≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Nonafluoro- tert -butyl alcohol is also referred as perfluoro tertiary butanol and ′artificial blood′.
Application
Nonafluoro- tert -butyl alcohol was employed as a precursor for the preparation of appropriate bis (polyfluoroalkoxymethyl)carbinols and their corresponding mesylates.
| Pubchem Sid | 504752788 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752788 |
| Sonrisas canónicas | C(C(F)(F)F)(C(F)(F)F)(C(F)(F)F)O |
| IUPAC Name | 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol |
| InChIKey | XZNOAVNRSFURIR-UHFFFAOYSA-N |
| INCHI | 1S/C4HF9O/c5-2(6,7)1(14,3(8,9)10)4(11,12)13/h14H |
| Isómeros SMILES | C(C(F)(F)F)(C(F)(F)F)(C(F)(F)F)O |
| RTECS | UB6452700 |
| Peso molecular | 236.04 |
| Reaxy-Rn | 1841640 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1841640&ln= |
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 |
| Clase | 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 |
| Descripción | 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 |
| Índice de refracción | n20/D 1.3 (lit.) |
|---|---|
| Punto de ebullición (°C) | 45 °C |
| Punto de fusión (°C) | -17°C |
| Peso molecular | 236.040 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 0 |
| Exact Mass | 235.988 Da |
| Monoisotopic Mass | 235.988 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 170.000 |
| 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 |
| 1. Pei Yang, Huihui Liu, Shuang Wang, Linghui Meng, Yongping Bai, Jinmei He. (2024) Functional energetic materials: Simple preparation of fluorinated materials to improve safety, preservation and energy release performance of energetic materials. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, [PMID:] [10.1016/j.colsurfa.2024.134144] |
H2307884