D2157

1,3-Dipalmitoyl-2-oleoylglycerol

≥99%

• Sinónimos: 1,3-Dihexadecanoyl-2-(cis-9-octadecenoyl)glycerol
• Fórmula empírica (notación de Hill): C₅₃H₁₀₀O₆
• Número CAS: 2190-25-2
• Peso molecular: 833.36
• NACRES: NA.25
• PubChem Substance ID: 24893645
• UNSPSC Code: 12352211
• MDL number: MFCD00673528

Propiedades

• biological source: synthetic (organic)
• Quality Segment: 200
• assay: ≥99%
• form: powder
• functional group: ester
• lipid type: neutral glycerides
• shipped in: ambient
• storage temp.: −20°C
• SMILES string: CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC
• InChI: 1S/C53H100O6/c1-4-7-10-13-16-19-22-25-26-29-32-35-38-41-44-47-53(56)59-50(48-57-51(54)45-42-39-36-33-30-27-23-20-17-14-11-8-5-2)49-58-52(55)46-43-40-37-34-31-28-24-21-18-15-12-9-6-3/h25-26,50H,4-24,27-49H2,1-3H3/b26-25-
• InChI key: FDCOHGHEADZEGF-QPLCGJKRSA-N

Descripción

Application

• Oxidative lipidomics to elucidate the non-volatile derivatives of four typical triglycerides in vegetable oils under simulated frying conditions: This research underscores the pivotal role of 1,3-Dipalmitoyl-2-oleoylglycerol in understanding the oxidative stability and decomposition products of triglycerides under high-heat conditions, relevant in food science and lipidomics (Hu et al., 2023).


• Stearic acids at sn-1, 3 positions of TAG are more efficient at limiting fat deposition than palmitic and oleic acids in C57BL/6 mice: This research examines the impact of specific triglyceride configurations, including 1,3-Dipalmitoyl-2-oleoylglycerol, on lipid metabolism and fat accumulation in experimental models, which is crucial for understanding lipid-related diseases and for developing lipid-based therapeutics (Gouk et al., 2014).

Información de seguridad

• hcodes: H413
• Hazard Classifications: Aquatic Chronic 4
• Clase de almacenamiento: 11 - Combustible Solids
• wgk: WGK 3
• ppe: Eyeshields, Gloves, type N95 (US)