| CAS No. | 15445-77-9 |
| Molecular Formula | 2*C14H10Cl2N2O3S |
| Molecular Weight | N/A |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
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.
O-(3-Nitrophenyl) (3,4-dichlorobenzyl)carbamothioate compound with 1,1'-(piperazine-1,4-diyl)bis(ethan-1-one) (2:1) (CAS 15445-77-9) is a high-purity analytical reference standard with the molecular formula C14H10Cl2N2O3SC8H14N2O2 and a molecular weight of 527.42 g/mol.
The molecular framework of O-(3-Nitrophenyl) (3,4-dichlorobenzyl)carbamothioate compound with 1,1'-(piperazine-1,4-diyl)bis(ethan-1-one) (2:1) (C14H10Cl2N2O3SC8H14N2O2) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.
CATO manufactures O-(3-Nitrophenyl) (3,4-dichlorobenzyl)carbamothioate compound with 1,1'-(piperazine-1,4-diyl)bis(ethan-1-one) (2:1) 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 | 2*C14H10Cl2N2O3S C8H14N2O2 |
| Molecular Weight | 527.42 g/mol |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| 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) | 12.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1961 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 4 |
| Sulfur Atoms | 1 |