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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)-

b-Alanine, N-(2-carboxyethyl)-N-dodecyl-

CCCCCCCCCCCCN(CCC(=O)O)CCC(=O)O Request for Quotation
Chemical Name: b-Alanine, N-(2-carboxyethyl)-N-dodecyl-
CAS Number: 17066-08-9
Product Number: AG003ADW(AGN-PC-0Q9RN3)
Synonyms:
MDL No:
Molecular Formula: C18H35NO4
Molecular Weight: 329.4748

Identification/Properties

Computed Properties
Molecular Weight:
329.481g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
17
Exact Mass:
329.257g/mol
Monoisotopic Mass:
329.257g/mol
Topological Polar Surface Area:
77.8A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
289
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-Carboxyethyl)-N-dodecyl-beta-alanine, also known as $name$, serves as a versatile compound in chemical synthesis due to its unique properties. This compound is frequently utilized as a surfactant in various reactions and processes, functioning as an effective emulsifier and dispersant. Its amphiphilic nature enables it to lower the surface tension between different phases, making it an ideal choice for enhancing the solubility of hydrophobic substances in aqueous environments.In chemical synthesis, $name$ plays a crucial role in facilitating reactions that involve hydrophobic compounds by aiding in their dispersion and stabilization in aqueous solutions. Its ability to form micelles and interact with both hydrophobic and hydrophilic molecules makes it a valuable tool in emulsion polymerization, nanoparticle synthesis, and drug delivery systems.Furthermore, the presence of the carboxylic acid group in N-(2-Carboxyethyl)-N-dodecyl-beta-alanine allows for potential chemical modifications, enabling the introduction of functional groups that can further tailor its properties for specific applications in synthesis. Its compatibility with a wide range of organic compounds and its stability under varying conditions make it a desirable choice for researchers and chemists seeking to optimize their synthetic pathways.$name$ has proven to be an indispensable component in the toolkit of synthetic chemists, offering versatile applications in the synthesis of complex organic molecules, polymers, and nanomaterials. Its role as a surfactant and emulsifier extends its functionality beyond traditional surfactants, opening up new possibilities for innovative chemical processes and product development.