Wusu, Tacheng Prefecture, Xinjiang, China sales7@sinochem-nanjing.com
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2,3-Dimethylaniline

    • Product Name 2,3-Dimethylaniline
    • Alias o-Toluidine
    • Einecs 202-455-6
    • Mininmum Order 1 g
    • Factory Site Wusu, Tacheng Prefecture, Xinjiang, China
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    687966

    Cas Number 87-59-2
    Molecular Formula C8H11N
    Molecular Weight 121.18 g/mol
    Iupac Name 2,3-Dimethylaniline
    Appearance Colorless to pale yellow liquid
    Melting Point 3-6 °C
    Boiling Point 216-218 °C
    Density 0.995 g/cm³ at 25 °C
    Solubility In Water Slightly soluble
    Flash Point 98 °C
    Refractive Index 1.557 (20 °C)
    Pubchem Cid 7371
    Odor Aromatic

    As an accredited 2,3-Dimethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,3-Dimethylaniline is packaged in a 500 mL amber glass bottle with a secure cap, labeled with hazard and handling information.
    Shipping **2,3-Dimethylaniline** should be shipped in tightly sealed containers, clearly labeled, and compliant with local and international hazardous materials regulations. Store and transport it under cool, dry conditions, away from incompatible substances. Handle with proper protective gear and maintain documentation for safety and emergency procedures during transit.
    Storage 2,3-Dimethylaniline should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep away from sources of ignition, heat, and direct sunlight. Store in a flammable chemical storage cabinet if possible. Use secondary containment to prevent spills and clearly label the storage area.
    Application of 2,3-Dimethylaniline

    Applications of 2,3-Dimethylaniline in Industrial Manufacturing

    As a manufacturer deeply engaged in the production of 2,3-Dimethylaniline, we supply this compound to industries where precise formulation, compliance, and integration into downstream processes are vital for high-quality chemical manufacturing. Below, we detail main application fields, focusing on genuine downstream market practices and technical benchmarks.

    1. Synthesis of Disperse Dyes for Polyester Fibers

    Major dye producers employ 2,3-Dimethylaniline as a building block during the production of specific azo and anthraquinone disperse dyes, tailored for high-performance polyester fiber coloration. Its introduction at the diazotization or coupling step impacts shade uniformity, thermal stability, and dye fastness. Our quality commitment ensures stable composition for consistent batch results, aligning with the requirements of advanced textile coloration plants.

    Industry compliance standards

    • ISO 16373-2:2020 (Textiles – Dyestuffs – Analytical Methods for Dyed Textile Products)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • OEKO-TEX Standard 100 Annex 6 Class I – Dye Input
    • REACH Regulation (EC) No 1907/2006 Annex XVII for Aromatic Amines

    Typical usage ratio

    • 10–30% by molar proportion in dye intermediate syntheses; actual quantity adjusted based on azo coupling stoichiometry, target chromophore, and required batch size.

    Downstream process integration

    • Introduced after initial sulfonation or nitration, reacting with coupling components under controlled temperature and pH in stirred reactors; purification precedes dye isolation or spray drying.

    Final product types

    • Azo-based disperse dyes (e.g., Disperse Orange 30, Disperse Red 60)
    • Anthraquinone disperse dyes
    • Finished masterbatch pigments for polyester fiber spinning

    2. Agrochemical Intermediate for Herbicide Manufacturing

    Producers of selective herbicides for cereal and rice agriculture utilize 2,3-Dimethylaniline as an intermediate in the multi-step synthesis of active ingredients, particularly in the aniline-condensation stage. The compound facilitates substitution patterns in benzoic acid derivatives, impacting selectivity and environmental fate, making precision handling and product consistency essential for compliance in crop protection chemical lines.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 (Quality Systems for Agrochemical Manufacturing)
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)

    Typical usage ratio

    • 5–18% of total reactant weight in the aniline condensation step; dosage optimized per reaction yield and desired substituent pattern for the active ingredient.

    Downstream process integration

    • Added to solvent-based condensation reactors during key steps of herbicide active ingredient synthesis, followed by caustic neutralization, filtration, and multi-stage purification ahead of formulation blending.

    Final product types

    • Technical grade herbicide actives (e.g., mefenacet, bromobutide derivatives)
    • 53–75% SC (Suspension Concentrate) herbicidal formulations
    • EC (Emulsifiable Concentrate) and WG (Water Dispersible Granule) finished goods

    3. Raw Material for Pharmaceutical Intermediate Synthesis

    2,3-Dimethylaniline serves pharmaceutical manufacturers as a core starting material in the stepwise construction of intermediate scaffolds for non-steroidal anti-inflammatory drugs (NSAIDs) and select CNS agents. The compound’s methylation pattern allows targeted substitution, influencing pharmacokinetic properties in downstream synthetic active pharmaceutical ingredient (API) routes. Strict quality control and full traceability help companies fulfill validated process and regulatory obligations.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • USP/NF and Ph. Eur. specifications for intermediates
    • 21 CFR Part 211 (Good Manufacturing Practice for Finished Pharmaceuticals)
    • EDQM CEP requirements for API pathway documentation

    Typical usage ratio

    • 8–22% by molar proportion in API precursor reactions; final dose determined by stoichiometry with acid chlorides or sulfonylating agents, route-dependent.

    Downstream process integration

    • Deployed in early-stage batch or continuous reactors for the synthesis of mono- or di-substituted aniline derivatives; product is then isolated as an intermediate, designated for later coupling or ring closure steps.

    Final product types

    • Intermediate scaffolds for NSAIDs (e.g., tolfenamic acid-type derivatives)
    • Precursors for CNS-related compounds (e.g., methylated aromatic amines)
    • API building blocks processed for global regulatory markets

    4. Intermediate in the Production of Specialty Rubber Accelerators

    Manufacturers of specialty vulcanization accelerators and antidegradants for high-performance rubber formulations incorporate 2,3-Dimethylaniline as a starting aromatic amine, enabling tailored reaction pathways that influence accelerator activity and polymer crosslinking behavior. The compound is critical in preparing rubber chemicals for demanding tire and industrial goods segments, where product traceability and impurity profiles affect final compound consistency.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management in Chemicals)
    • ASTM D4678 (Rubber Chemicals Test Methods)
    • REACH pre-registration and SVHC notification, if applicable
    • Global Automotive OEM chemical approval lists

    Typical usage ratio

    • 15–28% by weight in accelerator synthesis, tailored to final activity specification, reaction yield, and target impurity content.

    Downstream process integration

    • Metered into reactor vessels with carbon disulfide or sulfenyl chloride for the formation of sulfenamide-type accelerators; further purified before integration into solid or liquid rubber additive carriers.

    Final product types

    • Specialty rubber accelerators (e.g., N,N’-dimethyl derivative grades)
    • Antidegradants for light-colored rubber goods
    • Pre-dispersed masterbatch additives for high-performance tire and industrial rubber production

    5. Base Material in High-Temperature Polymerization Initiators

    Specialty chemical plants use 2,3-Dimethylaniline in the manufacture of polymerization initiators for engineering thermoplastics production, where tailored substituted aromatic amines help adjust initiation rates, color stability, and resistance to high-temperature processing. Accurate dosing and controlled impurity content are monitored according to each polymerization technology’s specific reactivity and end-use market requirements.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (Quality and Environmental Management)
    • EU REACH compliance for polymer additive usage
    • Chemical control requirements (TSCA for US production)
    • Polymer industry product stewardship programs

    Typical usage ratio

    • 6–14% by weight, dependent on end polymer grade, initiator system formulation, and targeted polymerization kinetics.

    Downstream process integration

    • Introduced in the early initiator synthesis as a reduction or functionalization agent; after final blending and purification, initiators are delivered to polymerization reactor charging tanks.

    Final product types

    • High-performance initiators for polycarbonate and specialty polyester resins
    • Polymer additives for engineering plastics extrusion
    • Stabilizers for advanced copolymer systems
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    Certification & Compliance
    More Introduction

    2,3-Dimethylaniline: Raising the Bar in Chemical Synthesis

    Our Experience with 2,3-Dimethylaniline in Plant Operations

    Running a chemical manufacturing plant demands a reliable backbone of intermediates, and 2,3-Dimethylaniline has always stood out for its strong performance in downstream synthesis. In our facility, we consistently see how the purity and tight specification of 2,3-dimethylaniline play crucial roles for our customers' production lines, especially those pursuing dyes, pigments, and pharmaceutical compounds. Every batch we produce must match very precise grades, with typical specifications like a molecular weight of 121.18 g/mol, a melting point near 9°C, and a boiling range around 231°C. We maintain GC purity over 99.5% because even a small deviation can ripple through finished-goods quality.

    Handling this aromatic amine, C8H11N, taught us a few things: small changes in methyl group position create major differences in performance. The 2,3- isomer we make brings specific reactivity in certain coupling and acylation reactions that the 2,4-dimethylaniline or 3,4-dimethylaniline models can’t quite match. The ortho and meta methyl groups present in our product result in less steric hindrance compared to the 2,4- isomer, which often tilts reaction pathways in favor of higher yields for targeted applications.

    Key Applications and Insights from Production

    The majority of our annual output goes to downstream users involved in the synthesis of azo dyes, where color consistency and reproducible shade are must-haves. Here, the high-purity 2,3-dimethylaniline supports batch-to-batch color matching, without introducing trace impurities that might otherwise change tone, shift reaction rates, or impact fastness. In pharmaceuticals, research teams value this isomer when building core scaffolds for antihypertensives, antifungals, and some local anesthetics. Its selectivity and defined reaction profile are valuable, especially in tightly regulated manufacturing processes where rejects translate into sunk costs.

    We observed that other dimethylaniline variants, such as the 2,4- or 3,5- isomers, often struggle to deliver the same intermediate profile as the 2,3-. On the plant floor, switching between isomers means recalibrating processes, adjusting purification protocols, and often facing an uptick in off-spec product. Our experienced team fields regular technical questions from long-time partners who appreciate details: a 2,3-dimethylaniline feedstock tolerates somewhat broader reaction conditions and shows fewer side reactions in halogenation and sulfonation processes, compared to 2,4- or 3,4- types. This subtle but fundamental difference continuously saves time and resources downstream.

    Rigorous Product Controls: Beyond Specification Sheets

    Spec-sheets only tell part of the story. From years of operation, we know that controlling residual moisture, low-level metal ions, and trace nitro impurities makes all the difference in plant-scale syntheses. We invest heavily in distillation and drying stages, eliminating batch memory and minimizing carryover between runs. In our plant, active vapor-phase monitoring and inline chromatography make sure the product meets these high standards so our partners never face catalyst poisoning or unplanned downtime in their reactors.

    Where some see 2,3-dimethylaniline as a commodity, experience tells us that details matter. For instance, the presence of even a few ppm of 2,4-dimethylaniline as a cross-contaminant can trigger off-colors in high-end pigments or negatively impact pharmaceutical intermediates. We focus on single-isomer runs and ongoing line cleaning, making sure what goes into our drums is exactly what our label says—no more, no less.

    The Benefits 2,3-Dimethylaniline Brings to Dye Manufacturers

    Large-scale dye production faces plenty of complexities, particularly as the market demands higher purity, lower toxicity profiles, and consistent environmental compliance. From the early days of our dye industry partnerships, we've heard consistent feedback: switching to our 2,3-dimethylaniline input improved dyeing reproducibility and reduced the number of process interruptions due to insoluble byproducts. Its consistent molecular structure and low trace impurity content cut down on process variability and minimize waste streams—key for meeting today’s zero-discharge objectives.

    Batch records from our leading clients show that the fewer fluctuations in input, the fewer unexpected color shifts or yield drops follow downstream. Some pigments are sensitive to even minor inputs of analogous amines, and we have plenty of data revealing that unwanted isomeric content can block further functionalization or lead to dull, less saturated color shades. Using a consistent, high-purity 2,3-dimethylaniline feedstock keeps high-throughput systems running without unplanned maintenance or discarded product, giving our customers more uptime and less scrap.

    Pharmaceutical Intermediates: Meeting Precise Needs

    Pharmaceutical-grade chemical intermediates live under some of the toughest regulatory scrutiny in the entire industry. Our years supplying this sector with 2,3-dimethylaniline taught us that customers need much more than ‘basic purity.’ They look for absolute traceability, exceptional batch-to-batch reproducibility, and full analytical support.

    Each lot leaves our site accompanied by a complete COA, as well as residual solvent and impurity profiling with detection limits well below pharmacopoeial requirements. We partner with manufacturers who use our material to build heterocyclic compounds and aromatic active ingredients. They know from experience: introducing other isomers or off-purity intermediates even at trace levels might feed unexpected side reactions or generate impurities that require costly downstream removal.

    While some suppliers focus on volume, our approach emphasizes consistency and documented assurance, supported by years of customer audits and performance feedback. Regulatory filings often reference our lot numbers directly. Unlike 2,4-dimethylaniline, where para substitution often means higher risk of N-oxidation during certain coupling reactions, the 2,3- provides tighter control of the intermediate’s electron density—this can make the crucial difference between an efficient scale-up and a stalled project.

    Differences Between 2,3-Dimethylaniline and Other Dimethylaniline Isomers

    Many users new to aromatic amine chemistry think the various dimethylaniline isomers are interchangeable. Our plant’s record books and customer feedback say otherwise. The 2,3-dimethylaniline’s methyl groups at adjacent ortho and meta positions tweak both steric and electronic effects versus, say, the 2,4- or 3,5- isomers. These differences translate directly to practical chemistry: reactivity in electrophilic substitution shifts, formation of key intermediates proceeds more cleanly, and certain unwanted byproducts simply do not appear.

    Some pigment makers switched from 2,4- to 2,3-dimethylaniline and quickly noticed a drop in batch rejects caused by shade drift or spotty fastness. Peering into reaction mixtures with NMR and GC-MS, our technical team documented how the 2,3- isomer participates more predictably in nitration, halogenation, and condensation routes. Its ortho-meta arrangement blocks over-substitution in the aromatic ring, helping downstream reactions target the right positions.

    Comparing it to 3,4-dimethylaniline or others, we see altered melting and boiling points, with ours offering more convenient handling for automated dosing or continuous flow processes. The oil-like character and low melting temperature cut out handling headaches; the sharp boiling point supports easier separation, helping clean up the process. Practically, switching isomers means revalidating your syntheses—a prospect buyers rarely wish to revisit after optimizing with our product.

    Operational Realities: Handling and Storage from the Manufacturer’s View

    Manufacturing, storing, and shipping 2,3-dimethylaniline brings its own set of operational realities. The amine’s clear, slightly yellowish liquid form means we use corrosion-resistant piping and tanks, mainly stainless steel, to avoid contamination and ensure long shelf life. Bulk storage employs nitrogen blanketing to protect from oxidation, and our loading teams are trained to prevent spills and undetected contamination.

    We support each shipment with stability data and shelf-life tracking, as some customers depend on batch scheduling over several months. Regular monitoring of peroxide levels, color, and trace acid values keeps product within customer acceptance limits, based on their downstream quality protocols. We run short distribution lines and operate our own fleet for regional customers so that, from batch finishing to end-user delivery, there’s no risk of product degradation or contamination.

    Environmental and Safety Considerations in Modern Production

    Across all chemical manufacturing, responsible stewardship shapes everything we do. 2,3-dimethylaniline’s aromatic nature means waste streams require close monitoring. We run closed-loop off-gas treatment, capture amine vapors, and treat all aqueous effluent to meet strict local limits before discharge.

    Our plant teams undergo routine safety training on amine handling, with personal monitoring for air exposure during drum filling and tank transfers. Regular audits, informed by incidents industry-wide, have led us to invest in smart sensors on valves and transfer lines, reducing the chance for leaks. Our environmental controls meet or exceed current regional and global standards because we recognize the long-term value of regulatory harmony and local community trust.

    We connect with other manufacturers and technology providers to exchange best practices in solvent recovery and emissions reduction. For our end-user partners, we share guidelines for safe storage, prompt use, and proper disposal of both product and packaging—recognizing our shared responsibility for environmental management.

    Supporting Innovation with Reliable Building Blocks

    Research groups at R&D labs, dye houses, and pharma firms often push us with questions about 2,3-dimethylaniline’s compatibility, long-term stability, and impact across new reaction types. Our technical support team runs pilot reactions, interfaces with process chemists, and regularly publishes process case studies that allow customers to anticipate integration challenges before plant trials. Direct dialogue, open data sharing, and timely sample support forge deeper partnerships—faster than transactional sales ever could.

    Working closely with downstream innovation teams, we've documented improvements in continuous process yield, sharper endpoint detection in nitration, and quicker cycle times for amide formation—all made possible by the reliability and reactivity of 2,3-dimethylaniline. Researchers reach better results not because the chemistry is easy, but because the feedstock stays consistent, sample after sample.

    Troubleshooting and Continuous Improvement on the Factory Floor

    From experience, we know there’s no such thing as a ‘finished’ process. Some of our plant’s best improvements started with challenges in the 2,3-dimethylaniline line: unwanted color in a pigment batch, pressure drops during distillation, or unexpected batch-to-batch reactivity swings. Our operators, chemists, and engineers work as one: troubleshooting from refining reaction times to rethinking solvent systems to keep final product quality high.

    Historically, standardization of raw materials across long production runs made the biggest impact on reducing costs and increasing yields. We track critical parameters—color index, trace impurity content, GC area percentage—linking every step from incoming aniline base to final packaging. Every issue flagged, either by in-house QC or customer feedback, turns into a project: we reevaluate equipment, process flows, or even modify standard operating procedures to lock in improvements.

    Addressing Industry Concerns: Purity, Safety, and Regulatory Shifts

    Market requirements for aromatic amines like 2,3-dimethylaniline evolve fast. Demand for increased analytical transparency, more sustainable manufacturing, and minimized impurity profiles shows no sign of slowing. We actively expand our in-house analytical labs, updating MS, GC, and HPLC platforms to identify trace-level contaminants, delivering actionable data both to customers and regulators.

    Every new regulatory proposal or change – from REACH restrictions to new toxicology studies – gets immediate review in our compliance and product management teams. We register every batch produced; comprehensive documentation supports customers during audits, filings, and any regulatory review. By providing our customers with advance notice of any anticipated changes, and facilitating transition to improved production methods or alternate grades, we build forward-looking partnerships rather than just putting product in drums.

    Continuous Investment for Tomorrow’s Applications

    Upgrading technology in chemical manufacturing always brings practical and financial challenges. Over the years, we have directed capital toward automation, precision dosing, real-time reactor analytics, and inline quality monitoring. These investments paid off in shorter lead times, higher spec adherence, and less unplanned downtime.

    As new markets arise—advanced functional materials, specialty pharmaceuticals, and high-performance pigments—our technical and production teams share a goal to adapt 2,3-dimethylaniline production quickly and safely for new regulatory and technical demands. We support trial campaigns, offer custom packaging, and fine-tune storage strategies for global and new-industry partners, understanding tomorrow’s needs may not look like yesterday’s.

    Strong Relationships Lead to Reliable Supply

    Years of hands-on work taught us that relationships drive long-term success. By remaining open to site audits, technical dialogues, and collaborative troubleshooting, we’ve built trust with major downstream users. They rely on our 2,3-dimethylaniline not just for its consistent molecular profile, but because our people stand behind every shipment.

    As global supply chains tighten and customers demand credible, reliable, and responsible manufacturing partners, we see the value multiply. Whether facing logistic bottlenecks, new regulatory hurdles, or technical scale-up challenges, our people draw from rich operational experience and a continuous commitment to product and process improvement.

    Final Thoughts from a Manufacturer's Standpoint

    Producing 2,3-dimethylaniline for diverse markets means more than just hitting a purity target. It’s about decades of practical knowledge, from the details of how isomer purity shifts reaction profiles, to the day-to-day realities of inventory management, logistics, and technical support. Our team remains eager to share this expertise and committed to being part of every project’s success, from pilot scale to full production.