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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

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)

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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
L G McGirr et al.
Chemico-biological interactions, 61(1), 61-74 (1987-01-01)
The mechanism of peroxidative N-dealkylation of alkylamines proceeds via one-electron oxidation to the iminium cation which reacts with water to give the N-hydroxymethyl derivative which decomposes to formaldehyde and the N-demethylated product. This reaction is normally inhibited by glutathione by
S Kusunoki et al.
Journal of clinical microbiology, 29(8), 1596-1603 (1991-08-01)
Quantitative microdilution plate hybridization was used to identify 22 Mycobacterium species. DNAs of clinical strains were rapidly extracted and labeled with photoreactive biotin. Labeled DNAs were distributed into wells of a microdilution plate in which reference DNAs had been immobilized.
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