3,3′,5,5′-Tetramethylbenzidine
Line Structure
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)
ChEMBL
ChemSpider
ECHA InfoCard 100.053.949
EC Number
  • 259-364-6
UNII
  • InChI=1S/C16H20N2/c1-9-5-13(6-10(2)15(9)17)14-7-11(3)16(18)12(4)8-14/h5-8H,17-18H2,1-4H3 checkY
    Key: UAIUNKRWKOVEES-UHFFFAOYSA-N checkY
  • InChI=1/C16H20N2/c1-9-5-13(6-10(2)15(9)17)14-7-11(3)16(18)12(4)8-14/h5-8H,17-18H2,1-4H3
    Key: UAIUNKRWKOVEES-UHFFFAOYAM
  • Cc1cc(cc(c1N)C)c2cc(c(c(c2)C)N)C
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:
GHS07: Exclamation mark
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).
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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).[1] 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.

Enzymatic assay

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

Oxidation of TMB
Shows the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) to 3,3',5,5'-tetramethylbenzidine diimine

The resulting one-electron oxidation product is a diimine-diamine complex, which causes the solution to take on a blue colour,[2] 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.[3]

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,[4][5][6][7] and did not induce formation of tumors in a single-arm study of 24 rats.[4] On that evidence, it has been used as a replacement for carcinogenic compounds such as benzidine[8] and o-phenylenediamine.

References

  1. ↑ Sigma Aldrich Catalog Entry for 3,3′,5,5′-Tetramethylbenzidine
  2. ↑ Zhang X; Yang Q; Lang Y; Jiang X; Wu P (2020). "Rationale of 3,3',5,5'-Tetramethylbenzidine as the Chromogenic Substrate in Colorimetric Analysis". Anal. Chem. 92 (18): 12400–12406. doi:10.1021/acs.analchem.0c02149. PMID 32794705. S2CID 221132691.
  3. ↑ "TMB Substrate Solution".
  4. 1 2 Holland VR; Saunders BC; Rose FL; Walpole AL (1974). "A safer substitute for benzidine in the detection of blood". Tetrahedron. 30 (18): 3299. doi:10.1016/S0040-4020(01)97504-0.
  5. ↑ Ashby J; Paton D; Lefevre PA; Styles JA; Rose FL (1982). "Evaluation of two suggested methods of deactivating organic carcinogens by molecular modification". Carcinogenesis. 3 (11): 1277–1282. doi:10.1093/carcin/3.11.1277. PMID 6758975.
  6. ↑ Chung K-T; Chen S-C; Wong TY; Li YS; Wei CI; Chou MW (2000). "Mutagenicity studies of benzidine and its analogs: Structure-activity relationships". Toxicol Sci. 56 (2): 351–356. doi:10.1093/toxsci/56.2.351. PMID 10910993.
  7. ↑ Chung K-T; Chen S-C; Claxton LD (2006). "Review of the Salmonella typhimurium mutagenicity of benzidine, benzidine analogues, and benzidine-based dyes". Mutation Research/Reviews in Mutation Research. 612 (1): 58–76. doi:10.1016/j.mrrev.2005.08.001. PMID 16198141.
  8. ↑ Yang J; Wang H; Zhang H (2008). "One-pot synthesis of silver nanoplates and charge-transfer complex nanofibers". J Phys Chem C. 112 (34): 13065–13069. doi:10.1021/jp802604d.
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