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TMPD dihydrochloride
CAS No. 637-01-4
TMPD dihydrochloride( —— )
Catalog No. M28331 CAS No. 637-01-4
TMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | 27 | In Stock |
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Biological Information
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Product NameTMPD dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionTMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.
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DescriptionTMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.(In Vitro):TMPD dihydrochloride differentiates organisms that exhibit CYP C oxidase activity and distinguishes between Gram-negative and Gram-positive pathogenic and non-pathogenic bacteria. TMPD dihydrochloride can be used as a colorimetric indicator.
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In VitroTMPD (N,N,N′,N′-tetramethyl-para-phenylene-diamine) is used in cell culture and microbiology to differentiate organisms that exhibit cytochrome c oxidase activity and to distinguish between Gram-negative and Gram-positive pathogenic and non-pathogenic bacteria.The concept of TMPD oxidation by microorganisms is widely used and is known as a successful colorimetric indicator for bacterial oxidases, as the radical cation TMPD+˙, formed by oxidation, shows a characteristic deep blue colour. The electrochemical recognition of the TMPD oxidation by bacterial oxidases can be applied to a variety of pathogens.
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number637-01-4
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Formula Weight237.17
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Molecular FormulaC10H18Cl2N2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 100 mg/mL (421.64 mM)
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SMILESCN(C)C1=CC=C(N(C)C)C=C1.Cl.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Weber U, Schmid H. Synthese und biologische Aktivit?t des Dekapeptids Gly-Pro-Cys-Lys-Ala-Arg-Phe-Gly-Gly-Cys als Modell für das aktive Zentrum des basischen Trypsininhibitors aus Rinderorganen (Kunitz-Inhibitor [Synthesis and biological activity of the decapeptide Gly-Pro-Cys-Lys-Ala-Arg-Phe-Gly-Gly-Cys as a model for the active center of the basic trypsin inhibitor from bovine organs (Kunitz inhibitor) (author's transl)]. Hoppe Seylers Z Physiol Chem. 1976 Dec;357(10):1359-63. German.
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