≥97% 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.
1-Cyclohexylethanol undergoes photocatalytic oxidation (PCO) using nanoparticles titanium dioxide (TiO2-P25) as a semiconductor photocatalyst in acetonitrile, under aerated conditions. It forms cyclohexylethanols by undergoing catalytic ring hydrogenation over several noble metal catalysts supported on charcoal, or on γ-alumina in supercritical carbon dioxide
| Kanonisches Lächeln | CC(C1CCCCC1)O |
|---|---|
| IUPAC Name | 1-cyclohexylethanol |
| InChIKey | JMSUNAQVHOHLMX-UHFFFAOYSA-N |
| INCHI | 1S/C8H16O/c1-7(9)8-5-3-2-4-6-8/h7-9H,2-6H2,1H3 |
| Isomere SMILES | CC(C1CCCCC1)O |
| WGK Deutschland | 2 |
| RTECS | GV5776500 |
| Molekulargewicht | 128.21 |
| Reaxy-Rn | 2322053 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2322053&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 |
| Klasse | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Secondary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Secondary alcohol - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). |
| External Descriptors | Not available |
| Brechungsindex | 1.465 |
|---|---|
| Flammpunkt (°F) | 163.4 °F |
| Flammpunkt (°C) | 73 °C |
| Siedepunkt (°C) | 189℃ |
| Molekulargewicht | 128.210 g/mol |
| XLogP3 | 2.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 128.12 Da |
| Monoisotopic Mass | 128.12 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 74.600 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
K2527077