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rac 1,2-Dioleoyl-3-chloropropanediol-13C36
For research use only. Not for therapeutic Use.
rac 1,2-Dioleoyl-3-chloropropanediol-13C36, a labeled derivative of 1,2-dioleoyl-3-chloropropanediol, is utilized as a stable isotope tracer in lipid metabolism studies. Its ^13C-labeled carbons enable precise tracking of metabolic pathways involving lipids. This compound is particularly useful in research focusing on lipid metabolism, phospholipid dynamics, and cellular membrane studies. Its applications span pharmaceutical development, particularly in understanding drug interactions with lipid membranes, as well as material chemistry, where it helps elucidate lipid-related chemical processes and interactions.
Catalog Number | R048010 |
CAS Number | NA |
Synonyms | (9Z)-9-Octadecenoic Acid 1,1’-[1-(Chloromethyl)-1,2-ethanediyl] Ester-13C36; Oleic Acid (Chloromethyl)ethylene Ester-13C36; 3-Chloro-1,2-propanediol Dioleate-13C36; |
Molecular Formula | C₃¹³C₃₆H₇₁ClO₄ |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | [(2S)-3-chloro-2-[(Z)-(1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18-13C18)octadec-9-enoyl]oxypropyl] (Z)-(1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18-13C18)octadec-9-enoate |
InChI | InChI=1S/C39H71ClO4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-36-37(35-40)44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20,37H,3-16,21-36H2,1-2H3/b19-17-,20-18-/t37-/m1/s1/i1+1,2+1,3+1,4+1,5+1,6+1,7+1,8+1,9+1,10+1,11+1,12+1,13+1,14+1,15+1,16+1,17+1,18+1,19+1,20+1,21+1,22+1,23+1,24+1,25+1,26+1,27+1,28+1,29+1,30+1,31+1,32+1,33+1,34+1,38+1,39+1 |
InChIKey | BLQSPZHGZHJLGB-ZDGIDXTESA-N |
SMILES | [13CH3][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2]/[13CH]=[13CH]\[13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C](=O)OC[C@@H](CCl)O[13C](=O)[13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2]/[13CH]=[13CH]\[13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH3] |