Tamsulosin impurity standards
For Tamsulosin, the Zemixal catalogue holds 34 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 16 pharmacopoeial impurities and 1 nitrosamine.
Batches are supplied with a certificate of analysis, and the supporting spectra can be sent ahead of a purchase order so your QA team can review them. Laboratories use them to validate related-substance methods, set specification limits under ICH Q3A and Q3B, and identify unknown peaks in stability samples. For nitrosamine risk evaluation, the N-nitroso standards allow confirmatory LC-MS testing against the acceptable intake limits.
By impurity type
Counts are based on product names. One compound can fall into more than one type.
All Tamsulosin reference materials
- CAS
- 35193-64-7
- Formula
- C20H13O4P
- MW
- 348.3 g/mol
- CAS
- 112101-77-6
- Formula
- C10H17ClN2O3S
- MW
- 280.77 g/mol
- CAS
- 1027854-97-2
- Formula
- C27H34N2O5S
- MW
- 498.6 g/mol
- CAS
- 133261-17-3
- Formula
- C20H26N2O6S
- MW
- 422.5 g/mol