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Home Impurity Midazolam CS-O-13591

Midazolam EP Impurity D

RFQ Review Required

Midazolam EP Impurity D

Impurity · API Family: Midazolam · CAT No. CS-O-13591 · CAS No. 59468-83-6 · Controlled Product
Controlled Product - RFQ Review Required

This product requires compliance review before availability, pricing or documentation can be shared. Please add this item to your RFQ basket. Our team will evaluate the request based on end-use, company details and applicable documentation.

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Controlled product. This item is supplied only after compliance review and applicable documentation. For Research & Analytical Purposes only. Not for personal use.
Clearsynth product packaging

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.
Storage: Refer MSDS for complete information.
Hazard: Refer MSDS for accurate information.

Midazolam EP Impurity D Product Information

Midazolam EP Impurity D is listed under Impurity and is intended for research and analytical applications. It is associated with Midazolam. This product is controlled and availability, pricing and documentation are shared only after RFQ and compliance review.

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
Midazolam EP Impurity D
CAS No.
59468-83-6
CAT No.
CS-O-13591
HSN Code
38229010
Country of Origin
Can be shipped from India, Canada and USA
Molecular Formula
C18H13ClFN3O
Molecular Weight
341.8
Category
API Family
Storage Condition
Refer MSDS for complete information.
Controlled Product
Yes - RFQ and compliance review required before pricing, availability or documentation can be shared.
Hazard Compound
Refer MSDS for accurate information.

Description

Regulatory Description
Midazolam EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Midazolam EP Impurity D 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 Midazolam.
Overview
Impurity in commercial preparations of Midazolam.
Synonyms
Midazolam EP Impurity D
Application Notes
Impurity in commercial preparations of Midazolam.
References

Product Applications & Regulatory Search Terms

Useful product, supplier and regulatory search terms for this reference standard.

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