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3-Amino-4-Methoxybenzamide

    • Product Name 3-Amino-4-Methoxybenzamide
    • Alias 3-Amino-4-methoxybenzenecarboxamide
    • Einecs 629-022-6
    • 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

    742362

    Iupac Name 3-amino-4-methoxybenzamide
    Molecular Formula C8H10N2O2
    Molecular Weight 166.18 g/mol
    Cas Number 5036-46-6
    Appearance Off-white to light yellow solid
    Melting Point 180-184 °C
    Solubility Slightly soluble in water, soluble in organic solvents like DMSO
    Smiles COC1=CC(=CC(=C1)C(=O)N)N
    Inchi InChI=1S/C8H10N2O2/c1-12-6-3-2-5(8(11)10)7(9)4-6/h2-4H,9H2,1H3,(H2,10,11)
    Purity Typically >97% (commercial)
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 4-Methoxy-m-anthranilamide; 3-Amino-p-anisamide

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

    Packing & Storage
    Packing The 25g amber glass bottle features a secure screw cap, clear hazard labeling, and a printed chemical name: 3-Amino-4-Methoxybenzamide.
    Shipping 3-Amino-4-Methoxybenzamide is shipped in tightly sealed containers to prevent moisture and contamination. Packages are clearly labeled with appropriate hazard information. The chemical is handled in compliance with regulatory requirements, transported under ambient conditions, and accompanied by a safety data sheet (SDS) for safe transit and storage.
    Storage 3-Amino-4-Methoxybenzamide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Store at room temperature and protect from light and moisture. Follow all relevant safety protocols and local regulations for handling and disposal of chemicals.
    Application of 3-Amino-4-Methoxybenzamide

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

    As a direct manufacturer of 3-Amino-4-Methoxybenzamide, we ensure strict quality control and reliable supply to customers specializing in high-value chemical synthesis. The following sections detail proven, industrial-scale application areas for this material, highlighting relevant compliance frameworks, precise integration protocols, proportion guidelines, and definitive end-product categories for each scenario.

    1. Pharmaceutical API Intermediate for Kinase Inhibitor Development

    3-Amino-4-Methoxybenzamide serves as a key intermediate in the synthesis of specific kinase inhibitors used in oncology portfolio pipelines. Our technical support team works with pharmaceutical manufacturing partners to incorporate this compound at the heterocyclic building-block assembly stage, promoting controlled reactivity and high yield. Our manufacturing facility ensures qualified traceability for every batch supporting GMP supply chains and regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph compliance for starting materials
    • US FDA 21 CFR Part 211 Current Good Manufacturing Practice
    • WHO Good Manufacturing Practices for pharmaceutical raw materials

    Typical usage ratio

    • Applied at 1.2–2.5 molar equivalents depending on the targeted coupling reaction and optimization for impurity profile

    Downstream process integration

    • Introduced after initial ring system construction; participates in amide coupling or nucleophilic aromatic substitution during multi-step API synthesis under strictly anhydrous conditions

    Final product types

    • Anticancer kinase inhibitor drug substance (API)
    • Pilot-scale investigational medicinal products (IMPs)
    • Advanced drug candidate intermediates for oral solid dosage forms

    2. Active Ingredient Precursor for Azo and Heterocyclic Dye Manufacturing

    In specialty dye synthesis, 3-Amino-4-Methoxybenzamide functions as a primary aromatic amine donor for constructing high-purity azo and heterocyclic dye structures. Downstream users implement carefully controlled diazotization and coupling steps to maximize chromophore intensity and batch-to-batch reproducibility for textile and industrial dye finishing lines.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted amine residues in textile dyes
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • EU REACH Regulation (EC) No 1907/2006 for registration and use in dye compounds
    • ISO 9001:2015 certified quality management systems for auxiliary chemicals

    Typical usage ratio

    • Incorporated at 0.5–1.7% (w/w) relative to the total batch mass; optimized for desired color strength and minimal side-product formation

    Downstream process integration

    • Added during aqueous diazotization under chilled, acidic conditions before coupling with coupling components or heterocyclic precursors

    Final product types

    • Reactive and direct dyes for cotton and viscose fibers
    • Metal-complex dyes for heavy-duty technical textiles
    • Intermediate azo dye building blocks for further downstream modifications

    3. Building Block for Custom Agrochemical Synthesis

    In crop protection R&D and production, 3-Amino-4-Methoxybenzamide acts as a customizable aromatic amide source for the creation of specific herbicide and fungicide structures. Agrochemical formulators select this material for its predictable reactivity in constructing targeted aromatic frameworks, supporting precise mode-of-action design and minimization of off-target effects during field applications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO JMPS)
    • EU Regulation (EC) No 1107/2009 on the placing of plant protection products on the market
    • US EPA 40 CFR Part 158 Data requirements for pesticide registration
    • ISO 17025-accredited analytical testing of residue and byproducts

    Typical usage ratio

    • Introduced at 0.8–2.3 molar equivalents in final coupling or cyclization stages depending on the target scaffold complexity

    Downstream process integration

    • Utilized during amide condensation or regioselective nitration prior to further functionalization and formulation into technical-grade actives

    Final product types

    • Herbicide technical concentrates (TCs)
    • Fungicide wettable powder premixes (WP)
    • Active substance intermediates for registration dossiers

    4. Intermediate for Specialty Fluorescent Sensor Synthesis

    Research and advanced manufacturing facilities employ 3-Amino-4-Methoxybenzamide as a strategic intermediate for assembling core structures used in fluorescent and colorimetric sensor molecules. These sensors, commonly implemented in analytical chemistry and biochemical monitoring, require feedstock with high purity profiles and documented residual solvent controls to achieve reliable signal response and regulatory acceptance.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for toxic substances in laboratory equipment
    • ISO 13485:2016 for quality management in medical device components
    • USP General Chapter <1040> Ancillary Materials
    • ASTM D6751 specifications for auxiliary testing chemicals

    Typical usage ratio

    • Deployed at 1.0–1.5 molar equivalents in condensation or cross-coupling steps according to desired sensor platform and yield optimization

    Downstream process integration

    • Fed during palladium-catalyzed C–N or C–C coupling sequences, with final fluorophore purification via preparative HPLC

    Final product types

    • Fluorescent probe conjugates for in vitro diagnostics
    • Colorimetric sensor molecules for field detection kits
    • Research-grade analyte detection compounds

    5. Precursor for Benzamide-Based API Impurity Reference Standards

    Analytical laboratories and reference standard manufacturers use 3-Amino-4-Methoxybenzamide as a reproducible precursor in generating bespoke impurity reference materials, especially for drug substance impurity profiling mandated by global health authorities. Its controlled purity and low trace kontaminant levels provide benchmark consistency and facilitate accurate QC testing during regulatory submissions.

    Industry compliance standards

    • USP <1086> Impurities in Drug Substances and Drug Products
    • European Pharmacopoeia General Monograph 2034
    • ICH Q3A/B(R2) guidelines for impurity limits
    • ISO/IEC 17025 for testing and calibration labs

    Typical usage ratio

    • Employed at stoichiometric levels based on targeted impurity synthesis protocols; typical scales range from 10 mg to 10 g per batch

    Downstream process integration

    • Inserted in last synthetic step or stress-test degradation conditions to generate certified reference impurity standards for analytical validation

    Final product types

    • Pharmacopoeial impurity reference standards
    • Certified impurity markers for LC/MS, HPLC, and GC validation
    • Documented impurity mixtures for regulatory compliance batches
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    Certification & Compliance
    More Introduction

    3-Amino-4-Methoxybenzamide: Practical Experience, Real Value

    Overview

    As a chemical manufacturer, we have witnessed how a compound’s story unfolds not just in technical literature but at the bench and reactor. 3-Amino-4-Methoxybenzamide has always belonged in a select group of intermediates that deliver reliable performance when margins for error stand thin. Every kilo shipped represents repeated production batches, thorough testing, and constant review of both process and practical value. We engage with formulators, research chemists, and process engineers every year. Their input, coupled with our hands-on process refinement, shapes the way we view this molecule—not just as an abstract structure but as a practical, tangible solution.

    Experience reveals that not all aromatic amide derivatives respond the same to process stress or to downstream function. 3-Amino-4-Methoxybenzamide, with its CAS number 6375-47-9, strikes an unusual balance between reactivity and stability. The combination of an amino group at the third position and a methoxy at the fourth crafts a unique electron density profile on the benzamide ring. This is not mere jargon. In decades of batch histories, this arrangement stands out for providing distinctive selectivity in reactions, observable not only in the raw data but also in improved yields and reduced purification steps.

    Product Variants and Formulation Insight

    We offer 3-Amino-4-Methoxybenzamide under several in-house models, with the most mature version delivering 99% minimum purity by HPLC and less than 0.5% moisture. Each batch faces full-spectrum quality tests, covering not just chromatographic analysis but also critical performance characteristics like color stability in storage, particle size distribution, and actual downstream reactivity. Why obsess over these factors? Our own experience managing scale-ups for pharma and specialty chemical producers has proven that minuscule impurities or water content can cause process fouling, inconsistent product profile, and in extreme cases, total run failures.

    We keep lots available as both free-flowing crystalline powder and as wet cakes for customers who find that solution-phase transformations favor an altogether different physical profile. It is never just about pushing a single grade. Whether you aim for API intermediates, dye precursors, or specialty catalysts, 3-Amino-4-Methoxybenzamide’s sulfonation and acylation behaviors diverge noticeably from close relatives such as 4-Amino-3-Methoxybenzamide. We have seen outsourcing partners request the “mirror isomer,” only to report solubility mismatches or irreproducible product color. Those cases highlight why this particular orientation matters in large-scale protocols—solubility, stability, reactivity barriers, and process robustness all tie directly to where the substituents actually land on the ring.

    Application Lessons from the Field

    In pharmaceutical synthesis, 3-Amino-4-Methoxybenzamide emerges most frequently in the making of intermediates for central nervous system candidates and certain anti-inflammatory actives. Our field partners report that, compared to other substituted benzamides, this molecule enables more predictable N-acylation and condensation outcomes, sparing hours normally lost to impurity purges and trial runs. One major customer, frustrated by unpredictability with the para-methoxy isomer in their coupling steps, switched to our recommended grade of 3-Amino-4-Methoxybenzamide and saw not just fewer side reactions, but a jump in downstream crystallinity, making separation and drying far easier.

    For dye and pigment intermediates, batch-to-batch color reliability is non-negotiable. Small variations in process, particularly solvent-wash and drying details, can nudge the intrinsic color from pale beige into off-tones that compromise bulk blending in color-sensitive end products. Feedback from multiple application labs, confirmed by our on-site QA techs, demonstrates that our focus on lot uniformity helps stabilize finished pigment tone across full-scale output. These conversations have shown us that everyday problems—filter pressing, washing, and final micronizing—can undermine product quality more than any specification sheet ever admits. It takes constant adjustment and dialog to ensure 3-Amino-4-Methoxybenzamide supports seamless operations downstream.

    Comparing 3-Amino-4-Methoxybenzamide to Related Compounds

    Competitors often compare 3-Amino-4-Methoxybenzamide to close analogs like 3-Methoxy-4-aminobenzamide and 4-Amino-3-Methoxybenzamide. Our real-world experience reveals differences that may not jump out from catalog listings. The relative position of the amino and methoxy groups profoundly shapes solubility in organic and aqueous media, and even more, affects synthetic path development. Batch data from the last decade uncovers that the meta position (amino at C3) paired with para-methoxy at C4 reduces the risk of side chain migration reactions in condensation processes. Researchers in advanced pharmaceutical labs tell us this difference alone cuts down on time wasted in rework, especially in scale-up conditions that never quite behave like a one-liter flask.

    Trying to substitute a positional isomer disrupts not just solubility but overall process rhythm. Once-infrequent issues—like unexpected gel-phase formation, inconsistent dissolution rates, or incomplete nitration—start showing up in early production runs. Our technical team’s troubleshooting logs, compiled from dozens of site visits, underline that adopting a different substitution pattern usually means requalifying almost every step, from raw material feeding right through to reactor workup and filtration. Manufacturers attempting to cut corners by exchanging one isomer for another often come up against dead ends that eat up time and resources.

    Supply Reliability and Quality Lessons

    Long-term partnerships have shown us that product quality stands and falls on process discipline. Sourcing from faceless vendors or resellers rarely works when your process tolerates little variance. We control synthesis parameters, solvent recovery, and drying to keep batch drift within narrow windows. After every scale-up, we revisit every operation for yield, impurity profile, and, above all, consistency. Many partners come to us after seeing off-spec lots from brokers or bulk traders who prioritize turnover above reliability. Standardizing on a controlled product line minimizes unforeseen hiccups at each formula update or site expansion.

    We incorporate customer feedback directly into daily production reviews. A few years back, a pharmaceuticals customer detected unexpected yellowing in their final intermediate. They investigated their upstream controls, only to find that the deviation stemmed from a subtle solvent change made without adjusting drying times. Since then, we review solvent policy on every shift and flag any deviation, no matter how slight. This isn’t process rigidity—it’s accumulated routine from years of responding to what actually happens under plant conditions, not just what’s written on a spec sheet.

    Challenges in Handling and Storage

    No intermediate truly avoids handling challenges, and 3-Amino-4-Methoxybenzamide, with its crystalline structure, demands its own procedures. Moisture control remains one of the biggest sources of batch loss. In our facilities, material moves from final centrifuge to vacuum dryer within strict timing. Even small delays let surface moisture climb, affecting not just shelf life but also downstream hydrogenation or acetylation steps. In our central QA archive, records show that less vigilance leads to clumping, hard-to-redisperse cakes, and inaccurate dosing. Tech staff run constant loss-on-drying checks and monitor every lot through to packing. Partners who transport in high-humidity climates benefit from this pre-emptive control, as the product’s flow quality and dose accuracy matter more the further it travels.

    Containers and liners also form a surprisingly important link in batch quality. Even trace amounts of previous residues or mismatched materials can cause off-odors or unexpected discoloration in extended storage. This seems mundane, but in the real world, such details often go missed until they cause failed runs in high-value downstream applications. We address this with dedicated cleaning cycles, batch-coded liners, and in-line sampling. Years of deliveries confirm that these “small” steps preserve a lot more value than any fancy equipment ever could.

    Environmental and Safety Considerations

    Operating chemical synthesis on scale brings major responsibilities. Our risk management policies come from practical experience, bolstered by regulator audits and internal near-miss reviews. 3-Amino-4-Methoxybenzamide does not pose many acute hazards, but dust generation and handling always require scrupulous respect. Respiratory protection, grounded dispensing stations, and real-time particulate monitoring form the backbone of our worker safety program. Periodic training, updated after every incident anywhere in the industry, ensures that plant staff treat each transfer, each blending, like it could cause a shutdown the next day. Facility upgrades over the years have included specialized dust extractors and improved seals, based not on marketing but on actual, observed improvement in air quality logs and near-miss documentation.

    Waste minimization has shifted from phrase to practice over the past decade. We treat mother liquors and process filtrates to recover solvents and any unreacted starting material. Recycled streams power not only cost savings but compliance with the evolving global regulatory picture—where restrictions on aromatic amides continue to tighten. By proactively reassessing solvent choice, process temperatures, and reaction yield at every campaign, we sustain output while slashing residual discharge. Progress here is measured not just in permits, but in lower supply chain disruptions and minimal audit flags. We know that our customers ask about green credentials and real-world impact these days; recycled solvent runs and careful wastewater management form the basis of every new process route.

    How Ongoing R&D Improves Product Value

    Our experience tells us that waiting on old technology closes doors. Over the years, our process chemists have worked to reduce not just impurity levels but also to squeeze time and risk out of every stage. Switching to a continuous-flow hydrogenation process a few seasons ago dropped batch times and nearly eliminated the rare but persistent trace impurity associated with batch mode reduction. This wasn’t motivated by abstract improvement goals—customers’ actual problems drove new investments. Our R&D team maintains a direct customer hotline, ensuring even the smallest complaint or request triggers a feasibility review. These reports accumulate into trends, sparking pilot trials well before commercial scale-up. Small changes—chelator selection, buffer swaps, even out-of-the-box filtration tweaks—turn into material savings for end users. The long feedback loop between shop floor, customer site, and lab gradient elutes has become our most valuable tool for improvement.

    We encourage partners to share their full process context, not just specifications. In practice, customers who collaborate openly tend to resolve process bottlenecks faster than those who treat every request as a black box. Exchanging pilot run reports, blending observations, and even failure analyses speeds up improvement cycles. Years of shared results show that as soon as upstream and downstream teams share what works and what goes wrong, rejects drop and batch-to-batch consistency rises. 3-Amino-4-Methoxybenzamide, because of its central place in several synthetic trees, regularly benefits from this kind of transparency.

    Supporting Your Process, Not Just Selling Commodity

    While catalog listings might make everything look like a commodity, real-world consequences come from the intersection of lab data, plant runs, and site-specific hardware. 3-Amino-4-Methoxybenzamide has survived in our catalog through hundreds of compound evaluations because it holds up against shifting regulations, changing plant hardware, and varied downstream needs. We draw not just on process simulations or marketing briefs, but on accident logs, shift leader notes, and daily batch reviews. This boots-on-the-ground perspective lets us recommend not just the right variant, but also packaging, shipping, and storage tweaks, often catching problems before they wander downstream. Each technical interaction tells us that long-term value comes from consistent follow-through, batch after batch.

    Export and logistics regulations change fast. Our in-house team tracks new classifications and customs issues so finished goods never get stuck at the dock for want of the right paperwork. Only direct experience teaches how to navigate seemingly minor compliance changes, like shipping classification shifts for aromatic compounds, that can interrupt deliveries international partners count on.

    Final Thoughts From the Factory Floor

    Through decades of production and direct problem-solving, we have seen that product quality does not start and stop at the molecule. Every step, from raw material mgmt to drum filling to final QA signoff, accumulates into a product that meets not just technical sheet numbers but actual field needs. 3-Amino-4-Methoxybenzamide has proven itself across diverse uses, far beyond generic applications lists. Returning customers and their hard-won improvements give meaning to every incremental change we put in place.

    Our ongoing challenge is to remain sensitive to real input, keep adjusting controls, and stay open to field lessons. The result is a product history defined less by perfect stability and more by measured improvement, shared knowledge, and practical reliability. 3-Amino-4-Methoxybenzamide continues to unlock possibilities in both tried-and-true and new applications—rooted in hard data, field stories, and a manufacturing tradition that values practical results over empty claims.