Rivaroxaban EP Impurity H
Added to RFQ
For Research & Analytical Purposes. Not for Personal use.
Packaging & Handling
Indicative product packaging is shown for visual reference. Actual packaging may vary based on pack size, quantity, storage condition and shipping requirements.
Documentation Available
Detailed specifications, certificates, and supporting documents are available upon request.
Detailed specifications, certificates, and supporting documents are available upon request.
Storage: Refer MSDS for complete information.
Hazard: Refer MSDS for accurate information.
Rivaroxaban EP Impurity H Product Information
Rivaroxaban EP Impurity H is listed under Impurity and is intended for analytical research, quality control and pharmaceutical reference standard applications. It is associated with Rivaroxaban. The product is supplied by Clearsynth under CAT No. CS-O-16749.
Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight and product enquiry details.
Technical Data
Product Name
Rivaroxaban EP Impurity H
CAS No.
1770812-37-7
CAT No.
CS-O-16749
HSN Code
38229010
Country of Origin
Can be shipped from India, Canada and USA
Molecular Formula
C19H17Cl2N3O5S
Molecular Weight
470.33
Category
API Family
Storage Condition
Refer MSDS for complete information.
Hazard Compound
Refer MSDS for accurate information.
Description
Regulatory Description
Rivaroxaban EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Rivaroxaban EP Impurity H can be used for analytical method development, method validation (AMV), Quality Control (QC) application for Abbreviated New Drug Application (ANDA), or during commercial production of Rivaroxaban.
Overview
Impurity of Rivaroxaban
Synonyms
Rivaroxaban EP Impurity H
Application Notes
Impurity of Rivaroxaban
Product Applications & Regulatory Search Terms
Useful product, supplier and regulatory search terms for this reference standard.