Ziprasidone EP Impurity E
| Catalog No. | KMZ002017 |
|---|---|
| CAS No. | 1159977-04-4 |
| Alt. name | Ziprasidone USP Related Compound D |
| Formula | C28H24ClN5OS2 |
| FW | 546.1 |
| Unit | Price | Stock |
|---|---|---|
| 100 mg | Enquire | Enquire |
| Chemical Name: | 3-(1,2-Benzisothiazol-3-yl)-5-[2-[4-(1,2-benzisothiazol-3-yl)piperazin-1-yl]ethyl]-6-chloro-1,3-dihydro-2H-indol-2-one (as per EP) ; 3-(Benzoisothiazol-3-yl)-5-{2-[4-(benzoisothiazol-3-yl)piperazin-1-yl]ethyl}-6-chloroindolin-2-one (as per USP) |
|---|---|
| Purity: | >95% |
| Storage: | Store at 2-8 deg. C for long term storage |
| Shipping: | Product is stable to be Shipped at Room Temperature |
Ziprasidone EP Impurity E is chemically 3-(1,2-Benzisothiazol-3-yl)-5-[2-[4-(1,2-benzisothiazol-3-yl)piperazin-1-yl]ethyl]-6-chloro-1,3-dihydro-2H-indol-2-one (as per EP) ; 3-(Benzoisothiazol-3-yl)-5-{2-[4-(benzoisothiazol-3-yl)piperazin-1-yl]ethyl}-6-chloroindolin-2-one (as per USP) .
Ziprasidone EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline.
Ziprasidone EP Impurity E can be used for the analytical method development, method validation (AMV), Quality Controlled (QC)
application for Abbreviated New Drug Application (ANDA) or during commercial production of Ziprasidone EP Impurity E.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. K.M.Pharma products are for analytical purpose only and not for human use.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. K.M.Pharma products are for analytical purpose only and not for human use.
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