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Phenol, 2-(hydroxyamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91367-87-2

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91367-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91367-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91367-87:
(7*9)+(6*1)+(5*3)+(4*6)+(3*7)+(2*8)+(1*7)=152
152 % 10 = 2
So 91367-87-2 is a valid CAS Registry Number.

91367-87-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxyamino)phenol

1.2 Other means of identification

Product number -
Other names Phenol,2-(hydroxyamino)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91367-87-2 SDS

91367-87-2Upstream product

91367-87-2Relevant academic research and scientific papers

Investigations on the Kinetics and Mechanism of Polarigraphic Reduction of o-, m- and p-Nitrotoluenes and o-, m- and p-Nitrophenols in the presence of Ionic and non-Ionic Surfactants

Singh, M.,Chandra, K.

, p. 977 - 989 (2007/10/02)

Polarographic behaviour of o-, m- and p-nitrotoluenes (4percent, V/V, ethanolic solution) in the presence of ionic and non-ionic surfactants at their concentrations just sufficient to suppress the maxima has been studied as a function of pH of Britton-Robinson (BR) buffer.The present study aims at investigating the kinetics and mechanism of the reduction of these compounds at the d.m.e. which has been found to be diffusion-controlled and irreversible.The potential-dependent rate constant, kf,h has been calculated by Koutecky's method at different pH values of BR buffer and the values of kinetic parameters (αna and kf,h0) have been calculated from log kf,h Vs Ed.e. plots which are linear thereby suggesting that only a single rate-determining step is involved in the reduction of each depolarizer.Based on the values of kinetic parameter, αna and the variation of E1/2 with pH, the stoichiometry of the rate-determinig step, in each case, has been established thereby leading to the postulation of a mechanism for the polarographic reduction of each depolarizer.

Kinetics and Mechanism of Polarographic Reduction of Aromatic Nitro Compounds in Aqueous Alcoholic Medium

Ratan, Ram,Rani, Rama,Singh, Mukhtar

, p. 664 - 670 (2007/10/02)

Polarographic reduction of nitrobenzene, ortho-, meta- and para- chloronitrobenzenes, nitrotoluenes, nitrophenols and nitrobenzaldehydes has been studied in 25percent (v/v) aqueous ethanolic solutions, using Britton-Robinson (BR) buffer of varying pH values.KCl (0.1 M) has been used as the supporting electrolyte and Triton X-100 (0.001percent) as the maxima suppressor.The potential-dependent rate constant, kf,h has been calculated by Koutecky's method at different pH values and the values of kinetic parameters (αna and kf,h) have been calculated from logkf,h versus Ed.e. plots which are linear thereby suggesting that only a single rate-determining step is involved in the electrode process of each depolarizer.Based on the values of kinetic parameter, αna and the variation of E1/2 with pH, the stoichiometry of the rate-determining step has been established.This has led to the postulation of a tentative mechanism for the polarographic reduction of each depolarizer.Besides, the effect of the nature and position of various substituents, viz.Cl, CH3, OH and CHO on the kinetics of the polarographic reduction of NO2 group has been investigated.

Polarographic Behaviour of Some ortho-Substituted Nitrobenzenes: Evaluation of Polarographic ortho-Shift

Ganapathy, K,Ramanujam, M

, p. 1087 - 1089 (2007/10/02)

The polarographic characteristics of thirteen ortho-substituted nitrobenzenes have been studied at 35 deg C +/- 0.1 deg C in a well-buffered medium of 50percent (v/v) aqueous ethanol, having pH 5.8.Reduction process for all the compounds is found to be ir

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