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2-Amino-3-Chloro-5-Nitrobenzonitrile

    • Product Name 2-Amino-3-Chloro-5-Nitrobenzonitrile
    • Alias 3-Chloro-5-nitro-2-aminobenzonitrile
    • Einecs EINECS 612-976-8
    • 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

    590634

    Productname 2-Amino-3-Chloro-5-Nitrobenzonitrile
    Casnumber 38734-54-4
    Molecularformula C7H4ClN3O2
    Molecularweight 197.58
    Appearance Yellow crystalline powder
    Meltingpoint 163-167°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Density Approx. 1.57 g/cm3
    Synonyms 2-Amino-3-chloro-5-nitrobenzenecarbonitrile
    Structuralformula NC1=CC(Cl)=C(C=N1)N(2)NO2
    Storageconditions Store in a cool, dry place, away from direct sunlight
    Hazardclass Irritant

    As an accredited 2-Amino-3-Chloro-5-Nitrobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Amino-3-Chloro-5-Nitrobenzonitrile is packaged in a sealed 25g amber glass bottle with a tamper-evident cap.
    Shipping 2-Amino-3-Chloro-5-Nitrobenzonitrile is shipped in tightly sealed containers, protected from light and moisture. Handle with care, using appropriate personal protective equipment. The chemical is classified as hazardous; transport must comply with local, national, and international regulations. Store at room temperature in a ventilated area, away from incompatible materials and sources of ignition.
    Storage **Storage Description for 2-Amino-3-Chloro-5-Nitrobenzonitrile:** Store 2-Amino-3-Chloro-5-Nitrobenzonitrile in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from direct sunlight, heat, and sources of ignition. Segregate from incompatible substances such as strong oxidizers and acids. Use proper labeling, and ensure access is restricted to trained personnel. Handle with appropriate protective equipment.
    Application of 2-Amino-3-Chloro-5-Nitrobenzonitrile

    Applications of 2-Amino-3-Chloro-5-Nitrobenzonitrile in Industrial Manufacturing

    2-Amino-3-Chloro-5-Nitrobenzonitrile serves as a critical intermediate in specialized chemical synthesis for sectors requiring high-purity building blocks. Our vertically integrated production facilities support downstream manufacturers seeking consistent quality, traceable supply chains, and documented compliance for advanced chemical preparations. Below are the focused industrial applications where our material meets the demanding requirements of global industrial operators.

    1. Agrochemical Intermediate Production

    Major agrochemical formulators rely on this compound as a key starting material for synthesizing several classes of selective herbicides. Its unique substitution pattern provides high compatibility in nucleophilic aromatic substitution reactions, facilitating downstream chlorination or further functionalization steps. Companies in this field utilize it in multi-step manufacturing of active ingredients for pre-emergence weed control, supporting robust acreage-scale deployment.

    Industry compliance standards

    • FAO/WHO Maximum Residue Limits (MRLs)
    • US EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemical Residues in Food)
    • REACH Annex XVII for Hazardous Substances
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing

    Typical usage ratio

    • 2-10% by mass in herbicide active ingredient synthesis; final charge level depends on targeted end-molecule, typically adjusted according to stoichiometric requirement outlined in validated route-of-synthesis protocols.

    Downstream process integration

    • Charged as the principal aromatic nucleophile during heterocycle or ether bridge formation—commonly in the first or second chemical transformation after initial hydrolysis or reduction; followed by condensation, halogenation or sulfonation prior to formulation.

    Final product types

    • Triazine and pyridine-based herbicides
    • Chloronitrobenzonitrile-derived weed control agents
    • Intermediates for safener compounds
    • Actives for crop protection emulsifiable concentrates and water dispersible granules

    2. Pharmaceuticals: Advanced API Intermediates

    Pharmaceutical companies use this compound selectively in the synthesis of complex heterocyclic intermediates, especially for small-molecule active pharmaceutical ingredients (APIs) where electron-withdrawing groups influence regioselectivity. It enables precise functionalization in nitroaromatic-to-amino conversions and is integral to manufacturing steps for certain antihypertensive, antitumor, and antiviral candidates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
    • EU GMP Directive 2003/94/EC for APIs
    • USP/NF and Ph. Eur. requirements for raw material traceability

    Typical usage ratio

    • Often 1.5-8% of the total synthetic batch input, based on molecular mass balance; process chemists adjust according to yield optimization and impurity profile control, particularly for multi-step transformations.

    Downstream process integration

    • Acts as the core aromatic precursor during initial nitro group manipulations, including reduction and amide coupling; typically introduced in the second or third step of multi-stage API intermediate manufacture, followed by purification and conversion toward the final API framework.

    Final product types

    • Pyrimidine and pyridine derivative API intermediates
    • Precursors for anti-infective and oncology drug substances
    • Specialty nitrogen-containing heterocycles for finished medicine synthesis
    • Key building block for generic and branded pharmaceutical intermediates

    3. Dyes and Pigments: Specialty Colorants Manufacturing

    Dye houses and pigment producers employ this compound as an essential feedstock for synthesizing high-performance disperse dyes and specialty colorants. Its integrated electron-withdrawing groups enable formation of vivid, stable colorant structures, particularly in the manufacture of azo and anthraquinone-based dyes used for demanding textile and plastic industry applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textile colorants
    • EU REACH Regulation (EC) No 1907/2006 requirements for registration and safety data
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 certification for colorant chemical plants

    Typical usage ratio

    • Generally 3-12% of total mass in dye synthesis reactions, with specific loading determined by desired shade depth, chromophore structure, and intended substrate reactivity.

    Downstream process integration

    • Charged during initial diazotization or coupling stages; forms core aromatic skeletons for further modifications such as sulfonation or alkylation, prior to granulation or dispersion processing for end-use pigment preparations.

    Final product types

    • Disperse and reactive dyes for polyester and blended fabrics
    • Technical pigments for plastics and industrial coatings
    • Colorants for high-resistance inkjet and toner systems
    • Specialty dyes for high-temperature print and dyeing processes

    4. Specialty Chemical Synthesis: Electronic Chemicals and Fine Chemicals

    This intermediate finds strategic use in the preparation of fine chemicals for liquid crystal display (LCD) intermediates, photoresist compounds, and custom synthesis projects where halogenated, nitrated aromatics are vital. Electronics-grade manufacturers rely on its consistent purity to ensure downstream yields and minimize side reactions in highly controlled, cleanroom-based synthetic operations.

    Industry compliance standards

    • SEMI C93 for chemical purity requirements in microelectronics
    • ISO 9001:2015 and ISO 14001:2015 Quality and Environmental Management for fine chemical manufacture
    • IECQ QC 080000 Hazardous Substance Process Management System
    • RoHS Directive 2011/65/EU regarding restricted halogenated materials

    Typical usage ratio

    • Ranges from 1-6% depending on the structural complexity of the target molecule; formulation engineers typically optimize according to impurity profile management and desired performance attributes in end-use electronics applications.

    Downstream process integration

    • Introduced as a primary or secondary precursor in batch or continuous flow syntheses for specialty halogen/nitro-aromatic intermediates; incorporated before cyclization or etching-resistant functionalization steps in advanced electronic materials production.

    Final product types

    • Liquid crystal intermediates for display technologies
    • Photoresist base materials for semiconductor lithography
    • Fine chemical precursors for specialty polymers
    • Custom research molecules for electronics and materials science sectors
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    Certification & Compliance
    More Introduction

    2-Amino-3-Chloro-5-Nitrobenzonitrile: Precision from the Manufacturer’s Bench

    Understanding the Substance

    Producing 2-Amino-3-Chloro-5-Nitrobenzonitrile seems straightforward from the outside, but those who work with it know this molecule demands real diligence at every step. We have years of experience in handling aromatic nitrile synthesis, and this compound sits right at the intersection of complexity and utility. By carefully adjusting temperature, pH, and choice of reagents, a consistent product emerges, one with balanced purity, color, and granularity. Over multiple production cycles, feedback from end-users shaped our processes: persistence with purification methods, patience in crystallization, and tight control over reagent quality.

    Chemically, 2-Amino-3-Chloro-5-Nitrobenzonitrile carries an aromatic ring decorated with four functional groups. The amino, chloro, and nitro substituents, combined with a cyano group, create distinct electron-rich and electron-deficient sites on the molecule. Each function changes the compound’s reactivity in downstream syntheses. Over time, we’ve fine-tuned the reaction stages to avoid unwanted side products, especially considering how nitro-group orientation can trigger unexpected rearrangements during coupling. The refined methods lead to material that holds up under scrutiny and performs in specialized transformations.

    From Bench to Industry: Why This Compound Matters

    Looking at the market, 2-Amino-3-Chloro-5-Nitrobenzonitrile carves out its identity as more than just an intermediate. Pharmaceutical research draws on this molecule for a starting scaffold during heterocyclic ring assembly. Both the electron-donating amino and electron-withdrawing nitro group make it a versatile building block for constructing substituted anilines, diazonium salts, or even certain pyridine derivatives. Agrochemical developers ask for this product by name as they design crop-protection agents, and pigment chemists rely on it for synthesizing high-stability colorants.

    Our colleagues in the lab often point out that not all benzonitriles offer the same resilience during demanding multi-step syntheses. We see regular requests for this specific chloro-nitro arrangement since it holds up better when exposed to reductive or nucleophilic conditions. Customers working on target-oriented syntheses reported stronger yields when switching to our material, remarking that the purity and consistent crystal habits minimize unpredictable side reactions down the line.

    Specification and Consistency: What Sets Our Material Apart

    Down to the specifics, we manufacture 2-Amino-3-Chloro-5-Nitrobenzonitrile targeting a purity of no less than 99%. Melting point range and HPLC chromatograms are posted with every lot for full transparency. Our team goes beyond mere compliance with compendial standards; batch records and process change logs are accessible for audit upon request. This traceability reflects deep engagement with the production process that third-party handlers simply don’t offer.

    By controlling the entire synthetic route, starting from precisely chosen precursors, we ensure minimal carryover of chloro or nitro byproducts. End users benefit from consistently white to light yellow crystalline solids, with no streaking or dark discoloration, which often signals incomplete purification. We run additional vacuum-drying sessions to reduce residual moisture to below 0.5%, based entirely on hands-on experience that even a slight increase can jeopardize downstream reactions.

    Over the years, we’ve compared our product’s performance against other offerings on the market. Some samples sourced from brokers reveal off-odors, sticky caking, or spectral impurities—all problems traced back to shortcut-laden processes or insufficient environmental controls. Field feedback revealed that certain trace organics negatively impact high-yielding couplings or render pilot-scale batches unworkable. By maintaining granular oversight from raw material input to packaged output, we sidestep common bottlenecks and ensure batch reproducibility.

    End-Uses and Industry Feedback

    Practical application drives every improvement in our workflow. Pharmaceutical chemists testing library expansions depend on intermediates that won’t stall or introduce side products in late-stage modifications. Sample requests prompted our team to pilot smaller, more frequent batches to guarantee freshness and prompt, stable delivery schedules. Agrochemical formulators use feedback about compatibility with different catalytic systems to suggest minor process adjustments, which we’ve incorporated without sacrificing scale.

    A leading polymer additive developer visited our plant last year. Their technical lead expressed relief that our benzonitrile derivative resisted cross-reactivity during high-temperature curing—outperforming a competing batch sourced from a general-purpose trader. The experience led to a joint quality review and, ultimately, expanded cooperation between our technical departments. End-user observation remains the truest metric: improved shelf stability, visual uniformity, and reduced requalification work for every new lot.

    Lessons from Synthesis and What They Mean

    Synthesis of this molecule requires careful manipulation at each ring substitution step. Early mistakes in reaction sequence, especially with nitro-group directionality or overchlorination, translate directly into lower yields or challenging separations. Years ago, we struggled with inconsistent batch color and aromatic overchlorination until a more finely metered addition was implemented. Adjusting pH during amino group introduction created a marked improvement, seen firsthand by our purification technicians as clearer filtrate and less fouling on filter media.

    Those practical improvements make a difference where operators and chemists work side by side, scrutinizing every lot before release. Regular in-process controls, visual checks, and hands-on sampling drive day-to-day decisions—a contrast to more hands-off or batch-blind approaches seen in bulk-trade environments. Every adjustment, whether in cooling rates or endpoint detection, comes from direct observations and data, rather than theoretical paper yields. These lessons find their way into our site-specific manufacturing protocol, reducing rework and building trust with buyers who demand more than just “compliant” product.

    Comparison With Similar Compounds

    It’s tempting to assume all substituted benzonitriles behave similarly, but years of feedback show otherwise. Swap the positions of the amino, nitro, or chloro group and photostability, reactivity, and solubility can change unexpectedly. The 3-chloro, 5-nitro, and 2-amino arrangement produces unique cross-coupling and cyclization behaviors not found in para- or ortho-substituted analogs. Customers exploring neighboring compounds soon discover drift in color development, inconsistent filtration rates, or unexpected byproduct formation.

    Working hands-on with different substituted benzonitriles, our chemists noticed better compatibility with both basic and acidic reagents in this configuration. Attempts to use similar nitrile intermediates either slowed process development or increased the cost of downstream purification by requiring more solvent or longer recrystallization schedules. Chemical differences, while subtle on paper, translate into meaningful productivity gains for synthetic teams charged with both innovation and throughput.

    Challenges and Solutions in Production

    Raw material sourcing plays a major role in consistency. Long ago, inconsistent lot performance exposed weaknesses in our nitrochlorination step; batches produced from unvetted suppliers led to visible clumping and non-uniform color. Engineers worked with our procurement team, establishing strict vendor audits and backup sources to keep supplies uninterrupted. Where others opt for the cheapest available inputs, we select based on supplier transparency and their documented quality measures.

    Process safety also matters. Nitro-containing aromatics require precise temperature and pressure control, not just for quality, but for plant safety. We invested in automated monitoring, and our skilled crew watches for foaming or runaway reaction signatures at each critical stage. Incidents dropped dramatically after integrating dynamic feedback controls, and lost-time accidents from fugitive exposures became rare. Other manufacturers, focused mainly on batch volume, sometimes shortchange investment in robust controls or operator training. By contrast, we see both product quality and workplace safety as linked goals, learned from direct experience rather than after-the-fact fixes.

    Dealing with waste streams from aromatic nitrile production requires a commitment to responsible stewardship. Early refinements focused on recycling wash solvents and optimizing reaction sequences to minimize bleed-through of unwanted organics into plant effluent. We track every kilogram of reagent and product, always looking for new routes to reduce overall footprint and comply with the latest environmental benchmarks.

    Batch-to-Batch Consistency: The Details That Matter

    Across thousands of kilograms shipped to research, manufacturing, and pilot plants, attention to detail defines our planning. Each batch undergoes checks for water content, melting point, residual catalyst, and spectroscopic properties. In some cases, a single degree cooler during crystallization dialed down insoluble particle count on QC. We learned to record each experiment, update process windows, and adapt based on customer and internal feedback. Flexibility in operating procedures avoids the “one-size-fits-all” approach that leads to production hiccups as scale increases.

    Packaging is kept clear and consistent to prevent exposure to light and moisture, with double-bagging as our standard practice. Operators cycle storage-room samples into real production environments to anticipate temperature swings or humidity spikes. Material destined for global shipment receives an additional round of environmental stress testing, based on firsthand experience with product sensitivity at extended transit times.

    Dialog with Application Experts

    Our long-term clients in the fine chemical and pharmaceutical industry care about more than just paperwork. Routine calls between our product managers and a customer’s synthetic team become chances to share new observations, both strengths and weaknesses. On several projects, observing catalyst fouling or color change before full scale-up proved invaluable, allowing us to adjust particle size distribution or adjust lot sequencing. The result is not simply a “sale” but an ongoing technical partnership, informed by accurate record-keeping, field visits, and honest feedback.

    Once, a researcher flagged subtle lot-to-lot differences in performance, which we traced back to a minor alteration in bath temperature control. In-house trials duplicated their findings, and we made the corresponding changes before shipping the next order. Such troubleshooting demonstrates respect for the technical skills of both producer and user, strengthening a feedback loop that keeps standards high long after certificates expire.

    Solutions to Recurring Issues in the Field

    Handling, storage, and use often throw up more challenges than any bench experiment predicts. Over time, field technicians reported dusting and slight clumping for shipments exposed to prolonged humidity. We responded with modified storage protocols, improved barrier linings, and a direct channel for customer troubleshooting. Several synthetic chemists faced problems with batch carryover into aqueous extractions. We helped optimize their protocols, even supplying mock contaminated samples to simulate “worst-case” scenarios. Other companies offering the same product can’t always close that loop with hands-on advice.

    Many production hiccups arise from trying to force a single protocol on all facilities. Our style emphasizes adaptability—finding a solution that works for large industrial reactors or smaller academic pilot lines without compromising product integrity. The experience that comes from repeated observation, collaborative troubleshooting, and mutual learning with users establishes a level of insight that bulk resellers rarely match.

    Looking Forward: Partnerships and Innovation

    Beyond refining our own process, we listen carefully to R&D teams pushing boundaries in both established and emerging applications. The trend in “green synthesis” pushed us to test alternative, less hazardous solvents; a shift from batch to continuous production in several facilities prompted further automation upgrades. These changes allowed for sharper reaction control, safer operator conditions, and better overall yields. Our company recognizes that successful adaptation comes from open communication at all levels of the supply chain—from engineers on the plant floor to principal investigators designing novel synthetic routes.

    Growth in fine and specialty chemical production calls for more than technical knowledge. Keeping pace means investing in state-of-the-art equipment, regular skills training, and robust data collection. Annual audits of production logs by seasoned staff catch small variations before they turn into big issues. We pass those lessons back to customers through transparent documentation and updates to our manufacturing standards.

    As more industries look to advanced intermediates like 2-Amino-3-Chloro-5-Nitrobenzonitrile, we stand ready with both the experience and infrastructure required for ongoing collaboration. Direct sourcing from a dedicated manufacturer builds trust: the technical questions get immediate answers, unexpected challenges receive practical support, and everyone benefits from open, honest communication.

    Conclusion

    Operators on the production line and chemists at the bench know the difference between off-the-shelf and purpose-prepared chemical intermediates. Each lot of 2-Amino-3-Chloro-5-Nitrobenzonitrile carries the collective knowledge of continuous improvement, field learning, and straightforward commitment to chemical craftsmanship. Reliable supply, technical transparency, and long-term partnership distinguish the manufacturer’s approach—qualities that matter for every experiment and every process scale.