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Ethanaminium, N-ethyl-N-(4-imino-3-methyl-2,5-cyclohexadien-1-ylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33624-85-0

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33624-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33624-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33624-85:
(7*3)+(6*3)+(5*6)+(4*2)+(3*4)+(2*8)+(1*5)=110
110 % 10 = 0
So 33624-85-0 is a valid CAS Registry Number.

33624-85-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl(4-imino-3-methyl-2,5-cyclohexylidene)ammonium salt

1.2 Other means of identification

Product number -
Other names Diethyl-(4-imino-3-methyl-cyclohexa-2,5-dienylidene)-ammonium

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:33624-85-0 SDS

33624-85-0Upstream product

33624-85-0Downstream Products

33624-85-0Relevant academic research and scientific papers

Activation parameters and mechanism of the deamination of N-substituted quinone monoimines and di-imines

Nickel, Ulrich,Jaenicke, Walther

, p. 1601 - 1605 (1980)

The deamination rates of six N-substituted quinone monoimines in aqueous solution were measured by a stopped-flow method at temperatures between 278 and 323 K in the pH range between 1 and 9 using u.v. spectra. The observed rate constants are given by k = k′[H2O] + k″[OH-]; k′ and k″ differ by 12 orders of magnitude. The enthalpies of activation of k′ and k″ are nearly equal; the entropies of activation are strongly negative for k′ and strongly positive for k″. The activation parameters of the acid and alkaline deamination of N-substituted quinone di-imines were also measured. With regard to the activation entropies similar results were found as for the quinone monoimines. For all deaminations a common mechanism with a preceding solvation equilibrium is proposed.

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