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Anthranilamide

    • Product Name Anthranilamide
    • Alias 2-aminobenzamide
    • Einecs 207-696-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    687053

    Chemical Name Anthranilamide
    Iupac Name 2-aminobenzamide
    Molecular Formula C7H8N2O
    Molar Mass 136.15 g/mol
    Cas Number 88-68-6
    Appearance White to off-white crystalline solid
    Melting Point 147-150 °C
    Solubility In Water Slightly soluble
    Boiling Point 382.5 °C at 760 mmHg
    Density 1.31 g/cm³
    Smiles C1=CC=C(C(=C1)C(=O)N)N
    Pubchem Cid 6796

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

    Packing & Storage
    Packing Anthranilamide, 100 grams, is packaged in a sealed amber glass bottle with a secure cap and clear hazard labeling for safety.
    Shipping Anthranilamide is typically shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be transported following regulations for chemical safety, often as a non-hazardous material, but appropriate labeling and documentation are required. Standard shipping conditions involve ambient temperature and cushioning to prevent breakage or leakage during transit.
    Storage Anthranilamide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it separate from incompatible substances such as strong oxidizing agents. Use appropriate safety precautions, including gloves and eye protection, when handling. Follow all local, regional, and national regulations for storage and disposal.
    Application of Anthranilamide

    Applications of Anthranilamide in Industrial Manufacturing

    Anthranilamide (2-aminobenzamide) is widely employed across selected industrial segments, serving specialized roles in high-value chemical synthesis, polymer modification, crop protection intermediates, and dyestuff manufacturing. As a dedicated chemical raw material producer, we deliver batch-consistent anthranilamide fully traceable to production origin, supporting downstream processors with technical documentation and compliance transparency for every application area detailed below.

    1. Pharmaceutical Intermediate Synthesis

    Anthranilamide is a core building block for the synthesis of various heterocyclic compounds, antidiabetic agent intermediates, and anticonvulsant analogues. Its ortho-substitution pattern, combined with reactive amide and amino groups, facilitates ring closure and acylation reactions that underpin the commercial routes to several regulated APIs and their intermediates. Manufacturers use it in multi-step batch and flow chemistry syntheses within cGMP-compliant environments, tightly monitored for impurity profiles and trace elements that impact downstream medicinal compound purity.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF General Chapters & Monographs for intermediates
    • EDQM CEP/DMF referencing for API synthesis
    • 21 CFR Part 211 (US FDA GMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.05–0.5 molar equivalents versus target API, adjusted according to stoichiometry of each specific synthetic step; precise ratios calculated per validated process protocol.

    Downstream process integration

    • Charged directly into ring cyclizations, amidation, or condensed into functionalized aromatic cores during early to mid-stage synthesis prior to final API assembly.

    Final product types

    • Anticonvulsant pharmaceutical intermediates
    • Antidiabetic agent precursors
    • Specialty heterocyclic building blocks

    2. Agrochemical Intermediate Production

    Agrochemical manufacturers incorporate anthranilamide in the synthesis of active ingredient intermediates, particularly those used in phenylamide, aniline, and benzimidazole crop protection agents. The compound's functional groups participate in nucleophilic substitution and condensation reactions, enabling routes to complex pesticide molecules. Plant facilities operate under crop protection GMP systems to satisfy regulatory residue and safety assessments, requiring precise control over input purity, trace contaminants, and batch uniformity for reproducibility in downstream application.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • OECD Principles of Good Laboratory Practice (GLP) for toxicology traceability
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 for substance registration in the EU

    Typical usage ratio

    • 0.1–0.8 molar equivalents per batch, adjusted based on target intermediate yield; the precise loading depends on desired conversion rate and downstream yield optimization datasets.

    Downstream process integration

    • Introduced in intermediate coupling or condensation steps for synthesis of amide-linked crop protection precursors. Forms part of closed-system batch or continuous flow processes subject to in-process QC for residual amines and byproducts.

    Final product types

    • Fungicide intermediates (e.g. precursor to benzimidazole group agents)
    • Herbicide synthetic intermediates
    • Pesticide formulation actives

    3. Polymer Additive Manufacturing

    Chemical processors use anthranilamide as a reactive additive and chain modifier in specialty polymer production, including the enhancement of polyamide, polyester, and acrylic resin performance characteristics. Its amide functionality contributes to improved chain structure and increased crystallinity, supporting finished materials with targeted mechanical and thermal properties. Process engineers introduce anthranilamide during melt blending or solution-phase copolymerization, applying relevant quality and environmental compliance systems specific to polymer production.

    Industry compliance standards

    • ISO 9001/14001 (Quality and Environmental Management for plastics manufacturing)
    • EU RoHS Directive 2011/65/EU (if downstream polymers for electronics)
    • FDA 21 CFR 177.1500 (if used in polymers with food contact applications, where permitted)
    • GB/T 2410-2008, GB 4806 (China food-contact plastics, if applicable)

    Typical usage ratio

    • 0.1–3.0% by weight, adjusted based on the desired modification to tensile strength, transparency, thermal stability, and processing flow attributes. The exact ratio is driven by resin target properties, application method, and regulatory restrictions.

    Downstream process integration

    • Added during polymer melt compounding, extrusion, or batch copolymerization reactions. May be introduced as a masterbatch in highly filled concentrates for subsequent let-down during plastic part fabrication.

    Final product types

    • Enhanced polyamide engineering plastics
    • Modified acrylic resins for automotive and optical use
    • Specialty polyester films and fibers

    4. Dye and Pigment Manufacturing

    Colorant manufacturers leverage anthranilamide as an intermediate for synthesis of disperse and reactive dyes, utilizing its aromatic amide and primary amine groups as points of functionalization in diazotization, condensation, and coupling reactions. These processes require strict adherence to environmental and consumer safety standards regulating colorant residuals for use in textile, leather, and plastic coloration sectors. Input material traceability and impurity management are essential for ensuring the final dye’s compliance with textile and ecological labeling schemes.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile dye applications)
    • REACH Annex XVII & SVHC (restrictions on hazardous substances in dyes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, for textile supply chain)
    • ISO 9001:2015 (Colorant manufacturer quality assurance)

    Typical usage ratio

    • 0.2–1.2 molar equivalents, depending on the dye chromophore and color depth required; formulations adjusted per batch synthesis design and shade matching requirements.

    Downstream process integration

    • Fed into primary aromatic amine derivatization or as a coupling partner during diazo dye synthesis steps. Incorporated in early organic synthesis sequences, prior to dye purification and standardization.

    Final product types

    • Disperse dyes for polyester fiber dyeing
    • Reactive dyes for cellulosic textile substrates
    • Functional dye intermediates for ink and plastics

    5. Specialty Metal Complex Ligand Synthesis

    In industrial chelate chemistry, anthranilamide enables manufacture of custom metal-complex ligands for use in analytical reagents, metal extraction, and formulation of homogeneous catalysts. Its bifunctional structure provides strong binding motifs for transition metals, contributing to ligand sets utilized in fine chemical analysis and industrial water treatment. This segment requires documentation of trace metal impurity levels and robust supply chain transparency to fulfill stringent international specifications governing analytical reagent production.

    Industry compliance standards

    • ISO 17034 (Reference material producer competence, relevant for analytical reagents)
    • ISO 14001 (environmental controls in chelate synthesis)
    • REACH substance registration for custom ligand chemicals
    • International Council for Harmonisation (ICH) Q6A (if analytical intermediates enter pharma QC pipelines)

    Typical usage ratio

    • 0.5–1.5 equivalents relative to metal ion content; stoichiometry tailored to achieve targeted complex stability or extraction efficiency depending on application.

    Downstream process integration

    • Charged into ligand synthesis reactors, forming part of direct metal complexation or pre-ligand activation in controlled-pH, oxygen-exclusion environments; processed to remove trace contaminants before final chelate extraction and concentration.

    Final product types

    • Analytical-grade metal-complex ligands
    • Homogeneous catalyst components (e.g., for polyesterification or hydrogenation)
    • Water treatment chelating agent intermediates
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    Certification & Compliance
    More Introduction

    Introducing Anthranilamide: Experience from the Factory Floor

    Real Work, Real Results: Our Anthranilamide Story

    Every season, new orders for dyes, crop protection solutions, and pharmaceutical materials flow into the production halls. Over the years, Anthranilamide became a cornerstone compound for all sorts of specialty synthesis. As the manufacturer, we stand over each batch, checking the color, grain, consistency, and even the smell because we know what long hours and tough customers have taught us: quality starts at the source, not the shelf.

    Unpacking the Substance: What Makes Our Anthranilamide Different

    Raw Anthranilamide rolls off the reactor line as a white to off-white crystalline powder. Each lot matches only one standard: the one set inside our own plant. Our typical specification holds the active content above 99% by HPLC. Moisture hovers under 0.2%. Ash residue drops below 0.1%. These numbers reflect hard-earned know-how from decades of tightening controls, testing each production run, and working hand-in-hand with chemists and engineers on-site—not at desks miles away.

    Traceability Begins in the Reactor Vessel

    Every drum of Anthranilamide has a story that begins at a steel-clad vessel with a trained operator logging temperatures and adding reactants ounce by ounce. No automation replaces the technician who recognizes by sight when a crystalline slurry is ready or when it needs more time. Production runs in this business can’t hide behind slipshod labeling or vague paperwork; we track batches down to the hour they left filtration. Knowing where and when a drum was filled backs every ton we ship with a record that follows it clear to the customer’s plant.

    Why Purity Sets the Margin for Manufacturers

    In the dye industry, a trace impurity translates into shades drifting off tone. For pharmaceutical middlemen, excess moisture or inconsistent crystal size eats into yields during downstream reactions. Our team doesn't just hit textbook specs. We watch for full dissolution rates and inspect granule formation to ensure that when you weigh out Anthranilamide in your operation, it acts precisely as your own QC team expects every single time.

    What Our Experience Taught Us about Handling Anthranilamide

    Partners ask how to work with Anthranilamide, and we give it to them straight. This material flows easily from sealed bags but holds a knack for sticking if left exposed on humid days. Workers in our plant never skip desiccant use, and we keep drums closed tight. One misstep and the quality slides, so we only fill containers inside a climate-controlled suite. Each batch leaves the warehouse with silica packs and the kind of sealing we’d expect if we were receiving it ourselves.

    Getting the Particle Right

    Some customers want as fine a grade as we can make without pushing costs through the roof. Years back, a leading pigment factory gave us feedback—the coarser form settled too slowly in their tanks. We altered the crystal growth step, dialed in the particle size, and swapped filter meshes. That adjustment cut their process time by hours. That’s not a trick from a textbook. It comes from trial, error, and direct conversation with the people who put their name on the end product.

    How Usage Shapes Design

    Among the dye producers, Anthranilamide serves as a key intermediate in producing azo compounds and certain disperse dyes. In agrochemical lines, it slots into the crafting of fungicides and herbicides that require a clean, non-reactive amide group. Pharmaceutical operations depend on our product for reliably yielding downstream amination and condensation reactions—especially where regulatory filings require process repeatability. The point is this: we know exactly where our product lands because we’ve toured these customer plants, seen their benches and production lines, and fielded their rawest, toughest process complaints.

    Consistency from Batch to Batch: What QA Really Means in Practice

    Outside labs don’t run our QA program; our own technicians sign off every lot before it clears the dock. Batch sheets stay accessible long after shipping in case a traceability audit crops up. Customers sometimes ask for full spectral files or wet chemistry proofs, and we scan, print, or prepare fresh ones as needed.

    Old-Fashioned Know-How Meets Modern Compliance

    Regulatory challenges build new hurdles every year. We remember the day when only local checks mattered; today, a shipment can stall if the certificate or safety data isn’t flawless. Our compliance department works side by side with the production crew. Instead of dumping paperwork on a separate office, we train everyone—lab techs, packers, even forklift operators—to know what new standards look like. Tracking each lot against European, US, and local regulations becomes a living part of every shift.

    What Goes Wrong—and How We Handle It

    No seasoned manufacturer gets through a decade without slip-ups. Sometimes a filter fouls and a batch runs off spec, or we find a stray impurity on a retention sample that sailed through visual checks. No cover-ups, no delays—senior staff lock down that batch, rerun every test, and call out the root cause before resuming shipments. Lessons learned in sweat—every one of them winds up written in the process guide, right where new staff can see how to dodge past mistakes.

    Comparing Anthranilamide to the Competition: Honesty and Open Eyes

    We’ve handled plenty of alternatives—both home-grown and imported. Some producers chase the lowest cost with recycled solvents or relaxed crystallization conditions. These shortcuts creep into the product, showing up months later as clogs in customer lines or off-odors in stored material. Years ago, a client returned a large lot sourced elsewhere due to plate-out on their reactors. We opened both bags: one with a fine, free-flowing powder, ours with no visible residue after hours exposed to air. That moment said more than any marketing brochure.

    Roots in Customer Collaboration

    Open dialogue makes a difference. A client aiming to scale up their dye run flew in for a walkthrough. Days on-site, in boots, sampling at every step gave them the answer: the problem came not from our shipment, but from a leaky pipe diluting their dissolution tank. Problem fixed, business kept humming. Real support doesn’t end at the order confirmation.

    The Backbone Behind Every Specification

    Some users don’t sweat granular size, purity, or dampness—but the toughest customers stand behind the most exacting processes. We track not just what our product is, but how it acts after weeks in storage or a thousand miles in a hot shipping container. We store retention samples and welcome surprise audits. The best antidote to errors is expecting them, preparing for them, and tracking changes with exactness.

    The Model You Receive Comes from the Floor, Not from a Brochure

    We calibrate every detail—degree of dryness, content by titration and HPLC, bulk density—on the samples your operators pull on their own lines. Sometimes we get requests for material with special melting points or slightly altered granularity. Instead of turning these away or making bland promises, we bring R&D right to the line and test changes at pilot scale, tweaking just as much as the application demands. Flexibility in production, paired with practical skill, brings more value than generic assurances.

    Why Serious Partners Don’t Gamble on Unknown Quality

    Real buyers know poor consistency eats up more cash in downtime and remediation than any imaginary savings from budget vendors. Over-dependence on spot suppliers or souped-up middlemen links the fate of your whole process to someone who’s never seen how the raw material acts during an overnight run or in a mixer at full scale. Our plant’s proximity to our own supply chain helps avoid those letdowns. In our experience, old-fashioned partnership, backed by data and transparency, trumps fast talk every single time.

    Supply Security Is Not a Buzzword to a Plant Operator

    Stories pour in from buyers caught short during global shortages—supplies strangled, prices doubled, deliveries missed. In those days, we keep the lines rolling and stock up buffer inventory. While others chase substitutions or filtered-down blends, our customers get full-strength Anthranilamide without the risk of recipe changes or defensive explanations to their end buyers. Consistent operation keeps not just our staff paid but our partners’ processes whole.

    Packaging Is Not an Afterthought

    Every time a truck leaves our yard, we walk the line—seals checked, drums double-wrapped, and pallets braced for long hauls. Field stories about torn bags or powder streaking out the back of containers keep our team alert. Nothing ruins a high-purity batch faster than careless handling in freight. We use thick polybags, triple-layered, and only food-grade ties. From the filling station to your loading dock, we carry the liability for every shipment.

    Safety and Environmental Accountability Come from the Production Hall

    Decades handling Anthranilamide built muscle memory in our team—goggles on, dust controls running, careful tracking of every spill or sweep. Waste streams see double-redundant checks before discharge. Our environmental monitors cross-verify with official standards daily. Staff rotate through ongoing environmental and safety classes. Not just to check boxes—because a single mistake could ruin reputations and relationships built over years.

    Why Trust Grows Through Unfiltered Feedback

    We appreciate the unvarnished complaints, sometimes more than the praise. One loud phone call about a batch that wouldn’t dissolve right had our QA running extra solubility checks until root cause came clear. Every correction nudges us closer to zero-defect shipments. We post feedback forms right on every invoice and answer every call in real-time, pulling staff away from paperwork if needed. No question too small, no hour too late.

    Tightening the Process Every Year

    Improvement isn’t a one-off project. Five years ago, we shifted from solvent-based to cleaner water-based purification. Energy savings followed, and so did a drop in trace residues. Another round of investment brought in new chromatographs, letting us slice impurities that rode through older methodologies. Vendor evaluations run every season—not for show, but to catch trading partners who lose focus on raw material clean-up. Our Anthranilamide didn’t just ‘meet the market;’ it keeps moving with the market needs.

    Anticipating the Next Challenge: Customization, Not Commoditization

    Standard products fill the bulk orders, but unique requirements come through quieter channels. Once, a large client came with a pharma-grade request: tighter than any generic producer would even consider. We shut down a whole line, refitted filtration gear, and fine-tuned our crystallization cascade batch by batch until the spectra fell into lockstep. Those kinds of custom runs keep the crew sharp, the lab busy, and the product ahead of outside substitutes.

    Listening at Every Step

    Clients sometimes share what works and what doesn’t—process steps that make or break their conversion yields. We dive into their struggle, running side-by-side trials or duplicating conditions inside our pilot labs. Every real-world adjustment turns into the next improvement loop in our documentation. Managing Anthranilamide for years, we learned that the customer’s process becomes part of our expertise the minute we step into their plant or receive samples for troubleshooting.

    Reflections from Years in the Trenches

    Ask any member of our crew about a memorable batch, and you’ll hear stories of hot summer days, power bumps, impossible targets, and last-minute fixes that staved off disaster. Pride doesn’t grow from keeping up with the market—it comes from fixing what went wrong, stretching what’s possible, and keeping the bar higher with every shipment. Our Anthranilamide doesn’t claim a miracle; it grows better from every test, every phone call, and every pound packed by a crew that takes their job personally.

    Built for Real Users, Not Checkboxes

    Looking back over tens of thousands of tons shipped, what stands out isn’t just numbers on a page. It’s the faces behind the process—operators, lab techs, clients who risk their own reputation on our materials. Making Anthranilamide at this scale means investing both in smarter processes and sturdier relationships. Experience spanning generations taught us not to treat quality, safety, or traceability as a marketing boast, but as a daily, living practice.

    The Next Shipment Ships with Our Own Reputation Inside

    Not every customer demands full profile tests, humidity logs, or updated compliance files, but we run them as a matter of routine. Our track record with Anthranilamide stands as the result of thousands of small corrections, late hours, and a culture of accountability. Each new order refines the process. That’s not just manufacturing; that’s partnership—the best kind, earned honestly, batch by batch.