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H-DL-ASP(OME)-OME HCL

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H-DL-ASP(OME)-OME HCL Basic information

Product Name:
H-DL-ASP(OME)-OME HCL
Synonyms:
  • DL-ASPARTIC ACID DIMETHYL ESTER HYDROCHLORIDE
  • DL-ASPARTIC ACID(OME)-OME HCL
  • DL-ASPARTIC ACID ALPHA,BETA-DIMETHYL ESTER HYDROCHLORIDE
  • H-DL-ASP(OME)-OME HCL
  • DL-ASPARTIC ACID DIMETHYL ESTERHYDROCHLO RIDE CRYST
  • dl-asparticaciddimethylesterHCl
  • DL-Asp(OMe)-OMe·HCl
  • DL-ASPARTIC ACID A,B-DIMETHYLESTER HYDROCHLORIDE
CAS:
14358-33-9
MF:
C6H12ClNO4
MW:
197.62
Mol File:
14358-33-9.mol
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H-DL-ASP(OME)-OME HCL Chemical Properties

Melting point:
115-116.5℃ (ethanol ethyl acetate )
storage temp. 
Inert atmosphere,2-8°C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Powder
color 
White to off-white
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Safety Information

Hazard Codes 
Xi
Risk Statements 
42/43
Safety Statements 
36/37
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H-DL-ASP(OME)-OME HCL Usage And Synthesis

Chemical Properties

White or off-white crystal

Uses

DL-Aspartic acid dimethyl ester hydrochloride is an aspartic acid derivative[1].

Synthesis

67-56-1

1783-96-6

14358-33-9

106.8 g (0.8 mol) of D-aspartic acid and 700 ml of methanol were added to the reaction vessel, and 84.4 ml (1.2 mol) of thionyl chloride was slowly added dropwise under stirring conditions, with the reaction temperature controlled at 0 °C. After the dropwise addition, the reaction mixture was warmed up to room temperature (about 29°C) and the reaction was continued with stirring for 30 hours. Upon completion of the reaction, excess methanol and thionyl chloride were removed from the reaction solution by distillation. The remaining oily substance was dissolved in 3.5 times the volume of ether for crystallization to obtain white crystals. After filtration, the crystals were washed with ether three times and dried to finally obtain 107.8 g of white solid product DL-aspartic acid dimethyl ester hydrochloride.

Purification Methods

Crystallise it from absolute MeOH. [Kovach et al. J Am Chem Soc 107 7360 1985.] The diethyl ester has pK25 6.4.

References

[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368

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