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Ethylenediamine
(redirected from Ethylene diamine)

   Also found in: Medical, Wikipedia 0.01 sec.
ethylenediamine [¦eth·ə·‚lēn′dī·ə‚mēn]
(organic chemistry)
NH2CH2CH2NH2Colorless liquid, melting at 8.5°C, soluble in water; used as a solvent, corrosion inhibitor, and resin and in adhesive manufacture.

Ethylenediamine 

(also called 1,2-diaminoethane), H2NCH2CH2NH2, a colorless liquid that has the odor of ammonia.

Ethylenediamine has a boiling point of 116.5°C, a melting point of 8.5°C, and a density of 0.899 g/cm3 at 20°C. It is soluble in water and alcohol and slightly soluble in ether, but it is insoluble in benzene. It is a strong base.

The salts of ethylenediamine and fatty acids are used in the textile industry as softeners, and ethylenediamine tartrate has piezoelectric properties. Ethylenediaminetetraacetic acid is produced by reacting ethylenediamine with chloroacetic acid. Ethylenediamine is used in the manufacture of such products as fungicides, dyes, latex stabilizers, emulsifiers, and plasticizers, and it is also used as a curing agent for epoxy resins. It is produced mainly by the action of ammonia on dichloroethane.

Ethylenediamine is toxic. The maximum permissible concentration of its vapors in the air is 0.001 mg per liter.



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The chief element in chelation treatment is EDTA that is ethylene diamine tetra-acetic acid that is a protein similar to molecule when gradually introduced into the blood stream connects with raw materials such as lead, iron, calcium and copper and takes them to the kidney where they are emitted.
In this study, we synthesized PUFs from 4,4'-diphenylmethane diisocyanate (PMDI) and polypropylene glycols (PPG), which were prepared from four different types of initiators such as sorbitol and its combinations with toluene diamine (TDA), ethylene diamine (EDA), and sucrose/ glycerin.
Many of them produce toxic or hazardous side effects, but she has had success with ethylene diamine used in combination with thiocyanate salts.
 
 
 
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