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1,2-Dinonanoyl-sn-glycero-3-phosphocholine

Selected Variant

HY-W339206

Size: 1 Each

1,2-Dinonanoyl-sn-glycero-3-phosphocholine, a specific phosphatidylcholine, features fatty acyl configurations that can influence the physical properties of membranes, making it a key component for generating eicosanoids. As a phospholipid abundant in membranes, it has fatty acids attached to glycerol at the sn-1 and sn-2 positions via ester bonds.

Product Specifications

CAS Number

27869-45-0

UNSPSC

12352211

Hazard Statement

H301-H311-H315-H319-H331-H335-H350

Target

Endogenous Metabolite

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/1-2-dinonanoyl-sn-glycero-3-phosphocholine.html

Smiles

C[N+](C)(C)CCOP(OC[C@H](OC(CCCCCCCC)=O)COC(CCCCCCCC)=O)([O-])=O

Molecular Formula

C26H52NO8P

Molecular Weight

537.67

Precautions

P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P362+P364-P405-P501

References & Citations

[1]Enhanced charge separation in ternary P3HT/PCBM/CuInS2 nanocrystals hybrid solar cells|[2]Triarylamine-containing poly (perfluorocyclobutane) as hole-transporting material for polymer light-emitting diodes|[3]Characterization of thick film poly (triarylamine) semiconductor diodes for direct x-ray detection|[4]Solvent engineering for high-performance inorganic-organic hybrid perovskite solar cells|[5]High-efficiency inverted semi-transparent planar perovskite solar cells in substrate configuration|[6]Dielectric function and degradation process of poly (triarylamine) (PTAA) |[7]Enhanced infrared spectroscopy of organic field effect transistor (OFET) materialsSendner M and Pucci AAIP Conference Proceedings2015

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

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