Home » Active Pharmaceuticals Ingredients » Oxyclozanide
| Product Name | Oxyclozanide BP/EP/USP |
| Chemical Name | 2,3,5-Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxybenzamide |
| CAS Number | 2277-92-1 |
| Chemical Formula | C13H6Cl5NO3 |
| Molecular Mass | 401.46 g/mol |
| Therapeutic Category | Anthelmintic |
Specification of Oxyclozanide :
| Test | Specification |
| Nature | A pale, cream colour odourless powder |
| Solubility | Slightly soluble in water, freely soluble in acetone, soluble in ethanol (96%),slightly soluble in chloroform |
| Identification | As per BP Vet |
| Melting Point | About 208 ºC |
| Ionisable chlorine | NMT 0.25% |
| Related substance by HPLC A) Individual Impurity B) Total Impurity |
NMT 0.3% NMT 1% |
| Loss on Drying (At 60ºC under vacuum) | NMT 1% w/w |
| Moisture content | NMT 0.5% |
| Sulphated Ash | NMT 0.2% w/w |
| Assay (Dry Basis) | NLT 98.00% & NMT 101.00% |
We are leading manufacturer and exporter of Olanzapine and our product is made up of good quality.
Olanzapine is a Yellow Crystalline Powder and an atypical antipsychotic. It is used for the treatment of schizophrenia and bipolar disorder.
| NAME OF PRODUCT : Olanzapine | |
| CAS NO | 132539-06-1 |
| Chemical Formula | C17H20N4S |
| MOL. WEIGHT | 312.439 g/mol |
| NAME OF PRODUCT : Orlistat Pellets | ||
| Description | a white to off-white powder | |
| Solubility | Freely soluble in Chloroform. Insoluble in Water | |
| Identification a) By HPLC b) By I.R. Absorption |
The retention time of Orlistat peak in the sample chromatogram of assay test should match with that of laboratory standard. The IR Spectrum of sample should be concordant with that of the laboratory standard. |
|
| Melting Range | Between 40°C to 48°C | |
| Water content(by KF Titration) | NMT 1.00% W/W | |
| Specific Optical Rotation (in Chloroform) | Between -30.0° and -40.0° | |
| Residue on Ignition | NMT 0.20% W/W | |
| Heavy Metals | NMT 0.002% (20 ppm) | |
| Related substances (by HPLC ) | Isopentyl Analog Dimethyl Orlistat Any other single maximum impurity Total Impurity |
NMT 1.00% NMT 1.00% NMT 1.00% NMT 3.00% |
| Assay Content of Orlistat(by HPLC) | Between 95.0% W/W and 100% W/W | |
Our Product Range : Active Pharmaceuticals Ingredients |Drug Intermediates | Finished Formulation
Home|About Us|Our Product Range|Media Gallery|Contact Us|Enquiry
©
Yashica Pharmaceuticals Private Limited. All Rights Reserved (Terms
of Use)
