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3-Methoxybenzonitrile

    • Product Name 3-Methoxybenzonitrile
    • Alias m-Anisnitrile
    • Einecs 211-852-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    105929

    Chemical Name 3-Methoxybenzonitrile
    Cas Number 1527-89-5
    Molecular Formula C8H7NO
    Molecular Weight 133.15
    Appearance Colorless to pale yellow liquid
    Boiling Point 259-260 °C
    Melting Point 11-14 °C
    Density 1.098 g/cm3
    Refractive Index 1.532
    Flash Point 133 °C
    Solubility In Water Low
    Synonyms m-Anisyl cyanide; m-Methoxybenzonitrile; 1-Cyano-3-methoxybenzene

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

    Packing & Storage
    Packing 3-Methoxybenzonitrile is packaged in a 100g amber glass bottle with a secure screw cap, labeled with hazard and identification details.
    Shipping 3-Methoxybenzonitrile is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package should be labeled according to local regulations and handled with care, avoiding exposure to heat and moisture. Appropriate hazardous material documentation must accompany the shipment if applicable. Store in a cool, dry place during transit.
    Storage 3-Methoxybenzonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Proper chemical labeling and segregation are essential to prevent cross-contamination, and it should be handled in accordance with standard laboratory safety protocols.
    Application of 3-Methoxybenzonitrile

    Applications of 3-Methoxybenzonitrile in Industrial Manufacturing

    3-Methoxybenzonitrile is a specialized intermediate widely employed by manufacturers within fine chemical synthesis. Its principal applications focus on downstream sectors such as pharmaceutical intermediate synthesis, agrochemical development, specialty pigment manufacturing, advanced organic synthesis, and liquid crystal precursor development. Our industrial-grade product meets the stringent technical and regulatory requirements set by international industry leaders, supporting stable, reliable integration into established manufacturing chains.

    1. Pharmaceutical Intermediate Synthesis for API Production

    Regulated pharmaceutical companies leverage 3-Methoxybenzonitrile for the synthesis of active pharmaceutical ingredient intermediates, particularly within the process routes for selective serotonin reuptake inhibitors and new-generation antihistamines. Production integrates this material at early aromatic nitrile formation steps, enabling precise downstream functional group transformations. Pharmaceutical manufacturers conduct rigorous in-process testing according to pharmacopeial monographs before scaling up, ensuring traceability and compliance throughout the lifecycle from initial reaction to final API crystallization, filtration, and drying.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia 11.0 monograph reference
    • 21 CFR Part 211 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs
    • USP General Chapter <767>

    Typical usage ratio

    • 5% – 15% by mass in nitrile stage intermediates, tuned by API target and process step
    • Adjusts based on stoichiometry and targeted molecular substitution patterns

    Downstream process integration

    • Introduced during aromatic ring nitrilation and methoxylation stage
    • Feeds into catalytic hydrogenation, reduction, and amide coupling units
    • Subjected to chromatographic purification and final recrystallization

    Final product types

    • Active pharmaceutical ingredients (API) — e.g., fluoxetine-type compounds
    • Antihistamine intermediates
    • Specialty intermediate blocks for new molecular entities

    2. Agrochemical Synthesis for Selective Herbicides and Growth Regulators

    Manufacturers in the agrochemical sector utilize 3-Methoxybenzonitrile as a core nitrile building block for coupling and cyclization reactions leading to new heterocyclic herbicide and plant growth regulator actives. Process engineers optimize batch and continuous protocols with proprietary catalysts to maximize ring closure efficiency and maintain cost-effective yields. Material traceability and impurity control remain essential to meet international pesticide residue and registration requirements for downstream formulated products.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • China Ministry of Agriculture GB 2763 National Food Safety Standard for Maximum Residue Limits for Pesticides
    • ISO 17025 laboratory accreditation for impurity and residue testing
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 7% – 18% by mass of total input in the nitrile arylation and cyclization synthesis stage
    • Refined based on downstream substitution and scale-up reactor conditions

    Downstream process integration

    • Entry at early step during aromatic cyanation and methoxy addition
    • Subsequent condensation and ring cyclization for herbicide molecule assembly
    • Final purification and technical grade formulation steps

    Final product types

    • Selective herbicide actives (e.g., oxadiazole, triazine derivatives)
    • Plant growth regulator intermediates
    • Active ingredient precursors for custom agrochemical blends

    3. Specialty Pigment and Dye Intermediate Manufacturing

    Producers in the pigments and dyes sector employ 3-Methoxybenzonitrile as a key aromatic intermediate that enables high-purity synthesis of specialty azo, anthraquinone, and phthalocyanine pigments. The nitrile’s electronic structure supports tailored aromatic substitution patterns, allowing precise control of chromophore characteristics and color fastness properties. Strict analytical monitoring ensures batch-to-batch consistency, meeting the formulation requirements of advanced printing, coatings, and textile dyeing manufacturers in regulated markets.

    Industry compliance standards

    • EN 71-3 Safety of Toys. Migration of Certain Elements for colorant safety
    • OEKO-TEX® STANDARD 100 for textile pigment safety
    • Quality Management System ISO 9001:2015
    • REACH Annex XVII for restricted aromatic amines

    Typical usage ratio

    • 4% – 10% by mass in initial nitroaromatic preparation
    • Varies according to pigment depth, color shade, and downstream conversion rate

    Downstream process integration

    • Charged in early aromatic nitrile introduction for core dye building blocks
    • Carried through diazotization and coupling reactions for azo pigment synthesis
    • Final isolation via filtration, drying, and micronization units

    Final product types

    • High-performance azo pigments
    • Anthraquinone dyes
    • Textile functional colorants and technical pigment dispersions

    4. Liquid Crystal Material Synthesis for Display Technologies

    Advanced electronics materials manufacturers deploy 3-Methoxybenzonitrile as a precursor for custom-designed liquid crystal molecules used in LCD and OLED screen production. The methoxy and nitrile functionality afford high-order electronic and mesogenic properties essential to manufacturer specifications. Production lines incorporate this intermediate at targeted substitution stages, enabling modification of viscosity, clearing point, and molecular orientation to fit narrow device tolerances. Strict quality control ensures minimal trace impurities to avoid drift in optical performance.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics chemical safety
    • IEC 61249-2-21:2017 Requirements for base materials in electronics
    • ISO 14001:2015 Environmental Management System for electronics supply
    • Industry-specific material restriction lists (major display panel OEMs)

    Typical usage ratio

    • 2% – 8% by mass during final mesogen precursor condensation
    • Tuned by target molecular geometry and electronic requirements for display class

    Downstream process integration

    • Input during core liquid crystal intermediate synthesis
    • Feeds into end-stage hydrogenation, esterification, and high-purity refinement
    • Final-stage blending with other mesogenic units for application-specific tuning

    Final product types

    • Liquid crystal display (LCD) panel liquid crystals
    • OLED display pre-materials
    • Specialty high-stability liquid crystal compounds for advanced screens

    5. Advanced Organic Synthesis in Research and Custom Manufacturing

    Chemical manufacturers and custom synthesis contractors adopt 3-Methoxybenzonitrile for research and pilot development of complex molecules, structure-activity relationship studies, and lead structure modifications. Its defined reactivity and clean aromatic profile allow for controlled functionalization and subsequent derivatization steps. Process development teams monitor reactivity, color, and impurity profiles using robust analytical methods to expedite transfer from laboratory-scale reactions to 100 L or larger pilot campaigns. Material lot traceability and documentation ensure conformity when scaling up for regulated markets and contract manufacturing agreements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for synthesis scale-up
    • Responsible Care® chemical management requirements
    • Documentation practices according to GLP (Good Laboratory Practice)
    • Customer-specific technical and safety specifications

    Typical usage ratio

    • Ranges widely, 1% – 25% as per desired substitution and targeted novel compound yield
    • Optimized via design of experiment (DoE) methods in process development

    Downstream process integration

    • Charged at initial aromatic nitrile synthesis or for late-stage methoxylation
    • Feeds into multi-step, tailor-made synthesis routes including acylation, hydrolysis, or nucleophilic substitution
    • Allows for rapid iteration and impurity profiling before pilot expansion

    Final product types

    • Research quantity fine chemicals
    • Custom small-molecule libraries
    • Lead compound intermediates for pharmaceutical and materials science research
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    Certification & Compliance
    More Introduction

    3-Methoxybenzonitrile—A Practical Foundation for Diverse Chemical Synthesis

    Decades of Direct Manufacturing Experience with 3-Methoxybenzonitrile

    Years of hands-on work with aromatics and nitriles reveal that not every intermediate answers the same set of needs. 3-Methoxybenzonitrile stands out with its unique arrangement—a methoxy group on the benzene ring, sitting at the meta position, and a cyano group completing its chemical identity. Chemists favor this compound for its smart balance of reactivity and selectivity, making it an essential anchor in multiple synthetic chains. Its CAS number, 1527-89-5, serves as a clear identifier for tracking quality and batch lineage. Our teams focus on delivering high-purity material, typically at or above 99%, crystallized as a white or faintly off-white powder. Moisture content and trace impurity levels, notably, receive tight control from the batch outset.

    The Role of Chemical Structure in Practical Applications

    The methoxy group’s electron-donating effect brings targeted reactivity in organic synthesis. Our crew finds 3-Methoxybenzonitrile especially valuable when crafting more complex pharmaceutical intermediates. The cyano group imparts pronounced polarity, opening doors in coupling reactions, amidine transformations, and heterocycle construction. For manufacturers committed to API development, this molecule offers a level of reliability not always present in less rigid aromatics. Chemists often use it to introduce controlled substitution patterns that resist unwanted side reactions.

    Every kilogram reflects several inspection steps. Beyond HPLC results, we look for consistent melting ranges, low ash content, and steady flow properties. Hundreds of pilot and production runs sharpened our understanding of solvent interactions and filtration strategies, culminating in improved yields from large-scale production. The staff tracks not only physical appearance but also batch-resolved analytical signatures.

    Clear Differences from Ortho and Para Methoxy Isomers

    Discussions about benzonitriles often circle back to substitution patterns. 3-Methoxybenzonitrile takes its spot alongside the ortho (2-methoxybenzonitrile) and para (4-methoxybenzonitrile) isomers. From our viewpoint, the meta isomer draws less attention but carries unique properties. Electron flow changes across the ring—handled differently than in the ortho and para variants. In downstream synthesis, especially nucleophilic aromatic substitution, the meta isomer delivers higher site selectivity. For those scaling up pharmaceutical or agrochemical syntheses, the ability to dial in electronic effects without over-activating a ring matters.

    Our process engineers notice significant variations in solubility and reactivity profiles between these isomers. 4-Methoxybenzonitrile, commonly used for dye and pigment work, cannot mimic the regioselectivity we see in the meta version. Ortho variants tend to cyclize under certain conditions; the meta isomer resists this tendency. Handling protocols change accordingly. In our experience, unwanted byproducts drop when shifting from para to meta, especially during functional group interconversions. As a direct producer, we appreciate the value of reproducible, controllable outcomes over speed or mere availability.

    Main Applications from Field Experience

    Pharmaceutical research represents the most consistent demand for 3-Methoxybenzonitrile. Large discovery teams rely on its stability as a building block for aromatic amides, triazines, and even complex active molecules. We routinely ship production batches for generics programs and early-phase research. The molecule’s controlled reactivity supports regioselective methylation, acylation, and nucleophile introduction—tools every medicinal chemist values. Our staff works closely with teams scaling from grams to multi-kilo, updating drying, grinding, and packaging protocols as needs evolve.

    Agrochemical formulators depend heavily on clean intermediates. 3-Methoxybenzonitrile feeds into herbicide candidates and selected insecticides requiring aromatic cyano functions. The highest efficacy arrives only when source purity exceeds standard trade material. Custom protocols applied in our plant clear out residual chlorides and acid traces, which can otherwise break reaction pathways later on.

    Dye and pigment makers find selective use cases as well, especially where color-fastness relies on the ring’s electron-donating structure. While para isomers often dominate this industry, the meta structure brings thermal stability and controlled hue adjustment. Process steps such as condensation with aminophenols run smoother and deliver brighter, more durable colors with controlled starting material.

    We witness a smaller but steady interest among material science teams. Polymer research groups build specialty monomers using meta-substituted benzonitriles, counting on their resistance to hydrolysis and their flexibility in copolymerization. Our technical liaisons accumulate feedback from these labs, feeding improvements back into purification and stability studies.

    Factory Protocols Ensuring Consistent Quality

    Manufacturing specialty chemicals starts at the reactor, not in a catalogue. Our days revolve around cycle control, raw material inspection, and process analytics. The temperature ramp during reaction sets yield and impurity levels; even a few degrees shift the product slate. We rely on direct feedback from shift supervisors and plant analytics teams to tune cycle times and crystallization points.

    Material traceability provides confidence. Each batch earns a unique identifier, mapped through solvent receipt, charging sequence, solvent recovery, and filtration. Analytical checkpoints—initial GC and HPLC, then moisture and residue tests—carry out across all lots. In our experience, deviations emerge most during the post-crystallization filtration stage, where particle size and sticking point affect drying and product uniformity. By tracking these trends, our process engineers tweak agitation rates or filter media to improve future runs.

    Handling practices matter just as much downstream. The solid form, as handled in our facility, flows easily but absorbs ambient moisture if left exposed. Workers package fresh material with low-humidity liners, heat-sealed within hours of final QC clearance. Not every plant touches these details, but our field audits show fewer customer complaints—and longer shelf life—when these steps get close attention.

    Laboratory feedback closes our loop. User labs occasionally detect trace color or by-products not visible at the bulk scale. Sharing these findings with production supervisors drives tweaks to quench conditions or wash cycles. Ongoing collaboration with application chemists outside our own factory feeds a cycle of learning and incremental refinement.

    Supporting Safe and Effective Use

    Safety comes from knowledge and planning. Teams on our floor engage with the material daily, and their insight shapes storage protocols and PPE selection. Spillage at the kilo scale rarely presents acute hazard, but chronic exposure or improper ventilation increases risk. Routine training runs through transfer procedures, fume hood operation, and correct spill neutralization.

    Compared with benzene or toluene derivatives, 3-Methoxybenzonitrile presents a lower flash point but higher affinity for skin barriers. Our maintenance crew checks closed-transfer lines and verifies integrity. Packaging gets robust enough to withstand repeated handling during storage and overseas shipment. Secondary containment and documented spill response hold fast across logistics and warehouse teams.

    Most inquiries from industrial users revolve around reactivity—not toxicity. Our engineering advisors document response to acids, bases, oxidizers, and reducing agents based on real incidents and laboratory simulations. The material keeps stable under standard conditions. As a practical rule, it stays far from strong caustics and oxidizing agents, especially in scale-up. Our technical staff maintains records of any off-normal findings, sharing knowledge with long-term clients.

    Practical Tips for Successful Application

    Many laboratory and process failures trace to overlooked physical properties. 3-Methoxybenzonitrile dissolves best in acetone, ethyl acetate, or chlorinated hydrocarbons—water brings only minimal uptake. Stirring and agitation promote clean dissolution; clumps signal subpar temperature or excessive solid loading. Small crystal habits aid in fast dissolution but may powder if transported roughly. Our shipping team reinforces cartons for extended transit, knowing fine material handles differently than granular forms.

    Reactions calling for cyano group activation respond to heat and chosen catalysts; not all protocols transfer smoothly across scales. Our in-house chemists recommend starting trials at bench scale before doubling or tripling batch sizes in a pilot reactor. We maintain ongoing dialogue with R&D teams across industries, passing along collected practical notes—always based on actual run data rather than theoretical predictions. Any new application, such as introduction into condensation steps or cross-coupling, benefits from staged temperature ramps and solvent compatibility testing.

    Addressing Supply Consistency and Quality Concerns

    Global markets absorb increasing volumes of substituted benzonitriles. Fluctuating raw costs, labor shortages, and logistics backlog affect timelines. From our vantage point, sourcing quality starts long before tonnage procurement. By building direct relationships with raw aromatic producers and solvent vendors, our purchasing keeps contamination risk low. Periodic audits and lot testing keep the feedback honest. Multiple site locations within the region split risk—unusual disruptions in one plant rarely impact all output.

    Final users—especially in high-margin pharmaceutical or electronics applications—consistently demand tighter impurity specs, micron-level control, and documentation trails. Our document control teams log analytical, manufacturing, and shipping records from batch start to customer delivery. On-demand customer audits, commonplace these days, receive open access to production logs. Unexpected findings become triggers for root-cause analysis and workflow adjustment. Batch recalls rarely appear, but our staff runs drills several times a year, tuned to lessons learned from both our sector and other fine chemical operations.

    Continuous Improvement and Collaborative Problem Solving

    Process chemists and production managers seldom rest on yesterday’s protocols. Annual internal reviews, driven by production outcomes and customer feedback, steer protocols toward improved yield, reduced solvent losses, and lower energy consumption. Teams test alternate crystallization schemes, filtration techniques, and product drying methods. Data from each campaign filters back into SOP changes for subsequent operations.

    Should recurring process bottlenecks emerge—such as filtration blinding, reactor fouling, or solvent loss—cross-functional groups meet to brainstorm and pilot alternatives. These sessions might yield subtle changes: swapping filter grades, timing reactor quenching differently, or providing extra operator training. Improvement happens batch by batch. Long-standing clients count on our willingness to bring emerging issues into the open and share practical learnings rather than theoretical generalities.

    Specific projects highlight the value of repeated experimentation. In one multi-year partnership with an API manufacturer, small but persistent trace impurities disrupted their downstream synthesis. Our team, working with theirs, ran split-batch purifications, compared wash solvents, and tested several alternative precipitation routes over dozens of cycles. Neither party accepted “good enough”—eventual results raised purity by over 0.8% and dropped a troublesome side impurity below detection. No distant distributor matches that level of iterative, cooperative problem-solving, and the whole production base benefits from lessons earned on the line.

    Commitment to Long-Term Reliability and Value Creation

    Every shipment of 3-Methoxybenzonitrile tells a story beyond specifications. Many clients first arrive with urgent requests—tight deadlines, custom particle size, or analytical support for scale-up. The root of a successful partnership emerges in steady, open dialogue about observed challenges. Our team listens closely, adapting production, packaging, or documentation where it counts. Instead of chasing lowest cost per kilo, we concentrate effort where it safeguards process reliability and product fit for use.

    Long-term programs, such as regulatory documentation or multi-year research trials, benefit from this kind of producer touch. Clients rely on us to keep analytical trends steady year after year, easing paperwork for DMF filings or international registrations. The stability of a known, trusted material—the ability to trace each drum, each lot, directly back to originating process logs—forms the backbone of regulatory and supply smoothness.

    Smaller users also value access to direct advice. Early-stage researchers and pilot-scale engineers ask for tailored batch sizes, custom drying cycles, or technical clarification on by-product handling. Our customer support crew—drawn from our own process teams, not outside reps—fields these questions, drawing from direct knowledge and established best practice. Relationships grow more resilient where feedback flows both ways.

    Looking Forward—Sustainable Manufacturing

    The growing push for cleaner synthesis and responsible production brings changes to how every plant approaches aromatic and nitrile intermediates. Volatile Organic Compounds, solvent recycling, and energy-use audits shape investment in new production technologies. Our team spearheads upgrades that favor closed-loop solvent management, lower emissions, and increased yield per reactor cycle. These changes grow out of both regulatory compliance and practical observation. Lower waste streams result in fewer plant shutdowns and less hazardous waste shipping—cost savings transfer directly to final pricing and long-term supply stability.

    Efforts don’t stop at the factory gate. Technical staff work with customer safety, environmental, and R&D teams to develop end-to-end “best use” profiles—helping to minimize environmental release and improve recovery, not only at batch start but all the way through to finished goods. This cycle, repeated year after year, builds real value: more reliable starting material, reduced compliance risk, and a reduced environmental footprint—shaping not just how we make, but how we advise downstream users to handle, react, and recover.

    Direct Insights Born on the Factory Floor

    Making 3-Methoxybenzonitrile brings practical lessons for anyone in specialty chemicals. Efficiency looks different at the scale of a thousand-liter reactor compared to a fume hood. Skilled operators know small deviations cost more in time, cleanup, and lost batch than any theoretical gain might promise. Experienced staff—many with decades at the same lines—read flows, react to unplanned shifts, and dig into analytical printouts for the patterns that matter. No distant procurement office substitutes this know-how.

    Client needs keep evolving. Regulatory bars creep up; shipping rules tighten; downstream applications demand tighter consistency. By drawing on stable, far-reaching internal expertise, direct producer feedback, and years of iterative process tuning, our factory supports these changing requirements with fewer supply interruptions and less risk during innovation. Partnerships built around this core advantage gain most: deeper technical service, faster troubleshooting, and a foundation for both routine and novel applications.

    No single compound shapes every synthesis, but the careful, hands-on craftsmanship behind 3-Methoxybenzonitrile delivers steady value for researchers, process chemists, and product teams seeking dependable, adaptable building blocks for future growth.