PRODUCTS

ETHYLENEDIAMINE EDA

Ethylenediamine EDA is used in the formulation of chelating agents, corrosion inhibitors, and scale removers.
Ethylenediamine EDA serves as a precursor in the synthesis of herbicides, pesticides, and fungicides.
Ethylenediamine EDA is utilized in drug synthesis and specialty chemical formulations.

CAS Number: 107-15-3
EC Number: 203-468-6
IUPAC Name: Ethane-1,2-diamine
Molecular Formula: C₂H₈N₂
Molecular Weight: 60.10 g/mol

SYNONYMS:
Ethylenediamine (USP/JP14), Edamine, 1,2-ethanediamine, ethane-1,2-diamine, Ethylendiamin, NCI-C60402, EthylenediamineAnhydrous, Ethyliminum, EDA, EDA, ETHANE-1,2-DIAMINE, 1,2-DIAMINOETHANE, YEA, 1,2-ETHANEDIAMINE, Ethylendiamine, 1,2-Ethylenediamine, Diaminoethane, H2NCH2CH2NH2, Ethyleendiamine, Ethylenediamine, Ethane-1,2-diamine, 1,2-Diaminoethane, 1,2-Ethanediamine, Dimethylenediamine, “en”, Ethylendiaminum, beta-Aminoethylamine, Ethane-1,2-diamine Edamine, 1,2-Diaminoethane, 'en' when a ligand 1,2-Diaminoethane, 1,2-Ethylenediamine, Ethane-1,2-diamine, EDA, Aethaldiamine ethylenediamine Ethane-1,2-diamine 107-15-3 1,2-Ethanediamine 1,2-Diaminoethane Ethylene diamine Ethylendiamine edamine Dimethylenediamine 1,2-Ethylenediamine Aethaldiamin Aethylenediamin Ethyleendiamine Ethylene-diamine beta-Aminoethylamine 1,2-Diaminoaethan Algicode 106L Amerstat 274 1,2-Diamino-ethaan 1,2-Diamino-ethano NCI-C60402 CHEBI:30347 EPA Pesticide Chemical Code 004205 60V9STC53F DTXSID5021881 AI3-24231 DTXCID501881 PB05721 PB-05721 Ethylenediamine (anhydrous) ethyl diamine RefChem:5818 2-aminoethan-1-aminium 203-468-6 Ethylenediamine [JAN] ETHYLENEDIAMINE ANHYDROUS Edamine [INN] MFCD00008204 CHEMBL816 H2NCH2CH2NH2 ETHANE,1,2-DIAMINO NCGC00091527-01 ethane, 1,2-diamino- 1,2-diaminoethane phase II EN 1,2-diaminoethane phase I beta Aethaldiamin [German] Caswell No. 437 1,2-diaminoethane phase I alpha Ethyleendiamine [Dutch] Aethylenediamin [German] Ethylenediamine; Ethane-1,2-diamine Ethylene-diamine [French] Ethane-1,2-diammonium bromide CAS-107-15-3 Ethylenediamine, ReagentPlus(R), >=99% 1,2-Diaminoaethan [German] 1,2-Diamino-ethaan [Dutch] CCRIS 5224 HSDB 535 1,2-Diamino-ethano [Italian] Aminophylline Injection EINECS 203-468-6 UN1604 Ethylenediamine [USP:JAN] BRN 0605263 UNII-60V9STC53F Edamina ethylenediarnine 2-aminoethylamine ethylene di amine 1,4-diazabutane 1,2-diaminoethan ethylene - diamine EDN 1,2-ethylendiamine 1,2-diamino-ethane ethane 1,2-diamine N,N'-ethylenediamine Ethylenediamine, 8CI 1,2-ethylene diamine 1,2-ethylene-diamine Ethylenediamine [UN1604] [Corrosive] .beta.-Aminoethylamine ethane-1, 2-diamine N,N'-ethylene diamine Ethylenediamine, BioXtra 1,2-Diaminoethane;EDA Epitope ID:117724 EC 203-468-6 SCHEMBL3083 ETHYLENEDIAMINE [II] ETHYLENEDIAMINE [MI] SCHEMBL69372 4-04-00-01166 (Beilstein Handbook Reference) Ethylenediamine (USP/JP15) Ethylenediamine (USP/JP17) ETHYLENEDIAMINE [HSDB] SCHEMBL189756 SCHEMBL190090 SCHEMBL228843 BDBM7972 NH2(CH2)2NH2 SCHEMBL3907065 SCHEMBL4425938 ETHYLENEDIAMINE [MART.] ETHYLENEDIAMINE [WHO-DD] 624-59-9 (di-hydrobromide) 333-18-6 (di-hydrochloride) 5700-49-2 (di-hydriodide) Ethylenediamine, analytical standard STR00309 Tox21_111145 Tox21_201202 STL264241 ETHYLENEDIAMINE [EP MONOGRAPH] AKOS000118850 DB14189 ETHYLENEDIAMINE [USP MONOGRAPH] FE04155 UN 1604 Ethylenediamine, for synthesis, 99.0% NCGC00091527-02 NCGC00258754-01 BP-20367 Ethylenediamine [UN1604] [Corrosive] E0077 E0081 NS00003922 EN300-19398 InChI=1/C2H8N2/c3-1-2-4/h1-4H D01114 Ethylenediamine, SAJ special grade, >=99.0% Ethylenediamine, meets USP testing specifications Ethylenediamine, Vetec(TM) reagent grade, >=98% F043401 Q411362 Ethylenediamine, purified by redistillation, >=99.5% TIZANIDINE HYDROCHLORIDE IMPURITY H [EP IMPURITY] Z104473714 Ethylenediamine, puriss. p.a., absolute, >=99.5% (GC) QuadraPure(R) AEA, 100-400 mum particle size, extent of labeling: 1.3 mmol/g loading, 1 % cross-linked with divinylbenzene

Ethylenediamine EDA (EDA; 1,2-diaminoethane; CAS 107-15-3) is the ethyleneamine with the lowest molecular weight.
Ethylenediamine EDA contains two primary amine groups and appears as a colourless liquid.
Ethylenediamine EDA is a highly reactive and versatile molecule.

Ethylenediamine EDA (CAS #000107-15-3, 1,2-diaminoethane) is the lowest molecular weight ethylenediamine.
Ethylenediamine EDA is a single-component product with two primary nitrogens.
Ethylenediamine EDA has an ammonia-like odor and is clear and colorless.

Ethylenediamine EDA, with the chemical formula C2H8N2, is a typical aliphatic diamine and is a colorless or pale yellow oily or watery transparent liquid that produces fumes in the air, with an ammonia-like odor and hygroscopic properties.
Ethylenediamine EDA's molecular weight is 60.10, melting point is 8.5°C, and autoignition point is 385°C.

Ethylenediamine EDA is classified as a basic substance, highly soluble in water and ethanol, slightly soluble in ether, and insoluble in benzene unless absolutely dry.
Ethylenediamine EDA can form azeotropic mixtures with water, n-butanol, and toluene.

Ethylenediamine EDA is flammable when encountering heat, open flames, or oxidizers, posing a moderate risk during combustion.
Ethylenediamine EDA can be sterilized by high pressure or filtration.

Ethylenediamine EDA (EDA) is a highly reactive, colorless liquid with a strong ammonia-like odor, widely used as a building block in various industrial applications.
As a versatile diamine, Ethylenediamine EDA plays a crucial role in chemical synthesis, coatings, water treatment, and pharmaceutical formulations.

Ethylenediamine EDA is a BSE-free single component product with two primary nitrogens.
Ethylenediamine EDA has an ammonia-like odor and is clear and colorless.
Ethylenediamine EDA is versatile and has low vapor pressure, high viscosity, low environmental viscosity, low sensitivity.

Ethylenediamine EDA is REACH compliant.
Ethylenediamine EDA is the organic compound with the formula C₂H₄(NH₂)₂.
This colorless liquid, Ethylenediamine EDA, with an ammonia-like odor is a basic amine.

Ethylenediamine EDA is the first member of the so-called polyethylene amines.
Ethylenediamine EDA is the ethyleneamine with the lowest molecular weight.
Ethylenediamine EDA contains two primary amine groups and is a colorless liquid.

Ethylenediamine EDA (abbreviated as en when a ligand) is the organic compound with the formula C2H4(NH2)2.
Ethylenediamine EDA with an ammonia-like odor is a basic amine.
Ethylenediamine EDA is the first member of the so-called polyethylene amines.

Ethylenediamine EDA is a chelating agent, corrosion inhibitor, mineral & rubber processing aid and plastic lubricant.
Ethylenediamine EDA is the lowest molecular weight ethylenediamine.
Ethylenediamine EDA is a single-component product with two primary nitrogens.

Ethylenediamine EDA is the ethyleneamine with the lowest molecular weight.
Ethylenediamine EDA contains two primary amine groups and is a colorless liquid.
Ethylenediamine EDA appears as a clear colorless liquid with an ammonia-like odor.

Flash point 91 °F and a melting point of Ethylenediamine EDA is 47 °F.
Density of Ethylenediamine EDA is 7.5 lb / gal.
Ethylenediamine EDA is an alkane-alpha,omega-diamine in which the alkane is ethane.

Ethylenediamine EDA has a role as a GABA agonist.
Ethylenediamine EDA derives from a hydride of an ethane.
Ethylenediamine EDA is an organic compound that is used as a building block for the production of many other chemical products.

Ethylenediamine EDA is also used as an excipient in many pharmacological preparations such as creams.
Notably, Ethylenediamine EDA is a contact sensitizer capable of producing local and generalized reactions.
Sensitivity to Ethylenediamine EDA may be identified with a clinical patch test.

Ethylenediamine EDA is a metabolite found in or produced by Escherichia coli.
Ethylenediamine EDA is a small molecule drug with a maximum clinical trial phase of III (across all indications) and has 2 investigational indications.

RN given refers to parent cpd; edamine is the recommended contraction for the Ethylenediamine EDA radical.
The lowest molecular weight ethylenediamine.
Ethylenediamine EDA is a single-component product with two primary nitrogens.

Ethylenediamine EDA has an ammonia-like odor and is clear and colorless.
Ethylenediamine EDA is the lowest molecular weight ethyleneamine.
Ethylenediamine EDA contains two primary nitrogens.

Ethylenediamine EDA is a single-component product that is clear and colorless, with an ammonia-like odor.
Ethylenediamine EDA is the lowest molecular weight ethylenediamine.
Ethylenediamine EDA is a single-component product with two primary nitrogens.

Ethylenediamine EDA has an ammonia-like odor and is clear and colorless.
Ethylenediamine EDA can be found in epoxy-resin hardeners, cooling oils, fungicides, and waxes.
Contact dermatitis from Ethylenediamine EDA is almost exclusively due to topical medicaments.

Occupational contact dermatitis in epoxy-resin systems is rather infrequent.
Ethylenediamine EDA can cross react with triethylenetetramine and diethylenetriamine.
Ethylenediamine EDA was responsible for sensitization in pharmacists handling aminophylline suppositories, in nurses preparing and administering injectable theophylline, and in a laboratory technician in the manufacture of aminophylline tab lets.

Ethylenediamine EDA is an organic compound with the chemical formula H2N(CH2)2NH2.
Ethylenediamine EDA is a colorless liquid with a strong, ammonia-like odor.
Ethylenediamine EDA is a colorless to yellow liquid ammonia-like odor

Ethylenediamine EDA is an alkane-alpha,omega-diamine in which the alkane is ethane.
Ethylenediamine EDA is an organic compound, H2NCH2CH2NH2.
Ethylenediamine EDA is important in inorganic chemistry because it may function as a bidentantate ligand, coordinating to a metal ion by the lone pairs on the two nitrogen atoms.

In the names of complexes Ethylenediamine EDA is given the abbreviation en.
Ethylenediamine EDA is a colorless to yellow liquid with an ammonia-like odor.

Ethylenediamine EDA is a single component pure product that is mainly used as a raw material for crop protection products, in the synthesis of chelating agents and for low-temperature-active bleaching agents.
Ethylenediamine EDA is a clear and colorless product at normal temperature and pressure which has a characteristic smell of an amine.

Ethylenediamine EDA is strongly alkaline and is miscible with water and alcohol.
Ethylenediamine EDA is air sensitive and hygroscopic and absorbs carbon dioxide from the air.

Ethylenediamine EDA is incompatible with aldehydes, phosphorus halides, organic halides, oxidising agents, strong acids, copper, its alloys, and its salts.
Ethylenediamine EDA is a linear aliphatic diamine, widely used as a building block in organic synthesis.

Ethylenediamine EDA readily forms heterocyclic imidazolidine derivatives, because of its bifunctional nature, having two amines.
Ethylenediamine EDA is a clear colourless liquid with an amine smell.
Ethylenediamine EDA is an example of a diamine, a chemical compound with two primary amine groups.

Ethylenediamine EDA has a very specific type of reactivity, and it plays an important role as an intermediate in the synthesis of numerous chemicals.

Ethylenediamine EDA (according to IUPAC nomenclature : ethane-1,2-diamine , often abbreviated as EDA ) is an organic chemical compound belonging to the group of aliphatic primary amines.
More specifically, Ethylenediamine EDA is a diamine.

USES and APPLICATIONS of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is used mainly as a building block for crop protection products, in the synthesis of chelating agents and for low-temperature-active bleaching agents.
The many other applications of Ethylenediamine EDA include polyamides, lubricants, fuel additives and textiles.

Ethylenediamine EDA is used as a building block for the synthesis of bleach activators, chelates and crop protection products.
Furthermore, Ethylenediamine EDA is used as an intermediate in applications like corrosion inhibitors, polyamide resins and lubricants/fuel additives.

Chain extender in the production of poyurethane resin for the water PU Dispersion (PUD).
Products derived from Ethylenediamine EDA are frequently used for bleach activators and chelates in detergents and for fungicides in crop protection area.

Polyamide resins find wide use as binders in printing inks for flexogravure application on certain paper, film, and foil webs and in hot-melt, pressure-sensitive, and heat-seal adhesives for leather, paper, plastic, and metal.
The main polyamide resin type, in addition to the liquid resins used as epoxy hardeners, is prepared generally by the condensation reaction of diamines with di- and polybasic fatty acids.

Thermoplastic polyamides are similarly used in formulating glossy, abrasion-resistant, overprint varnishes.
Ethylenediamine EDA is available as pure substance.
Ethylenediamine EDA is commonly used as an intermediary to produce detergents, paper chemicals, textile auxiliaries, fungicides and polyamides.

Epoxy Curing Agents: Ethylenediamine EDA enhances adhesion, flexibility, and chemical resistance in epoxy coatings and adhesives.
Water Treatment: Ethylenediamine EDA is used in the formulation of chelating agents, corrosion inhibitors, and scale removers.
Agrochemicals: Ethylenediamine EDA serves as a precursor in the synthesis of herbicides, pesticides, and fungicides.

Pharmaceuticals: Ethylenediamine EDA is utilized in drug synthesis and specialty chemical formulations.
Polymers & Resins: Ethylenediamine EDA acts as a key component in polyamide and polyurethane production.
Textiles & Leather: Ethylenediamine EDA improves fabric treatment processes and dyeing applications.

Applications of Ethylenediamine EDA: Bleach Activator, Chelating Agents, Corrosion Inhibitors, Elastomeric Fibers, Fungicides, Fuel Additives, Mineral Processing Aids, Pharmaceutical Intermediate, Plastic Lubricants, Polyamide Resins, Rubber Processing additives,
Textile Additives, and Urethane Chemicals.

Ethylenediamine EDA finds diverse applications in various industries across Europe.
Chemical Intermediates: Ethylenediamine EDA is widely used as a chemical intermediate in synthesizing various organic compounds, including resins, adhesives, and polyamide polymers.

Pharmaceuticals: Ethylenediamine EDA is used in the pharmaceutical industry to produce certain drugs and medications.
Textile Industry: Ethylenediamine EDA is employed in the textile industry as a chemical modifier and fabric softener.
Chemical Synthesis: Ethylenediamine EDA serves as a precursor in the production of various chemicals, including ethylenediaminetetraacetic acid (EDTA), a chelating agent.

Polymer Industry: Ethylenediamine EDA is used in the production of polyurethanes and epoxy resins.
Pharmaceuticals: Ethylenediamine EDA acts as a solubilizing agent in certain drug formulations.
Agriculture: Ethylenediamine EDA is utilized in the synthesis of pesticides and fungicides.

Corrosion Inhibition: Ethylenediamine EDA is employed as a corrosion inhibitor in water treatment processes.
Ethylenediamine EDA is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998.
Ethylenediamine EDA is commonly used as an intermediate to produce detergents, chelates, textile auxiliaries, agrochemicals and polyamides.

Applications of Ethylenediamine EDA: Detergents, Lubricant, Petroleum Additive, Pigments, Polymer Polyols, Printing Ink, Bleaching, Textile Auxiliary, Textile Softeners, Epoxy Coating, Urethane Catalysts, Adhesives.
Ethylenediamine EDA is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998.

Uses of Ethylenediamine EDA: Corrosion inhibitors, Wet-strength resins, Fabric softeners, Epoxy curing agents, Polyamide resins, Fuel additives, Lube oil additives, Asphalt additives, Ore flotation, Corrosion inhibitors, and Ore flotation.

Ethylenediamine EDA is used Asphalt, Additives, Corrosion inhibitors, Epoxy curing agents, Hydrocarbon purification, Lube oil & fuel additives, Mineral processing aids, Polyamide resins, Surfactants, Textile additives-paper wet-strength resins, Fabric softeners, Surfactants, Coatings, Urethanes, Fuel additives, Chemical intermediates, Epoxy curing agents, Lube oils, and Wet strength resins.

Ethylenediamine EDA is used to make other chemicals and as a fungicide.
As a solvent, Ethylenediamine EDA is miscible with polar solvents and is used to solubilize proteins such as albumins and casein.
Ethylenediamine EDA is also used in certain electroplating baths.

Ethylenediamine EDA is used as a corrosion inhibitor in paints and coolants.
Ethylenediamine dihydroiodide (EDDI) is added to animal feeds as a source of iodide.
Chemicals for color photography developing, binders, adhesives, fabric softeners, curing agents for epoxies, and dyes.

Ethylenediamine EDA is used as a compound to sensitize nitromethane into an explosive.
This mixture was used at Picatinny Arsenal during World War II, giving the nitromethane and Ethylenediamine EDA mixture the nickname PLX, or Picatinny Liquid Explosive.

Ethylenediamine EDA is commonly used as an intermediate to produce detergents, chelates, textile auxiliaries, agrochemicals and polyamides.
Ethylenediamine EDA is used in elastomeric fiber and textile.
Ethylenediamine EDA is used in large quantities for production of many industrial chemicals.

Ethylenediamine EDA forms derivatives with carboxylic acids (including fatty acids), nitriles, alcohols (at elevated temperatures), alkylating agents, carbon disulfide, and aldehydes and ketones.
Because of its bifunctional nature, having two amino groups, Ethylenediamine EDA readily forms heterocycles such as imidazolidines.

Ethylenediamine EDA is used as a building block in the synthesis of various chemicals such as polyamides, polyurethanes, and chelating agents.
Ethylenediamine EDA is also used as an intermediate in the production of pesticides, pharmaceuticals, and corrosion inhibitors.
Ethylenediamine EDA is also found in such applications as lubricants, fuel additives, textiles and polyamide resins.

Applications of Ethylenediamine EDA: Chemical Intermediate
Recommended Use of Ethylenediamine EDA: Bleach Activators, Chelating Agents, Corrosion Inhibitors, Fungicides, Fuel additives, Plastic lubricants, Textile additives, Pharmaceutical intermediates,

Elastomeric fibers, Mineral processing aids, Polyamide resins, Surfactants, and Urethane chemicals.
Ethylenediamine EDA is used in numerous industrial proces ses as a solvent for casein or albumin, as a stabilizer in rubber latex and as a textile lubricant.

Intermediate in the manufacture of EDTA; catalytic agent in epoxy resins; dyes, solvent stabilizer; neutralizer in rubber products
Ethylenediamine EDA is used as a stabilizerfor rubber latex, as an emulsifier, as aninhibitor in antifreeze solutions, and intextile lubricants.
Ethylenediamine EDA is also used as a solvent for albumin, shellac, sulfur, and othersubstances.

Edamine is the recommended contraction for the Ethylenediamine EDA radical.
Ethylenediamine EDA is in the manufacture of organic flocculants, urea resins, and fatty bisamides.
Ethylenediamine EDA is used in the production of formulations for use in the printed circuit board and metal finishing industries.

Ethylenediamine EDA is used as intermediate in the production of crop protection agents, hardeners for epoxy resins, leather industry, paint industry, fungicides in crop protection area, and textile industry.
Ethylenediamine EDA is also used as solvent and for the analytical chemistry.

Ethylenediamine EDA is used to produce photographic fixer additive.
For many years, Ethylenediamine EDA has been used in agriculture for the synthesis of herbicides and pesticides that are now key inputs in crop protection and higher agricultural yields.

Ethylenediamine EDA is also utilized as a raw material for the synthesis of chelating agents, polymers, agrochemicals and pharmaceutical intermediates.
Ethylenediamine EDA is commonly used in fungicides, chelating agents like EDTA, resins, textiles, lubricants, and as a solvent and emulsifying agent.

Ethylenediamine EDA is particularly used in complex chemistry for the synthesis of chelating agents (e.g., ethylenediaminetetraacetic acid).
Ethylenediamine EDA is also used as a solvent , stabilizer , and for acid neutralization in oils.

Ethylenediamine EDA is also used in the production of synthetic resins, rubber chemicals, pharmaceuticals, pesticides, inhibitors, and detergents and cleaning agents.
In organic chemistry, Ethylenediamine EDA is also used as a base for the isomerization of allyl alcohols into aldehydes , for the reduction of nitroarenes to azo compounds , and in many other reactions.

Ethylenediamine EDA also serves as an intermediate in the fields of corrosion protection, polyamide resins , and lubricant and fuel additives.
Ethylenediamine EDA is an organic compound that is used as a building block for the production of many other chemical products.

Ethylenediamine EDA is also used as an excipient in many pharmacological preparations such as creams.
Notably, Ethylenediamine EDA is a contact sensitizer capable of producing local and generalized reactions 1.
Sensitivity to Ethylenediamine EDA may be identified with a clinical patch test.

-Ligands in coordination chemistry uses of Ethylenediamine EDA:
With the two nitrogen atoms, which can donate their lone pairs of electrons, Ethylenediamine EDA is widely used as a chelating ligand for coordination chemistry to form bonds to a transition-metal ion such as nickel (II).
The bonds form between the metal ion and the nitrogen atoms of ethylenediamine.

Ethylenediaminetetraacetic acid (EDTA) is a derivate of Ethylenediamine EDA and it is a versatile chelating agent, which could form chelates with both transition-metal ions and main-group ions.
Ethylenediamine EDA is mainly used to synthesize ethylenediaminetetraacetic acid.

EDTA is frequently used in soaps and detergents to form complexes with calcium and magnesium ions in hard water to improve the cleaning efficiency.
Furthermore, EDTA is used extensively as a stabilizing agent in the food industry to promote color retention, to improve flavor retention, and to inhibit rancidity.

-Pharmaceutical ingredient uses of Ethylenediamine EDA:
Ethylenediamine EDA is used to facilitate the dissolution of theophylline.

This combination is known as aminophylline and used to treat and prevent wheezing and trouble breathing caused by ongoing lung disease (e.g. asthma, emphysema, chronic bronchitis).

It is evidenced that there is no molecular association between theophylline and Ethylenediamine EDA in biological media.
The bioavailability of Ethylenediamine EDA is approximately 34% and of theophylline is about 88%.

-Tetraacetylethylenediamine uses of Ethylenediamine EDA:
Ethylenediamine EDA is used as an intermediate in the manufacture of tetraacetyl Ethylenediamine EDA (TAED), a bleaching activator, which is used in detergents and additives for laundry washing and dishwashing.
The amount of TAED used in household cleaning products in Europe was estimated to be 61,000 t in 2001.

-Application of Ethylenediamine EDA in Agriculture:
The application of EDA in Agriculture sector mainly as raw materials for different agrochemicals productions.

That is, the Ethylenediamine EDA would be ued in herbicides, fungicides and insecticides synthesis.
Ethylenediamine EDA will help in the crop management and improve the productions, in this way leads to increase in agricultural productivity and practices in the sustainable farming.

-Other Significant Industries' uses of Ethylenediamine EDA:
● Food & Nutrition:
Ethylenediamine EDA acts as a stabilizer in diverse food formulations.

● Personal Care:
Ethylenediamine EDA is used in the production of surfactants and conditioning agents.

● Construction:
Ethylenediamine EDA is essential for developing high-quality epoxy resins and curing agents.
CASE (Coatings, Adhesives, Sealants, and Elastomers):
Ethylenediamine EDA acts as a curing (hardening) or cross-linking agent in coatings and adhesives.

● Pharmaceutical:
Ethylenediamine EDA serves as a key intermediate in drug synthesis and formulations.

● Industrial Hygiene & Cleaning:
Ethylenediamine EDA is included in formulations for effective cleaning agents.

● Plastics and Rubber:
Ethylenediamine EDA is used in the production of flexible polyurethane foams.

● Petroleum & Gas:
Ethylenediamine EDA functions in the refining process as a valuable chemical additive.

● Lubricants & Greases:
Ethylenediamine EDA is used in formulating high-performance lubricants for various applications.

-Surfactant uses of Ethylenediamine EDA:
*Emulsification:
Ethylenediamine EDA can react with certain acids to form corresponding salts, which have surfactant properties and can be used as emulsifiers.
In industries such as cosmetics and food, they are used to prepare emulsions, creams, and other products, allowing the oil phase and water phase to mix evenly, improving the stability and effectiveness of the products.

*Dispersing effect:
In the industries of coatings and pigments, Ethylenediamine EDA and its derivatives can serve as dispersants to ensure that pigment particles are evenly distributed in the medium, preventing pigment agglomeration and enhancing the opacity and coloring power of the coatings.

*Epoxy resin curing agent:
Ethylenediamine EDA can undergo a cross-linking reaction with the epoxy groups in the epoxy resin, resulting in the curing of the epoxy resin to form a three-dimensional network structure.

The cured epoxy resin has good mechanical properties, chemical resistance, and insulation performance, and Ethylenediamine EDA is widely used in fields such as coatings, adhesives, and electronic packaging.
For example, epoxy resin coatings cured with Ethylenediamine EDA exhibit excellent weather resistance and anti-corrosion properties, making them suitable for the protection of building exteriors, bridges, and more.

Ethylenediamine hydrate, with the CAS number 6780-13-8, is a chemical compound that consists of Ethylenediamine EDA combined with water molecules.
Ethylenediamine EDA is a colorless, viscous liquid with a strong ammonia-like odor, and it is known for its ability to form chelates with metal ions due to its two amine functional groups.

In its hydrated form, Ethylenediamine EDA typically exists as a colorless to pale yellow liquid or solid, depending on the concentration of water.
Ethylenediamine EDA is hygroscopic, meaning it can absorb moisture from the air.

Ethylenediamine EDA hydrate is soluble in water and polar organic solvents, making it useful in various applications, including as a building block in organic synthesis, in the production of pharmaceuticals, and as a complexing agent in analytical chemistry.
However, Ethylenediamine EDA is important to handle this compound with care, as it can be irritating to the skin, eyes, and respiratory system.
Proper safety precautions should be taken when working with Ethylenediamine EDA hydrate.

-Industrial uses of Ethylenediamine EDA:
Ethylenediamine EDA functions as a reactive intermediate in the synthesis of carbamate fungicides and in the preparation of dyes, synthetic waxes, resins, insecticides and asphalt wetting agents.

Ethylenediamine EDA is a solvent for casein, albumin, shellac, and sulfur; an emulsifier; a stabilizer for rubber latex; an inhibitor in antifreeze solutions; and a pharmaceutic aid (aminophylline injection stabilizer).
Ethylenediamine EDA is also an important ingredient in hair-settings, cold wave lotions, and nail polish.

-Chemical raw materials uses of Ethylenediamine EDA:
*Synthetic Polymers:
Ethylenediamine EDA is an important raw material for the synthesis of polyamides, polyurethanes, and other polymers.
For example, Ethylenediamine EDA can react with diacids to produce polyamides, which have excellent mechanical properties, wear resistance, and corrosion resistance, and are widely used in fields such as fibers and engineering plastics.

*Production of pesticides and pharmaceutical intermediates:
In pesticide production, Ethylenediamine EDA can be used to synthesize certain fungicides and insecticides.
In the pharmaceutical field, Ethylenediamine EDA serves as an intermediary in the synthesis of various drugs, such as those used to produce aminophylline, which can be used to treat respiratory difficulties caused by bronchial asthma and cardiogenic pulmonary edema.

-Metal ion chelating agent uses of Ethylenediamine EDA:
*Industrial Cleaning:
Ethylenediamine EDA can form stable chelates with many metal ions, and it can be used in industrial cleaning to remove rust and scale from metal surfaces, preventing metal corrosion.
For example, in the cleaning of car engines, Ethylenediamine EDA can effectively remove scale and rust from within the engine, ensuring the normal operation of the engine.

*Electroplating Industry:
In the electroplating process, Ethylenediamine EDA acts as a chelating agent to regulate the concentration and stability of metal ions in the plating solution, making the electroplated layer more uniform and dense, thereby improving the quality of electroplated products.

-Alkaline reagent uses of Ethylenediamine EDA:
*Acid-base neutralization:
Ethylenediamine EDA is basic and can act as a basic reagent in some chemical reactions to adjust the acidity and alkalinity of the reaction system.

For example, in certain organic synthesis reactions, Ethylenediamine EDA is necessary to carry out the reaction under basic conditions, and Ethylenediamine EDA can provide the alkaline environment.

*Deacidification reaction:
In oil processing, Ethylenediamine EDA can be used to remove free fatty acids from fats and oils, improving the quality of the fats.

CHEMICAL PROPERTIES of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA, a polyamine, is a strongly alkaline, colorless, clear, thick liquid.
Ethylenediamine EDA has ammonia odor.
Ethylenediamine EDA is a solid below 8.5 ℃.
The Odor Threshold of Ethylenediamine EDA is 1.0 ppm

PHYSICAL PROPERTIES of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA islear, colorless, volatile, slight viscous, hygroscopic liquid with a sweet, ammonia-like odor.
The average least detectable odor threshold concentrations in water at 60 °C and in air at 40 °C were 12 and 52 mg/L, respectively.

BENEFITS & CHARACTERISTICS of ETHYLENEDIAMINE EDA:
*Versatility:
Due to its bifunctional nature, Ethylenediamine EDA can react with a wide range of compounds, making it a valuable intermediate in chemical synthesis.

*Reactivity:
The amino groups in Ethylenediamine EDA can form complexes with metal ions, enhancing its utility in various applications.

*Solubility:
Ethylenediamine EDA's miscibility with water allows for easy incorporation into aqueous formulations.

*Stability:
Ethylenediamine EDA is stable under standard conditions, facilitating its handling and storage.

PHYSICAL DETAILS AND PROPERTIES of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is an organic compound with the chemical formula C₂H₈N₂ and a 60.10 g/mol molecular weight.
Ethylenediamine EDA appears as a colorless, hygroscopic liquid with a strong ammonia-like odor.
Ethylenediamine EDA is miscible with water and soluble in many organic solvents.

PRODUCTION METHODS of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is primarily produced through the reaction of ethylene dichloride with aqueous ammonia.
The reaction results in the formation of Ethylenediamine EDA, which can be further processed and purified.

FEATURES & BENEFITS of ETHYLENEDIAMINE EDA:
*Highly reactive diamine with strong chelating properties.
*Excellent solubility in water and organic solvents.
*Ethylenediamine EDA improves performance in coatings, adhesives, and polymers.
*Versatile applications across multiple industries.

PRECURSOR TO CHELATION AGENTS, DRUGS, AND AGROCHEMICALS of ETHYLENEDIAMINE EDA:
A most prominent derivative of Ethylenediamine EDA is the chelating agent EDTA, which is derived from Ethylenediamine EDA via a Strecker synthesis involving cyanide and formaldehyde.
HydroxyethylEthylenediamine is another commercially significant chelating agent.

Numerous bio-active compounds and drugs contain the N–CH2–CH2–N linkage, including some antihistamines.
Salts of ethylenebisdithiocarbamate are commercially significant fungicides under the brand names Maneb, Mancozeb, Zineb, and Metiram.
Some imidazoline-containing fungicides are derived from ethylenediamine.

PHARMACEUTICAL INGREDIENT of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is an ingredient in the common bronchodilator drug aminophylline, where it serves to solubilize the active ingredient theophylline.
Ethylenediamine EDA has also been used in dermatologic preparations, but has been removed from some because of causing contact dermatitis.

When used as a pharmaceutical excipient, after oral administration Ethylenediamine EDA's bioavailability is about 0.34, due to a substantial first-pass effect.
Less than 20% is eliminated by renal excretion.

Ethylenediamine EDA-derived antihistamines are the oldest of the five classes of first-generation antihistamines, beginning with piperoxan, aka benodain, discovered in 1933 at the Pasteur Institute in France, and also including mepyramine, tripelennamine, and antazoline.

The other classes are derivatives of ethanolamine, alkylamine, piperazine, and others (primarily tricyclic and tetracyclic compounds related to phenothiazines, tricyclic antidepressants, as well as the cyproheptadine-phenindamine family)

ROLE IN POLYMERS of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA, because it contains two amine groups, is a widely used precursor to various polymers.
Condensates derived from formaldehyde are plasticizers.
Ethylenediamine EDA is widely used in the production of polyurethane fibers.
The PAMAM class of dendrimers are derived from ethylenediamine.

PRODUCTION METHODS of ETHYLENEDIAMINE EDA:
The production of Ethylenediamine EDA is by the catalytic amination of monoethanolamine or the reaction of aqueous ammonia with 1,2-dichloroethane.
U.S. Production is estimated at greater than 33,000 tons in 1975.

BENEFITS of ETHYLENEDIAMINE EDA:
*Consistent and predictable reaction products
*Easily derivatized
*Low vapor pressure
*High viscosity
*Low environmental impact
*Suitable for harsh conditions
*Low sensitivity
*Versatile

RELATED COMPOUNDS of ETHYLENEDIAMINE EDA:
-Related alkanamines
*1,2-Diaminopropane, 1,3-Diaminopropane

-Related compounds
*Ethylamine, Ethylenedinitramine

FUNCTIONS of ETHYLENEDIAMINE EDA:
*Raw Material,
*Scale inhibitor,
*Chemical Intermediate,
*Chemical Reagent,
*Dispersing Agent,
*Scale Removal and Control.

SYNTHESIS of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is produced industrially by treating 1,2-dichloroethane with ammonia under pressure at 180 °C in an aqueous medium (EDC process).
In this reaction, hydrogen chloride is generated, which forms a salt with the amine.

Ethylenediamine EDA is liberated by addition of sodium hydroxide and can then be recovered by fractional distillation.
Diethylenetriamine (DETA) and triethylenetetramine (TETA) are formed as by-products.

Another industrial route to Ethylenediamine EDA involves the reaction of ethanolamine and ammonia.
This process involves passing the gaseous reactants over a bed of nickel heterogeneous catalysts.

Ethylenediamine EDA can be prepared in the lab by the reaction of either ethylene glycol or ethanolamine and urea, followed by decarboxylation of the ethyleneurea intermediate.
Ethylenediamine EDA can be purified by treatment with sodium hydroxide to remove water followed by distillation.

Ethylenediamine EDA is a basic amine with two amino groups attached to a two-carbon ethylene chain.
Ethylenediamine EDA is a widely used building block in chemical synthesis, with applications in various industries due to its reactivity and versatility.

AIR & WATER REACTIONS of ETHYLENEDIAMINE EDA:
*Hygroscopic.
*Fumes in the air.
*Water soluble.
*Biodegrades readily.

REACTIVITY PROFILE of ETHYLENEDIAMINE EDA:
A base.
Highly reactive with many compounds.

Can react violently with acetic acid, acetic anhydride, acrolein, acrylic acid, acrylonitrile, allyl chloride, carbon disulfide, chlorosulfonic acid, epichlorohydrin, ethylene chlorohydrin, hydrogen chloride, mesityl oxide, nitric acid, oleum, AgClO4, sulfuric acid, beta-propiolactone and vinyl acetate.

Incompatible with strong acids, strong oxidizers (perchlorate salts), and chlorinated organic compounds.
Ethylenediamine EDA is also incompatible with halogenated organic compounds and metal halides.

Readily absorbs carbon dioxide from the air to give crusty solid deposits.
Ethylenediamine EDA reacts violently with ethylene chlorohydrin.

CHARACTERISTICS of ETHYLENEDIAMINE EDA:
PHYSICAL PROPERTIES of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA has a relative gas density of 2.07 (density ratio to dry air at the same temperature and pressure).
A relative density of the vapor-air mixture of 1.01 (density ratio to dry air at 20 °C and atmospheric pressure).
The density is 0.90 g cm−3 at 20 °C.
Ethylenediamine EDA also has a vapor pressure of 12.4 hPa at 20 °C, 22.6 hPa at 30 °C, 39.4 hPa at 40 °C, and 66.3 hPa at 50 °C.

CHEMICAL PROPERTIES of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is a flammable liquid belonging to the group of aliphatic primary amines.
Ethylenediamine EDA is completely miscible with water, forming a hydrate.
Aqueous solutions of Ethylenediamine EDA are strongly basic.

Furthermore, diaminoethane is hygroscopic and fumes in humid air.
Ethylenediamine EDA is considered to be moderately to highly volatile.
An aqueous solution with a concentration of 100 g l−1 has a pH of 12.2 at 25 °C.

SYNTHESIS of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA can be synthesized from ethanolamine (EA) with ammonia over acidic types of zeolite catalyst.2
Ethylenediamine EDA is produced industrially by the reaction of 1,2-dichloroethane with ammonia in a liquid base under high temperature and high presseure.

The synthesis of Ethylenediamine EDA from 1,2-dichloroethane is ClCH2CH2Cl + 2NH3 → NH2CH2CH2NH22HCl
ClCH2CH2Cl + NH2CH2CH2NH22HCl + 2NH3 → NH2CH2C H2NHCH2CH2NH3*3HCl + NH4HCl
Nevertheless, there are too many byproducts during the reaction.

The key of this synthesis is to improve the selectivity of reaction product and the application of advanced separation methods to obtain high product purity.

CHEMICAL REACTIVITY of ETHYLENEDIAMINE EDA:
*Reactivity with Water Gives off heat, but reaction is not hazardous;
*Reactivity with Common Materials: No reaction;
*Stability During Transport: Stable;
*Neutralizing Agents for Acids and Caustics: Flush with water;
*Polymerization: Not pertinent;
*Inhibitor of Polymerization: Not pertinent.

PHYSICAL PROPERTIES of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is a hygroscopic liquid that is water‑ and most organic solvent-soluble.
Ethylenediamine EDA is highly reactive and forms chelates.
Ethylenediamine EDA is an important starting material in chemical synthesis and agriculture.

EXTRACTION AND PRESENTATION of ETHYLENEDIAMINE EDA:
There are several processes and process variants in the chemical industry for the large-scale production of ethylenediamine.
The most commonly used method for the synthesis of Ethylenediamine EDA today is the reaction of monoethanolamine with ammonia at temperatures of 160–230 °C and pressures of 150–250 bar in the presence of hydrogen over transition metal oxide catalysts , which consist essentially of nickel and copper oxide as well as zirconium dioxide and are supported on aluminum oxide (Al 2 O 3 ), in the liquid phase.

Reaction of monoethanolamine with ammonia to form Ethylenediamine EDA and water in the presence of a nickel oxide/zirconium dioxide catalyst supported on alumina
The reaction is preferably carried out in fixed-bed reactors.

Tubular reactors and tube bundle reactors are particularly suitable , as molten salts maintain a nearly constant temperature throughout the reaction.
In this process, byproducts such as diethylenetriamine (DETA) and triethylenetetramine (TETA) are formed in addition to ethylenediamine.

These byproducts are separated by multi-stage distillation under pressure.
Ethylene glycol can also be used instead of monoethanolamine.

However , ammonia must be used in a twofold molar excess.
A second large-scale process for the production of Ethylenediamine EDA involves the reaction of 1,2-dichloroethane with ammonia under pressure at 180 °C in an aqueous medium.

Copper or nickel catalysts arranged as a fixed bed are also used as catalysts.
Reaction of 1,2-dichloroethane with ammonia to Ethylenediamine EDA and hydrochloric acid
This produces hydrogen chloride , which is initially present in bound form as the hydrochloride of the amine.

Ethylenediamine EDA is converted into its free form by addition of sodium hydroxide and can then be isolated from the mixture by rectification.
Diethylenetriamine (DETA) and triethylenetetramine (TETA) are also formed as by-products.
Ethylenediamine EDA (EDA) is a colorless, alkaline liquid with an ammonia-like odor.

Ethylenediamine EDA is a strong base that’s soluble in water, alcohol, ether, and insoluble in benzene.
Ethylenediamine EDA readily absorbs carbon dioxide from the air.

COORDINATION CHEMISTRY of ETHYLENEDIAMINE EDA:
Ethylenediamine EDA is a well-known bidentate chelating ligand for coordination compounds, with the two nitrogen atoms donating their lone pairs of electrons when Ethylenediamine EDA acts as a ligand.

Ethylenediamine EDA is often abbreviated "en" in inorganic chemistry.
The complex [Co(en)3]3+ is a well studied example.
Schiff base ligands easily form from ethylenediamine.

For example, the diamine condenses with 4-Trifluoromethylbenzaldehyde to give to the diimine.
The salen ligands, some of which are used in catalysis, are derived from the condensation of salicylaldehydes and ethylenediamine.

RELATED LIGANDS of ETHYLENEDIAMINE EDA:
Related derivatives of Ethylenediamine EDA include ethylenediaminetetraacetic acid (EDTA), tetramethylEthylenediamine (TMEDA), and tetraethylEthylenediamine (TEEDA).
Chiral analogs of Ethylenediamine EDA include 1,2-diaminopropane and trans-diaminocyclohexane.

PHYSICAL and CHEMICAL PROPERTIES of ETHYLENEDIAMINE EDA:
Chemical Formula: C2H8N2
Molecular Weight: 60.10 g/mol
Molar Mass: 60.100 g·mol−1
Appearance: Colourless to pale yellow liquid
Odor: Ammoniacal
Density: 0.90 g/cm³
Melting Point: 8 °C
Boiling Point: 116 °C
Solubility in Water: Miscible

Flash Point: 34 °C
Autoignition Temperature: 385 °C
Vapor Pressure: 1.3 kPa at 20 °C
Log P (Octanol/Water): −2.057
Refractive Index: 1.4565
Explosive Limits: 2.7–16%
Molecular Properties:
XLogP3: −2
Hydrogen Bond Donor Count: 2

Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 1
Exact Mass: 60.068748264 Da
Monoisotopic Mass: 60.068748264 Da
Topological Polar Surface Area: 52 Å²
Heavy Atom Count: 4
Formal Charge: 0
Complexity: 6

Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Thermodynamic Properties:

Heat Capacity (C): 172.59 J·K⁻¹·mol⁻¹
Standard Molar Entropy (S°298): 202.42 J·K⁻¹·mol⁻¹
Standard Enthalpy of Formation (ΔfH°298): −63.55 to −62.47 kJ·mol⁻¹
Standard Enthalpy of Combustion (ΔcH°298): −1.8678 to −1.8668 MJ·mol⁻¹
Chemical Formula: C2H8N2
Molecular Weight: 60.12 g/mol
Appearance: Clear liquid, colorless to pale yellow
Odor: Strong ammoniacal / amine-like

Physical State: Liquid
pH (100 g/L, 20 °C): 12.2
Density: 0.899 g/mL at 25 °C
Melting Point: 8.5 °C
Boiling Point: 118–119.7 °C
Flash Point: 38–93 °C (closed cup / literature)
Autoignition Temperature: 405 °C
Decomposition Temperature: >120 °C

Viscosity: Dynamic 1,265–1,725 mPa·s at 25 °C;
kinematic not available
Water Solubility: Miscible (~1,000 g/L)
Solubility in Ethanol: Soluble
Vapor Pressure: 10–12 hPa at 20 °C
Relative Vapor Density: 2.07 (vs air)
Partition Coefficient (Log P, n-octanol/water): −2.04
Upper/Lower Explosive Limits: 2–17% (V)
Explosive Properties: Not classified as explosive

Oxidizing Properties: None
Refractive Index: 1.4565 (n20/D)
Specific Gravity: 0.899
Form: Liquid, fuming in air
Air Sensitivity: Sensitive
Registry and Reference IDs:
EINECS: 203-468-6
CBNumber: CB2127811

MDL Number: MFCD00008204
Merck Index: 14,3795
BRN: 605263
Chemical Formula: C2H8N2
Molecular Weight: 60.10 g/mol
Appearance: Colorless to pale yellow liquid
Odor: Strong ammoniacal / ammonia-like
Physical State: Liquid

pH (100 g/L, 20 °C): 12.2
Density: 0.899–0.90 g/cm³ at 20–25 °C
Melting Point: 8–8.5 °C
Boiling Point: 116–118 °C
Flash Point: 93 °F (38–93 °C) closed cup
Autoignition Temperature: 405 °C
Decomposition Temperature: >120 °C
Viscosity: Dynamic 1,265–1,725 mPa·s at 25 °C

Water Solubility: Miscible (~1,000 g/L)
Solubility in Ethanol: Soluble
Vapor Pressure: 10–12.4 hPa at 20 °C; increases with temperature
(22.6 hPa at 30 °C; 39.4 hPa at 40 °C; 66.3 hPa at 50 °C)
Relative Vapor Density: 2.07 (vs air)
Refractive Index: 1.4565 (n20/D, 20 °C)
LogP (Octanol/Water): −1.6 to −2.057
Henry’s Law Constant: 1.69 × 10⁻⁹ atm·m³/mol at 25 °C

Dielectric Constant: 16.0 (18 °C)
pKa / Protonation: pKa1 ≈ 6.90, pKa2 ≈ 9.95 for the doubly protonated molecule;
literature pKa ~10.7 at 0 °C
Explosive Limits: 2–17% (V)
Form: Liquid, fuming in air
Air Sensitivity: Sensitive
Storage Conditions: Flammables area, cool, protected from air
Regulatory / Reference Data:
CAS Number: 107-15-3

EINECS: 203-468-6
InChIKey: PIICEJLVQHRZGT-UHFFFAOYSA-N
Merck Index: 14,3795
BRN: 605263
FDA EAFUS / Food Additive: Ethylenediamine
FDA 21 CFR: 173.320; 175.105; 175.300; 176.180; 176.300; 178.3120
NIST Chemistry Reference: Ethylenediamine (107-15-3)
EPA Substance Registry System: Ethylenediamine (107-15-3)
UNSPSC Code: 41116107
NACRES: NA.25

FIRST AID MEASURES of ETHYLENEDIAMINE EDA:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available

ACCIDENTAL RELEASE MEASURES of ETHYLENEDIAMINE EDA:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of ETHYLENEDIAMINE EDA:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of ETHYLENEDIAMINE EDA:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of ETHYLENEDIAMINE EDA:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.

STABILITY and REACTIVITY of ETHYLENEDIAMINE EDA:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Possibility of hazardous reactions:
No data available