Determine the necessary mass, volume, or concentration for preparing a solution.
≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-Trifluoromethyl-2-propanol is a fluorinated aliphatic alcohol. It can be prepared by reacting methyllithium, trifluoroacetone and trifluorovinyl bromide in ether.This can also be synthesized from the reaction between methylmagnesium bromide and 1,1,1-trifluoroacetone in ether.
Application:
2-Trifluoromethyl-2-propanol may be employed as a solvent for the preparation of [18F]fluorothymidine. It may also be used in the synthesis of [2-(trifluoromethyl)-2-propyl nitrate] through nitration in nitric acid/trifluoroacetic anhydride.
| Pubchem Sid | 504754265 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754265 |
| Sorrisi canonici | CC(C)(C(F)(F)F)O |
| IUPAC Name | 1,1,1-trifluoro-2-methylpropan-2-ol |
| InChIKey | OCGWWLDZAFOHGD-UHFFFAOYSA-N |
| INCHI | 1S/C4H7F3O/c1-3(2,8)4(5,6)7/h8H,1-2H3 |
| Isomeri SMILES | CC(C)(C(F)(F)F)O |
| WGK Germania | 3 |
| PubChem CID | 68182 |
| Peso molecolare | 128.09 |
| Reaxy-Rn | 1736196 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tertiary alcohols |
| Alternative Parents | Fluorohydrins Organofluorides Hydrocarbon derivatives Alkyl fluorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tertiary alcohol - Halohydrin - Fluorohydrin - Hydrocarbon derivative - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as tertiary alcohols. These are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Jul 30, 2026 | T161663 | |
| Certificate of Analysis | Jul 30, 2026 | T161663 | |
| Certificate of Analysis | Jul 30, 2026 | T161663 | |
| Certificate of Analysis | Jul 09, 2024 | T161663 | |
| Certificate of Analysis | Jul 09, 2024 | T161663 | |
| Certificate of Analysis | Apr 13, 2024 | T161663 | |
| Certificate of Analysis | Oct 30, 2023 | T161663 | |
| Certificate of Analysis | Oct 30, 2023 | T161663 | |
| Certificate of Analysis | Oct 30, 2023 | T161663 |
| Indice di rifrazione | 1.33 |
|---|---|
| Punto di infiammabilità (°F) | 59 °F |
| Punto di infiammabilità (°C) | 15°C(lit.) |
| Punto di ebollizione (°C) | 82°C(lit.) |
| Peso molecolare | 128.090 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 128.045 Da |
| Monoisotopic Mass | 128.045 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 83.800 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |