(2-Aminoethyl)trimethylazanium chloride

Base Information

• Chemical Name: (2-Aminoethyl)trimethylazanium chloride
• CAS No.: 10256-43-6
• Molecular Formula: C5H15 N2 . Cl
• Molecular Weight: 138.641
• European Community (EC) Number: 222-266-9
• DSSTox Substance ID: DTXSID30955574
• Wikipedia: Cholamine_chloride_hydrochloride
• Mol file: 10256-43-6.mol

Synonyms:10256-43-6;(2-aminoethyl)trimethylazanium chloride;(2-Aminoethyl)trimethyl chloride hydrochloride;Ethanaminium, 2-amino-N,N,N-trimethyl-, chloride (1:1);cholamine chloride hydrochloride;EINECS 222-266-9;(2-Aminoethyl)trimethyl chloride HCl;Ethanaminium, 2-amino-N,N,N-trimethyl-, chloride;SCHEMBL234179;DTXSID30955574;2-aminoethyltrimethylammonium chloride

Chemical Property of (2-Aminoethyl)trimethylazanium chloride

Chemical Property:

• PSA: 26.02000
• LogP: -2.64440
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 138.0923762
• Heavy Atom Count: 8
• Complexity: 44.5

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[N+](C)(C)CCN.[Cl-]

Technology Process of (2-Aminoethyl)trimethylazanium chloride

There total 1 articles about (2-Aminoethyl)trimethylazanium chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C16H27N2O4P + C16H36N(1+)*C18H21NO4P(1-) + 2-phenylacetylhydrazine (937-39-3) → C16H36N(1+)*C19H22N2O5P(1-) + 2-AMINOETHYL TRIMETHYLAMMONIUM CHLORIDE (10256-43-6) + benzylamine (100-46-9)

Guidance literature:

In d⁽⁴⁾-methanol; [D₃]acetonitrile; at 26.84 ℃; for 120h; Equilibrium constant; Thermodynamic data;

DOI:10.1039/c1cc15295e

Reference yield: 87.5%

1,3,5-trichloro-2,4,6-triazine (108-77-0) + 1-amino-4-(benzoylamino)-5-nitroanthraquinone + 2-AMINOETHYL TRIMETHYLAMMONIUM CHLORIDE (10256-43-6) + 1-amino-3-(dimethylamino)propane (109-55-7) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → C36H42N10O6(2+)*2Cl(1-)

Guidance literature:

1,3,5-trichloro-2,4,6-triazine; 1-amino-4-(benzoylamino)-5-nitroanthraquinone; With sodium carbonate; In water; acetonitrile; at 0 - 5 ℃; for 3h; pH=5-6; Cooling with ice;

2-AMINOETHYL TRIMETHYLAMMONIUM CHLORIDE; With sodium carbonate; In water; acetonitrile; at 35 - 40 ℃; for 4h; pH=5-6;

1-amino-3-(dimethylamino)propane; epichlorohydrin; Further stages;

Reference yield: 86.3%

1,3,5-trichloro-2,4,6-triazine (108-77-0) + 1-amino-4-benzamidoanthraquinone (81-46-9) + 2-AMINOETHYL TRIMETHYLAMMONIUM CHLORIDE (10256-43-6) + 1-amino-3-(dimethylamino)propane (109-55-7) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → C37H45N9O4(2+)*2Cl(1-)

Guidance literature:

1,3,5-trichloro-2,4,6-triazine; 1-amino-4-benzamidoanthraquinone; With sodium carbonate; In water; acetonitrile; at 0 - 5 ℃; for 3h; pH=5-6; Cooling with ice;

2-AMINOETHYL TRIMETHYLAMMONIUM CHLORIDE; With sodium carbonate; In water; acetonitrile; at 35 - 40 ℃; for 4h; pH=5-6;

1-amino-3-(dimethylamino)propane; epichlorohydrin; Further stages;

upstream raw materials:

2-phenylacetylhydrazine

Downstream raw materials:

4-{3-[2-(trimethylamino)ethylaminocarbonyl]propoxy}phenyl-4',4''-dimethoxytritanol chloride

2-(biotinamidyl)ethyltrimethylammonium chloride

C₁₂⁽¹³⁾CH₂₁N₂O⁽¹⁺⁾*Cl^(1-)

2-phenylacetylhydrazine