N-Benzyl-N-methylethanolamine Chemical Properties

Boiling point:

95-105 °C2 mm Hg(lit.)

Density 

1.017 g/mL at 25 °C(lit.)

refractive index 

n20/D 1.529(lit.)

Flash point:

>230 °F

storage temp. 

Sealed in dry,Room Temperature

solubility 

Chloroform (Slightly), Methanol (Slightly)

pka

14.75±0.10(Predicted)

form 

Oil

color 

Colourless

BRN 

366412

CAS DataBase Reference

101-98-4(CAS DataBase Reference)

NIST Chemistry Reference

Ethanol, 2-[methyl(phenylmethyl)amino]-(101-98-4)

EPA Substance Registry System

Ethanol, 2-[methyl(phenylmethyl)amino]- (101-98-4)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26-37/39-24/25

WGK Germany 

3

HS Code 

29214990

MSDS

• Language:English Provider:N-Benzyl-N-methylethanolamine
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

N-Benzyl-N-methylethanolamine Usage And Synthesis

Description

N-Benzyl-N-methylethanolamine is a surfactant that has a high capacity for adsorbing proteins. It is used as an efficient method to remove impurities from human immunoglobulin preparations and as an adsorbent in chromatographic methods. N-Benzyl-N-methylethanolamine has also been used as a diagnostic agent for the detection of chromatographically separated monoclonal antibodies, which are produced by activated B cells in culture. The antibody binds to the target protein and then the antibody-protein complex is isolated using a particle agglomeration technique. This method can be repeated multiple times and produce high concentrations of pure monoclonal antibodies.

Chemical Properties

clear yellowish liquid

Uses

2-[Methyl(phenylmethyl)amino]ethanol is used in the preparation of dihydropyrimidinones as sodium iodide symporter inhibitors used to regulate the accumulation of iodide in the thyroid gland. Also used in the synthesis of new class of pseudopeptides as potential inhibitors of β-sheet aggregation.

General Description

N-Benzyl-N-methylethanolamine is a tertiary benzylamine. Electrochemical alkoxylation of N-benzyl-N-methylethanolamine is reported. Rate of proton exchange of N-benzyl-N-methylethanolamine in aqueous HCl has been reported.

N-Benzyl-N-methylethanolamine(101-98-4)Related Product Information

• N-Phenylmaleimide
• 4-(DICHLOROMETHYL)PYRIDINE HCL
• N-Benzylmaleimide
• N-Hydroxyethylphthalimide
• Thymolphthalein Complexone
• ALPHA-(4-MORPHOLINO)PHENYLACETONITRILE
• N-(2,3-EPOXYPROPYL)PHTHALIMIDE
• 2,5-DIMETHYL-4-(MORPHOLINOMETHYL)PHENOL HYDROCHLORIDE
• 1-(MORPHOLINOMETHYL)-2-NAPHTHOL
• XYLENOL ORANGE
• N-BENZYLIMINODIACETIC ACID
• N-Benzyl-N-methylethanolamine
• METHYL BENZETHONIUM CHLORIDE
• o-Cresolphthalein Complexone
• Xylenol Orange sodium salt
• PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL
• 2,2'-(BENZYLIMINO)DIETHANOL
• Benzethonium chloride