| CAS No. | CATO-C4X-131637 |
| Molecular Formula | C7H17O5P |
| Molecular Weight | 212.18 g/mol |
| Category | Pharmacopoeial Impurity Standards / EP Impurities |
| Availability | In Stock |
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 process- or degradation-related impurity, Fosfomycin Impurity 37 (CAS CATO-C4X-131637, C7H17O5P) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.
Structurally, Fosfomycin Impurity 37 (C7H17O5P) contains a phosphate ester group, a carboxylic acid group, a hydroxyl group, an ether linkage. 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 212.18 g/mol, it falls into the medium-molecular-weight range.
CATO manufactures Fosfomycin Impurity 37 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
| Molecular Formula | C7H17O5P |
| Molecular Weight | 212.18 g/mol |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°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 |