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2-Chloro-6-Nitroaniline

    • Product Name 2-Chloro-6-Nitroaniline
    • Alias 2-Chloro-6-nitrobenzenamine
    • Einecs 221-633-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    771646

    Chemical Name 2-Chloro-6-Nitroaniline
    Cas Number 89-63-4
    Molecular Formula C6H5ClN2O2
    Molecular Weight 172.57
    Appearance Yellow to brown crystalline powder
    Melting Point 118-122°C
    Boiling Point No data available
    Solubility Slightly soluble in water
    Density 1.56 g/cm3
    Pka No data available
    Pubchem Cid 85748
    Smiles CC1=CC(=CC(=C1)[N+](=O)[O-])Cl
    Inchi InChI=1S/C6H5ClN2O2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H,8H2
    Synonyms 2-Chloro-6-nitrobenzenamine
    Ec Number 201-928-0

    As an accredited 2-Chloro-6-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 g of 2-Chloro-6-Nitroaniline, sealed with a screw cap, labeled with hazard and chemical information.
    Shipping 2-Chloro-6-nitroaniline should be shipped in tightly sealed containers under dry, cool, and well-ventilated conditions. Label packaging according to regulatory guidelines, indicating its hazardous nature. Protect from physical damage, moisture, and direct sunlight. During transit, handle with care to prevent leaks or spills and comply with all applicable chemical transport regulations.
    Storage 2-Chloro-6-nitroaniline should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from direct sunlight. Separate it from incompatible substances such as oxidizers and strong acids. Protect from moisture, heat, and sources of ignition. Clearly label containers and store them according to relevant chemical safety regulations to ensure safe handling and minimize hazards.
    Application of 2-Chloro-6-Nitroaniline

    Applications of 2-Chloro-6-Nitroaniline in Industrial Manufacturing

    As a direct manufacturer of 2-Chloro-6-Nitroaniline, we supply this specialty intermediate to key production segments in dyes, pigments, pharmaceutical intermediates, agrochemical synthesis, and polymer additive manufacturing. Below is an industry-focused overview of the primary sectors we serve and the real industrial processes in which our material is deployed.

    1. Azo Dye Synthesis for Textile Coloring

    2-Chloro-6-Nitroaniline functions as a diazo component in the synthesis of selected azo dyes, mainly for cotton and viscose textile applications. Dyers use this intermediate during the coupling stage for arylamine-based colorants, achieving precise shade control and bath stability. The nitro and chloro groups allow for enhanced tinctorial strength and washfastness, meeting industrial color quality demands for global textile producers.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 6
    • ZDH Quality Management for Reactive Dyes
    • EU REACH Regulation (EC) No 1907/2006
    • China GB/T 7571.2-2009 for Textile Dye Safety

    Typical usage ratio

    • 0.8–2.5% by weight in dye coupling mixtures, adjusted by substrate affinity and shade target

    Downstream process integration

    • Entry during the diazotization and coupling stage; reacts with coupling components such as resorcinol or naphthols in aqueous or alkaline medium

    Final product types

    • Direct dyes for cotton
    • Reactive dyes for cellulosic fibers
    • Disperse dyes for synthetics
    • Acid dyes for protein fibers

    2. Pigment Intermediate for High-Performance Colored Pigments

    Major pigment producers employ 2-Chloro-6-Nitroaniline to synthesize high-purity pigmented compounds such as Pigment Yellow 17 and related arylide pigments. These pigments see use in coatings, high-grade plastics, and inkjet ink formulations. The intermediate reacts in coupling with acetoacetarylide derivatives, providing superior light and solvent resistance profiles favored in automotive and industrial paint systems.

    Industry compliance standards

    • ASTM D3723 for Organic Pigments in Coatings
    • EN 71-3 Toy Safety (heavy metal migration limits)
    • ISO 9001:2015 Quality Management for Pigment Production
    • RoHS Directive 2011/65/EU (for uses in plastics and electronics)

    Typical usage ratio

    • 1.2–2.8 molar equivalents based on target pigment load and hue strength desired

    Downstream process integration

    • Chemical reduction or coupling with acetoacetanilide derivatives; enters the pigment synthesis reactor after precise milling for homogeneous reaction environment

    Final product types

    • Pigment Yellow 17 and similar diarylide pigments
    • Polymer color concentrates
    • Industrial coatings (powder, automotive, protective)
    • Printing inks (digital, offset, flexo)

    3. Pharmaceutical Intermediate for Antimicrobial Synthesis

    Pharmaceutical manufacturers use 2-Chloro-6-Nitroaniline as an advanced intermediate in the multi-step synthesis of active pharmaceutical ingredients (API) such as anti-tubercular and antibacterial drug precursors. The compound supplies a stable nitroaniline scaffold, enabling regioselective transformations essential to achieve the purity and activity required under ICH guidelines. Our production adheres strictly to cGMP and traceability protocols demanded for pharmaceutical supply.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 for Finished Pharmaceuticals
    • EU GMP Part II for APIs
    • Pharmacopoeia standards (USP/NF, Ph.Eur., JP)

    Typical usage ratio

    • Typically 0.5–1.4 molar equivalents at selective nitration, adjusted per API yield and side product minimization

    Downstream process integration

    • Acylation, reduction, or amination steps initiated with purified 2-Chloro-6-Nitroaniline as the main aromatic amine component

    Final product types

    • Antimicrobial drug intermediates
    • Synthons for anti-tubercular compounds
    • Active intermediates for finished pharmaceutical APIs
    • Building blocks for further chemical elaboration

    4. Agrochemical Precursor for Selective Herbicides

    Agrochemical synthesis plants use 2-Chloro-6-Nitroaniline to manufacture selective herbicide actives such as certain aniline-derived pre-emergence and post-emergence weed control agents. The molecular structure offers functional sites for etherification and condensation reactions, allowing precise molecular tailoring. Quality control encompasses isomer purity and low trace contaminants to comply with crop safety and environmental release guidelines.

    Industry compliance standards

    • FAO/WHO Guidelines on Pesticide Specification
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • US EPA Pesticide Registration requirements (FIFRA)
    • ISO 17025 Laboratory Accreditation for Agrochemical QC

    Typical usage ratio

    • 0.9–2.3 equivalents, batch-adjusted for molecular target and residual monomer control

    Downstream process integration

    • Enters amidation or etherification reactors as a pre-condensed arylamine intermediate during the synthesis of active herbicidal compounds

    Final product types

    • Aniline-derived selective herbicides
    • Early-stage agrochemical intermediates
    • Chemical scaffolds for further sulfonation or alkylation
    • Registered active ingredient pre-cursors

    5. Polymer Additive Manufacturing for UV Stabilizers

    Producers of specialty polymers and plastics utilize 2-Chloro-6-Nitroaniline to synthesize UV absorbers and stabilizer intermediates. The compound contributes to benzotriazole derivative manufacturing, acting as a coupling reagent or monomer in controlled addition reactions. Stabilizers derived enhance photostability and lifespan of PVC, polyolefins, and polyurethane coatings, especially for outdoor construction or automotive applications where weathering resistance is critical.

    Industry compliance standards

    • ISO 4892-2 for Plastics – UV Exposure Testing
    • ASTM D2565 for Polymeric Weathering Resistance
    • EU Directive (EU) No 10/2011 on Plastic Materials for Food Contact (where applicable)
    • REACH Annex XVII for Limitation of Hazardous Substances

    Typical usage ratio

    • 0.5–1.7% by resin mass for intermediate synthesis, subject to polymer matrix and stabilizer target concentration

    Downstream process integration

    • Introduced in step-growth or condensation polymerization; reacts during stabilizer molecule formation prior to compounding or masterbatch extrusion

    Final product types

    • UV absorber intermediates for plastics
    • Industrial polymer additives
    • Weathering-resistant coating compounds
    • Additive packages for construction and automotive plastics
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    Certification & Compliance
    More Introduction

    2-Chloro-6-Nitroaniline: A Closer Look at a Core Intermediate

    Understanding 2-Chloro-6-Nitroaniline from a Manufacturer’s Bench

    Years of running production lines for fine chemicals provide an unfiltered view into the strengths and practical challenges of making specialty intermediates like 2-Chloro-6-Nitroaniline. Hands-on experience with this compound reveals both its key properties and what sets it apart from similar nitroaniline derivatives. Our process engineers and synthesis chemists, working from raw feedstock through crystallization, know where its specific traits count in real industrial settings.

    Specifications That Matter in the Real World

    We produce 2-Chloro-6-Nitroaniline with a molecular formula of C6H5ClN2O2 and a molecular weight of 172.57 g/mol. This compound has a pale yellow to bright yellow crystalline appearance, faintly bitter odor, and a defined melting point that typically falls between 135 to 140°C under standard atmospheric pressure. Purity always runs greater than 99% by HPLC, with water content well below 0.5% and trace metals tightly controlled through the entire production batch. Chloride and sulfonate impurities fall below quantifiable levels because margin for error in downstream syntheses is slim.

    We keep the particle size distribution tight to limit dusting in the cutter mill and rotary dryer—handling the dust in production can cause both loss and discomfort for operators, and uncontrolled particle sizes can slow down reactions for our customers downstream. Our real efforts go into reproducibility, avoiding batch-to-batch differences that throw process development labs off. Customers running continuous dye synthesis or API intermediate steps need a product that acts the same every time.

    Why This Compound Stands Out on the Line

    Within the nitroaniline family, you’ll find a range of ortho, meta, and para isomers—chemically distinct variants with functionally different applications. 2-Chloro-6-Nitroaniline’s value comes from its dual substitution: the electron-withdrawing nitro group at the six-position, and the chloro group at the ortho position. This pairing underpins its reactivity profile, selectivity in coupling, and solubility when matched to solvents like chlorobenzene or DMF. Most coloring intermediates can’t offer this combination.

    During direct nitration, the challenge lies in driving high selectivity for the 6-nitro isomer without a side reaction at the 4-position. As a manufacturer, we fine-tune the acid mix and control temperature precisely with real-time analytics—what may sound abstract becomes very tangible on full-scale vessels when an exotherm threatens to run away. Continuous temperature probes and closed-loop vacuum distillation keep the process in check, and the end result justifies the careful control.

    Targeted Usage in Synthesis Applications

    2-Chloro-6-Nitroaniline finds its central role in downstream production of azo and anthraquinone dyes, as well as in making pharmaceutical building blocks. Specific coupling reactions demand that particular electron density profile—something para-nitro or mono-chloro anilines simply can’t mimic. In azo dye synthesis, it supports a faster diazotization and gives better color strength to pigments used for polyamide and polyester fibers.

    From our long-term supply relationships, we know formulators in textile and plastics pigmentation prize this compound because it enables higher tinctorial value and deeper, more resistant color shades. Synthetic routes to disperse dyes use 2-Chloro-6-Nitroaniline for its ability to anchor on aromatic frameworks, yielding stable hues that resist fading, washing, and bleaching—critical in reactive dye systems. Color fastness for polyesters rises with its use, and the cost per colored batch lowers because less pigment can achieve the same shade intensity.

    Pharmaceutical manufacturers also come to us for this intermediate when building blocks for active ingredients require substitution patterns that fend off metabolic degradation. As an example, it feeds into key steps for certain anti-infective medicines where specific halogen-nitro synergies support the stability needed through formulation and shelf life.

    Differences That Directly Affect Use and Process Safety

    Lab results have their place, but actual day-to-day plant operations uncover the subtle but significant differences among nitroaniline compounds. Pure 2-chloroaniline or pure 6-nitroaniline each lack the combined performance profile: the chloro group increases resistance to hydrolysis, and the nitro group opens the door for safer, more controlled reduction reactions. In correcting any misconceptions, you’ll find 2-Chloro-6-Nitroaniline allows more predictable diazotization than 4-nitrochloroaniline, with less risk of uncontrolled by-product formation. Its melting point fits optimally above typical ambient plant temperatures, so it transports and stores solidly without caking—unlike lower melting meta isomers prone to setting in drums.

    We once worked with a partner shifting their blend from a para-nitro to 2-Chloro-6-Nitroaniline, aiming to improve shade retention for acrylic fibers. The difference showed itself not only in superior color but also in batch-to-batch reliability; results matched target shade and strength every time, streamlining their own QC cycle. Downstream reactivity also improved—less unreacted intermediate, fewer solvents needed, and reduced heat input during final coupling.

    In terms of safety, there is a clear benefit. We have identified and minimized risk from residual organics and chlorinated by-products, which can be persistent issues with lower grade material. Our newer filtration methods ensure that our product contains minimal contaminant load—environmental teams at downstream plants cite this as a major reason for switching to direct supply from our production site. Fewer contaminants mean less process troubleshooting, and emission limits are easier to meet. Batch failures and effluent surges shrink with better input material.

    From the Reactor to Our Customers: Practical Handling Observations

    Walking the plant where 2-Chloro-6-Nitroaniline is synthesized highlights practical concerns beyond the chemistry. Bulk bags require careful loading to avoid airborne particulate, so we’ve moved to semi-automated unloading systems in recent years—cutting visible emissions and reducing losses. Our floor staff appreciate that the product doesn’t cake or bridge, even after weeks of storage at non-climate-controlled docks. That counts for something in places without round-the-clock environmental controls.

    Research and pilot plant customers tell us our material dissolves more smoothly in both polar and non-polar solvents than older, less pure grades. We attribute this in part to the targeted drying method, which minimizes occluded moisture and residual solvent. For high-volume users, these handling differences translate to easier batch prepping and faster process throughput. It’s a quiet but tangible productivity gain.

    Long-Term Partnership Brings Continuous Improvements

    We treat every customer issue and suggestion as a source of improvement. Over many years, requests from dye companies, pigment processors, and pharma customers led to upgrades in both QA and plant operations. One major dye house challenged our particle size variance. In response, we invested in finer hammer milling and inline particle analysis, cutting down oversize crystals and dust. Many of our longer-term clients cite this as directly improving their own consistency on the shop floor.

    Early on, we faced persistent color purity issues. Detailed impurity analysis—performed concurrently with continuous improvement—revealed that minor process tweaks, like holding pH within a one-tenth band at the coupling tank, dropped off-color batches to near zero. It took months of hands-on effort from our lead operator team, not a consultant, to integrate these insights across our production shifts.

    We remain on direct call with partners introducing new application areas. In recent years, we’ve supplied innovators exploring specialty polymers and high-performance coatings. The direct technical link—operator to chemist to process engineer—powers faster troubleshooting and lets us tweak drying, storage, and packaging when new challenges arise. In several cases, an early flag from an in-house QC professional at a customer’s plant led us to refine purification cycles; these rapid responses have meant fewer process stoppages and delayed shipments for everybody involved.

    Addressing Market Issues Through Direct Manufacturing Experience

    No global chemical supply chain stays perfectly smooth. Shifting local and national regulations, environmental rules, and raw material price jumps test every manufacturing operation. We have weathered volatility in both feedstock aniline and nitric acid pricing by optimizing inventory levels and contracting for off-peak delivery schedules—logistical decisions rooted in factory experience rather than broker models. This planning lets us continue supplying core intermediates even during external shocks.

    Factory-site control over emissions and wastewater output protects both workers and community. We no longer use older chlorinated solvents at critical steps, avoiding persistent organic pollutants at the source. Instead, recycling systems within the plant recover process water and separate halogenated organics for safe destruction. These programs began well before regulatory deadlines, reflecting active collaboration with downstream users and local authorities. Responsibly managed supply chains protect long-standing business as much as regulatory compliance.

    Time brings new questions about biodegradability and process residue, especially among multinational buyers adopting stricter green chemistry guidelines. We have partnered directly with university teams to monitor both acute and chronic aquatic toxicity in the region. In collaboration with partners, we contribute product and process data to industry-wide databases guiding safer chemical practices. Balancing process efficiency with responsible manufacturing isn’t a one-off—each production campaign brings lessons to feed forward into plant upgrades and process documentation.

    Continued Advancements in Quality and Application Support

    Supporting changing customer needs goes beyond stable supply. We field technical queries about process adaptation, from solvent switching to reaction scale-up. Years of hands-on synthesis work have shown us which grades and handling methods improve yields in dye or drug production. We provide detailed residue and impurity profiles, not just a certificate of analysis, so QC teams can tune their own acceptance criteria. Many customers with specific process challenges come back for batch samples and guidance, knowing we do not rely on stock answers or solutions that only fit on paper.

    Recognizing the growth of advanced materials and specialty applications, our R&D and process scale teams continually experiment with new drying, screening, and blending approaches to meet demands for ultra-low metal content, tailored moisture levels, or unique particle morphologies. Each advance stems from questions that pop up in scaling or integrating 2-Chloro-6-Nitroaniline into newer, more complex formulations for both performance chemicals and medical intermediates.

    We have experienced that a well-documented supply chain, supported by plant-based monitoring and technical records, wins confidence and clears certification audits. Several major clients in regulated sectors invite our teams on-site to survey receiving and handling protocols, cross-checking how our product blends into their closed systems. Transparent records serve everyone—operator, manager, auditor, or regulator. They eliminate surprises when rare deviations arise, keeping both product integrity and business relationships strong.

    The Value of Close Customer Partnership

    Market expansion and shifting technical parameters constantly redefine what “quality” means in specialty chemicals. Instead of chasing trends, we stick to direct feedback from customers who use and process our 2-Chloro-6-Nitroaniline daily. Every new facility trial or end-product specification yields another layer of know-how, helping both our team and our customers adapt to new formulations or compliance challenges. Direct manufacturing contact makes adaptation and troubleshooting far more effective than relying on third-party suppliers removed from the actual plant floor.

    Our commitment to responsible production, open collaboration, and steady improvement shapes how we produce, test, store, and deliver every batch. From the first bag leaving our warehouse to the final application in dyes, drugs, or advanced materials, the focus remains on actual performance where it matters: real chemistry, experienced hands, and continuous engagement with every user that brings our product into their process.