1,2-dipalmitoyl-sn-glycero-3-succinate - ≥99% , CAS No.108032-13-9

CAS: 108032-13-9 Cat. No.: D130741 Molecular Weight: 668.984

GRADE & PURITY ≥99%

Synonyms

1,2-Dipalmitoyl-3-succinylglycerol|108032-13-9|4-[(2R)-2,3-di(hexadecanoyloxy)propoxy]-4-oxobutanoic acid|1,2-Dpsg|1,2-dipalmitoyl-sn-glycero-3-succinate|SCHEMBL4862128|DTXSID10148366|GNENAKXIVCYCIZ-PGUFJCEWSA-N|16:0 DGS, 1,2-dipalmitoyl-sn-glycero-3-succ

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Application

228,229

Overview

application：

16:0 DGS may be used in the liposomes preparation.

Specifications

Synonyms

1, 2-Dipalmitoyl-3-succinylglycerol | 108032-13-9 | 4-[(2R)-2, 3-di(hexadecanoyloxy)propoxy]-4-oxobutanoic acid | 1, 2-Dpsg | 1, 2-dipalmitoyl-sn-glycero-3-succinate | SCHEMBL4862128 | DTXSID10148366 | GNENAKXIVCYCIZ-PGUFJCEWSA-N | 16:0 DGS, 1, 2-dipalmitoyl-sn-glycero-3-succ

Specifications & Purity

≥99%

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: 504756999
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756999
• Canonical Smiles: CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCC(=O)O)OC(=O)CCCCCCCCCCCCCCC
• IUPAC Name: 4-[(2R)-2,3-di(hexadecanoyloxy)propoxy]-4-oxobutanoic acid
• InChIKey: GNENAKXIVCYCIZ-PGUFJCEWSA-N
• INCHI: 1S/C39H72O8/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-37(42)45-33-35(34-46-38(43)32-31-36(40)41)47-39(44)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h35H,3-34H2,1-2H3,(H,40,41)/t35-/m1/s1
• Isomeric SMILES: CCCCCCCCCCCCCCCC(=O)OC[C@H](COC(=O)CCC(=O)O)OC(=O)CCCCCCCCCCCCCCC
• Molecular Weight: 668.984
• Reaxy-Rn: 12770112
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12770112&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Glycerolipids
      • Subclass Triradylcglycerols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Glycerolipids
• Subclass: Triradylcglycerols
• Intermediate Tree Nodes: Not available
• Direct Parent: Triacylglycerols
• Alternative Parents: Tetracarboxylic acids and derivatives Fatty acid esters Carboxylic acid esters Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Triacyl-sn-glycerol - Tetracarboxylic acid or derivatives - Fatty acid ester - Fatty acyl - Carboxylic acid ester - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.
• 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

Chemical and Physical Properties

• Molecular Weight: 669.000 g/mol
• XLogP3: 14.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 39
• Exact Mass: 668.523 Da
• Monoisotopic Mass: 668.523 Da
• Topological Polar Surface Area: 116.000 Ų
• Heavy Atom Count: 47
• Formal Charge: 0
• Complexity: 753.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1