Molecular structure of Diethyldithiocarbamic acid sodium salt trihydrate, CAS Number: 148-18-5
Diethyldithiocarbamic acid sodium salt trihydrate (CAS 20624-25-3)
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Alternate Names:
Sodium diethyldithiocarbamate trihydrate
Application:
Diethyldithiocarbamic acid sodium salt trihydrate is a Nitric oxide (NO) spin-trapping reagent
CAS Number:
20624-25-3
Purity:
≥98%
Molecular Weight:
225.31
Molecular Formula:
C5H10NS2•Na•3H2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Diethyldithiocarbamic acid sodium salt trihydrate is a dithiol compound that forms an NO-reactive spin-trapping agent when complexed with Fe2+. The Fe2+-DETC complex is described to be an efficient selective NO trap for EPR experiments, and the nitrosyl-iron-dithiocarbamate NOFe(DETC)2 reacted compound is identifiable with a characteristic triplet EPR signature. Diethyldithiocarbamic acid sodium salt trihydrate is an inhibitor of SOD and NF kappa B. Diethyldithiocarbamic acid sodium salt trihydrate is a versatile white crystalline powder utilized in biochemistry. Its significance lies in its potent catalytic properties, enabling the synthesis of a diverse array of compounds.
Diethyldithiocarbamic acid sodium salt trihydrate (CAS 20624-25-3) References
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- Self-Assembly of NaOL-DDA Mixtures in Aqueous Solution: A Molecular Dynamics Simulation Study. | Wang, L., et al. 2021. Molecules. 26: PMID: 34885699
- DDA-imaging with structural identification of lipid molecules on an Orbitrap Velos Pro mass spectrometer. | Khalil, SM., et al. 2022. J Mass Spectrom. 57: e4882. PMID: 36055222
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- In vivo spin trapping of nitric oxide generated in the small intestine, liver, and kidney during the development of endotoxemia: a time-course study. | Wallis, G., et al. 1996. Shock. 6: 274-8. PMID: 8902945
- Complexes of Fe2+ with diethyldithiocarbamate or N-methyl-D-glucamine dithiocarbamate as traps of nitric oxide in animal tissues: comparative investigations. | Mikoyan, VD., et al. 1997. Biochim Biophys Acta. 1336: 225-34. PMID: 9305794
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- Deoxygenation of oxovanadium(IV) complexes under mild conditions: Synthesis and structural characterization of cis- dihalobis(diakyldithiocarbamato)vanadium(IV) | Edward L. Jones, John G. Reynolds, John C. Huffman, George Christou. 1991. Polyhedron. 10: 1817-1825.
- Synthesis of poly(p-phenylene vinylene) and derivatives via a new precursor route, the dithiocarbamate route | A. Henckens a b, I. Duyssens b, L. Lutsen b, D. Vanderzande a b, T.J. Cleij a. 2006. Polymer. 47: 123-131.
- Electrochemical Studies of Ochratoxin A Mycotoxin at Gold Electrodes Modified with Cysteamine Self-Assembled Monolayers. Its Ultrasensitive Quantification in Red Wine Samples | Patricio René Perrotta, Nelio Roberto Vettorazzi, Fernando Javier Arévalo, Adrián Marcelo Granero, Sofía Noemí Chulze, María Alicia Zón, Héctor Fernández. 2011. Electroanalysis. 23: 1585-1592.
- Synthesis of Ni3S4/NiS2/FeS2 nanoparticles for hydrogen and oxygen evolution reaction | Wenpin Wang a, Weijie Wang a, Yue Xu b, Xiaoxuan Ren b, Xien Liu b, Zhongcheng Li b. 2021. Applied Surface Science. 560: 149985.
Inhibitor of:
CYP1A1, Grx2, MOXD2, NF kappa B, SOD, SOD-1, STEAP, TMTSP, ZNF202, and ZnT-1.Activator of:
ATP7A, catalase, and COMMD10.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Diethyldithiocarbamic acid sodium salt trihydrate, 5 g | sc-202576 | 5 g | $19.00 | |||
Diethyldithiocarbamic acid sodium salt trihydrate, 25 g | sc-202576A | 25 g | $59.00 |