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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Avoid ingestion and inhalation. If breathing is difficult, give oxygen. Wear appropriate protective gloves to prevent skin exposure. LD 50 median dose.
Complete a full risk assessment for your workplace so that you can map out all the hazards into a single comprehensive COSHH assessment. The salen ligandssome of which are used in catalysis, are derived from the condensation of salicylaldehydes and ethylenediamine.
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This process involves passing the gaseous reactants over a bed of nickel heterogeneous catalysts. Media related to Ethylenediamine at Wikimedia Commons. Please select either yes or no to receiving news and offers from us.
It forms derivatives with carboxylic acids including fatty acidsnitrilesalcohols at elevated temperaturesalkylating agents, carbon disulfideand aldehydes and ketones. It is often abbreviated “en” in inorganic chemistry.
If conscious and alert, rinse mouth and drink cupfuls of milk or mdss. Ethylenediamine-derived antihistamines are the oldest of the five classes of first-generation antihistaminesbeginning with piperoxan aka benodain, discovered in at the Pasteur Institute in France, and also including mepyraminetripelennamineand antazoline. How it works – 1.
Describes the effects when workers come into contact with the chemical and how to proceed in case of an accident. I strongly believe that health and safety is the responsibility of every single employer. If not breathing, give artificial respiration. Do NOT induce vomiting. I have made myself a promise to ensure that employers’ and the public are provided with the necessary knowledge and tools to make their workplaces safer.
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Ethylenediamine – Wikipedia
Unless tightly contained, liquid etuylenediamine will release toxic and irritating vapors into its surroundings, especially on heating. It is a widely used building block in chemical synthesis, with approximatelytonnes produced in Hydroxyethylethylenediamine is another commercially significant chelating agent. Butyl rubber Butylated hydroxytoluene 1,2-Dibromoethane 1,2-Dichloroethane Dimethyl methylphosphonate 2,4-Dimethyltert-butylphenol Dinonylnaphthylsulfonic acid 2,6-Di-tert-butylphenol Ecalene Ethylenediamine Metal deactivator Methyl tert-butyl ether Nitromethane Tetraethyllead Tetranitromethane.
Ethylenediamine is a well-known bidentate chelating ligand for coordination compoundswith the two nitrogen atoms donating their lone pairs of electrons when ethylenediamine acts as a ligand. The other classes are derivatives of ethanolaminealkylaminepiperazineand others primarily tricyclic and tetracyclic compounds related to phenothiazinestricyclic antidepressantsas well as the cyproheptadine – phenindamine family.
The toxicological properties of this substance have not been fully investigated. Contact permission We’d love to send you exclusive offers and the latest info relating to health and safety ethyelnediamine 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. This colorless liquid with an ammonia -like odor is a strongly basic amine.
Ethylenediamine is an ingredient in etjylenediamine common bronchodilator drug aminophyllinewhere it serves to solubilize the active ingredient theophylline. Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA’s eye and face protection regulations in 29 CFR Beijing Ouhe Technology Co.
It is widely used in the production of polyurethane fibers. Wash clothing before reuse. Views Read Edit View history. Ethylenediamine, like ammonia and other low-molecular weight aminesis a skin and respiratory irritant. Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes.
Chiral analogs of ethylenediamine include 1,2-diaminopropane and trans -diaminocyclohexane. Minimize dust generation and accumulation.