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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)-

1-Propanaminium, N,N,N-tripropyl-, bromide

CCC[N+](CCC)(CCC)CCC.[Br-] Request for Quotation
Chemical Name: 1-Propanaminium, N,N,N-tripropyl-, bromide
CAS Number: 1941-30-6
Product Number: AG0035ON(AGN-PC-00UNWM)
Synonyms:
MDL No:
Molecular Formula: C12H28BrN
Molecular Weight: 266.2614

Identification/Properties

Properties
MP:
266-272 °C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Hygroscopic
Refractive Index:
1.5260 (estimate)
Solubility:
H2O: 0.1 g/mL, clear
Computed Properties
Molecular Weight:
266.267g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
8
Exact Mass:
265.141g/mol
Monoisotopic Mass:
265.141g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
80.2
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

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tetrapropylammonium bromide is a versatile quaternary ammonium salt commonly utilized in chemical synthesis as a phase transfer catalyst. With its ability to enhance the transfer of anions between immiscible phases, Tetrapropylammonium bromide is instrumental in promoting reactions that would otherwise proceed slowly or inefficiently. Its high solubility in both organic solvents and water makes it an ideal choice for a wide range of synthetic transformations, including nucleophilic substitutions, oxidations, and Wittig reactions. By facilitating the transport of reactants and products across liquid-liquid interfaces, Tetrapropylammonium bromide significantly accelerates reaction rates and enhances overall yields in complex organic syntheses.