Gabapentin EP Impurity A; Gabapentin USP Related Compound A

CAS No.: 64744-50-9 - Gabapentin EP Impurity A; Gabapentin USP Related Compound A
CAS No. : 64744-50-9
Mol F. : C9H15NO
Mol W. : 153.22
Cat No. : SA22801
SKU: bde6f3b68265 Categories: , Tags: ,
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Description

Product NameGabapentin EP Impurity A; Gabapentin USP Related Compound A
SynonymsGabapentin USP Related Compound A

Gabapentin Lactam

3-Azaspiro-[4,5]decan-3-one

3,3-Pentamethylene-5-butyrolactam

4,4-Pentamethylene-2-pyrrolidinone

Related APIGabapentin
CategoryImpurities

Order Gabapentin EP Impurity A; Gabapentin USP Related Compound A product with CAS: 64744-50-9 and speed up your project. This product is also known as Gabapentin USP Related Compound A; Gabapentin Lactam and can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Gabapentin EP Impurity A; Gabapentin USP Related Compound A is used in Gabapentin impurity profiling as per limits and threshold values specified by respective drug legislations, FDA and pharmacopoeial guidelines during commercial production of Gabapentin and its related formulations. Moreover, Gabapentin USP Related Compound A 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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Certificate of Analysis (CoA) and Characterization Data:

All products are provided with a certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS, etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply). 

This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This product provided by SynThink is generally used for Abbreviated New Drug Application (ANDA) filing to FDA, toxicity study of respective drug formulation, Quality Control (QC) and analytical studies during commercial production of the API]. Please also find out process impurities, degradation impurities, potential impurities of related api/drug developed by our R&D.

Products provide by SynThink are for research and development (R&D) use only

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