Tetrafluoroborato de tetrapropilamonio - ≥98% , CAS No.338-38-5

CAS: 338-38-5 Cat. No.: T169686 Peso molecular: 273.16 Beilstein Registry Number: 3637590 Número EC: 206-416-0 PubChem CID: 9558

GRADE & PURITY ≥98%

Synonyms

FT-0631981 | tetrapropilazonio;tetrafluoroborato | 1-Propanaminio,N,N-tripropil-, tetrafluoroborato(1-) | MFCD00031619 | WLN: 3K3&3&3 &.B-F4 | Tetrafluoroborato de tetrapropilamonio, >=98,0% | 1-Propanaminio, N,N,N-tripropil-, tetrafluoroborato(1-) | Am

Storage

Temperatura ambiente

Shipped In

Normal

Descripción general

Aplicación del producto：

El tetrafluoroborato de tetrapropilamonio (Pr4NBF4 o TPABF4) puede utilizarse como:Un electrolito en la determinación de compuestos fenólicos de extractos de semillas de uva por método electroforético capilar. Un electrolito de soporte en la hidrogenación electroquímica de dimetilformamida (DMF) a trimetilamina (TMA)

Specifications

Sinónimos

FT-0631981 | tetrapropilazonio;tetrafluoroborato | 1-Propanaminio, N, N-tripropil-, tetrafluoroborato(1-) | MFCD00031619 | WLN: 3K3&3&3 &.B-F4 | Tetrafluoroborato de tetrapropilamonio, >=98, 0% | 1-Propanaminio, N, N, N-tripropil-, tetrafluoroborato(1-) | Am

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Temperatura ambiente

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504751843
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751843
• Sonrisas canónicas: [B-](F)(F)(F)F.CCC[N+](CCC)(CCC)CCC
• IUPAC Name: tetrapropylazanium;tetrafluoroborate
• InChIKey: ADADJCUTHQJPCB-UHFFFAOYSA-N
• INCHI: 1S/C12H28N.BF4/c1-5-9-13(10-6-2,11-7-3)12-8-4;2-1(3,4)5/h5-12H2,1-4H3;/q+1;-1
• Isómeros SMILES: [B-](F)(F)(F)F.CCC[N+](CCC)(CCC)CCC
• WGK Alemania: 3
• RTECS: BS8420000
• PubChem CID: 9558
• Peso molecular: 273.16
• Beilstein: 3637590

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylammonium salts
• Alternative Parents: Organic metalloid salts Organopnictogen compounds Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organic metalloid salt - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with 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

• Punto de fusión (°C): 245-247 °C
• Peso molecular: 273.160 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 8
• Exact Mass: 273.225 Da
• Monoisotopic Mass: 273.225 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 99.300
• 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

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