Basic information Safety Supplier Related

N-Methyl-N-(4-methylbenzyl)amine

Basic information Safety Supplier Related

N-Methyl-N-(4-methylbenzyl)amine Basic information

Product Name:
N-Methyl-N-(4-methylbenzyl)amine
Synonyms:
  • CHEMBRDG-BB 4004536
  • N-METHYL-N-(4-METHYLBENZYL)AMINE
  • 4-Methyl-N-methylbenzylamine
  • (4-Methylbenzyl)methylamine
  • N-Methyl-N-(4-methyl
  • N-Methyl-4-methylbenzylamine
  • N-methyl-1-(4-methylphenyl)methanamine(SALTDATA: HCl)
  • 4-[(Methylamino)methyl]toluene
CAS:
699-04-7
MF:
C9H13N
MW:
135.21
Mol File:
699-04-7.mol
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N-Methyl-N-(4-methylbenzyl)amine Chemical Properties

Melting point:
70°C
Boiling point:
70 ºC (1 MMHG)
Density 
0.917±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
liquid
pka
9.98±0.10(Predicted)
color 
Colorless
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
22-34-36
Safety Statements 
36/37/39-26-23
HS Code 
2921490090
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N-Methyl-N-(4-methylbenzyl)amine Usage And Synthesis

Synthesis

104-82-5

74-89-5

699-04-7

To a stirred solution of 4-methylbenzyl chloride (2.5 g, 17.85 mmol) in ethanol (15 ml) was slowly added 40% aqueous methylamine (5 ml) and stirred continuously for 4 h at room temperature. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove the solvent and subsequently quenched with deionized water (30 ml). The aqueous phase was extracted with dichloromethane (2 x 25 ml) and the organic phases were combined and dried with anhydrous sodium sulfate. The dried organic phase was concentrated under reduced pressure to afford N-methyl-N-(4-methylbenzyl)amine as a yellow oil (2.1 g, 87% yield).

References

[1] Patent: WO2009/109998, 2009, A1. Location in patent: Page/Page column 50
[2] Patent: WO2009/109999, 2009, A1. Location in patent: Page/Page column 70
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 20, p. 8073 - 8088
[4] Justus Liebigs Annalen der Chemie, 1931, vol. 490, p. 189,200
[5] Journal of Medicinal Chemistry, 1983, vol. 26, # 3, p. 309 - 312

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