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T5513

Sigma-Aldrich

N,N,N′,N′-Tetramethylbenzidine

≥95% (HPLC)

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About This Item

Linear Formula:
[-C6H4-4-N(CH3)2]2
CAS Number:
366-29-0
Molecular Weight:
240.34
EC Number:
206-676-5
MDL number:
MFCD00008310
UNSPSC Code:
12352103
PubChem Substance ID:
24900288
NACRES:
NA.32

Quality Level

100

Assay

≥95% (HPLC)

form

powder

mp

193-195 °C (lit.)

SMILES string

CN(C)c1ccc(cc1)-c2ccc(cc2)N(C)C

InChI

1S/C16H20N2/c1-17(2)15-9-5-13(6-10-15)14-7-11-16(12-8-14)18(3)4/h5-12H,1-4H3

InChI key

YRNWIFYIFSBPAU-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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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D I Metelitsa et al.
Biokhimiia (Moscow, Russia), 61(2), 308-321 (1996-02-01)
The tetramethylbenzidine (TMB) oxidation kinetics dependent on spleen ferritin (FERR) has been studied in TMB-FERR-H2O2 (1) and TMB-FERR-O2 (2) systems at pH 4.2 and 6.0. At TMB concentrations below 6 mM, the dependencies of the initial rate for protein oxidation
F H Pujol et al.
Journal of immunoassay, 14(1-2), 21-31 (1993-03-01)
An enzyme immunoassay for detection of hepatitis B surface antigen based on the use of 3 monoclonal antibodies (mAbs) was developed: an IgM as capture and 2 IgG1 for detection. The system biotin-streptavidin was compared with direct conjugation of mAbs
T Wolff et al.
Photochemistry and photobiology, 62(1), 82-86 (1995-07-01)
After UV irradiation of rapidly frozen solutions of N,N,N',N'-tetramethylbenzidine (TMB) in dilute aqueous micellar cetyltrimethylammonium bromide at 80 K, the ESR signal corresponding to the TMB+ cation was detected indicating photoionization. This signal was monitored as a function of time
D I Metelitza et al.
Biochemistry. Biokhimiia, 64(10), 1200-1209 (1999-11-24)
Polydisulfides of urea (PDSU), thiourea (PDSTU), biuret (PDSB), and gallic acid (PDSG) and their monomer analogues (urea, biuret, and gallic acid) inhibited (in a competitive manner) tetramethylbenzidine (TMB) peroxidation catalyzed by ferritin in 0.1 M acetate buffer, pH 4.2, containing
M E Rivière et al.
Archives of biochemistry and biophysics, 277(1), 130-136 (1990-02-15)
Photoionization of hydrophobic probes has been developed in micelles or synthetic vesicles. Studies of the yields, compartmentation, and lifetimes of the photo-produced charged species have gathered reliable information on the interfacial and structural properties of these assemblies. Such an approach
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