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4-Nitro-O-Phenylenediamine

    • Product Name 4-Nitro-O-Phenylenediamine
    • Alias 4-nitro-1,2-benzenediamine
    • Einecs 202-870-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    630725

    Product Name 4-Nitro-o-phenylenediamine
    Cas Number 99-56-9
    Molecular Formula C6H7N3O2
    Molecular Weight 153.14 g/mol
    Appearance Orange to brown crystalline powder
    Melting Point 173-177 °C
    Solubility In Water Slightly soluble
    Density 1.48 g/cm3
    Purity Typically ≥98%
    Synonyms 4-Nitro-1,2-phenylenediamine; 4-Nitrobenzene-1,2-diamine
    Smiles C1=CC(=C(C(=C1)N)[N+](=O)[O-])N
    Inchi InChI=1S/C6H7N3O2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H,7-8H2
    Ec Number 202-768-6
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 4-Nitro-O-Phenylenediamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package of 4-Nitro-O-Phenylenediamine is supplied in a sealed amber glass bottle with detailed hazard labeling.
    Shipping 4-Nitro-O-Phenylenediamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. The packaging complies with relevant regulations for hazardous chemicals, including correct labeling and documentation. Transport typically requires ground or air shipment with appropriate safety measures to minimize risk of spillage, exposure, or environmental contamination.
    Storage **4-Nitro-O-Phenylenediamine** should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Ensure storage in clearly labeled containers, and avoid elevated temperatures to prevent decomposition. Handle with appropriate protective equipment to avoid inhalation, ingestion, or skin contact.
    Application of 4-Nitro-O-Phenylenediamine

    Applications of 4-Nitro-O-Phenylenediamine in Industrial Manufacturing

    4-Nitro-O-Phenylenediamine serves as a core intermediate in several advanced chemical manufacturing sectors. As the direct source manufacturer, we supply this compound for downstream processes that require high purity and precision in synthesis, contributing to the performance and safety of end products. Below, we highlight key industrial application segments, including detailed compliance, process, and end-use product information.

    1. Organic Dye Intermediates for Textile Industry

    In textile dye manufacturing, our material acts as a critical building block for producing various azo and anthraquinone dyes. These dye classes require consistent intermediate quality to ensure stable color development and resistance properties. End users depend on our tight quality control to avoid off-shades, insoluble residues, and excessive impurities in dye formulations. Typical application routes include multi-step diazotization and coupling reactions, where batch-to-batch consistency minimizes wastage and rework in large-scale production.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Regulation (EC No. 1907/2006) compliance
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • Employed at 1–5% of total dye intermediate mass during synthesis, adjustable based on targeted chromophore structure, bath ratio, and dye purity demands.

    Downstream process integration

    • Feeds into primary diazotization step, followed by coupling with aromatic amines or phenols under acid or neutral conditions to construct the dye molecule framework.

    Final product types

    • Azo disperse dyes for polyester and acetate fibers
    • Anthraquinone acid dyes for wool and silk
    • Pre-metallized fast dyes used in nylon fabric processing
    • Direct dyes for cellulosic fibers

    2. Specialty Pigment Synthesis for Automotive Coatings

    Our chemical intermediate is used to create advanced pigments in the automotive paint sector, ensuring color stability, UV resistance, and precise particle dispersion for OEM finishes. Automotive pigment manufacturers integrate it during controlled high-temperature condensation reactions, where reliable traceability and absence of byproducts prevent shade variation and defects in multilayer coating systems. Downstream operations include surface modification and final pigment dispersion into resin systems.

    Industry compliance standards

    • Global Automotive Declarable Substance List (GADSL)
    • ISO 12944-6:2018 for corrosion protection paints
    • Automotive industry supply chain standards (IATF 16949)
    • RoHS (2011/65/EU) for heavy metal limits

    Typical usage ratio

    • Utilized at 2–7% relative to combined pigment precursor mass, proportional to targeted pigment particle size and color shade required by end paint systems.

    Downstream process integration

    • Introduced in the nucleation stage of pigment synthesis, followed by calcination and controlled surface treatment to enhance dispersibility in coating resin matrices.

    Final product types

    • Solid automotive basecoat pigments
    • Pearlescent pigments for luxury vehicles
    • Micronized effect pigments for metallic finishes
    • OEM repair coating raw materials

    3. Pharmaceutical Intermediates for API Synthesis

    Pharmaceutical ingredient manufacturers use this raw material for constructing key heterocyclic scaffolds in non-steroidal anti-inflammatory drugs and antibacterial agents. Compliance with pharmacopeial trace impurity limits is essential, as the compound’s amine-nitro structure offers a route to highly selective ring-closure and reduction reactions. Our controlled synthesis minimizes genotoxic and nitrosamine impurities, allowing direct use in GMP-compliant active pharmaceutical ingredient chains.

    Industry compliance standards

    • ICH Q3A/B Guidelines on impurities in new drug substances and products
    • European Pharmacopoeia (Ph.Eur.) and United States Pharmacopeia (USP)
    • 21 CFR Part 210/211 cGMP for finished pharmaceuticals
    • ISO 22716 for cosmetic GMP (where applicable)

    Typical usage ratio

    • Charged at 0.8–3% of total API batch mass during multi-step heterocyclic assembly, adjusted by route efficiency, tolerance of byproduct levels, and downstream crystallization yields.

    Downstream process integration

    • Feeds initial ring-closing reaction; often followed by catalytic hydrogenation, acylation, or condensation for final API formation.

    Final product types

    • Intermediates for fluoroquinolone antibiotics
    • NSAID scaffolds for pain management APIs
    • Precursor to active benzodiazepine derivatives
    • Bulk pharmaceutical intermediates for contract manufacturing

    4. Photographic Chemical Manufacturing

    This compound supports the synthesis of key dyes and developing agents used in emulsified photographic and X-ray films. Film material suppliers require stable, low-impurity intermediates to prevent fogging, color drift, and precipitation during film casting and photographic development. Our high-purity grade material is processed under conditions designed for controlled batch reproducibility, critical for downstream emulsion blending and micro-encapsulation.

    Industry compliance standards

    • ANSI IT9.2 and ISO 18902 for imaging material preservation
    • DIN EN ISO 14001 for environmental management in chemical manufacturing
    • RoHS and REACH compliance for hazardous content control
    • Internal QC protocols for silver halide film production

    Typical usage ratio

    • Incorporated at 0.5–2% of the total developing agent or dye mass; adjusted based on film sensitivity, image density requirements, and desired shelf-life extension.

    Downstream process integration

    • Added during forming or stabilizing of color-coupler chemistry in film emulsion tanks, with careful control of pH and redox potential.

    Final product types

    • Color-coupler for photographic films
    • Sensitizing dyes in X-ray and medical imaging films
    • Emulsion stabilizers for archival photo materials
    • Developer bath concentrates for professional use

    5. Advanced Polymer Additives

    In specialty polymer synthesis, our product functions as an antioxidant precursor and UV stabilizer component, primarily for engineering plastics and high-performance polymer films. Resin compounders use this intermediate for in situ modification and to create functional additives by chemical grafting processes. Precise upstream quality control allows for reproducible additive performance, maintaining required transparency, mechanical integrity, and aging resistance in demanding service environments.

    Industry compliance standards

    • FDA 21 CFR 177.1520 for additives in food-contact polymers (when applicable)
    • ISO 4892 Weathering Test Protocols for polymers
    • UL 94 flammability standard for plastic components
    • REACH registration, evaluation, and authorization

    Typical usage ratio

    • Blended at 0.2–1.5% relative to total resin batch; selection based on required UV resistance, processing temperature, and intended end-use lifetime.

    Downstream process integration

    • Introduced into melt-phase polymerization or post-polymerization grafting, then compounded into masterbatches or directly into matrix resins before extrusion or molding.

    Final product types

    • Polyolefin films for packaging
    • Engineering resin parts for electronics
    • Anti-aging additives for outdoor-use plastics
    • Specialty fiber spinning ingredient for technical textiles

    6. Corrosion Inhibitor Precursors for Metal Treatment

    Metalworking fluid and surface treatment compound manufacturers rely on this chemical as a precursor for several corrosion inhibitor molecules. The controlled reactivity of the amine groups under nitration or subsequent diazotization provides a tailored path to high-affinity metal protective agents. Our precision synthesis supports downstream blending into high-performance anti-corrosion coatings and pickling inhibitors, essential for extending equipment lifespan and preventing surface failure in harsh environments.

    Industry compliance standards

    • ASTM D6109 for water-based metal cleaners
    • ISO 8044 for corrosion management in industrial sectors
    • REACH compliance for precursor chemicals in corrosion inhibitors
    • Applicable local environmental protection regulations

    Typical usage ratio

    • Reacted at 0.5–4% of total concentrate weight in inhibitor synthesis; ratio chosen based on target substrate (steel, copper, aluminum), aggressiveness of service fluid, and required inhibitor residual film thickness.

    Downstream process integration

    • Converted to active inhibitor species by further diazotization or condensation; then incorporated into concentrate batches for blending with aqueous or oil-based metalworking fluids.

    Final product types

    • Acid pickling inhibitors for steel pipes
    • Corrosion-inhibiting additives for circulating water systems
    • Protective surface treatments for industrial machinery
    • Metalworking emulsifier concentrates
    Free Quote

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    Email: sales7@sinochem-nanjing.com

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    Certification & Compliance
    More Introduction

    Practical Insights on 4-Nitro-O-Phenylenediamine from a Manufacturer’s View

    Understanding 4-Nitro-O-Phenylenediamine in Real Factory Terms

    On the production floor, 4-Nitro-O-Phenylenediamine never comes across as an obscure chemical destined for niche benches. It lands in our hands raw, and we understand how small adjustments in reaction conditions change its crystal form, texture, and the depth of yellow-brown that tells us purity even before a GC trace confirms it. This aromatic diamine has built its reputation as a sharp tool across several industries because it responds predictably to strong organic transformations. Back in our labs, every new run means more real-world feedback: stability at scale, resilience to temperature shifts, and its unwavering nucleophilicity in highly substituted ring systems.

    In-house, we produce 4-Nitro-O-Phenylenediamine under the model designation 4NOD-99. Our team runs the synthesis by direct nitration, using pure o-phenylenediamine and carefully monitored nitric acid feeds. This gives us tight control over the position and extent of nitration, so the product always lands with a nitro group on the para position relative to one amino group and ortho to the other. Minor impurities get chased out at each clean-up, leaving material with assays regularly above 99% by HPLC. This is not just a number; chemists downstream know a trace contaminant can poison a whole batch.

    Real Value in Synthesis and Applications

    Anyone who works with dyes, research reagents, or sensor chemistry soon runs into 4-Nitro-O-Phenylenediamine. What we see, year after year, are returning inquiries not from textbook researchers but from hands-on technologists fixing color-fading inks, improving fastness in polyamide dyeing, or troubleshooting polymer batches when lesser intermediates stall mid-polymerization. Chemists trust 4NOD-99 for the comfort in its strong activating and electron-donating amino groups, balanced by a single electron-withdrawing nitro group. This subtle tuning opens up pathways that other diamines, even close analogues such as 2,4-dinitroaniline or m-phenylenediamine, simply cannot offer. It provides a different palette: one that resists over-oxidation yet offers good solubility under many conditions.

    Many asked if 4-Nitro-O-Phenylenediamine stands apart from related intermediates because of price, availability, or just academic curiosity. Our real answer always comes back to its role enabling specific reactions where mono-nitrated, ortho-substituted phenylenediamines give better selectivity, particularly in azo coupling and heterocycle formation. Where dinitro- or mixed chloro-derivatives choke progress with steric hindrance, 4NOD-99’s clean substitution pattern clears the way. Polymer chemists enjoy its performance as a chain-extension monomer for specialty materials, where alternative diamines either kill flexibility or tip the process into runaway rates. The balance between reactivity, color depth, and compatibility—especially for high-performance coatings and functional dyes—makes it a staple, not just another option.

    Packing and Handling: What Actually Matters in Operation

    We never just ship out powder and walk away. Most clients, especially those running at production levels, care intensely about how a batch will handle inside their own plant. We pack 4NOD-99 in lined, anti-static fiber drums or heat-sealed PE bags, minimizing clumping and moisture uptake because everyone remembers the day a cheap bag ruined a reactor feed. A good chemist remembers not only the reaction recipe but also what the bag looked like—too many cost overruns stem from missed handling details. Our workers weigh out by eye, by feel, double-check the load, and keep track of color shade, because any drift sometimes hints at an upstream minor process hiccup. Communication goes deep; we update clients about any process tweak that might affect downstream reactivity, color, or trace metal content.

    On the factory floor and in the shipping bay, there's zero patience for wordy safety tips or abstract paperwork; what actually keeps workers safe is hard-won experience seeing how the nitro-amino system responds to humidity, light, or accidental mixing with strong oxidizers. We've learned not to cut corners here. Anything more than mild exposure—especially to skin and mucous membranes—causes strong irritation, so our standard practice involves gloves, face mask, and routine air extraction. Pipelines get flushed if the batch runs hot, and storage always happens in cool, dry, inert conditions. Mistakes have taught us more about temperature excursions than a thousand theoretical protocols—residual solvent or ammonia can jumpstart a runaway reaction nobody wants to clean up on a Friday.

    Why Quality and Traceability Change Everything

    Plenty of buyers try to compare 4-Nitro-O-Phenylenediamine to “commodity” diamines—something off a global trade platform, cut with untold residuals or stale from months parked in sea containers. This is a false economy in real chemistry. From our own failures and those of our competitors, it’s easy to spot the problem: even a hint of dinitro impurity or residual sulfate affects color stability, dyeing reproducibility, and sensor sensitivity. Technical teams in R&D departments send us requests for granular batch data—trace metal analysis, residual chloride, particle size distribution—because critical syntheses fail otherwise. We’ve invested in regular batch fingerprinting: our automated Karl Fischer moisture test hits less than 0.1%, and GC qualifying checks for byproducts down to 10 ppm. We keep full logs on every run so customers aren’t chasing batch-to-batch surprises.

    We ship samples globally and have seen how climate and warehousing can affect shelf life and usability. Most resellers can’t trace a lot number; our practice is to register every outgoing consignment with a digital profile so repeated orders never drift from specification. We've had emergency calls about competitor failures: substitution gone wrong in textile pigmentation or lost yield for pre-polymer prep. Sometimes, only close technical backup avoids outright production downtime. You don’t gain trust with certificates alone—real reliability comes through consistency, open data, and fast response in troubleshooting.

    Getting the Most from 4-Nitro-O-Phenylenediamine in Formulations

    We work alongside customers running textile dyes, specialty pigments, high-precision electronics, and advanced polymers. They look to 4-Nitro-O-Phenylenediamine not for generic performance, but to push what’s possible: deeper color, sharper contrast, higher response in sensors, or stronger chain-building in resins. Years of feedback cycle into our process: controlling residual acidity improves downstream coupling for azo dyes; matching granule size with intake systems cuts dust and waste; and narrowing polymorph ratios keeps reactivity within strict tolerances.

    The technical handbooks may say phenylenediamines are interchangeable, but in continuous chemical lines or high-value batch runs, subtle differences have dramatic effects on cost, yield, and product reliability. For instance, in chemosensor assembly, the stiffness of the aromatic backbone in 4-Nitro-O-Phenylenediamine means electronic transfer runs cleaner, while the ortho arrangement adds resilience against photobleaching over repeated cycles. Compared to m-phenylenediamine or 2,4-dinitroaniline, the response curve under stress or pH shift stays flatter, and that’s what matters in real-world performance—not just formula-vs-formula claims.

    The Chemical Manufacturer’s Eye: How Production and Scale Influence Outcomes

    Production scale alters not only economics but often the very chemical behavior of intermediates. For small lots, batch reactions provide fine control, but at scale, bandwidth widens and so does risk. Our process engineers learned early the difference between a manageable nitration and a runaway one; automated dosing was not a luxury but a necessity. We calibrate feed rates, pH, agitation, and temperature window for every batch of 4-Nitro-O-Phenylenediamine. Small differences in acid content or ammonia neutralization—often overlooked on pilot scale—reshape particle size, filterability, and the way the end product integrates with fast-moving lines on our clients’ side.

    Close collaboration with partner labs and commercial buyers drove us toward more stringent internal standards. For every hundred kilos made, we track spent reagents and waste streams with same focus as the main product. Not because it’s regulatory box-ticking, but because every mishandled wash stage or incomplete neutralization in the final drying shifts the end properties. Technical users don't trust assurances—they run parallel tests, compare yields, and expect us to deliver not just a specification, but a performance promise as solid as engineering steel.

    Environmental Responsibility Grounded in Practice

    Chemical manufacturing—especially nitration chemistry—puts real pressure on environmental safety. The old days of unchecked effluent and airborne emissions have ended. We capture all spent acid and organics from the 4-Nitro-O-Phenylenediamine process and feed them through neutralization and carbon scrubbing. Trace byproducts from nitroaromatic syntheses (like nitrosamines or spent phosphates) get separated and contained onsite, with regular testing against thresholds that reflect both community health and regulatory limits. Our operators find that diligence in waste handling is as crucial as raw material purity. The real cost of ignoring compliance is unpredictable shutdown, so careful monitoring isn’t ‘optional’, it’s the foundation for uninterrupted production.

    Customers increasingly demand proof of greener process choices. Many industries ask for detailed lifecycle data: what percentage of input solvents are recycled, what methods remove trace organic content. Our routine includes waste stream distillation and solvent recovery with over 70% efficiency, a standard we set not for image but because it cushions against volatility in both regulatory and raw material pricing. The investment in closed-system handling cuts costs in insurance, waste, and failed batches. These are lessons written not in compliance office memos, but in savings and prevented incidents tracked through years of wary production and high-stakes delivery deadlines.

    Common Client Questions and How We Keep Improving

    Some users want 4-Nitro-O-Phenylenediamine pellets, others need it fine-ground; a few specify zero silica anti-caking agents for ultra-pure work. Our team responds by controlling milling, sieving, and packing right on the main line. Handling feedback and product adjustments never feels like a hassle; it’s how we keep the process robust and the customer’s trust intact. Market trends shift—demand for conductive polymers grows, and others decline as pigment lines move to new color bases. Our approach isn’t to hoard data but share process tweaks and even failures, so everyone downstream benefits. Some process changes have even originated from client-side improvements—improved feed hoppers, line cleaning tips that make handling easier for both parties.

    Global shipping creates unique challenges. Customs pre-clearance, temperature variations, and even small time-zone misalignments can throw deliveries off schedule. We mitigate these with staggered production and redundant confirmation systems, not just for compliance, but because every lost day means delayed manufacturing, wasted labor in someone else’s plant, and potential batch failures.

    Why 4-Nitro-O-Phenylenediamine Earns its Place

    On paper, anyone can list uses for this intermediate: dye and pigment chemistry, electronics, specialty polymer synthesis. On the ground, most genuinely new applications emerge where three needs collide—one, a strong donor-acceptor molecule is needed on an aromatic backbone; two, scale and purity must match sensitive downstream catalysts; three, every shift in production runs through the hands of teams that rely on repeatable quality and truthful technical support. Synthetic chemists who have suffered from faint yellowing or inconsistent performance in final materials remember both the problem and who solved it. Many clients return after trialing alternatives and realizing that subtle molecular differences have outsize impact on product shelf life, appearance, or durability.

    The chemical market changes, and regulatory environments tighten. What doesn’t change is the rate at which real-world manufacturing exposes the strengths and weaknesses of intermediates. 4-Nitro-O-Phenylenediamine remains essential not simply because it is a reactant, but because in capable hands, it enables breakthroughs and withstands the unpredictable nature of bulk-scale chemistry. For every compound fighting to replace it, chemists come back to this one for its reliability, reactivity, and the hard-won knowledge accumulated over many thousands of kilos, hundreds of reactors, and decades of process troubleshooting.

    Manufacturing, like chemistry itself, is a long game. The careful, detail-driven approach with 4-Nitro-O-Phenylenediamine has built trust and kept our facility on call for the world’s most exacting makers of specialty materials, dyes, and advanced polymers. Each kilogram carries with it lessons learned, problems solved, and the expectation of future challenges—exactly the way real products, and real progress, have always been made.