Material Safety Data Sheet. Ethylenediamine. MSDS# Section 1 – Chemical Product and Company Identification. MSDS Name: Ethylenediamine. Etyléndiamín Ethylenediamine for synthesis. CAS , EC Number -6, chemical formula H₂NCH₂CH₂NH₂. – Find MSDS or SDS, a COA, data. Information on: Ethylenediamine Ethylenediamine is corrosive to the eyes and skin. See MSDS section 11 – Toxicological information.

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Ethylenediamine More Suppliers. Edamine [1] 1,2-Diaminoethane, ‘en’ when a ligand.

Ethylenediamine (EDA)

Beijing dtftchem Technology Co. Condensates derived from formaldehyde are plasticizers.

Instructions on what protective equipments should be used to handle the materials. Simply fill in your email address below and click ‘Send To My Email’ get your data sheet emailed to you.

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How it works – 1. Physical and Chemical Properties.



Remove contaminated clothing and wash before reuse. This process involves passing the gaseous reactants over a bed of nickel heterogeneous catalysts. Ethylenediamine is used in large quantities for production of many industrial chemicals. This page was last edited on 19 Octoberat This colorless liquid with an ammonia -like odor is a strongly basic amine. In other projects Wikimedia Commons. Wash clothing before reuse. The derivative NN -ethylenebis stearamide EBS is a commercially significant mold- release agent and a surfactant in gasoline and motor oil.

Other names Edamine [1] 1,2-Diaminoethane, ‘en’ when a ligand. LD 50 median dose. Because of its bifunctional nature, having two amines, it readily forms heterocycles such as imidazolidines.

MSDS shows how the material reacts to environment and how to store it properly. Ethylenediamine is an ingredient in the common bronchodilator drug aminophyllinewhere it serves to solubilize the active ingredient theophylline.

Yes please, I’d like to hear about offers and services. Another industrial route to ethylenediamine involves the reaction of ethanolamine and ammonia: Some imidazoline -containing fungicides are derived from ethylenediamine. Hydroxyethylethylenediamine is another commercially significant chelating agent.

Retrieved 3 May The salen ligandssome of which are used in catalysis, are derived from the condensation of salicylaldehydes and ethylenediamine. Please select either yes or no to receiving news and offers from us.

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Ethylenediamine() MSDS Melting Point Boiling Point Density Storage Transport

If breathing is difficult, give oxygen. Ethylenediamine, like ammonia and other low-molecular weight aminesis a skin and respiratory irritant. The toxicological properties of this substance have not been fully investigated. Wear appropriate protective gloves to prevent skin exposure.

Ethylenediamine has also been used in dermatologic preparations, but has been removed from some because of causing contact dermatitis. Refractive index n D. Safe handling and storage The right first aid measures Protect people close to you. Keep container tightly closed. We’d love to send you exclusive offers and the latest info relating to health and safety and safety data sheets by email and other electronic means. A most prominent derivative of ethylenediamine is the chelating agent EDTAwhich is derived from ethylenediamine via a Strecker synthesis involving cyanide and formaldehyde.