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3-Amino-4-Chlorobenzamide

    • Product Name 3-Amino-4-Chlorobenzamide
    • Alias 4-Chloroanthranilamide
    • Einecs 617-089-4
    • 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

    623229

    Chemical Name 3-Amino-4-Chlorobenzamide
    Molecular Formula C7H7ClN2O
    Molecular Weight 170.6 g/mol
    Cas Number 36839-65-7
    Appearance White to off-white solid
    Melting Point 208-211°C
    Solubility Slightly soluble in water
    Synonyms 4-Chloro-3-aminobenzamide
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, in a dry place
    Smiles NC1=CC(Cl)=CC=C1C(=O)N

    As an accredited 3-Amino-4-Chlorobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Amino-4-Chlorobenzamide, 25g, is supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping 3-Amino-4-Chlorobenzamide is shipped in tightly sealed containers, protected from light and moisture. All packages comply with applicable chemical safety and regulatory guidelines. Transportation is conducted via ground or air, following appropriate hazardous material protocols to ensure safe and secure delivery. Material Safety Data Sheet (MSDS) accompanies each shipment for reference.
    Storage 3-Amino-4-Chlorobenzamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from moisture, direct sunlight, and sources of ignition. Store away from incompatible materials, such as strong oxidizing agents, acids, and bases. Label the container clearly and keep it in a designated chemical storage cabinet.
    Application of 3-Amino-4-Chlorobenzamide

    Applications of 3-Amino-4-Chlorobenzamide in Industrial Manufacturing

    3-Amino-4-chlorobenzamide plays a critical role as an intermediate in several specialized downstream manufacturing processes. Its chemical attributes enable precise formulation in active pharmaceutical synthesis, agrochemical production, pigment manufacturing, and specialty polymer development. As the direct manufacturer, we ensure consistent specification control matched to sectoral requirements.

    1. Pharmaceutical Intermediate for Antipsychotic Synthesis

    Major pharmaceutical producers use 3-amino-4-chlorobenzamide as a key intermediate during the synthesis of specific antipsychotic agents within the substituted benzamide chemical class. The material enters the synthesis in initial amide-coupling stages, where tight control of impurities and residual solvents is critical to meet international monograph specifications for regulated APIs. Material purity, trace metal control, and compliance with residual solvent guidelines are mandatory due to subsequent downstream conversion into high-dose oral pharmaceuticals subjected to stringent batch release testing.

    Industry compliance standards

    • Ph. Eur., USP, JP relevant monographs for intermediates
    • ICH Q7 GMP for active pharmaceutical ingredient manufacturing
    • 19th Edition Chinese Pharmacopoeia acceptance criteria for intermediates
    • FDA 21 CFR Part 211 process and validation controls

    Typical usage ratio

    • 1.00–1.25 molar equivalents relative to principal precursor amines, adjusted according to target yield and downstream conversion requirements.

    Downstream process integration

    • Material added at step 2 or 3 in multi-step batch synthesis schemes, following protection/deprotection or amidation reactions. Precise handling under nitrogen to prevent hydrolysis. Purity check via HPLC before further coupling with secondary substrates.

    Final product types

    • API for antipsychotic medications (e.g., amisulpride analogues)
    • Benzamide-based therapeutic agents supplied as bulk pharmaceutical chemicals

    2. Agrochemical Synthesis for Herbicide Intermediates

    Leading agrochemical groups incorporate 3-amino-4-chlorobenzamide as a precursor in sulfonylurea- and anilide-type herbicides. Its function lies in selective chlorination/amidation stages, producing active fieldspraying compounds. The compound’s reliable reactivity profile supports process optimization and efficient effluent management. Stringent pesticide material controls ensure minimal cross-contamination, critical when supplying multi-purpose plants. All supply streams serve strictly non-food crop applications where validated traceability from starting material remains essential throughout formulation runs.

    Industry compliance standards

    • China GB 2763 residue standards for technical pesticides
    • ISO 9001:2015 certified production controls
    • EU REACH Annex VII registration for intermediates
    • OECD pesticide manufacturing guidance for industrial hygiene

    Typical usage ratio

    • 0.85–1.10 molar equivalents per downstream formation batch, depending on yield optimization during chlorination or amidation for target herbicides.

    Downstream process integration

    • Consumable at critical precursor synthesis steps. Integrated before ring closure/elaboration or during coupling with sulfonyl or alkyl groups after amide activation, with in-process LC-MS purity monitoring to meet export compliance.

    Final product types

    • Sulfonylurea herbicide technical concentrate
    • Anilide herbicide intermediates for further on-site finishing
    • Bulk herbicidal active ingredient exports for crop application

    3. Pigment and Dye Intermediate Formulation

    Specialty pigment and dye formulators draw on the strong electron-withdrawing and donator effects of this raw material to synthesize high-performance azo and anthraquinone colorants. During production, 3-amino-4-chlorobenzamide reacts with diazonium salts or carboxyl group activators to create chromophoric structures used in plastics and technical fibers. Purity and color strength depend on precise molecular feed ratios and minimization of residual sulfur, which otherwise impacts final shade quality and fastness, especially for synthetic yarn and automotive applications.

    Industry compliance standards

    • EN ISO 105-X12 color fastness testing for textiles
    • CFR Title 21, Part 73 for synthetic colorant safety
    • REACH SVHC exclusion for colorant intermediates
    • ZDHC MRSL list conformance for zero discharge production

    Typical usage ratio

    • 0.6–0.95 molar equivalents, determined by chromophore development curves and desired pigment intensity for batch or continuous dyeing systems.

    Downstream process integration

    • Charged at primary diazo-coupling stages or amidation steps; post-synthesis purification by solvent extraction and crystallization for enhanced yield and color selectivity.

    Final product types

    • Azo pigments for plastics, inks and coatings
    • Textile colorants for polyester and polyamide fibers
    • Anthraquinone-based dyes for synthetic yarn

    4. Specialty Polymer and Resin Additive Synthesis

    Technical resin and engineering polymer producers employ 3-amino-4-chlorobenzamide as a chain stopper, comonomer, or nucleation additive for custom performance resins. Its amide and amino substituents support molecular tailoring in high-gloss coatings, structural adhesives, and occasionally heat-resistant polyamides, where exact chain composition determines mechanical and thermal end-properties. QC protocols require incoming analytical verification to avoid byproduct clustering, especially for electronics and automotive molding compounds.

    Industry compliance standards

    • UL 94 flammability standards for high-performance polymers
    • ISO 9001:2015 for specialty resin production
    • ASTM D638 tensile testing for finished plastics
    • EU RoHS directive for electronics polymers

    Typical usage ratio

    • 0.02–0.12 weight percent as a chain stopper or up to 1.5 mol% as an active comonomer depending on degree of polymerization and targeted physical properties.

    Downstream process integration

    • Mixed into bulk monomer streams before thermal initiation or polycondensation. Acts at specific macromolecule growth step; residual monomer removed after post-polymerization washing or devolatilization.

    Final product types

    • Gloss-modified epoxy coatings for automotive OEM
    • Electrical encapsulant resins for semiconductor assembly
    • Specialty polyamide engineering plastics for molded technical parts
    Free Quote

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    Certification & Compliance
    More Introduction

    3-Amino-4-Chlorobenzamide: Building Confidence with Reliable Synthesis

    Real Chemical Experience: Why Our 3-Amino-4-Chlorobenzamide Makes a Difference

    Daily production at our facility shapes the story behind each molecule of 3-Amino-4-Chlorobenzamide. Over the years, we’ve handled this aromatic compound from batch development through to ton-scale distribution, learning the ins and outs of delivering reproducibility and reliability. This substance, which goes by the model designation 3A4CB, serves as a key component in specific chemical syntheses, especially in pharmaceutical and research segments.

    Consistent Structure, Trusted Results

    3A4CB’s chemical structure—an amide adorned with amino and chloro groups—offers a unique base for molecular building. With experience gained across hundreds of batches, we’ve adapted our parameters to yield material that reliably matches published standards for purity, clarity, and solubility. Recent runs, for instance, achieve a purity consistently above 99% (HPLC), leaving users with predictability in their downstream reactions. Color, odor, melting point, and loss-on-drying get checked and rechecked for each lot. We maintain this routine because chemical research can’t afford surprises, and impurities present even at small amounts could compromise entire syntheses.

    Reliable supply of this intermediate helps labs speed up exploratory projects, build new libraries, and develop active pharmaceutical ingredients. In my early years on site, tasks like filtering out trace synthetic byproducts and confirming single-digit ppm levels of residual solvents took many hours and sharp focus. Today’s automated tracking and precise control of reaction conditions, together with modern analytical equipment, let us dial in the fine details faster than ever. Each step serves the same goal: giving clients confidence rather than raising questions about their foundation chemicals.

    From Gram-Scale Research to Multi-Ton Orders

    Small-scale research and commercial manufacturing both depend on uniform supply. Shipments leave our warehouses in tailored packaging, ranging from glass vials for gram-scale discovery up to fiber drums for progressive scale-up. Packing methods, inert atmospheric control, and shipment scheduling come from years of feedback from repeat users. We learned, not from theory but from real mishaps—a small breach in drum packaging during the humid summer of 2011 taught us about robust closure and effective moisture barrier systems.

    We keep documentation ready for every lot, including certificates of analysis, spectral data, and chain-of-custody records. This is not just about regulatory checks; researchers count on traceability in case their work calls for ever-deeper scrutiny. Early in our production journey, we faced a request from a team progressing to patent stage; ready access to historical records, including archived analytical data, let us assist their intellectual property application process without a hitch.

    The Role of 3-Amino-4-Chlorobenzamide in Modern Chemistry

    Customers describe 3A4CB as a high-yielding intermediate. It enters multi-step syntheses leading to various biologically active structures, especially where its amide backbone can take part in further coupling or cyclization. Scientists aiming for selective substitution reactions appreciate the regioselectivity our material provides, owing to the reliable arrangement of electron-donating and -withdrawing groups. Our in-house chemists themselves have used in-house 3A4CB in contract synthesis programs underpinning antihypertensive and anti-infective candidate pipelines.

    While some products come and go with fleeting demand, this one remains a steady workhorse in our catalog. Unlike simpler anilines or diamines, the presence of both amino and chloro groups on the benzamide core offers extra synthetic handles. Skilled chemists can execute transformations ranging from direct acylations and cross-couplings to selective dehalogenation, tweaking reaction conditions with confidence that they’re starting from a dependable, single-spot reactant.

    Purity and Consistency: Not Just a Label

    Achieving high content of 3-Amino-4-Chlorobenzamide demands close attention. During early pilot runs, trace-matrix interference sometimes crept in—this meant some customers struggled with unexpected outcomes or separation problems. Over time, we optimized workup and purification; judicious choices between recrystallization and chromatography, guided by up-to-date equipment, allowed us to drive contaminants down and standardize crystallinity. This consistency shifted the perception of our product; instead of being a “sometimes-passable option,” it’s now routinely specified for high-stakes projects.

    The market has seen lower-grade material from less experienced shops: darker color, lingering trace solvents, inconsistent melting ranges. Our crew learned by troubleshooting such missteps. For us, every outgoing batch earns a green light from someone with experience in hands-on bench chemistry, not just an analyst working a prescribed checklist. Regular communication with users, from researchers in university settings to process development teams at multinational pharma firms, comes back to quality. This is not a one-and-done process—the bar shifts every year as partners raise expectations.

    Direct Feedback Shapes the Product

    Nothing teaches better than real-world feedback. Several years back, a long-term customer reported minor issues with solubility in their novel solvent system. After reviewing their data and our analytical records, we traced it to a subtle batch-to-batch density variation rooted in ambient humidity uptake during packaging on an unusually damp week. We revisited the packaging line, improved both environmental control and monitoring, and the issue hasn’t returned since. The result: stability in both our product and our long-term relationships.

    As global markets adapt and competition intensifies, direct, transparent feedback from customers continues to guide how we approach quality. Site audits, open chemist-to-chemist conversations, and joint troubleshooting sessions let us refine process controls. This approach helps us tweak not only the final product, but also the steps that ensure bench-to-bulk-scale reliability. Every hiccup and every triumph trace back to the hands-on adjustments we’ve made together with partners who value more than just the lowest bid.

    Comparing 3-Amino-4-Chlorobenzamide with Similar Compounds

    Having produced more than a dozen functionalized benzamides, we understand where 3A4CB stands apart. For instance, compared with 4-Aminobenzamide, which lacks the chloro substitution, 3A4CB opens new reaction possibilities; electrophilic aromatic substitution or metal-catalyzed cross-coupling proceeds more selectively due to the ortho-chloro’s directing effect. Conversely, 4-Chlorobenzamide, missing the amino group, limits downstream functionalization. Once, a customer attempted to “upgrade” from 4-Chlorobenzamide by introducing the amino functionality in situ, but met with low yields and high labor costs. Dedicated 3A4CB from our production offered better efficiency and reproducibility.

    Material stability is another factor. Unprotected aromatic amines sometimes suffer from oxidation or discoloration during poor storage. Our 3A4CB, properly dried, consistently stores well under moderate, dry conditions. We’ve monitored stability both for routine shipments and under accelerated aging—real data rather than assumed shelf-life figures. Whether the end use involves small molecule construction or complex scaffolds, reliable performance pays off through fewer surprises and less waste.

    Why Process Know-How Matters for Safety and Compliance

    Safety steps into every process we run. 3A4CB’s controlled synthesis involves safe handling of potentially hazardous reagents—chlorinating agents and strong acids demand discipline. Our facilities operate under local and international chemical management standards, supported by years of in-house training. This foundation isn’t about regulatory box-ticking. Real accidents or near-misses in the world of chlorinated aromatics are powerful reminders; we’ve used such events as training cases, helping new generations of operators learn the standards borne from lived experience.

    Transport and storage bring their own set of demands. Aromatic amides don’t typically generate hazardous vapors, but fine particulates can cause dust problems if mishandled. Our approach, informed by actual shipment incidents and customer feedback, focuses on robust, tamper-evident packaging and careful labeling.

    Supporting Large-Scale API and Custom Synthesis Projects

    In contract manufacturing and process R&D, supplier reliability often spells the difference between project success and missed deadlines. Process teams need to count on secure reordering—stock-outs can stall an entire campaign. We saw this firsthand during a major GMP API project, where a delay in a key intermediate derailed three months of development. That lesson led to the implementation of our dual-sourcing and advanced planning system, ensuring uninterrupted availability for recurring 3A4CB needs.

    Process transfer from bench to kilo to tons brings new challenges. Scale introduces temperature control, mixing, and phase transfer limitations that aren’t visible at the 10-gram flask stage. We work side-by-side with clients' technical staff, offering not just supply but process input based on hundreds of runs at multiple scales. Conversations range from preferred solvent systems to filtration aids, always based on grounded experience rather than generic prescriptions. There’s no substitute for the experience gained troubleshooting and optimizing real reactions in real reactors.

    Transparency, Traceability, and Ethical Manufacturing

    Chemical manufacturing isn’t just pushing molecules from one flask to another. Trust builds over time as customers see the hands guiding the process, the records kept, and the concrete steps taken to improve. From early analytical missteps to careful inventory controls, we’ve invested in the details that give researchers a reliable product, free of unwelcome variables.

    We maintain full traceability for starting materials, solvents, and each transformation step. This effort came into sharp focus during a client’s regulatory audit, where full process transparency averted costly delays. Being direct about our capacity, timelines, and batch history pays off. It’s the difference between making a sale and creating a partnership rooted in reliability.

    Responsibility extends to the community and environment. Handling aromatic and halogenated intermediates creates specific waste and disposal issues. On our production floor, we’ve built solvent recovery and targeted waste treatment protocols—moving from basic compliance to a routine that conserves cost and limits impact. Periodic reviews by local authorities keep us sharp, but the bigger driver has always been knowing our work impacts more than just our own team.

    Improvement Never Stops

    Client demands shape our operations more than R&D wish lists or textbook recipes. Each feedback loop brings better methods: cleaner work-ups, faster filtration, stable packaging, easier inventory tracking. With a team that’s lived through the highs and lows of commercial chemical production, fresh energy pairs with hard-won wisdom to drive improvements, from the first order of the day through the last shipment of the month.

    Providing 3-Amino-4-Chlorobenzamide isn't simply a matter of filling drums. It means being a dependable partner for chemists tackling high-stakes synthesis goals, whether for a single experiment or a major pharmaceutical pipeline. Listening, iterating, and delivering—on time, to spec, and with clarity—have kept us at the forefront of specialty chemicals. Trust grows from real performance, not from generic promises. With every batch, we reinforce the value of long-term collaboration, grounded in the experience only real manufacturing brings.