3,3',5,5'-Tetramethylbenzidine
| Names | |
|---|---|
| Preferred IUPAC name
3,3′,5,5′-Tetramethyl[1,1′-biphenyl]-4,4′-diamine | |
| Other names
3,3′,5,5′-Tetramethylbiphenyl-4,4'-diamine | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.053.949 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C16H20N2 | |
| Molar mass | 240.3482 g/mol |
| Melting point | 168 to 171 °C (334 to 340 °F; 441 to 444 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H302, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
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 solid that forms a pale blue-green liquid in solution with ethyl acetate. TMB is degraded by sunlight and by fluorescent lights. Used to detect hematuria as it turns blue in contact with hemoglobin.