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1,2-Dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt - >99%, high purity , CAS No.67254-28-8

COA

Grade & Purity:

≥99%

Cas Number: 67254-28-8
Molecular Weight: 797.03
EC Number: 200-663-8
PubChem CID: 23702460

In stock

Item Number

D130353

Grouped product items
SKU	Size	Availability	Price
D130353-25mg	25mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$87.90
D130353-100mg	100mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$158.90
D130353-500mg	500mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$713.90

View related series

Element classified compounds (2014) Lipid metabolism (1912) Phospholipid (111) Phosphorus compounds (460)

Basic Description

Synonyms	(9Z)-9-Octadecenoic acid 1-[[[(2,3-dihydroxypropoxy)hydroxyphosphinyl]oxy]methyl]-1,2-ethanediyl ester monosodium salt \| 1,2-Di(9Z-octadecenoyl)-sn-glycero-3-phospho-(1'-rac-glycerol) sodium salt \| DOPG-Na \| PG(18:1(9Z)/18:1(9Z)) \| DOPG-Na, r- \| 1,2-di-(9
Specifications & Purity	≥99%
Biochemical and Physiological Mechanisms	Remodeling of diacylphosphatidylglycerols by transesterification was studied in a phosphatidylglycerol-deficient microbe grown with exogenous DOPG.
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	The lipid DOPG has significant influence on multidrug transport. The DOPG membrane content can alter substrate transport of small multidrug transporters (SMR) proteins by an order of magnitude.

Taxonomic Classification

Taxonomy Tree

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

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Glycerophospholipids
Subclass	Glycerophosphoglycerols
Intermediate Tree Nodes	Not available
Direct Parent	Phosphatidylglycerols
Alternative Parents	Fatty acid esters Dialkyl phosphates Dicarboxylic acids and derivatives Secondary alcohols Carboxylic acid esters 1,2-diols Primary alcohols Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
Molecular Framework	Aliphatic acyclic compounds
Substituents	1,2-diacylglycerophosphoglycerol - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Secondary alcohol - 1,2-diol - Carboxylic acid ester - Carboxylic acid derivative - Organic alkali metal salt - Hydrocarbon derivative - Carbonyl group - Primary alcohol - Organic oxide - Organooxygen compound - Alcohol - 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 phosphatidylglycerols. These are glycerophosphoglycerols in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages.
External Descriptors	Not available
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

Names and Identifiers

IUPAC Name	sodium;[(2R)-2,3-bis[[(Z)-octadec-9-enoyl]oxy]propyl] 2,3-dihydroxypropyl phosphate
INCHI	InChI=1S/C42H79O10P.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-41(45)49-37-40(38-51-53(47,48)50-36-39(44)35-43)52-42(46)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;/h17-20,39-40,43-44H,3-16,21-38H2,1-2H3,(H,47,48);/q;+1/p-1/b19-17-,20-18-;/t39?,40-;/m1./s1
InChIKey	IUVFCFQZFCOKRC-IPKKNMRRSA-M
Smiles	CCCCCCCCC=CCCCCCCCC(=O)OCC(COP(=O)([O-])OCC(CO)O)OC(=O)CCCCCCCC=CCCCCCCCC.[Na+]
Isomeric SMILES	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC(CO)O)OC(=O)CCCCCCC/C=C\CCCCCCCC.[Na+]
WGK Germany	3
Molecular Weight	797.03
Reaxy-Rn	28872212
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=28872212&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot Number	Certificate Type	Date	Item
E2507270	Certificate of Analysis	Apr 26, 2025	D130353
E2507272	Certificate of Analysis	Apr 26, 2025	D130353
E2114112	Certificate of Analysis	Sep 22, 2023	D130353
E2114110	Certificate of Analysis	Sep 22, 2023	D130353
H2203356	Certificate of Analysis	Feb 13, 2023	D130353
H2203332	Certificate of Analysis	Feb 13, 2023	D130353
H2203338	Certificate of Analysis	Feb 13, 2023	D130353
H2202186	Certificate of Analysis	Jun 30, 2022	D130353
E2114111	Certificate of Analysis	Jun 22, 2022	D130353

Chemical and Physical Properties

Sensitivity	Heat Sensitive；Air sensitive；Moisture sensitive；Light sensitive
Specific Rotation[α]	9° (C=2,EtOH)
Flash Point(°F)	>392 °F
Flash Point(°C)	>200 °C
Molecular Weight	797.000 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	10
Rotatable Bond Count	42
Exact Mass	796.523 Da
Monoisotopic Mass	796.523 Da
Topological Polar Surface Area	152.000 Å²
Heavy Atom Count	54
Formal Charge	0
Complexity	948.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	2
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	2
Covalently-Bonded Unit Count	2

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