| CAS No. | 2835499-20-0 |
| Molecular Formula | C6H16N3O2PS |
| Molecular Weight | 225.25 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
As a certified reference material (CRM), Thiotepa Impurity 12 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
CATO supplies Thiotepa Impurity 12 (CAS 2835499-20-0), a pharmacopoeial impurity reference standard (molecular formula C6H16N3O2PS, MW 225.25 g/mol) used for the identification and quantification of trace impurities in APIs.
Owing to an amide group, a sulfone group, organophosphorus functionality, a carboxylic acid group, a hydroxyl group, an ether linkage, Thiotepa Impurity 12 is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 225.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.
This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.
| Molecular Formula | C6H16N3O2PS |
| Molecular Weight | 225.25 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 0.5 |
| CAS Registry Year (est.) | 2003 |
| Nitrogen Atoms | 3 |
| Sulfur Atoms | 1 |