Levodopa Levodopa,C9H11NO4 59-92-7,chemical
Product Name: | Levodopa |
Synonyms: | BETA-(3,4-DIHYDROXYPHENYL)-L-ALANINE;HYDROXYTYROSINE;H-PHE(3,4-DI-HYDROXY)-OH;H-PHE(3,4-DI-OH)-OH;H-TYR(3-HYDROXY)-OH;L-BETA-(3,4-DIHYDROXYPHENYL)ALANINE;L-DOPA;L-DOPA, L-3-HYDROXYTYROSINE |
CAS: | 59-92-7 |
MF: | C9H11NO4 |
MW: | 197.19 |
EINECS: | 200-445-2 |
Product Categories: | Pharmaceutical;Amino Acids;Biochemistry;Biological-modified Amino Acids;Nutritional Supplements;Natural Plant Extract;Amino Acids & Derivatives;Chiral Reagents;Intermediates & Fine Chemicals;Neurochemicals;Pharmaceuticals;Dopamine receptor;plant extract;Plant extracts;Herb extract;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;LARADOPA;Inhibitors |
Levodopa Chemical Properties |
mp | 276-278 °C(lit.) |
alpha | -11.7 º (c=5.3, 1N HCl) |
refractive index | -12 ° (C=5, 1mol/L HCl) |
storage temp. | 2-8°C |
Merck | 14,5464 |
BRN | 2215169 |
Stability: | Stable. Incompatible with strong oxidizing agents. Light and air sensitive. |
CAS DataBase Reference | 59-92-7(CAS DataBase Reference) |
NIST Chemistry Reference | Levodopa(59-92-7) |
EPA Substance Registry System | L-Tyrosine, 3-hydroxy-(59-92-7) |
Levodopa Usage And Synthesis |
Chemical Properties | Colorless Crystalline Powder |
Usage | Natural isomer of the immediate precursor of dopamine; product of tyrsine hydroxylase |
Usage | antiparkinsonian |
Biological Activity | Immediate precursor of dopamine, produced by tyrosine hydroxylase. Displays antiParkinsonian activity. |
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