Palmitic acid-13C16

Base Information

• Chemical Name: Palmitic acid-13C16
• CAS No.: 56599-85-0
• Molecular Formula: 13CH3(13CH2)1413CO2H
• Molecular Weight: 0
• European Community (EC) Number: 622-162-7
• DSSTox Substance ID: DTXSID60584437
• Wikidata: Q82476097
• Mol file: 56599-85-0.mol

Synonyms:Palmitic acid-13C16;56599-85-0;Hexadecanoic acid-13C16;(1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16-13C16)Hexadecanoic acid;Palmitic acid-13C??;Palmitic Acid-?13C16;SCHEMBL1331318;DTXSID60584437;(~13~C_16_)Hexadecanoic acid;HY-N0830S6;Hexadecanoic acid-13c16(algal source)(;MS-23863;CS-0226384;G12397;CP pound masculine98% pound not98 atom % 13C;Palmitic acid-13C16, 99 atom % 13C, 99% (CP);Palmitic acid-13C16, S & P tested, 99 atom % 13C

Chemical Property of Palmitic acid-13C16

Chemical Property:

• Melting Point: 61-64 °C
• Boiling Point: 271.5 °C/100 mmHg(lit.)
• Flash Point: 206℃
• PSA: 37.30000
• Density: 0.904 g/mL at 25 °C
• LogP: 5.55230
• Storage Temp.: Refrigerator
• Solubility.: Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
• XLogP3: 6.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 272.29390762
• Heavy Atom Count: 18
• Complexity: 178

Purity/Quality:

NLT 98% ^*data from raw suppliers

Palmitic acid-13C16 ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38-36
• Safety Statements: 26-37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCC(=O)O
• Isomeric SMILES: [13CH3][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C](=O)O
• Uses: Palmitic Acid-?13C16 is an analytical agent for analysis of sphingolipid biosynthesis by tandem mass spectrometry.

Technology Process of Palmitic acid-13C16

There total 1 articles about Palmitic acid-13C16 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

[1,2-13C]acetyl-CoA (140701-77-5) + [(13)C4]malonyl-CoA → [U-13C]palmitic acid (56599-85-0)

Guidance literature:

With ethylenediaminetetraacetic acid; recombinant rat fatty acid synthase; NADH; diothiothreitol; at 37 ℃; pH=7; aq. phosphate buffer; Enzymatic reaction;

DOI:10.1016/j.ab.2012.06.013

upstream raw materials:

[1,2-¹³C]acetyl-CoA

Refernces