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この商品について
化学式:
CH3(CH2)14COOH
CAS番号:
分子量:
256.42
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-312-9
MDL number:
Beilstein/REAXYS Number:
607489
Assay:
≥98% palmitic acid basis (GC)
Form:
flakes, powder or crystals
製品名
パルミチン酸, ≥98% palmitic acid basis (GC)
vapor pressure
10 mmHg ( 210 °C)
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.)
functional group
carboxylic acid
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
human ... FABP2(2169), FABP3(2170), FABP4(2167), FABP5(2171)
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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.
保管分類
11 - Combustible Solids
wgk
nwg
flash_point_f
235.4 °F
flash_point_c
113 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
Catalytic deoxygenation of stearic acid and palmitic acid in semibatch mode.
Lestari S, et al.
Catalysis Letters, 130(1-2), 48-51 (2009)
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%).
Xiaozhe Yin et al.
Cell reports, 33(3), 108278-108278 (2020-10-22)
Dendritic cells (DCs) orchestrate the initiation, programming, and regulation of anti-tumor immune responses. Emerging evidence indicates that the tumor microenvironment (TME) induces immune dysfunctional tumor-infiltrating DCs (TIDCs), characterized with both increased intracellular lipid content and mitochondrial respiration. The underlying mechanism
B Vessby et al.
Diabetologia, 37(10), 1044-1050 (1994-10-01)
Recent data indicate that peripheral insulin sensitivity may be influenced by dietary fat quality and skeletal muscle phospholipid fatty acid composition. During a health survey of 70-year-old men insulin sensitivity was measured by the euglycaemic hyperinsulinaemic clamp technique and the
Jonas Sieber et al.
The American journal of pathology, 183(3), 735-744 (2013-07-23)
Type 2 diabetes mellitus is characterized by dyslipidemia with elevated free fatty acids (FFAs). Loss of podocytes is a hallmark of diabetic nephropathy, and podocytes are highly susceptible to saturated FFAs but not to protective, monounsaturated FFAs. We report that
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