1H,1H,2H,2H-Perfluorohexan-1-ol - ≥98% , CAS No.2043-47-2

CAS: 2043-47-2 Cat. No.: P122276 Fórmula: CF₃(CF₂)₃(CH₂)₂OH Peso molecular: 264.09 Número EC: 218-050-9

GRADE & PURITY ≥98%

Synonyms

C6H5F9O | MFCD00039543 | 2-Naphthalenol, 1-(1-piperidinylmethyl)- | 2-Octyl dodecanol | 2-perfluorobutyl ethanol (4:2) | 1h,1h,2h,2h-nonafluorohexan-1-ol | N0600 | 4:2 FTOH | 1H, 1H, 2H, 2H-perfluorohexan-1-ol, 98% | AS-48920 | n:2 fluorotelomer alcohols,

Storage

Room temperature,Argon charged

Shipped In

Normal

Descripción general

application：

1H,1H,2H,2H-Perfluorohexanol is used in the synthesis of polymer coatings with controlled surface topography. As well used in the preparation of star polymers as fluorous nanocapsules for the encapsulation and release of perfluorinated compounds.

Specifications

Sinónimos

C6H5F9O | MFCD00039543 | 2-Naphthalenol, 1-(1-piperidinylmethyl)- | 2-Octyl dodecanol | 2-perfluorobutyl ethanol (4:2) | 1h,1h,2h,2h-nonafluorohexan-1-ol | N0600 | 4:2 FTOH | 1H, 1H, 2H, 2H-perfluorohexan-1-ol, 98% | AS-48920 | n:2 fluorotelomer alcohols,

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

504754880

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504754880

Sonrisas canónicas

C(CO)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F

IUPAC Name

3,3,4,4,5,5,6,6,6-nonafluorohexan-1-ol

InChIKey

JCMNMOBHVPONLD-UHFFFAOYSA-N

INCHI

1S/C6H5F9O/c7-3(8,1-2-16)4(9,10)5(11,12)6(13,14)15/h16H,1-2H2

Isómeros SMILES

C(CO)C(C(C(C(F)(F)F)(F)F)(F)F)(F)F

WGK Alemania

3

Peso molecular

264.09

Reaxy-Rn

2095198

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2095198&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Clase Alkyl halides
      • Subclass Alkyl fluorides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Clase: Alkyl halides
• Subclass: Alkyl fluorides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorotelomer alcohols
• Alternative Parents: Primary alcohols Organofluorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fluorotelomer alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organofluoride - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fluorotelomer alcohols. These are fluorocarbon-based oligomers linked to an alcohol chain.
• External Descriptors: Not available

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

• Sensibilidad: Heat sensitive；Air sensitive
• Índice de refracción: 1.314
• Punto de inflamación (°F): 163.4 °F
• Punto de inflamación (°C): 73°C(Lit.)
• Punto de ebullición (°C): 76°C/50mmHg
• Peso molecular: 264.090 g/mol
• XLogP3: 3.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 4
• Exact Mass: 264.02 Da
• Monoisotopic Mass: 264.02 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 243.000
• 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