1-Hexadecene - ≥94% , CAS No.629-73-2

CAS: 629-73-2 Cat. No.: H103614 Summenformel: C₁₆H₃₂ Molekulargewicht: 224.43 Beilstein Registry Number: 1753401 EG-Nummer: 211-105-8

GRADE & PURITY ≥94%

Synonyms

1-Hexadecene 10 microg/mL in Cyclohexane | Gulftene 16 | 1-Hexadecene, >=98.5% | 97T015M2UX | Alkenes, C14-18 .alpha.- | 1-Hexadecene | 1-Hexadecene, analytical standard | ?1-Hexadecene | Hexadecene-1 | Hexadecene, 1- | .alpha.-Hexadecene | Hexadecylene-1

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyme

1-Hexadecene 10 microg/mL in Cyclohexane | Gulftene 16 | 1-Hexadecene, >=98.5% | 97T015M2UX | Alkenes, C14-18 .alpha.- | 1-Hexadecene | 1-Hexadecene, analytical standard | ?1-Hexadecene | Hexadecene-1 | Hexadecene, 1- | .alpha.-Hexadecene | Hexadecylene-1

Spezifikationen & Reinheit

≥94%

Storage

Argon charged,Room temperature

Verschickt in

Normal

Reinheit

≥94%

Namen und Kennungen

• Pubchem Sid: 488181654
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181654
• Kanonisches Lächeln: CCCCCCCCCCCCCCC=C
• IUPAC Name: hexadec-1-ene
• InChIKey: GQEZCXVZFLOKMC-UHFFFAOYSA-N
• INCHI: 1S/C16H32/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3H,1,4-16H2,2H3
• Isomere SMILES: CCCCCCCCCCCCCCC=C
• WGK Deutschland: 1
• RTECS: MM0479000
• Molekulargewicht: 224.43
• Beilstein: 1753401
• Reaxy-Rn: 1753401
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1753401&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Hydrocarbons
• Klasse: 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
• Beschreibung: 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: alkene

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

Chemische und physikalische Eigenschaften

• Löslichkeit: Insoluble in water; Soluble in Ether,Alcohol
• Brechungsindex: 1.44
• Flammpunkt (°F): 269.6 °F
• Flammpunkt (°C): 132 °C
• Siedepunkt (°C): 285°C
• Schmelzpunkt (°C): 4 °C
• Molekulargewicht: 224.420 g/mol
• XLogP3: 8.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 13
• Exact Mass: 224.25 Da
• Monoisotopic Mass: 224.25 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 126.000
• 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

Referenzen

1. Dan Zhao, Shibo Peng, Hanzhang Xiao, Qilong Li, Yahong Chai, Hongxia Sun, Ruping Liu, Li Yao, Lin Ma.  (2023)  High-Performance T1–T2 Dual-Modal MRI Contrast Agents through Interface Engineering.  ACS Applied Bio Materials,      [PMID:37229527] [10.1021/acsabm.3c00007]

2. Bin Sun, Fengfei Chen, Hualin Lin, Yuan Xue, Sheng Han.  (2022)  Influence of comb type terpolymers of methyl benzyl acrylate-co-hexadecene-maleic anhydride with tetradecyl pendant on cold flow properties of diesel fuel.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2022.130636]

3. Lunqiang Jin, Yusha Gao, Yanping Huang, Minghui Ou, Zhen Liu, Xiang Zhang, Chao He, Baihai Su, Weifeng Zhao, Changsheng Zhao.  (2022)  Mussel-Inspired and In Situ Polymerization-Modified Commercial Sponge for Efficient Crude Oil and Organic Solvent Adsorption.  ACS Applied Materials & Interfaces,      [PMID:34984908] [10.1021/acsami.1c16230]

4. Xueying Li, Jing Zhao, Beijiao Cui, Yiming Li, Doudou Zhang, Haiyan Liu, Ligai Bai, Hongyuan Yan, Yong Wang.  (2017)  Preparation of hemin polymer monolithic column and its application in the separation of proteins and small molecules.  International Journal of Polymeric Materials and Polymeric Biomaterials,      [PMID:] [10.1080/00914037.2017.1354207]

5. Hong-Bin Ju, Li-Zhi Zhang, De-Bao Li, Tao Geng, Ya-Jie Jiang, Ya-Kui Wang.  (2024)  The influence of hydrogen bonding on the structure of organic–inorganic hybrid catalysts and its application in the solvent-free epoxidation of α-olefins.  RSC Advances,  14  (18): (12853-12863).  [PMID:38650685] [10.1039/D4RA01399A]

6. Junyu Chen, Lian Duan, Jinlei Xu, Xinjian Cheng.  (2025)  Chitosan based fluorescent interpenetrating network polymeric probes for the sensitive detection and efficient removal of Hg+ ions.  CARBOHYDRATE POLYMERS,      [PMID:40368552] [10.1016/j.carbpol.2025.123624]

7. Haijiao Bai, Zimeng Wei, Zexiang Bi, Xuejiao Song, Lining Bao, Xu Li, Jinxiang Dong.  (2025)  Isomeric olefin sulfonate surfactants with varied branched hydrocarbon architectures: Effect of the chain branching degree.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2025.122070]

8. Yinzhi Wang, Yunqing Zhou, Zhenzhen Wu, Hualiang Li, Chuanqi Shi, Siyi Bao, Jianhua Yan, Hao Zhang.  (2026)  In-situ mechanistic elucidation of 1-hexadecene pyrolysis as a polyethylene model compound.  JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS,      [PMID:] [10.1016/j.jaap.2026.107606]

9. Qingfu Wang, Jiaming Zhao, Zening Wang, Liuke Zhang, Lei Li, Yibo Ning, Zhipeng Jing, Pengfei Yang, Yongzhen Zhao, Changtong Lu.  (2026)  Study on the enhancement of volatile components extraction from Lysimachia foenum-graecum Hance essential oil by metal salts.  Frontiers in Chemistry,      [PMID:42482699] [10.3389/fchem.2026.1869613]

Häufig gestellte Fragen

What is the purity of this product?

This product is supplied at ≥94% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 629-73-2, the molecular formula is C16H32, and the molecular weight is 224.43 g/mol. InChIKey GQEZCXVZFLOKMC-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.