D8394

1,2-Dioleoyl-rac-glycerol

≥97%

• Synonyme(s) : (9Z)-9-Octadecenoic acid 1,1′-[1-(hydroxymethyl)-1,2-ethanediyl] ester, (±)-1,2-Diolein, 1,2-Di(cis-9-octadecenoyl)-rac-glycerol, rac-1,2-Dioleoylglycerol, rac-Glycerol 1,2-dioleate, DG(18:1(9Z)/18:1(9Z)/0:0)[rac]
• Formule empirique (notation de Hill) : C₃₉H₇₂O₅
• Numéro CAS: 2442-61-7
• Poids moléculaire : 620.99
• UNSPSC Code: 12352211
• NACRES: NA.25
• PubChem Substance ID: 24894210
• MDL number: MFCD00043031
• Beilstein/REAXYS Number: 1917687

Propriétés

• biological source: synthetic (organic)
• Quality Segment: 200
• assay: ≥97%
• form: liquid
• impurities: ≤3% 1,3-isomer
• functional group: ester
• lipid type: neutral glycerides
• shipped in: dry ice
• storage temp.: −20°C
• SMILES string: CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCC\C=C/CCCCCCCC
• InChI: 1S/C39H72O5/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/h17-20,37,40H,3-16,21-36H2,1-2H3/b19-17-,20-18-
• InChI key: AFSHUZFNMVJNKX-CLFAGFIQSA-N

Description

Application

• Diacylglycerol acyltransferases from Vernonia and Stokesia prefer substrates with vernolic acid.: Studies enzyme preferences for 1,2-Dioleoyl-rac-glycerol in the biosynthesis of industrially important oils, offering pathways to enhance bio-oil production using specific enzymatic processes (Yu et al., 2006).

Disclaimer

Some isomerization may occur in storage or in solution.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)