Production Method 1

873-71-2

Reaction Conditions

1.1 100 °C

Reference

Isolating the role of hydrogen bonding in hydroxyl-functionalized ionic liquids by means of vaporization enthalpies, infrared spectroscopy and molecular dynamics simulations

Zaitsau, Dzmitry H.; Neumann, Jan; Niemann, Thomas; Strate, Anne; Paschek, Dietmar; et al, Physical Chemistry Chemical Physics, 2019, 21(36), 20308-20314

Production Method 2

873-71-2

Reaction Conditions

1.1 18 h, 70 °C

Reference

Effects of Synthesis Variables on SAPO-34 Crystallization Templated Using Pyridinium Supramolecule and Its Catalytic Activity in Microwave Esterification Synthesis of Propyl Levulinate

Ma, Yik-Ken; Alomar, Taghrid S. ; AlMasoud, Najla; El-Bahy, Zeinhom M.; Chia, Stephen; et al, Catalysts, 2023, 13(4),

Production Method 3

873-71-2

Reaction Conditions

1.1 20 h, 70 °C

Reference

Ionothermal Crystallization of SAPO-11 Using Novel Pyridinium Ionic Liquid and Its Catalytic Activity in Esterification of Levulinic Acid into Ethyl Levulinate

Mohammad, Al Issa Jehad Moh'dFathi; Saminathan, Vinithaa; El-Bahy, Zeinhom M.; Michelin, Laure; Ling, Tau Chuan; et al, Catalysts, 2023, 13(2),

Propylpyridiniumbromide Preparation Products

• Propylpyridiniumbromide (873-71-2)

• 1. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 2. Fe(iii)-mediated isomerization of α,α-diarylallylic alcohols to ketones via radical 1,2-aryl migration?
  Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
• 3. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 4. Enabling stable MnO2 matrix for aqueous zinc-ion battery cathodes?
  Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
• 5. Enabling high-throughput single-animal gene-expression studies with molecular and micro-scale technologies
  Jason Wan Lab Chip, 2020,20, 4528-4538

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinium derivatives

• 140-72-7(Hexadecyl pyridinium bromide)
• 874-80-6(1-Butylpyridinium Bromide)
• 104-73-4(1-Dodecylpyridinium bromide)
• 143715-91-7(n-Hexadecylpyridinium-d5 Bromide)
• 14208-08-3(1-4-(pyridin-1-ium-1-yl)butylpyridin-1-ium dibromide)
• 14208-07-2(Pyridinium,1,1'-(1,3-propanediyl)bis-, bromide (1:2))
• 1155-74-4(1-Tetradecylpyridin-1-ium bromide)
• 2534-66-9(1-Octylpyridinium bromide)
• 2534-65-8(Pyridinium, 1-decyl-,bromide (1:1))
• 23271-47-8(1-Propylpyridinium Chloride)