Nonadecano - ≥99% , CAS No.629-92-5

CAS: 629-92-5 Cat. No.: N100269 Formula: C₁₉H₄₀ Peso molecolare: 268.52 Beilstein Registry Number: 1742892 Numero EC: 211-116-8

GRADE & PURITY ≥99%

Synonyms

NONADECANE|n-Nonadecane|629-92-5|Nonadekan|UNII-NMY21D3Y5T|NMY21D3Y5T|ISTD|NONADECANE, N-|EINECS 211-116-8|NSC 77136|NSC-77136|AI3-36122|DTXSID9047170|Nonadecane-d40 98 atom % D|CHEBI:32927|HSDB 8349|CH3-[CH2]17-CH3|MFCD00009012|n-Nonadecane 10000 microg/

Storage

Conservare a 2-8°C, al riparo dalla luce, disidratato

Shipped In

Ghiaccio umido

Panoramica

Insolubile in acqua, leggermente solubile in etanolo e facilmente solubile in etere.

Il nonadecano è generalmente utilizzato come soggetto nella spettroscopia del tempo di vita dell'annichilazione di positroni (PALS).

Specifications

Sinonimi

NONADECANE | n-Nonadecane | 629-92-5 | Nonadekan | UNII-NMY21D3Y5T | NMY21D3Y5T | ISTD | NONADECANE, N- | EINECS 211-116-8 | NSC 77136 | NSC-77136 | AI3-36122 | DTXSID9047170 | Nonadecane-d40 98 atom % D | CHEBI:32927 | HSDB 8349 | CH3-[CH2]17-CH3 | MFCD00009012 | n-Nonadecane 10000 microg/

Specifiche e purezza

≥99%

Condizioni di conservazione di stoccaggio

Conservare a 2-8°C, al riparo dalla luce, disidratato

Spedito in

Ghiaccio umido

Purezza

≥99%

Nomi e identificatori

• Pubchem Sid: 508812540
• Sorrisi canonici: CCCCCCCCCCCCCCCCCCC
• IUPAC Name: nonadecane
• InChIKey: LQERIDTXQFOHKA-UHFFFAOYSA-N
• INCHI: 1S/C19H40/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h3-19H2,1-2H3
• Isomeri SMILES: CCCCCCCCCCCCCCCCCCC
• WGK Germania: 3
• Numero UN: 1325
• Gruppo di imballaggio: II
• Peso molecolare: 268.52
• Beilstein: 1742892
• Reaxy-Rn: 1742892
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1742892&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbons
    • Classe Saturated hydrocarbons
      • Subclass Alkanes

• Kingdom: Organic compounds
• Superclass: Hydrocarbons
• Classe: Saturated hydrocarbons
• Subclass: Alkanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkanes
• Alternative Parents: Not available
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acyclic alkane - Alkane - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alkanes. These are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.
• External Descriptors: an alkane

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

Proprietà chimiche e fisiche

• Solubilità: Soluble in Chloroform, Hexane.
• Punto di infiammabilità (°F): 212 °F
• Punto di infiammabilità (°C): 168.3℃
• Punto di ebollizione (°C): 330.6°C
• Punto di fusione (°C): 31.9°C
• Peso molecolare: 268.500 g/mol
• XLogP3: 9.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 16
• Exact Mass: 268.313 Da
• Monoisotopic Mass: 268.313 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 123.000
• 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

Riferimenti

1. Liangguang Chen, Huiwen Li, Junying Fu, Changlin Miao, Pengmei Lv, Zhenhong Yuan.  (2015)  Catalytic hydroprocessing of fatty acid methyl esters to renewable alkane fuels over Ni/HZSM-5 catalyst.  CATALYSIS TODAY,      [PMID:] [10.1016/j.cattod.2015.08.023]

2. Qing-Jie Cao, Jia Yu, Ya-Li Ran, De-Fu Chi.  (2015)  Effects of plant volatiles on electrophysiological and behavioral responses of Cryptorrhynchus lapathi.  ENTOMOLOGIA EXPERIMENTALIS ET APPLICATA,  156  (2): (105-116).  [PMID:] [10.1111/eea.12322]

3. Miaojia Song, Xinghua Zhang, Qi Zhang, Lungang Chen, Yubao Chen, Jianguo Liu, Longlong Ma.  (2024)  Hydrodeoxygenation of Fatty Acid Esters over Nitrogen-Functionalized Bimetallic Oxides Catalyst.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c01443]

4. Xinzhe Zhang, Aipeng Li, Xiaohan Huang, Shuqi Guo, Chenyue Zhang, Ramon Gonzalez, Qiang Fei.  (2025)  Metabolic Engineering of Methanotrophic Bacteria for De Novo Production of Taxadiene from Methane.  ACS Synthetic Biology,      [PMID:40658032] [10.1021/acssynbio.5c00109]

5. Xue Xiong, Meiling Qi.  (2020)  A novel column fabrication approach for capillary gas chromatography via a cross-linked organogel network with high stability and inertness.  NEW JOURNAL OF CHEMISTRY,  44  (25): (10621-10627).  [PMID:] [10.1039/D0NJ02185G]

6. Nian Cao, Yubo Yang, Xiaoling Xiong, Bohan Zhang, Ping Xiang, Fan Yang.  (2026)  Dynamic sensory mapping: how sip volume shapes sensory perception and drinking comfort of Jiangxiangxing Baijiu.  INTERNATIONAL JOURNAL OF FOOD PROPERTIES,      [PMID:] [10.1080/10942912.2026.2618833]

7. Yuwei Chen, Mingxin Zhong, Yujie Xu, Sijie Hua, Lingxin Bao, Yongsheng Fan, Jianchun Jiang, Feng Long, Xincheng Cao, Junming Xu.  (2026)  Green diesel production via biodiesel upgrading over Ru/nitrogen-doped carbon catalysts derived from yeast cell wall waste.  RENEWABLE ENERGY,      [PMID:] [10.1016/j.renene.2026.126393]