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2-Acetamido-6-Chlorobenzoic Acid

    • Product Name 2-Acetamido-6-Chlorobenzoic Acid
    • Alias 2-Acetamido-6-chlorobenzoic acid
    • Einecs 248-609-1
    • 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
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    Specifications

    HS Code

    448746

    Chemical Name 2-Acetamido-6-Chlorobenzoic Acid
    Cas Number 15307-28-7
    Molecular Formula C9H8ClNO3
    Molecular Weight 213.62
    Appearance White to off-white solid
    Melting Point 220-224°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Synonyms 6-Chloro-2-acetamidobenzoic acid
    Storage Temperature 2-8°C
    Inchi Key KFOXVLMHZCEBMP-UHFFFAOYSA-N

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

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 25 grams of 2-Acetamido-6-Chlorobenzoic Acid, labeled with safety and identification details.
    Shipping **Shipping Description:** 2-Acetamido-6-Chlorobenzoic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. The packaging complies with chemical safety guidelines, clearly labeled with hazard information. During transit, it is handled as a non-hazardous solid but stored away from incompatible substances and extreme temperatures to maintain product integrity.
    Storage 2-Acetamido-6-Chlorobenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Avoid exposure to moisture and incompatible substances such as strong oxidizing agents. Store at room temperature, and ensure that the container is clearly labeled to prevent accidental misuse or contamination.
    Application of 2-Acetamido-6-Chlorobenzoic Acid

    Applications of 2-Acetamido-6-Chlorobenzoic Acid in Industrial Manufacturing

    2-Acetamido-6-Chlorobenzoic Acid serves as a key specialty intermediate that supports advanced synthesis routes in select industries. As the direct manufacturer, we supply this raw material to global partners whose final applications demand precise control of process quality, compliance to industry protocols, and tailored integration into established compound production flows. Below we outline the principal industrial segments where this compound is used for proven, large-scale outputs, detailing specific end-uses and considerations at each production stage.

    1. Pharmaceutical Intermediate for Cephalosporin Antibiotic Synthesis

    This raw material is primarily introduced as a vital building block during the synthesis of certain cephalosporin antibiotics, especially those with extended-spectrum activity. In commercial pharmaceutical manufacturing, it functions as a protected aromatic acid and undergoes further functionalization in multi-step organic reactions. Its use directly impacts the downstream quality of beta-lactam core structures, thus making it integral to API development for anti-infective therapies.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and EP guidelines for pharmaceutical raw materials
    • 21 CFR Part 210/211 (FDA cGMP regulations)
    • ISO 9001 Quality Management System certification

    Typical usage ratio

    • 0.9–1.1 molar equivalents relative to the intended cephalosporin core (adjusted for reaction stoichiometry and batch size)

    Downstream process integration

    • Charged into the initial condensation reaction involving 7-aminocephalosporanic acid (7-ACA) derivatives to install the chlorinated aromatic moiety
    • Undergoes controlled acylation and subsequent deprotection steps prior to isolation of the antibiotic precursor

    Final product types

    • Semi-synthetic cephalosporin Active Pharmaceutical Ingredients (APIs), including extended-spectrum injectable antibiotics
    • Antibiotic bulk powder for oral suspensions and parenteral solutions

    2. Agrochemical Synthesis Intermediate for Fungicide Production

    Selective agrochemical manufacturers employ this intermediate in the creation of chlorinated benzamide-based fungicides. The compound’s unique aromatic structure aligns with the developmental chemistry required for highly regulated crop protection agents, and its controlled reactions facilitate substitution patterns not readily achievable through direct chlorination of other benzoic acid precursors.

    Industry compliance standards

    • FAO/WHO Code of Conduct for the Distribution and Use of Pesticides
    • ISO 9001 Quality Management for production facilities
    • REACH registration for intermediate handling in Europe
    • OECD guidelines for chemical intermediates safety

    Typical usage ratio

    • 0.8–1.2 molar equivalents per batch, adjusted according to target fungicide molecular weight and target yield

    Downstream process integration

    • Added in controlled addition steps for amide-bond formation, preceding halogenation and ring-closing reactions
    • Serves as the backbone for further upstream elaboration into triazole or benzimidazole ring systems typical in modern fungicides

    Final product types

    • Active fungicidal ingredient bulk crystals
    • Formulated crop protection emulsifiable concentrates and water-dispersible granules

    3. Chemical Intermediate for Dyes and Pigment Manufacturing

    Leading specialty chemical producers utilize this compound in the tailored synthesis of high-performance azo and anthraquinone dyes. Its selectively substituted benzene ring introduces halogen and amide functionalities that modify pigment binding affinity and color fastness, especially for fibres subjected to rigorous industrial dyeing procedures.

    Industry compliance standards

    • Oeko-Tex Standard 100 restricted substances list
    • REACH Annex XVII compliance for dye precursors
    • ISO 9001/14001 for pigment manufacturing and environmental management
    • EN 71-3 (Safety of Toys – migration of certain elements) where dyes are used in toy and textile industries

    Typical usage ratio

    • 0.5–0.9 parts by weight per 1 part of diamine or anthraquinone core; varies with final pigment intensity requirement

    Downstream process integration

    • Introduced in the coupling stage for azo dye production after diazotization of aromatic amines
    • Integrated into high-temperature condensation reactors for anthraquinone dye synthesis

    Final product types

    • Reactive, acid, and disperse dyes for synthetic and natural fibres
    • High-stability color pigments for plastics, inks, and coatings

    4. Intermediate for Veterinary Drug Active Substance Synthesis

    Within the animal health sector, this material supports the production of select veterinary cephalosporins and related pharmaceutical agents. Its function as an intermediate ensures lot-to-lot consistency for veterinary preparations, where supply chain monitoring and cross-contamination prevention are prioritized during bulk pharma compound manufacturing.

    Industry compliance standards

    • VICH GL guidelines for Good Manufacturing Practice
    • Ph. Eur. (European Pharmacopoeia) veterinary appendices
    • APVMA (Australia) and US FDA: Center for Veterinary Medicine raw material registration
    • ISO 22000 (Food safety management, where veterinary drugs co-exist with feed production lines)

    Typical usage ratio

    • 0.95–1.1 molar equivalents per equivalent of core cephalosporin, dependent on synthetic route optimization

    Downstream process integration

    • Added to intermediate vessel immediately prior to final amidation in veterinary antibiotic biosynthesis route
    • Cleanroom charging protocols observed to avoid cross-contamination with food-grade substances

    Final product types

    • Veterinary injectable antibiotic APIs
    • Bottled or sacheted oral suspensions for animal health use

    5. Precursor for Specialty Chemical Synthesis in Research and Development

    Advanced material development laboratories and specialty synthesis facilities incorporate this compound as a customizable aromatic platform for small-series synthesis projects. Its reactive positions enable introduction of additional functional groups, supporting both scale-up trials and pilot runs for innovative molecules not yet produced on bulk scale.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Quality Management
    • OECD Principles of Good Laboratory Practice (GLP) for research trials
    • REACH notification for R&D substances
    • Internal SOP compliance for traceability and impurity control

    Typical usage ratio

    • Experimental: typically 0.4–1.5 equivalents, scaled per research protocol and molecular modification targets

    Downstream process integration

    • Functionalization at bench-scale reactors or small pilot vessels during lead compound or library synthesis
    • Reacted under mild or controlled temperature as a precursor for further modification, including halogen exchange and amide hydrolysis

    Final product types

    • Prototype pharmaceutical and agrochemical candidates
    • Specialty organic building blocks for patent application compounds
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    Certification & Compliance
    More Introduction

    2-Acetamido-6-Chlorobenzoic Acid: A Closer Look from the Manufacturer’s Perspective

    Introduction to 2-Acetamido-6-Chlorobenzoic Acid

    Every day at our facility, dozens of raw materials move through reactors, filtration setups, and crystallizers—the tools of our trade. One compound that consistently comes off our lines is 2-Acetamido-6-Chlorobenzoic Acid, also referred to in research and industry as a specialty aromatic carboxylic acid. Our production team has worked closely with process engineers to ensure the output hits the specifications demanded by downstream users in pharmaceutical research, intermediates development, and certain fine chemical syntheses.

    The typical batch leaves our reactors as a crystalline powder, white to light beige in color, with a chemical structure defined by an acetamido group at the second position and a chlorine at the sixth position of the benzoic acid ring. We analyze our product for purity, which regularly exceeds 99%. Impurity profiles, including related chlorinated and acetamido isomers, remain closely monitored—a demand that’s come directly from conversations with lab managers and process chemists we supply.

    Why Manufacturing Precision Matters

    Our experience tells us sloppy synthesis leads to unpredictable outcomes downstream. Early on, we competed with lower-cost imports that traded on price, but we watched customers struggle with variable impurity content, inconsistent melting points, and poor solubility behavior. Several of our regular clients, frustrated with unwanted side reactions in their research, requested tighter controls on residual solvents, especially concerning chlorinated byproducts and acetic acid traces. This feedback pushed us to invest in analytical hardware and robust SOPs for every batch.

    Purity and batch consistency drive almost every discussion we have about this compound. Quality checks—including HPLC, NMR, and mass spectrometry—don’t just generate paperwork, they let us guarantee a product that doesn’t cause unexpected results in the hands of a research chemist. In one instance, a customer synthesizing a novel amide found inferior grade 2-acetamido-6-chlorobenzoic acid left behind trace contaminants that affected their biological assays. After we shared batch analysis and discussed their protocols, they switched to our higher grade product and measured a dramatic drop in background interference.

    Specifications in Practice

    Our batches hit a melting range between 195 and 200°C. Water content usually sits below 0.2%, and residual solvents, such as DMF or acetic acid, are tightly regulated—numbers we confirm by GC. We pay close attention not just to overall purity, but to isomeric and oxidative degradation products. Storage conditions in our plant are optimized for stability, but once the material ships, our technical team regularly discusses best practices with our customers: sealed containers, controlled humidity, away from strong oxidizers. This repetitive feedback loop between our lab and the field helps us tweak process variables to meet what end-users actually need on the bench or in the plant.

    Applications: Research, Synthesis, and More

    Pharmaceutical chemists are the most frequent users of 2-Acetamido-6-Chlorobenzoic Acid. Our compound often goes into the early-stage synthesis of novel active pharmaceutical ingredients, as well as reference libraries for drug screening. Process chemistry teams tell us they value predictability—they need to scale up without surprises. Stable reactivity, consistent melting point, and low levels of colored impurities can save weeks of troubleshooting. In several specialty segments, like agrochemical development and pigment research, the compound’s halogenated aromatic backbone gives unique reactivity and physical properties that are hard to replicate.

    We also see this acid as a building block for more complex amides and heterocyclic systems. One global peptide synthesis group we supply reported that the acetamido group—delivered intact and unhydrolyzed—plays a crucial role in forming robust linkages under surprisingly harsh coupling conditions. This isn’t possible if residual moisture or hydrolyzed impurities sneak in, so we take great care during drying and packaging.

    Key Differences From Other Benzoic Acid Derivatives

    The chemistry community works with a spectrum of benzoic acid derivatives, but subtle differences can create major changes in downstream processes. For instance, 2-acetamidobenzoic acid (also known as N-acetylanthranilic acid) lacks the chlorine substituent and serves as a gentler reactant. In contrast, our 2-acetamido-6-chlorobenzoic acid introduces an ortho-chloro group, which can activate or deactivate the aromatic ring for electrophilic or nucleophilic substitution—something our customers in medicinal chemistry take advantage of when designing next-generation molecules.

    A couple of process developers in pilot plants have told us how the electron-withdrawing nature of the chlorine atom provides unique selectivity in multi-step syntheses, especially when managing oxidative transformations or selective halogen exchange. This specificity is not just a matter of academic interest; these subtle electronic effects can govern yield, purity, and scalability. For users considering alternatives, either for patent circumvention or cost, we explain that swapping out the 6-chloro for a hydrogen may seem like an incremental change, but in synthesis everything hinges on the details. Our experience bears this out: in certain Suzuki couplings or amidation reactions, reaction rates and byproduct profiles shift dramatically.

    Production: Hands-On Experience With Process Optimization

    Our plant started synthesizing this compound with glass-lined reactors, manually charged with acetanilide, chlorobenzoic acid, and acid chlorides under precise temperature control. Today, with solvent recovery and in-line filtration, we cut down on waste and control exothermic runs much more smoothly. We’ve learned that temperature ramp rates make a difference for color and filterability, so we monitor every batch reaction with tight process control.

    Most issues—like dark-colored byproducts or sub-par crystallinity—have been solved through operator vigilance and feedback from end users who flagged our early attempts as substandard. One large-scale synth used to face bottlenecks during work-up due to insoluble material, but shifting our drafting sequence and crystallization solvent fixed this. By iterating on these small but critical details, we have managed to make a product that customers say drops right into their flow chemistry setups or batch reactors with minimal rework.

    Logistics and On-the-Ground Support

    We don’t just load drums onto pallets and consider the job done. Shipping regulations related to chlorinated aromatics require certain labeling and packaging; nobody wants delays at customs over paperwork or specification disputes. Over time, we’ve taken feedback from import managers and compliance teams to ensure documentation matches requirements and full traceability gets documented—right down to batch-level impurity data. This has helped several pharmaceutical supply chains stay smooth, even amid sudden audits and regulatory scrutiny.

    Even the small details—humidity in shipping containers, inner linings of packaging, or secondary contamination risks—matter for a product like this. Our technical support team regularly fields questions from new users on storage, shelf life, and handling minor material clumping. Sometimes there’s not a universal answer: someone in a humid tropic will face different challenges than a user in a dry climate, so we stay in touch after delivery and document lessons as we go.

    Sustainability and Handling of Process Residues

    Scale brings new challenges. As production rose, our waste streams shifted—mainly, increased volumes of chlorinated process water and acetic acid residues. These couldn’t be ignored any longer; regulatory demands at the local and international level now demand waste minimization and safe treatment. We invested in solvent recovery and neutralization beds not only to meet compliance but also to control operating costs. When major off-takers began asking for documented “greener” alternatives, we experimented with batch parameter tweaks that cut the solvent load by a measurable margin without compromising product quality.

    There is no magic bullet to waste, but by collaborating with other local manufacturers, we’ve formed a consortium to share best practices around waste reduction and byproduct valorization. This includes on-site solvent recycling and periodic third-party audits—a move which over time has both cut corners off our utility bills and helped make compliance audits smoother.

    Challenges We’ve Overcome—And Ongoing Issues

    Manufacturing chemistry is never static. Our journey with 2-acetamido-6-chlorobenzoic acid has seen quality issues, processing delays, raw material price jumps, and occasionally hard-to-predict batch failures tied to minute changes in upstream feedstock. These problems are not unique to this compound, but the tight tolerances and regulatory pressure in the pharmaceutical market make any glitch costly. Staffing continuous improvement teams and maintaining a robust relationship with our upstream suppliers helps prevent surprises.

    Supply chain disruptions do not always announce themselves. For a spell, an upstream supplier of acetanilide shut down for maintenance, causing tightness in the market and some delay for our customers. Rather than source from unvetted suppliers, we kept communication clear and transparent—sharing updates, adjusting schedules, and providing technical documentation so our downstream clients could plan around the shortfall. This open-book approach, learned over years, builds trust and typically turns short-term roadblocks into repeat business, coming from users who prefer reliability over cost-cutting.

    A handful of customers in regulated spaces have requested additional documentation to support their internal audits. We work directly with their regulatory teams, providing signed batch certificates, impurity breakdowns, and even historical deviation records. Being open about lab findings—good or bad—has forged stronger customer relationships. These users show us that manufacturing goes far beyond pushing a good-looking powder out the door.

    Opportunities for Future Improvement

    No process stays perfect forever. Our R&D group continues to investigate alternative synthetic routes, including lower temperature coupling methods and greener chlorination steps. There is interest in continuous flow chemistry, which could reduce batch times and decrease waste. Feedback from our largest customers has encouraged us to focus on shelf life extension, which ties directly to better stability formulations during packaging.

    Recent conversations in the industry have focused on process intensification—reducing the number of synthetic steps and implementing in-line analytical monitoring. We believe this will cut down on batch-to-batch deviations and reduce the overall energy footprint. Our team is launching pilot runs exploring these new process technologies, hoping to deliver even tighter impurity profiles and lower environmental impact.

    Feedback Loop: Manufacturer and End User

    Chemists doing hands-on synthesis have little patience for fluff. They want reliable materials, straightforward data, and real communication from suppliers. Our experience making 2-acetamido-6-chlorobenzoic acid has shown us that successful supply doesn’t end with the shipping manifest. It continues through tech support calls, shared troubleshooting, and honest conversations about what is and isn’t working. This feedback loop, built over years with polymer, pharma, and pesticide development groups, keeps us improving batch after batch.

    Recently, an early-stage biotech firm flagged a minor issue: lots from a particular production window had slightly altered color. Our QA team dug into archived batch records, traced back to a subtle pH variation in a precursor step, and quickly adjusted the process. This collaborative approach meant current and future batches went out with improved specs, and the customer responded by placing an extended order—proof that open lines and a willingness to fix issues yield real results.

    Comparing Direct Alternatives

    Alternatives with minor changes—whether swapping the position of the acetamido group, removing the chloride, or using an unsubstituted benzoic acid—do not always translate in real-world experiments. Colleagues in pharma mention attempts to replace our product with lower-cost 2-acetamidobenzoic acid; in many cases, downstream conversion steps fail, yields suffer, or isolation becomes a bottleneck. The ortho-chloro group’s unique electronic influence precisely tunes reactivity, offering a window to otherwise challenging synthetic targets.

    Direct side-by-side testing in our own applications lab has demonstrated the difference. Using 2-acetamido-6-chlorobenzoic acid as a precursor in multi-step aminolysis consistently produces higher yields and purities versus more basic benzoic acids. Not every customer needs this edge, but for those scaling up complex syntheses, this difference can push a project from pilot scale into full production.

    Final Reflections from the Manufacturing Floor

    2-Acetamido-6-chlorobenzoic acid is not just a chemical registry number—making it involves careful raw material selection, process optimization, real-world troubleshooting, and close customer dialogue. Each drum tells the story of operators making temperature calls, lab staff troubleshooting signals, and support teams juggling paperwork and compliance. Industry remains driven by stories like these, and from our side, it is the steady feedback and evolving challenges that keep us innovating and investing.

    As downstream uses diversify—from medicinal chemistry to materials science—users will continue to demand ever-tighter specifications, greener credentials, and a manufacturer who understands the product not just as numbers on a sheet, but through the lens of hands-on experience. We see our future in this space built on trust, technical rigor, and a willingness to share what success—and the occasional setback—looks like behind the scenes.