| Weight | 240.35 g/mol |
|---|---|
| Formula | C16H20N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
54827-17-7 (54827-17-7)
tetramethyl benzidine · 3,3',5,5'-tetramethylbenzidine · tetramethylbenzidine dihydrochloride
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- Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: a non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents. (Journal of Histochemistry and Cytochemistry, 1978)
- Additional Factors Influencing Sensitivity in the Tetramethyl Benzidine Method for Horseradish Peroxidase Neurohistochemistry (Journal of Histochemistry and Cytochemistry, 1980)
- A new stabilizing agent for the tetramethyl benzidine (TMB) reaction product in the histochemical detection of horseradish peroxidase (HRP) (Journal of Neuroscience Methods, 1985)
- Brain stem projections of the aortic nerve in the cat: a study using tetramethyl benzidine as the substrate for horseradish peroxidase. (Brain Research, 1980)
- Lead-selective fluorescent optode membrane based on 3,3,5,5-tetramethyl-N-(9-anthrylmethyl)benzidine (Analytica Chimica Acta, 2002)
- Electron microscopic visualization of tetramethyl benzidine reaction product on horseradish peroxidase neurohistochemistry. (Cellular and molecular biology, including cyto-enzymology, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tetramethyl benzidine
- 3,3',5,5'-tetramethylbenzidine
- tetramethylbenzidine dihydrochloride
- 3,3',5,5'-TMP
-
SMILESCC1=CC(=CC(=C1N)C)C2=CC(=C(C(=C2)C)N)C
-
InChIKeyUAIUNKRWKOVEES-UHFFFAOYSA-N
- Pubchem - 54827-17-7
- Wikipedia - 3,3',5,5'-tetramethylbenzidine
3,3,5,5-Tetramethylbenzidine or TMB is a chromogenic substrate used in staining procedures in immunohistochemistry as well as being a visualising reagent used in enzyme-linked immunosorbent assays (ELISA). TMB is a white crystal powder that forms a pale blue-green liquid in solution with ethyl acetate. TMB is degraded by sunlight and by fluorescent lights.
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