| Identification | Back Directory | [Name]
Palmitic acid-1,2,3,4-13C4 | [CAS]
287100-89-4 | [Synonyms]
Palmitic Acid-13C (C1, C2, C3, and C4 labeled) | [Molecular Formula]
CH3(CH2)11(CH2)3COOH | [MOL File]
287100-89-4.mol | [Molecular Weight]
260.46 |
| Chemical Properties | Back Directory | [Melting point ]
61-64 °C (lit.) | [storage temp. ]
Store at -20°C | [solubility ]
DMF: 15 mg/ml,DMSO: 10 mg/ml,Ethanol: 1 mg/ml | [form ]
A crystalline solid | [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)/i13+1,14+1,15+1,16+1 | [InChIKey]
IPCSVZSSVZVIGE-FIZPRHLTSA-N | [SMILES]
CCCCCCCCCCCC[13CH2][13CH2][13CH2][13C](O)=O | [CAS Number Unlabeled]
57-10-3 |
| Hazard Information | Back Directory | [Uses]
Palmitic acid-1,2,3,4-13C4 is the 13C-labeled Palmitic acid. Palmitic acid is a long-chain saturated fatty acid commonly found in both animals and plants. Palmitic acid can induce the expression of glucose-regulated protein 78 (GRP78) and CCAAT/enhancer binding protein homologous protein (CHOP) in in mouse granulosa cells[1][2]. | [Definition]
ChEBI: Hexadecanoic acid-13C4 is a long-chain fatty acid. | [References]
[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Harada H, et al. Antitumor activity of palmitic acid found as a selective cytotoxic substance in a marine red alga. Anticancer Res. 2002 Sep-Oct;22(5):2587-90. PMID:12529968 |
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