1,1'-Diethyl-4,4'-bipyridinium dibromide

Base Information

• Chemical Name: 1,1'-Diethyl-4,4'-bipyridinium dibromide
• CAS No.: 53721-12-3
• Molecular Formula: 2Br*C₁₄H₁₈N₂
• Molecular Weight: 374.118
• European Community (EC) Number: 626-504-6
• DSSTox Substance ID: DTXSID40467092
• Mol file: 53721-12-3.mol

Synonyms:53721-12-3;1,1'-Diethyl-4,4'-bipyridinium dibromide;Ethyl viologen dibromide;Ethylviologen Dibromide;1,1'-Diethyl-[4,4'-bipyridine]-1,1'-diium bromide;1-ethyl-4-(1-ethylpyridin-1-ium-4-yl)pyridin-1-ium;dibromide;MFCD00134590;1,1'-Diethyl-[4,4'-bipyridine]-1,1'-diiumbromide;4,4'-Bipyridinium, 1,1'-diethyl-, dibromide;Ethylviologendibromide;YSWG424;SCHEMBL483094;Ethyl viologen dibromide, 99%;DTXSID40467092;LCEBDKLPALDQPV-UHFFFAOYSA-L;AKOS024283397;CS-W011785;s12407;AS-19987;SY316627;E1430;FT-0640187;1,1'-diethyl-4,4'-bipyridine-1,1'-diium bromide;1,1 inverted exclamation mark -Diethyl-[4,4 inverted exclamation mark -bipyridine]-1,1 inverted exclamation mark -diium Bromide

Chemical Property of 1,1'-Diethyl-4,4'-bipyridinium dibromide

Chemical Property:

• Melting Point: 278ºC
• PSA: 7.76000
• LogP: -4.02360
• Storage Temp.: Inert atmosphere,Room Temperature
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 373.98162
• Heavy Atom Count: 18
• Complexity: 167

Purity/Quality:

98%Min ^*data from raw suppliers

Ethyl viologen dibromide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[N+]1=CC=C(C=C1)C2=CC=[N+](C=C2)CC.[Br-].[Br-]
• Uses: Ethylviologen Dibromide maintains the ability to be genotoxic to cells and their corresponding DNA.

Technology Process of 1,1'-Diethyl-4,4'-bipyridinium dibromide

There total 1 articles about 1,1'-Diethyl-4,4'-bipyridinium dibromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

4,4'-bipyridine (553-26-4) + ethyl bromide (74-96-4) → 1,1′-diethyl-[4,4′-bipyridine]-1,1′-diium dibromide (53721-12-3)

Guidance literature:

In acetonitrile; for 6h; Reflux;

DOI:10.1021/ja903778d

upstream raw materials:

4,4'-bipyridine

ethyl bromide

Refernces

• 1、 Tanaka, Rikako,Okazawa, Atsushi,Konaka, Hisashi,Sasaki, Akito,Kojima, Norimichi,Matsushita, Nobuyuki. "Unique Hydration/Dehydration-Induced Vapochromic Behavior of a Charge-Transfer Salt Comprising Viologen and Hexacyanidoferrate(II)". . p. 2209 - 2217. Retrieved 2018.
• 2、 Pramanik, Bapan,Mondal, Julfikar Hassan,Singha, Nilotpal,Ahmed, Sahnawaz,Mohanty, Jyotirmayee,Das, Debapratim. "A Viologen–Perylenediimide Conjugate as an Efficient Base Sensor with Solvatochromic Property". . p. 245 - 252. Retrieved 2017.
• 3、 Chen, Hongning,Chen, Mao,Liu, Lei,Zhang, Peiyao. "A low-cost and high-loading viologen-based organic electrode for rechargeable lithium batteries". . p. 24429 - 24435. Retrieved 2021.
• 4、 Cheng, Si-Yuan,Qu, Yun-Xia,Tao, Zhu,Zhou, Kai-Zhi,Wei, Lian-Tong,Wang, Cong,Zhao, Wei-Wei,Jiang, Dao-Fa,Ma, Pei-Hua. "The Host-Guest Properties Observed between the Viologens and Cyclopentanocucurbit[6]uril". . p. 601 - 607. Retrieved 2020/01/24.