| CAS No. | CATO-C4X-131657 |
| Molecular Formula | C5H13O5P |
| Molecular Weight | 184.13 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Fosfomycin Impurity 57.
CATO supplies Fosfomycin Impurity 57 (CAS CATO-C4X-131657), a pharmacopoeial impurity reference standard (molecular formula C5H13O5P, MW 184.13 g/mol) used for the identification and quantification of trace impurities in APIs.
Structurally, Fosfomycin Impurity 57 (C5H13O5P) contains a carbohydrate-derived structure, a phosphate ester group. The molecule exhibits a degree of unsaturation (DBE) of -0.5, corresponding to approximately 0 ring(s) or double-bond equivalent(s). With a molecular weight of 184.13 g/mol, it falls into the medium-molecular-weight range.
Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.
As a certified reference material (CRM), Fosfomycin Impurity 57 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.
| Molecular Formula | C5H13O5P |
| Molecular Weight | 184.13 g/mol |
| Purity | >95% |
| Storage | Store at 2-8°C, keep sealed and dry |
| Solubility (reference) | Soluble in methanol, ethanol, DMSO, water |
| Stability | Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | -0.5 |