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Chlorinated Aniline Derivative · CAS 636-30-6

2,4,5-Trichloroaniline

C6H4Cl3N Molar mass 196.46 g/mol

A trichlorinated aniline intermediate supplied by Chelora Chemicals for azo dye, herbicide and pharmaceutical synthesis — exported from Indonesia in technical and high-purity grades, with full batch documentation on every shipment.

Identification Sheet REP.
IUPAC name2,4,5-Trichloroaniline
CAS number636-30-6
EC / EINECS number211-254-9
Molecular formulaC₆H₄Cl₃N
Molar mass196.46 g/mol
AppearanceGrey-brown crystalline powder
Common synonyms1-Amino-2,4,5-trichlorobenzene
Melting Point93 – 95 °Clit.
Boiling Point270 °Clit.
Density1.68 g/cm³typical
Flash Point175 °Cclosed cup
SolubilityLow in watersoluble in acetone, ethanol, benzene
Purity Offered97% / 99%+technical & high-purity
01 / PRODUCT DOSSIER

What 2,4,5-Trichloroaniline is, and why buyers source it

A working overview of the compound's chemistry, its place in the chlorinated aniline family, and the grades Chelora Chemicals keeps in regular supply.

2,4,5-Trichloroaniline is a trichlorinated derivative of aniline, carrying chlorine atoms at the 2-, 4- and 5-ring positions relative to the amino group. With three chlorines contributing inductive electron withdrawal but none directly conjugated through the ring in a way that fully shuts down the amine's reactivity, the nitrogen retains enough nucleophilicity for the standard primary-arylamine reactions — diazotization, acylation and further substitution — while the heavily chlorinated ring itself gives the finished molecules built from it good chemical and biological stability, a property widely exploited in agrochemical and antimicrobial chemistry.

At room temperature it is a grey-brown crystalline solid, only sparingly soluble in water but soluble in common organic solvents such as acetone, ethanol and benzene.

Where it fits in the synthesis chain

Like other chlorinated anilines, 2,4,5-trichloroaniline is used almost exclusively as a synthesis intermediate. Its amino group is diazotized and coupled to build azo dye chromophores, or acylated and otherwise elaborated to build herbicide, insecticide and antiviral agent structures. The particular 2,4,5-trichloro substitution pattern recurs across several classes of crop-protection and pharmaceutical chemistry, which is why this specific isomer — rather than a different trichloroaniline — is the one most consistently in demand.

Grades we supply

Chelora Chemicals offers 2,4,5-Trichloroaniline in technical grade (≈97% assay) for standard industrial synthesis, and high-purity grade (99%+) for applications sensitive to isomer carryover or trace metal content. Both grades are supplied with a batch-wise certificate of analysis so your incoming QC team can verify the parameters you ordered against.

02 / MANUFACTURING ROUTE

How 2,4,5-Trichloroaniline is made

An overview of the production route for orientation purposes. Our manufacturing partners' own process parameters and in-process controls are proprietary and are not disclosed beyond what is needed to interpret the certificate of analysis.

Commercial-scale 2,4,5-trichloroaniline is produced by the catalytic reduction of 2,4,5-trichloronitrobenzene, following the same general pattern used for other chlorinated anilines in our range. The starting nitro compound is obtained by chlorination and nitration of benzene in a controlled sequence that fixes the three chlorines in the 2,4,5-relationship to the eventual amino group.

Reduction of 2,4,5-trichloronitrobenzene to the amine is most commonly carried out by catalytic hydrogenation (Pd/C or Raney nickel under hydrogen), with an older iron/acid (Béchamp-type) reduction also used on a smaller scale. As with other polychlorinated nitrobenzenes, hydrogenation conditions are controlled to minimize hydrodechlorination — the loss of a ring chlorine under overly aggressive reduction conditions — which would otherwise generate dichloroaniline impurities.

After reduction, the crude amine is washed and vacuum-distilled or recrystallized to remove unreacted starting material, partially dechlorinated by-products and residual catalyst metals before drying and packing. This purification step is where technical grade and high-purity grade material part ways.

Why the chlorination/nitration sequence matters

As with the other chlorinated anilines we supply, the positions of the three chlorines are fixed at the chlorination and nitration stage of the starting benzene, well before the amine is ever formed. This is why 2,4,5-trichloroaniline and other trichloroaniline isomers are sourced from distinct manufacturing streams, and why isomer purity is reported on the certificate of analysis as a core specification.

03 / APPLICATIONS

Industries and processes that use it

2,4,5-Trichloroaniline is consumed almost entirely as a synthesis intermediate. The fields below account for most of the global demand we see through our export desk.

Field 01

Azo Dyes

Diazotized and coupled to build azo dye chromophores, where the trichlorinated ring contributes to the finished colourant's shade and lightfastness.

Field 02

Herbicides & Insecticides

A building block in the synthesis of chlorinated herbicide and insecticide active ingredients, where the stability of the trichlorinated ring is part of the target structure.

Field 03

Antiviral & Pharmaceutical Intermediates

Used in the synthesis of antiviral agents and other pharmaceutical intermediates that call for a trichlorinated aniline core.

Field 04

Specialty & Chlorinated Aromatics

A starting material for further chlorinated aromatic compounds used across process and research chemistry.

04 / REACTION CHEMISTRY

How the molecule is typically carried forward

The primary amine remains the reactive handle, with the three ring chlorines moderating its reactivity by induction. Reaction classes below account for most of the ways 2,4,5-Trichloroaniline is converted into a finished intermediate downstream.

Diazotization

Reaction of the amino group with nitrous acid (generated in situ, held below 5 °C) converts the amine into a diazonium salt — the entry point for azo-coupling and Sandmeyer-type substitution chemistry.

Azo Coupling

The diazonium intermediate is coupled with an electron-rich aromatic partner to build the azo (–N=N–) linkage that forms the chromophore core of dye structures.

Acylation

Reaction with an acid chloride or anhydride converts the amine to an amide, a step used in building herbicide, insecticide and pharmaceutical active-ingredient scaffolds from this intermediate.

Further Ring Substitution

Under suitable conditions, one of the ring chlorines can itself be displaced by a nucleophile, a route used to access further substituted aniline intermediates from the same starting material.

05 / RELATED BUILDING BLOCKS

2,4,5-Trichloroaniline against other chlorinated anilines we supply

Buyers sourcing 2,4,5-trichloroaniline often need a related chlorinated or nitro-chlorinated aniline for a neighbouring step in the same process. A quick reference to what else is on our regular supply list.

ProductCAS NumberCategoryNotes
2,4,5-Trichloroaniline636-30-6Trichlorinated primary arylamineThe product on this page — our most regularly stocked trichloroaniline.
2,4-Dichloroaniline554-00-7Dichlorinated primary arylamineA less-chlorinated analogue in the same intermediate class — see its product page.
Ortho Chloro Para Nitro Aniline121-87-9Chloro-nitro primary arylamineA diazo-component building block for a different downstream chemistry — see its product page.
2,6-Dichloro-4-Nitroaniline99-30-9Dichloro mono-nitro primary arylamineAlso supplied as the Dichloran fungicide active — see its product page.

Exact physical constants and purity specifications are confirmed per batch on the certificate of analysis — treat the notes above as a sourcing guide, not a specification sheet, for products other than 2,4,5-Trichloroaniline.

06 / HAZARD & HANDLING

Safety classification at a glance

Based on GHS classification as commonly listed for this substance. This is a summary for orientation only — always work from the current safety data sheet supplied with your specific batch.

H301 / H311 / H331

Toxic if swallowed, in contact with skin or if inhaled.

H373

May cause damage to organs through prolonged or repeated exposure.

H410

Very toxic to aquatic life, with long-lasting effects.

Storage Note

Keep away from strong oxidizers and reducing agents.

Dust Handling

Avoid generating or inhaling dust during transfer and weighing.

Colour Check

Significant darkening on receipt can indicate degradation; verify against the batch CoA.

Combined Statement

H301+H311+H331: a single combined acute-toxicity classification covering all three exposure routes.

Signal word

Danger — GHS06 toxic, GHS08 health hazard and GHS09 environmental pictograms commonly apply.

Handle with chemical-resistant gloves, eye/face protection and adequate ventilation or respiratory protection; avoid release to drains and waterways given its aquatic toxicity profile. Full first-aid, storage, spill and PPE guidance is in the MSDS issued with every shipment.

07 / STORAGE & SHELF LIFE

Keeping it on spec between delivery and use

General storage guidance for this grade. Site-specific storage rules, segregation requirements and re-test intervals should follow your own EHS procedures and the MSDS issued with your batch.

Storage TemperatureCool, ambient
ContainerOriginal sealed drum / bag
Typical Shelf Life24 months, unopened
Keep Away FromOxidizers, strong acids
Beyond Shelf LifeRe-assay before use

Store in a dry, well-ventilated area out of direct sunlight, in tightly closed original packaging, segregated from strong oxidizing and acidic materials. Once a container is opened, reseal it promptly to limit moisture pickup, which can affect both the measured assay and handling characteristics. If a batch is held past its retest date, re-check assay and moisture before use.

08 / PACKING & EXPORT

How it ships from Indonesia

Standard packing and export terms for this product. Confirm exact figures against your order — they vary slightly by destination and quantity.

Standard Packing25 kg bags
Bulk PackingDrums / jumbo bags
Min. OrderFrom 1 drum
Lead Time2 – 4 weeks
Export TermsFOB · CFR · CIF
09 / QUALITY & DOCUMENTATION

What travels with every batch

Specification is agreed before the purchase order, not discovered on arrival. Every shipment of 2,4,5-Trichloroaniline leaves with a documented, checkable paper trail.

Doc 01

Certificate of Analysis

Batch-wise assay (by GC), isomer purity, melting point range and moisture, issued against the agreed specification so your QC team can check it, not just file it.

Doc 02

Safety Data Sheet

GHS-format SDS in English covering hazard classification, handling, storage, first-aid and spill response for the exact grade shipped.

Doc 03

Technical Data Sheet

Reference physical and chemical properties, recommended storage and typical applications, for internal circulation to your process or R&D teams.

Doc 04

Certificate of Origin

Confirms Indonesian origin for customs clearance and any preferential-duty claim at your destination port.

Doc 05

Dangerous Goods Declaration

UN packing group, classification and shipper's declaration prepared ahead of loading so documentation never holds up customs.

Doc 06

Third-Party Inspection

Independent pre-shipment inspection and re-sampling can be arranged on request, at your cost, for buyers who require it as a matter of policy.

10 / FAQ

Frequently asked questions

What buyers most often ask our sales desk about this grade.

01What is 2,4,5-Trichloroaniline used for?+
It is used mainly as a chemical intermediate in the manufacture of azo dyes, chlorinated herbicide and insecticide active ingredients, and antiviral and other pharmaceutical intermediates.
02What is the CAS number of 2,4,5-Trichloroaniline?+
Its CAS Registry Number is 636-30-6, with molecular formula C₆H₄Cl₃N and a molar mass of 196.46 g/mol.
03What purity grades does Chelora Chemicals supply?+
We supply technical grade (around 97% assay) for standard industrial synthesis, and high-purity grade (99%+) for processes sensitive to isomer carryover or trace impurities. Each batch is shipped with a certificate of analysis.
04Is 2,4,5-Trichloroaniline hazardous?+
Yes. It carries a GHS “Danger” signal word with hazard statements covering acute toxicity (oral, dermal, inhalation), organ damage on repeated exposure, and toxicity to aquatic life. It should be handled with appropriate PPE and in line with the MSDS supplied with each shipment.
05How does 2,4,5-Trichloroaniline compare to 2,4-Dichloroaniline?+
Both are chlorinated primary anilines used in similar downstream chemistry (diazotization, acylation), but the extra ring chlorine in the trichloro version further moderates the amine's reactivity and adds chemical stability to the finished molecule, which is why process chemists specify one or the other depending on the target structure.
06What packing options are available?+
Standard packing is 25 kg bags, with drums and jumbo bags available for bulk orders. Trial quantities from a single drum can usually be arranged before you commit to larger volumes.
07How long does delivery take?+
Typical lead time is two to four weeks plus transit, depending on whether the grade is ex-stock or made to order and your destination port. A firm date is confirmed in the written quotation.
08Can I get a sample before placing a bulk order?+
Yes. Pre-shipment samples and a batch certificate of analysis can be arranged so your QC team can verify the specification before committing to volume.
09Do you supply other chlorinated anilines?+
Yes, we also supply 2,4-Dichloroaniline and several chloronitroaniline diazo components, and can source other chlorinated aniline building blocks on request.
10How is 2,4,5-Trichloroaniline manufactured?+
It is produced by reducing 2,4,5-trichloronitrobenzene, most commonly by catalytic hydrogenation, followed by washing and distillation or recrystallisation to remove partially dechlorinated by-products and trace catalyst metals before packing.
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