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N,N,N'-Trimethylbenzidine (TMB) is an organic compound with the chemical formula C15H21N3. It is a derivative of benzidine, a known carcinogen, and is used as a chemical intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. TMB is a colorless to pale yellow crystalline solid that is soluble in organic solvents. It is also used as a substrate in enzyme-linked immunosorbent assays (ELISA) to produce a colorimetric reaction, indicating the presence of specific antibodies or antigens. Due to its potential health risks, handling TMB requires proper safety measures, including the use of personal protective equipment and adherence to proper disposal procedures.

2655-66-5

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2655-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2655-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2655-66:
(6*2)+(5*6)+(4*5)+(3*5)+(2*6)+(1*6)=95
95 % 10 = 5
So 2655-66-5 is a valid CAS Registry Number.

2655-66-5Downstream Products

2655-66-5Relevant academic research and scientific papers

Electron Spin Resonance, Electron Spin Echo Modulation, and Electron Nuclear Double Resonance Studies on the Photoionization of N-Alkyl-N,N',N'-trimethylbenzidine in Anionic and Cationic Micelles

Stenland, Chris,Kevan, Larry

, p. 5177 - 5184 (1993)

N-Alkyl-N,N',N'-trimethylbenzidines (CnTMB, n = 1-6, 8) were synthesized and photoionized in rapidly frozen anionic and cationic micelles.The photoyields of the cation radicals were investigated by electron spin resonance spectroscopy.Electron spin echo modulation spectroscopy and proton matrix electron nuclear double resonance were used to determine the relative location of the photoproduced cation radical with respect to the deuterated aqueous interface.No dependence on the photoyield as a function of the electron donor alkyl chain length is observed, although increasing the alkyl chain length on the benzidine moiety moves its location toward the aqueous interface.The lack of a photoyield trend is interpreted in terms of the solubilization geometry, which determines the paths of electron escape to form charge-separated products.An electron escape cone defined as the solid angle formed from the center of the electron donor moiety through the width of the spin distribution that intersects the interface changes only slowly as a function of radical location over a limited range.Hence, the photoyield is little changed.

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