조직 및 계약 가격을 보려면 로그인를 클릭합니다.
크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)14COOH
CAS 번호:
Molecular Weight:
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
제품 이름
Palmitic acid, ≥98% palmitic acid basis (GC)
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.)
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)
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.
저장 등급
11 - Combustible Solids
wgk
nwg
flash_point_f
235.4 °F
flash_point_c
113 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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.
Lestari S, et al.
Catalysis Letters, 130(1-2), 48-51 (2009)
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