturalsources, such as animal fats and plant oils.

Application

Palmitic acid may be employed in the preparation of palmitic anhydride, via reaction with dicyclohexylcarbodiimide (DCC) in carbon tetrachloride. It undergoes deoxygenation in the presence of 4%wt Pd/C mesoporous catalyst at 300°C and pressure of 17bar of 5% H2 in argon. Aliphatic chain length hydrocarbons containing one less carbon than the corresponding acid were obtained as major products.

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

235.4 °F

flash_point_c

113 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Los clientes también vieron

Z Selinger et al.
Journal of lipid research, 7(1), 174-175 (1966-01-01)
A simple method is described for the preparation of caprylic, palmitic, stearic, and oleic anhydrides. Reaction of the free fatty acid and dicyclohexylcarbodiimide in carbon tetrachloride at room temperature gives the corresponding anhydrides in high yield (87-94%).
Catalytic deoxygenation of stearic acid and palmitic acid in semibatch mode.
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