1,2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (Sodium Salt) - ≥99% , CAS No.474923-39-2

CAS: 474923-39-2 Cat. No.: D130725 Molecular Weight: 730.991

GRADE & PURITY ≥99%

Synonyms

ZTA92339 | Sodium (R)-2,3-bis(palmitoyloxy)propyl (2-mercaptoethyl) phosphate | 16:0 Ptd Thioethanol, 1,2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (Sodium Salt), chloroform | 16:0 Ptd Thioethanol, 1,2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (Sodium

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

general description：

1,2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (DPPTE) or 16:0 Ptd Thioethanol is a thiol modified phospholipid.

application：

16:0 Ptd Thioethanol has been used in the preparation of unilamellar liposomes and supported lipid bilayers (SLB).

Specifications

Synonyms

ZTA92339 | Sodium (R)-2, 3-bis(palmitoyloxy)propyl (2-mercaptoethyl) phosphate | 16:0 Ptd Thioethanol, 1, 2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (Sodium Salt), chloroform | 16:0 Ptd Thioethanol, 1, 2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (Sodium

Specifications & Purity

≥99%

Biochemical and Physiological Mechanisms

1, 2-Dipalmitoyl-sn-Glycero-3-Phosphothioethanol (DPPTE) or 16:0 Ptd Thioethanol facilitates the liposome formation by building the lipid layers with the assistance of thiol-anchors at the lipid headgroups.

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 488201395
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488201395
• Canonical Smiles: CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCCS)OC(=O)CCCCCCCCCCCCCCC.[Na+]
• IUPAC Name: sodium;[(2R)-2,3-di(hexadecanoyloxy)propyl] 2-sulfanylethyl phosphate
• InChIKey: AKETWRINAWSUQU-RUQJKXHKSA-M
• INCHI: 1S/C37H73O8PS.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-36(38)42-33-35(34-44-46(40,41)43-31-32-47)45-37(39)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;/h35,47H,3-34H2,1-2H3,(H,40,41);/q;+1/p-1/t35-;/m1./s1
• Isomeric SMILES: CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCCS)OC(=O)CCCCCCCCCCCCCCC.[Na+]
• Molecular Weight: 730.991

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Glycerophospholipids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Glycerophospholipids
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Glycerophospholipids
• Alternative Parents: Fatty acid esters Dialkyl phosphates Dicarboxylic acids and derivatives Carboxylic acid esters Alkylthiols Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Glycerophospholipid - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Carboxylic acid ester - Carboxylic acid derivative - Alkylthiol - Organic alkali metal salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organosulfur compound - Organooxygen compound - Organic oxygen compound - Organic salt - Organic sodium salt - Organic cation - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as glycerophospholipids. These are derivatives of glycerophosphoric acid that contains at least one O-acyl, or O-alkyl, or O-(1-alkenyl) group attached to the glycerol residue.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

References

1. Jin Ji, Zijie Chen, Tingting Jiang, Yuhua Feng, Hongyu Chen.  (2024)  Two-dimensional active surface growth of Ag nanoplates.  Inorganic Chemistry Frontiers,  11  (14): (4288-4296).  [PMID:] [10.1039/D4QI00620H]