4-tert-butyl-2,6-bis(hydroxymethyl)phenol (CHEM167645)
| Record Information | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Version | 1.0 | ||||||||
| Creation Date | 2026-08-18 19:46:41 UTC | ||||||||
| Update Date | 2026-08-18 19:46:41 UTC | ||||||||
| Accession Number | CHEM167645 | ||||||||
| Identification | |||||||||
| Common Name | 4-tert-butyl-2,6-bis(hydroxymethyl)phenol | ||||||||
| Class | Small Molecule | ||||||||
| Description | 4-tert-butyl-2,6-bis(hydroxymethyl)phenol is an organic compound with the formula C12H18O3 and an average molecular weight of 210.27 g/mol. 4-tert-butyl-2,6-bis(hydroxymethyl)phenol belongs to the phenylpropanes, a subclass of benzene and substituted derivatives within the organic compounds. This benzenoid compound has been identified in or released from one recorded source: Electrical & Electronic Equipment (Auxiliary Devices). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C12H18O3 | ||||||||
| Average Molecular Mass | 210.270 g/mol | ||||||||
| Monoisotopic Mass | 210.126 g/mol | ||||||||
| CAS Registry Number | 2203-14-7 | ||||||||
| IUPAC Name | 4-tert-butyl-2,6-bis(hydroxymethyl)phenol | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | Not Available | ||||||||
| InChI Identifier | InChI=1S/C12H18O3/c1-12(2,3)10-4-8(6-13)11(15)9(5-10)7-14/h4-5,13-15H,6-7H2,1-3H3 | ||||||||
| InChI Key | SIBBGGADHQDMHI-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
| ||||||||
| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
| ||||||||
| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
