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ChemicalBook >  Product Catalog >  Analytical Chemistry >  Standard >  Pharmaceutical Impurity Reference Standards >  LEVODOPA RELATED COMPOUND A (50 MG) (3-(3,4,6-TRIHYDROXYPHENYL)-ALANINE)

LEVODOPA RELATED COMPOUND A (50 MG) (3-(3,4,6-TRIHYDROXYPHENYL)-ALANINE)

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LEVODOPA RELATED COMPOUND A (50 MG) (3-(3,4,6-TRIHYDROXYPHENYL)-ALANINE) Basic information

Product Name:
LEVODOPA RELATED COMPOUND A (50 MG) (3-(3,4,6-TRIHYDROXYPHENYL)-ALANINE)
Synonyms:
  • 2,5-dihydroxy-l-tyrosine
  • 4,5-trihydroxyphenyl)-3-(l-alanin
  • 6-oh-dopa
  • l-2,4,5-trihydroxyphenylalanine
  • l-6-hydroxydopa
  • 3-(3,4,6-Tirhydroxyphenyl)-alanine
  • (2S)-2-Amino-3-(2,4,5-trihydroxyphenyl)propanoic acid
  • l-hydroxydopa
CAS:
27244-64-0
MF:
C9H11NO5
MW:
213.19
Product Categories:
  • Amino Acids & Derivatives, Aromatics, Neurochemicals, Pharmaceuticals, Intermediates & Fine Chemicals
Mol File:
27244-64-0.mol
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LEVODOPA RELATED COMPOUND A (50 MG) (3-(3,4,6-TRIHYDROXYPHENYL)-ALANINE) Chemical Properties

Melting point:
>190°C (dec.)
Boiling point:
515.2±38.0 °C(Predicted)
Density 
1.606±0.06 g/cm3(Predicted)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
Aqueous Acid (Slightly, Sonicated), Water (Slightly, Heated, Sonicated)
pka
2.34±0.25(Predicted)
color 
Brown to Black
Stability:
Air Sensitive, Hygroscopic
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Safety Information

HS Code 
2922504500
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LEVODOPA RELATED COMPOUND A (50 MG) (3-(3,4,6-TRIHYDROXYPHENYL)-ALANINE) Usage And Synthesis

Uses

6-Hydroxy-L-DOPA (Levodopa EP Impurity A; Levodopa USP Related Compound A) is the 6-hydroxy derivative of the amino acid L-DOPA (D533751) with neurotoxic properties. Studies show that exogenously administered 6-Hydroxy-L-DOPA is biotransformed by amino acid decarboxylase to the highly potent and catecholamine-selective neurotoxin, 6-Hydroxydopamine. The treatment of 6-Hydroxy-L-DOPA in rats resulted in the stimulation of acetylcholinesterase.

Uses

6-Hydroxy-L-DOPA is the 6-hydroxy derivative of the amino acid L-DOPA (D533751) with neurotoxic properties. Studies show that exogenously administered 6-Hydroxy-L-DOPA is biotransformed by amino acid decarboxylase to the highly potent and catecholamine-selective neurotoxin, 6-Hydroxydopamine. The treatment of 6-Hydroxy-L-DOPA in rats resulted in the stimulation of acetylcholinesterase.

Definition

ChEBI: An L-alpha-amino acid that is L-dopa carrying an additional hydroxy substituent at position 6.

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