| Specification
 |      According to European Pharmacopoeia 7.8 | 
		
			| Items | Specification | Results | 
		
			| Appearance | White or slightly yellowish crystalline powder | White crystalline powder | 
		
			| Solubility | Should meet the requirement | Conforms | 
		
			| IR Identification | Should correspond to the RS Infrared Absorption | Correspond to the reference substance | 
		
			| Appearance of solution | Should meet the requirement | Conforms | 
		
			| Related substance | Impurity A | ≤0.15% | 0.05% | 
		
			| Impurity B | ≤0.15% | 0.02% | 
		
			| Impurity C | ≤0.2% | 0.03% | 
		
			| Impurity D | ≤0.2% | 0.05% | 
		
			| Unspecified Ims. | ≤0.1% | 0.06% | 
		
			| Total | ≤1.0% | 0.30% | 
		
			| Residual solvents | 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 | ≤0.5% | 0.20% | 
		
			| Sulphated ash | ≤0.1% | Conforms | 
		
			| Melting point |     261 ºC -263 ºC |      261.1 ºC -262.2 ºC | 
		
			| Particle size |     90% Less than 200um |      Conforms | 
		
			| Assay |     99.0%~101.0% |      99.9% | 
		
			| Conclusion |    It conforms to European Pharmacopoeia 7.0 |