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1-Ethylpyridinium bromide

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1-Ethylpyridinium bromide Basic information

Product Name:
1-Ethylpyridinium bromide
Synonyms:
  • ETHYLPYRIDINIUM BROMIDE
  • 1-ethyl-pyridiniubromide
  • N-ETHYLPYRIDINIUM BROMIDE
  • 1-ETHYLPYRIDINIUM BROMIDE
  • Pyridinium, 1-ethyl-, bromide
  • PYRIDINEETHOBROMIDE
  • 1-Ethylpyridin-1-ium bromide
  • 1-Ethylpyridinium bromide,98%
CAS:
1906-79-2
MF:
C7H10BrN
MW:
188.07
EINECS:
217-607-3
Product Categories:
  • Ionic Liquids
  • Pyridinium Compounds
  • Pyridinium Compounds (Ionic Liquids)
  • Synthetic Organic Chemistry
Mol File:
1906-79-2.mol
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1-Ethylpyridinium bromide Chemical Properties

Melting point:
117-121 °C
Density 
1.4194 (rough estimate)
refractive index 
1.6190 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Almost white
Water Solubility 
almost transparency
Sensitive 
Hygroscopic
InChI
InChI=1S/C7H10N.BrH/c1-2-8-6-4-3-5-7-8;/h3-7H,2H2,1H3;1H/q+1;/p-1
InChIKey
ABFDKXBSQCTIKH-UHFFFAOYSA-M
SMILES
[N+]1(CC)C=CC=CC=1.[Br-]
CAS DataBase Reference
1906-79-2(CAS DataBase Reference)
NIST Chemistry Reference
Ethyl pyridinium bromide(1906-79-2)
EPA Substance Registry System
Pyridinium, 1-ethyl-, bromide (1906-79-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26-37
TSCA 
Yes
HS Code 
29333990

MSDS

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1-Ethylpyridinium bromide Usage And Synthesis

Chemical Properties

white agglomerated crystalline powder or crystals

Synthesis

110-86-1

74-96-4

1906-79-2

The one-step synthesis of 1-ethylpyridin-1-ium bromide ([EPy]Br) proceeded as follows: 4.2 mol of ethyl bromide and 4.0 mol of pyridine were added to a 1000 mL round-bottom flask. The reaction mixture was placed in a combined ultrasound-microwave reactor, and the loss of volatile bromoethane was controlled by a cooling water condensation system. The ultrasonic power was set at 1000 W, the microwave heating power was set at 800 W, the reaction temperature was maintained at 50 °C, and the reaction time was 60 min. Upon completion of the reaction, the yield of 1-ethylpyridin-1-ium bromide was calculated to be 89%.

References

[1] Bulletin of the Chemical Society of Japan, 1986, vol. 59, # 3, p. 757 - 762
[2] Journal of the American Chemical Society, 1985, vol. 107, # 16, p. 4655 - 4662
[3] Journal of Physical Chemistry, 1986, vol. 90, # 4, p. 641 - 644
[4] Journal of Physical Chemistry A, 2010, vol. 114, # 11, p. 3782 - 3787
[5] Green Chemistry, 2011, vol. 13, # 6, p. 1527 - 1535

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