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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phosphonium, tributyloctyl-, bromide

CCCCCCCC[P+](CCCC)(CCCC)CCCC.[Br-] Request for Quotation
Chemical Name: Phosphonium, tributyloctyl-, bromide
CAS Number: 57702-65-5
Product Number: AG003T9N(AGN-PC-03UJP5)
Synonyms:
MDL No:
Molecular Formula: C20H44BrP
Molecular Weight: 395.4411

Identification/Properties

Properties
MP:
25℃
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
395.45g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
16
Exact Mass:
394.236g/mol
Monoisotopic Mass:
394.236g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
178
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

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tributyl(octyl)phosphonium bromide, a versatile quaternary ammonium salt, plays a pivotal role in chemical synthesis as a powerful phase transfer catalyst. 
It facilitates the transfer of reagents between two immiscible phases, typically between aqueous and organic solvents, enhancing reaction efficiency and yield. 
This property makes Tributyl(octyl)phosphonium bromide ideal for various organic transformations such as nucleophilic substitutions, Wittig reactions, and alkylations. 
Additionally, its high solubility and stability make it a preferred choice for promoting the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals in both industrial and academic settings.