Chemodex

N,N,N',N'-Tetramethyl-p-phenylenediamine dihydrochloride

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Product Details
Synonyms TMPD; Tetramethyl-p-phenylenediamine dihydrochloride; Wurster's reagent dihydrochloride; 1,4-Bis(dimethylamino)benzene dihydrochloride
Product Type Chemical
Properties
Formula C10H18Cl2N2
MW 237.17
CAS 637-01-4
Source/Host Chemicals Synthetic
Purity Chemicals ≥95% (NMR)
Appearance Pale-yellow solid.
Solubility Soluble in water (50mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturer's product datasheet.

InChi Key FBHKTSXMTASXFJ-UHFFFAOYSA-N
Smiles N(C)(C)C1=CC=C(N(C)C)C=C1.Cl
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
N,N,N',N'-Tetramethyl-p-phenylenediamine dihydrochloride (TMPD) is a redox-active aromatic amine compound, widely used in biochemical and analytical applications, particularly as a chromogenic redox indicator. TMPD is commonly used in redox titrations and biochemical assays. It is colorless in its reduced form and turns blue or purple (called Wurster's Blue) upon oxidation, indicating electron transfer activity. This makes it valuable for detecting the presence or activity of oxidases or cytochromes. TMPD serves as an artificial electron donor, particularly to cytochrome c oxidase (complex IV) in the mitochondrial electron transport chain. It's often used in combination with ascorbate to assess respiratory chain function. TMPD is used in colorimetric assays for peroxidase activity or other oxidoreductases, where a color change signals enzyme action.
Product References
(1) M.G. Mustafa & T.E. King; Arch. Biochem. Biophys. 122, 501 (1967) | (2) H.K. Kimelberg & P. Nicholls; Arch. Biochem. Biophys. 133, 327 (1969) | (3) S. Papa, et al.; FEBS Lett. 157, 15 (1983) | (4) R. Munday; Chem. Biol. Interact. 65, 133 (1988) | (5) R.M. Lorence, et al.; J. Biol. Chem. 263, 5271 (1988) | (6) E.W. de Vrind-de Jong, et al.; Appl. Environ. Microbiol. 56, 3458 (1990) | (7) C. Storle & P. Eyer; Chem. Biol. Interact. 78, 321 (1991) | (8) N. Petrovic & M. Murray; Methods Mol. Biol. 594, 129 (2010)
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