Skip to the beginning of the images gallery

1,2-dilauroyl-sn-glycero-3-phosphoethanolamine - >99%, high purity , CAS No.59752-57-7

COA

Grade & Purity:

≥99%

Cas Number: 59752-57-7
Molecular Weight: 579.746
Beilstein Registry Number: 1810614
EC Number: 261-912-4
MDL number: MFCD00042828
PubChem CID: 9546801

In stock

Item Number

D130467

Grouped product items
SKU	Size	Availability	Price
D130467-25mg	25mg	2	$245.90
D130467-100mg	100mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$480.90
D130467-500mg	500mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,957.90

View related series

Activated Lipid (124) Lipid metabolism (1912) Phospholipid (111)

Basic Description

Synonyms	12:0 PE \| DLPE \| PE(12:0/12:0) \| beta,gamma-Dilauroyl-L-alpha-phosphatidylethanolamine \| UNII-D1O2S89PCE \| DLPE \| PE(12:0/12:0) \| [(2R)-3-[2-aminoethoxy(hydroxy)phosphoryl]oxy-2-dodecanoyloxypropyl] dodecanoate \| C29H58NO8P \| 1,2-didodecanoyl-sn-glycero-3
Specifications & Purity	≥99%
Biochemical and Physiological Mechanisms	Phosphatidylethanolamine (PE) plays a vital role in the structure and function of eukaryotic membranes.
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	Description Phosphatidylethanolamine (PE) is one of the widely distributed glycerophospholipid in eukaryotic cells. 1,2-dilauroyl-sn-glycero-3-phosphoethanolamine (12:0 PE/DLPE) possess an ammonium head group (RNH3+) and has alkyl chains made of 11 carbon atoms. Application 1,2-dilauroyl-sn-glycero-3-phosphoethanolamine (12:0 PE): has been used as a lipid standard in the optimization of the liquid chromatography−mass spectrometry (LC-MS) method conditions, may be used as a phospholipid (PL) standard to quantify phosphatidylethanolamine (PE) from plant lipids, may be used to prepare anionic liposomes, may be used to prepare binary giant unilamellar vesicles (GUVs).

Taxonomic Classification

Taxonomy Tree

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

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Glycerophospholipids
Subclass	Glycerophosphoethanolamines
Intermediate Tree Nodes	Not available
Direct Parent	Phosphatidylethanolamines
Alternative Parents	Phosphoethanolamines Fatty acid esters Dialkyl phosphates Dicarboxylic acids and derivatives Carboxylic acid esters Amino acids and derivatives Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Diacylglycero-3-phosphoethanolamine - Phosphoethanolamine - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organic nitrogen compound - Primary amine - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as phosphatidylethanolamines. These are glycerophosphoetahnolamines in which two fatty acids are bonded to the glycerol moiety through ester linkages.
External Descriptors	Diacylglycerophosphoethanolamines
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	[(2R)-3-[2-aminoethoxy(hydroxy)phosphoryl]oxy-2-dodecanoyloxypropyl] dodecanoate
INCHI	InChI=1S/C29H58NO8P/c1-3-5-7-9-11-13-15-17-19-21-28(31)35-25-27(26-37-39(33,34)36-24-23-30)38-29(32)22-20-18-16-14-12-10-8-6-4-2/h27H,3-26,30H2,1-2H3,(H,33,34)/t27-/m1/s1
InChIKey	ZLGYVWRJIZPQMM-HHHXNRCGSA-N
Smiles	CCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCCN)OC(=O)CCCCCCCCCCC
Isomeric SMILES	CCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN)OC(=O)CCCCCCCCCCC
Molecular Weight	579.746
Beilstein	1810614
Reaxy-Rn	1810614
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1810614&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.

5 results found

Lot Number	Certificate Type	Date	Item
K2005178	Certificate of Analysis	Jul 09, 2025	D130467
K2005176	Certificate of Analysis	Jul 09, 2025	D130467
E2431068	Certificate of Analysis	Mar 13, 2024	D130467
L2115499	Certificate of Analysis	Jun 14, 2023	D130467
L2115539	Certificate of Analysis	Jun 14, 2023	D130467

Chemical and Physical Properties

Molecular Weight	579.700 g/mol
XLogP3	5.900
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	9
Rotatable Bond Count	31
Exact Mass	579.39 Da
Monoisotopic Mass	579.39 Da
Topological Polar Surface Area	134.000 Å²
Heavy Atom Count	39
Formal Charge	0
Complexity	634.000
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

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration