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Methanaminium, N-methyl-N-(4-oxo-2,5-cyclohexadien-1-ylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62972-60-5

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62972-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62972-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62972-60:
(7*6)+(6*2)+(5*9)+(4*7)+(3*2)+(2*6)+(1*0)=145
145 % 10 = 5
So 62972-60-5 is a valid CAS Registry Number.

62972-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-(4-oxocyclohexa-2,5-dien-1-ylidene)azanium

1.2 Other means of identification

Product number -
Other names Methanaminium,N-methyl-N-(4-oxo-2,5-cyclohexadien-1-ylidene)

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:62972-60-5 SDS

62972-60-5Downstream Products

62972-60-5Relevant academic research and scientific papers

Spectrophotometric determination of H2-receptor antagonists via their oxidation with cerium(IV)

Darwish, Ibrahim A.,Hussein, Samiha A.,Mahmoud, Ashraf M.,Hassan, Ahmed I.

, p. 33 - 40 (2008/09/17)

A simple, accurate and sensitive spectrophotometric method has been developed and validated for determination of H2-receptor antagonists: cimetidine, famotidine, nizatidine and ranitidine hydrochloride. The method was based on the oxidation of these drugs with cerium(IV) in presence of perchloric acid and subsequent measurement of the excess Ce(IV) by its reaction with p-dimethylaminobenzaldehyde to give a red colored product (λmax at 464 nm). The decrease in the absorption intensity of the colored product (ΔA), due to the presence of the drug was correlated with its concentration in the sample solution. Different variables affecting the reaction were carefully studied and optimized. Under the optimum conditions, linear relationships with good correlation coefficients (0.9990-0.9994) were found between ΔA values and the concentrations of the drugs in a concentration range of 1-20 μg ml-1. The assay limits of detection and quantitation were 0.18-0.60 and 0.54-1.53 μg ml-1, respectively. The method was validated, in terms of accuracy, precision, ruggedness and robustness; the results were satisfactory. The proposed method was successfully applied to the determination of the investigated drugs in pure and pharmaceutical dosage forms (recovery was 98.3-102.6 ± 0.57-1.90%) without interference from the common excipients. The results obtained by the proposed method were comparable with those obtained by the official methods.

Kinetics and mechanism of the heterogeneous oxidation of N-substituted-p-phenylenediamines over supported zinc oxide

Salem, Ibrahim A.

, p. 249 - 261 (2007/10/03)

The kinetics and mechanism of the oxidation of some N-substituted-p-phenylenediamines over ZnO supported with some transition metal sulfates were investigated at 25°C. The rate of reaction decreased in the following order; N,N,N′,N′-tetramethyl-p-phenylenediamine, TMPPD > N,N-diethyl-p-phenylenediamine, DEPPD > N,N-dimethyl-p-phenylenediamine, DMPPD, due to the positive inductive effect of alkyl groups. For the oxidation of DEPPD, the rate of reaction was observed to have the order: Cu(II) > Fe(III) > Ni(II) > Cr(III) > Mn(II) > Co(II). The initial rate of reaction was decreased with decreasing pH as a result of the protonation of the diamine nitrogen atoms. Also, it follows a first order dependence of the initial concentration of the diamine and attained a maximum at higher concentrations. Moreover, it increased with increasing amount of the oxidant. Greater amounts, however, reduced the rate of reaction as a result of the adsorption of the formed p-semiquinonediimine, S+, by the support. A mechanism is proposed which implies two consecutive electron transfer steps as well as a synproportionation reaction between the diamine and the totally oxidized p-quinonediimine, T.

A Frontier Orbital Study of Substituent Effects in the Deamination of N-Substitued Quinone Di-imines

Grampp, Guenter

, p. 2001 - 2004 (2007/10/02)

The substituent effects on the rate constant of the acid and alkaline deamination of quinone di-imines are explained, using the frontier orbital (FO) perturbation theory.The main contributions to the pertubation energy are electrostatic and orbital interactions.The alkaline deamination is both orbital and charge controlled, whereas the acid deamination is only an orbital-controlled reaction.

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