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Z-D-MET-OH

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Z-D-MET-OH Basic information

Product Name:
Z-D-MET-OH
Synonyms:
  • N-CBZ-D-METHIONINE
  • N-CARBOBENZOXY-D-METHIONINE
  • N-ALPHA-CBZ-D-METHIONINE
  • N-ALPHA-CARBOBENZOXY-D-METHIONINE
  • N-ALPHA-BENZYLOXYCARBONYL-D-METHIONINE
  • Z-D-MET-OH
  • Z-D-METHIONINE
  • Z-D-METHIONINE extrapure
CAS:
28862-80-8
MF:
C13H17NO4S
MW:
283.34
Product Categories:
  • Amino Acids
  • Amino Acids (N-Protected)
  • Biochemistry
  • Cbz-Amino Acids
Mol File:
28862-80-8.mol
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Z-D-MET-OH Chemical Properties

Melting point:
67-69°C
Density 
1.253
refractive index 
26 ° (C=1, MeOH)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
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Safety Information

Safety Statements 
24/25
HS Code 
29225090
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Z-D-MET-OH Usage And Synthesis

Chemical Properties

White solid

Uses

N-Cbz-D-methionine is an N-Cbz-protected form of D-Methionine (M260550). D-Methionine is an isomer of L-Methionine (M260440), and is known to be a cytoprotectant against Cisplatin (C499500), an anticancer agent. D-Methionine is also used to prevent noise- and drug-induced hearing loss, as well as hair loss (all of which may also be caused by Cisplatin or aminoglycosides).

Synthesis

348-67-4

501-53-1

1152-62-1

General procedure for the synthesis of Z-L-methionine from D-methionine and benzyl chloroformate: (2R)-2-Amino-4-(methylthioalkyl)butyric acid (4.90 g, 32.84 mmol) and sodium carbonate (16.91 g, 159.54 mmol) were dissolved in water (100 mL) at room temperature. Subsequently, a solution of benzyl chloroformate (5.59 g, 32.74 mmol) in dioxane (50 mL) was added slowly and dropwise over 10 minutes. The resulting reaction mixture was stirred at room temperature for 5 hours. Upon completion of the reaction, the reaction was quenched by the addition of water (100 mL). The reaction mixture was extracted with ethyl acetate (300 mL x 3) and the organic phases were combined, washed with brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the residue was purified by chromatography on a C18 reversed-phase column using gradient elution with aqueous acetonitrile (0 to 50% acetonitrile, 30 min) to afford (2R)-2-[[(benzyloxy)carbonyl]amino]-4-(methylsulfanyl)butanoic acid as a yellow oil (3.48 g, 36% yield).

References

[1] Journal of Agricultural and Food Chemistry, 1995, vol. 43, # 10, p. 2728 - 2734
[2] Canadian Journal of Chemistry, 2003, vol. 81, # 8, p. 937 - 960
[3] Patent: WO2017/106607, 2017, A1. Location in patent: Paragraph 00400

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