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4-Bromo-2-Methylbenzonitrile

    • Product Name 4-Bromo-2-Methylbenzonitrile
    • Alias 4-Bromo-o-tolunitrile
    • Einecs 819-084-2
    • 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

    517563

    Productname 4-Bromo-2-Methylbenzonitrile
    Casnumber 7073-61-2
    Molecularformula C8H6BrN
    Molecularweight 196.05 g/mol
    Appearance White to off-white solid
    Meltingpoint 66-69 °C
    Boilingpoint 283-285 °C
    Density 1.53 g/cm³
    Purity Typically ≥98%
    Synonyms 2-Methyl-4-bromobenzonitrile
    Smiles CC1=CC=C(C#N)C=C1Br
    Inchi InChI=1S/C8H6BrN/c1-6-3-2-7(5-10)4-8(6)9/h2-4H,1H3
    Solubility Slightly soluble in water, soluble in organic solvents
    Storagetemperature Store at 2-8°C
    Hazardclass Irritant

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

    Packing & Storage
    Packing Amber glass bottle labeled "4-Bromo-2-Methylbenzonitrile, 25g." Features hazard symbols and CAS number; securely sealed for laboratory use.
    Shipping 4-Bromo-2-Methylbenzonitrile is shipped in sealed, chemical-resistant containers, protected from moisture and extreme temperatures. It is classified as a hazardous material and must be handled with care, adhering to all regulatory guidelines for transport. Appropriate labeling and documentation are required to ensure safe and compliant delivery.
    Storage 4-Bromo-2-Methylbenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition or heat. Keep away from incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature, and ensure the storage area is equipped to handle chemical spills or leaks safely.
    Application of 4-Bromo-2-Methylbenzonitrile

    Applications of 4-Bromo-2-Methylbenzonitrile in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Bromo-2-Methylbenzonitrile to multiple industries demanding advanced aromatic intermediates. This material supports specific synthesis routes in pharmaceuticals, agrochemicals, specialty dyes, advanced materials, and custom fine chemicals, with dedicated handling processes and industry-driven compliance frameworks.

    1. Pharmaceutical Intermediate Synthesis

    This compound supports active pharmaceutical ingredient (API) production, serving as a key intermediate during the synthesis of substituted benzonitrile-based drug molecules, especially in the development of non-steroidal anti-inflammatory drugs, antihypertensives, and CNS agents. Customers incorporate this material at the early or mid-stage of API routes that require controlled halogenation and nitrile group retention. Strict traceability and batch documentation govern each step.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA: finished pharmaceuticals)
    • EU EudraLex Volume 4 - GMP Guidelines
    • Supplier QMS per ISO 9001:2015

    Typical usage ratio

    • Typically 0.7–1.2 molar equivalents per mol of final API intermediate, adjusted based on target substitution pattern and coupling efficiency

    Downstream process integration

    • Charged to the coupling reactor after solvent charging and catalyst addition; reacts with amines or other aromatic substrates under controlled temperature and inert atmosphere

    Final product types

    • Pharmaceutical intermediates for anti-inflammatory compounds
    • Raw material for antihypertensive drug synthesis
    • CNS-active molecule intermediates

    2. Agrochemical Synthesis (Herbicide and Pesticide Intermediates)

    Downstream agrochemical producers utilize the product as a nitrile- and bromo-functionalized aromatic core for next-generation herbicide, fungicide, and insecticide molecule construction. It supports step-growth synthesis where a brominated nitrile confers selectivity and optimum activity spectrum in custom formulations. Reactivity control is crucial during halide exchange and further functionalization.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH Regulation (EC 1907/2006) registration
    • ISO 9001:2015 Quality Management System
    • Compliance with US EPA Pesticide Chemical Regulation (40 CFR)

    Typical usage ratio

    • Usage varies from 8–18% by weight in stepwise synthesis batches, depending on the molecular structure of target active ingredient and desired bromine/nitrile content

    Downstream process integration

    • Introduced during base-catalyzed substitution or Suzuki-type cross-coupling reactions to form the core scaffold of agrochemical actives

    Final product types

    • Herbicide intermediates for aryl-nitrile scaffolds
    • Precursors to systemic fungicides
    • Custom intermediates for insecticides used in seed treatment formulations

    3. Specialty Dye and Pigment Manufacture

    Manufacturers of specialty dyes and pigments value this intermediate for introducing bromo and nitrile substituents on aromatic rings, crucial in colorant stability and solubility modification. The material enhances chromophore structures during high-temperature condensation and diazotization steps in the dye industry. Strict purity and trace metal content specification are maintained to guarantee reproducibility and batch consistency.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • OEKO-TEX Standard 100 (applicable for textile colorants)
    • ISO 9001:2015 QMS for colorant intermediates
    • Restricted Substance List (RSL) protocols as required by textile brands

    Typical usage ratio

    • Typically employed at 5–12% by weight of total dye intermediate mass, variable per pigment shade and synthesis pathway

    Downstream process integration

    • Added after initial aromatic amination for coupling in diazo condensation, or utilized as the starting unit for brominated azo pigment synthesis

    Final product types

    • Disperse and solvent dyes for synthetic fibers
    • Organic pigments for plastics and coatings
    • Specialty textile colorants

    4. Advanced Material Monomer Production

    High-performance material producers employ this compound as a monomer precursor for specialty polymers, resins, and electronic material backbones. Its halide and nitrile groups offer reactivity for subsequent cross-coupling or polycondensation, leading to high glass transition temperature (Tg) polymer matrices. Strict contamination control and process validation are in place due to applications in electronic and optical-grade materials.

    Industry compliance standards

    • IPC-4101 (laminate and prepreg materials standards)
    • RoHS Directive (2011/65/EU) for electronics
    • REACH (EC 1907/2006) SVHC criteria for polymer raw materials
    • ISO 14001 Environmental Management (if implemented)

    Typical usage ratio

    • Monomer input ranges from 15–28% by weight of batch, depending on target density and crosslinking requirements in advanced composites

    Downstream process integration

    • Blended at the start of polycondensation, or fed during Grignard cross-coupling in semiconductive polymer synthesis

    Final product types

    • High-performance polymer resins for printed circuit boards and electronic films
    • UV-curable resins for optical applications
    • Specialty engineering plastics with halogenated aromatic domains

    5. Custom Fine Chemical Synthesis

    Research and pilot production facilities utilize this intermediate for building blocks in heterocyclic and aromatic molecule libraries. It supports rapid analog development, SAR studies, and custom reaction design thanks to its dual functional groups, offering reliable selectivity in transition metal-catalyzed and nucleophilic aromatic substitution reactions. We supply high-purity and custom-packaged quantities for reproducible lab-to-pilot scale transitions.

    Industry compliance standards

    • ISO 9001:2015 for lab and pilot chemicals
    • Custom ERP and traceability protocols for research-grade materials
    • Local and international transport regulations (IATA, IMDG)

    Typical usage ratio

    • Usually varies from 1–10 mmol scale, or 2–10% by weight per reaction batch depending on study design and reaction pathway

    Downstream process integration

    • Charged as a primary substrate or coupling partner in exploratory synthesis, structure–activity optimization, and analog creation pipelines

    Final product types

    • New heterocyclic building blocks
    • Library analogs for discovery research
    • Specialty intermediates for contract synthesis projects
    Free Quote

    Competitive 4-Bromo-2-Methylbenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2-Methylbenzonitrile Direct from the Manufacturer

    Real Experience with 4-Bromo-2-Methylbenzonitrile

    We have been synthesizing and supplying 4-Bromo-2-methylbenzonitrile for years, and every batch comes off our reactors with a story that matters to both researchers and industrial users. This compound, which many chemists call 2-Methyl-4-bromobenzonitrile in the lab, holds a unique niche in chemical synthesis. We use model number 4723-33-9 as a reference because it reflects high purity batches produced through controlled bromination and cyanation steps. The structure, as its name suggests, gives a distinguishing blend of reactivity and selectivity that our partners appreciate. Every lot we dispatch draws on our team’s diligence in the upstream synthesis and downstream purification, which means users find minimal need to clean up impurities before applying it to their own research or intermediate manufacture.

    We Care About What Goes Into the Drum

    From the start, our focus has centered on consistency. In practical terms, 4-Bromo-2-methylbenzonitrile leaves our facility as a white to pale off-white crystalline powder, with purity levels hitting above 98 percent. This material behaves in a predictable way during handling thanks to our standardized drying and packaging. Moisture control during packing means no unnecessary clumping, and the particle size remains fine enough for reliable weighing and transfer. These may look like minor advantages, yet we know from our work with drug discovery teams and agrochemical groups that even a small clump can throw off doses or reactions. That’s why our investment goes into well-maintained filtration and oven systems at the last production step rather than just relying on paperwork to certify the specification sheet looks good.

    Why Chemists Choose This Nitrile for Complex Syntheses

    What makes 4-Bromo-2-methylbenzonitrile different from its isomers and related benzyl derivatives starts at the molecular level. The pair of functional groups—a nitrile and a bromine on specific positions—creates a handle for aggressive transformations. The methyl group in the 2-position blocks certain side reactions, keeping the bromine exposed for cross-coupling or substitution chemistry. Working in the fine chemical industry, we have seen firsthand how developers rely on the reactivity of the aryl bromide group; it couples smoothly with palladium catalysts in Suzuki and Buchwald-Hartwig reactions, making it an efficient tool for constructing more elaborate molecules in fewer steps. This saves time and lowers the cost for customers scaling up heterocyclic compounds or drug candidates in early clinical trials.

    We have watched several agrochemical innovators use our 4-Bromo-2-methylbenzonitrile to introduce the nitrile moiety into challenging scaffolds that must withstand harsh processing. The electron-withdrawing effect of the nitrile, combined with the sterics of the methyl and the modifiable bromine, lets chemists tune reactivity for exacting needs. For example, synthetic routes aiming for selective functionalization will often fail when using closely related compounds, such as 2-bromo-4-methylbenzonitrile. The position of the methyl group in our product changes the electronics and pharmacophore profile, yielding higher conversion rates and cleaner separations in chromatography.

    Specifications That Matter in Real Labs and Plants

    High-purity specification isn’t just a phrase on a label for us—it means less downtime in process development. Our trusted workflow starts from bromotoluene intermediates, with our team closely monitoring exothermic bromination and careful temperature controls to keep byproducts out of the product stream. Our 4-Bromo-2-methylbenzonitrile comes consistently with melting points between 55°C and 60°C. Each drum or small pack is checked for identity and purity using HPLC and NMR, not just titration or TLC. Impurities such as dibromo or oxidative byproducts remain below 1 percent, usually less than half a percent, reducing the risk of catalytic poisoning further down a synthetic path. A research chemist can treat our product as a reliable building block rather than a troubleshooting headache.

    Our process lines now rely on stainless steel vessels dedicated to nitrile handling. This approach prevents cross-contamination which can plague plants juggling multiple aromatic intermediates. Years ago, we encountered a case with a client trying to use 4-Bromo-2-methylbenzonitrile sourced from a generic supplier: the impurity profile was inconsistent, and their in-house purification caused yield loss and a week’s delay. We rebuilt their experience with them, starting with our own QA-tested lots. Issues ceased. This type of feedback keeps our QA and plant teams vigilant, and we document every production run down to spectral fingerprints confirmed with archived samples.

    Differentiation from Other Aromatic Nitriles and Bromides

    Many buyers group bromobenzonitriles together, but each isomer runs differently through a reactor and impacts downstream processes. We do not substitute our 4-Bromo-2-methylbenzonitrile with either meta‑ or para‑brominated versions, despite the naming confusion common in trade channels. Synthetic chemists who have experimented with 3-Bromo-2-methylbenzonitrile or 4-Bromo-3-methylbenzonitrile share that the pattern of activation and steric hindrance alters pathways in straightforward cross-coupling steps. Any switch from our compound to a positional isomer means risking totally different yields and selectivity, especially if a late-stage route relies on a well-placed methyl group shielding a reactive site. We stock and supply these distinctions because we know the pain-points that arise from mislabeling or mix-ups in the supply chain.

    Our product also contrasts sharply with unsubstituted benzonitrile or 4-bromobenzonitrile. The second substituent (the methyl at the 2-position) locks in secondary effects, tightening up selectivity in both metal-based couplings and functional group additions. For large scale manufacturers, this difference is not academic. A client from the dyes industry once attempted a substitution using less expensive alternatives. The result failed both solubility and color-fastness tests, sending their process back to the drawing board until they returned to our direct-supplied 4-Bromo-2-methylbenzonitrile. Price alone can't correct for the subtleties in structure and reactivity needed in specialty synthesis.

    Users often compare our grade with resold or down-purified competitors that cut corners on moisture, left-over solvents, or packaging. Reliability in melt behavior and purity makes a difference in automated dosing and continuous flow setups, which now dominate modern pharmaceutical and materials pipelines. We learned to handle and store the product in sealed HDPE or steel-lined containers, which keeps both substrate and finished goods safe from contamination or degradation. Cases of off-odor or discoloration due to repackaging from less disciplined sources provided hard lessons for the entire team years ago.

    Impact on Workflow, Productivity, and Safety

    As a manufacturer, we see daily how the wrong starting material can cascade into rework, lost raw materials, and production slowdowns. Our clients benefit from tighter spectra, less need to rerun analytics, and simpler downstream filtration. 4-Bromo-2-methylbenzonitrile arrives consistently in the expected form: stable, finely powdered, and free from dust or crystalline lumps. In research settings, chemists feedback that reactions “just work” without adjustments. In kilo-scale plants, productivity jumps when raw material reproducibility becomes a non-issue.

    Operators on our floor always handle this compound in full PPE with local vacuum extraction—real-world practice, not just paperwork. Methylbenzonitriles carry moderate toxicity and the bromine atom can sensitize the skin or respiratory tract. We train our staff with hands-on drills, keep raw material moving in closed systems, and maintain our MSDS up to date with trade regulations. Being on the ground, we don’t gloss over risk: we have caught low-level spills quickly and treated them in our waste neutralization tanks, preventing problems for neighboring downstream lines. Bigger distributors don’t offer this level of perspective; we own each batch from reaction to pack-out.

    Key Applications Defined by Industry, Not Catalog

    4-Bromo-2-methylbenzonitrile stands out as more than a generic intermediate, as shown in the diverse end uses we see every month. Pharmaceutical clients trust it as an intermediate for benzyl amine derivatives and pyridine scaffolds, both in lead development and process routes moving toward scale-up. The specific placement of substituents in our compound allows for palladium-catalyzed amination to run cleanly to product, without troublesome rearrangement side chains appearing in the HPLC. QA teams at contract manufacturing organizations have cited our material in their regulatory filings, due to its effect on downstream impurity profiles and overall process reproducibility.

    Agrochemical companies use our 4-Bromo-2-methylbenzonitrile to feed high-value pesticides and fungicides that require robust intermediates. Stability during storage at warm warehouses and compatibility with organometallic reagents both underlie their repeat orders. We have seen this compound used to tailor physical properties—solubility, lipo- or hydro-philicity, UV-resistance—when attached to target molecules for specialty polymers as well. In academic chemistry, researchers focused on step-economical synthesis gravitate to it for methods development and structure–activity relationship explorations. If a research director aims to avoid unneeded protection–deprotection steps, our product’s substituent pattern lets them get there sooner.

    Over the past five years, we have shipped 4-Bromo-2-methylbenzonitrile to pilot programs in dyes, pigments, materials science and next-generation electronic components. Polymer modifiers built from this intermediate perform better under thermal cycling, and dye manufacturers have commented on color sharpness and consistency. The simplicity of handling—especially in controlled environments, gloveboxes or dry box settings—means minimal waste and reliable mass balances.

    Our Lessons Learned in Manufacturing and Distribution

    Manufacturing this product has required us to refine our operational discipline. The bromination and cyanation steps demand relentless attention to reaction conditions. Years ago, an unchecked pressure spike led to a flurry of emergency responses and minor residue contamination; since then, every reactor run is supervised by experienced chemists who anchor critical controls. We take pride in batch-to-batch traceability, using digital logging and barcoded sample archives.

    Shipping boxes and drums go through internal inspection for tamper-evidence and seal integrity. We have learned from logistics setbacks too: an early shipment went awry due to mismarked containers that let in moisture and caused caking. Today, desiccant packs and robust linings are standard, not afterthoughts. This hands-on vigilance translates to higher confidence for our partners, who expect each drum to arrive in identical condition, no matter the season or shipping route. Supply chain trust is built batch by batch, and as genuine manufacturers, we directly put our reputation on the line with every kilogram we produce and send out.

    Looking Beyond Today’s Batches—How We Shape Quality for the Future

    Our investment in in-house reactor and analytical equipment continues to deepen our ability to offer leading quality. Relying on off-the-shelf automation never reached the consistency or scale we needed, so our engineering teams built bespoke reactors with real-time sensor feedback. This allows us to witness small upswings in temperature or pH and catch impurity profiles before they can grow. With each synthesis campaign, we revalidate NMR and HPLC calibration against reference standards, not just company benchmarks. Clients benefit through fewer “out-of-spec” investigations, fewer regulatory headaches, and shorter down times.

    Environmental responsibility comes natural to us, not as an afterthought for compliance. Scrubbing columns, solvent recovery, and controlled waste treatment are integrated into our workflow. We reprocess byproducts and keep emissions well below regulatory limits. We learned from tough early audits, and now our green chemistry initiatives mean every run of 4-Bromo-2-methylbenzonitrile leaves a smaller environmental footprint. Our team members share these best practices with other departments, spurring ideas for solvent substitution and energy efficiency in line with corporate values.

    Supporting Innovation and Customer Success

    Feedback from the labs and process lines using our 4-Bromo-2-methylbenzonitrile forms the backbone of our production strategy. Whether it is a challenging gram-scale pilot or a multi-tonne rollout, we see the real world impact of reliable intermediates. Production upsets fall when users can take consistency for granted. Researchers trying out a new synthetic methodology know our product’s impurity profile supports innovation, rather than stalling it.

    In conversations with scientists and plant managers, discussion turns to cost of changeovers and revalidation if a new supplier is considered. Our detailed batch records, traceable analytics, and stable supply lines anchor those relationships. Joint trouble-shooting efforts revealed that small adjustments in drying or storage could mean the difference between regular QA holds and non-stop manufacturing. Sharing those lessons with clients reduces their time spent troubleshooting and increases their yield.

    Perspectives from Our Manufacturing Team

    Day-to-day production of 4-Bromo-2-methylbenzonitrile brings both routine and challenge. The plant hums with distillation columns and reactors, but real satisfaction comes from seeing a flawless powder reach a customer without hitches. New team members learn the significance of every test—be it powder flowability or bromine content—because even minor deviations show up downstream, sometimes in a client’s product loss or delayed launch. Our work builds on previous runs; we track each process tweak and review it for improvements. Over years, this cycle has cut our off-grade material and made the product central to the portfolios of many pharmaceutical and materials innovators.

    The Road Ahead for 4-Bromo-2-Methylbenzonitrile

    Making and perfecting 4-Bromo-2-methylbenzonitrile is more than filling orders. By keeping quality high, impurity levels low, and batch records traceable, we support industries where failure is not an option. We plan to deepen collaboration with customers by developing new grades tailored for emerging applications, analyzing use patterns, and investing in workflow innovation. Our bottom line: a strong batch benefits everyone.