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2-Amino-4,5-Dimethoxybenzonitrile

    • Product Name 2-Amino-4,5-Dimethoxybenzonitrile
    • Alias 2,4,5-DMAn
    • Einecs 629-022-7
    • 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

    649454

    Chemicalname 2-Amino-4,5-Dimethoxybenzonitrile
    Casnumber 13434-13-4
    Molecularformula C9H10N2O2
    Molecularweight 178.19 g/mol
    Appearance Off-white to light yellow solid
    Meltingpoint 115-118°C
    Solubility Soluble in organic solvents like ethanol, DMSO
    Purity Typically ≥98%
    Smiles COC1=C(C=C(C(=C1N)C#N)OC)
    Inchi InChI=1S/C9H10N2O2/c1-12-7-3-6(5-10)9(11)8(4-7)13-2/h3-4H,11H2,1-2H3
    Storageconditions Store at 2-8°C, protected from light and moisture

    As an accredited 2-Amino-4,5-Dimethoxybenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25-gram brown glass bottle is tightly sealed, labeled "2-Amino-4,5-Dimethoxybenzonitrile," and features hazard and handling instructions.
    Shipping 2-Amino-4,5-Dimethoxybenzonitrile is shipped in tightly sealed containers to prevent contamination and moisture ingress. The chemical is packed according to regulatory requirements for hazardous materials, typically using secondary protective packaging. Handling and shipping comply with relevant safety guidelines, including labeling and documentation, to ensure safe transportation and delivery to the customer.
    Storage Store **2-Amino-4,5-dimethoxybenzonitrile** in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizing agents. Protect from direct sunlight, moisture, and sources of ignition. Use appropriate chemical storage cabinets and label the container clearly. Follow relevant safety protocols and local regulations for handling and disposal.
    Application of 2-Amino-4,5-Dimethoxybenzonitrile

    Applications of 2-Amino-4,5-Dimethoxybenzonitrile in Industrial Manufacturing

    2-Amino-4,5-Dimethoxybenzonitrile serves as a high-purity chemical intermediate adopted by industrial partners in targeted sectors including pharmaceutical active ingredient synthesis, advanced dye manufacturing, photoinitiator production, and specialty agrochemical formulation. Below we outline real downstream processes with key compliance requirements, industrial ratios, technical integration points, and representative final products.

    1. Pharmaceutical Intermediate for API Synthesis (Benzonitrile Derivatives)

    Our material is selected by innovators and generics manufacturers for multi-step synthesis of benzoxazole- and quinazoline-based active pharmaceutical ingredients. Its electron-rich aromatic structure and defined amine/nitrile functionalities allow site-specific substitution in key intermediate steps, supporting stringent cGMP compliance and batch traceability. Users leverage our QC support for process validation, batch homogeneity, and impurity profiling aligned with regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • United States Pharmacopeia (USP) Monograph referencing intermediates
    • 21 CFR Part 211 (FDA current GMP for finished pharmaceuticals)
    • EU GMP Annex 1 traceability and impurity control

    Typical usage ratio

    • 15%–35% of molar input for heterocyclic step—final ratio determined by labeling requirements, impurity thresholds, route-specific yield optimization, and endpoint API scale

    Downstream process integration

    • Introduced in the early condensation or nucleophilic substitution stage, preceding ring-closure and subsequent hydrolysis
    • Molecule remains traceable through purification and crystallization steps
    • Intermediate QC routinely samples for isomer and residual solvent content after its addition
    • Included in analytical validation for process-oriented registration dossiers

    Final product types

    • Quinazoline anti-tumor drug substance (e.g., gefitinib intermediates)
    • Benzoxazole anti-infective APIs
    • CNS-active compound intermediates
    • Precursor to antihypertensive API building blocks

    2. Dye and Pigment Synthesis (Methoxybenzene Intermediates)

    Formulators in the dye sector use our compound as a building block for methoxy-substituted anthraquinone and azo dye classes. Its controlled reactivity and consistent purity assist in stepwise coupling and cyclization reactions, allowing for bright, high-performing pigments suitable for printing and textile coloration. Leading pigment manufacturers rely on us for COA-backed supply and impurity control above industry standard.

    Industry compliance standards

    • EN 71-3 for pigments used in printed children’s articles
    • OEKO-TEX® Standard 100 for textile dye safety
    • REACH Annex XVII (restricted aromatic amines in consumer dyes)
    • ISO 9001 Quality Management Systems for batch traceability

    Typical usage ratio

    • 10%–30% by mass in coupling stages—optimized by targeted shade, molar efficiency, and environmental discharge limits

    Downstream process integration

    • Charged to the diazotization reactor post-diazonium salt preparation
    • Enters as main aromatic core or substitution point for subsequent sulfonation/halogenation
    • Monitored for color consistency and migration during pigment precipitation
    • QC sampling at exit of final synthesis and before blend/milling stage

    Final product types

    • Disperse dyes for synthetic fibers
    • Anthraquinone-based textile paints
    • Organic pigments for solvent-based inks
    • Azo pigments for plastic color masterbatches

    3. Photoinitiator and Electronic Chemical Precursor

    Manufacturers producing photoinitiators and photoresist chemicals for circuit boards and UV-cured coatings utilize 2-amino-4,5-dimethoxybenzonitrile for specialized condensation reactions. Its chemical profile enhances absorption characteristics and promotes specific photoreactive properties required in electronics manufacture. Strict impurity limits support sensitive downstream photolithography yields.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94 Flammability Testing for plastics
    • ISO 14001 Environmental Management for process chemicals
    • IEC 62474 declarable substance list for electronic components

    Typical usage ratio

    • 5%–20% incorporated into resin blends; adjusted for targeted absorption spectrum and UV-initiated polymerization kinetics

    Downstream process integration

    • Added at the photoinitiator synthesis stage prior to final distillation/purification
    • Introduced as a radical-forming substrate in polymer matrix adjustments
    • Subjected to melt-compounding and UV-reactivity tests during final QC
    • Verified by HPLC for trace impurities before formulation into photoresist paste

    Final product types

    • Photoresist chemicals for PCB fabrication
    • UV-curable ink photoinitiators
    • High-spec electronics-grade coatings
    • Photopatternable resins for microelectronics

    4. Agrochemical Intermediate for Herbicide Synthesis

    Agrochemical companies source this compound as an intermediate for nitrogen- and methoxy-substituted herbicide molecules. Its reactivity enables key nucleophilic steps in safe, selective herbicidal agents targeting broadleaf and grass weeds. Strict batch documentation and impurity characterization match field-application regulations and international registration file requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA FIFRA (40 CFR Part 158) composition and residues
    • ISO 17025 for analytical testing of pesticide actives
    • China GB2763 Maximum Residue Limits in Food

    Typical usage ratio

    • 12%–28% relative to total reactant load; ratio refined for required biological selectivity, field stability data, and byproduct minimization

    Downstream process integration

    • Incorporated at first cyclization or amidation phase of herbicide precursor synthesis
    • Followed by multi-step purification before downstream bulk blend
    • Samples analyzed via GC-MS for nitro and methoxy group integrity preformulation
    • Accompanied by impurity profile documentation for international registration

    Final product types

    • Selective herbicide actives (e.g., substituted benzoxazolinone herbicides)
    • Pre-emergent weed control formulations
    • Agricultural chemical blends for custom application rates
    • Bulk technical-grade herbicidal intermediates
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    Certification & Compliance
    More Introduction

    Hands-On Perspective: 2-Amino-4,5-Dimethoxybenzonitrile in Production and Application

    Practical Experience on the Plant Floor

    Standing at our reactors, I spend my days with chemical intermediates that rarely make headlines, but drive innovation for countless lab and industrial workflows. Among these, 2-Amino-4,5-Dimethoxybenzonitrile stands out—not for its glamour, but for its reliability in multistep organic synthesis. After years of scaling up batches, I’ve come to recognize the small differences that matter to chemists downstream and the manufacturing quirks that impact what arrives in each drum.

    What we call 2-Amino-4,5-Dimethoxybenzonitrile exhibits a pale off-white appearance, a straightforward crystalline solid under room conditions. Each batch needs to pass strict HPLC and NMR checks, which might seem standard, but it is small peaks and residuals that slow a whole project. Homogeneity in the crystals makes a real difference for anyone using the material in pharmaceutical or dye intermediate research. Chemically, we're looking at a benzonitrile core with two methoxy groups at the 4 and 5 positions, and an amino group at the 2 position, delivering both electron-rich aromatic reactivity and functional-group diversity.

    Why are these subtle details so important? Nitrile building blocks often set the stage for amide or heterocycle introduction, commonly through nucleophilic aromatic substitution or condensation. Our 2-Amino-4,5-Dimethoxybenzonitrile, with high purity and a carefully controlled moisture profile, resists premature degradation through hydrolysis. We keep water content below industry benchmarks—something you notice in high-precision transformations, where unexpected moisture can tank costly downstream coupling reactions.

    Reliability Rooted in Process Design

    As a manufacturer, not a re-bottler, my stake in the properties of 2-Amino-4,5-Dimethoxybenzonitrile isn't just business—it’s pride in repeatable production. Scaling up from liters in the lab to thousands of liters in plant reactors, each step needs monitoring. Residual solvents, trace acids or base, and potential byproducts from the O-methylation stage require removal. Through in-process controls and skilled plant operators, we hit purity levels consistently above 99%. Once every so often, a chromatography check catches something unexpected—a signal to pause, not push ahead and hope for the best.

    Other manufacturers sometimes settle for lower-purity output, banking on the idea that customers will tolerate a few tenths of a percent of unknowns. Our partners working in regulated sectors, especially custom synthesis for pharmaceuticals, will not. In my experience, even a small impurity can become a forensic headache when an unexpected signal shows up during scale-up in another facility halfway around the globe. We minimize batch-to-batch variation by using a stable source of starting benzaldehyde and strict environmental controls. Even basic factors like particle size distribution receive attention; small discrepancies in grinding can affect how quickly—and even whether—the solid goes into solution for the next synthetic step.

    End-Use Realities: From Synthesis Bench to Final Molecule

    Our main customers use 2-Amino-4,5-Dimethoxybenzonitrile as a precursor for drug molecule frameworks, advanced materials, and custom heterocycles. In these advanced syntheses, the position of amino, methoxy, and nitrile matters: migration, elimination, or uncontrolled rearrangement risk entire batches. Some buyers focus on dye chemistry—cyanine dye systems, for example, rely on the reactivity of substituted aminobenzonitriles. Others work in medicinal chemistry, motivated by the pharmacological profiles built around this scaffold.

    You would not believe how much a single percent of residual moisture or a spectral impurity impacts a multistep campaign costing hundreds of thousands of euros. Chemists grinding through repetitive work can't afford to repeat weeks of synthesis because a building block fell short. We get frequent feedback from project leaders who have chased purity problems across continents, only to find the root in a single intermediate. That is why attention to purification—through recrystallization, continuous column chromatography, or solvent-system adjustments—never feels wasted. It defines the difference between a roll of the dice and a predictable, project-friendly material.

    Comparisons with Other Substituted Benzonitriles

    There are hundreds of benzonitrile derivatives on the commercial market, but 2-Amino-4,5-Dimethoxybenzonitrile brings its own value. Many competing intermediates, such as the 3,5-dimethoxy-, 2,4-diamino-, or 2,6-dimethoxybenzonitriles, possess different electronic or steric properties. Change the position of a methoxy group, and reactivity can shift; move the amino group, and coupling partners may not fit as intended downstream.

    What distinguishes our product is careful placement of substituents, which tunes both solubility and reactivity. The 4,5-methoxy configuration, along with the ortho amino group, gives a distinct advantage in certain custom synthesis applications where regioselectivity and functional-group tolerance determine the success of the next stage. I have seen cases where a seemingly minor change—a methyl or an amino moved—throws off the intended azole ring closure or influences the vibrancy of dye precursors. These are not theoretical distinctions; synthetic teams regularly share reaction outcomes that diverged because of such differences.

    Some intermediates lack the desired stability or introduce side-products during hydrogenation, halogenation, or amidation. Our production methods reduce these risks by avoiding common contaminants and offering a consistent melting range. It can feel like splitting hairs, but these subtle physicochemical differences end up shaping entire development programs. Laboratories in Europe and Asia have detailed instances where batch-to-batch variation frustratingly altered compound profiles. We tackle those frustrations with vigilant crystallization parameters, routine microanalysis, and robust supplier relationships for every upstream reagent.

    Facing Challenges: Scale, Consistency, and Downstream Demands

    Making specialty intermediates isn't simply running a reaction and filling bottles. Once, a drop in solvent quality triggered an end-of-line impurity spike. I saw firsthand how hard it was to trace the problem. We learned to automate certain purification steps but keep human eyes on the process—automation can’t catch everything. 

    Recent years brought unpredictable swings in raw materials. Cautious procurement and resilient logistics allow us to keep 2-Amino-4,5-Dimethoxybenzonitrile supply steady. A massive buffer stock, plus guaranteed backup suppliers, help us meet contracts even as global shipping stumbles along. During COVID disruptions, we ran double shifts to keep key pharmaceutical partners running, sending batches by air—expensive, but learning what works under pressure matters. 

    The biggest frustrations arise during scale-up. A reaction that looks flawless in a flask suddenly misbehaves in a large reactor: more exotherm, unpredictable crystallization, and filtration hiccups. Our approach involves pilot runs for every change, coupled with intensive in-plant analytics. We don’t ever want process drift to send bad product out the door. Teams dedicated to process engineering, synthesis, and troubleshooting make a tangible difference. We collect feedback not only from our client’s QA department but also directly from on-the-ground chemists who run reactions day and night. They don’t sugarcoat problems, and we don’t pretend not to hear them.

    Seemingly minor controls—such as maintaining exacting control over temperature during the O-methylation phase or using fresh, tested ammonia sources for introduction of the amino group—translate into confidence at the customer’s bench. We take pride in rendering a tight melting point (often within 1-2 degrees Celsius) and batch-level NMR spectra available on demand. Our lot numbers aren’t just for traceability but an open invitation for clients to ask for reference samples or supporting data.

    Our Role: Partnership Beyond Transaction

    Looking back, most relationships with large firms started with a single small order—just a hundred grams, maybe a kilo. That first trial batch brings scrutiny: does the solid flow cleanly? Does the powder dissolve with minimal heating? Are trace byproducts—a persistent threat for any aromatic amine—absent to a rigorous degree? Delivering positive answers opened doors. Researchers requested additional analytical support: extended mass spectra, photostability data, even guidance on safe handling or alternative solvents when regulatory trends shifted away from older toxic species.

    We do not operate in isolation. Our teams routinely participate in technical calls to troubleshoot applications: refining a purification routine, swapping buffer systems, or simply sharing “tribal knowledge” of how our material interacts with rare reagents. Sometimes, our engineers visit partner sites to see real-world bottlenecks up close. Years in, these collaborations yield process improvements that ripple back to our plant, prompting us to re-examine everything from reactor materials to the speed of the final centrifuge run.

    We don’t just ship drums and step aside. If something isn’t right, we work alongside customers—sometimes late into their night and our morning, ensuring the next step goes as planned. If batch documentation needs updating to meet a new regulatory region’s standards, we provide it, drawing on extensive archives of production and testing. Having been burned by incomplete upstream documentation earlier in my career, I know how imperative full and open analytical transparency is for any regulated end-use.

    Supporting Sustainability and Ethical Commitments

    The chemistry sector faces rising pressure to demonstrate responsible stewardship—both for safety and sustainability. We minimize waste streams by investing in closed-loop solvent recovery and careful energy management. Regulatory agencies check our systems routinely, but internal audits catch trouble far sooner. Staff have standing instructions to flag anything out of the ordinary. Heat exchangers, emission scrubbers, and advanced wastewater treatment systems aren’t optional or afterthoughts—they’re as integral as the reaction vessel itself.

    We actively revise processes to minimize use of problematic raw materials, researching greener methylation reagents and piloting alternative routes that replace legacy chemicals flagged by REACH or other governing bodies. Some improvements slow output in the short term. But in the long term, they ensure a more reliable and acceptable solution for everyone involved. For example, trials with solid-supported reagents resulted in gentler reaction conditions, producing less airborne emission and safer working spaces for our staff. Customers appreciate learning that these changes don’t sacrifice purity, yield, or analytical consistency.

    Employees undergo ongoing training, not just to meet compliance, but to foster problem-solving skills. Over the past year, we’ve hosted knowledge swaps—cross-discipline sessions drawing on synthetic chemists, analysts, and even logistics managers. That’s how process bottlenecks are uncovered and addressed before the line goes live. Our approach to ESG stands in daily practice, not website declarations.

    Looking Ahead: Building on Experience With Each Batch

    Every day spent in manufacturing shapes how we think about improvement. Years ago, we struggled with product caking in long-term storage, frustrating customers who needed free-flowing powder. Now, we screen particle size before packaging and control warehouse humidity. Small changes, but they’ve reduced complaints. Feedback loops run both ways; what customers experience in their syntheses gets fed back into our quality review. In the laboratory, we continue to test alternative reaction routes—sometimes inspired by our customers’ synthetic challenges.

    We record, study, and share every process deviation. Problems are not punishable offenses; they mark opportunities for tighter controls or smarter automation. Regulatory scrutiny gets more intense year by year, meaning our documentation systems must be bulletproof and our analytics fast and thorough. We invite customers to review our quality protocols firsthand, knowing that the real test is not in what’s written on a spec sheet, but in the consistency of material delivered order after order.

    My own experience shows the significance of expertise over generic promises. Highly specific knowledge of feedstock fluctuations, analytical interpretation, and flexible logistics keeps the supply chain running smoothly. If a problem can happen, it likely already has in our plant—or will in time. The best approach remains open communication, proactive problem-solving, and real technical partnership.

    Two decades in, we recognize that no synthetic intermediate, no matter how routine, becomes “just another commodity” for the chemists trying to innovate with it. Our 2-Amino-4,5-Dimethoxybenzonitrile reflects that perspective: it’s an ingredient with history, context, and cumulative experience from bench to bulk scale. We know precisely how much accuracy, transparency, and pride each kilo should carry, and we act accordingly every day.