1,2-Dipalmitoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt - ≥99%(TLC) , CAS No.67232-81-9

CAS: 67232-81-9 Cat. No.: D433257 Molecular Weight: 744.95
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Synonyms
AKOS037646929 | DPPG-Na | EN300-19735887 | sodium 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) | MG-6060LS | R-DPPG-Na | Sodium (R)-2,3-bis(palmitoyloxy)propyl (2,3-dihydroxypropyl) phosphate | DPPG | BP-26314 | DPPG-NA, R- | sodium (2R)-1-[(2,3
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25mg
D433257-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$340.90
100mg
D433257-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$1,099.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥99%(TLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

General Description

Forms classical lipid bilayers. At low temperature, however, an unusual and much thinner bilayer forms where the hydrocarbon chains are interdigitated.


Other Notes

PG(16:0/16:0)

Specifications

Synonyms
AKOS037646929 | DPPG-Na | EN300-19735887 | sodium 1, 2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) | MG-6060LS | R-DPPG-Na | Sodium (R)-2, 3-bis(palmitoyloxy)propyl (2, 3-dihydroxypropyl) phosphate | DPPG | BP-26314 | DPPG-NA, R- | sodium (2R)-1-[(2, 3
Specifications & Purity
≥99%(TLC)
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.
Names and Identifiers
Canonical SmilesCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC(CO)O)OC(=O)CCCCCCCCCCCCCCC.[Na+]
IUPAC Namesodium;[(2R)-2,3-di(hexadecanoyloxy)propyl] 2,3-dihydroxypropyl phosphate
InChIKeyLDWIWSHBGAIIMV-ODZMYOIVSA-M
INCHI1S/C38H75O10P.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-37(41)45-33-36(34-47-49(43,44)46-32-35(40)31-39)48-38(42)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;/h35-36,39-40H,3-34H2,1-2H3,(H,43,44);/q;+1/p-1/t35?,36-;/m1./s1
Isomeric SMILES CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC(CO)O)OC(=O)CCCCCCCCCCCCCCC.[Na+]
WGK Germany 3
Molecular Weight 744.95
Reaxy-Rn 9249367
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9249367&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassGlycerophospholipids
SubclassGlycerophosphoglycerols
Intermediate Tree Nodes Not available
Direct ParentPhosphatidylglycerols
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 FrameworkAliphatic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Molecular Weight745.000 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count10
Rotatable Bond Count40
Exact Mass744.492 Da
Monoisotopic Mass744.492 Da
Topological Polar Surface Area152.000 Ų
Heavy Atom Count50
Formal Charge0
Complexity804.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Documents & Articles
Citations of This Product
References
1. Chu Wang, Chenxi Hou, Jiayou Pu, Siyu Li, Shiao Luo, Xiaofeng Han, Xiaolin Lu.  (2023)  Differentiating Two Adsorption Modes of Membrane-Bound Antimicrobial Peptides via Sum Frequency Generation.  LANGMUIR,      [PMID:37417367] [10.1021/acs.langmuir.3c01117]
2. Ruicheng Xu, Jing Tang, Roja Hadianamrei, Suyu Liu, Songwei Lv, Rongrong You, Fang Pan, Peng Zhang, Nan Wang, Zhiqiang Cai, Xiubo Zhao.  (2023)  Antifungal activity of designed α-helical antimicrobial peptides.  Biomaterials Science,  11  (8): (2845-2859).  [PMID:36857655] [10.1039/D2BM01797K]
3. Fang Pan, Yueping Li, Yujie Ding, Songwei Lv, Rongrong You, Roja Hadianamrei, Mhd Anas Tomeh, Xiubo Zhao.  (2022)  Anticancer effect of rationally designed α-helical amphiphilic peptides.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:36174494] [10.1016/j.colsurfb.2022.112841]
4. Songwei Lv, Jingfang Wang, Rongrong You, Suyu Liu, Yujie Ding, Roja Hadianamrei, Mhd Anas Tomeh, Fang Pan, Zhiqiang Cai, Xiubo Zhao.  (2022)  Highly selective performance of rationally designed antimicrobial peptides based on ponericin-W1.  Biomaterials Science,  10  (17): (4848-4865).  [PMID:35861280] [10.1039/D2BM00744D]
5. Lechuan Wang, Lisha Li, Nuo Xu, Weiqing Sun, Baomiao Ding, Wei Xu, Zhenshun Li.  (2019)  Effect of carboxymethylcellulose on the affinity between lysozyme and liposome monolayers:evidence for its bacteriostatic mechanism.  FOOD HYDROCOLLOIDS,      [PMID:] [10.1016/j.foodhyd.2019.105263]
6. Shuang Cui, Bo Wang, Zheng Zhou, Yuying Zhang, Dayong Zhou, Xuhui Huang, Lei Qin.  (2024)  Integrated volatolomics and lipidomics analysis reveal the characteristic flavor formation mechanism in steamed large yellow croaker (Pseudosciaena crocea).  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.105113]
7. Zheng Zhou, Guoan Jing, Liang Wang, Shuang Cui, Lei Qin, Xuhui Huang.  (2025)  Lipid nutritional variances in thermal-treated egg yolks and their influence on flavor formation.  FOOD CHEMISTRY,      [PMID:39933354] [10.1016/j.foodchem.2025.143185]
8. Zheng Zhou, Shuang Cui, Jing Che, Yuying Zhang, Dayong Zhou, Xuhui Huang, Lei Qin.  (2024)  Unraveling the Formation Mechanism of Egg’s Unique Flavor via Flavoromics and Lipidomics.  Foods,  13  (2): (226).  [PMID:38254527] [10.3390/foods13020226]
Solution Calculators
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