2,2,3,3-Tetrafluoro-1-propanol - ≥98% , CAS No.76-37-9

CAS: 76-37-9 Cat. No.: T101367 Peso molecular: 132.06 Beilstein Registry Number: 1738264 Número EC: 200-955-5 PubChem CID: 6441

GRADE & PURITY ≥98%

Synonyms

2,2,3,3-Tetrafluoropropyl alcohol | UNII-RNO513716P | AI3-23784 | Q23978438 | C3-Fluoroalcohol | W-104366 | 1-Propanol,2,3,3-tetrafluoro- | 2,2,3,3-Tetrafluoro-propanol-1 | 2,2,3,3-tetrafluoropropanol-1 | 1,1,2,2-TETRAFLUORO-3-HYDROXYPROPANE | 2,3,3-Tetra

Storage

Room temperature,Desiccated,Cool

Shipped In

Normal

Descripción general

2,2,3,3-Tetrafluoro-1-propanol (TFP) is extensively used as the solvent.

Mineralization and defluoridation of TFP by UV oxidation in a novel three-phase fluidized bed reactor was reported.

Desorption of activated carbon loaded with TFP by supercritical carbon dioxide in a rotating packed bed was investigated.

Specifications

Sinónimos

2, 2, 3, 3-Tetrafluoropropyl alcohol | UNII-RNO513716P | AI3-23784 | Q23978438 | C3-Fluoroalcohol | W-104366 | 1-Propanol, 2, 3, 3-tetrafluoro- | 2, 2, 3, 3-Tetrafluoro-propanol-1 | 2, 2, 3, 3-tetrafluoropropanol-1 | 1, 1, 2, 2-TETRAFLUORO-3-HYDROXYPROPANE | 2, 3, 3-Tetra

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Desiccated, Cool

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488180066
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180066
• Sonrisas canónicas: C(C(C(F)F)(F)F)O
• IUPAC Name: 2,2,3,3-tetrafluoropropan-1-ol
• InChIKey: NBUKAOOFKZFCGD-UHFFFAOYSA-N
• INCHI: 1S/C3H4F4O/c4-2(5)3(6,7)1-8/h2,8H,1H2
• Isómeros SMILES: C(C(C(F)F)(F)F)O
• WGK Alemania: 1
• RTECS: UB9400000
• PubChem CID: 6441
• Número ONU: 1993
• Grupo de embalaje: III
• Peso molecular: 132.06
• Beilstein: 1738264
• Reaxy-Rn: 1738264

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

Propiedades químicas y físicas

• Solubilidad: Soluble in water.
• Índice de refracción: 1.32-1.322
• Punto de inflamación (°F): 114.8 °F
• Punto de inflamación (°C): 43°C
• Punto de ebullición (°C): 107-109°C
• Peso molecular: 132.060 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 132.02 Da
• Monoisotopic Mass: 132.02 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 71.700
• 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. Zhichang Liu, Pengcheng Hu, Xianghai Meng, Rui Zhang, Huiqing Yue, Chunming Xu, Yufeng Hu.  (2014)  Synthesis and properties of switchable polarity ionic liquids based on organic superbases and fluoroalcohols.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2013.12.040]