Specification |
According to European Pharmacopoeia 7.8
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Items
|
Specification
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Results
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Appearance
|
White or slightly yellowish crystalline powder
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White crystalline powder
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Solubility
|
Should meet the requirement
|
Conforms
|
IR Identification
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Should correspond to the RS Infrared Absorption
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Correspond to the reference substance
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Appearance of solution
|
Should meet the requirement
|
Conforms
|
Related substance
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Impurity A
|
≤0.15%
|
0.05%
|
Impurity B
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≤0.15%
|
0.02%
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Impurity C
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≤0.2%
|
0.03%
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Impurity D
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≤0.2%
|
0.05%
|
Unspecified Ims.
|
≤0.1%
|
0.06%
|
Total
|
≤1.0%
|
0.30%
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Residual solvents
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Methanol
|
≤0.3%
|
Not detected
|
Ethanol
|
≤0.5%
|
0.031%
|
Methylene dichloride
|
≤0.06%
|
Not detected
|
n-hexane
|
≤0.029%
|
Not detected
|
Acetic acid ethyl ester
|
≤0.5%
|
Not detected
|
Toluene
|
≤0.089%
|
0.025%
|
Acetic acid
|
≤0.5%
|
0.036%
|
Loss on drying
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≤0.5%
|
0.20%
|
Sulphated ash
|
≤0.1%
|
Conforms
|
Melting point
|
261 ºC -263 ºC
|
261.1 ºC -262.2 ºC
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Particle size
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90% Less than 200um
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Conforms
|
Assay
|
99.0%~101.0%
|
99.9%
|
Conclusion
|
It conforms to European Pharmacopoeia 7.0
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