Farnesal (Mixture of Isomers） - ≥85% , CAS No.19317-11-4

CAS: 19317-11-4 Cat. No.: F334908 Peso molecular: 220.35 Número EC: 242-957-9

GRADE & PURITY ≥85%

Synonyms

(2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrienal | G4E58106EW | 2,6,10-Dodecatrienal, 3,7,11-trimethyl-, (2E,6E)- | farnesal, pract. | C03461 | EINECS 242-957-9 | Farnesal | E,E-Farnesal | (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrienal | UNII-G4E58106EW | UNII-

Storage

Store at 2-8°C,Protected from light,Argon charged,Desiccated

Shipped In

Wet ice

Descripción general

Farnesal es un aldehído insaturado de cadena larga para la investigación proteómica

Specifications

Sinónimos

(2E, 6E)-3, 7, 11-Trimethyl-2, 6, 10-dodecatrienal | G4E58106EW | 2, 6, 10-Dodecatrienal, 3, 7, 11-trimethyl-, (2E, 6E)- | farnesal, pract. | C03461 | EINECS 242-957-9 | Farnesal | E, E-Farnesal | (E, E)-3, 7, 11-Trimethyl-2, 6, 10-dodecatrienal | UNII-G4E58106EW | UNII-

Especificaciones y pureza

≥85%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged, Desiccated

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥85%

Nombres e identificadores

• Pubchem Sid: 488195213
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488195213
• Sonrisas canónicas: CC(=CCCC(=CCCC(=CC=O)C)C)C
• IUPAC Name: (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal
• InChIKey: YHRUHBBTQZKMEX-YFVJMOTDSA-N
• INCHI: 1S/C15H24O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11-12H,5-6,8,10H2,1-4H3/b14-9+,15-11+
• Isómeros SMILES: CC(=CCC/C(=C/CC/C(=C/C=O)/C)/C)C
• WGK Alemania: 2
• Peso molecular: 220.35
• Reaxy-Rn: 1723427
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723427&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Prenol lipids
      • Subclass Sesquiterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Sesquiterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Sesquiterpenoids
• Alternative Parents: Medium-chain aldehydes Enals Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Farsesane sesquiterpenoid - Sesquiterpenoid - Medium-chain aldehyde - Enal - Alpha,beta-unsaturated aldehyde - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.
• External Descriptors: Acyclic farnesane sesquiterpenoids

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Chloroform (Slightly), Methanol (Slightly)
• Sensibilidad: Light sensitive
• Índice de refracción: n20/D >1.4920(lit.)
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 126-129° C (lit.) at 3.5 mmHg
• Punto de fusión (°C): 16.65° C (Predicted)
• Peso molecular: 220.350 g/mol
• XLogP3: 4.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 220.183 Da
• Monoisotopic Mass: 220.183 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 289.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 2
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 2
• Covalently-Bonded Unit Count: 1

Referencias

1. Kefa Hu, Zhipeng Qi, Xiaode Huang, Lei Wang, Xiaomeng Zhang, Shaoheng Tang.  (2026)  De novo biosynthesis of lavandulol and lavandulyl acetate in Escherichia coli.  JOURNAL OF BIOTECHNOLOGY,      [PMID:41619942] [10.1016/j.jbiotec.2026.01.014]