| CAS No. | 1992957-06-8 |
| Molecular Formula | C13H15ClO4S |
| Molecular Weight | 302.77 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| 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 4-(2-Chlorobenzyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide.
CATO supplies 4-(2-Chlorobenzyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide (CAS 1992957-06-8), a certified reference material (molecular formula C13H15ClO4S, MW 302.77 g/mol) for analytical method development and quality control.
The molecular framework of 4-(2-Chlorobenzyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide (C13H15ClO4S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
CATO manufactures 4-(2-Chlorobenzyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide 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 | C13H15ClO4S |
| Molecular Weight | 302.77 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 6.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1996 |
| Halogen Content | Cl-containing |
| Sulfur Atoms | 1 |