Basic information Safety Supplier Related

1-Dodecylpyridinium bromide

Basic information Safety Supplier Related

1-Dodecylpyridinium bromide Basic information

Product Name:
1-Dodecylpyridinium bromide
Synonyms:
  • laurosept
  • DODECYLPYRIDINIUM BROMIDE
  • LauryL Pyridinium Bromide
  • Dodecylpyridinum Bromide
  • 1-DodecylpyridinuUM BROMIDE
  • 1-Dodecylpyridin-1-ium bromide
  • Pyridinium, 1-dodecyl-,bromide (1:1)
  • 1-dodecylpyridinium bromide
CAS:
104-73-4
MF:
C17H30BrN
MW:
328.33
EINECS:
203-231-7
Mol File:
104-73-4.mol
More
Less

1-Dodecylpyridinium bromide Chemical Properties

Melting point:
125 °C
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
CAS DataBase Reference
104-73-4(CAS DataBase Reference)
EPA Substance Registry System
Pyridinium, 1-dodecyl-, bromide (104-73-4)
More
Less

1-Dodecylpyridinium bromide Usage And Synthesis

Synthesis

110-86-1

143-15-7

104-73-4

Ionic liquids (ILs) were synthesized from pyridine and dodecyl bromide by direct alkylation reaction in a round-bottomed flask (5.4 cm in diameter and 60 mL in total volume) equipped with a reflux condenser, a magnetic stirrer (250 rpm), and a heating device. The reaction was carried out in an oil bath at 80 °C with continuous stirring of the reaction mixture for 3 h to 17 h. The reaction was carried out under the protection of N2 atmosphere. During the reaction, the formation of a second lower phase containing the ionic liquid was observed. After completion of the reaction, the mixture was cooled to room temperature. For different bromo alkanes the synthesis conditions were as follows: 1. n-Butylpyridinium bromide: Heating for 3 hours. After the reaction, excess reagent was removed under reduced pressure and the resulting solid pyridinium salt was washed with ether and dried to give 17.3 g of the target product [BuPy][Br] in 80% chemical yield. 2. n-Hexylpyridinium bromide: Heated for 3 hours. After cooling, the white precipitate formed was filtered, washed and dried with about 350 mL of diethyl ether to give 21.2 g of [HePy][Br] ionic liquid in 87% chemical yield. 3. n-Octylpyridinium bromide: heated for 3 hours. 21.4 g [OcPy][Br] was obtained as a light brown liquid in 79% chemical yield. 4. n-Dodecylpyridinium bromide: Heated for 17 hours. After cooling, the white precipitate formed was filtered, washed and dried with 100 mL of ether to give 22.0 g of [DoDePy][Br] ionic liquid in 67% chemical yield.

References

[1] Molecules, 2010, vol. 15, # 3, p. 1967 - 1972
[2] Tetrahedron Letters, 2012, vol. 53, # 27, p. 3474 - 3477
[3] Journal of Physical Chemistry, 1986, vol. 90, # 4, p. 641 - 644
[4] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1952, vol. 291, p. 1,4
[5] Journal of the Chemical Society, 1938, p. 682

1-Dodecylpyridinium bromideSupplier

Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Email
isenchem@163.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Email
shyysw007@163.com
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611