637-01-4
637-01-4
Chemical Structure
TMPD dihydrochloride
- CAS No.: 637-01-4
- Formula:C10H18Cl2N2
- Molecular Weight:237.17
IUPAC Name: N1,N1,N4,N4-tetramethylbenzene-1,4-diamine dihydrochloride
InChIKey: FBHKTSXMTASXFJ-UHFFFAOYSA-N
SMILES: CN(C)C1=CC=C(N(C)C)C=C1.[H]Cl.[H]Cl
Biological Activity: TMPD dihydrochloride, a readily oxidizable compound, is an enzymatically convert redox active substrate molecule. TMPD dihydrochloride is also an electron donor and serves as a reducing cosubstrate for heme peroxidases[1][2]. TMPD dihydrochloride is also a complex IV substrate[3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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TMPD dihydrochloride | 99.33% | TMPD dihydrochloride, a readily oxidizable compound, is an enzymatically convert redox active substrate molecule. TMPD dihydrochloride is also an electron donor and serves as a reducing cosubstrate for heme peroxidases. TMPD dihydrochloride is also a complex IV substrate. | ||||||||||||||||||||
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References
- [1]. S Kuss, et al. Electrochemical recognition and quantification of cytochrome c expression in Bacillus subtilis and aerobe/anaerobe Escherichia coli using N, N, N', N'-tetramethyl- para-phenylene-diamine (TMPD). Chem Sci. 2017 Nov 1;8(11):7682-7688. [Content Brief]
- [2]. Nenad Petrovic, et al. Using N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD) to assay cyclooxygenase activity in vitro. Methods Mol Biol. 2010;594:129-40. [Content Brief]
- [3]. Franco A Rossato, et al. Fatty acid synthase inhibitors induce apoptosis in non-tumorigenic melan-a cells associated with inhibition of mitochondrial respiration. PLoS One. 2014 Jun 25;9(6):e101060. [Content Brief]
Keywords
