2,2-Dichloropentane-1,1,5-triyl triacetate CAS 141942-61-2
| CAS No. | 141942-61-2 |
| Molecular Formula | C11H16Cl2O6 |
| Molecular Weight | 315.15 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
2,2-Dichloropentane-1,1,5-triyl triacetate (CAS 141942-61-2) is a high-purity analytical reference standard with the molecular formula C11H16Cl2O6 and a molecular weight of 315.15 g/mol.
Based on its molecular formula C11H16Cl2O6, 2,2-Dichloropentane-1,1,5-triyl triacetate contains a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 315.15 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).
CATO manufactures 2,2-Dichloropentane-1,1,5-triyl triacetate 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.
Physical & Chemical Properties
| Molecular Formula | C11H16Cl2O6 |
| Molecular Weight | 315.15 g/mol |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), keep sealed and dry |
| Solubility (reference) | Soluble in methanol, ethanol, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 3.0 |
| UV Absorption | UV-absorbing |
| CAS Registry Year (est.) | 1997 |
| Halogen Content | Cl-containing |
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Why CATO?
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