| CAS No. | 1025707-86-1 |
| Molecular Formula | C20H24N3S |
| Molecular Weight | N/A |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
The occurrence of 4-({[(2Z)-3-tert-butyl-4-phenyl-2,3-dihydro-1,3-thiazol-2-ylidene]amino}methyl)-1-methylpyridin-1-ium iodide is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies 4-({[(2Z)-3-tert-butyl-4-phenyl-2,3-dihydro-1,3-thiazol-2-ylidene]amino}methyl)-1-methylpyridin-1-ium iodide (CAS 1025707-86-1), a certified reference material (molecular formula C20H24N3SI, MW 465.39 g/mol) for analytical method development and quality control.
4-({[(2Z)-3-tert-butyl-4-phenyl-2,3-dihydro-1,3-thiazol-2-ylidene]amino}methyl)-1-methylpyridin-1-ium iodide (C20H24N3SI) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, iodine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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.
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.
| Molecular Formula | C20H24N3S I |
| Molecular Weight | 465.39 g/mol |
| Purity | 97%+ |
| Storage | Store at room temperature, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 10.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1988 |
| Halogen Content | I-containing |
| Nitrogen Atoms | 3 |
| Sulfur Atoms | 1 |