2,2,3,3,4,4,5,5-Octafluoro-1-pentanol - ≥98%(GC) , CAS No.355-80-6

CAS: 355-80-6 Cat. No.: O159995 Peso molecular: 232.07 Número EC: 206-593-4

GRADE & PURITY ≥98%(GC)

Synonyms

EINECS 206-593-4 | WLN: Q1XFFXFFXFFYFF | 1,1,5-Trihydrooctafluoropentyl alcohol | 1,5-Trihydrooctafluoropentan-1-ol | 2,2,3,3,4,4,5,5-octafluoro-pentan-1-ol | 2,2,3,3,4,4,5,5-Octafluoropentan-1-ol | 1,1,5-Trihydrooctafluoropentan-1-ol | 1h,1h,5h-octafluor

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

2,2,3,3,4,4,5,5-Octafluoro-1-pentanol was used as a cosurfactant in the synthesis of silver and silver iodide nanocrystals. It was also used in the synthesis of Ag2S nanocrystals with a characteristic surface plasmon resonance absorption at 330nm

Specifications

Sinónimos

EINECS 206-593-4 | WLN: Q1XFFXFFXFFYFF | 1, 1, 5-Trihydrooctafluoropentyl alcohol | 1, 5-Trihydrooctafluoropentan-1-ol | 2, 2, 3, 3, 4, 4, 5, 5-octafluoro-pentan-1-ol | 2, 2, 3, 3, 4, 4, 5, 5-Octafluoropentan-1-ol | 1, 1, 5-Trihydrooctafluoropentan-1-ol | 1h, 1h, 5h-octafluor

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 488181007
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181007
• Sonrisas canónicas: C(C(C(C(C(F)F)(F)F)(F)F)(F)F)O
• IUPAC Name: 2,2,3,3,4,4,5,5-octafluoropentan-1-ol
• InChIKey: JUGSKHLZINSXPQ-UHFFFAOYSA-N
• INCHI: 1S/C5H4F8O/c6-2(7)4(10,11)5(12,13)3(8,9)1-14/h2,14H,1H2
• Isómeros SMILES: C(C(C(C(C(F)F)(F)F)(F)F)(F)F)O
• WGK Alemania: 3
• RTECS: SA7650000
• Peso molecular: 232.07
• Reaxy-Rn: 1773494
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1773494&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Clase Halohydrins
      • Subclass Fluorohydrins

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Clase: Halohydrins
• Subclass: Fluorohydrins
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorohydrins
• Alternative Parents: Primary alcohols Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fluorohydrin - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organofluoride - Alkyl halide - Alkyl fluoride - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fluorohydrins. These are alcohols substituted by a fluorine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
• 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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water.
• Sensibilidad: air sensitive；light sensitive
• Índice de refracción: 1.318
• Punto de inflamación (°F): 167°F
• Punto de inflamación (°C): 75°C
• Punto de ebullición (°C): 141-142°C
• Punto de fusión (°C): <-50℃
• Peso molecular: 232.070 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 4
• Exact Mass: 232.013 Da
• Monoisotopic Mass: 232.013 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 200.000
• 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

Referencias

1. Xinyu Yin, Liying Liu, Yuanyang Yan, Kangquan Yang, Pihui Pi, Xiaoe Peng, Xiufang Wen.  (2023)  Superamphiphobic surface with high aperture ratio interconnected pore structures for anti−condensation and repelling hot fluids.  Materials Today Nano,      [PMID:] [10.1016/j.mtnano.2023.100417]

2. Yang Zheng, Changbo Wang, Wei Liu, Xinfang Zhang, Shuangkun Zhang, Zhanpeng Wu.  (2024)  Effects of Fluorinated Side Groups on the Insulation Performances of Polyphosphazenes with Organic Fiber Reinforcement.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.3c02937]

3. Jiannan Cheng, Jiyun Tang, Zongkui Li, Xiaowei An, Qi Li, Liwei Liu, Chunyang Wei.  (2026)  Polyurea-based hydrophobic durable coatings with carbon nanotubes for passive anti-icing and active de-icing.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2026.110122]