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(2S,4S)-4-Methylglutamic acid

Base Information
  • Chemical Name:(2S,4S)-4-Methylglutamic acid
  • CAS No.:6141-27-1
  • Molecular Formula:C6H11NO4
  • Molecular Weight:161.158
  • Hs Code.:2922499990
  • UNII:NPW4ZK5UGA,G44Q8UU4V9
  • DSSTox Substance ID:DTXSID70390561
  • Nikkaji Number:J686.917C
  • Wikidata:Q82187421
  • ChEMBL ID:CHEMBL41221
  • Mol file:6141-27-1.mol
(2S,4S)-4-Methylglutamic acid

Synonyms:6141-27-1;(2S,4S)-4-METHYLGLUTAMIC ACID;(2S,4S)-2-amino-4-methylpentanedioic acid;(4S)-4-Methyl-L-glutamic Acid;NPW4ZK5UGA;CHEMBL41221;2S,4S-4-Methylglutamic acid;G44Q8UU4V9;4-Methyl-DL-glutamic acid, threo-;4-Methyl-L-glutamic acid, (4S)-;DL-Glutamic acid, 4-methyl-, threo-;L-Glutamic acid, 4-methyl-, (4S)-;D-Glutamic acid, 4-methyl-, (4R)-rel-;38523-28-3;NSC-41355;starbld0018205;UNII-NPW4ZK5UGA;NCIStruc1_000060;NCIStruc2_000006;UNII-G44Q8UU4V9;SCHEMBL2263577;DTXSID70390561;NCI41355;BDBM50031703;CCG-36834;NCGC00013482;AKOS006275456;NCGC00013482-02;NCGC00013482-03;NCGC00096596-01;NCGC00096596-02;(2S,4S)-2-Amino-4-methyl-pentanedioic acid;2-Amino-4-methyl-pentanedioic acid(S-Me-Glu)

Suppliers and Price of (2S,4S)-4-Methylglutamic acid
Supply Marketing:
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,4S)-4-MethylglutamicAcid
  • 10mg
  • $ 250.00
  • Medical Isotopes, Inc.
  • (2S,4S)-4-MethylglutamicAcid
  • 25 mg
  • $ 2000.00
  • American Custom Chemicals Corporation
  • (2S,4S)-4-METHYLGLUTAMIC ACID 95.00%
  • 50MG
  • $ 1732.50
  • American Custom Chemicals Corporation
  • (2S,4S)-4-METHYLGLUTAMIC ACID 95.00%
  • 5MG
  • $ 756.25
Total 9 raw suppliers
Chemical Property of (2S,4S)-4-Methylglutamic acid
Chemical Property:
  • PSA:100.62000 
  • LogP:0.20940 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Methanol (Slightly), Water (Soluble) 
  • XLogP3:-2.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:161.06880783
  • Heavy Atom Count:11
  • Complexity:168
Purity/Quality:

97% *data from raw suppliers

(2S,4S)-4-MethylglutamicAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CC(C(=O)O)N)C(=O)O
  • Isomeric SMILES:C[C@@H](C[C@@H](C(=O)O)N)C(=O)O
  • Uses A highly selective and potent agonist for metabotropic receptors (2S,4S)-4-Methylglutamic Acid is a potent and selective kainate receptor agonist (1). It has been shown that (2S,4S)-4-Methylglutamic Acid can desensitize kainate receptors and also attenuate capsaicin and inflammatory hyperalgesia (2).
Technology Process of (2S,4S)-4-Methylglutamic acid

There total 29 articles about (2S,4S)-4-Methylglutamic 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:
dimethyl (2S,4S)-N-(tert-butoxycarbonyl)-4-methylglutamate; With hydrogenchloride; In water; at 80 ℃; for 6h; Inert atmosphere;
With methyloxirane; at 20 ℃; for 0.5h;
DOI:10.1002/chem.201903725
Guidance literature:
With Cysteine sulfinic acid; pyridoxal 5'-phosphate; glutamic oxalacetic transaminase; In water; at 20 ℃; for 24h; pH=7; Enzymatic reaction;
DOI:10.1002/(SICI)1099-0690(199912)1999:12<3403::AID-EJOC3403>3.0.CO;2-U
Guidance literature:
4-methyl-2-ketoglutaric acid; In water; at 20 ℃; for 2h; pH=7.6; Enzymatic reaction;
With pyridoxal 5'-phosphate; Escherichia coli branched chain aminotransferase; Escherichia coli aspartate aminotransferase; In sodium hydroxide; at 20 ℃; for 15h; pH=7.6; Further stages.; Enzymatic reaction;
DOI:10.1021/jo070805q
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