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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-Hexanaminium, N,N,N-trihexyl-, iodide

CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC.[I-] Request for Quotation
Chemical Name: 1-Hexanaminium, N,N,N-trihexyl-, iodide
CAS Number: 2138-24-1
Product Number: AG003UQS(AGN-PC-0JLP3T)
Synonyms:
MDL No:
Molecular Formula: C24H52IN
Molecular Weight: 481.5808

Identification/Properties

Properties
MP:
99-101℃
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
481.591g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
20
Exact Mass:
481.314g/mol
Monoisotopic Mass:
481.314g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
195
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


Tetrahexylammonium iodide is a versatile chemical compound commonly used in organic synthesis as a phase-transfer catalyst. This compound plays a crucial role in facilitating various chemical reactions by promoting the transfer of ions between immiscible phases, such as aqueous and organic solvents. Due to its unique properties, Tetrahexylammonium iodide is particularly valuable in reactions that involve the conversion of insoluble or poorly soluble substrates.In chemical synthesis, Tetrahexylammonium iodide can enhance the efficiency and selectivity of reactions by aiding in the transport of reagents and products across different phases. This catalyst is especially useful in organic transformations that require efficient mixing of reactants that would otherwise remain unreacted or form undesired byproducts. By acting as a mediator between phases, Tetrahexylammonium iodide enables better control over reaction conditions and allows chemists to achieve higher yields and purities in their final products.Overall, Tetrahexylammonium iodide serves as a valuable tool in the realm of chemical synthesis, providing a means to overcome challenging reaction limitations and advance the development of novel compounds with tailored properties. Its versatile applications make it a fundamental component in the toolbox of organic chemists seeking to explore new synthetic routes and optimize existing methodologies.