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L-Glutamic acid dimethyl ester hydrochloride

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L-Glutamic acid dimethyl ester hydrochloride manufacturers

L-Glutamic acid dimethyl ester hydrochloride Basic information
Product Name:L-Glutamic acid dimethyl ester hydrochloride
Synonyms:H-GLU(OME)-OME HCL;GLUTAMIC ACID(OME)-OME HCL;Dimethyl L-glutamate hydrochloride~H-Glu(OMe)-OMe.HCl;dimethyl L-2-aminoglutarate hydrochloride;L-GUTAMINSAURE-DIMETHYLESTER HYDROCHLORIDE;DimethylL-glutamateHCl~H-Glu(OMe)-OMe.HCl;GLU(OME)-OMEHCL;H-L-Glu(Me)-OMe*HCl
CAS:23150-65-4
MF:C7H14ClNO4
MW:211.64
EINECS:245-461-0
Product Categories:Amino Acid Derivatives;Glutamic Acid;Peptide Synthesis;Glutamic acid [Glu, E];Amino Acids and Derivatives;Amino hydrochloride;Amino Acid Methyl Esters;Amino Acids (C-Protected);Biochemistry;chiral;Amino Acids
Mol File:23150-65-4.mol
L-Glutamic acid dimethyl ester hydrochloride Structure
L-Glutamic acid dimethyl ester hydrochloride Chemical Properties
Melting point 89-90°C
alpha 26 º (c=5% in H2O)
refractive index 26 ° (C=5, H2O)
storage temp. 2-8°C
solubility Methanol, Water
form Powder
color White
Optical Rotation[α]20/D +26.0±1°, c = 5% in H2O
Water Solubility Soluble in water, methanol (50 mg/ml).
Sensitive Hygroscopic
BRN 4238829
Stability:Hygroscopic
Major Applicationpeptide synthesis
InChIInChI=1/C7H13NO4.ClH/c1-11-6(9)4-3-5(8)7(10)12-2;/h5H,3-4,8H2,1-2H3;1H/t5-;/s3
InChIKeyMFUPLHQOVIUESQ-JEDNCBNOSA-N
SMILES[C@@H](N)(C(=O)OC)CCC(=O)OC.Cl |&1:0,r|
CAS DataBase Reference23150-65-4(CAS DataBase Reference)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
HS Code 29224999
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
L-Glutamic acid dimethyl ester hydrochloride Usage And Synthesis
Chemical PropertiesCrystalline
UsesL-Glutamic Acid Dimethyl Ester is a diester analogue of L-Glutamic Acid, a non-essential amino acid. L-Glutamic Acid Dimethyl Ester has been shown to antagonize the effects of morphine sulfate.
UsesL-Glutamic acid dimethyl ester hydrochloride is used as a pharmaceutical intermediate.
reaction suitabilityreaction type: solution phase peptide synthesis
Synthesis
Methanol

67-56-1

L-Glutamic acid

56-86-0

L-Glutamic acid dimethyl ester hydrochloride

23150-65-4

To a 500 mL four-necked flask equipped with a stirrer, thermometer and reflux condenser (connected to a 30% aqueous sodium hydroxide solution absorption unit), 300 g of methanol, 14.7 g (0.10 mol) of L-glutamic acid, and 30.0 g (0.25 mol) of thionyl chloride were added sequentially. The reaction mixture was heated to 60-63 °C and the reaction was stirred at this temperature for 7 hours. Upon completion of the reaction, the system was cooled to 20-25 °C, followed by the passage of nitrogen to displace the hydrogen chloride gas in the system for 30 min. Next, the excess thionyl chloride and methanol were recovered by distillation. To the residue, 100 g of methyl tert-butyl ether was added and pulped, followed by filtration to collect the solid. Upon drying, 20.8 g of L-glutamic acid dimethyl ester hydrochloride was obtained as a white solid. The product was analyzed by high performance liquid chromatography (HPLC) with 99.5% purity and 98.1% yield.

References[1] Journal of Medicinal Chemistry, 2007, vol. 50, # 24, p. 6144 - 6153
[2] Archiv der Pharmazie, 2005, vol. 338, # 5-6, p. 281 - 290
[3] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 18, p. 6273 - 6290
[4] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 2, p. 777 - 793
[5] Patent: CN107602436, 2018, A. Location in patent: Paragraph 0053; 0054
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