Products

2-Methylbenzonitrile

    • Product Name: 2-Methylbenzonitrile
    • Alias: o-Tolunitrile
    • Einecs: 208-315-9
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    140409

    Cas Number 611-16-7
    Molecular Formula C8H7N
    Molar Mass 117.15 g/mol
    Iupac Name 2-Methylbenzonitrile
    Appearance Colorless liquid
    Boiling Point 218-219 °C
    Melting Point -14 °C
    Density 1.015 g/cm3
    Refractive Index 1.528
    Flash Point 92 °C (closed cup)
    Solubility In Water Insoluble
    Smiles Cc1ccccc1C#N
    Pubchem Cid 11896

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

    Packing & Storage
    Packing The 2-Methylbenzonitrile is packaged in a 100 mL amber glass bottle, clearly labeled with hazard warnings and product details.
    Shipping 2-Methylbenzonitrile is shipped in tightly sealed containers, typically glass or high-density polyethylene bottles, to prevent leaks and contamination. It should be labeled as a hazardous material, transported under cool, dry conditions, and handled according to relevant regulations due to its flammability and toxicity. Ensure proper documentation accompanies the shipment.
    Storage 2-Methylbenzonitrile should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and moisture. Keep the container tightly closed when not in use. Store separately from incompatible substances such as strong oxidizers and acids. Ensure proper chemical labeling and use storage containers made of compatible materials, such as glass or high-density polyethylene.
    Application of 2-Methylbenzonitrile

    Applications of 2-Methylbenzonitrile in Industrial Manufacturing

    2-Methylbenzonitrile serves as a specialized intermediate in several chemical production sectors, primarily for the synthesis of high-value molecules and performance products. As a manufacturer, we support strict specification control and supply stability for advanced downstream integrations.

    1. Agrochemical Intermediate Synthesis

    Crop protection manufacturers rely on this aromatic nitrile as a building block in targeted herbicide and insecticide syntheses. The methyl-substituted aromatic ring enhances molecular reactivity for constructing substituted pyridines, phenoxyacetic acids, and other actives through amination, hydrolysis, or coupling reactions. Accurate dosage meets reactivity needs and minimizes impurity carryover for regulatory approval.

    Industry compliance standards

    • REACH compliance (EU)
    • EPA TSCA Inventory (US)
    • ISO 9001:2015 Quality Management
    • FAO/WHO Technical Specifications for Pesticides

    Typical usage ratio

    • 5–15% by mass in active ingredient intermediate batch, adjusted based on ring substitution pattern required

    Downstream process integration

    • First- or second-step condensation with other functionalized aromatics
    • Subsequent hydrolysis for carboxylic acid intermediates
    • Direct amination for heterocycle core formation
    • Final purification by crystallization before blending with adjuvants

    Final product types

    • Selective rice herbicides (e.g., pyridinecarboxylic acids)
    • Systemic insecticides
    • Precursor for phenoxy herbicide formulations
    • Specialty agro intermediates for export

    2. Pharmaceutical Intermediate Production

    Specialty API producers incorporate this compound for the manufacture of advanced pharmaceutical intermediates, especially where ortho-substitution improves binding specificity in target molecules. Controlled addition and careful reaction monitoring help achieve high-purity intermediates, supporting subsequent synthetic steps and batch traceability for regulated markets.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • Ph. Eur. Monographs where applicable
    • FDA cGMP (21 CFR Part 210/211)
    • ISO 14644-1 for controlled environments

    Typical usage ratio

    • 3–12% by theoretical yield, adjusted according to coupling reaction efficiency and impurity clearance needs

    Downstream process integration

    • Key starting material in nucleophilic aromatic substitution
    • Hydrolysis and reduction for amide or amine intermediates
    • Direct integration into ring-closing processes during API assembly
    • High-purity distillation and in-process control sampling

    Final product types

    • Intermediates for antipsychotic APIs
    • Precursors for antihypertensive compounds
    • Selective metabolite standards
    • Reference substances for R&D and quality control

    3. Dye and Pigment Manufacturing

    Producers of high-stability dyes and organic pigments use this material during Friedel–Crafts and condensation syntheses for specialty colorants. The methyl group’s ortho position contributes to color fastness and migration resistance, ensuring product consistency in applications such as fiber and polymer coloring.

    Industry compliance standards

    • EN 71-3: Safety of Toys (migration of certain elements)
    • Oeko-Tex® Standard 100 (textile safety)
    • ISO 9001:2015 Quality Control in Batch Processing
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)

    Typical usage ratio

    • 2–8% by mass in dyestuff intermediate blends, based on chromophore requirements and batch scale

    Downstream process integration

    • Condensation with aromatic amines for azo dye core synthesis
    • Oxidative coupling to enhance lightfastness in pigments
    • Colorant microencapsulation and purification through filtration
    • Integration in heat- and light-resistant formulation lines

    Final product types

    • Disperse dyes for synthetic fibers
    • Solvent-based printing inks
    • Organic pigments for plastics compounding
    • High-performance textile dye solutions

    4. Liquid Crystal and Advanced Materials Synthesis

    Manufacturers of liquid crystal materials select this compound as a precursor for key aromatic core units, influencing mesophase temperature ranges and dielectric behavior in display applications. The methyl group contributes to rigid molecular packing needed in TN and STN displays. Process control ensures homogeneity and strict exclusion of byproducts, critical for electro-optical performance.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Hazardous Substances Restriction)
    • IEC 60412 for display component materials
    • China GB/T 26362 (liquid crystal chemical standards)
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • 3–10% by mole in mixture formulation, adjusted according to host-guest mesogen system and desired electro-optical properties

    Downstream process integration

    • Initial aryl nitrile introduction for core unit formation
    • Esterification or etherification with flexible spacers
    • Pilot-scale blending with other LC precursors
    • Final purification via column chromatography

    Final product types

    • Twisted nematic (TN) and super-twisted nematic (STN) liquid crystals
    • Specialty LC mixtures for automotive displays
    • Organic photoconductors
    • Dielectric alignment films for electronics

    5. Fragrance and Aroma Chemical Production

    Aroma manufacturers employ this nitrile in the construction of complex aromatic compounds for perfumery and flavors. Ortho-methyl substitution helps create unique musk and floral notes, particularly after reduction and further functional modification routes. Stringent quality control ensures the absence of hazardous residuals for IFRA compliance.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • 21 CFR Part 172.515 (US FDA flavor and fragrance substances)
    • Kosher and Halal certificate requirements for certain markets
    • ISO 22716 Cosmetics GMP

    Typical usage ratio

    • 0.5–2.5% by mass in aroma intermediate blends, tuned according to strength and finished product requirements

    Downstream process integration

    • Hydrogenation step to convert nitrile to aldehyde or alcohol intermediates
    • Further chain extension and etherification for musk building
    • Concentration and stabilization for fragrance oil bases
    • Sensory evaluation batchwise under GMP

    Final product types

    • Artificial musk and floral aroma compounds
    • Flavor ingredients for beverages
    • Fine fragrance blends
    • Functional aroma chemicals for detergent and personal care

    Free Quote

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

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Methylbenzonitrile: Experience Derived Quality, Purposeful Applications

    Understanding the Character of 2-Methylbenzonitrile

    Benzonitrile derivatives carry a quiet strength across the specialty chemicals market—among them, 2-Methylbenzonitrile stands as a reliable choice, both for its consistent performance and its ability to anchor high-value processes. As a direct manufacturer with a decades-long legacy in aromatic nitrile synthesis, we’ve watched 2-Methylbenzonitrile evolve from a niche laboratory chemical to a core intermediate in large-scale production settings. In demand by both the pharmaceutical and fine chemical sectors, this compound offers a purity and compositional stability that laboratories and industrial sites have counted on for a generation.

    Our team crafts 2-Methylbenzonitrile using carefully calibrated conditions in closed systems. The controlled process yields a pale, aromatic liquid with a distinct, pleasant odor—often overlooked, but well-known to those who have spent time at a bench or pilot facility. Rigorous distillation and analytics highlight its precise composition: a methyl side group at the ortho position to the nitrile, bringing both reactivity and compatibility. Product batches display repeatable assay levels, low moisture, and minimal side products, attributes sustained by round-the-clock monitoring. This reliability undergirds every ton of material shipped, as we know end users cannot afford deviation, whether scaling up from grams to kilograms or embarking on full campaign production.

    Distinctive Roles and Performance in Synthesis

    2-Methylbenzonitrile, sometimes known by its common name o-Tolunitrile, features a single methyl group adjacent to the nitrile. While this may seem a minor shift compared to unsubstituted benzonitrile, the difference speaks for itself in chemical reactivity and downstream utility. In practical terms, the ortho-methyl confers unique electronic and steric characteristics—subtle enough that experts value it as a gateway to specific target molecules, yet robust enough that it behaves with notable consistency every run. Experienced chemists and engineers routinely choose our product for hydrogenation, Grignard, and amination reactions, recognizing the reliability that originates from tight process control.

    Each drum and bulk delivery reflects a routine that leaves nothing to luck. Our operators understand the risks of trace impurities—especially in pharmaceutical routes where any off-target reaction can strain yields or, worse, demand repeated validation. After repeated conversations and site visits with customers, we’ve come to appreciate how much trust the industry places in the transparency and reproducibility of our supply. A minor change in a process parameter here can ripple into days of troubleshooting in someone else’s reactor. That feedback loop stays at the front of our minds during every shift.

    Industry Uses: Pharmaceuticals, Agrochemicals, and Beyond

    When the industry talks about functional building blocks, 2-Methylbenzonitrile consistently ranks high for purpose-built molecules. Our product finds its way into pharmaceutical intermediates, agrochemical actives, dyes, and specialty polymers. Medicinal chemistry teams turn to the methyl group as both a solubility and metabolic tuning handle, while the nitrile provides a resilient anchor for diverse further transformations. In our experience, agrochemical clients prize the methyl group’s contribution to target molecule selectivity—plant metabolism and binding profiles often change notably with the ortho-methyl shift. Such nuances are not lost on analytical chemists who stress over batch purity and chromatographic profiles, or on process engineers facing scale-up risks.

    Manufacturers of fine chemicals turn to our 2-Methylbenzonitrile when looking to build more complex aromatic systems. In practical batch operations, the compound’s boiling and melting points support easy handling—our technical support team fielding questions about storage and transport always emphasizes its manageable volatility and consistent liquid phase at typical warehouses. While benzonitrile itself is better known as a solvent, the methylated version plays better as an intermediate, holding its structure in harsh conditions, including high-temperature hydrogenations and classic nucleophilic additions.

    Comparisons and Differences That Matter

    Most inquiries we receive involve comparisons with benzonitrile, o-toluidine, and meta or para methylbenzonitrile derivatives. Chemists want a clear-eyed view of how substituent positions affect reactivity, selectivity, and operational safety. We’ve run these comparisons at scale—side-by-side pilot lots, routine GC and NMR analysis, yield monitoring—and our results point to some recurring conclusions. The ortho-methyl group in 2-Methylbenzonitrile often slows certain nucleophilic additions compared to the unsubstituted counterpart, but this sluggishness transforms into an advantage when seeking selectivity or when aiming to avoid overreaction. In contrast, its isomers—meta and para versions—often change boiling points and migration rates, and can complicate recoveries and downstream purification.

    Some end users mistakenly reach for 2-Methylbenzonitrile as a direct solvent replacement for benzonitrile. Our engineers have tested these cases at the bench: the results reveal notable differences in viscosity, odor, and miscibility with polar and nonpolar co-solvents. While benzonitrile’s planar structure grants it broad solvent power, the ortho-methyl addition narrows its utility, making 2-Methylbenzonitrile more at home as a synthetic intermediate, rather than a general-purpose solvent. Our regular technical conversations uncover cases where the methyl group reduces byproduct formation or grants a shorter route to a pharmaceutical core—benefits that pay off in campaign time and waste reduction.

    Operational Considerations—From Plant to End Application

    Years of refining production have taught us that fine aromatic nitrile chemistry rewards vigilance. All the way from nitration and reduction steps to dehydration and refining, we have learned that every batch tells a story—one where even minor variances in raw material or ambient humidity can affect crystallinity, color, and downstream performance. Plant operators, QC analysts, and logistics coordinators know that the unpredictable weather impacts, power interruptions, and raw material variability require both preventive design and resilience born from experience.

    Customers count on us for just-in-time deliveries where shelf life and cold-chain logistics can make or break a project. We have seen the real-world impact of improper storage—trace hydrolysis leading to amide contamination, off-odors developing in open drums, or vapor losses during rough transfers. In our warehouses, technicians monitor drum seals, verify stock with near-IR probes, and confirm documentation, rejecting anything short of the norm. Such diligence and openness underwrite the reliability laboratories and plants count on—helping researchers avoid reruns, lost material, or non-conforming lots.

    Practical Paths to Improved Product Safety and Compliance

    Safety comes from experience and from an unwavering commitment to transparency. The nitrile functional group confers both value and toxicity; seasoned handlers know to work under good ventilation, wearing the right gloves and eye protection, and following guidelines from certificate to use point. On more than one occasion, we’ve traced back laboratory headaches to improper ventilation or to lack of familiarity with the compound’s mild but persistent odor. Companies who value rigorous training and documentation see fewer interruptions and safer, more consistent outcomes. We share best practices openly, helping procurement and EH&S teams wave off risky shortcuts.

    Our documentation keeps pace with the changing regulatory landscape—each lot accompanied by transparent test results and material details, revised as compliance standards develop. Communication with downstream users in Europe, North America, and Asia often reveals subtle differences in local regulations; we respond with clear labeling and support so each facility can adopt safe handling in line with local requirements, eliminating ambiguity. We encourage regular feedback from our customers, using it to further refine both process design and frontline safety guidance.

    Quality Assurance Drawn from Direct Experience

    Quality in manufacturing has no shortcuts. Since moving to our current synthesis protocol over a decade ago, our team has tracked every lot of 2-Methylbenzonitrile from the first step to final shipment, learning directly from the rare but instructive lessons of unexpected impurity or variable color. Corrective actions—like tightening nitrogen blanketing, optimizing reflux times, or fortifying drum liners—have all arisen out of direct failures, not from armchair theorizing.

    Batch control begins at the raw material stage. We source toluidine precursors from trusted suppliers, using in-house spectroscopy and chromatography to identify any deviation, then follow up with real-time monitoring during reactor runs. Dedicated purging routines at the end of each shift clear reactors to minimize cross-contamination. Final product is tested both internally and by third-party labs for purity, color, GC-MS profile, and residual moisture—criteria that reflect the practical concerns of both lab chemists and plant scale users.

    Our goal remains predictable: ship every kilogram as described, without compromise or surprise. Regular engagement with customers—factory visits, conference calls, and shared round-robin testing—helps align our internal targets with customer needs. The technical team participates in troubleshooting calls with both process development chemists and quality managers, sharing candid findings so each batch fits smoothly into its end use.

    Supporting Sustainability and Responsible Manufacturing

    Today’s market expects more than technical competence; it demands responsible stewardship of materials and waste streams. In our own experience, the journey to greener chemistry often starts with basic questions: can a process step generate fewer byproducts, can a solvent be recycled efficiently, can drums be reused, and can energy be minimized without sacrificing product profile? The path toward environmental responsibility has often been incremental, grounded in trial, error, and iteration.

    Wastewater from 2-Methylbenzonitrile production is managed using closed-loop systems and on-site treatment—decisions made not just for compliance, but to maintain trust in local communities who neighbor our sites. Efforts to minimize air emissions and energy use stem from simple observations made on the plant floor. Operators notice when a column fouls, or a vent condenser loses effectiveness; incremental upgrades—slurry filters, improved seals, and energy monitoring—prove their worth over months and years, not in a single, showy investment.

    Feedback from multinational clients increasingly pushes us to adopt more sustainable logistics as well. We carefully coordinate shipment frequencies, drum return, and bulk transfer options, always seeking to reduce both transit emissions and end-of-life disposal risks. Every improvement feeds a sense of pride among our team—from production hand to logistics planner—knowing that our practices measure up to the rising expectations of the marketplace. Moving forward, we collaborate with research partners and clients to run life-cycle assessments, seeking further areas for improvement that go beyond compliance.

    Partnerships Across the Supply Chain

    End-to-end reliability means working collaboratively—no manufacturer can afford isolation, especially with a versatile input like 2-Methylbenzonitrile. Our technical support staff maintains open lines with R&D chemists, contract manufacturers, and even competitors, trading observations and practical tips that keep product quality high and troubleshooting efficient. We have learned the value of sharing lessons openly; trade secrets may confer a short-term edge, but long-term trust grows from transparency and accountability.

    Mutual site visits bring engineers face to face with the intricacies and quirks of each implementation. These experiences directly inform both product improvements and custom solutions—be it modified packaging, alternative lot release protocols, or enhanced documentation for rare applications such as pigment synthesis or novel ligand formation. Each partnership, built on a foundation of demonstrated reliability, ensures that feedback on real-world use reaches the plant floor, not just a sales inbox.

    Our role as a manufacturer carries unique responsibilities—to customers, to team members, and to the industry as a whole. By maintaining stringent quality and safety practices, adapting to process challenges, and prioritizing sustainability, we deliver a product that research, manufacturing, and regulatory partners alike can trust. Our long-term clients measure our commitment not in marketing claims, but in the track record of on-time, on-spec deliveries and in our willingness to engage constructively with every batch or process campaign.

    Continuous Learning: Evolution in Practice

    No plant or product remains static. Over the years, we’ve invested in both people and technology, ensuring each batch of 2-Methylbenzonitrile benefits from a workforce that brings both expertise and curiosity. Regular training sessions, skill exchanges, and hands-on mentoring create an environment where operational discipline pairs with a readiness to adapt and rethink assumptions. We bring in external experts to audit and challenge our own procedures, and we send our best operators out to customer sites to learn firsthand about new trends or emerging challenges.

    Regulatory and technical environments continue to shift: process conditions may change, impurity thresholds tighten, or new applications emerge. Our technical teams catch potential issues early, updating control strategies, adjusting purification procedures, or refining analytical methods on the fly. Customer feedback often signals changes before they become industry standard. This loop—spanning shop floor to end application—keeps quality, safety, and customer satisfaction aligned with changing needs.

    Looking Forward: Proven Chemistry, Adaptive Solutions

    2-Methylbenzonitrile stands as an engine for innovation across pharmaceuticals, agrochemicals, and specialty sectors. Our experience as a direct manufacturer shapes every lot, as we adjust, improve, and tailor production through a steady commitment to quality, safety, and accountability. The differences between methylated and non-methylated benzonitriles, or among positional isomers, may feel subtle on the spec sheet; in reality, they drive profound changes in laboratory and manufacturing performance.

    Long-term relationships with customers and partners drive us to share knowledge, compare approaches, and avoid shortcuts. We regularly benchmark our product against both international standards and customer benchmarks, never settling for good-enough. As new uses for 2-Methylbenzonitrile develop—whether as a specialized intermediate, a metabolic probe, or the core of a green chemistry initiative—we continue to invest in expertise, technology, and training. This approach forms the backbone of our reliability and the enduring value our product delivers to each user, from R&D to full-scale plants.

    Top