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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)-

Ethanaminium, N,N,N-trimethyl-2-[(1-oxododecyl)oxy]-, chloride

CCCCCCCCCCCC(=O)OCC[N+](C)(C)C.[Cl-] Request for Quotation
Chemical Name: Ethanaminium, N,N,N-trimethyl-2-[(1-oxododecyl)oxy]-, chloride
CAS Number: 25234-60-0
Product Number: AG003R8E(AGN-PC-0JLZ4T)
Synonyms:
MDL No:
Molecular Formula: C17H36ClNO2
Molecular Weight: 321.9262

Identification/Properties

Properties
MP:
205-207ºC
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
321.93g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
14
Exact Mass:
321.243g/mol
Monoisotopic Mass:
321.243g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
234
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Lauroylcholine Chloride is commonly used in chemical synthesis as a versatile building block for the production of various organic compounds. This compound serves as an important intermediate in the synthesis of surfactants, emulsifiers, and pharmaceuticals, among other products. Due to its unique chemical properties, Lauroylcholine Chloride can be utilized in reactions to introduce the lauroyl group, which consists of a 12-carbon chain, into molecules, thereby altering their physical and chemical properties. Its ability to form stable complexes and participate in esterification, amidation, and other key reactions make it a valuable tool in the hands of synthetic chemists. Furthermore, Lauroylcholine Chloride's compatibility with a wide range of solvents and reaction conditions enhances its utility in various chemical processes.