≥98% 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
2-Methyl-2-heptene undergoes oxidation by singlet oxygen generated by the excitation of thiazine dyes cation to form hydroperoxides.2-Methyl-2-heptene was used in the functionalization of ethylene/5,7-dimethyl-1,6-diene copolymer with maleic anhydride via Alder Ene reaction.
| Sorrisi canonici | CCCCC=C(C)C |
|---|---|
| IUPAC Name | 2-methylhept-2-ene |
| InChIKey | WEPNJTDVIIKRIK-UHFFFAOYSA-N |
| INCHI | 1S/C8H16/c1-4-5-6-7-8(2)3/h7H,4-6H2,1-3H3 |
| Isomeri SMILES | CCCCC=C(C)C |
| WGK Germania | 3 |
| Peso molecolare | 112.21 |
| Reaxy-Rn | 1732139 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732139&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 | Hydrocarbons |
| Classe | Unsaturated hydrocarbons |
| Subclass | Branched unsaturated hydrocarbons |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Branched unsaturated hydrocarbons |
| Alternative Parents | Unsaturated aliphatic hydrocarbons Alkenes |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Branched unsaturated hydrocarbon - Unsaturated aliphatic hydrocarbon - Olefin - Alkene - Acyclic olefin - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch. |
| External Descriptors | Not available |
| Punto di infiammabilità (°F) | 53.6 °F |
|---|---|
| Punto di infiammabilità (°C) | 12 °C |
| Peso molecolare | 112.210 g/mol |
| XLogP3 | 3.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 3 |
| Exact Mass | 112.125 Da |
| Monoisotopic Mass | 112.125 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 66.100 |
| 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 |
