1-Heptadecene [Standard Material for GC] - ≥99.5%(GC) , CAS No.6765-39-5

CAS: 6765-39-5 Cat. No.: H157278 Peso molecular: 238.46 Beilstein Registry Number: 1758490 Número EC: 229-825-6

GRADE & PURITY ≥99.5%(GC)

Synonyms

1-HEPTADECENE|heptadec-1-ene|6765-39-5|HEPTADECENE|Hexahydroaplotaxene|26266-05-7|NSC 77132|NSC-77132|P33057D09T|64743-02-8|heptadecen|UNII-P33057D09T|EINECS 229-825-6|EINECS 247-567-2|EINECS 265-207-2|MFCD00009000|C30-38 olefin|1-Heptadecene, 98%|AI3-364

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

1-HEPTADECENE | heptadec-1-ene | 6765-39-5 | HEPTADECENE | Hexahydroaplotaxene | 26266-05-7 | NSC 77132 | NSC-77132 | P33057D09T | 64743-02-8 | heptadecen | UNII-P33057D09T | EINECS 229-825-6 | EINECS 247-567-2 | EINECS 265-207-2 | MFCD00009000 | C30-38 olefin | 1-Heptadecene, 98% | AI3-364

Especificaciones y pureza

≥99.5%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99.5%(GC)

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCCCCCCCC=C
• IUPAC Name: heptadec-1-ene
• InChIKey: ADOBXTDBFNCOBN-UHFFFAOYSA-N
• INCHI: 1S/C17H34/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3H,1,4-17H2,2H3
• Isómeros SMILES: CCCCCCCCCCCCCCCC=C
• WGK Alemania: 3
• Peso molecular: 238.46
• Beilstein: 1758490
• Reaxy-Rn: 1758486
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1758486&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbons
    • Clase Unsaturated hydrocarbons
      • Subclass Unsaturated aliphatic hydrocarbons

• Kingdom: Organic compounds
• Superclass: Hydrocarbons
• Clase: 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
• Descripción: 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Índice de refracción: 1.44
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 300°C(lit.)
• Punto de fusión (°C): 10-11 °C
• Peso molecular: 238.500 g/mol
• XLogP3: 9.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 14
• Exact Mass: 238.266 Da
• Monoisotopic Mass: 238.266 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 137.000
• 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

Referencias

1. Bin Chen, Zining Zhou, Yuze Li, Kok Bing Tan, Youting Wang, Xiaoping Rao, Jiale Huang, Xiaodong Zhang, Qingbiao Li, Guowu Zhan.  (2023)  Catalytic pyrolysis of fatty acids and oils into liquid biofuels and chemicals over supported Ni catalysts on biomass-derived carbon.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2023.123067]

2. Jin Zhong, Qiang Deng, Taimei Cai, Xiang Li, Rui Gao, Jun Wang, Zheling Zeng, Guiping Dai, Shuguang Deng.  (2021)  Graphitic carbon embedded FeNi nanoparticles for efficient deoxygenation of stearic acid without using hydrogen and solvent.  FUEL,      [PMID:] [10.1016/j.fuel.2021.120248]

3. Bin Chen, Xingwen Cha, Xuexue Dong, Juanjuan Bian, Jiale Huang, Qingbiao Li, Xiaoqing Huang, Guowu Zhan.  (2025)  Biochar assembled Ni atom-clusters for hydrogen-free and solvent-free deoxygenation of fatty acids.  AICHE JOURNAL,      [PMID:] [10.1002/aic.18821]

4. Bin Chen, Shui Yang, Longmei Shang, Yiling Wu, Youting Wang, Jian Tian, Jiale Huang, Xiaodong Zhang, Qingbiao Li, Guowu Zhan.  (2024)  Catalytic pyrolysis of biomass to aromatics over bifunctional Ni/ZSM-5 catalysts assembled on rice husk-derived silica platform.  Chem Catalysis,      [PMID:] [10.1016/j.checat.2024.100958]

5. Kok Bing Tan, Yueming Qiu, Yuze Li, Bin Chen, Lingxing Xia, Dongren Cai, Sajid Ali, Jiale Huang, Guowu Zhan.  (2024)  Enhanced catalytic deoxygenation of stearic acid into biofuels over supported FeNi catalysts.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.114361]

6. Xuwen Zhang, Xuexue Dong, Youting Wang, Juanjuan Bian, Sajid Ali, Dongren Cai, Kang Sun, Xiaoping Rao, Jianchun Jiang, Guowu Zhan.  (2025)  Metal–Organic Frameworks-Derived Cobalt Catalyst Supported on Biochar for Efficient Deoxygenation of Stearic Acid.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c03679]