Ethylenediamine (EDA) CAS 107-15-3
Chelora Chemicals is a supplier of high-purity Ethylenediamine, shipping worldwide to chelating agent manufacturers, agrochemical plants, detergent intermediate producers and epoxy and resin formulators. Every consignment leaves with a batch-specific COA and the current SDS.
Also known as: EDA · 1,2-Diaminoethane · Ethane-1,2-diamine · 1,2-Ethanediamine · Dimethylenediamine · EDA 99%
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Price, lead time and a sample COA for Ethylenediamine (EDA), usually within one working day. We ship worldwide.
Request a Quote Email the DeskDocumentation
- Batch-specific COA
- Safety Data Sheet (SDS)
- Technical Data Sheet
- Dangerous-goods papers
- Certificate of origin
What is Ethylenediamine (EDA)?
Ethylenediamine is the first and simplest ethyleneamine — two primary amines joined by a two-carbon bridge, H2NCH2CH2NH2. Four active amine hydrogens on a very small molecule makes it unusually functional for its size, and the two-carbon spacing is exactly right for chelating a metal ion through both nitrogens at once.
It is a clear, colourless liquid boiling at about 116 °C with a strong ammoniacal odour, freezing near 8 °C and a flash point around 34 °C. It is fully miscible with water, strongly hygroscopic, and absorbs carbon dioxide from air readily to form a solid carbamate — which is why an open drum crusts around the closure.
The chelating geometry is the key to its largest market. Two nitrogens two carbons apart form a stable five-membered ring with a metal ion, and building four acetic acid arms onto those nitrogens gives EDTA — the most widely used synthetic chelating agent in the world.
Beyond chelants, EDA is the amine half of the ethylenebisdithiocarbamate fungicides used across global agriculture, the backbone of the bleach activator in most European laundry powders, and a building block for epoxy hardeners, polyamide resins, fabric softeners, corrosion inhibitors and pharmaceutical intermediates.
Why ethylenediamine specifically
- Ideal chelating geometry. Two nitrogens separated by two carbons form a stable five-membered chelate ring with a metal ion. Longer or shorter spacing binds far less strongly, which is why EDTA has no serious structural rival.
- Four active hydrogens on a tiny molecule. Very high functionality per unit weight, which matters in crosslinking and in building multi-armed derivatives.
- Two identical primary amines. Symmetrical, so reactions give clean products rather than isomer mixtures.
- Upstream of the whole ethyleneamine family. The higher ethyleneamines are built on the same ethylene bridge, so EDA availability signals the family's.
How EDA is Manufactured
Ethylenediamine is made by two quite different industrial routes, and they leave different signatures on the product. Both also produce the higher ethyleneamines as co-products.
- Ethylene dichloride route. Ethylene dichloride is reacted with excess ammonia under pressure. The chloride is displaced and the resulting amine hydrochloride is neutralised with caustic. This route is older and produces a salt by-product stream, and residual chloride is its characteristic trace.
- Ethanolamine route. Monoethanolamine is aminated with ammonia and hydrogen over a supported metal catalyst. This is the cleaner modern route — no chloride, no salt stream — and it is why chelant-grade and low-chloride material generally comes from this process.
- Co-product formation. Both routes produce DETA, TETA, piperazine and the higher ethyleneamines alongside EDA. The distribution is set by ammonia ratio and catalyst, and producers swing between products rather than making one exclusively.
- Separation. The mixture is resolved by distillation, partly under vacuum. EDA forms an azeotrope with water, so drying to a low-water specification is a separate operation.
Typical Commercial Specification
Figures below are representative of standard commercial grade. Chelant-grade, low-chloride and low-colour material is available — send us the specification you work to and we will quote against it.
| Parameter | Typical Value |
|---|---|
| Appearance | Clear, colourless liquid, free of suspended matter |
| Assay (GC) | 99.5% min |
| Diethylenetriamine | 0.2% max |
| Piperazine | 0.2% max |
| Aminoethylethanolamine | 0.1% max |
| Water (Karl Fischer) | 0.3% max |
| Colour (APHA) | 20 max |
| Freezing point | approx. 8 °C |
| Total amine value | 1840 – 1870 mg KOH/g |
| Chloride | 5 ppm max (route dependent — specify if critical) |
| Iron (Fe) | 1 ppm max |
| Non-volatile residue | 0.02% max |
Physical & Chemical Properties
| Property | Value |
|---|---|
| Molecular formula | H2NCH2CH2NH2 (C2H8N2) |
| Molecular weight | 60.10 g/mol |
| Appearance | Clear, colourless liquid |
| Odour | Strong ammoniacal |
| Freezing point | approx. 8 °C — may solidify in cold storage |
| Boiling point | approx. 116 °C at 760 mmHg |
| Vapour pressure | approx. 1.4 kPa at 20 °C |
| Relative density | approx. 0.90 g/cm³ at 20 °C |
| Flash point | approx. 34 °C (closed cup) |
| Autoignition temperature | approx. 385 °C |
| Explosive limits in air | approx. 2.7 – 16.6 vol% |
| Solubility in water | Miscible in all proportions; strongly hygroscopic |
| Basicity | Two basic nitrogens; conjugate acid pKa values approx. 10.7 and 7.6 |
| Functionality | Two primary amines; four active amine hydrogens |
| Carbon dioxide uptake | Absorbs CO₂ from air to form a solid carbamate |
| Incompatibilities | Strong oxidisers, strong acids, acid chlorides, nitrites, isocyanates, copper and its alloys |
| Decomposition products | Oxides of nitrogen, carbon monoxide, carbon dioxide, ammonia |
Reactivity in practice
Two primary amines two carbons apart. That geometry, and the four hydrogens it carries, define everything:
- Chelate formation. The two nitrogens bind a metal ion simultaneously to form a stable five-membered ring. Carboxymethylating them gives EDTA and the wider aminopolycarboxylate chelant family.
- Dithiocarbamate formation. With carbon disulphide and a metal base it gives ethylenebisdithiocarbamates — the manganese and zinc salts of which are major protectant fungicides.
- Acylation and cyclisation. Reaction with acetic anhydride gives the tetraacetyl derivative used as a bleach activator; with other partners it closes to imidazolines and related heterocycles.
- Epoxy curing and polyamide formation. Four active hydrogens crosslink epoxy resin; condensation with dibasic and dimer acids gives polyamide resins.
EDA vs DETA, TETA and TEPA
The ethyleneamines form a ladder: each step adds one more ethylene bridge and one more nitrogen. Going up it, the boiling point and viscosity rise steeply, the number of active amine hydrogens increases, and — importantly — the product stops being a single compound and becomes a distribution of linear, branched and cyclic isomers. They all come off the same plant and move together on availability.
| Ethyleneamine | CAS | Functionality & principal use |
|---|---|---|
| Ethylenediamine (EDA) | 107-15-3 | 2 N, 4 active H — EDTA chelants, dithiocarbamate fungicides, bleach activators, epoxy chemistry |
| Diethylenetriamine (DETA) | 111-40-0 | 3 N, 5 active H — epoxy hardeners, DTPA chelants, fuel and lube additives, wet-strength resins |
| Triethylenetetramine (TETA) | 112-24-3 | 4 N, 6 active H — epoxy hardeners, asphalt additives; supplied as an isomer distribution |
| Tetraethylenepentamine (TEPA) | 112-57-2 | 5 N, 7 active H — lubricant dispersants, epoxy hardeners, CO₂ sorbents; also a distribution |
Stated plainly: EDA and DETA are genuine single compounds; TETA and TEPA as sold are distributions of isomers with a nominal name, and the linear content is what a formulator actually pays for. Going up the ladder, each additional nitrogen adds crosslink functionality and basicity while raising viscosity and lowering volatility — so a lower member cures faster and smells more, and a higher one builds a denser network and stays where it is put. Substituting across the ladder is always a reformulation.
Industries We Supply EDA To
The same molecule leaves our warehouse for very different factories. What changes between them is not the CAS number but the grade — chloride, colour and distribution — and the documentation each sector expects.
Where EDA is Used
EDA is a genuine platform chemical with several large and unrelated markets. These are the end uses our customers buy it for, roughly in order of volume.
In chelating agent manufacture
This is the largest outlet and the clearest demonstration of why EDA's geometry matters. Two nitrogens separated by two carbons can both bind to a single metal ion, forming a stable five-membered ring — a geometry that longer or shorter spacing does not achieve nearly as well. Adding four acetic acid arms gives EDTA, which wraps a metal ion in six coordination points and holds it in solution across a wide pH range. EDTA and its relatives appear in detergents, textile processing, photographic chemistry, agriculture and industrial cleaning. Chelant producers care about chloride and about the ethyleneamine distribution more than about the headline assay.
In fungicide manufacture
EDA reacted with carbon disulphide gives ethylenebisdithiocarbamate, isolated as the manganese, zinc or mixed salt. These are protectant fungicides used at large scale across potato, vine, vegetable and fruit crops worldwide, valued because their multi-site mode of action makes resistance development slow. Plants running these actives specify consistency of the amine distribution, since DETA and piperazine carry-over give structurally different dithiocarbamates.
In bleach activators
Acetylating all four amine hydrogens gives tetraacetylethylenediamine, the compound that makes low-temperature oxygen bleaching work. Percarbonate and perborate bleaches release hydrogen peroxide, which is only effective at high wash temperatures; the activator reacts with it to generate peracetic acid in situ, which bleaches effectively at 30 or 40 degrees. It is a quietly significant chemical in domestic laundry across Europe.
In epoxy and polyamide chemistry
Four active hydrogens on a small molecule make EDA a high-functionality, fast curing agent — quick ambient cure and a high crosslink density, at the cost of a short pot life, a strong odour and a tendency to blush. In practice it is more often used as a building block for modified hardeners and polyamide resins than neat, with DETA and TETA taking the direct curing agent role.
Need EDA for a specific grade or volume?
Tell us the grade, the chloride and distribution limits you work to and the annual quantity. We will come back with a price, a lead time and a sample COA — delivered to any port worldwide.
Quality Control & Testing
Every lot is released against a batch-specific Certificate of Analysis. The methods behind the numbers are standard across the industry, and we are happy to share them or to work to your own in-house test protocol.
- Assay and ethyleneamine distribution — gas chromatography quantifying DETA, piperazine, AEEA and the other close relatives.
- Chloride — ion chromatography. Route-dependent and critical in chelant and high-purity service.
- Total amine value — titration, the figure formulators charge against.
- Water content — Karl Fischer titration. EDA is strongly hygroscopic and also absorbs carbon dioxide, so an open drum drifts on two fronts.
- Colour — APHA / Hazen against a standard. The ethyleneamines darken readily on air contact.
- Freezing point — a quick practical check correlating with water and cross-contamination.
Common Process Problems & Likely Causes
When EDA misbehaves in a plant, the cause is usually one of a short list of things. This table is the shortcut our technical desk works through before anyone opens a complaint file.
| Symptom | Likely cause | What to check |
|---|---|---|
| Chloride found in a chelant product | Ethylene dichloride route material carrying residual chloride | Chloride figure on the COA; specify ethanolamine-route material if critical |
| Drum solid or slushy on arrival | Freezing point near 8 °C against cold transit — normal behaviour | Warm gently and homogenise; this is physical, not degradation |
| White crust around the closure | Carbon dioxide absorbed from air forming a solid carbamate | Seal integrity, drum breathing, nitrogen blanket — this also consumes amine value |
| Amine value below the certificate | Carbon dioxide and water pickup after the drum was opened | Water content and amine value now versus on the COA; reseal discipline |
| Different dithiocarbamate species in a fungicide batch | DETA or piperazine carry-over reacting differently with carbon disulphide | Full ethyleneamine distribution on the COA |
| Epoxy pot life shorter than expected | EDA is inherently fast — four active hydrogens on a small molecule | Formulation design; blend with a slower hardener rather than expecting EDA to be slow |
| Material darkened in storage | Air contact, accelerated by warmth | Blanket gas, headspace, storage temperature |
| Corrosion on transfer fittings | Copper, brass, bronze or aluminium in contact with the amine | Materials of construction — stainless steel or lined equipment |
Packaging, Storage & Shipping
- Standard packing. 180 kg net in lined steel or HDPE drums, with 1000 L IBCs for larger users.
- Bulk packing. Road tankers and ISO tank containers for chelant, fungicide and detergent producers.
- Cold weather handling. The freezing point is near 8 °C, so drums can solidify or go slushy in winter transit. Warm gently and homogenise before use.
- Carbon dioxide exclusion. EDA absorbs carbon dioxide from air to form a solid carbamate, which crusts around closures and consumes amine functionality. Keep containers sealed and blanket bulk storage — this is not just a colour issue.
- Inert blanketing. Nitrogen-blanketed at fill where colour matters. The ethyleneamines darken on air contact more readily than most amines, and they also absorb carbon dioxide to form carbamate.
- Materials of construction. Stainless steel or suitable lined vessels. Avoid copper, brass, bronze, aluminium and mercury.
- Shelf life. Typically 12 months in unopened original packing under those conditions. Beyond that, re-test rather than assume.
- Fire precautions. The flash point is near 34 °C, so a warm store or heated transfer can bring the headspace into the flammable range. Classify the zone accordingly.
- Transport classification. UN 1604, Ethylenediamine, Class 8 corrosive with subsidiary risk 3 flammable, Packing Group II — shipped with full dangerous-goods documentation.
Hazards & Safe Handling
Ethylenediamine is corrosive, flammable and a skin and respiratory sensitiser. It must be handled by trained personnel under a proper risk assessment. The classifications below are indicative — the current SDS supplied with your consignment is the governing document.
- Sensitisation. The ethyleneamines are recognised skin sensitisers, and several are respiratory sensitisers as well. Once a worker is sensitised, exposures previously tolerated can provoke a reaction, so preventing first contact matters far more than managing repeat contact. This is the dominant occupational concern across this whole family.
- Exposure control. Handle in a closed system or under local exhaust ventilation. Where the material is warmed or sprayed, vapour and mist exposure rise sharply and need their own controls.
- PPE. Chemical-resistant gloves rated for amines, chemical goggles and face shield, and chemical-resistant clothing. Glove breakthrough time is worth checking rather than assuming.
- Mixed-system handling. In a two-part epoxy system the uncured mixture carries the hazards of both hardener and resin. Applicators handling mixed material need controls for both, which is often where site assessments fall short.
- Incompatibilities. Strong oxidising agents, strong acids, acid chlorides, nitrites and isocyanates — the amine-isocyanate reaction is violently exothermic. Also copper, brass, bronze and aluminium.
- Spill response. Contain, absorb with inert non-combustible material and collect in a labelled closed container. Ventilate. Do not wash to drain.
- Environment. Harmful to aquatic life. Do not allow to enter drains, surface water or groundwater. Dispose through a licensed chemical waste contractor.
- First aid. Remove contaminated clothing immediately, wash skin with plenty of water and soap, flush eyes for at least 15 minutes, and seek medical attention with the SDS to hand. Report any skin or breathing reaction, which may indicate developing sensitisation.
Regulatory & Compliance Notes
Ethylenediamine is a long-established industrial chemical listed on the major national inventories, but its respiratory sensitiser classification gives it a heavier occupational profile than most amines of its size. The notes below are orientation rather than legal advice — confirm your own position with your regulatory adviser before importing.
- Inventory status. Listed on the principal chemical inventories in the major importing regions. Ask us for the inventory confirmation relevant to your destination country.
- Import registration. Several territories require the importer to hold a registration or notification before a consignment lands. Start that process early — it is the most common cause of delay at destination.
- Hazard communication. Supplied with an SDS compliant with the format applicable to your region, and labelled in line with the GHS classification for the product.
- Respiratory sensitiser classification. Classified as a respiratory sensitiser, which triggers specific labelling and, in several jurisdictions, exposure control and health surveillance obligations for exposed workers. These apply downstream as well as at the formulator.
- Agrochemical end use. Where the material feeds a registered fungicide active, the destination authority will generally require traceability on the intermediate. Keep the batch COA with your production records.
- Family supply dynamics. EDA comes out of the ethyleneamine train with DETA, TETA, TEPA and piperazine, so availability moves across the family rather than product by product.
- Dangerous goods. UN 1604, Ethylenediamine, Class 8 with subsidiary risk 3, Packing Group II. Declarations prepared for IMDG (sea) or IATA (air) as appropriate.
We Supply EDA Worldwide
Chelora Chemicals is a supplier and export partner, not a single-plant trader. We ship Ethylenediamine (EDA) from India to customers across Asia, Europe, the Middle East, Africa, and North and South America, handling the export documentation, dangerous-goods paperwork and freight so the material arrives ready to use.
- Incoterms. EXW, FOB, CIF, CFR and DAP quoted to suit your purchasing terms and freight arrangements.
- Ports. Regular shipments through Nhava Sheva (JNPT) and Mundra, with other Indian ports arranged where it suits the routing.
- Documentation. Commercial invoice, packing list, certificate of origin, COA, SDS and dangerous-goods declaration issued as a complete set.
- Flexible volumes. A single drum for laboratory qualification, through LCL consolidations, up to repeat full loads on a supply contract.
- Supply continuity. Because we are independent of any one producer, a plant turnaround or a shipping disruption at one source does not have to become your stock-out.
Buying EDA from Chelora
We are an independent sourcing and supply partner. For EDA that means establishing the production route before quoting, because chloride content follows directly from it — and in chelant and high-purity service that single figure can decide whether a lot is usable.
- Documentation on every lot. Batch-specific COA including chloride and distribution, current SDS and TDS.
- Samples before commitment. Trial quantities for process qualification ahead of a commercial order.
- Quantities. From a single 180 kg drum through to repeat tank loads on contract supply.
- Export experience. Class 8 dangerous-goods documentation, packing and labelling handled for sea and road freight.
- Technical support. Direct access to people who know the chemistry, for questions on production route, amine value or carbamate formation.
- Related intermediates. DETA, TETA, TEPA, piperazine, AEEA and the wider ethyleneamine range from one supplier.
How ordering works
- Send the enquiry. Product, grade or specification, quantity, destination port and the Incoterm you buy on. If you have a spec sheet, attach it — it saves a round trip.
- We quote. Price, lead time, packing and a sample COA, normally within one working day.
- Sample and qualify. For first orders or critical applications, we send a trial quantity so your lab can sign off before you commit.
- Confirm the order. Proforma invoice issued; payment terms agreed against the volume and the relationship.
- Production and QC. Material allocated and released against a batch-specific COA, with a pre-shipment sample where the application calls for it.
- Ship and document. Packed, labelled and loaded with the full export and dangerous-goods document set, and tracked through to arrival.
Related Ethyleneamines & Intermediates
Buyers of EDA usually source several of these alongside it — they come off the same plant and move together on availability. Consolidating them on one order cuts freight cost and gives you a single point of contact for documentation.
Ethylenediamine (EDA) — Common Questions
The questions our technical desk is asked most often about EDA. If yours isn't here, call or email and you will reach someone who knows the chemistry.
What is the CAS number of Ethylenediamine?
The CAS number for Ethylenediamine is 107-15-3, and its EC number is 203-468-6. It is also listed as EDA, 1,2-diaminoethane and ethane-1,2-diamine. The molecular formula is H2NCH2CH2NH2 with a molecular weight of 60.10 g/mol.
What is ethylenediamine used for?
Its largest outlet is chelating agents — carboxymethylated to EDTA, the most widely used synthetic chelant in the world. It is also the amine half of the ethylenebisdithiocarbamate protectant fungicides used across global agriculture, and the backbone of tetraacetylethylenediamine, the bleach activator in most low-temperature laundry powders. Beyond that it is used in epoxy hardeners, polyamide resins, fabric softeners, corrosion inhibitors and pharmaceutical intermediates.
Do you supply ethylenediamine worldwide?
Yes. Chelora Chemicals supplies and exports ethylenediamine worldwide — across Asia Pacific, Europe, the Middle East, Africa and the Americas, as well as throughout India. We quote on EXW, FOB, CIF, CFR and DAP terms, ship mainly through Nhava Sheva and Mundra, and handle the commercial invoice, packing list, certificate of origin, COA, SDS and dangerous-goods declaration as a complete document set.
Why is EDA so good at chelating metals?
Geometry. Two nitrogens separated by exactly two carbons can both reach the same metal ion and form a five-membered ring, which is the most stable arrangement available. A longer or shorter bridge binds far less strongly. Building four acetic acid arms onto those two nitrogens gives EDTA, which wraps a metal ion in six coordination points and holds it in solution across a wide pH range — a performance no structurally different chelant has matched at comparable cost.
Does the production route matter?
It does if chloride matters to you. EDA is made either by reacting ethylene dichloride with ammonia, which leaves residual chloride, or by aminating monoethanolamine, which does not. In chelant manufacture, in high-purity applications and in any system with stainless steel at temperature, chloride is a genuine specification rather than a curiosity. Ask which route your material came from and get the chloride figure on the batch certificate.
Why does my EDA form a white crust around the closure?
It absorbs carbon dioxide from air to form a solid carbamate. This is more than a cosmetic nuisance: the reaction consumes amine functionality, so an open drum quietly drifts below its certified amine value while the crust builds. A formulator charging to the original figure then ends up short with nothing on the certificate to explain it. Keep containers sealed, blanket bulk storage, and re-check amine value on a part-used drum that has been open a while.
How is ethylenediamine manufactured?
Two routes. The older one reacts ethylene dichloride with excess ammonia under pressure, then neutralises the resulting amine hydrochloride with caustic — producing a salt by-product stream and leaving residual chloride. The modern route aminates monoethanolamine with ammonia and hydrogen over a supported metal catalyst, with no chloride and no salt stream. Both produce DETA, piperazine and the higher ethyleneamines as co-products, separated by distillation.
What purity does Chelora supply, and can you meet a tighter specification?
Standard commercial grade is 99.5% minimum assay by GC, with DETA and piperazine each held to 0.2% maximum, water to 0.3% maximum and a total amine value of 1840–1870 mg KOH/g. Chelant-grade, low-chloride and low-colour material is available — send us the specification you work to and we will quote against it.
My drum has solidified — is the product damaged?
No. EDA freezes at about 8 °C, so drums commonly solidify or go slushy in winter transit and unheated storage. Warm gently and homogenise thoroughly before use. This is normal physical behaviour, not degradation, provided the material has not been left open to air while warm.
Is ethylenediamine a sensitiser?
Yes, and it is the most important health point about the product. EDA is classified as both a skin and a respiratory sensitiser, and it is a recognised cause of occupational asthma. Once a worker is sensitised, very low exposures can provoke a reaction, so preventing first contact matters far more than managing repeat contact. Several jurisdictions require health surveillance for exposed workers. The same applies in varying degrees across the whole ethyleneamine family.
How should EDA be stored, and what is its shelf life?
Store in a cool, dry, well-ventilated and bunded area away from heat and ignition sources, acids, oxidisers and isocyanates, with containers tightly sealed and ideally nitrogen-blanketed — sealing matters more here than for most amines because of the carbon dioxide uptake. Keep above the freezing point where practical. Use stainless steel or suitably lined equipment and avoid copper, brass, bronze and aluminium. Unopened original packing typically carries a 12-month shelf life.
What are the hazards of handling EDA?
It causes severe skin burns and serious eye damage, is a skin and respiratory sensitiser, and is a flammable liquid with a flash point near 34 °C. Sensitisation is the dominant concern. Handle in a closed system or under local exhaust ventilation with gloves rated for amines, goggles and face shield, and chemical-resistant clothing, in an area classified for the flammability risk. Always work from the current SDS.
How is EDA classified for transport?
It ships as UN 1604, Ethylenediamine, Class 8 corrosive with subsidiary risk 3 flammable, Packing Group II. We supply the full dangerous-goods documentation, packing and labelling for both sea and road freight.
What is a bleach activator and why does EDA make one?
Oxygen bleaches such as percarbonate and perborate release hydrogen peroxide in the wash, but peroxide only bleaches effectively at high temperature. A bleach activator reacts with it to form peracetic acid in situ, which works at 30 or 40 degrees. Acetylating all four amine hydrogens of EDA gives tetraacetylethylenediamine, the activator used in most European low-temperature laundry powders. It is a quietly significant outlet and a good illustration of EDA's high functionality per unit weight.
What packing sizes and order quantities are available?
Standard packing is 180 kg net in lined steel or HDPE drums, with 1000 L IBCs for larger users and road tankers or ISO tanks for chelant, fungicide and detergent producers. Orders run from a single drum for trial work up to repeat tank loads on contract supply.
Do you provide a COA and SDS, and can I get a sample first?
Yes to both. Every consignment ships with a batch-specific Certificate of Analysis including chloride and the ethyleneamine distribution, the current Safety Data Sheet and a Technical Data Sheet. Trial samples for process qualification are available before you place a commercial order — request one through the contact form or email source@chelorachemicals.com.
Can EDA be substituted with another diamine?
In chelant chemistry, essentially not — the two-carbon bridge is what makes the chelate ring stable, and 1,3-propanediamine or hexamethylenediamine give measurably weaker binding. In epoxy curing, DETA and TETA substitute readily and are usually preferred anyway, since EDA cures very fast with a short pot life. In fungicide manufacture the ethylenebisdithiocarbamate structure is the registered active, so there is no substitution at all.
Ready to source Ethylenediamine (EDA)?
Send us your specification, grade and annual volume. You will get a price, a realistic lead time and a sample COA from someone who understands what the material has to do in your process — delivered anywhere in the world.
