| CAS No. | 52892-98-5 |
| Molecular Formula | C16H24O4 |
| Molecular Weight | 280.36 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 2,2,4,4-Tetramethylcyclobutane-1,3-diyl bis(2-methylacrylate).
CATO supplies 2,2,4,4-Tetramethylcyclobutane-1,3-diyl bis(2-methylacrylate) (CAS 52892-98-5), a certified reference material (molecular formula C16H24O4, MW 280.36 g/mol) for analytical method development and quality control.
2,2,4,4-Tetramethylcyclobutane-1,3-diyl bis(2-methylacrylate) (C16H24O4) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.
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 2,2,4,4-Tetramethylcyclobutane-1,3-diyl bis(2-methylacrylate) 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 | C16H24O4 |
| Molecular Weight | 280.36 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store at room temperature, keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure |
| Degree of Unsaturation (DBE) | 5.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1972 |