TRI-N-BUTYLPHOSPHONIUM TETRAFLUOROBORATE

Product Information

Molecular Formula:
C12H28BF4P
Molecular Weight:
290.13
Description
TRI-N-BUTYLPHOSPHONIUM TETRAFLUOROBORATE is a pharmaceutical compound widely used in the biomedicine industry. It has proven efficacy as an ionic liquid and catalyst in various drug synthesis processes. This compound is extensively employed in the drug development of diseases related to the central nervous system, such as neurodegenerative disorders and psychiatric illnesses. Additionally, it plays a crucial role in the development of novel drug delivery systems due to its unique physicochemical properties.
Synonyms
TRI-N-BUTYLPHOSPHONIUM TETRAFLUOROBORATE; TRI-N-BUTYLPHOSPHINE TETRAFLUOROBORATE,&; Tri-n-butylphosphoniumtetrafluoroborate,99%; tributylphosphine tetrafluoroborate
IUPAC Name
tributylphosphaniumtetrafluoroborate
Canonical SMILES
[B-](F)(F)(F)F.CCCC[PH+](CCCC)CCCC
InChI
InChI=1S/C12H27P.BF4/c1-4-7-10-13(11-8-5-2)12-9-6-3;2-1(3,4)5/h4-12H2,1-3H3;/q;-1/p+1
InChI Key
NCHAZLRRIGGCER-UHFFFAOYSA-O
Melting Point
50-53°C(lit.)
Flash Point
Not applicable
Purity
95%
Appearance
White powder

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
9
Exact Mass
290.1957807 g/mol
Monoisotopic Mass
290.1957807 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
91.2
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113214137-A Aryl ketone peptide deformylase inhibitor and application thereof in antibacterial and antitumor aspects 2021-05-19
TW-202138363-A Substituted thiophene carboxamides and derivatives thereof 2019-12-20
CN-110981889-A Hole transport material and preparation method and application thereof 2019-12-11
CN-111019404-A Modified attapulgite for rubber reinforcement and preparation method thereof 2019-11-29
ES-2822398-A1 3 - ((R) -2- (Amino-2-phenylethyl) -1- (2-fluoro-6-trifluoromethylbenzyl) -5-iodo-6-methyl-1H-pyrimidine-2,4-dione or a salt of the same, procedure for its preparation and its use in the synthesis of elagolix 2019-10-30
WO-2021083554-A1 3-((r)-2-(amino-2-phenylethyl)-1-(2-fluoro-6-trifluoromethyl benzyl)-5-iodo-6-methyl-1h-pyrimidine-2,4-dione or a salt thereof, process for its preparation, and its use in the synthesis of elagolix 2019-10-30
JP-2021024815-A Method for producing olefin compound 2019-08-06
JP-2021024816-A A method for purifying a phosphorus-containing olefin compound salt and a method for producing an olefin compound using the purified product obtained thereby. 2019-08-06
JP-6863421-B2 Method for producing olefin compound 2019-08-06
JP-6863422-B2 A method for purifying a phosphorus-containing olefin compound salt and a method for producing an olefin compound using the purified product obtained thereby. 2019-08-06
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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