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Aliphatic & Specialty Amines · CAS 100-97-0

Hexamethylenetetramine (HMTA) supplier and exporter

Hexamine · methenamine · urotropine · Powder, granules and crystals

Hexamethylenetetramine is the odd one out in any list of amines. It is not a chain with amino groups on the ends — it is a rigid cage of four nitrogens bridged by six methylene groups, with no N–H bond anywhere on the molecule. That structure makes it almost inert at room temperature and a generous source of both formaldehyde and ammonia when heated or acidified, which is exactly what a novolac phenolic resin needs to crosslink. It is also a reportable explosives precursor in the European Union and controlled in a number of other markets, so it is supplied against a confirmed end use. Chelora Amines supplies HMTA as powder, granules and crystals, with a batch-wise COA and SDS on every dispatch.

Molecular formulaC₆H₁₂N₄
Molecular weight140.19 g/mol
Physical stateWhite crystalline solid
Usual technical grade≥ 99.0% assay
Powder, granular and crystal grades Batch-wise COA with every dispatch Supplied against end-use and regulatory checks
(CH₂)₆N₄ CAS 100-97-0 C C C C C C N N N N four tertiary nitrogens CH₂ bridge a cage, not a chain six methylene bridges and no N–H bond anywhere
  • C₆ Six methylene carbons, each bridging two nitrogens 6 × 12.011
  • H₁₂ Two on every carbon — and none at all on the nitrogens 12 × 1.008
  • N₄ Four tertiary nitrogens at the corners of a tetrahedron 4 × 14.01

72.06 + 12.10 + 56.03 = 140.19 g/mol

Hexamine, (CH₂)₆N₄ — a cage built from formaldehyde and ammonia Four nitrogens sit at the corners of a tetrahedron and six methylene groups bridge every possible pair, giving an adamantane-like cage with no free N–H and no exposed lone pair geometry that behaves like an ordinary amine. The molecule is essentially six molecules of formaldehyde and four of ammonia locked into a stable, solid, easily handled form — and acid or heat will release them again, which is the basis of nearly every industrial use.
100-97-0CAS number
2933 69HS / HSN tariff code
≥ 99.0%Assay, technical grade
UN 1328Class 4.1, PG III
Annex IIEU reportable precursor
24 hrsTypical quote response
What it is

Hexamethylenetetramine at a glance

Hexamethylenetetramine — hexamine, methenamine, urotropine, HMTA — is a white crystalline solid, odourless to faintly amine-like, freely soluble in water and giving a mildly alkaline solution. It does not melt: heated strongly it sublimes and decomposes from around 260 °C. It burns readily with an almost smokeless flame, which is both why it is classified as a flammable solid and why it has been used for decades in solid fuel tablets.

Chemically it behaves nothing like the amines it sits alongside. There is no N–H bond on the molecule, so it does not cure epoxy, does not react with isocyanates as an amine and is a very weak base. What it does instead is store formaldehyde and ammonia in a stable, free-flowing solid and release them on heating or in acid. That is the whole basis of its biggest use: mixed into a novolac phenolic resin, it supplies the methylene bridges that crosslink the resin when the part is cured.

It also has a serious regulatory profile that has nothing to do with toxicity. Hexamine is listed in Annex II of the EU explosives precursors regulation as a reportable substance, which places duties on suppliers and users around suspicious transactions, disappearances and thefts, and a number of other jurisdictions impose their own controls. We supply it for industrial and professional use against a confirmed end use.

Why formulators specify hexamine

  • A solid formaldehyde source. Stable, free-flowing and dust-manageable, with none of the handling problems of formalin.
  • Latent reactivity. Essentially inert in the mix, fully reactive at cure temperature — the definition of a one-pack hardener.
  • Ammonia as well. The nitrogen released catalyses the crosslinking reaction as it goes.
  • Decades of process data. One of the most thoroughly characterised hardeners in the phenolic resin industry.
Identification and physical properties
Chemical nameHexamethylenetetramine
Common synonymsHMTA, hexamine, methenamine, urotropine, 1,3,5,7-tetraazaadamantane, formin
CAS number100-97-0
EC / EINECS number202-905-8
HS / HSN code2933 69 (heterocyclic compounds with nitrogen hetero-atoms only; HSN 2933 69 90 on Indian invoices)
Molecular formulaC₆H₁₂N₄ ((CH₂)₆N₄)
Molecular weight140.19 g/mol
AppearanceWhite crystalline powder, granules or crystals
OdourOdourless to faintly amine-like
Melting behaviourDoes not melt; sublimes and decomposes from about 260 °C
DensityAbout 1.33 g/cm³
Solubility in waterFreely soluble — roughly 85 g per 100 mL at 20 °C
pH, 10% aqueous solutionAbout 7–10
BasicityVery weak base — no N–H, tertiary nitrogens only
Decomposition productsFormaldehyde and ammonia, on heating or in acid
UN numberUN 1328, Hexamethylenetetramine, Class 4.1 (flammable solid), Packing Group III
Regulatory statusEU Regulation 2019/1148 Annex II — reportable explosives precursor; controls vary by jurisdiction

Figures are typical values for the technical grade. Pharmacopoeial and food-grade material is tested against its own monograph. All values for the material you order are stated on its Certificate of Analysis and Safety Data Sheet.

Chemistry and reactivity

How hexamine behaves in a formulation

Almost everything hexamine does industrially comes back to one fact: the cage is stable until you heat it or acidify it, and then it gives up formaldehyde and ammonia.

Novolac crosslinking

Blended into a novolac resin, hexamine decomposes at cure temperature and supplies the methylene bridges that link the phenolic chains — with the ammonia released acting as catalyst.

novolac + HMTA → cured resole network

Acid hydrolysis

In acid the cage breaks down cleanly to formaldehyde and ammonium salt. This is the basis of its analytical determination and of its action as a urinary antiseptic.

(CH₂)₆N₄ + acid → 6 HCHO + 4 NH₄⁺

Thermal decomposition

On heating it sublimes and breaks down rather than melting, releasing formaldehyde and ammonia — the behaviour exploited in resin cure, foundry binders and refractory systems.

heat → HCHO + NH₃

Rubber bonding systems

Paired with resorcinol and silica in the classic three-part bonding system, hexamine provides the methylene donor that builds the resin in situ during vulcanisation.

methylene donor in HRH bonding

Duff formylation

Formylates activated aromatic rings ortho to a phenolic hydroxyl — a standard laboratory and fine-chemical route to salicylaldehyde derivatives.

ArOH + HMTA → ortho-aldehyde

Sommelet reaction

Converts benzylic halides to the corresponding aldehydes through the quaternary hexaminium salt, under mild conditions and without over-oxidation.

ArCH₂X → ArCHO

Delépine reaction

Converts alkyl halides to primary amines through the same quaternary salt followed by acid cleavage — a clean alternative to direct ammonia alkylation.

RX → RNH₂

Acid inhibition

Adsorbs on steel surfaces in acid, slowing attack on the metal while leaving scale dissolution largely unaffected — hence its use in pickling and acidising inhibitor packages.

inhibitor film on steel in acid

Hexamine is a formaldehyde source, and that has two consequences worth planning for. In the process, the formaldehyde and ammonia it releases have to go somewhere — cure ovens, presses and foundry lines need extraction sized for it. In the product, residual free formaldehyde may be subject to emission limits depending on where the finished article ends up. Both are easier to design for than to retrofit.

Discuss your process
How it is made

From formalin and ammonia to a finished bag

Hexamine is made in one step, by reacting formaldehyde with ammonia. The chemistry is simple; the work is in crystallisation and in keeping the product dry and free-flowing.

Stage 1

Feedstock

Aqueous formaldehyde and ammonia, in the ratio the stoichiometry demands — six molecules of formaldehyde to four of ammonia.

Stage 2

Reaction

Ammonia is absorbed into formalin under controlled temperature and pH; the cage assembles directly, with water as the only by-product.

Stage 3

Concentration

The solution is evaporated under vacuum, keeping temperature low enough that the product does not begin to decompose.

Stage 4

Crystallisation

Crystals are grown, separated by centrifuge and washed; crystal size here sets whether the product behaves as a dusty powder or free-flowing granules.

Stage 5

Drying and filling

Material is dried to specification, screened to the grade's particle size and bagged or filled into bulk bags in a dust-controlled plant.

Powder, granules or crystals

Particle size is not a cosmetic choice with hexamine, and it is the specification most often left off an enquiry. Fine powder disperses quickly and evenly into a novolac resin or a friction compound, which is what a moulding or brake pad formulator wants, but it dusts badly and dust is both a nuisance and a flammability consideration. Granular and crystalline grades flow cleanly, charge with far less airborne dust and suit automated weighing, but they take longer to disperse and can leave unreacted hexamine in a short mixing cycle. Pick on the mixing time you actually have, and if you are moving from one form to another, expect to re-check your cure profile rather than assuming it carries across.

Storage and stability

Hexamine is stable in storage if it is kept dry and away from acids. Moisture causes caking and, over time, slow hydrolysis releasing formaldehyde; acid contact does the same thing quickly, so it must be segregated from acids in both storage and spill planning. It is a flammable solid that ignites readily and burns with an almost invisible flame, so ignition sources need controlling and a fire in a hexamine store will not look like a fire until you are close to it. Keep packs sealed, palletised and under cover, store below about 30 °C, and treat the material as dust-explosive in handling design where the powder grade is used in quantity.

Grades and specification

Grades matched to your process

Assay and ash separate the industrial grades from each other; particle size separates them in practice.

≥99.0%

Technical grade

Powder, granular or crystal for phenolic resins, friction materials, abrasives, foundry binders and rubber bonding systems.

Form
Powder to crystal
Packs
Bags, FIBC
Low ash

High-purity grade

Tighter ash, chloride and heavy metal limits for electronic-grade resins, analytical use and demanding resin systems.

Ash
Tightly limited
Chloride
Controlled
Pharma / food

Monograph grades

Material tested against the applicable pharmacopoeial or food-additive monograph, supplied with the corresponding documentation.

Testing
Per monograph
Availability
On enquiry
Typical specification — Hexamethylenetetramine, technical grade
ParameterTest methodTypical specification
AppearanceVisualWhite crystalline powder, granules or crystals
Assay, dry basisAcid back-titration≥ 99.0% w/w
Loss on drying105 °C, 4 h≤ 0.5% w/w
Residue on ignition (ash)Gravimetric≤ 0.03% w/w
pH, 10% solutionpH meter7.0 – 10.0
ChloridesTurbidimetric≤ 0.015% w/w
SulphatesTurbidimetric≤ 0.02% w/w
Heavy metals (as Pb)Colorimetric≤ 10 ppm
Particle sizeSieve analysisTo the grade ordered

Indicative specification for planning. The controlling document is the Certificate of Analysis issued for your batch. State the particle size you need at enquiry stage — it is the parameter most often omitted and the one most likely to affect your process.

Applications

Where hexamine is used

Phenolic resin chemistry takes most of the volume, and a surprisingly wide tail takes the rest.

Novolac resin hardener

The dominant outlet. Blended into novolac phenolic resins as the crosslinker for moulding compounds, laminates, binders and composite systems.

Friction materials

The hardener in phenolic-bonded brake pads, brake linings and clutch facings, where the cured resin has to hold its strength hot.

Abrasives and refractories

Resin-bonded grinding wheels, cutting discs and coated abrasives, and phenolic-bonded refractory shapes and ramming masses.

Foundry binders

The hardener in resin-coated sand for shell moulding and core making, giving fast, reliable cure on a hot pattern.

Rubber bonding and vulcanisation

The methylene donor in resorcinol-based bonding systems for steel cord and textile adhesion, and a secondary accelerator in some compounds.

Corrosion inhibition in acid

Used in pickling and acidising inhibitor packages, where it slows attack on steel while leaving scale removal largely unaffected.

Pharmaceutical use

As methenamine and its salts, a long-established urinary antiseptic that works by releasing formaldehyde in acidic urine. Requires monograph-grade material.

Organic synthesis

The reagent behind the Duff, Sommelet and Delépine reactions, and a standard buffer and reagent in analytical chemistry.

Downstream chemistry

What hexamine goes into

From brake pads to grinding wheels — the value chain downstream of hexamethylenetetramine.

Principal outlets and what they produce
ApplicationWhat hexamine doesEnd product
Novolac moulding compoundsSupplies methylene bridges and catalytic ammonia at cure temperatureElectrical components, closures, handles, engineering mouldings
Friction materialsCures the phenolic binder that holds the friction formulation togetherBrake pads, brake linings, clutch facings
Resin-bonded abrasivesHardens the phenolic bond that holds the grainGrinding wheels, cutting discs, coated abrasives
Shell moulding sandCures the resin coating on hot pattern contactFoundry shells and cores for metal casting
Rubber bonding systemsActs as the methylene donor alongside resorcinol and silicaSteel cord and textile adhesion in tyres and belting
Methenamine saltsSalt formation with hippuric or mandelic acidUrinary antiseptic pharmaceutical products
Synthetic intermediatesFormylating, aminating and oxidising reagent in named reactionsAldehydes, primary amines and fine-chemical intermediates
Packing and supply

Packs for a dry, flammable solid

Every container carries the Chelora Amines label with product name, grade, net weight, batch number, manufacturing date, UN number and hazard pictograms, including the flame pictogram. Packs are sealed against moisture.

25 kg

Bags

PE-lined paper or polywoven bags, heat-sealed and palletised under shrink wrap. The standard pack for resin and compound producers.

500 / 1000 kg

Jumbo bags

Lined FIBCs with a discharge spout for contained charging — the better option wherever the powder grade is used in quantity.

Drums / LR

Drums and small packs

Lined fibre or steel drums where a rigid moisture-tight pack is wanted, and 500 g to 5 kg containers for laboratory and trial use.

Two things to tell us at enquiry stage that buyers routinely leave out: the particle size you need, and the end use. The first decides whether the material disperses properly in your mix; the second we are required to establish before accepting an order. Export consignments are packed in UN-specification packaging with full dangerous goods documentation for a Class 4.1 flammable solid, and shipped FOB, CIF or CFR through Nhava Sheva and Mundra.

Plan my supply
Handling, storage and safety

A flammable solid and a skin sensitiser

Hexamine is a flammable solid and may cause an allergic skin reaction. It is not corrosive and not acutely toxic in the way most amines on this site are, but it burns readily with an almost invisible flame, the powder grade presents a dust hazard, and contact with acid releases formaldehyde. The notes below are a summary for planning only; always work to the Safety Data Sheet and your own site risk assessment.

Fire and dust control

  • Treat as a flammable solid: control ignition sources, no smoking, no hot work near open material.
  • Hexamine burns with an almost smokeless, nearly invisible flame — brief your fire response team specifically on this.
  • Design powder handling against dust explosion risk: earthing, dust extraction and housekeeping.
  • Local exhaust ventilation at charging, weighing and transfer points.

Storage and incompatibilities

  • Store dry, sealed and under cover, below about 30 °C; moisture causes caking and slow hydrolysis.
  • Segregate strictly from acids and oxidising agents — acid contact releases formaldehyde.
  • Restrict and record access to the store; stock reconciliation is part of the precursor obligations.
  • Keep away from food and feed, and from any area where formaldehyde release would be a problem.

Personal protection

  • Gloves, coveralls and eye protection; sensitisation is the main health risk for regular handlers.
  • Dust mask or respiratory protection appropriate to the task where the powder grade is handled.
  • Treat persistent dermatitis in a handler as a possible sensitisation event rather than rotating them back.
  • Extraction on cure ovens and presses sized for the formaldehyde and ammonia released during cure.
Flammable solid — burns with a nearly invisible flame
May cause an allergic skin reaction
Releases formaldehyde on contact with acid
Formaldehyde and ammonia released during cure
UN 1328 · Class 4.1 · PG III
EU reportable explosives precursor

Regulatory status. Hexamine is listed in Annex II of Regulation (EU) 2019/1148 as a reportable explosives precursor, because it can be diverted into the manufacture of military explosives. Annex II status does not restrict sale to professional users, but it does create duties: economic operators must inform the supply chain, and suspicious transactions, disappearances and thefts must be reported to the national contact point. Several other jurisdictions impose their own licensing, record-keeping or reporting requirements. We confirm the end use before accepting an order, keep records of supply, and expect buyers to control and reconcile stock on their own sites. Check the position that applies where you operate rather than relying on a page like this one.

Confirm compliance
Certificate of AnalysisHexamethylenetetramine, technical grade · CAS 100-97-0
ParameterSpecificationResult
AppearanceWhite crystalline solidComplies
Assay, dry basis≥ 99.0%Complies
Loss on drying≤ 0.5%Complies
Residue on ignition≤ 0.03%Complies
pH, 10% solution7.0 – 10.0Complies
Heavy metals (as Pb)≤ 10 ppmComplies
Sample layout. Parameters follow the grade you order.QC passed
Quality and documentation

Every bag traceable to a tested batch

Hexamine is checked before dispatch. Each consignment leaves with the paperwork your QC, EHS, stores and accounts teams need on day one — and, for this product, the records that the precursor obligations expect.

COACertificate of Analysis with the test results for your specific batch, including assay, moisture, ash and particle size.
SDSSafety Data Sheet covering hazard classification, fire precautions, exposure controls, handling, storage and first aid.
HSN / HS codeHSN 2933 69 90 on domestic invoices; matching HS code on export documents.
Batch labelsGrade, net weight, batch number, manufacturing date and full hazard marking on every pack.
Export setCommercial invoice, packing list, certificate of origin, dangerous goods declaration and bill of lading.
On requestPrecursor supply-chain information, monograph test reports and country-specific declarations.
How ordering works

From enquiry to plant gate

Five steps for a first order of hexamine. The end-use check in step two is specific to this product.

Step 1

Send your requirement

Grade, particle size, quantity, pack size, intended application and your delivery location.

Step 2

End use confirmed

We confirm the intended use and the regulatory position in the destination market before an order is accepted — this is a precursor obligation, not a formality.

Step 3

Quote and batch check

We quote, then the batch is tested — assay, moisture, ash, pH and particle size — and the COA and SDS are prepared.

Step 4

Packed and dispatched

Sealed, labelled bags, FIBCs or drums move under dangerous goods documentation for a Class 4.1 flammable solid.

Step 5

Delivered and repeated

Material reaches your gate and repeat dispatches are scheduled to your usage, with supply records kept on both sides.

Questions buyers ask

Hexamethylenetetramine FAQ

Short answers to what purchase, lab, EHS and plant teams ask us most. Anything else, ask us directly.

What is hexamethylenetetramine used for?
Mostly as the hardener for novolac phenolic resins — moulding compounds, laminates, friction materials such as brake pads and clutch facings, resin-bonded abrasives, foundry shell-moulding sand and refractory binders. It is also the methylene donor in resorcinol-based rubber bonding systems, a corrosion inhibitor in acid pickling, a reagent in the Duff, Sommelet and Delépine reactions, and, as methenamine, a urinary antiseptic.
Why does hexamine cure phenolic resins?
Because it is formaldehyde and ammonia locked into a stable solid. A novolac resin is deliberately short of methylene bridges, so it will not cure on its own. At cure temperature hexamine decomposes, supplying the methylene groups that link the phenolic chains while the ammonia released catalyses the reaction. That is why it works as a one-pack latent hardener: inert in the mix, fully reactive in the press.
Is hexamine actually an amine?
Not in any useful sense. It has four nitrogens but no N–H bond at all, so it will not cure epoxy, will not react with isocyanates the way an amine does, and is a very weak base. Structurally it is a rigid cage — four nitrogens at the corners of a tetrahedron with six methylene bridges between them. Treat it as a formaldehyde and ammonia source rather than as an amine.
Is hexamine a controlled substance?
It is a regulated explosives precursor in a number of markets. In the European Union it is listed in Annex II of Regulation (EU) 2019/1148 as a reportable precursor, which does not restrict sale to professional users but does require suppliers to inform the supply chain and requires suspicious transactions, disappearances and thefts to be reported to the national contact point. Other jurisdictions apply their own licensing, record-keeping or reporting rules. We confirm the end use before accepting an order.
Should I take powder, granules or crystals?
It depends on your mixing time. Fine powder disperses quickly and evenly into a resin or friction compound but dusts badly, which is both a housekeeping and a flammability issue. Granular and crystalline grades flow cleanly, charge with far less airborne dust and suit automated weighing, but need longer to disperse. If you switch form, re-check your cure profile rather than assuming it carries across.
Does hexamine melt?
No. It sublimes and decomposes from around 260 °C rather than melting, which is why you will see a decomposition temperature rather than a melting point on the datasheet. That behaviour is exactly what makes it useful — it stays solid and unreactive right up to the point where it breaks down and does its job.
Why does my hexamine cake in storage?
Moisture. The material is stable when dry but picks up water in a humid store, which causes caking and, over time, slow hydrolysis that releases formaldehyde. Keep packs sealed, palletised and under cover, store below about 30 °C, and keep it strictly away from acids — acid contact releases formaldehyde quickly rather than slowly.
What should my fire team know about it?
That it is a flammable solid which ignites readily and burns with an almost smokeless, nearly invisible flame. That is unusual enough to be worth a specific briefing, because a hexamine fire will not look like a fire from a distance. The powder grade also needs handling design against dust explosion risk — earthing, extraction and housekeeping.
Will hexamine cure my epoxy resin?
No. Epoxy curing needs active amine hydrogens and hexamine has none — every nitrogen is tertiary and fully substituted. If you are looking for an aliphatic epoxy hardener, DETA or TETA are the usual starting points; if you need an aromatic one, MDA or m-phenylenediamine. Hexamine's curing role is specific to novolac phenolic chemistry.
What is the HS code for hexamine?
Hexamethylenetetramine sits under heading 2933 69, heterocyclic compounds with nitrogen hetero-atoms only — not under 2921 with the acyclic amines, because the nitrogens are inside a ring system. HSN 2933 69 90 appears on Indian invoices, and the matching national code appears on export documents.
Do you supply pharmacopoeial or food-grade material?
On enquiry, tested against the applicable monograph with the corresponding documentation. Those grades are a different supply arrangement from technical material, so tell us at enquiry stage rather than after a technical-grade quote — the testing, documentation and lead time all differ.
How do I get a price?
Send the grade, particle size, quantity, pack size, intended end use and delivery location through our contact page, by email to source@cheloraamines.com or by phone on +91 98191 11179. A complete enquiry usually gets a quote within 24 hours.

Order hexamine from Chelora Amines

Send the grade, particle size, quantity, pack size, intended end use and your delivery address or destination port. We come back with a price, the documents that go with the batch and a dispatch or shipping plan, usually within 24 hours.

Contact Chelora Amines

Call us+91 98191 11179 Email ussource@cheloraamines.com
Office102, L1, Ashok Premises, Nicholas Road, Andheri (East), Mumbai 400069