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(2S,4R)-2-amino-4-hydroxypentanedioic acid

Base Information Edit
  • Chemical Name:(2S,4R)-2-amino-4-hydroxypentanedioic acid
  • CAS No.:2485-33-8
  • Molecular Formula:C5H9NO5
  • Molecular Weight:163.13
  • Hs Code.:2922509090
  • DSSTox Substance ID:DTXSID90331532
  • Nikkaji Number:J83.286C
  • Wikidata:Q82096649
  • Metabolomics Workbench ID:53837
  • ChEMBL ID:CHEMBL371946
  • Mol file:2485-33-8.mol
(2S,4R)-2-amino-4-hydroxypentanedioic acid

Synonyms:(2S,4R)-2-amino-4-hydroxypentanedioic acid;2485-33-8;erythro-4-hydroxy-L-glutamic acid;L-erythro-4-hydroxyglutamic acid;(2S,4R)-gamma-Hydroxyglutamic acid;L-erythro-4-Hydroxyglutamate;CHEBI:21285;(4S)-4-hydroxy-L-glutamic acid;erythro-4-hydroxy-L-glutamate;(2S,4R)-4-Hydroxy-L-glutamic Acid;erythro-4-hydroxyglutamate;L-erythro-4-hydroxy-glutamate;CHEMBL371946;SCHEMBL5819946;DTXSID90331532;H-(2S,4R)--Hydroxy-Glu-OH;(2S,4R)-4-Hydroxyglutamic Acid;H-(2S,4R)-g-Hydroxy-Glu-OH;L-Glutamic acid,4-hydroxy-,(4R)-;MFCD00672375;(2S,4R)-gamma-Hydroxy-glutamic acid;AKOS006271402;CS-W013253;HY-W012537;MS-22896;C05947;J-015700;(4R)-4-Hydroxy-L-glutamic acid, >=98.0% (TLC);1-Benzyl-4-trifluoromethyl-pyrrolidine-3-carboxylicacid

Suppliers and Price of (2S,4R)-2-amino-4-hydroxypentanedioic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (2S,4R)-4-Hydroxy-L-glutamicAcid
  • 10mg
  • $ 165.00
  • Sigma-Aldrich
  • (4R)-4-Hydroxy-L-glutamic acid ≥98.0% (TLC)
  • 50mg
  • $ 497.00
  • Sigma-Aldrich
  • (4R)-4-Hydroxy-L-glutamic acid ≥98.0% (TLC)
  • 10mg
  • $ 196.00
  • Medical Isotopes, Inc.
  • (2S,4R)-4-Hydroxy-L-glutamicAcid
  • 100 mg
  • $ 2200.00
  • Crysdot
  • (2S,4R)-2-Amino-4-hydroxypentanedioicacid 95+%
  • 1g
  • $ 1376.00
  • Chem-Impex
  • (2S,4R)-γ-Hydroxy-L-glutamicacid,≥98%(TLC) ≥98%(TLC)
  • 1G
  • $ 1615.58
  • Chem-Impex
  • (2,4)-γ-Hydroxy-L-glutamic acid ≥ 98% (TLC)
  • 25MG
  • $ 166.00
  • Chem-Impex
  • (2S,4R)-γ-Hydroxy-L-glutamicacid,≥98%(TLC) ≥98%(TLC)
  • 250MG
  • $ 783.91
  • American Custom Chemicals Corporation
  • (2S,4R)-2-AMINO-4-HYDROXYPENTANEDIOIC ACID 95.00%
  • 10MG
  • $ 750.75
  • AK Scientific
  • H-(2S,4R)-Gamma-Hydroxy-Glu-OH
  • 250mg
  • $ 958.00
Total 7 raw suppliers
Chemical Property of (2S,4R)-2-amino-4-hydroxypentanedioic acid Edit
Chemical Property:
  • Boiling Point:458.7 °C at 760 mmHg 
  • PKA:2.15±0.10(Predicted) 
  • Flash Point:231.2 °C 
  • PSA:120.85000 
  • Density:1.595 g/cm3 
  • LogP:-1.06580 
  • Storage Temp.:-15°C 
  • Solubility.:DMSO (Slightly), Water (Slightly) 
  • XLogP3:-4.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:4
  • Exact Mass:163.04807239
  • Heavy Atom Count:11
  • Complexity:168
Purity/Quality:

99% *data from raw suppliers

(2S,4R)-4-Hydroxy-L-glutamicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(C(=O)O)N)C(C(=O)O)O
  • Isomeric SMILES:C([C@@H](C(=O)O)N)[C@H](C(=O)O)O
  • Uses (2S,4R)-4-Hydroxy-L-glutamic Acid is a metabolite of Glutamic acid (G596960).
Technology Process of (2S,4R)-2-amino-4-hydroxypentanedioic acid

There total 10 articles about (2S,4R)-2-amino-4-hydroxypentanedioic 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:
Guidance literature:
With L-asparagine; Escherichia coli aspartate transaminase; Pseudomonas aeruginosa A0A081HJP9 aldolase; water; magnesium chloride; In aq. phosphate buffer; at 20 ℃; for 24h; stereoselective reaction; Kinetics; Enzymatic reaction;
DOI:10.1039/c7cc00742f
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