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DIETHYLENETRIAMINE (DETA)

Diethylenetriamine is the structural analog of diethylene glycol. Diethylenetriamine appears as a yellow liquid with an ammonia-like odor.

DIETHYLENETRIAMINE (DETA)

Diethylenetriamine CAS number: 111-40-0

Diethylenetriamine EC number: 203-865-4

Diethylenetriamine IUPAC name: N '- (2-aminoethyl) ethane-1,2-diamine

Synonyms;

DETA; dietilentriamin; dietilen triamin; diethylenetriamine; diethylenetriamin; dıethylenetrıamıne; dıethylenetrıamın; diethylene triamine; diethylenetriamin; di ethylene tri amine; di etilen tri amin; DİETİLENTRİAMİN; DİETİLEN TRİAMİN; DİETHYLENETRİAMİNE; DİETHYLENETRİAMİN; DIETHYLENETRIAMINE; DIETHYLENETRIAMIN; DİETHYLENE TRİAMİNE; DİETHYLENETRİAMİN; Dİ ETHYLENE TRİ AMİNE; Dİ ETİLEN TRİ AMİN; Dietilentriamin; Dietilen Triamin; Diethylenetriamine; Diethylenetriamin; Dıethylenetrıamıne; Dıethylenetrıamın; Diethylene Triamine; Diethylenetriamin; Di Ethylene Tri Amine; Di Etilen Tri Amin; N-(2-aminoetil)-1,2-etandiamin; 2,2ı-diaminodietilen amin; diethylene triamine; diethylenetriamine; diethylenetriamine diacetate; diethylenetriamine hydrochloride; diethylenetriamine monohydrochloride; diethylenetriamine trihydrofluoride; DIETHYLENETRIAMINE; Bis(2-aminoethyl)amine; 111-40-0; 2,2'-Diaminodiethylamine; Diethylene triamine; Barsamide 115; N,N-Bis(2-aminoethyl)amine; 1,4,7-Triazaheptane; 2,2'-Iminodiethylamine; (Aminoetil) etandiamin; 1,4,7-Triazaheptan; 1,5-Diamino-3-azapentan; 2,2'-Diaminodietilamin; 2,2'-Iminobisethylamine; 2,2'-Iminodietilamin; 2,2-Iminodietilamin; 3-Azapentan-1,5-diamin; Aminoetiletandiamin; Bis (2-aminoetil) amin; Bis [«beta» -aminoetil] amin; DETA; Dietilamin, 2,2'-diamino-; Dietilentriamin; Dietilentriamin eklentisi; Etilamin, 2,2'-iminobis-; Etilendiamin, N- (2-aminoetil) -; N- (2-Aminoetil) -1,2-etandiamin; N- (2-Aminoetil) etilendiamin; N, N-Bis (2-aminoetil) amin; 2- (2-AMİNOETİLAMİNO) ETİLAMİN; AMİNOETİLETANEDİAMİN; ANKAMİN DETA; 3-AZAPENTAN-1,5-DİAMİN; BETA, BETA'-DİAMİNODİETİLAMİN; BİS (2-AMİNOETİL) AMİN; BİS (BETA-AMİNOETİL) AMİN; BIS- (2-AMİNOETİL) AMİN; CHS-P 1; DEH 20; DETA; 1,5-DİAMİNO-3-AZAPENTAN; 2,2' DİAMİNODİETİLAMİN; Dietilentriamin; DETA; dietilentriamin; dietilen triamin; diethylenetriamine; diethylenetriamin; dıethylenetrıamıne; dıethylenetrıamın; diethylene triamine; diethylenetriamin; di ethylene tri amine; di etilen tri amin; DİETİLENTRİAMİN; DİETİLEN TRİAMİN; DİETHYLENETRİAMİNE; DİETHYLENETRİAMİN; DIETHYLENETRIAMINE; DIETHYLENETRIAMIN; DİETHYLENE TRİAMİNE; DİETHYLENETRİAMİN; Dİ ETHYLENE TRİ AMİNE; Dİ ETİLEN TRİ AMİN; Dietilentriamin; Dietilen Triamin; Diethylenetriamine; Diethylenetriamin; Dıethylenetrıamıne; Dıethylenetrıamın; Diethylene Triamine; Diethylenetriamin; Di Ethylene Tri Amine; Di Etilen Tri Amin; 2,2'-İMİNOBİS (ETANAMİN); 2,2'-İMİNOBİSETİLAMİN; N, N-BIS (2-AMİNOETİL) AMİN; N- (2-AMİNOETİL) -1,2-ETANDİAMİN; N- (2-AMİNOETİL) 1,2-ETANDİAMİN; N- (2-AMİNOETİL) ETİLENDİAMİN; 1,4,7-TRİAZAHEPTAN; Dietilentriamin; CAS111-40-0; Bis (2-aminoetil) amin; Dietilen triamin; 2,2'-Diaminodietilamin; Barsamide 115; Epikür T; Ancamine DETA; 1,4,7-Triazaheptan; 2,2'-Iminodietilamin; N, N-Bis (2-aminoetil) amin; Aminoetiletandiamin; 1,2-Ethanediamin, N- (2-aminoetil) -; 3-Azapentan-1,5-diamin; İmino-bis-etilamin; N- (2-Aminoetil) -1,2-etandiamin; N- (2-aminoetil) etan-1,2-diamin; 1,5-Diamino-3-azapentan; 2,2'-Iminodi (etilamin); 2,2'-Iminobis (etanamin); Bis (beta-aminoetil) amin; 2- (2-Aminoetilamino) etilamin; Epon 3223; Etilamin, 2,2'-iminobis-; dien; Dietilamin, 2,2'-diamino-; DEH 20; (Aminoetil) etandiamin; dietilentriamin; NSC 446; UNII-03K6SX4V2J; Texacure EA-20; CCRIS 4794; HSDB 525; N- (2-Aminoetil) etilendiamin; C4H13N3; 2,2'-Iminobisethylamine; EINECS 203-865-4; N '- (2-aminoetil) etan-1,2-diamin; N1- (2-aminoetil) etan-1,2-diamin; BRN 0605314; Bis [--aminoetil] amin; 1,2-Ethanediamin, N1- (2-aminoetil) -; 03K6SX4V2J; CHEMBL303429; DETA; dietilentriamin; dietilen triamin; diethylenetriamine; diethylenetriamin; dıethylenetrıamıne; dıethylenetrıamın; diethylene triamine; diethylenetriamin; di ethylene tri amine; di etilen tri amin; DİETİLENTRİAMİN; DİETİLEN TRİAMİN; DİETHYLENETRİAMİNE; DİETHYLENETRİAMİN; DIETHYLENETRIAMINE; DIETHYLENETRIAMIN; DİETHYLENE TRİAMİNE; DİETHYLENETRİAMİN; Dİ ETHYLENE TRİ AMİNE; Dİ ETİLEN TRİ AMİN; Dietilentriamin; Dietilen Triamin; Diethylenetriamine; Diethylenetriamin; Dıethylenetrıamıne; Dıethylenetrıamın; Diethylene Triamine; Diethylenetriamin; Di Ethylene Tri Amine; Di Etilen Tri Amin;  CHEBI: 30629; Etilendiamin, N- (2-aminoetil) -; Dietilentriamin; DSSTox_CID_5050; Dietilentriamin,% 98 +; DSSTox_RID_77641; DSSTox_GSID_25050; CAS-111-40-0; bis (2-amino-etil) -amin; di-etilentriamin; di (2-aminoetil) amin; 2,2-Iminodietilamin; Dietilentriamin eklentisi; 1,4,7-triaza-heptan; Etilamin, 2'-iminobis-; 2,2-iminodi (etilamin); Dietilamin, 2'-diamino-; 2,2'-diamino-dietilamin; 2,2'-Iminobis-Etilamin; 3-aza-1,5-pentandiamin; EC 203-865-4; 1, N-(2-aminoethyl)-; 2, 2'-Diaminodiethylamine; 3-Aza-1,5-diaminopentane; bis-(2-amino-ethyl)-amine; beta ,beta '; diaminodiethylamine; n-(2-aminoethyl)-ethylenediamine; beta.,.beta.'-Diaminodiethylamine; n1-(2-aminoethyl)-1,2-ethanediamine; MCULE-4803305991; n-(2-Aminoethyl)-1, 2-ethanediamine; Diethylenetriamine, ReagentPlus(R), 99%; Diethylenetriamine [UN2079] [Corrosive]; N-(2-Aminoethyl)-1,2-ethanediamine, 9CI; N * 1 * - (2-Amino-etil) -etan-1,2-diamin; N- (2-Aminoetil) -1,2-etandiamin; bis (2-Aminoetil) amin; DETA; 2,2'-Diaminodietilamin; Di etilen triamin; diethylene triamine; dietilentriamin; DETA; N-(2-aminoethyl-1,2-ethanediamine); di ethylene tri amine; di etilen tri amin; dietilen triamine; etilentriamin; 2,2'-Iminobis (ethylamine); Bis(2-aminoethyl)amine; 2,2'-Diaminodiethylamine (Aminoetil) etandiamin; DETA; dietilentriamin; dietilen triamin; diethylenetriamine; diethylenetriamin; dıethylenetrıamıne; dıethylenetrıamın; diethylene triamine; diethylenetriamin; di ethylene tri amine; di etilen tri amin; DİETİLENTRİAMİN; DİETİLEN TRİAMİN; DİETHYLENETRİAMİNE; DİETHYLENETRİAMİN; DIETHYLENETRIAMINE; DIETHYLENETRIAMIN; DİETHYLENE TRİAMİNE; DİETHYLENETRİAMİN; Dİ ETHYLENE TRİ AMİNE; Dİ ETİLEN TRİ AMİN; Dietilentriamin; Dietilen Triamin; Diethylenetriamine; Diethylenetriamin; Dıethylenetrıamıne; Dıethylenetrıamın; Diethylene Triamine; Diethylenetriamin; Di Ethylene Tri Amine; Di Etilen Tri Amin; 1,2-Etanediamin, N- (2-aminoetil) -; 1,4,7-Triazaheptane; 1,5-Diamino-3-azapentan; 2,2'-diamino-dietilamin; 2,2'-iminobis (etanamin); 2,2'-iminobis-etilamin; 2,2'-iminobis-etilendiamin, n- (2-aminoetil) –etilamin; bis (2-Aminoetil) amin, N- (2-Aminoetil) -1,2-etandiamin, DETA, 2,2'-Diaminodietilamin; bis (2-aminoetil) amin; Dietilentriamin; IE1225000; MFCD00008171; N- (2-Aminoetil) -1, 2-etandiamin; N- (2-Aminoetil) -1, 2-etandiamin; N- (2-Aminoetil) -1, 2-etandiamin; N- (2-aminoetil) et ane-1,2-diamin; (Aminoetil) ethaned iamine; [111-40-0]; 1,2-Ethanediamin, N- (2-aminoetil) -; 1,2-Etanediamin, N1- (2-aminoetil) -; 2,2′-Diaminodietil amin; 2,2′-Iminodiethylam ine; 2,2'-diamino-Diethy ilamin; 2,2'-Iminobis (etan amin); 2,2'-iminobisethyla; 2,2'-Iminobis-Etil amin; 2,2'-Iminodi (ethyla mine); 2,2-Iminodiethylami ne; bütan-1,3 –diamin; Ancamine DETA; Barsamide 115; Bis (2-amino-etil) – amin; Bis (β-aminoetil) amin; DETA; dietilentriamin; dietilen triamin; diethylenetriamine; diethylenetriamin; dıethylenetrıamıne; dıethylenetrıamın; diethylene triamine; diethylenetriamin; di ethylene tri amine; di etilen tri amin; DİETİLENTRİAMİN; DİETİLEN TRİAMİN; DİETHYLENETRİAMİNE; DİETHYLENETRİAMİN; DIETHYLENETRIAMINE; DIETHYLENETRIAMIN; DİETHYLENE TRİAMİNE; DİETHYLENETRİAMİN; Dİ ETHYLENE TRİ AMİNE; Dİ ETİLEN TRİ AMİN; Dietilentriamin; Dietilen Triamin; Diethylenetriamine; Diethylenetriamin; Dıethylenetrıamıne; Dıethylenetrıamın; Diethylene Triamine; Diethylenetriamin; Di Ethylene Tri Amine; Di Etilen Tri Amin; Bis [β-aminoetil] amin; DETA; Di (2-aminoetil) amino ne; -Diaminodietilamin; Dien; Dietil enetriamin; Dietilamin, 2,2'- diamino-; dietilen triamin; DİETİLENETRİAMİN; Dietilentriamin; Etilamin, 2,2'-im inobis-; Etilendiamin, N- (2-aminoetil) -; İmino-bis-etilamin; -Iminodietilamin; InChI = 1 / C4H13N3 / c5- 1-3-7-4-2-6 / h7H, 1-6H; N- (2-Aminoetil) -1; N- (2-Aminoetil) -1,2 -etandiamin, 9CI; N '- (2-aminoetil) etan-1,2-diamin; N- (2-Aminoetil) etilendiamin; N- (2-Aminoetil) -Et hylenediamin; N * 1 * - (2-Amino-etil ) -etan-1,2-diamin; N, N-BIS (2-AMINOETHY L) AMİN; N1- (2-aminoetil) -1,2 –Etandiamin; N1- (2-aminoetil) etan-1,2-diamin; β '-diaminodieth ylamine; β, β'-Diaminodietil amin; DETA; dietilentriamin; dietilen triamin; diethylenetriamine; diethylenetriamin; dıethylenetrıamıne; dıethylenetrıamın; diethylene triamine; diethylenetriamin; di ethylene tri amine; di etilen tri amin; DİETİLENTRİAMİN; DİETİLEN TRİAMİN; DİETHYLENETRİAMİNE; DİETHYLENETRİAMİN; DIETHYLENETRIAMINE; DIETHYLENETRIAMIN; DİETHYLENE TRİAMİNE; DİETHYLENETRİAMİN; Dİ ETHYLENE TRİ AMİNE; Dİ ETİLEN TRİ AMİN; Dietilentriamin; Dietilen Triamin; Diethylenetriamine; Diethylenetriamin; Dıethylenetrıamıne; Dıethylenetrıamın; Diethylene Triamine; Diethylenetriamin; Di Ethylene Tri Amine; Di Etilen Tri Amin;

 

DIETHYLENETRIAMINE (DETA)

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine;

DETA (diethylenetriamine) is formed as a result of the reaction of ethylenediamine and ethylene dichloride. DETA (diethylenetriamine) wet strength resins are used in corrosion inhibitors, fuel additives, epoxy curing agents, textile detergents, softeners, asphalt additives formulations. Diethylenetriamine is the second linear member of the ethyleneamine family. It is seen that the difference in boiling and melting point is wider compared to ethylenediamine in our stocks. Diethylenetriamine is available in barrels from our stocks.

Diethylenetriamine is an analog of diethylene glycol. It has similar chemical behavior and uses similar to ethylene diamine. It is a weak base and its aqueous solution is alkaline. It is used as a solvent for the extraction of sulfur and acid gas in the oil industry. Diethylenetriamine has been shown to exhibit diuretic function. Diethylenetriamine belongs to the Polyamine family. These are compounds containing more than one amine group. It belongs to the class of organic compounds known as dialkylamines. These are organic compounds that contain a dialkylamine group, characterized by two alkyl groups attached to the amino nitrogen.

Diethylenetriamine appears as a yellow liquid with an ammonia-like odor. Diethylenetriamine less dense than water. Diethylenetriamine is corrosive to metals and tissues. Vapors heavier than air. Burns, though probably difficult to ignite. Toxic nitrogen oxides formed during combustion. Diethylenetriamine is used as a solvent for plastics and dyes and in chemical synthesis. Diethylenetriamine is a triamine and a polazaalkane. Diethylenetriamine (DETA), a secondary amine, is synthesized from ethanol. The ability of diethylenetriamine to retain carbon monoxide from aqueous solutions has been studied. The toxicity of diethylenetriamine DETA was evaluated. The coupling reaction of diethylenetriamine DETA with carboxyl-terminated magnetic particles was analyzed.

Diethylenetriamine is a collector that enhances the buoyancy separation for use in the recovery of iron and other metals and for certain ore types including gold and pyrite. Diethylenetriamine is also used as an anti-shrinkage agent in concrete, which reduces surface tension and minimizes shrinkage / cracking as water evaporates from the concrete. Diethylenetriamine is also a building block for asphalt modification additives and in the production of imidazoline-based corrosion inhibitors. Diethylenetriamine is a building block in the production of imidazoline based corrosion inhibitors.

DETA is a weak base and its aqueous solution is alkaline. Asphalt is used to produce anti-stripping agents, emulsifiers, chelating agents, epoxy curing agents and wet strength resins. DETA can be used to produce polyamide resins for application in paints and adhesives. Diethylenetriamine neutralizes acids in exothermic reactions, forming salts plus water. It may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides and acid halides. Combustible gaseous hydrogen can be produced in combination with strong reducing agents such as hydrides.

Uses and properties: It is the simplest cyclic ethylene amine with two secondary amine groups. It is a moisture-penetrating crystal. Soluble in water, alcohol, glycerol, hydrocarbons and glycols. DETA; It is the main component of anthelmintics and psychoactive drugs. It is used as a solvent for sulfur, acidic gas, resin, as a component in the field of fuel and oil (modified polyamides, corrosion inhibitors, fuel additives, epoxy, curing agents, texture softeners and adhesion promoters) and as a saponification agent of acidic materials. It is used in pharmaceuticals, pesticides, hardeners for epoxy resins, additives for fuel and lubricants, corrosion inhibitors, paper and textile industry. These products are widely used in textile auxiliaries, detergents, cosmetics, paper, agriculture, medicine and many other sectors.

Diethylenetriamine (abbreviated as Diene or DETA) and also known as 2,2'-Iminodi (ethylamine)) is an organic compound of formula HN (CH 2 CH 2, NH 2) 2. This colorless hygroscopic liquid is soluble in water and polar organic solvents, but not simple hydrocarbons. Diethylenetriamine is the structural analog of diethylene glycol. Its chemical properties are similar to those for ethylene diamine and it has similar uses. This is a weak base and aqueous solution is alkali. (Diethylenetriamine) Ethylene dichloride from ethylenediamine, which is a byproduct of DETA production. Diethylenetriamine is a common curing agent for epoxy resins in epoxy adhesives and other thermosets. Diethylenetriamine is N-alkylated upon reaction with epoxide groups forming crosslinking.

Diethylenetriamine appears as a yellow liquid with an ammonia-like odor. Less dense than water. It is corrosive to metals and tissues. Vapors heavier than air. Burns, though probably difficult to ignite. Toxic nitrogen oxides formed during combustion. It is used as a solvent for plastics and paints and in chemical synthesis.

Diethylenetriamine neutralizes acids in exothermic reactions, forming salts plus water. It may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides and acid halides. Combustible gaseous hydrogen can be produced in combination with strong reducing agents such as hydrides. Prolonged inhalation of vapors may cause asthma. The liquid burns the skin and eyes. Skin rash may occur. Short-term contact with concentrated diethylenetriamine can cause serious local injury to the eyes and skin, similar to the action of strong base. Human subjects are susceptible to sensitization responses as a response to dermatitis or asthma. A time-weighted average restart for diethylenetriamine of 1 ppm (ACGIH 1986). Special Hazards of Combustion Products: When heated, irritating vapors are produced. Poisoning by skin contact and intraperitoneal routes. Moderately toxic if swallowed. Caustic. Seriously irritating to skin and eyes. In high concentrations, vapor causes irritation, nausea and vomiting in the respiratory tract. Repeated exposure may cause asthma and skin sensitization. Burn when exposed to heat or flame; May react with oxidizing agents. Mixture with nitromethane is a shock sensitive explosive. Cellulose with high surface area ignites in contact with nitrate. Use alcohol foam to fight fire. Emits toxic NOx fumes when heated to decomposition. See also AMINS. DETA has a strong odor similar to ammonia, but does not provide enough warning for dangerous concentrations.

The chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. The DIETHYLENETRIAMINE molecule contains a total of 19 bonds, there are 6 non-H bond (s), 4 rotatable bond (s), 2 primary amine (s) (aliphatic) and 1 secondary amine (s) (aliphatic).

Ethylenediamine is a colorless to yellowish strongly alkaline liquid that melts at 8.5 ° C, boils at 116 ° C; It is completely soluble in water and soluble alcohol. It is a manufactured chemical that does not occur naturally. It has two primary amine groups. Ethylenediamines have a homologous odd-numbered amine (on an even-numbered linear carbon chain) series; diethylenetriamine (linear C-4 diamine), triethylenetetramine (linear C-6 triamine), tetraethylenepentamine (linear C-8 pentamine), and pentaethylenehexamine (linear C-10 hexamine).

Diethylenediamine is the simplest cyclic ethyleneamine (C-4) called piperazine. It has two secondary amine groups in the cyclic system. It is a crystalline compound that melts at 105 ° C; Soluble in water, alcohol, glycerol and glycols. It is used as the main ingredient of anthelmintics and psychoactive drugs. Aminoethylpiperazine is also a member of C-6 cyclic ethyleneamine containing aminoethyl linked to a nitrogen in piperazine. Accordingly, it has a primary, a secondary and a tertiary nitrogen atom. It is used in the synthesis of catalysts, epoxy curing agents and corrosion inhibitors. Aminoethylethanolamine (AEEA) is an analogue of diethylenetriamine. A hydroxyl group replaces a primary amine group. AEEA has a primary amine, a secondary amine, and a primary hydroxyl group. AEEA is a useful intermediate in the production of surfactants, chelating agents and curing agents. Other branched or cyclic ethylenediamines include N, N'-Bis- (2-aminoethyl) piperazine) [CAS #: 6531-38-0], N - [(2-aminoethyl) 2-aminoethyl] piperazine) [CAS #: 24028 -46-4], tris (2-aminoethyl) amine [CAS No: 4097-89-6].

Ethylenediamines are produced by reacting aqueous ammonia with 1,2-dichloroethane. This process gives the polyamine mixture in the form of hydrochloride salts. The next step is to neutralize the salts with aqueous caustic soda to separate free amines. Individual free amines are isolated by fractional distillation. Ethylenediamines can undergo various reactions due to their combination of reactivity, basicity and surface activity and the basic functionality of the nitrogen atom. Therefore, they are important intermediates for a wide variety of chemical syntheses. Examples of products obtained by reacting amines are as follows:

With carboxylic acid derivatives (acids, esters, anhydrides or acyl halides): amides and amidoamines

With fatty acid: imidazoline

With cyanide or nitrile: with amidoamines, polyamides, imidazolines

With urea: substituted urea and ammonia

With ethyleneimines: hydroxyalkyl amine derivatives

With aliphatic alcohols and glycols: alkylated ethyleneamines or cyclic ethyleneamines

With alkyl or aryl halides: substituted amines

With aliphatic aldehydes: imidazolidine substituted

With carbon disulfide: thiocarbamates

With carbon dioxide: carbamate

With inorganic acids: water soluble salts

Ethylenediamine is used as chelating agents that form a very important bidentate ligand. The main application is to produce chelating agents such as ethylenediaminetetraacetic acid (EDTA). Carbamate is used in the production of fungicides, surfactants and paints. It is also useful in the production of accelerators or curing agents in the epoxy industry. Additional applications include photographic enhancement chemicals and cutting oils, especially bleach activators for low temperature wash powders, lubricant and fuel additives for plastics and polyamide processing.

Diethylenetriamine is a yellow, hygroscopic liquid; Boiling point of 206 ° C; It is soluble in water and hydrocarbons. It is used as a solvent for sulfur, acidic gas, resin, and as a fuel and oil field component. It is used as an intermediate product as saponification agent for organic synthesis (modified polyamides, corrosion inhibitors, fuel additives, epoxy curing agents, fabric softeners and adhesion enhancers) and acidic materials.

Triethylenetetramine is a clear to yellowish oily liquid; melting point 12 C, boiling point 280 C. Miscible with water and the solution is alkaline ((pH 10 at 10% solution). Reacts with ketones, halogenated hydrocarbons, nitriles, epoxides and strong oxidants. Commercial triethylenetetramine linear TETA (typically 60%) and Branched or cyclic TETA mixture such as N, N'-Bis (2-aminoethyl) piperazine, N- [1- (2-piperazin-1-yl-ethyl)] ethane-1, 2-diamine, tris- (2-aminoethyl) ) -amine TETA and its derivatives are used as epoxy curing agents, their applications are similar to ethylenediamine and diethylenetriamine.

End uses of ethylenediamine family products include:

Dispenser-detergent

• Modified Polyamides

Fabric softeners

Ore Flotation Agents

Emulsifiers

Corrosion inhibitors

Adhesives

• Binding Agents

Chelating Agents

• Bleach Activators

• Epoxy Curing Agent

 

BENEFITS OF DIETHYLENETRIAMINE (DETA)

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine;

Diethylenetriamine is an analog of diethylene glycol. It has similar chemical behavior and uses similar to ethylene diamine. It is a weak base and its aqueous solution is alkaline. It is used as a solvent for the extraction of sulfur and acid gas in the oil industry. Diethylenetriamine has been shown to exhibit diuretic function. Diethylenetriamine belongs to the Polyamine family. These are compounds containing more than one amine group. It belongs to the class of organic compounds known as dialkylamines. These are organic compounds that contain a dialkylamine group, characterized by two alkyl groups attached to the amino nitrogen.

Diethylenetriamine creates consistent and predictable reaction products. Diethylenetriamine is readily derived. Diethylenetriamine has a low vapor pressure. Diethylenetriamine has high viscosity. Diethylenetriamine has a low environmental impact. Diethylenetriamine is suitable for harsh conditions. Diethylenetriamine has low sensitivity. Diethylenetriamine is versatile.

DIETHYLENETRIAMINE (DETA) USAGE AREAS

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine

Diethylenetriamine is used as corrosion inhibitors. Diethylenetriamine is used in wet strength resins. Diethylenetriamine is used in fabric softeners. Diethylenetriamine is used as epoxy curing agents. Diethylenetriamine is used in polyamide resins. Diethylenetriamine is used as fuel additives. Diethylenetriamine lubricating oil is used as additives. Diethylenetriamine Asphalt is used as additives. Diethylenetriamine is used in ore flotation. Diethylenetriamine is used as corrosion inhibitors. Diethylenetriamine is used in ore flotation. Diethylenetriamine is used in asphalt. Diethylenetriamine is used as weft materials. Diethylenetriamine is used in hydrocarbon purification. Diethylenetriamine is used as mineral oil and fuel additives. Diethylenetriamine is used as mineral processing aids. Diethylenetriamine is used as surfactants. Diethylenetriamine textile additives-paper is used in wet strength resins. It is used in diethylenetriamine coatings. Diethylenetriamine is used as chemical intermediates. Diethylenetriamine is a hardener in Bisphenol A type epoxy resins. It has been reported as a sensitizer in ultrasonic baths, synthetic lubricants and carbonless copy paper for cleaning jewelery. Diethylenetriamine is a corrosive liquid and a solvent. Diethylenetriamine is produced by reacting ethylene dichloride and ammonia. It is used as a solvent, in organic synthesis, and in a variety of industrial applications, including use as a fuel component. Diethylenetriamine is a solvent for sulfur, acidic gas, resin and dye intermediates for organic synthesis; saponification agent for acidic materials; fuel component; hardener for epoxy resins. Hardener and stabilizer for epoxy resins; Used as a solvent for paints, acid gases and sulfur. Diethylenetriamine is produced by the reaction of ethylene dichloride with ammonia. A yellow liquid with an ammonia-like odor. Less dense than water. It is corrosive to metals and tissues. Vapors heavier than air. Burns, though probably hard to ignite. Toxic nitrogen oxides formed during combustion. It is used as a solvent for plastics and paints and in chemical synthesis. Diethylenetriamine is water soluble.

Uses and properties: It is the simplest cyclic ethylene amine with two secondary amine groups. It is a moisture-penetrating crystal. Soluble in water, alcohol, glycerol, hydrocarbons and glycols. DETA; It is the main component of anthelmintics and psychoactive drugs. It is used as a solvent for sulfur, acidic gas, resin, as a component in the field of fuel and oil (modified polyamides, corrosion inhibitors, fuel additives, epoxy, curing agents, texture softeners and adhesion promoters) and as a saponification agent of acidic materials. It is used in pharmaceuticals, pesticides, hardeners for epoxy resins, additives for fuel and lubricants, corrosion inhibitors, paper and textile industry. These products are widely used in textile auxiliaries, detergents, cosmetics, paper, agriculture, medicine and many other sectors.

DETA is a weak base and its aqueous solution is alkaline. Asphalt is used to produce anti-stripping agents, emulsifiers, chelating agents, epoxy curing agents and wet strength resins. DETA can be used to produce polyamide resins for application in paints and adhesives.

Diethylenetriamine is used as a solvent for plastics, dyes and chemical synthesis. It acts as a curing agent for epoxy resins. As a triangular ligand, it forms complexes like Co (diene) (NO 2) 3 in coordination chemistry. It is also used as a fuel additive. It reacts with fatty acid and causes the formation of amidoamines used as corrosion inhibitors in the petroleum industry. It is associated with the unsymmetrical dimethylhydrazine to prepare the hydride, a propellant for liquid fuel rockets. Diethylenetriamine is an analog of diethylene glycol. It has similar chemical behavior and uses similar to ethylene diamine. It is a weak base and its aqueous solution is alkaline. It is used as a solvent for the extraction of sulfur and acid gas in the oil industry. Diethylenetriamine has been shown to exhibit diuretic function. Diethylenetriamine belongs to the Polyamine family. These are compounds containing more than one amine group. It belongs to the class of organic compounds known as dialkylamines. These are organic compounds that contain a dialkylamine group, characterized by two alkyl groups attached to the amino nitrogen.

Diethylenetriamine (DETA), the component of ion exchange resins for use in food processing, for example in the production of grapefruit juice, is a colorless hygroscopic liquid soluble in water and hydrocarbons. Diethylenetriamine is an analog of diethylene glycol. It has similar chemical behavior and uses similar to ethylene diamine. It is a weak base and its aqueous solution is alkaline. It is used as a solvent for the extraction of sulfur and acid gas in the oil industry. Diethylenetriamine has been shown to exhibit diuretic function. Diethylenetriamine belongs to the Polyamine family. These are compounds containing more than one amine group. It belongs to the class of organic compounds known as dialkylamines. These are organic compounds that contain a dialkylamine group, characterized by two alkyl groups attached to the amino nitrogen.

Diethylenetriamine (DETA) is used in a wide range of applications. Diethylenetriamine (DETA) can be used directly as a hardener in Epoxy application or as a building block for Polyamidoamines.

Adhesives and Sealants

Its materials Diethylenetriamine (DETA) is used as a hardener for epoxy resins. Diethylenetriamine (DETA) finds application in hot melt, pressure sensitive and heat sealable adhesives for leather, paper, plastic and metal.

Coatings

Diethylenetriamine (DETA) is used as a hardener for epoxy resins. It can be accelerated by phenols, acids and some alcohols, which react with the epoxy group and form a cross-linked structure.

Detergents

Diethylenetriamine (DETA) Used in the synthesis of chelating agents, surfactants and fabric softeners.

Inks

Diethylenetriamine (DETA), which reacts with di- and polybasic fatty acids, is used in the production of polyamide resins used as a binder in flexographic printing inks in certain paper, film and foil webs. Diethylenetriamine (DETA) Thermoplastic polyamides are similarly used in formulating glossy, abrasion resistant, overprinting varnishes.

Pulp and Paper

Diethylenetriamine (DETA) is mainly used as a building block for wet strength resins for paper applications. Diethylenetriamine (DETA) It is converted with a dicarboxylic acid (eg adipic acid) to a polyaminoamide which is then crosslinked with epichlorohydrin.

 

Other Additional applications of diethylenetriamine (DETA) include asphalt additives, corrosion inhibitors, lubricating oil / fuel additives, and mineral processing aids.

Diethylenetriamine (DETA) is the imported chelate raw material in the chemistry of metal complexes. Bromine is converted by acetic acid to DTPA (Diethylenetriaminepentaacetic acid).

Diethylenetriamine is effective for the direct cleavage of unactivated carbamates and ureas without additional reagents and catalysts. Various carbamates and urea were split to obtain products with good yields and the reactions were not affected by air or moisture. Unique chemoselective cleavage of carbamate and urea was also achieved in the presence of amides.

N- (2-aminoethyl) -1,2 ethanediamine) with two primary and one secondary nitrogen. Used in asphalt additives, chelating agents, corrosion inhibitors, drainage aids, epoxy curing agents, fabric softeners, lubricating oil and fuel additives, mineral processing aids, polyamide resins, surfactants, textile additives, paper wet strength resins. It has a low molecular weight.

Diethylenetriamine (DETA) is a hygroscopic liquid and is soluble in water and polar organic solvents but not in simple hydrocarbons. DETA is the structural analog of diethylene glycol. Its chemical properties are similar to those for ethylene diamine and it has similar uses.

Diethylenetriamine (DETA) is used as a solvent for sulfur, acid gases, resins and dyes. Diethylenetriamine (DETA) can also be a saponification agent or a fuel component for acidic materials.

PHYSICAL AND CHEMICAL PROPERTIES OF DIETHYLENETRIAMINE (DIETHYLENETRIAMINE - DETA)

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine

Diethylenetriamine appears as a yellow liquid with an ammonia-like odor. Less dense than water. It is corrosive to metals and tissues. Vapors heavier than air. Burns, though probably difficult to ignite. Toxic nitrogen oxides formed during combustion. It is used as a solvent for plastics and paints and in chemical synthesis. Diethylenetriamine is an analog of diethylene glycol. It has similar chemical behavior and uses similar to ethylene diamine. It is a weak base and its aqueous solution is alkaline. It is used as a solvent for the extraction of sulfur and acid gas in the oil industry. Diethylenetriamine has been shown to exhibit diuretic function. Diethylenetriamine belongs to the Polyamine family. These are compounds containing more than one amine group. It belongs to the class of organic compounds known as dialkylamines. These are organic compounds that contain a dialkylamine group, characterized by two alkyl groups attached to the amino nitrogen.

Diethylenetriamine Physical State: Liquid

Diethylenetriamine Color: colorless to yellow

Diethylenetriamine Odor: amine-like

Diethylenetriamine pH: Strong alkali

Diethylenetriamine Vapor Pressure: 0.37 mm Hg @ 20C

Diethylenetriamine Viscosity: 0.0714 Ps 20 C

Diethylenetriamine Boiling Point: 207 ° C

Diethylenetriamine Freezing / Melting Point: -35 ° C

Diethylenetriamine Autoignition Temperature: 395 degrees C (743,00 degrees F)

Diethylenetriamine Flash Point: 102 degrees C (215,60 degrees F)

Diethylenetriamine Explosion Limits, lower: 2.0%

Diethylenetriamine Explosion Limits, upper: 11.6%

Diethylenetriamine Decomposition Temperature: None.

Diethylenetriamine Solubility in water: soluble in water.

Diethylenetriamine Specific Gravity / Density: .9586

Diethylenetriamine Molecular Formula: C4H13N3

Diethylenetriamine Molecular Weight: 103.1111

OVERVIEW OF EMERGENCIES

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine

Diethylenetriamine Harmful in contact with skin and if swallowed. Diethylenetriamine Causes burns. Diethylenetriamine May cause sensitization by skin contact. Diethylenetriamine Abrasive. Diethylenetriamine Causes eye burns. Diethylenetriamine May cause corneal damage. Diethylenetriamine May cause irreversible eye injuries. Diethylenetriamine Causes skin burns. Diethylenetriamine May cause skin sensitization, an allergic reaction that becomes evident on re-exposure to this material. Diethylenetriamine Causes gastrointestinal system burns. Diethylenetriamine May cause corrosion and permanent tissue damage in the esophagus and digestive tract. Diethylenetriamine May cause asthma attacks due to allergic sensitivity in the respiratory tract. Causes respiratory irritation with possible burns.

Prolonged or repeated skin contact, sensitivity may cause dermatitis and possible damage and / or ulcer. Repeated exposure may cause an allergic respiratory reaction (asthma).

HANDLING AND STORAGE

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine

Diethylenetriamine Wash thoroughly after handling. Take off contaminated clothing and wash before reuse. Use with adequate ventilation. Diethylenetriamine Do not get in eyes, on skin, or on clothing. Diethylenetriamine Do not ingest or inhale. Keep diethylenetriamine away from heat and flame. Store diethylenetriamine in a tightly closed container. Diethylenetriamine Keep away from contact with oxidizing materials. Store diethylenetriamine in a cool, dry and well-ventilated place away from incompatible materials. Area of ​​abrasives. Keep diethylenetriamine away from Acids.

DISPOSAL INFORMATION

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine;

Products considered to be dangerous for supply are classified as Special Waste and the disposal of such chemicals is covered by regulations that may vary depending on location. Contact a specialist disposal company or local waste regulator for advice. Empty containers must be decontaminated before sending for recycling.

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine

Diethylenetriamine is readily absorbed via the gastrointestinal tract and 96% of the administered dose is excreted within 48 hours. It is excreted in roughly equal amounts in feces and urine, and at least 4 metabolites are detected (but not identified) in the latter. Only a small fraction (<2%) was recovered as expired carbon dioxide. Any residue remaining in the animal was found primarily in the kidney, liver, bladder and large intestine.

CHARACTERIZATION OF DIETHYLENTRIAMINE (DETA) AS ABSORBAN FOR CO2

DETA; diethylenetriamine; diethylene triamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylenetriamine; diethylene triamine; diethylenetriamine; di ethylene tri amine; di ethylene tri amine

Diethylenetriamine is an analog of diethylene glycol. It has similar chemical behavior and uses similar to ethylene diamine. It is a weak base and its aqueous solution is alkaline. It is used as a solvent for the extraction of sulfur and acid gas in the oil industry. Diethylenetriamine has been shown to exhibit diuretic function. Diethylenetriamine belongs to the Polyamine family. These are compounds containing more than one amine group. It belongs to the class of organic compounds known as dialkylamines. These are organic compounds that contain a dialkylamine group, characterized by two alkyl groups attached to the amino nitrogen. CO2 absorption with amine-based absorbents is an established and proven technology. Unfortunately, it is still very energy intensive and has high capital costs. When aiming to use this technology for CO2 capture worldwide, the general challenge is to reduce these two factors with new and environmentally acceptable solvents. Prospective research can be accomplished through process design improvements or by finding new and better solvents. An ideal solvent should have a high capacity, high absorption rates, low absorption enthalpy, result in low vapor consumption, create negligible problems with degradation, corrosion and foaming, be non-volatile, and not harm the environment. The main purpose of this study is to gather more fundamental information (chemical, kinetics and equilibrium) regarding the characterization of diethylenetriamine (DETA) as a possible absorbent for CO2. The study was started by measuring physicochemical properties, density and viscosity for different concentrations, temperatures, loaded with CO2 and partially neutralized with H2SO4 in the Anton Paar Stabinger Viscometer SVM 3000. The results obtained for density and viscosity were compared to existing sources and a Redlich-Kister Model to determine thermodynamic properties (partial molar volume and partial molar volume at infinite dilution). The differences in the shape of the density and viscosity curves for the aqueous amine solution were found very interesting when compared with the different functionalities in molecular structures. N2O solubilities in various amine solutions were measured in a solubility cell. Validation of the apparatus and experimental procedure was done by measuring the solubility for N2O and CO2 in water and N2O in pure amines (MEA and MDEA). The results matched very well with the literature. Solubility measurements were performed for different diethylenetriamine (DETA) concentrations, temperatures or CO2 loaded DETA and partially neutralized with H2SO4. The commonly used 'N2O Analogy' has also been validated for fully neutralized amines (MEA and diethylenetriamine (DETA)) with H2SO4 in various concentrations.

Solubility model of Wang et al. (1992) applied in aqueous diethylenetriamine (DETA) solution but more parameters were proposed in this system, so the extended Wang model was proposed. The model based on the Redlich-Kister approach was developed and achieved a satisfactory fit. The effect of CO 2 on the solubility of N 2 O in diethylenetriamine (DETA) and 30 wt% MEA in aqueous was also performed to see the salting effect in solution. Both qualitative and quantitative measurements were made by NMR studies to elucidate the speciation in diethylenetriamine (DETA) -H2O-CO2 system. 22 species were found in the system, most of which could be detected other than tricarbamate and free CO2. Quantitative 13C NMR was performed to measure the concentrations of the species. The results showed that this method was reliable in measuring concentrations, but was experimentally time consuming, caused by the insensitivity and low natural abundance of carbon nuclei. Two important observations with this technique are the long relaxation time and the need to suppress enhanced signals from neighboring nuclei (NOE effect). In VLE modeling, a Deshmukh-Mater model was applied to the DETA-H2O-CO2 system at 2.5 M to estimate the CO2 partial pressures against loading at different temperatures. Two steps are required to comply with the parameters in the DM model. The first step was to determine the temperature dependence of the equilibrium constants by setting the short range interactions to zero. Second, to determine the ij b parameters which show significant sensitivity while keeping the equilibrium constants obtained from the first step. However, only the first step was taken in this work because, with the complexity of the DETA system, the available experimental data material was not large and variable enough to deserve to enter this procedure. Features from the VLE model were compared with the NMR results to check the quality of the model. The model that fits the CO2 partial pressure data became acceptable only after the DETA protonation constants were also fitted, demonstrating the importance of appropriate values ​​for these equilibrium constants. The kinetics of carbon dioxide reactions in aqueous amine systems were measured for uncharged solutions (MEA and diethylenetriamine (DETA)) and partially neutralized diethylenetriamine (DETA) with H2SO4. Measurements were performed on a series of disk contactors for different temperatures and amine concentrations. The so-called first-order approach was used to obtain the observed reaction rates, and two reaction mechanisms, namely thermolecular and zwitterion mechanisms, were used to interpret experimental data. Assuming that zwitterion deprotonation is rate determining and zwitterion formation rate constant is set to infinity, both mechanisms gave the same results in principle. However, the advantages of the thermolecular mechanism are that it has fewer parameters and is more robust, mainly in terms of statistical determination of parameters. The addition of an additional parameter, as in the zwitterion mechanism, creates noise in determining the parameters. Kinetic results show that diethylenetriamine (DETA) has significantly faster kinetics than AEEA, EDA, and MEA, but slower than Piperazine. The kinetic rate constant of the secondary amine group was also determined in DETA and was found to be approximately two orders of magnitude lower than the primary amine group. However, it should be noted that the measured secondary amine group rate constant may not represent the true value for CO2 absorption, as the neutralization of the two primary amine groups is done with H2SO4 and not CO2. In addition, a validation of the so-called first order approach was performed using the penetration model for fast amines MEA and DETA. The reduction in concentrations of MEA and diethylenetriamine (DETA) at the interface was found to be less than 1%. This showed that the so-called first-order approach was acceptable. The reduction in concentrations of MEA and diethylenetriamine (DETA) at the interface was found to be less than 1%. This showed that the so-called first order approach was acceptable. The reduction in concentrations of MEA and diethylenetriamine (DETA) at the interface was found to be less than 1%. This showed that the so-called first-order approach was acceptable.

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