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T8768

Sigma-Aldrich

3,3′,5,5′-Tetramethylbenzidine dihydrochloride hydrate

horseradish peroxidase substrate, chromogenic, ≥98%, powder

Synonym(s):

TMB dihydrochloride

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About This Item

Linear Formula:
[-C6H2(CH3)2-4-NH2]2·2HCl·xH2O
CAS Number:
Molecular Weight:
313.27 (anhydrous basis)
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.83

product name

3,3′,5,5′-Tetramethylbenzidine dihydrochloride hydrate, powder, ≥98%

Quality Level

Assay

≥98%

form

powder

solubility

acetic acid: water (1:2): 20 mg/mL, clear to slightly hazy

storage temp.

2-8°C

SMILES string

O.Cl.Cl.Cc1cc(cc(C)c1N)-c2cc(C)c(N)c(C)c2

InChI

1S/C16H20N2.2ClH.H2O/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;2*1H;1H2

InChI key

KVCWTKDFVVSVSJ-UHFFFAOYSA-N

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General description

3,3′,5,5′-Tetramethylbenzidine dihydrochloride hydrate (TMB-d) is a sensitive chromogen substrate for peroxidase. It is non- carcinogenic, hence, it can be used as a safe substitute for benzidine. TMB-d is useful in quantifying hemoglobin and in staining myeloperoxidase-containing granules in granulocytes.

Application

3,3′,5,5′-Tetramethylbenzidine dihydrochloride hydrate has also been used as a horseradish peroxidase substrate in enzyme linked immunosorbent assay and reverse dot blot (RDB).
Noncarcinogenic substitute for benzidine.

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 4 - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Quantitative determination of hemoglobin and cytochemical staining for peroxidase using 3, 3?, 5, 5?-tetramethylbenzidine dihydrochloride, a safe substitute for benzidine
Liem HH, et al.
Analytical biochemistry, 98(2), 388-393 (1979)
Robot Printing of Reverse Dot Blot Arrays for Human Mutation Detection
Lappin S, et al.
The Journal of Molecular Diagnostics : JMD, 3, 178-178 (2001)
Lymphocyte Homing to the Skin: Immunology, Immunopathology, and Therapeutic Perspectives (2004)
Detection of Antibodies Against DNA Polymerase of Hepatitis B Virus in HBsAg-Positive Sera Using ELISA
Rui LX, et al.
The Korean Journal of Internal Medicine, 13, 95-95 (1998)
R Piovesana et al.
Scientific reports, 10(1), 7159-7159 (2020-04-30)
Regenerative capability of the peripheral nervous system after injury is enhanced by Schwann cells (SCs) producing several growth factors. The clinical use of SCs in nerve regeneration strategies is hindered by the necessity of removing a healthy nerve to obtain

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