| CAS No. | 101920-13-2 |
| Molecular Formula | C22H22O2P |
| Molecular Weight | N/A |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
The occurrence of (2-Ethoxy-2-oxoethyl)triphenylphosphonium chloride hydrate is closely related to a steroid core, a phosphonate group, a hydroxyl group, an ether linkage, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.
(2-Ethoxy-2-oxoethyl)triphenylphosphonium chloride hydrate (CAS 101920-13-2) is a high-purity analytical reference standard with the molecular formula C22H22O2PClH2O and a molecular weight of 402.85 g/mol.
Owing to a steroid core, a phosphonate group, a hydroxyl group, an ether linkage, chlorine substitution, (2-Ethoxy-2-oxoethyl)triphenylphosphonium chloride hydrate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 402.85 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).
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-Ethoxy-2-oxoethyl)triphenylphosphonium chloride hydrate 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 | C22H22O2P Cl 2*H2O |
| Molecular Weight | 402.85 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 10.5 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1986 |
| Halogen Content | Cl-containing |