2-Nitroaniline

    • Product Name: 2-Nitroaniline
    • Alias: o-Nitroaniline
    • Einecs: 202-199-1
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    957512

    Cas Number 88-74-4
    Molecular Formula C6H6N2O2
    Molecular Weight 138.13 g/mol
    Iupac Name 2-nitroaniline
    Appearance Yellow to orange crystalline solid
    Melting Point 71-74 °C
    Boiling Point 284 °C
    Density 1.36 g/cm³
    Solubility In Water Slightly soluble
    Flash Point 169 °C
    Odor Odorless
    Pka 2.03
    Pubchem Cid 6987

    As an accredited 2-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500g amber glass bottle with a tightly sealed cap, labeled "2-Nitroaniline," hazard symbols, and detailed handling and safety information.
    Shipping 2-Nitroaniline should be shipped in tightly sealed containers, clearly labeled, and compliant with hazardous material regulations. It must be protected from heat, moisture, and incompatible substances. Transport is typically by ground or air, following UN 1662, Class 6.1 (toxic substance) guidelines. Only authorized personnel should handle shipping.
    Storage 2-Nitroaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. It must be kept separate from strong oxidizing agents, acids, and reducing agents to prevent hazardous reactions. Properly label storage containers, and use secondary containment to avoid spillage or contamination.
    Application of 2-Nitroaniline

    Applications of 2-Nitroaniline in Industrial Manufacturing

    As a committed manufacturer, we provide high-purity 2-Nitroaniline to support specialized production needs across several purpose-driven industrial value chains. The following scenarios detail established applications and precise technical roles of our material within recognized manufacturing environments.

    1. Azo Dye Intermediate for Textile and Leather Colorants

    Major dyestuff formulators utilize 2-Nitroaniline primarily as a diazo component in the synthesis of yellow, orange, and red azo dyes dedicated to the textile and leather markets. The aromatic amine function enables direct diazotization, followed by coupling with phenolic or naphtholic components to generate deep-shade, salt-stable dyes. Manufacturers precisely adjust raw material input based on target chroma, tinctorial strength, and batch scale, ensuring batch-to-batch reproducibility. Downstream, the integrated process includes sulfonation or alkylation for enhancement of migration resistance and lightfastness on final substrates.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Class I-IV for restricted amines)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals — limit for aniline derivatives)
    • REACH Regulation (EC) No 1907/2006 — Annex XVII entry 43 (aromatic amines restrictions for consumer textiles and leather articles)
    • ISO 105-C06 (Textiles—Tests for Colour Fastness)

    Typical usage ratio

    • 0.8–2.5% by weight of total dye batch; adjusted for target concentration and shade depth on a dry basis
    • Ratio determined by coupling efficiency and strength requirement, typically 1.2% for standard yellow/orange tones

    Downstream process integration

    • Charged into the primary diazotization reactor at 0–5°C in aqueous HCl solution
    • Further advanced in coupling stages for azo bond formation, followed by purification and granulation

    Final product types

    • Direct dyes for cotton and viscose
    • Acid dyes for polyamide fibers
    • Leather colorants with high UV stability
    • Granular and powder dye concentrates for textile mills and tanneries

    2. Synthesis of Agricultural Pesticide Intermediates

    Producers of herbicides and insecticidal actives employ 2-Nitroaniline as a select building block, supporting the manufacture of nitroaniline-based urea and sulfonamide classes. During intermediate production, the input material undergoes nucleophilic substitution or reduction prior to downstream coupling with carboxylates, forming the central pharmacophore required for selective weed control or crop protection. The percentage applied is based on target molecule structure, regulatory residue limits, and conversion yield for efficient process economy.

    Industry compliance standards

    • FAO/WHO JMPR pesticide specification (active ingredient quality and impurity profile)
    • ISO 9001:2015 (Quality management for crop protection intermediates)
    • Chinese GB 2763-2022 (MRL for pesticide residues in food)
    • ECHA REACH registration for all key synthetic intermediates in EU uses

    Typical usage ratio

    • 8–14% of total batch mass for intermediate formation; final level depends on stoichiometry toward urea or sulfonamide backbone
    • Adjusted for yield control in multi-step synthesis to minimize excess unconverted feedstock

    Downstream process integration

    • Added in batchwise synthesis of precursor; initiates substitution on pre-activated aliphatic or aromatic halides
    • Acts as starting reagent for reduction to amines before urea condensation

    Final product types

    • Nitroaniline/phenylurea herbicides (e.g., diuron, fluometuron)
    • Nitroaniline base intermediates for selective insecticides
    • Technical-grade active ingredient concentrates for agricultural blending
    • Wettable powder and suspension concentrate pesticide formulations

    3. Pharmaceutical Intermediate for Acetaminophen Synthesis

    Pharmaceutical API manufacturers rely on 2-Nitroaniline as a precursor in the multi-step process towards paracetamol (acetaminophen) and related active compounds. The robust reduction process yields 2-aminophenol, which is then acetylated under stringent cGMP protocols. Parameters on input levels relate to product purity targets, minimized by-product formation, and compliance with published pharmacopeial limits for residual nitro derivatives. Material integration must ensure traceability and batch segregation for medical-grade applications.

    Industry compliance standards

    • USP–NF (United States Pharmacopeia—National Formulary) for paracetamol
    • EU GMP EudraLex Volume 4, Part II: Basic requirements for active substances
    • ICH Q3A/B (Impurity limits for APIs)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for finished pharmaceuticals)

    Typical usage ratio

    • 0.7–1.1 molar equivalents based on desired output; generally 0.95–1.05 equivalent to minimize downstream purification steps
    • Adjusted to maximize 2-aminophenol yields and reduce unreacted residuals

    Downstream process integration

    • Fed into catalytic hydrogenation circuit at high differential pressure
    • Subsequent in situ acetylation to produce pharmaceutical intermediates meeting controlled impurity specifications

    Final product types

    • 2-Aminophenol API intermediates
    • Bulk paracetamol/acetaminophen for tableting
    • Pharmaceutical grade granules and finished dosages
    • Medical active precursor stocks for final API synthesis

    4. Rubber Chemical Accelerator and Antioxidant Precursor

    2-Nitroaniline is processed by rubber chemical manufacturers as an intermediate for creating certain accelerators and antioxidants, such as diphenylguanidine (DPG) and other substituted aniline derivatives. The integration involves staged reduction and condensation to attain high-purity aminobenzenes needed for vulcanization control. Ratio determination correlates tightly to batch scale and accelerator performance requirements, guided by the physical property profile needed in end-use compounded rubber goods.

    Industry compliance standards

    • ASTM D4678 (Rubber compounding materials—standard specification for preparation)
    • ISO 9001:2015 (Process controls for rubber chemical production)
    • EU REACH—Completion of registration dossier for chemical intermediates
    • US EPA TSCA (for new chemical notification in accelerator manufacturing)

    Typical usage ratio

    • 5–12% of total mass in precursor blend; ratio set relative to desired final accelerator purity and grade
    • Reduced for batch safety in high-temperature treatment and for low by-product generation

    Downstream process integration

    • Input during initial reduction step for aminated product generation
    • Directly incorporated into guanidination or sulfenamide synthesis pathways

    Final product types

    • Diphenylguanidine (DPG) accelerators for tire and industrial rubber compounding
    • Substituted aromatic amines as antioxidants
    • Masterbatch accelerator pellets for direct dispersion
    • Rubber compounding additives for technical rubber products

    5. Chemical Intermediate for Specialty Pigments

    Precision pigment manufacturers select 2-Nitroaniline as a strategic intermediate in the synthesis of yellow pigment lakes and certain complex organic chromophores, particularly for printing inks and plastics coloration. Process engineers manage the input closely, using it as a coupling or condensing agent to yield pigmentary molecules with desired particle size, hydrophobicity, and migration resistance. Strict process isolation ensures consistent chromatic index and dispersibility in various application polymers and liquid media.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys—Migration of certain elements in pigment formulations)
    • ISO 1248 (Pigments—Determination of coloring strength and tinting strength)
    • REACH Annex XVII (Restrictions on hazardous aromatic amines in consumer colorants)
    • US FDA 21 CFR 178 (Indirect food additives—Colorants in plastics)

    Typical usage ratio

    • 0.5–2.0% by weight in pigment synthesis batch; optimized for desired shade intensity and particle size
    • Adjusted on a per-formula basis to meet C.I. standard requirements

    Downstream process integration

    • Charged into the pigment precursor reactor for nitration and coupling reactions
    • Further processed via filtration, washing, and micronization prior to pigment dispersion

    Final product types

    • Yellow and orange pigment lakes (Color Index Pigment Yellow 49 & 74)
    • Organic pigment concentrates for flexographic and gravure inks
    • Plastic color masterbatches for PP, PE, and PVC applications
    • UV-stable organic pigment dispersions for paint and coatings

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    Certification & Compliance
    More Introduction

    2-Nitroaniline: Experience at the Source

    A Practical Introduction

    In our own manufacturing practice, true understanding of 2-nitroaniline comes not from reading a spec sheet, but from years standing by reactors, guiding crystal formation, tracking purity shifts, smelling those faintly sharp notes rising during filtration. At our facilities, we make 2-nitroaniline in its deep amber solid form with a focus on stability, consistency and on minimizing batch-to-batch differences that can cause trouble for our long-term buyers. Our standard material holds to a high purity level, maximizing reliability for downstream processes. Chemists, process engineers and lab managers know how even subtle deviations—like moisture remaining in the crystals or incomplete reduction in precursors—can lead to losses in yield and extra cost once the nitroaniline leaves our hands. That's why repeated investment in purification and crystal drying pays dividends along the whole supply chain, not just for one step.

    Key Characteristics from the Line

    The 2-nitroaniline we supply typically forms a dense, gold-brown crystalline powder when isolation and drying are managed well. Its reported melting point sits in the 70°C to 75°C range—a quick visual check in a glass capillary repeats itself batch after batch when procedures are steady. We monitor for off-hues and clumping, knowing instantly it indicates leftover solvent or incomplete drying, neither of which get past shipping. Trace impurity levels, especially unwanted isomers and residual starting aniline, are checked by in-house HPLC, not just for our own satisfaction, but because experienced customers run their own checks and usually call if levels step outside the expected window. The most valued batches, we’ve learned, always carry less than 0.5% detectable residue and leave no ammonia aroma behind. This obsessive internal discipline is tedious, but it keeps trust high; buyers who use 2-nitroaniline in dyes or pigment intermediates can’t afford wildcards.

    How 2-Nitroaniline Actually Works in Industry

    Most outsiders see 2-nitroaniline as just a chemical name, but for us, it’s directly linked to years of hands-on synthesis and troubleshooting. The major use for this compound traces back to dye and pigment production. Laboratories taking our material produce vivid azo dyes; textile dyers add the resulting colors to fabrics and inks. Even small differences in 2-nitroaniline’s particle size can change the final reproducibility in dyestuff coloration. Over time, we adjusted milling procedures and screen mesh numbers based on customer feedback. Nothing beats a direct call from a master dyer in Pakistan or a paint chemist in Germany asking for a batch that filters fast, dissolves clean, and leaves no strange spots on finished goods. These voices impact how we control temperature ramps in the nitration reactors, how long we let distillation run during work-up, and how we specify the shipment packaging. Downstream, even just a few extra milligrams of moisture or a trace of an undesired isomer will ripple outwards, slowing reactions, causing streaking, or even damaging equipment.

    Because the chemical structure—an aniline ring carrying a nitro group in the ortho position—dictates both reactivity and hazards, careful management at every step turns theory into practical success. 2-nitroaniline requires thoughtful handling, as the compound tends to oxidize if left unprotected, and trace peroxide formation can occur if air exposure is prolonged. That’s not academic concern: temperature-controlled storage and inert packaging prevent material loss and help meet buyers’ requests for material that arrives just as expected, even after weeks in transit or months on a warehouse shelf.

    Why Our Manufacturing Approach Matters

    We do not approach 2-nitroaniline as a commodity. Listening to the customers who run dye blend formulations, pigment syntheses, and fine chemical transformations, we keep the focus on reproducibility at scale. Each freshly isolated batch undergoes both automated and manual checks. A visual inspection can catch subtle changes—the edge of a glass drying pan sometimes gives away tiny, almost invisible, color gradients. The softer, almost floury batches often result from careful recrystallization, yielding better downstream solubility and mixing for those working with solvent-based processes. Laboratory-scale sample tests conducted on-site—parallel with production—let us anticipate user-side challenges before large-scale shipments ever leave the plant.

    Every week, we cross-check finished material against retained reference lots, looking for shifts in melting range, bulk density, flowability and solubility in the most frequently used solvents like ethanol and xylene. Feedback loops with our top end-users, especially those developing novel dyes or specialty chemicals, direct us to focus on characteristics that improve not just price per kilogram, but yield per process step and ease of workflow. The more consistently we deliver batches matched to prior shipments, the less our customers have to wonder about adjusting their own parameters.

    Comparing to Other Intermediates: How 2-Nitroaniline Stands Out

    A common question from purchasers and new partners revolves around the differences between 2-nitroaniline and other aromatic nitro compounds, especially 4-nitroaniline or 2,4-dinitroaniline. The difference lies not just in molecular placement of the nitro group, but in practical results: 2-nitroaniline provides unique reactivity for azo dye coupling thanks to the ortho substitution. This structure grants distinctive chromatic properties—tones richer and absorption stronger than many alternatives. Using 4-nitroaniline or 2,4-dinitroaniline in similar formulations yields noticeably different color brightness and may require rebalancing of additive concentrations or additional purification. From years of troubleshooting, we found that swapping intermediates for cost reasons often leads to problems down the line. 2-nitroaniline’s particular solubility and handling quirks also set it apart. Our compound typically dissolves at around 5 to 9 grams per 100 mL in boiling ethanol—a practical fact borne out in production lines, not just textbooks. Clogging or slow dissolution can halt an entire batch in colorant factories or fine chemical labs, as some operators using alternative nitroanilines found out the hard way.

    Another frequent comparison point touches on related compounds such as 3-nitroaniline. Having manufactured both on separate lines, we see how 2-nitroaniline maintains higher throughput yields due to fewer byproduct formation risks. Where 3-nitroaniline processes tend to produce more tarry residues, our 2-nitroaniline runs output cleaner crystals, creating less rework and lowering internal rejection rates. These are not marketing claims—they reflect ongoing analytical checks and process data maintained for our own QA records.

    Facing Practical Production Challenges

    Producing 2-nitroaniline involves more than selecting raw nitrobenzene and aniline sources. Quality hinges on steady control during acidic nitration, precisely managed pH drops for precipitation, and scrupulous solvent removal in vacuum dryers. These are shop-floor details; nobody learns them from a generic process guide. New operators at our plant spend months watching the color of nitroaniline slurries change during purification. Regular conversations between the production lead and the technical director help root out tiny inefficiencies—wasted solvent here, mis-set agitation there, slightly low yields traced back to an overlooked parameter. That’s years of accumulated discipline. On bad days, yield falls or off-specification product accumulates, and only a direct, hands-on response brings production back to target. We learned early that frequent batch checks during each stage—sampling the liquor, snapshotting the crystallized cake, monitoring the temperature with calibrated probes—delivers much better product than waiting for a final lab assay.

    Improving Sustainability and Worker Safety

    Over decades, safety issues have evolved as regulations grew stricter and client concerns grew sharper. 2-nitroaniline counts as a hazardous chemical, subject to specific environmental and safety controls, especially regarding exhaust emissions and spent mother liquor disposal. Our team upgraded solvent recovery systems and moved toward closed filtration cycles, cutting operator exposure. Regular training and real incident reviews bring sharper awareness—one missed glove, a poorly sealed barrel, and someone could suffer lasting effects. Honest dialogue between managers, bench chemists, and shipping teams keeps the focus where it matters: eliminating sources of injury and improving consistency across shifts.

    Environmental concerns have driven us to invest in higher-efficiency exhaust scrubbers and wastewater neutralization. We didn’t do this for cosmetic reasons. High penalties and real reputation risk follow lapses—anyone who’s spent years in chemical manufacturing knows the cost of local environmental complaints or regulatory findings. Careful control over nitrogen oxide emissions, and persistent reduction in phenolic trace pollutants, represent genuine commitments to sustainability. Process improvements rarely arrive overnight, but every tweak—recycling spent acid, switching to catalysts with lower environmental impact, automating drum washing—cumulatively improves both our workplace and customer product portfolios.

    Applications Beyond Dyes and Pigments

    While dye and pigment makers form our largest customer segment, demand for 2-nitroaniline continues to grow in pharmaceutical and fine chemical research. Small lots destined for R&D facilities sometimes call for special handling, custom lot certification, or even non-standard particle sizing. We’ve responded by forming a small technical services group focused on listening to researchers and adjusting protocols to match novel synthesis needs. In pharmaceutical labs, 2-nitroaniline acts as a versatile starting block for building heterocyclic compounds with antimicrobial or anticancer potential. Here, trace impurities affect not just color, but biological activity, so even stricter purity and packaging protocols apply.

    Other sectors use 2-nitroaniline as a reagent in analytical chemistry, such as colorimetric nitrate determination in environmental water testing. These applications require standard reference material-grade quality. Over the years, our teams have received challenging requests: calibrating batch quality to international pharmacopeial standards, supplying ultra-low moisture forms, or providing confirmatory NMR and IR spectra with every drum. This direct engagement with technically demanding customers keeps our crews motivated and our process knowledge fresh.

    Listening to End Users, Learning from Failures

    One of the key differences between working as the manufacturer and simply trading chemicals is the intimacy of feedback. Every failed batch—be it poor color strength, slow dissolution, excess dustiness or mislabeling—lands squarely at our door. We have received drums returned from halfway across the globe because of undetected caking or purity drift. Facing this feedback, not hiding it, shapes how our plant technicians learn to fine-tune every variable. We actively collect process feedback from industry users to continue improving—not just through online forms, but regular calls and face-to-face troubleshooting sessions.

    Dye makers and specialty chemical firms operating under tight timelines cannot afford downtime. If our 2-nitroaniline does not arrive on time or does not deliver promised specs, the real-world consequences—factory backups, wasted labor, lost revenue—stand in stark contrast to abstract cost-saving claims pushed by resellers. The cost of a failed batch far outweighs any marginal price saved by cutting corners at production. This understanding, forged by real-world experience and transparent data flows, has driven us to enforce a tightly regulated system from raw material reception to final drum closure.

    Adapting to Supply Chain Complexity

    In recent years, unpredictable global supply logistics and changing regulations have only underscored the value of in-house control. We source verified batches of aniline and nitric acid directly, avoiding recycling dubious intermediates from third parties. Production at our plant follows a schedule keyed to historical seasonal demand, building buffer stock for clients in fast-moving regions. At the same time, our logistics managers follow up with shipping partners, verifying that each outbound drum departs on time with sealed traceable tags. Documented chain-of-custody allows buyers to track their orders in real time, a system built not for show but in response to actual lost shipments and insurance claims.

    Contingency planning plays a real part in maintaining reliability. Natural events, trade policy changes, or border closures have all delayed raw material flows in the past. Disruption on this level led us to diversify warehouse locations. We maintain a ready-to-deploy team tasked with rerouting supply or shifting production priorities to support urgent customers—especially those with long-term contracts or who rely entirely on our product line. This flexibility, earned through years of hard learning, ensures our 2-nitroaniline keeps reaching those who actually run the world’s dyehouses, pigment plants and research labs.

    Quality Control: Earning Trust Batch by Batch

    Behind every shipment of 2-nitroaniline lies a sequence of repeated and rigorous checks. Each production run begins with standardized raw material assessment, often exceeding routine industry norms. Intermediate sampling—using both automatic and hand-grabbed techniques—helps pinpoint shifts in purity, particle size or color formation early, preventing compounding losses later. Our on-site QA team calibrates HPLC and GC-MS detectors weekly, sometimes daily when issues arise. This equipment, supported by experienced staff who have worked through multiple regulatory audits, gives us the data confidence to certify each outgoing drum.

    Calibrating internal standards from reference samples locked in our archive, our analysts remain alert to every minor deviation. When a shift in trace impurity profile appears, the response comes fast: technicians return to reactors, check pH, solvent flows, or agitation speed, resolving root causes before recertification for shipment. Documentation—a sometimes tedious task—remains meticulous, because our customers arrive with their own QC rigs and quickly flag inconsistencies. This open feedback culture lets us transparently improve internal procedures and build true buyer confidence, not just marketing gloss.

    Learning from Trends and Looking Ahead

    Rising expectations from global customers point not only to higher technical specs, but to transparency in provenance and shipping. Requests for region-specific documentation, carbon footprint tracking on each batch, and health risk disclosure layers add increasing responsibility for us as manufacturers. These external pressures drive us to refine both internal SOPs and external reporting. Our quality teams now draft carbon emission reports per lot, allowing downstream users to better calculate aggregate environmental impact in their supply chains.

    Looking forward, we take new challenges seriously. As demand for biodegradable dyes and environmentally benign intermediates increases, we research more green synthesis options—ionic liquid media, process-gas recycling, and lower-energy drying protocols. These investments do not translate into immediate profits, but they anticipate the next round of regulatory and market shifts. The push for reduced waste and better safety helps sustain both the business and the larger dye production ecosystem. Innovation is rarely a quick fix; it’s a constant investment.

    Summary: Direct Lessons from a Chemical Manufacturer

    Experience with 2-nitroaniline extends beyond formula sheets or third-party vendor pitches. Every step in its journey—from aniline and nitric acid sourcing through precise crystallization, granule drying, QA and on-time logistics—reflects the cumulative lessons of years spent in the plant and face-to-face with real-world users. Customer voices continue to shape every incremental improvement. The value our 2-nitroaniline brings does not rest on abstract claims, but on repeated demonstration of purity, reproducibility, process safety, and honest engagement when problems crop up.

    For those working in dye synthesis, pigment manufacture, research chemistry, or environmental applications, our attention to process detail makes 2-nitroaniline more than just another nitro-aniline. It means improved color quality, fewer batch losses, and a more predictable workflow. For us as chemical manufacturers, this shared success rests on shared reality—patience, feedback, and a willingness to adapt. Each shipment confirms a story written by dozens of hands and countless incremental improvements, building trust every step of the way.

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