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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Copolymers of 1-eicosene and ethene has been prepared using the methylaluminoxane activated dimethylsilanediyl(tetracyclopentadienyl)(tert-butylamido)-titanium dichloride catalyst system. It polymerizes in the presence of zirconocene and hafnocene catalyst to yield poly-1-eicosene
| Pubchem Sid | 488182514 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488182514 |
| Canonical Smiles | CCCCCCCCCCCCCCCCCCC=C |
| IUPAC Name | icos-1-ene |
| InChIKey | VAMFXQBUQXONLZ-UHFFFAOYSA-N |
| INCHI | 1S/C20H40/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3H,1,4-20H2,2H3 |
| Isomeric SMILES | CCCCCCCCCCCCCCCCCCC=C |
| Molecular Weight | 280.54 |
| Beilstein | 1(4)934 |
| Reaxy-Rn | 1768357 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1768357&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 |
| Class | Unsaturated hydrocarbons |
| Subclass | Unsaturated aliphatic hydrocarbons |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Unsaturated aliphatic hydrocarbons |
| Alternative Parents | Alkenes |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Unsaturated aliphatic hydrocarbon - Olefin - Alkene - Acyclic olefin - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as unsaturated aliphatic hydrocarbons. These are aliphatic Hydrocarbons that contains one or more unsaturated carbon atoms. These compounds contain one or more double or triple bonds. |
| External Descriptors | Hydrocarbons |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Dec 10, 2025 | E156121 | |
| Certificate of Analysis | Dec 10, 2025 | E156121 | |
| Certificate of Analysis | Aug 07, 2023 | E156121 | |
| Certificate of Analysis | Oct 13, 2022 | E156121 | |
| Certificate of Analysis | Oct 13, 2022 | E156121 | |
| Certificate of Analysis | Oct 13, 2022 | E156121 | |
| Certificate of Analysis | Oct 13, 2022 | E156121 | |
| Certificate of Analysis | Oct 13, 2022 | E156121 | |
| Certificate of Analysis | Feb 15, 2022 | E156121 | |
| Certificate of Analysis | Feb 15, 2022 | E156121 |
| Refractive Index | 1.45 |
|---|---|
| Boil Point(°C) | 151°C/1.5mmHg(lit.) |
| Melt Point(°C) | 29 °C |
| Molecular Weight | 280.500 g/mol |
| XLogP3 | 11.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 17 |
| Exact Mass | 280.313 Da |
| Monoisotopic Mass | 280.313 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 171.000 |
| 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. Weiwei Ge, Huihui Pai, Jiale Zhang, Chuanbo Zhang, Wenyu Lu. (2025) Construction of isopentenol utilization pathway and artificial multifunctional enzyme for miltiradiene synthesis in Saccharomyces cerevisiae. BIORESOURCE TECHNOLOGY, [PMID:39809383] [10.1016/j.biortech.2025.132065] |