3,3',5,5'-Tetramethylbenzidine

Enzymatic assay

TMB can act as a hydrogen donor for the reduction of hydrogen peroxide to water by peroxidase enzymes such as horseradish peroxidase.

The resulting one-electron oxidation product is a diimine-diamine complex, which causes the solution to take on a blue colour, and this colour change can be read on a spectrophotometer at the wavelengths of 370 and 650 nm.

The reaction can be halted by addition of acid or another stop reagent. Using sulfuric acid turns TMB yellow, with a peak absorbance of 450 nm. The amount of converted TMB may be indexed by the amount of 450 nm light it absorbs.

Material safety

TMB should be kept out of direct sunlight as it is photosensitive. It is not known if TMB is carcinogenic and the evidence is contradictory: TMB is not mutagenic by the Ames test, and did not induce formation of tumors in a single-arm study of 24 rats. On that evidence, it has been used as a replacement for carcinogenic compounds such as benzidine and o-phenylenediamine.

References

References

1. [http://www.sigmaaldrich.com/catalog/search/ProductDetail/ALDRICH/860336 Sigma Aldrich Catalog Entry for 3,3′,5,5′-Tetramethylbenzidine]
2. Zhang X. (2020). "Rationale of 3,3',5,5'-Tetramethylbenzidine as the Chromogenic Substrate in Colorimetric Analysis". Anal. Chem..
3. "TMB Substrate Solution".
4. Holland VR. (1974). "A safer substitute for benzidine in the detection of blood". Tetrahedron.
5. Ashby J. (1982). "Evaluation of two suggested methods of deactivating organic carcinogens by molecular modification". Carcinogenesis.
6. Chung K-T. (2000). "Mutagenicity studies of benzidine and its analogs: Structure-activity relationships". Toxicol Sci.
7. Chung K-T. (2006). "Review of the Salmonella typhimurium mutagenicity of benzidine, benzidine analogues, and benzidine-based dyes". Mutation Research/Reviews in Mutation Research.
8. Yang J. (2008). "One-pot synthesis of silver nanoplates and charge-transfer complex nanofibers". J Phys Chem C.