cis-9-Tricosene - ≥95% , CAS No.27519-02-4

CAS: 27519-02-4 Cat. No.: T140633 Peso molecular: 322.61 Beilstein Registry Number: 1841622 Número EC: 248-505-7 PubChem CID: 5365075

GRADE & PURITY ≥95%

Synonyms

BRN 1841622 | DTXSID0032653 | ENT 35349 | 6BSP6HFW73 | UNII-6BSP6HFW73 | (Z)-tricos-9-ene | Muscalure, PESTANAL(R), analytical standard | AM84868 | HY-W009165 | (9Z)-tricos-9-ene | cis-Tricos-9-ene | .alpha.-Methylbutyric acid | A819098 | 9Z-Tricosene | C

Storage

Room temperature

Shipped In

Normal

Descripción general

A molecule with potential for biochemical research.

Specifications

Sinónimos

BRN 1841622 | DTXSID0032653 | ENT 35349 | 6BSP6HFW73 | UNII-6BSP6HFW73 | (Z)-tricos-9-ene | Muscalure, PESTANAL(R), analytical standard | AM84868 | HY-W009165 | (9Z)-tricos-9-ene | cis-Tricos-9-ene | .alpha.-Methylbutyric acid | A819098 | 9Z-Tricosene | C

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504763746
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504763746
• Sonrisas canónicas: CCCCCCCCCCCCCC=CCCCCCCCC
• IUPAC Name: (Z)-tricos-9-ene
• InChIKey: IGOWHGRNPLFNDJ-ZPHPHTNESA-N
• INCHI: 1S/C23H46/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h17,19H,3-16,18,20-23H2,1-2H3/b19-17-
• Isómeros SMILES: CCCCCCCCCCCCC/C=C\CCCCCCCC
• WGK Alemania: 2
• RTECS: YD0807000
• PubChem CID: 5365075
• Peso molecular: 322.61
• Beilstein: 1841622

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

Objetivos asociados (humanos)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Miscible with water and hexane. Immiscible with alcohol.
• Punto de inflamación (°F): >235.4 °F
• Punto de inflamación (°C): >113 °C
• Punto de ebullición (°C): 300°C
• Peso molecular: 322.600 g/mol
• XLogP3: 11.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 19
• Exact Mass: 322.36 Da
• Monoisotopic Mass: 322.36 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 216.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Referencias

1. Shuai Xiao, Hai-ou Li, Meng-wei Xu, Ke Huang, Zhou-fei Luo, Lang-tao Xiao.  (2021)  A high-throughput method for profiling fatty acids in plant seeds based on one-step acid-catalyzed methylation followed by gas chromatography-mass spectrometry.  BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT,      [PMID:] [10.1080/13102818.2021.1954552]

2. Bo Luo, Wenbo Zhang, Shuangqing Hu, Kunyuan Liu, Leilei Cheng, Jing Gu, Haoran Yuan, Yong Chen.  (2025)  Product regulation mechanism in Joule flash pyrolysis of polyethylene for low carbon olefins and carbon nanospheres.  JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS,      [PMID:] [10.1016/j.jaap.2025.106963]