TMPD (dihydrochloride)

CAT: 0804-HY-W012145-01Size: 1 gDry Ice: NoHazardous: No
CAT#:0804-HY-W012145-01Size:1 g
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Description
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].
CAS Number
[637-01-4]
UNSPSC
12352005
Hazard Statement
H315, H319
Target
Biochemical Assay Reagents
Type
Reference compound
Related Pathways
Others
Applications
Metabolism-protein/nucleotide metabolism
Field of Research
Metabolic Disease
Assay Protocol
https://www.medchemexpress.com/tmpd-dihydrochloride.html
Purity
98.81
Solubility
DMSO : 16.67 mg/mL (ultrasonic) |H2O : 100 mg/mL (ultrasonic)
Smiles
CN(C)C1=CC=C(N(C)C)C=C1.[H]Cl.[H]Cl
Molecular Formula
C10H18Cl2N2
Molecular Weight
237.17
Precautions
H315, H319
References & Citations
[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.|[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.|[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.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture and light)
Scientific Category
Reference compound1
Clinical Information
Phase 3

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