| CAS No. | 104865-87-4 |
| Molecular Formula | C14H22O3 |
| Molecular Weight | 238.32 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 238.32 g/mol gives 1-(tert-Butyl)-4-(trimethoxymethyl)benzene distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
1-(tert-Butyl)-4-(trimethoxymethyl)benzene (CAS 104865-87-4), molecular formula C14H22O3 and molecular weight 238.32 g/mol, is a CATO reference standard with documented purity and traceability.
Structurally, 1-(tert-Butyl)-4-(trimethoxymethyl)benzene (C14H22O3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 238.32 g/mol, it falls into the medium-molecular-weight range. 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 1-(tert-Butyl)-4-(trimethoxymethyl)benzene 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 | C14H22O3 |
| Molecular Weight | 238.32 g/mol |
| Appearance | Off-white to pale yellow crystalline powder |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening |
| Degree of Unsaturation (DBE) | 4.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1986 |