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Ezetimibe Deprotected Impurity; SRS uncyclized ezetimibe impurity

Ezetimibe EP Impurity D; (S)-3-((2R,5S)-5-(4-fluorophenyl)-2-((S)-(4-fluorophenylaMino)(4-hydroxyphenyl)Methyl)-5-hydroxypentanoyl)-4-phenyloxazolidin-2-one;

Ezetimibe Deprotected Impurity; SRS uncyclized ezetimibe impurity | 1185883-40-2 | Ezetimibe

Specifications:

CAS No.

: 1185883-40-2

Mol F.

: C33H30F2N2O5

Mol W.

: 572.61

Cat No.

: SA14826

Appearance

Pack Size Price Availability
25 mg $200 In Stock
50 mg $350 In Stock
100 mg $650 In Stock
200 mg $995 In Stock
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Product Name

: Ezetimibe Deprotected Impurity; SRS uncyclized ezetimibe impurity

CAS No.

: 1185883-40-2

Mol F.

: C33H30F2N2O5

Mol W.

: 572.61

Cat No.

: SA14826

Appearance

Synonyms

: Ezetimibe EP Impurity D; (S)-3-((2R,5S)-5-(4-fluorophenyl)-2-((S)-(4-fluorophenylaMino)(4-hydroxyphenyl)Methyl)-5-hydroxypentanoyl)-4-phenyloxazolidin-2-one;

Related API

: Ezetimibe

Category

Ezetimibe Deprotected Impurity; SRS uncyclized ezetimibe impurity product with CAS: 1185883-40-2 is also known as Ezetimibe EP Impurity D. This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. It is used in Ezetimibe impurity profiling as per limits and threshold values specified by respective drug legislation, FDA, and pharmacopoeial guidelines. Moreover, Ezetimibe EP Impurity D is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

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Disclaimer

This impurity material may be used as a working standard or secondary reference standard, provided it is appropriately characterized, identified, and qualified for its intended use. Additional internal validation may be required in accordance with applicable FDA regulations and guidance documents.

These impurity standards are typically used for various regulatory and quality-related purposes, including: ANDA and DMF filings, Toxicological studies, Quality Control, Analytical method development and validation in pharmaceutical sector.

The product information provided on this webpage is based on the best available knowledge at the time of publication. However, accuracy and completeness are not guaranteed. The purchaser, user, or importer of record is responsible for verifying the product specifications and details at the time of ordering, as they may change without prior notice.

This product is intended strictly for research purposes and is not approved for human consumption.

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