sn-Glycerol 3-phosphate lithium salt - Moligand™, ≥95% , CAS No.17989-41-2

CAS: 17989-41-2 Cat. No.: G696252 Molecular Weight: 183.94
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥95%
Synonyms
Glycerol 3-phosphate | sn-Glycerol 3-phosphate
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Size
Status
Price
Qty
1mg
G696252-1mg
1
$126.90
5mg
G696252-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$379.90
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Why this grade

Moligand™, ≥95% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

sn-Glycerol 3-phosphate is an important intermediate in glycolysis and lipid metabolism. The cytosolic sn-Glycerol 3-phosphate dehydrogenase (GPDH) consumes NADH to generate sn-Glycerol 3-phosphate from dihydroxyacetone phosphate (DHAP). Glyceroneogenesis is an important supplier of sn-Glycerol 3-phosphate for lipid metabolism .

Specifications

Synonyms
Glycerol 3-phosphate | sn-Glycerol 3-phosphate
Specifications & Purity
Moligand™, ≥95%
Biochemical and Physiological Mechanisms
Glycerol 3-phosphate (G3P) is an important intermediate of carbohydrate and lipid metabolic pathways. It is produced from glycerol by glycerol kinase or from dihydroxyacetone phosphate by glycerol 3-phosphate dehydrogenase. G3P may enter the G3P shuttle t
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Purity
≥95%
Product Properties
ALogP-2.9
Names and Identifiers
Canonical SmilesC(C(COP(=O)(O)O)O)O
IUPAC Name[(2R)-2,3-dihydroxypropyl] dihydrogen phosphate
InChIKeyAWUCVROLDVIAJX-GSVOUGTGSA-N
INCHI1S/C3H9O6P/c4-1-3(5)2-9-10(6,7)8/h3-5H,1-2H2,(H2,6,7,8)/t3-/m1/s1
Isomeric SMILES C([C@H](COP(=O)(O)O)O)O
Molecular Weight 183.94
Reaxy-Rn 1723974
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723974&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.

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🔬 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
SubclassGlycerophosphates
Intermediate Tree Nodes Not available
Direct ParentGlycerophosphates
Alternative Parents Monoalkyl phosphates  Secondary alcohols  1,2-diols  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Sn-glycerol-3-phosphate - Monoalkyl phosphate - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Secondary alcohol - 1,2-diol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as glycerophosphates. These are compounds containing a glycerol linked to a phosphate group.
External Descriptors sn-glycerol 3-phosphates - glycerol 1-phosphate
3D Structure
Interactive Chemical Structure Model





Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

4 results found

Lot NumberCertificate TypeDateItem
E2608443Certificate of AnalysisMar 20, 2026 G696252
E2608459Certificate of AnalysisMar 20, 2026 G696252
K2514567Certificate of AnalysisNov 12, 2025 G696252
K2514568Certificate of AnalysisNov 12, 2025 G696252
Chemical and Physical Properties
SolubilityH2O: 50 mg/mL (271.83 mM; Ultrasonic-assisted dissolution)
SensitivityMoisture sensitive
Molecular Weight172.070 g/mol
XLogP3-2.900
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass172.014 Da
Monoisotopic Mass172.014 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity129.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Ming-Yan Wang, Meng-Xu Yi, Xing-Yu Mo, Shan-Jie Wei, Yu Qiao, Zheng Zhang, Zhao-Liang Su, Hong-Yan Lu.  (2024)  Over-activation of iNKT cells aggravate lung injury in bronchopulmonary dysplasia mice.  Redox Biology,      [PMID:39342744] [10.1016/j.redox.2024.103370]
Solution Calculators
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