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123-10-4

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123-10-4 Usage

General Description

N,N-Diethyl-N',N'-dimethylethylenediamine, also known as DEDMEDA, is a chemical compound commonly used in organic synthesis and as a catalyst in various chemical reactions. It is a diamine compound with two ethyl groups and two methyl groups attached to the nitrogen atoms. DEDMEDA is a clear, colorless liquid with a strong amine odor and is highly soluble in water. It is often used as a curing agent for epoxy resins, as a stabilizer in the production of polyurethane foams, and as a component in adhesives and coatings. Additionally, DEDMEDA is used in the manufacturing of pharmaceuticals, textiles, and rubber products. It is important to handle DEDMEDA with caution as it is a hazardous material and can cause skin and eye irritation and respiratory issues upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 123-10-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123-10:
(5*1)+(4*2)+(3*3)+(2*1)+(1*0)=24
24 % 10 = 4
So 123-10-4 is a valid CAS Registry Number.

123-10-4SDS

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 N',N'-diethyl-N,N-dimethylethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names N,N-diethyl-N',N'-dimethylethylenediamine

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:123-10-4 SDS

123-10-4Downstream Products

123-10-4Relevant articles and documents

Alkyl-substitution effect of the diamine on coordination geometry and ligand-field strength of niekel(ii) mixed-ligand complexes containing n-alkylethylenediamine, acetylacetonate, and nitrate ligands

Shirase, Hitoshi,Saito, Mariko,Machiko, Arakawa-Itoh,Fukuda, Yutaka

experimental part, p. 230 - 235 (2009/05/30)

Structures and spectral properties have been investigated for nickel(TI) mixed-ligand complexes, [Ni(Me4en)-(acac)(N03)] (1), [Ni(EtMe 3en)(acac)(NO3)] (2), [Ni(asym-Et2Me2en)(acac) (NO3)] (3), [Ni(Et

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