| CAS No. | 898787-82-1 |
| Molecular Formula | C16H15ClOS |
| Molecular Weight | 290.81 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
The occurrence of 3-(4-Chlorophenyl)-4-thiomethylpropiophenone is closely related to sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution, a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
CATO supplies 3-(4-Chlorophenyl)-4-thiomethylpropiophenone (CAS 898787-82-1), a certified reference material (molecular formula C16H15ClOS, MW 290.81 g/mol) for analytical method development and quality control.
Owing to sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution, a polycyclic aromatic system, 3-(4-Chlorophenyl)-4-thiomethylpropiophenone is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 290.81 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 3-(4-Chlorophenyl)-4-thiomethylpropiophenone 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 | C16H15ClOS |
| Molecular Weight | 290.81 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep tightly closed to prevent evaporation |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 9.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1987 |
| Halogen Content | Cl-containing |
| Sulfur Atoms | 1 |