D2157

1,3-Dipalmitoyl-2-Oleoylglycerin

≥99%

• Synonym(e): 1,3-Dihexadecanoyl-2-(cis-9-octadecenoyl)-glycerin
• Empirische Formel (Hill-System): C₅₃H₁₀₀O₆
• CAS-Nummer: 2190-25-2
• Molekulargewicht: 833.36
• MDL-Nummer: MFCD00673528
• UNSPSC-Code: 12352211
• PubChem Substanz-ID: 24893645
• NACRES: NA.25

Eigenschaften

• Biologische Quelle: synthetic (organic)
• Qualitätsniveau: 200
• Assay: ≥99%
• Form: powder
• Funktionelle Gruppe: ester
• Lipid-Typ: neutral glycerides
• Versandbedingung: ambient
• Lagertemp.: −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-
• InChIKey: FDCOHGHEADZEGF-QPLCGJKRSA-N

Beschreibung

Anwendung

• 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).

Sicherheitshinweise

• H-Sätze: H413
• Gefahreneinstufungen: Aquatic Chronic 4
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)