Basic information Safety Supplier Related

1-PYRIDIN-3-YL-ETHYLAMINE

Basic information Safety Supplier Related

1-PYRIDIN-3-YL-ETHYLAMINE Basic information

Product Name:
1-PYRIDIN-3-YL-ETHYLAMINE
Synonyms:
  • 3-(1-aminoethyl)pyridine
  • alpha-methyl-3-pyridinemethylamin
  • 1-(3-Pyridyl)ethylamine, 96%
  • 3-Pyridinemethylamine, alpha-methyl-
  • alpha-Methyl-3-pyridinemethylamine
  • Brn 0110124
  • 1-pyridin-3-ylethanamine (racemic-)
  • 1-(3-pyridinyl)ethanamine
CAS:
56129-55-6
MF:
C7H10N2
MW:
122.17
Mol File:
56129-55-6.mol
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1-PYRIDIN-3-YL-ETHYLAMINE Chemical Properties

Melting point:
63 °C
Boiling point:
118-120 °C(Press: 14 Torr)
Density 
1.014 g/cm3(Temp: 25 °C)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
8.81±0.29(Predicted)
form 
liquid
color 
Colourless
Sensitive 
Air Sensitive
CAS DataBase Reference
56129-55-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T,Xi
Risk Statements 
25-41-43-37/38
Safety Statements 
26-36/37/39-45-39
RIDADR 
UN2735
WGK Germany 
3
HazardClass 
8
PackingGroup 
III
HS Code 
2933399990
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1-PYRIDIN-3-YL-ETHYLAMINE Usage And Synthesis

Uses

1-pyridin-3-ylethanamine is mainly used in scientific research experiments.

Synthesis

350-03-8

56129-55-6

General procedure for the synthesis of 1-(3-pyridyl)ethylamine from 3-acetylpyridine: 1. 3-Acetylpyridine (0.5 g, 4.1 mmol), potassium carbonate (1.7 g, 12.3 mmol), hydroxylamine hydrochloride (342 mg, 5 mmol), and methanol (10 mL) were mixed and the reaction was stirred for 16 hours at room temperature. 2. After completion of the reaction, the mixture was filtered and the filtrate was collected. 3. Zinc powder (1.3 g, 21 mmol) and ammonium chloride (1.1 g, 21 mmol) were added to the filtrate and stirring was continued at room temperature for 24 hours. 4. At the end of the reaction, water (10 mL) was added to the reaction mixture and filtered again. 5. The filtrate was concentrated and dried to give the white solid product 1-(3-pyridyl)ethylamine in 300 mg yield and 60% yield. Product characterization data: 1H NMR (300 MHz, DMSO-d6) δ 8.52 (d, J = 4.9 Hz, 1H), 8.32 (td, J = 7.7, 1.9 Hz, 1H), 7.68 (d, J = 7.7 Hz, 1H), 7.28 (ddd, J = 7.5, 4.9, 1.1 Hz, 1H), 4.6 (q, J = 6.0 Hz, 1H) , 1.25 (d, J = 6.6 Hz, 3H); MS (ESI) m/z 123.4 [M + 1]+.

References

[1] Patent: WO2008/51493, 2008, A2. Location in patent: Page/Page column 105
[2] Patent: WO2003/99776, 2003, A1. Location in patent: Page 94-95
[3] Journal of the American Chemical Society, 1944, vol. 66, p. 1293
[4] Patent: WO2006/110668, 2006, A1. Location in patent: Page/Page column 54
[5] Patent: WO2009/42694, 2009, A1. Location in patent: Page/Page column 66

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