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3-Pyridineethaneamine

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3-Pyridineethaneamine Basic information

Product Name:
3-Pyridineethaneamine
Synonyms:
  • 3-AMINOETHYLPYRIDINE
  • 2-(3-PYRIDYL)ETHYLAMINE
  • 2-(PYRIDIN-3-YL)ETHANAMINE
  • 2-PYRIDIN-3-YL-ETHYLAMINE
  • 3-(2-AMINOETHYL)PYRIDINE
  • RARECHEM AL BW 0249
  • Aminoethylpyridine
  • 3-pyridineethaneamine
CAS:
20173-24-4
MF:
C7H10N2
MW:
122.17
EINECS:
671-720-6
Product Categories:
  • pharmacetical
  • Pyridines derivates
Mol File:
20173-24-4.mol
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3-Pyridineethaneamine Chemical Properties

Boiling point:
119-120°C 19mm
Density 
1.04
refractive index 
1.5518
Flash point:
119-120°C/19mm
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
clear liquid
pka
9.29±0.10(Predicted)
color 
Colorless to Almost colorless
Specific Gravity
1.04
Water Solubility 
Slightly soluble in water.
Sensitive 
Air Sensitive
BRN 
111288
CAS DataBase Reference
20173-24-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
34-41-37/38
Safety Statements 
26-36/37/39-39
RIDADR 
2735
WGK Germany 
3
HazardClass 
8
PackingGroup 
III
HS Code 
29333990

MSDS

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3-Pyridineethaneamine Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

3-(2-Aminoethyl)pyridine has been used in the synthesis of urea.

Synthesis

6443-85-2

20173-24-4

The general procedure for the synthesis of 3-(2-aminoethyl)pyridine from 3-pyridylacetonitrile was as follows: 2-(pyridin-3-yl)acetonitrile (1 g, 8.47 mmol, 1.00 eq.), nickel ryenne (1 g, 17.24 mmol, 1.00 eq.) and ammonium hydroxide (3 mL) were dissolved in methanol (15 mL). The mixture was stirred and reacted overnight at room temperature and 1 atm hydrogen atmosphere. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and washed several times with methanol. The filtrate and washings were combined and concentrated in vacuum to give 940 mg (45% yield) of 2-(pyridin-3-yl)ethylamine as a yellow oil.LC-MS analysis: (ES, m/z): 164 [M + CH3CN + H]+, 123 [M + H]+, 106.

References

[1] Patent: WO2013/155338, 2013, A2. Location in patent: Page/Page column 180
[2] Patent: US2015/329503, 2015, A1. Location in patent: Paragraph 0720; 0721
[3] Patent: US6017919, 2000, A
[4] Journal of the American Chemical Society, 1980, vol. 102, # 17, p. 5530 - 5538
[5] Journal of the American Chemical Society, 1955, vol. 77, p. 6554,6556

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