Efinaconazole impurities include process-related compounds, degradation products, and stereoisomeric variants formed during synthesis or storage. These impurities are monitored to ensure the safety and efficacy of this topical antifungal agent used in the treatment of onychomycosis. All materials are structurally confirmed and qualified under ICH guidelines for pharmaceutical analysis and toxicological evaluation.
We offer pharmacopeial and non-pharmacopeial Efinaconazole impurities that comply with European Pharmacopoeia (EP) specifications. These impurity standards are essential for method development, impurity profiling, and stability testing. Analytical techniques such as HPLC, LC-MS, and NMR are used for their identification and quantification. EP traceable standards are available upon request.
Our catalog includes Efinaconazole-related compounds such as epoxide intermediates, diol derivatives, and desfluoro analogs. These entries are used in forced degradation studies, impurity identification, and genotoxicity screening. All materials are thoroughly characterized and supported by detailed analytical documentation.
Efinaconazole impurity reference standards are supplied with validated analytical data including NMR, MS, and HPLC purity. These materials are used in pharmaceutical R&D, ANDA and DMF filings, method validation, and GMP-compliant quality control. EP/USP traceable entries are available upon request, and all products meet international regulatory expectations. Supplied materials are re-tested at regular intervals to ensure consistency.
![1-[[(2R,3S)-2-(2,4-Difluorophenyl)-3-methyloxiranyl]methyl]-1H-1,2,4-triazole | 127000-90-2 | Efinaconazole](https://synthinkchemicals.com/wp-content/uploads/2025/04/SA23618.png)
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