Allylestrenol Impurities & Reference Standards

Invenza supplies high-quality Allylestrenol Reference Standards, Allylestrenol impurities, pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine-related products for pharmaceutical research, analytical testing, and quality control applications.

Our Allylestrenol impurity reference standards are suitable for a wide range of pharmaceutical and analytical applications, including drug development, analytical method development and validation, quality control (QC), stability studies, impurity profiling, unknown impurity identification, regulatory submissions such as ANDA and DMF, and assessment of potential genotoxic impurities.

Allylestrenol-related reference standards are thoroughly characterized and supplied with Certificates of Analysis (COA) and supporting analytical data, subject to product availability and applicable specifications. We can also provide pharmacopeial and traceable reference standards, including EP/USP-related requirements, based on customer specifications

Our Allylestrenol impurity standards are manufactured, characterized, and handled to support reliable analytical testing and pharmaceutical research requirements. Products are periodically re-tested, where applicable, to help ensure consistent quality and dependable analytical performance.

CAT No. IR-A00586
CAS No. 432-60-0
Molecular Formula C21H32O
Molecular Weight 300.5
CAT No. IR-A00587
CAS No. 3646-28-4
Molecular Formula C18H26O
Molecular Weight 258.4
CAT No. IR-A00588
CAS No. NA
Molecular Formula C21H30O
Molecular Weight 298.5