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Home > Products >  Levodopa

Levodopa CAS NO.59-92-7

  • Min.Order: 1 Gram
  • Payment Terms: L/C,T/T,MoneyGram
  • Product Details

Keywords

  • Bendopa
  • Dopaston
  • Prodopa

Quick Details

  • ProName: Levodopa
  • CasNo: 59-92-7
  • Molecular Formula: C9H11NO4
  • Appearance: White to off- white powder
  • Application: Natural isomer of the immediate precur...
  • DeliveryTime: in stock
  • PackAge: 25kg fiber drum
  • Port: Shanghai , Nanjing , Hongkong
  • ProductionCapacity: 500 Metric Ton/Week
  • Purity: 99%
  • Transportation: storage temp. 2-8°C
  • LimitNum: 1 Gram

Superiority

1. Introduction of Levodopa

Levodopa, with the IUPAC Name of (2S)-2-Amino-3-(3,4-dihydroxyphenyl)propanoic acid, is one kind of colorless crystalline powder. This product belongs to the Product Category which include Pharmaceutical; Amino Acids; Biochemistry; Biological-modified Amino Acids; Nutritional Supplements; Natural Plant Extract. Besides, Levodopa could be stable under normal temperatures and pressures. It is not compatible with strong oxidizing agents, and you must not take it with incompatible materials. And also prevent it to broken down into hazardous decomposition products: Nitrogen oxides, carbon monoxide, irritating and toxic fumes and gases, carbon dioxide, nitrogen.

2. Properties of Levodopa

Levodopa has the following datas: (1)Index of Refraction: 1.654; (2)Molar Refractivity: 49.25 cm3; (3)Molar Volume: 134.2 cm3 ; (4)Surface Tension: 80.2 dyne/cm; (5)Density: 1.468 g/cm3; (6)Flash Point: 225 °C; (7)Enthalpy of Vaporization: 74.5 kJ/mol; (8)Boiling Point: 448.4 °C at 760 mmHg; (9)Vapour Pressure: 7.97E-09 mmHg at 25 °C; (10) Melting point: 276-278 °C(lit.); (11)Storage tempreture: 2-8 °C.

Details

Index Name

Index

Test results

Appearance

White to off- white powder

Conform

Identification

The retention time of the major peak of the sample solution to that the standard solution, as obtained in assay

Conform

Optical rotation

-160°~ -167°

-163.4°

Organic impurities

Levodopa related compound A0.1%

ND

 

L-Tyrosine %

ND

 

Levodopa related compound B0.5%

ND

 

Individual unkown impurity  0.1%

ND

 

Total impurities 1.0%

ND

Loss on drying %

 0.5

0.24

Residue on ignition %  

≤0.1

0.09

Heavy metal(pb)

20ppm

20ppm

 Assay ( HPLC)%

98.0-102.0

99.8

Conclusion

Qualified with USP standard 

 

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