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N,O-di-tert-butylhydroxylamine is an organic compound with the chemical formula C8H19NO. It is a derivative of hydroxylamine, where the hydroxyl group is replaced by two tert-butyl groups. N,O-di-tert-butylhydroxylamine is a colorless, oily liquid with a molecular weight of 143.24 g/mol. It is used as a stabilizer and antioxidant in various industrial applications, such as in the production of polymers and plastics, to prevent the degradation of materials caused by oxidation. Additionally, it serves as a reagent in organic synthesis, particularly in the preparation of other N-oxides and as a reducing agent in certain chemical reactions. Due to its reactivity, it is important to handle N,O-di-tert-butylhydroxylamine with care, as it can be sensitive to air and moisture.

4747-19-7

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4747-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4747-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4747-19:
(6*4)+(5*7)+(4*4)+(3*7)+(2*1)+(1*9)=107
107 % 10 = 7
So 4747-19-7 is a valid CAS Registry Number.

4747-19-7Relevant academic research and scientific papers

N-tert-Butoxy-N-tert-alkylaminyls. A New Class of Persistent Radicals

Woynar, Helmut,Ingold, K. U.

, p. 3813 - 3815 (1980)

N-tert-Butoxy-N-tert-butylaminyl (1.) and three related radicals have been generated from their parent hydroxylamines in hydrocarbon solution.In the absence of oxygen these radicals are extremely persistent.Their electronic structures, as indicated by their EPR parameters (a14N, a17O, and a13C, all determined without isotopic enrichment) and the N-H bond strength in 1-H (measured as 81.0 kcal/mol), show that the effectiveness of conjugative electron delocalization is reduced relative to that in the isomeric nitroxides.This effect is attributed to the greater electro negativity of oxygen compared with nitrogen.

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