| CAS No. | 1408279-90-2 |
| Molecular Formula | C7H2F6INS |
| Molecular Weight | 373.06 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 373.06 g/mol gives 2-Iodo-5-trifluoromethyl-4-trifluoromethylsulphanylpyridine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
2-Iodo-5-trifluoromethyl-4-trifluoromethylsulphanylpyridine (CAS 1408279-90-2), molecular formula C7H2F6INS and molecular weight 373.06 g/mol, is a CATO reference standard with documented purity and traceability.
2-Iodo-5-trifluoromethyl-4-trifluoromethylsulphanylpyridine (C7H2F6INS) contains a nitrile group, sulfur-containing functionality, fluorine/iodine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.
This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.
CATO manufactures 2-Iodo-5-trifluoromethyl-4-trifluoromethylsulphanylpyridine 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 | C7H2F6INS |
| Molecular Weight | 373.06 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 4.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1991 |
| Halogen Content | F/I-containing |
| Nitrogen Atoms | 1 |
| Sulfur Atoms | 1 |