≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normale 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488181395 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181395 |
| Sorrisi canonici | CCCCCC=C |
| IUPAC Name | hept-1-ene |
| InChIKey | ZGEGCLOFRBLKSE-UHFFFAOYSA-N |
| INCHI | 1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3 |
| Isomeri SMILES | CCCCCC=C |
| WGK Germania | 1 |
| RTECS | MJ8840000 |
| Numero UN | 2278 |
| Gruppo di imballaggio | II |
| Peso molecolare | 98.19 |
| Beilstein | 1098332 |
| Reaxy-Rn | 1098332 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098332&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 | 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 |
| Descrizione | 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 | Data | Oggetto |
|---|---|---|---|
 K2429127 | Certificate of Analysis | Sep 04, 2026 | H110653 |
| D2621087 | Certificate of Analysis | Apr 28, 2026 | H110653 |
| I2223571 | Certificate of Analysis | Apr 07, 2026 | H110653 |
| K1928227 | Certificate of Analysis | Mar 04, 2025 | H110653 |
| F2519136 | Certificate of Analysis | Jun 25, 2024 | H110653 |
| K2110187 | Certificate of Analysis | Aug 15, 2023 | H110653 |
| B2223571 | Certificate of Analysis | Aug 31, 2022 | H110653 |
| D2314553 | Certificate of Analysis | Aug 31, 2022 | H110653 |
| I2222848 | Certificate of Analysis | Aug 31, 2022 | H110653 |
| I2222849 | Certificate of Analysis | Aug 31, 2022 | H110653 |
| D2314562 | Certificate of Analysis | Jul 07, 2022 | H110653 |
| G2222309 | Certificate of Analysis | Jul 07, 2022 | H110653 |
| G2222325 | Certificate of Analysis | Jul 07, 2022 | H110653 |
| F2221114 | Certificate of Analysis | Jun 04, 2022 | H110653 |
| F2221222 | Certificate of Analysis | Jun 04, 2022 | H110653 |
| F2221505 | Certificate of Analysis | Jun 04, 2022 | H110653 |
| Indice di rifrazione | 1.3994 |
|---|---|
| Punto di infiammabilità (°F) | 15.8 °F |
| Punto di infiammabilità (°C) | -8℃ |
| Punto di ebollizione (°C) | 93.3°C |
| Punto di fusione (°C) | -119.2°C |
| Peso molecolare | 98.190 g/mol |
| XLogP3 | 4.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 4 |
| Exact Mass | 98.1096 Da |
| Monoisotopic Mass | 98.1096 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 37.300 |
| 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. Yang Xiao, Wang Yunbo, Cao Weihua, Jiang Ruizheng, Xie Guoxin, Cao Yuying, Qi Xiaowen. (2023) Adsorption limitation investigation on olefins for Cu-BTC. Friction, [PMID:] [10.1007/s40544-023-0763-5] |
| 2. Xu Li, Jiaqi Li, Xiaohong Wang, Lijun Yang, Hong Xu, Jinxiang Dong. (2022) Novel branched-chain sulfonate surfactants based on α-olefins from Fischer–Tropsch synthesis via reaction-separation-utilization integrated process. FUEL, [PMID:] [10.1016/j.fuel.2022.126961] |
| 3. Bao Jingxian, Fan Yonghui, Zhang Shuyi, Zhong Liangshu, Wu Minghong, Sun Yuhan. (2019) Hydrofunctionalization of Olefins to Higher Aliphatic Alcohols via Visible-Light Photocatalytic Coupling. CATALYSIS LETTERS, 149 (6): (1651-1659). [PMID:] [10.1007/s10562-019-02737-3] |
| 4. Tianjun Zhang, Xiaoxin Chen, Guangrui Chen, Mengyang Chen, Risheng Bai, Mingjun Jia, Jihong Yu. (2018) Synthesis of anatase-free nano-sized hierarchical TS-1 zeolites and their excellent catalytic performance in alkene epoxidation. Journal of Materials Chemistry A, 6 (20): (9473-9479). [PMID:] [10.1039/C8TA01439F] |
| 5. Shulan Yan, Xiufang Yan, Xuexiang Shao, Jie Liang. (2015) Porous polymeric antimicrobial resin containing N-halamine functional groups. REACTIVE & FUNCTIONAL POLYMERS, [PMID:] [10.1016/j.reactfunctpolym.2015.09.006] |
| 6. Geng Chen, Zexiang Bi, Xu Li, Jinxiang Dong. (2025) Hydroformylation of α-olefin dimers over Rh/C for synthesis of branched-chain fatty alcohols/acids. FUEL, [PMID:] [10.1016/j.fuel.2025.134552] |
| 7. Yuqing Wang, Miao Jiang, Na Liu, Tian Tian, Changdao Li, Zhao Sun, Gewen Yu, Yanming Wang, Wenxiu He, Jian Ding, Li Yan, Yunjie Ding. (2025) Constructing nitrogen-doped porous organic polymer- supported single-atom cobalt catalysts for highly efficient hydroformylation of internal olefins. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.166057] |
| 8. Shihao Su, Guojun Lv, Jialing Shen, Fuxin Wang, Lachgar Oussama, Yan Chen, Shengnan Xu. (2025) Pickering Interfacial Tandem Catalysis of Alkenes to 1,2-Diols over Manganese Oxide Catalysts at Room Temperature. ACS Catalysis, [PMID:] [10.1021/acscatal.4c06225] |
| 9. Shihao Su, Xuyang Zou, Guojun Lv, Fuxin Wang, Yangbin Shen. (2025) One-pot tandem conversion of alkenes into 1,2-diols over efficient bifunctional tin-tungsten oxide catalysts. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:40378450] [10.1016/j.jcis.2025.137875] |
