Tetrabutylphosphonium Hexafluorophosphate - ≥98% , CAS No.111928-21-3

CAS: 111928-21-3 Cat. No.: T162756 Peso molecular: 404.4 Número EC: 621-312-9 PubChem CID: 16218641

GRADE & PURITY ≥98%

Synonyms

J-002661 | DTXSID60584997 | Tetrabutylphosphanium hexafluorophosphate | tetrabutylphosphanium;hexafluorophosphate | Tetrabutylphosphonium hexafluorophosphate(V) | Tetrabutylphosphonium hexafluorophosphate, for electrochemical analysis, >=99.0% | A902524 |

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Novel organic electrolyte with high conductivity in high energy density electric double-layer capacitors (EDLC).

Specifications

Sinónimos

J-002661 | DTXSID60584997 | Tetrabutylphosphanium hexafluorophosphate | tetrabutylphosphanium;hexafluorophosphate | Tetrabutylphosphonium hexafluorophosphate(V) | Tetrabutylphosphonium hexafluorophosphate, for electrochemical analysis, >=99.0% | A902524 |

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488199319
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488199319
• Sonrisas canónicas: CCCC[P+](CCCC)(CCCC)CCCC.F[P-](F)(F)(F)(F)F
• IUPAC Name: tetrabutylphosphanium;hexafluorophosphate
• InChIKey: QLQAFNAPINCKBM-UHFFFAOYSA-N
• INCHI: 1S/C16H36P.F6P/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-7(2,3,4,5)6/h5-16H2,1-4H3;/q+1;-1
• Isómeros SMILES: CCCC[P+](CCCC)(CCCC)CCCC.F[P-](F)(F)(F)(F)F
• WGK Alemania: 3
• PubChem CID: 16218641
• Peso molecular: 404.4
• Reaxy-Rn: 5895425

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organophosphorus compounds
    • Clase Tetraalkylphosphonium compounds

• Kingdom: Organic compounds
• Superclass: Organophosphorus compounds
• Clase: Tetraalkylphosphonium compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylphosphonium compounds
• Alternative Parents: Organopnictogen compounds Organic salts Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylphosphonium compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetraalkylphosphonium compounds. These are organophosphorus compounds that contain a tetravalent phosphorus atom substituted to four alkyl chains.
• 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: Insoluble in water, soluble in methanol, chloroform, acetone
• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 226-228°C
• Peso molecular: 404.390 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 12
• Exact Mass: 404.22 Da
• Monoisotopic Mass: 404.22 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 179.000
• 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: 2

XLogP3

Referencias

1. Mengyang Xia, Ben Chong, Xiangjiao Gong, Hang Xiao, He Li, Honghui Ou, Bin Zhang, Guidong Yang.  (2023)  Ti2+ Site-Promoted N≡N Bond Activation in LaTiO3–x Nanosheets for Nitrogen Photofixation.  ACS Catalysis,      [PMID:] [10.1021/acscatal.3c02198]

2. Minyuan Han, Gaohui Liu, Chuanjie Fang, Liping Zhu.  (2024)  Robust superhydrophobic Poly(vinylidene fluoride) membranes with spherulitic surface morphology against wetting and scaling in membrane distillation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2024.123027]