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Aromatic Diamine · MDI Feedstock & High-Temperature Hardener

4,4′-Methylenedianiline (MDA) CAS 101-77-9

Chelora Chemicals supplies 4,4′-Methylenedianiline to isocyanate producers, high-performance epoxy formulators, polyurethane elastomer manufacturers and polyimide resin houses. This is a carcinogen-classified substance subject to authorisation in some territories — we establish the regulatory position before quoting. Every consignment leaves with a batch-specific COA and the current SDS.

Also known as: MDA · 4,4′-Diaminodiphenylmethane · DDM · DADPM · p,p′-Methylenedianiline · Bis(4-aminophenyl)methane

Worldwide supplyExport shipments to Asia, Europe, the Middle East and the Americas
Full documentationBatch COA, SDS, TDS and dangerous-goods papers with every lot
Enclosed handlingSealed bags, pre-weighed sachets and molten bulk, specified for closed transfer
Grade matchedMDI-feedstock, epoxy-hardener and polyimide grades to your specification

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Price, lead time and a sample COA for 4,4′-Methylenedianiline (MDA), usually within one working day. We ship worldwide.

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Documentation

  • Batch-specific COA
  • Safety Data Sheet (SDS)
  • Technical Data Sheet
  • Dangerous-goods papers
  • Certificate of origin
Overview

What is 4,4′-Methylenedianiline (MDA)?

4,4′-Methylenedianiline is an aromatic diamine — two aniline rings joined by a methylene bridge, CH2(C6H4NH2)2. It is made by condensing aniline with formaldehyde, and it is the direct precursor to methylene diphenyl diisocyanate.

That relationship explains both its enormous volume and its unusual commercial position. The overwhelming majority of MDA produced worldwide never leaves the plant that makes it — it is generated and immediately phosgenated to MDI within an integrated facility. The quantity traded as a free-standing product is a small fraction of total production.

Physically it is a light tan to brown crystalline solid melting at about 92 °C, supplied as flakes, pellets or molten bulk. It is practically insoluble in water and darkens readily on air and light exposure.

Where MDA is bought as a product rather than made as an intermediate, it is for its performance as a high-temperature epoxy curing agent and as a chain extender in cast polyurethane and polyurea elastomers, and as a monomer for polyimide and other high-performance polymers. The aromatic backbone gives cured systems heat resistance that aliphatic and cycloaliphatic hardeners cannot approach.

It must be said plainly that MDA carries a carcinogen classification and is subject to authorisation requirements in some territories. The regulatory section below sets out what that means in practice, and it is the first thing to settle on any enquiry.

Why 4,4′-methylenedianiline specifically

  • The direct precursor to MDI. Phosgenation of MDA and its polymeric homologues gives the aromatic isocyanate behind rigid insulation foam. No alternative feedstock serves this role.
  • Exceptional heat resistance in epoxy. The rigid aromatic backbone gives cured networks glass-transition temperatures and chemical resistance well beyond what aliphatic or cycloaliphatic hardeners deliver.
  • A polyimide monomer. Condensed with aromatic dianhydrides it gives polyimides and related high-temperature polymers used in electronics and aerospace.
  • Slow, controllable cure. The weakly basic aromatic amines react slowly at ambient and need heat, which gives long pot life and allows thick sections to be cast without runaway exotherm.
Production

How MDA is Manufactured

MDA is made by condensing aniline with formaldehyde under acid catalysis. The reaction is conceptually simple, and controlling what it produces is the whole of the technology.

  • Acid-catalysed condensation. Aniline and formaldehyde are reacted in the presence of hydrochloric acid. Formaldehyde bridges two aniline rings, and the reaction rearranges to place the amino groups predominantly in the 4,4′ positions.
  • Oligomer formation. The reaction does not stop at the two-ring product. Further condensation gives three-ring and higher polymeric methylene dianilines, and the ratio of two-ring to polymeric material is controlled by the aniline-to-formaldehyde ratio.
  • Isomer distribution. Alongside the 4,4′ isomer, the 2,4′ and 2,2′ isomers form in smaller amounts. For epoxy and polyimide use the 4,4′ content is a key specification; for MDI production the whole distribution is carried forward.
  • Neutralisation and separation. The acid is neutralised and the product separated. Material destined for MDI goes straight to phosgenation; material sold as a product is purified further and crystallised or flaked.
What this means commercially: the 4,4′ isomer content and the two-ring to polymeric ratio are what separate grades. For epoxy and polyimide use the 4,4′ isomer is what gives the symmetrical, high-melting, high-performance network, and 2,4′ carry-over disrupts it. For MDI the distribution is carried through deliberately to give polymeric MDI. Tell us which you need, because they are genuinely different products despite sharing a name.
Specification

Typical Commercial Specification

Figures below are representative of commercial grade for non-MDI use. Epoxy-hardener and polyimide grades with tighter isomer and colour limits are available — send us the specification you work to and we will quote against it.

ParameterTypical Value
AppearanceLight tan to brown crystalline flakes, pellets or molten liquid
Assay (4,4′ isomer, GC)99.0% min
2,4′-Methylenedianiline0.5% max
Polymeric methylene dianilines0.5% max
Free aniline0.1% max
Moisture0.2% max
Melting point90 – 93 °C
Amine value550 – 570 mg KOH/g
Amine hydrogen equivalent weight (AHEW)approx. 49.6 g/eq (theoretical)
Colour of meltTo grade specification
Ash / residue on ignition0.05% max
Iron (Fe)10 ppm max
Free aniline and the isomer split. Free aniline is the figure with the sharpest consequences: it is monofunctional so it caps chain growth and reduces crosslink density, and it brings its own severe toxicity and skin-absorption hazard into a workplace already handling a carcinogen-classified material. The 4,4′ isomer content is the second: symmetry is what gives the high-performance network, and 2,4′ carry-over lowers the glass-transition temperature of the cured system.
Properties

Physical & Chemical Properties

PropertyValue
Molecular formulaCH2(C6H4NH2)2 (C13H14N2)
Molecular weight198.26 g/mol
AppearanceLight tan to brown crystalline solid; flakes, pellets or molten
OdourFaint amine-like
Melting pointapprox. 92 °C
Boiling pointapprox. 398 °C at 760 mmHg
Vapour pressureNegligible at ambient temperature
Relative densityapprox. 1.15 g/cm³
Flash pointapprox. 220 °C (closed cup)
Solubility in waterPractically insoluble
Other solventsSoluble in alcohols, ethers, benzene and many polar organics
FunctionalityTwo primary aromatic amines; four active amine hydrogens
BasicityWeak, as for all aromatic amines
Health classificationCarcinogen classified; also a skin sensitiser and liver toxicant — see Safety
IncompatibilitiesStrong oxidisers, strong acids, acid chlorides, isocyanates (violent)
Decomposition productsOxides of nitrogen, carbon monoxide, carbon dioxide, aniline

Reactivity in practice

Four active hydrogens on a rigid aromatic backbone, with the weak basicity typical of aromatic amines. Four reaction types cover commercial use:

  • Phosgenation to MDI. Reaction with phosgene converts both amines to isocyanate groups, giving the aromatic diisocyanate behind rigid polyurethane foam. This is by far the largest outlet.
  • Epoxide ring opening. Four active hydrogens crosslink epoxy resin into a rigid aromatic network with very high heat-distortion temperature, cured with heat rather than at ambient.
  • Polyimide formation. Condensation with aromatic dianhydrides gives polyamic acids that cyclise to polyimides — high-temperature polymers used in electronics and aerospace.
  • Chain extension in elastomers. Reacts with isocyanate-terminated prepolymers to extend and crosslink cast polyurethane and polyurea elastomers.
Comparison

MDA vs MOCA, TDA and Aniline

These three aromatic amines are grouped together here for a reason that has nothing to do with their chemistry: all carry a carcinogen classification, and for all three the regulatory position rather than the technical specification usually decides whether a given use is possible in a given market. Understanding where each one stands is a prerequisite to buying it.

Aromatic amine CAS Principal use & regulatory position
4,4′-Methylenedianiline (MDA)101-77-9MDI feedstock and high-temperature epoxy hardener; carcinogen classified, EU authorisation list, with an intermediate-use exemption
MOCA / MBOCA101-14-4Cast polyurethane elastomer curative, essentially its only use; carcinogen classified, EU authorisation required
Toluenediamine (TDA)95-80-7TDI feedstock; carcinogen classified, prohibited in cosmetics, restricted as a releasable amine in textiles
Aniline62-53-3The parent compound; also carcinogen classified but not authorisation-listed — supplied far more freely

Stated plainly: the technical question of which curative or feedstock performs best is often settled long before the regulatory one, and it is the regulatory answer that determines whether you can proceed. For MDA and TDA, a very large majority of global volume is consumed as an isolated intermediate within integrated isocyanate plants, where different obligations apply from those on a free-standing industrial use. For MOCA, the position in Europe is specific and restrictive. Establish where your use sits before anything else.

Industries

Industries We Supply MDA To

MDA reaches a narrow set of industries, and in most of them it is handled in closed systems. What changes between them is the grade and, above all, the regulatory basis on which the use proceeds.

Isocyanates & polyurethaneMDI producers using it as an isolated intermediate within integrated plants
High-temperature compositesAerospace and industrial epoxy systems requiring maximum heat-distortion temperature
Cast polyurethane elastomersChain extender and curative in high-performance cast elastomer systems
High-performance polymersPolyimide, polybenzimidazole and specialty resin producers
Industrial coatingsTank lining and chemically resistant coating formulators
Dyes & specialitiesDye intermediate and specialty chemical producers, where permitted
Applications

Where MDA is Used

One application dominates by volume and the rest are specialist. These are the end uses our customers buy it for.

MDI production Phosgenated to methylene diphenyl diisocyanate — the aromatic isocyanate behind rigid polyurethane insulation foam. Almost all of this consumption is as an isolated intermediate within integrated plants.
High-temperature epoxy hardeners Heat-cured aromatic amine hardener giving the highest glass-transition temperatures and chemical resistance available from an amine cure.
Polyimide resins Condensed with aromatic dianhydrides for the polyimides used in flexible circuits, aerospace composites and high-temperature insulation.
Cast elastomer chain extenders Extends and crosslinks isocyanate-terminated prepolymers in high-performance cast polyurethane and polyurea.
Tank linings & chemical-resistant coatings Where maximum chemical and thermal resistance is required and the cured system is qualified for the service.
Specialty polymers Monomer for polybenzimidazole and other high-temperature polymer systems.
Composite tooling Heat-cured tooling resins requiring dimensional stability at elevated temperature.
Dye intermediates Specialty colourant intermediates, where the use is permitted at destination.

As MDI feedstock

This is the overwhelming majority of global MDA consumption, and it is worth understanding how it works commercially. In an integrated plant, aniline and formaldehyde are condensed to a mixture of MDA and its polymeric homologues, and that mixture goes directly to phosgenation without ever being isolated as a saleable product. The MDI produced is the foundation of the rigid insulation foam industry. Because the MDA exists only fleetingly inside a closed process, this use attracts different regulatory obligations from a free-standing industrial application — a distinction that matters a great deal to anyone assessing their position.

As a high-temperature epoxy hardener

Where a cured epoxy must hold its properties at high temperature, aromatic amine hardeners are the answer, and MDA is among the most effective. Four active hydrogens on a rigid two-ring backbone build a dense, stiff network with a glass-transition temperature well beyond what aliphatic or cycloaliphatic hardeners achieve. The trade-offs are a heat-required cure rather than ambient, and yellowing on UV exposure. In practice, formulators facing the regulatory position increasingly evaluate alternative aromatic hardeners, and that evaluation should be part of any new project rather than a response to a later restriction.

In polyimides and high-performance polymers

Condensing MDA with an aromatic dianhydride gives a polyamic acid that cyclises on heating to a polyimide — a class of polymer with exceptional thermal and chemical stability, used in flexible printed circuits, aerospace composites and high-temperature electrical insulation. These are low-volume, high-value applications where the material is handled in controlled laboratory and production environments and the quantities involved are small.

In cast polyurethane elastomers

MDA extends and crosslinks isocyanate-terminated prepolymers to give tough, high-modulus cast elastomers. It is less common in this role than MOCA, which it partly overlaps with, and the same regulatory considerations apply to both. Elastomer producers evaluating curatives today are generally working through the alternatives rather than specifying either as a default.

Need MDA for a specific grade or volume?

Tell us the intended use, the destination and the regulatory basis on which you will handle this material — intermediate use, authorised use or a territory where neither applies. Once that is settled we can discuss grade, quantity, price and lead time.

Quality

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 isomer distribution — gas chromatography quantifying the 4,4′, 2,4′ and 2,2′ isomers and the polymeric homologues.
  • Free aniline — reported explicitly. It caps chain growth, lowers crosslink density and adds its own severe toxicity to the workplace picture.
  • Amine value and AHEW — titration, the figure epoxy formulators mix against.
  • Melting point — a fast, sensitive check for isomer and oligomer carry-over.
  • Colour of melt — relevant where the cured system's appearance matters, though aromatic-cured systems yellow in service regardless.
  • Moisture, ash and metals — relevant in polyimide and electronic-grade service, where trace metals affect electrical properties.
Pre-shipment samples: for first orders and for any qualification-critical application, we send a sample from the actual lot before the consignment ships, so your lab signs off on the material you are going to receive rather than on a representative sample.
Troubleshooting

Common Process Problems & Likely Causes

When MDA 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
Glass-transition temperature below specification2,4′ isomer or free aniline reducing network symmetry and crosslink densityIsomer distribution and free aniline on the COA; post-cure schedule
Cure incomplete at the scheduled temperatureAromatic amines need heat — the cure schedule may be below what the system requiresCure profile against the formulation design; this is usually not a material issue
Cured system yellowing in serviceExpected — aromatic amine cures yellow on UV exposureHardener class; use a cycloaliphatic such as IPDA if colour stability is required
Mix ratio giving an under-crosslinked networkFree aniline capping chains, or AHEW assumed rather than measuredAmine value on the COA and the free aniline figure
Material darker than expectedAir and light exposure, or overheating during meltingMelt colour versus COA, packaging integrity, melting procedure
Biological monitoring result elevated in a workerSkin absorption — air monitoring alone will not detect thisGlove selection and change frequency, splash procedures, enclosure integrity
Consignment held at destinationAuthorisation or import clearance not in placeRegulatory basis for the use, registration, and any authorisation required at destination
Polyimide electrical properties below targetTrace metals or ionic contaminationAsh, iron and chloride figures; specify an electronic grade
Before you reject a batch: send us the lot number and the test result you are seeing. In most cases we can compare against the retained sample and the production COA within a day, which is faster than returning material and usually identifies whether the issue is the lot or the process.
Logistics

Packaging, Storage & Shipping

  • Enclosed packing. Supplied in sealed bags, lined drums, pre-weighed sachets designed to go into the reactor unopened, or as molten bulk — all chosen to avoid open handling of a carcinogen-classified solid.
  • Closed transfer. Where the process allows, pre-weighed sachets and melt-and-pump systems remove the weighing and charging exposure entirely. This is the single most effective control available and is worth designing in.
  • Storage. Cool, dry, dark, secure and well-ventilated, away from acids, oxidisers and isocyanates, with access controlled. Secondary containment and clear carcinogen labelling of the storage area are normal practice.
  • Waste handling. Contaminated packaging, PPE and cleaning materials should be treated as hazardous waste and consigned accordingly, not disposed of as general waste.
  • Materials of construction. Stainless steel or suitable lined vessels. Avoid copper, brass, bronze and aluminium.
  • Oxygen and light exclusion. Aromatic amines darken rapidly on exposure to air and light — a surface oxidation effect rather than bulk decomposition, but one that matters where colour is specified. Nitrogen blanketing and opaque packaging are standard.
  • Shelf life. Typically 12 months in unopened original packing under those conditions. Beyond that, re-test rather than assume.
  • Transport classification. UN 2651, 4,4′-Methylenedianiline, Class 6.1 toxic, Packing Group III — shipped with full dangerous-goods documentation.
Practical tip: design the charging step before you order the material. The single biggest determinant of exposure with a carcinogen-classified powder is whether anyone ever has to open a bag and weigh it. Pre-weighed sachets that go in unopened, or a melt-and-pump system, remove that step entirely — and they are far cheaper to specify at the design stage than to retrofit after an occupational hygiene survey.
Safety

Hazards & Safe Handling

4,4′-Methylenedianiline is classified as a carcinogen, a mutagen in some systems, a liver toxicant on repeated exposure and a skin sensitiser, and it is absorbed through intact skin. It must be handled only by trained personnel under a proper risk assessment with health surveillance. The classifications below are indicative — the current SDS supplied with your consignment is the governing document.

Carcinogen classified Suspected mutagen Liver damage on repeated exposure Skin sensitiser Skin absorption hazard Toxic to aquatic life
  • Carcinogen classification. This substance carries a carcinogen classification in major regulatory systems. That is the governing fact in any risk assessment and it should shape plant design, exposure control, worker selection and health surveillance — not sit as a line on a label. Exposure should be reduced to as low as reasonably practicable rather than merely kept below a limit value.
  • Closed handling. Open handling of a carcinogen-classified powder is difficult to justify where a closed or enclosed alternative exists. Bulk bags with enclosed discharge, pre-weighed sachets that go into the reactor unopened, and melt-and-pump systems are the normal approaches.
  • Health surveillance and biological monitoring. Most jurisdictions require health surveillance for workers exposed to carcinogen-classified aromatic amines. For some, biological monitoring of the substance or its metabolites in urine is established practice and gives a far better picture of real uptake than air sampling alone.
  • Skin absorption. Aromatic amines are commonly absorbed through intact skin, which means air monitoring can look acceptable while uptake continues. Glove selection with a verified breakthrough time, and procedures that treat any skin contact as a reportable event, matter more than ventilation alone.
  • PPE. Chemical-resistant gloves of a verified material, eye protection, protective clothing that is removed and laundered on site, and respiratory protection appropriate to a carcinogen-classified dust or vapour.
  • Hot and molten material. Melting raises vapour and mist exposure substantially and adds thermal burn risk. Treat heated handling as a distinct operation with its own assessment and controls.
  • Environment. Harmful or toxic to aquatic life. Do not allow to enter drains, surface water or groundwater. Dispose through a licensed chemical waste contractor, and treat contaminated PPE and packaging as hazardous waste.
  • First aid. Remove from exposure, remove contaminated clothing, wash skin thoroughly with soap and water, flush eyes for at least 15 minutes, and seek medical attention with the SDS to hand. Record any exposure incident — it may be relevant to long-term health surveillance.
Compliance

Regulatory & Compliance Notes

MDA's regulatory position is the first thing to establish on any enquiry, because in some territories it determines whether a use is lawful rather than merely how it must be controlled. The notes below are orientation and not legal advice — you must confirm your own position with your regulatory adviser before committing to a project, and we will ask you to tell us the basis on which you intend to handle it.

  • Carcinogen classification. MDA is classified as a carcinogen in the major regulatory systems, with additional classifications for mutagenicity, repeated-dose liver toxicity and skin sensitisation. This drives labelling, exposure control, worker health surveillance and, in several jurisdictions, substitution obligations.
  • Authorisation requirements. In the European Union MDA is included on the REACH authorisation list, meaning that non-exempt uses require a specific authorisation. Comparable restrictions exist in other territories. Confirm the current status and any applicable sunset or review dates with your regulatory adviser before planning a use.
  • Isolated intermediate exemption. Use as an isolated intermediate under strictly controlled conditions is treated differently from other uses under REACH, which is why the very large volumes consumed within integrated MDI plants proceed on a different basis from a free-standing industrial application. Whether your use qualifies is a question for your regulatory adviser, not an assumption to make.
  • Consumer and article restrictions. Aromatic amines of this class are restricted in articles in prolonged skin contact and in various consumer applications. Where a cured system will reach a consumer, residual monomer limits apply at destination.
  • Inventory and import. Listed on the principal chemical inventories, but import may additionally require registration specific to carcinogen-classified substances. Start that process well before the commercial discussion.
  • Dangerous goods. UN 2651, 4,4′-Methylenedianiline, Class 6.1 toxic, Packing Group III. Declarations prepared for IMDG (sea) or IATA (air) as appropriate.
End-use declarations: for MDA we will ask you to state the intended use and the regulatory basis for it before we quote — not as a formality but because the answer determines whether we can supply to your destination at all. If you are at the project design stage and the position is not yet settled, tell us that too; it is far better addressed now than after capital is committed.
Global Supply

We Supply MDA Worldwide

Chelora Chemicals is a supplier and export partner, not a single-plant trader. We ship 4,4′-Methylenedianiline (MDA) 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.

Asia PacificChina, Korea, Japan, Taiwan, Vietnam, Indonesia, Thailand
EuropeGermany, Italy, Spain, Turkey, Netherlands, Poland, UK
Middle EastUAE, Saudi Arabia, Oman, Qatar, Iran
AmericasUnited States, Mexico, Brazil, Argentina, Colombia
AfricaEgypt, Morocco, South Africa, Kenya, Nigeria
Domestic IndiaGujarat, Maharashtra, Tamil Nadu and all major industrial belts
  • 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.
Supply

Buying MDA from Chelora

We are an independent sourcing and supply partner, and for MDA that means the regulatory conversation genuinely comes first. We will want to understand the intended use, the destination, the basis on which you will handle the material, and what exposure controls exist at your site — before grade, price or lead time are useful topics.

  • Regulatory position established first. Intended use, destination and handling basis confirmed before we quote.
  • Documentation on every lot. Batch-specific COA including free aniline and isomer distribution, current SDS and TDS.
  • Enclosed packing options. Pre-weighed sachets, sealed liners and molten bulk to eliminate open handling where possible.
  • Export experience. Class 6.1 dangerous-goods documentation, packing and labelling handled for sea and road freight.
  • Technical support. Direct access to people who know the chemistry, including on alternative hardeners where substitution is being considered.
  • Related intermediates. Aniline, m-phenylenediamine, IPDA, DETA and the wider epoxy hardener 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.
FAQ

4,4′-Methylenedianiline (MDA) — Common Questions

The questions our technical desk is asked most often about MDA. If yours isn't here, call or email and you will reach someone who knows the chemistry.

What is the CAS number of 4,4′-Methylenedianiline?

The CAS number for 4,4′-Methylenedianiline is 101-77-9, and its EC number is 202-974-4. It is also listed as MDA, DDM, DADPM, 4,4′-diaminodiphenylmethane and bis(4-aminophenyl)methane. The molecular formula is CH2(C6H4NH2)2 with a molecular weight of 198.26 g/mol.

Is MDA restricted or subject to authorisation?

Yes, and this is the first thing to establish. MDA is classified as a carcinogen in the major regulatory systems and is included on the REACH authorisation list in the European Union, meaning non-exempt uses require a specific authorisation. Comparable restrictions exist in other territories. Use as an isolated intermediate under strictly controlled conditions is treated differently, which is why the very large volumes consumed inside integrated MDI plants proceed on a different basis. Confirm your own position with your regulatory adviser before planning a use — we will ask you to state it before quoting.

What is MDA used for?

Overwhelmingly as the direct precursor to MDI — it is phosgenated to the aromatic isocyanate behind rigid polyurethane insulation foam, almost always as an isolated intermediate within an integrated plant. Where it is bought as a product, it is used as a high-temperature epoxy curing agent, as a monomer for polyimide and other high-performance polymers, and as a chain extender in cast polyurethane and polyurea elastomers.

Do you supply MDA worldwide?

We supply MDA to destinations and uses where the regulatory position can be properly established. Because authorisation requirements and import restrictions differ substantially by territory, the destination and intended use determine what is possible before commercial terms are relevant. Tell us both with your first enquiry and we will tell you where things stand.

Why is MDA such an effective high-temperature epoxy hardener?

Because the backbone is rigid and aromatic. Four active amine hydrogens on two benzene rings joined by a methylene bridge build a dense, stiff crosslinked network, and the aromatic rings resist thermal motion in a way aliphatic chains do not — so the glass-transition temperature of the cured system is far higher than any aliphatic or cycloaliphatic hardener achieves. The costs are a heat-required cure rather than ambient, and yellowing on UV exposure.

What does the isolated intermediate exemption mean in practice?

Under REACH, substances used as isolated intermediates under strictly controlled conditions are treated differently from other uses, and authorisation requirements that apply to general industrial use do not apply in the same way. That is why MDA consumed inside an integrated MDI plant — where it is generated and immediately phosgenated within a closed process — is handled on a different regulatory basis from MDA bought as a hardener. Whether a particular use qualifies is a matter for your regulatory adviser rather than an assumption.

Why does free aniline matter?

For two separate reasons. Chemically it is monofunctional, so it reacts once and caps a growing chain, reducing crosslink density and lowering the glass-transition temperature of the cured network. Occupationally it brings its own severe toxicity, skin absorption and methaemoglobin hazard into a workplace that is already handling a carcinogen-classified material. It should be reported explicitly on every certificate.

How is MDA manufactured?

By condensing aniline with formaldehyde under acid catalysis, usually with hydrochloric acid. Formaldehyde bridges two aniline rings and the product rearranges to place the amino groups predominantly in the 4,4′ positions. The reaction does not stop there — further condensation gives three-ring and higher polymeric methylene dianilines — so the aniline-to-formaldehyde ratio controls how much two-ring product is formed relative to polymeric material.

What purity does Chelora supply, and can you meet a tighter specification?

Commercial grade for non-MDI use is 99.0% minimum 4,4′ isomer by GC, with the 2,4′ isomer held to 0.5% maximum, polymeric homologues to 0.5% maximum and free aniline to 0.1% maximum. Epoxy-hardener and polyimide grades with tighter isomer, colour and metals limits are available — send us the specification you work to, once the regulatory position is settled.

How should MDA be handled to control exposure?

Enclosed, wherever possible. The single largest determinant of exposure with a carcinogen-classified powder is whether anyone has to open a bag and weigh it — so pre-weighed sachets that go into the reactor unopened, sealed liners and melt-and-pump systems are the controls that matter. Beyond that: verified glove selection, because aromatic amines are absorbed through intact skin and air monitoring will not detect that; health surveillance; and treating contaminated PPE and packaging as hazardous waste.

Does MDA require health surveillance for workers?

In most jurisdictions handling carcinogen-classified aromatic amines, yes. Because skin absorption is a significant route, air monitoring alone gives an incomplete picture, and biological monitoring is established practice for some substances in this class. Treat health surveillance as part of the plant design rather than a compliance item added afterwards.

How is MDA classified for transport?

It ships as UN 2651, 4,4′-Methylenedianiline, Class 6.1 toxic, Packing Group III. We supply the full dangerous-goods documentation, packing and labelling for both sea and road freight.

What alternatives exist if MDA is not available for my use?

It depends what you are buying it for. For epoxy systems needing high heat resistance, other aromatic amine hardeners and some cycloaliphatics are candidates, each with different glass-transition temperature, cure schedule and regulatory profile — m-phenylenediamine and IPDA are the usual starting points for that evaluation. For polyimides the choice of diamine is part of the polymer design. For MDI there is no alternative feedstock. We are happy to discuss the options; substitution in this area is a qualification exercise rather than a purchasing decision.

Why does my MDA-cured epoxy yellow?

Because it is aromatic. Aromatic amine cures absorb UV and develop colour over time — it is inherent to the chemistry rather than a fault in the material or the cure. If colour stability matters, the answer is a cycloaliphatic hardener such as IPDA, accepting a lower glass-transition temperature in exchange. You cannot have maximum heat resistance and water-white colour stability from the same amine class.

Why does MDA need to be kept warm, and what happens if it solidifies?

MDA melts in the region of 90 °C, so grades supplied molten or as a melt-and-charge solid will set if the heating fails in transit or in the holding tank. Solidification itself does not damage the material — it can be remelted — but the remelt must be slow and uniform, because localised overheating against a hot surface darkens the product and can drive condensation reactions. Keep remelt temperatures modest, blanket the headspace with nitrogen, and avoid repeated freeze-thaw cycles. Flaked and bagged grades sidestep the problem entirely and are usually the better choice for intermittent users.

What packing options are available?

Sealed bags, lined drums, pre-weighed sachets designed to go into the reactor unopened, and molten bulk for continuous users — all chosen to minimise or eliminate open handling. We will discuss which suits your charging arrangement, because the packing choice and the exposure control design are the same conversation.

Do you provide a COA and SDS?

Yes. Every consignment ships with a batch-specific Certificate of Analysis including free aniline and the isomer distribution, the current Safety Data Sheet and a Technical Data Sheet. Given the hazard classification, we would expect your site to review the SDS and confirm the handling arrangements before any material is despatched.

Ready to source 4,4′-Methylenedianiline (MDA)?

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.