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5-Amino-2-(p-tolyl)-2H-benzotriazole is a chemical compound with the molecular formula C13H12N4. It is a derivative of benzotriazole, a heterocyclic compound with a benzene ring fused to a triazole ring. The compound features a p-tolyl group (a methyl-substituted phenyl group) attached to the benzene ring and an amino group on the triazole ring. This chemical is often used as a corrosion inhibitor, particularly in metalworking fluids, due to its ability to form stable complexes with metal ions, thereby preventing corrosion. It is also employed in various industrial applications, such as in the production of dyes and pigments, and as a reagent in organic synthesis. The compound is known for its effectiveness in protecting metals from corrosion, especially in acidic environments, and is valued for its low toxicity and environmental friendliness compared to some traditional corrosion inhibitors.

6659-91-2

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6659-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6659-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6659-91:
(6*6)+(5*6)+(4*5)+(3*9)+(2*9)+(1*1)=132
132 % 10 = 2
So 6659-91-2 is a valid CAS Registry Number.

6659-91-2Downstream Products

6659-91-2Relevant academic research and scientific papers

TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY

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Page/Page column 28; 43, (2010/11/28)

There are disclosed compound of Formula (I) or (II) wherein A1, A2, A3, A4and A5, which may be the same or different, represent N or CR1, R9 represents - L -R3, in whi

APPLICATION OF FLUORESCENT TRIAZOLES TO ANALYTICAL CHEMISTRY. III. FLUORESCENCE CHARACTERISTICS OF 2-PHENYLBENZOTRIAZOLYL-5-AMINE DERIVATIVES AS FLUORESCENT PROBES

Narita, Shigeru,Kitagawa, Takayasu

, p. 1005 - 1008 (2007/10/02)

2-Phenylbenzotriazole derivatives with a COCH3 or NH2 group on the 2-phenyl ring were synthesized and found to be applicable as fluorescent hydrophobic probes.The fluorescence intensities of these compounds, which were intense in non-polar solvents, were dramatically quenched in polar solvents.In particular, 2-(4-acetylphenyl)-2H-benzotriazolyl-5-amine (7) showed a much higher ratio of the fluorescence intensity in the organic solvent to that in water (Fo/Fw) than 8-anilino-1-naphthalenesulfonate (ANS): The Fo/Fw values of 7 were 470 for dioxane and 440 for acetone, while those of ANS were 100 for dioxane and 90 for acetone.We modified compound 7 to obtain water-soluble probes for use in drug-protein binding studies and examined the interaction of these probes with human serum albumin (HSA).All the compounds, which were practically non-fluorescent in the buffer solution, bound to HSA and fluoresced.Keywords: 2-phenylbenzotriazolyl-5-amine; fluorescence characteristies; solvent effect; fluorescent probe; protein binding

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