13171-25-0 Trimetazidine dihydrochloride Trimetazidine 2HCl
GMP (Good Manufacturing Practice)
DML (Drug Manufacturing License)
DMF (Drug Master File)
Stability Data
Quality Trimetazidine dihydrochloride 13171-25-0
1 Function :Bodybuilding
2 Quality: High quality
3 Product Group: API
ITEMS |
SPECIFICATIONS |
RESULTS |
Appearance |
White or almost white, crystalline powder, slightly hygroscopic. |
Conforms |
Identification |
A: Infrared absorption spectrophotometry. |
Conforms |
B: Dissolve 25mg in 5ml of water R. 2ml of the solution gives reaction (a) of chlorides. |
Conforms |
|
Solubility |
Freely soluble in water, sparingly soluble in alcohol. |
Conforms |
Appearance of solution |
Solution is clear and not more intensely coloured than reference solution BY6 |
Conforms |
Related substances |
Impurities A,B,C,D,E,F,H,I: for each impurity, not more than 0.1%. |
Not detected |
Any other impurity: for each impurity, not more than 0.1% |
0.07% |
|
Total: not more than 0.2% |
0.07% |
|
Impurity G: not more than 0.1%, expressed as anhydrous piperazine |
Conforms |
|
Sulphated ash |
0.1% Max, determined on 1.0g |
0.03% |
Loss on drying |
2.5%Max |
0.9% |
Assay |
98.5% to 101.5% (dried substance) |
99.6% |
CONCLUSION |
Complies with the standard of EP8.0 . |
Product Name Trimetazidine dihydrochloride
Catalog API
CAS No. 13171-25-0
DC No. DC00100013
Molecular Formula C14H22N2O3.2HCl
mp : 231-235 °C(lit.)
storage temp. : Refrigerator
Merck : 14,9705
Mole Weight: 338.12
Synonyms: s4004;vastarel;Takkmint;kyurinett;Vastarel F;Yoshimilon;Youmetazine;TRIMETAZIDINE 2HCL;Trimetazidine 3HCl;TRIMETAZIDINE DI HCL
CBNumber: CB6176226
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