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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ethyl viologen dibromide (1,1-diethyl- 4,4-bipyridinium dibromide) has been used as an internal standard in analysis of paraquat and diquat in the serum using high-performance liquid chromatography. It has also been used as as an internal standard in the quantitative analysis of paraquat in biological samples by liquid chromatography- electrospray ionization-mass spectrometry.
| Pubchem Sid | 504766468 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504766468 |
| Sonrisas canónicas | CC[N+]1=CC=C(C=C1)C2=CC=[N+](C=C2)CC.[Br-].[Br-] |
| IUPAC Name | 1-ethyl-4-(1-ethylpyridin-1-ium-4-yl)pyridin-1-ium;dibromide |
| InChIKey | LCEBDKLPALDQPV-UHFFFAOYSA-L |
| INCHI | 1S/C14H18N2.2BrH/c1-3-15-9-5-13(6-10-15)14-7-11-16(4-2)12-8-14;;/h5-12H,3-4H2,1-2H3;2*1H/q+2;;/p-2 |
| Isómeros SMILES | CC[N+]1=CC=C(C=C1)C2=CC=[N+](C=C2)CC.[Br-].[Br-] |
| WGK Alemania | 3 |
| CAS alternativo | 46713-38-6 |
| Peso molecular | 374.11 |
| Reaxy-Rn | 6946079 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6946079&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Pyridines and derivatives |
| Subclass | Bipyridines and oligopyridines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bipyridines and oligopyridines |
| Alternative Parents | Pyridinium derivatives Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic bromide salts Hydrocarbon derivatives Organic cations |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Bipyridine - 4,4p-bipyridinium - Pyridinium - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organonitrogen compound - Organic cation - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as bipyridines and oligopyridines. These are organic compounds containing two pyridine rings linked to each other. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 18, 2026 | E137263 | |
| Certificate of Analysis | Mar 11, 2026 | E137263 | |
| Certificate of Analysis | Mar 11, 2026 | E137263 | |
| Certificate of Analysis | Mar 11, 2026 | E137263 | |
| Certificate of Analysis | Feb 26, 2026 | E137263 | |
| Certificate of Analysis | May 27, 2025 | E137263 | |
| Certificate of Analysis | Jul 18, 2022 | E137263 |
| Sensibilidad | Hygroscopic |
|---|---|
| Punto de fusión (°C) | 278°C |
| Peso molecular | 374.110 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 373.982 Da |
| Monoisotopic Mass | 371.984 Da |
| Topological Polar Surface Area | 7.800 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 167.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 3 |
| 1. Liangliang Wu, Huajing Fang, Jiaqi Li, Lingqi Wu, Hong Wang. (2023) Catalyzing Viologen Electrochromic Reaction with CuOx Nanoparticles. Advanced Materials Technologies, 8 (22): (2301028). [PMID:] [10.1002/admt.202301028] |