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3-CHLORO-N-METHYLBENZYLAMINE

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3-CHLORO-N-METHYLBENZYLAMINE Basic information

Product Name:
3-CHLORO-N-METHYLBENZYLAMINE
Synonyms:
  • 3-CHLORO-N-METHYLBENZYLAMINE
  • M-CHLORO-N-METHYLBENZYLAMINE
  • 3-Chloro-N-methylbenzenemethanamine
  • N-Methyl-3-chlorobenzylamine
  • N-(3-CHLOROBENZYL)-N-METHYLAMINE
  • 1-(3-Chlorophenyl)-N-MethylMethanaMine
  • 3-Chloro-N-methylbenzylamine ,97%
  • 3-CHLORO-N-METHYLBEN
CAS:
39191-07-6
MF:
C8H10ClN
MW:
155.62
EINECS:
254-343-8
Product Categories:
  • Polyamines
  • Amines
  • C8
  • Nitrogen Compounds
Mol File:
39191-07-6.mol
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3-CHLORO-N-METHYLBENZYLAMINE Chemical Properties

Boiling point:
97 °C/0.6 mmHg (lit.)
Density 
1.072 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5395(lit.)
Flash point:
115 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
9.34±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
Sensitive 
Air Sensitive
NIST Chemistry Reference
N-methyl-m-chlorobenzylamine(39191-07-6)
EPA Substance Registry System
Benzenemethanamine, 3-chloro-N-methyl- (39191-07-6)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
10-22-38-41
Safety Statements 
16-26-36/37/39
RIDADR 
UN 1993 3/PG 1
WGK Germany 
2
TSCA 
Yes
HazardClass 
3
PackingGroup 
HS Code 
29214990

MSDS

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3-CHLORO-N-METHYLBENZYLAMINE Usage And Synthesis

Synthesis

104-83-6

74-89-5

39191-07-6

GENERAL STEPS: An ethanol solution of methylamine (33% w/v, 17 mL) was slowly added dropwise to 4-chlorobenzyl chloride (2.0 g, 12.42 mmol), followed by heating the reaction mixture to reflux overnight. Upon completion of the reaction, ethanol was removed by distillation under reduced pressure by rotary evaporator. The residue was diluted with deionized water (100 mL) and washed with ethyl acetate (150 mL × 2). The aqueous phase was adjusted to pH 8 with solid potassium carbonate and then extracted with ethyl acetate (100 mL × 2). All organic phases were combined, washed with deionized water (100 mL), dried over anhydrous sodium sulfate, and finally the target product, N-methyl-3-chlorobenzylamine (1.7 g), was obtained by concentration under reduced pressure. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 2.22 (s, 3H), 3.32 (br s, 1H), 3.62 (s, 2H), 7.25-7.38 (m, 4H); ESI-MS (m/z) 156 (M + H).

References

[1] Patent: WO2017/199103, 2017, A1. Location in patent: Page/Page column 28

3-CHLORO-N-METHYLBENZYLAMINE Preparation Products And Raw materials

Raw materials

3-CHLORO-N-METHYLBENZYLAMINESupplier

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