beta-Glycerophosphoric acid

Base Information

• Chemical Name: beta-Glycerophosphoric acid
• CAS No.: 17181-54-3
• Molecular Formula: C3H9O6P
• Molecular Weight: 172.075
• European Community (EC) Number: 241-228-2
• UNII: WWH06G87W6
• DSSTox Substance ID: DTXSID1023106
• Nikkaji Number: J135.242C
• Wikipedia: Glycerol_2-phosphate
• Wikidata: Q21099098
• Metabolomics Workbench ID: 38172
• ChEMBL ID: CHEMBL1232903
• Mol file: 17181-54-3.mol

Synonyms:2-glycerophosphoric acid;beta-glycerol phosphate;beta-glycerophosphate;beta-glycerophosphoric acid;beta-glycerophosphoric acid, calcium salt;beta-glycerophosphoric acid, calcium salt (1:1);beta-glycerophosphoric acid, disodium salt;beta-glycerophosphoric acid, iron salt;beta-glycerophosphoric acid, iron(3+) salt(3:2);beta-glycerophosphoric acid, sodium salt;Glycerol 2-phosphate

Chemical Property of beta-Glycerophosphoric acid

Chemical Property:

• Vapor Pressure: 1.33E-11mmHg at 25°C
• XLogP3: -2.9
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 172.01367500
• Heavy Atom Count: 10
• Complexity: 125

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(CO)OP(=O)(O)O)O

Technology Process of beta-Glycerophosphoric acid

There total 19 articles about beta-Glycerophosphoric acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethanol (64-17-5) + 1,2-di-O-stearoyl-rac-3-glycerophosphate (17966-25-5) → glycerol 2-phosphate, free acid (17181-54-3) + lysophosphatidic acid (57-03-4,1509-81-5,5746-57-6,17989-41-2) + stearic acid (57-11-4)

Guidance literature:

bei Raumtemperatur;

Reference yield:

→ glycerol 2-phosphate, free acid (17181-54-3) + lysophosphatidic acid (57-03-4,1509-81-5,5746-57-6,17989-41-2)

Guidance literature:

Hydrolysis;

DOI:10.1002/hlca.19260090101

Reference yield:

→ glycerol 2-phosphate, free acid (17181-54-3) + lysophosphatidic acid (57-03-4,1509-81-5,5746-57-6,17989-41-2)

Guidance literature:

Hydrolysis;

DOI:10.1002/hlca.19260090101

upstream raw materials:

ethanol

1,2-di-O-stearoyl-rac-3-glycerophosphate

(+/-)-phosphoric acid-(2,3-dihydroxy-propyl ester)-methyl ester

lysophosphatidic acid

Downstream raw materials:

lysophosphatidic acid

4-hydroxymethyl-2-oxo-2λ⁵-[1,3,2]dioxaphospholan-2-ol

phosphoric acid-(β,β'-dihydroxy-isopropyl ester)-(2,3-dihydroxy-propyl ester)

phosphoric acid

Refernces

• 1、 Gupta, Kalyan Kali Sen,Mahapatra, Ambikesh,Sanyal, Ankan. "Reactivities of some energy rich organic orthophosphates towards transition metal ion oxidants". . p. 332 - 334. Retrieved 2007/10/02.