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Dinitroaromatic · CAS 99-65-0

Meta Dinitrobenzene

C6H4N2O4 Molar mass 168.11 g/mol

A dinitroaromatic intermediate supplied by Chelora Chemicals as the meta-nitrated downstream step from Nitrobenzene — principally valued as the route into m-phenylenediamine and 3-nitroaniline chemistry — exported from Indonesia with full batch documentation on every shipment.

Identification Sheet REP.
IUPAC name1,3-Dinitrobenzene
CAS number99-65-0
Molecular formulaC₆H₄N₂O₄
Molar mass168.11 g/mol
AppearancePale yellow crystalline solid
Common synonymsm-Dinitrobenzene, 1,3-DNB
Melting Point89.6 °Clit.
Boiling Point297 °Cat 1 atm
Specific Gravity1.575at 20 °C
Flash Point149 °Cclosed cup
AppearancePale yellow crystals / flakestechnical grade
Purity Offered98% / 99%+technical & high-purity
01 / PRODUCT DOSSIER

What Meta Dinitrobenzene is, and why buyers source it

A working overview of the compound's chemistry, how it sits downstream of Nitrobenzene in our range, and the grades Chelora Chemicals keeps in regular supply.

Meta Dinitrobenzene (1,3-dinitrobenzene) is a benzene ring carrying two nitro groups in the 1,3 (meta) relationship. It is the direct product of nitrating Nitrobenzene a second time: the first nitro group is already a strong electron-withdrawing, meta-directing substituent, so the incoming second nitro group is channelled almost exclusively to the position meta to the first, which is why 1,3-dinitrobenzene so heavily dominates over the 1,2 and 1,4 isomers in the product mixture.

At room temperature it is a pale yellow crystalline solid, only slightly soluble in water but readily soluble in common organic solvents such as benzene, toluene and acetone. Like other nitroaromatics, it is handled as a toxic, environmentally persistent material rather than a benign commodity solid, and the hazard and handling information on this page should be read in full before it is ordered.

Where it fits in the synthesis chain

The commercially important chemistry of meta dinitrobenzene is almost entirely in the reduction of one or both nitro groups. Selective partial reduction of one nitro group gives 3-nitroaniline, an intermediate used in dye and pigment synthesis; full reduction of both nitro groups gives m-phenylenediamine, a key building block for aramid fibres (of the Kevlar/Nomex family) and for certain epoxy-resin curing agents. Chelora Chemicals supplies the dinitro starting material into both of these downstream chains.

Grades we supply

We offer Meta Dinitrobenzene in technical grade (≈98% assay) for standard reduction chemistry, and high-purity grade (99%+) for buyers whose downstream amine product is sensitive to isomeric (ortho/para-dinitrobenzene) carryover. Both grades ship with a batch-wise certificate of analysis.

02 / MANUFACTURING ROUTE

How Meta Dinitrobenzene 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.

Meta Dinitrobenzene is manufactured by the nitration of Nitrobenzene with a mixed nitric/sulfuric acid system, using sulfuric acid as catalyst and dehydrating agent in the same way as the first nitration step that makes nitrobenzene itself. Because the existing nitro group is a powerful meta-director, this second nitration is highly selective: the literature reports roughly 93% of the product forming at the meta position relative to the first nitro group, with only minor amounts of the ortho and para dinitrobenzene isomers formed alongside it.

After nitration, the crude product is separated from the spent acid, washed, and crystallised or distilled to the required purity before packing. The isomer separation step is what distinguishes technical grade from high-purity grade material.

Why the starting material matters

Starting from nitrobenzene rather than from benzene directly is what gives such strong control over which dinitrobenzene isomer dominates; attempting to introduce both nitro groups independently, without the first group's directing influence already in place, would give a far less selective and less useful isomer mixture.

03 / APPLICATIONS

Industries and processes that use it

Meta Dinitrobenzene is consumed almost entirely as a reduction-chemistry intermediate. The fields below account for most of the global demand we see through our export desk.

Field 01

Aramid Fibre Intermediate (m-Phenylenediamine)

Full reduction of both nitro groups gives m-phenylenediamine, a key monomer for aramid fibres of the Kevlar/Nomex family and for certain high-performance polymer chemistry.

Field 02

3-Nitroaniline Intermediate

Selective partial reduction of one nitro group gives 3-nitroaniline, used as an intermediate in dye and pigment synthesis.

Field 03

Epoxy Curing-Agent Chemistry

m-Phenylenediamine derived from this material is also used as a curing agent in certain epoxy-resin systems requiring high thermal performance.

Field 04

Dye & Pigment Intermediate Chemistry

Serves as a building block in broader nitroaromatic and amine-based dye and pigment intermediate synthesis.

04 / REACTION CHEMISTRY

How the molecule is typically carried forward

Both nitro groups are reduction handles, and which one (or both) is reduced determines the downstream product. Reaction classes below account for most of the ways Meta Dinitrobenzene is converted into a finished intermediate.

Selective Partial Reduction

Controlled catalytic or chemical reduction of a single nitro group gives 3-nitroaniline, leaving the second nitro group intact for further chemistry or isolation as the finished intermediate.

Full Reduction to m-Phenylenediamine

Complete catalytic hydrogenation of both nitro groups gives m-phenylenediamine, the aramid-fibre and epoxy-curing-agent building block that represents the largest downstream use of this material.

Diazotization of the Reduced Amine

Once reduced to an amine, the resulting aniline derivative can be diazotized under standard cold, acidic conditions for azo-coupling chemistry in dye and pigment manufacture.

Acid-Base & Salt Formation

Both 3-nitroaniline and m-phenylenediamine form well-characterised salts with mineral acids, used in some purification and formulation steps downstream.

05 / RELATED BUILDING BLOCKS

Meta Dinitrobenzene against other nitroaromatic building blocks we supply

Buyers sourcing meta dinitrobenzene often need Nitrobenzene itself for an earlier step, or a chloronitrobenzene isomer for a parallel process. A quick reference to what else is on our regular supply list.

ProductCAS NumberCategoryNotes
Meta Dinitrobenzene99-65-0Di-nitro aromaticThe product on this page — made by a second, meta-directed nitration of Nitrobenzene.
Nitrobenzene98-95-3Mono-nitro aromaticThe foundational starting material for this product — see its product page.
Ortho Nitrochlorobenzene88-73-3Mono-chloro mono-nitro aromaticMade from chlorobenzene nitration (ortho/para mixture) — see its product page.
Meta Nitrochlorobenzene121-73-3Mono-chloro mono-nitro aromaticMade from nitrobenzene chlorination (meta-directed) — 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 Meta Dinitrobenzene.

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.

H300 / H310 / H330

Fatal 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.

Blood & Organ Effects

Nitroaromatic amines and their precursors are associated with methaemoglobinaemia and other blood-related effects on overexposure.

Environmental Handling

Treat as persistent in the aquatic environment; avoid any release to drains or waterways.

PPE Standard

Impervious gloves, splash-proof eye protection and suitable respiratory protection are the baseline for routine handling.

Dust Control

Technical-grade flake/crystal material can generate dust; local exhaust ventilation is recommended during transfer and weighing.

Signal word

Danger — GHS06 acute toxicity and GHS09 environmental hazard pictograms apply.

This is a severely acutely toxic material by all three exposure routes, and must be handled with impervious gloves, full eye/face protection and suitable respiratory protection at all times; avoid any skin contact or inhalation of dust. It is also very toxic to aquatic life with long-lasting effects, so spill and waste handling must prevent any release to drains or waterways. Full first-aid, storage, spill and PPE guidance is in the MSDS issued with every shipment, and should be read in full before this material is handled.

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, dry
ContainerOriginal sealed packaging
Typical Shelf Life24 months, unopened
Keep Away FromStrong oxidizers, strong reducing agents
Beyond Shelf LifeRe-assay before use

Store in a cool, dry, well-ventilated area away from direct sunlight and ignition sources, in tightly closed original packaging, segregated from strong oxidizing and strong reducing materials. Avoid generating or accumulating dust during handling. If a batch is held past its retest date, re-check assay, melting point and colour 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 fibre drums / bags
Bulk Packing500 kg / 1,000 kg 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 Meta Dinitrobenzene leaves with a documented, checkable paper trail.

Doc 01

Certificate of Analysis

Batch-wise assay, melting point range, isomer content and colour, 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 Meta Dinitrobenzene used for?+
Its main use is as a reduction-chemistry intermediate: selective partial reduction gives 3-nitroaniline, a dye and pigment intermediate, while full reduction of both nitro groups gives m-phenylenediamine, a key monomer for aramid fibres (Kevlar/Nomex-type) and certain epoxy curing agents.
02What is the CAS number of Meta Dinitrobenzene?+
Its CAS Registry Number is 99-65-0, with molecular formula C₆H₄N₂O₄ and a molar mass of 168.11 g/mol.
03How is Meta Dinitrobenzene made?+
It is manufactured by nitrating Nitrobenzene a second time with a mixed nitric/sulfuric acid system. The first nitro group strongly directs the second nitration to the meta position, giving roughly 93% selectivity for the 1,3-dinitrobenzene isomer.
04What purity grades does Chelora Chemicals supply?+
We supply technical grade (around 98% assay) for standard reduction chemistry, and high-purity grade (99%+) for applications sensitive to isomeric dinitrobenzene carryover. Each batch ships with a certificate of analysis.
05Is Meta Dinitrobenzene hazardous?+
Yes, significantly so. It carries a GHS “Danger” signal word with hazard statements covering fatal acute toxicity by all three exposure routes, organ damage on repeated exposure, and very toxic, long-lasting effects on aquatic life. It must be handled with the PPE and precautions specified in the MSDS supplied with each shipment.
06What is m-phenylenediamine and why does it matter here?+
m-Phenylenediamine is the fully reduced form of this material (both nitro groups converted to amines). It is a key monomer for aramid fibres of the Kevlar/Nomex family and is used as a curing agent in certain high-performance epoxy systems.
07What packing options are available?+
Standard packing is 25 kg fibre drums or bags, with 500 kg or 1,000 kg jumbo bags available for bulk orders. Trial quantities can usually be arranged before you commit to larger volumes.
08How 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.
09Can 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.
10Do you supply other nitroaromatic building blocks?+
Yes, we also supply Nitrobenzene, Ortho Nitrochlorobenzene and Meta Nitrochlorobenzene, and can source other nitroaromatic intermediates on request.
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