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Home > Encyclopedia > L-Methionine, methyl ester, hydrochloride

L-Methionine, methyl ester, hydrochloride

L-Methionine, methyl ester, hydrochloride structure

L-Methionine, methyl ester, hydrochloride 

structure
  • CAS No:

    2491-18-1

  • Formula:

    C6H13NO2S.ClH

  • Chemical Name:

    L-Methionine, methyl ester, hydrochloride

  • Synonyms:

    L-Methionine,methyl ester,hydrochloride (1:1);L-Methionine,methyl ester,hydrochloride;Methionine,methyl ester,hydrochloride,L-;Methionine methyl ester hydrochloride;Methyl (S)-methioninate hydrochloride;(S)-Methionine methyl ester hydrochloride;Methyl L-methioninate hydrochloride;NSC 522231;(S)-2-Amino-4-methylsulfanylbutanoic acid methyl ester hydrochloride

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

Crystalline

L-Methionine, methyl ester, hydrochloride Basic Attributes

199.7

199.043381

3913214

219-651-9

29309090

Characteristics

77.6

1.74210

White to beige Powder

1.094g/cm3

159-161 °C

277.6ºC at 760 mmHg

121.7ºC

26 ° (C=1, H2O)

soluble in water.

−20°C

0.0388mmHg at 25°C

26 º (c=5, H2O 24 ºC)

Safety Information

NONH for all modes of transport

3

36/37/38

24/25-26

Xi

P261-P305 + P351 + P338

H315-H319-H335

L-Methionine, methyl ester, hydrochloride Use and Manufacturing

Synthesis \ , L-Methionine (0.5g, 1 equivalent) was suspended in methanol (30ml C = 0.1M) in a 100ml flask equipped with a magnetic stirrer and placed under nitrogen. Thionyl chloride (0.5ml, 2 equivalents) was added to the solution dropwise at 0°C then heated under reflux for 16 hours. The reaction mixture was then evaporated to yield a pale yellow solid. The solid was triturated with hot diethyl ether and the solution discarded to leave the title compound 2 as a white solid which was further dried under vacuum. (0.65561 g, 98percent yield).L-Methionine (0.5 g, 1 equivalent) was suspended in methanol (30 ml C=0.1M) in a 100 ml flask equipped with a magnetic stirrer and placed under nitrogen. Thionyl chloride (0.5 ml, 2 equivalents) was added to the solution dropwise at 0° C. then heated under reflux for 16 hours. The reaction mixture was then evaporated to yield a pale yellow solid. The solid was triturated with hot diethyl ether and the solution discarded to leave the title compound 2′ a white solid which was further dried under vacuum. (0.65561 g, 98percent yield). [0377] Using the general methyl esterification conditions, L-methionine (8, 2.00 g, 13.4 mmol) was treated with thionyl chloride (2.00 mL, 26.8 mmol) in methanol(20 mL) to afford the title compound as a white powder (1.95 g, 89percent); νmax (KBr pellet): 3080 (s), 1747(s), 2840 (w), 1236 (s); δH (300 MHz, CDClGeneral procedure: This compound has previously been described

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