Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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.
1,4-Diazabicyclo[2.2.2]octane bis(sulfur dioxide) (DABSO) is a charge transfer complex that can be used as a sulfur dioxide surrogate:
· In palladium-catalyzed aminosulfonylation process.
· In reaction with aryl bromides to synthesize sodium aryl sulfinates.
It can also be used to activate DMSO and o-vinylanilines for the synthesis of N-aryl-1H-benzo[d]imidazol-1-amine and 4-aryl quinolines, respectively
| Sonrisas canónicas | C1C[N+]2(CC[N+]1(CC2)S(=O)[O-])S(=O)[O-] |
|---|---|
| IUPAC Name | 1,4-diazoniabicyclo[2.2.2]octane-1,4-disulfinate |
| InChIKey | RWISEVUOFYXWFO-UHFFFAOYSA-N |
| INCHI | 1S/C6H12N2O4S2/c9-13(10)7-1-2-8(5-3-7,6-4-7)14(11)12/h1-6H2 |
| Isómeros SMILES | C1C[N+]2(CC[N+]1(CC2)S(=O)[O-])S(=O)[O-] |
| WGK Alemania | 3 |
| Peso molecular | 240.3 |
| Reaxy-Rn | 21980336 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=21980336&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Diazinanes |
| Subclass | Piperazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | N-alkylpiperazines |
| Alternative Parents | Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | N-alkylpiperazine - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aliphatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group. |
| 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 | Aug 11, 2025 | D166360 | |
| Certificate of Analysis | Aug 11, 2025 | D166360 | |
| Certificate of Analysis | Aug 11, 2025 | D166360 | |
| Certificate of Analysis | Apr 28, 2024 | D166360 | |
| Certificate of Analysis | Apr 28, 2024 | D166360 | |
| Certificate of Analysis | Sep 14, 2023 | D166360 | |
| Certificate of Analysis | Sep 14, 2023 | D166360 | |
| Certificate of Analysis | Sep 12, 2023 | D166360 |
| Solubilidad | Soluble in water |
|---|---|
| Sensibilidad | air and heat and moisture sensitive |
| Punto de fusión (°C) | 180 °C |
| Peso molecular | 240.300 g/mol |
| XLogP3 | -2.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 0 |
| Exact Mass | 240.024 Da |
| Monoisotopic Mass | 240.024 Da |
| Topological Polar Surface Area | 119.000 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 243.000 |
| 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 | 1 |
| 1. Wei Xiao, Jian-Qiang Chen, Jie Wu. (2025) Radical sulfonylation with sulfur dioxide surrogates. CHEMICAL SOCIETY REVIEWS, [PMID:40498470] [10.1039/D4CS01312C] |