Codergocrine Mesilate Impurity – F
N-[(2S)-1-hydroxypropan-2-yl]-6-methylergoline-8βcarboxamide (dihydroergometrine)
| Chemical Name | N-[(2S)-1-hydroxypropan-2-yl]-6-methylergoline-8βcarboxamide (dihydroergometrine) |
|---|---|
| CAS No. | 62841-02-5 |
| Molecular Formula | C19H25N3O2 |
| Molecular Weight | 327.43 |
| Chemical Structure |
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Codergocrine Mesilate Impurity – F
Codergocrine Mesilate Impurity – F represents a known degradation or process impurity of Codergocrine Mesilate, recognized under the EP monograph. Chemically, it is described as N-[(2S)-1-hydroxypropan-2-yl]-6-methylergoline-8βcarboxamide (dihydroergometrine). It has the molecular formula C19H25N3O2 and a molecular weight of 327.43 g/mol. Laboratories use this reference standard for impurity identification, method validation, and batch release testing related to Codergocrine Mesilate. Available with a Certificate of Analysis (CoA) as a high-purity reference standard suitable for HPLC and LC-MS applications.
Codergocrine Mesilate impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.
We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Codergocrine Mesilate impurities that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related impurities.
This related products or Impurities are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.
BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.
BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.
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