Iohexol EP Impurity A
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.
Iohexol EP Impurity A Product Information
Iohexol EP Impurity A is listed under Impurity and is intended for analytical research, quality control and pharmaceutical reference standard applications. It is associated with Iohexol. The product is supplied by Clearsynth under CAT No. CS-O-13730.
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
Iohexol EP Impurity A
CAS No.
31127-80-7
CAT No.
CS-O-13730
HSN Code
38229010
Country of Origin
Can be shipped from India, Canada and USA
Molecular Formula
C16H20I3N3O7
Molecular Weight
747.06
Category
API Family
Storage Condition
Refer MSDS for complete information.
Hazard Compound
Refer MSDS for accurate information.
Description
Regulatory Description
Iohexol EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Iohexol EP Impurity A 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 Iohexol.
Overview
Impurity in commercial preparation of Iohexol.
Synonyms
Iohexol EP Impurity A
Application Notes
Impurity in commercial preparation of Iohexol.
Product Applications & Regulatory Search Terms
Useful product, supplier and regulatory search terms for this reference standard.