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2,4,6-Trimethylaniline

    • Product Name 2,4,6-Trimethylaniline
    • Alias 2,4,6-Trimethylaniline
    • Einecs 202-423-8
    • 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

    251096

    Cas Number 88-05-1
    Molecular Formula C9H13N
    Molecular Weight 135.21 g/mol
    Appearance Colorless to pale yellow liquid
    Melting Point 1-3 °C
    Boiling Point 230-232 °C
    Density 0.984 g/mL at 25 °C
    Solubility In Water Insoluble
    Flash Point 100 °C (closed cup)
    Purity Typically ≥99%
    Synonyms 2,4,6-Trimethylaniline, Mesidine
    Refractive Index 1.553-1.556 at 20 °C

    As an accredited 2,4,6-Trimethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with tightly sealed cap, hazard label, and clear product name. Contains 100 grams of 2,4,6-Trimethylaniline.
    Shipping 2,4,6-Trimethylaniline should be shipped in tightly sealed containers made of compatible materials, protected from moisture and heat. It must be labeled according to hazardous material regulations, including UN number 2810 (if applicable). Transport via ground, air, or sea should adhere to local, national, and international chemical shipping guidelines to ensure safety.
    Storage 2,4,6-Trimethylaniline 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. Keep it out of direct sunlight and moisture. Storage in a flammable chemicals cabinet is recommended. Always handle with proper personal protective equipment to prevent exposure.
    Application of 2,4,6-Trimethylaniline

    Applications of 2,4,6-Trimethylaniline in Industrial Manufacturing

    As a direct manufacturer of 2,4,6-Trimethylaniline, we supply this key raw material to specialized downstream sectors that require traceable quality and compliance support. The following application sections detail real-world integration of 2,4,6-Trimethylaniline in value-added manufacturing with a focus on distinct fields, formula quantities, regulatory frameworks, production workflows, and finished products.

    1. Dye and Pigment Intermediate Production

    2,4,6-Trimethylaniline is a critical building block in the synthesis of azo and anthraquinone dyes, where it introduces methyl functionalities to enhance color fastness, solubility, and resistance profiles for specialty pigments. It reacts in diazotization and coupling stages, specifically selected for its minimal side reactivity and high conversion yield in manufacturing high-performance textile dyes and organic pigments for plastics processing industries.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • REACH (EC No 1907/2006) registration for import and use within EU
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EN 71-3 (Safety of toys – migration of certain elements) for pigments in toys

    Typical usage ratio

    • 5%–18% by weight in dye synthesis, depending on the chromophore structure and targeted substitution degree; exact proportion adjusted based on final product color intensity and substrate compatibility.

    Downstream process integration

    • Added to reaction vessels prior to or during diazotization and coupling for azo dyes; incorporated in the condensation stage for anthraquinone derivatives.

    Final product types

    • High-purity textile disperse dyes
    • Organic pigments for plastics and coatings
    • Printing inks for industrial applications
    • Colorants for synthetic fibers and films

    2. Pharmaceutical Intermediate Synthesis (API Manufacturing)

    Within the pharmaceutical sector, 2,4,6-Trimethylaniline serves as a selective intermediate in custom syntheses, particularly for active pharmaceutical ingredients (APIs) that require specific methylaniline motifs. Its defined substitution pattern enables medicinal chemists to build drug molecules with targeted activity profiles and favorable pharmacokinetics. It is typically introduced in early or mid-stage synthetic routes, where structural integrity and minimal byproduct formation are essential.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) – ICH Q7 for API intermediates
    • USP-NF (United States Pharmacopeia – National Formulary) for purity control where applicable
    • EDQM (European Directorate for the Quality of Medicines) monographs and CEP procedures
    • 21 CFR Part 210/211 (US FDA current Good Manufacturing Practice)

    Typical usage ratio

    • Typically 0.8–1.25 molar equivalents relative to the targeted drug nucleus on a multi-kilogram to tonnage batch scale; stoichiometry varies with substituent requirements and process yield optimization.

    Downstream process integration

    • Inserted as a key intermediate in the early functionalization stage or in ring closure reactions during the assembly of complex aromatic pharmaceuticals. Used in both batch and continuous flow synthesis settings.

    Final product types

    • Benzoxazole and benzothiazole-based APIs
    • Antimicrobial and anti-inflammatory drug precursors
    • Specialty cardiovascular drugs
    • Proprietary pharmaceutical R&D intermediates

    3. Antioxidant and Stabilizer Manufacture for Polymer Additives

    This raw material finds specialized use as a precursor or co-reactant in the manufacture of hindered amine light stabilizers (HALS) and antioxidant blends for polyolefin, polystyrene, and engineering thermoplastics. It modifies performance characteristics by providing tertiary amino structure for radical scavenging systems, thereby extending plastic lifetime under UV and thermal stress in end-use applications.

    Industry compliance standards

    • Food Contact Compliance: EU Regulation No. 10/2011 for plastics intended to contact food (where applicable)
    • US FDA 21 CFR 177.1520 (polyolefins additives in food packaging)
    • ISO 14021 (Self-declared environmental claims – additive release test guidance)
    • DIN EN ISO 4892-2 (Plastics – Methods of exposure to laboratory light sources)

    Typical usage ratio

    • 1%–4% by weight in finished additive masterbatch formulations. Exact level is determined by polymer matrix type, UV stability demands, and end-use exposure conditions.

    Downstream process integration

    • Reacted in intermediate synthesis of HALS core structures; subsequently blended into additive concentrates during polymer compounding or directly dosed during polymerization.

    Final product types

    • HALS masterbatch for polyolefins
    • Antioxidant blends for styrenics and engineering resins
    • UV stabilization packages for automotive and outdoor plastics
    • Food packaging additives (where permitted)

    4. Agrochemical Synthesis (Herbicide and Plant Growth Regulator Intermediates)

    Our material integrates into agrochemical production workflows as a precursor in synthesizing substituted aniline-based herbicides and certain plant growth regulators. Its methyl-substituted aromatic ring enhances biological selectivity in targeted agrochemicals and facilitates downstream derivatization steps essential for active ingredient manufacture.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material intermediate purity
    • ISO 9001:2015 Quality Management for chemical synthesis
    • EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) for US-market agrochemical raw materials
    • Chinese GB/T 1600–2001 (Technical Requirements for Pesticide Intermediates)

    Typical usage ratio

    • Varies from 2% to 8% by weight in formulation of active intermediate phase, depending on the chemistry route and selectivity demands of the finished molecule.

    Downstream process integration

    • Charged during the initial condensation, amidation, or urea formation step in technical grade herbicide synthesis. Also incorporated into multi-step flow reactions for plant regulator actives.

    Final product types

    • Methylated aniline herbicide mother liquor
    • Plant growth regulator intermediates
    • Agrochemical actives for cereal, oilseed, and specialty crop protection markets
    • Pre-emergent and post-emergent herbicide formulations

    5. Photographic Chemical Synthesis

    This material plays a role as a substituent-building intermediate in the preparation of color developer agents and couplers used in photographic and imaging industries. Its unique methylation pattern provides enhanced processing stability for color developers and assists in tuning spectral absorption ranges for advanced imaging emulsions.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical synthesis
    • ISO 18902 (Imaging materials – Photographic films – General requirements)
    • RoHS Directive (for restrictions relevant to imaging electronics integration)
    • Photographic Industry Technical Standards for chemical supply purity (by local associations)

    Typical usage ratio

    • Ranges from 3% to 7% by mass basis in developer and stabilizer chemical formulas; exact dose established through pilot runs based on developer lifetime and imaging performance requirements.

    Downstream process integration

    • Incorporated into the developer/coupler synthesis step via nucleophilic aromatic substitution; final blends prepared for use in color film and paper processing solutions.

    Final product types

    • Color film developer concentrates
    • Stabilizer solutions for photographic processing
    • Photographic color couplers supporting digital imaging workflows
    • Archival microfilm chemical systems

    6. Specialty Chemical Catalysts and Ligand Synthesis

    2,4,6-Trimethylaniline is utilized in high-value specialty chemical workflows to construct ligands for homogeneous catalysis and as a directed precursor for organocatalyst design in asymmetric synthesis. The methyl groups confer specific steric and electronic properties crucial for modern catalytic transformations in fine chemical and performance material production.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for specialty chemical manufacture)
    • Responsible Care global charter for safe handling of process catalysts
    • Local chemical safety data sheet compliance (EU, US, and APAC)
    • In-house traceability and purity audit standards

    Typical usage ratio

    • Usually 0.2–1 molar equivalent as a ligand precursor in metal-complex formation; precise level adjusted to match targeted activity and catalyst recovery performance.

    Downstream process integration

    • Introduced in the early-stage ligand assembly or complexation step; subsequent purification and metalation executed as part of homogeneous catalyst kit preparation or direct batch charging in fine chemical synthesis.

    Final product types

    • Palladium and ruthenium coordination catalysts
    • Custom organic ligands for asymmetric transformations
    • Homogeneous organometallic catalyst systems for fine chemicals
    • Chiral synthesis auxiliary materials
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    Certification & Compliance
    More Introduction

    2,4,6-Trimethylaniline: A Vital Building Block in Modern Chemistry

    Introducing Our Journey with 2,4,6-Trimethylaniline

    Every time we pour a batch of 2,4,6-Trimethylaniline through our reactors, we know we are contributing a core ingredient that supports production lines all over the world. At the plant, we see this aromatic amine not just as a raw chemical but as a material that reflects decades of chemistry know-how, tested procedures, and hard-earned manufacturing experience. This compound, with the formula C9H13N and CAS number 88-05-1, comes clear or pale yellow. Its sharp, almond-like odor makes it recognizable in the production area, reminding us and our technical team to handle it with the respect that precise work demands.

    2,4,6-Trimethylaniline goes by several names in labs and commercial lots: mesidine, 2,4,6-trimethylbenzenamine, and sometimes tmesidine by those who’ve been in the industry long enough to use the shorthand. It saw widespread use as early as the postwar chemical expansion and never left the scene, thanks to its clean reactivity and dependable output across a variety of synthetic pathways.

    Specifications We Stand By

    In manufacturing, delivering a reliable product goes well beyond published specs. Markets expect that 2,4,6-Trimethylaniline arrives clear of visible particulates, bringing an assay above 99.0% by GC for the majority of fine chemical and pharma clients. Moisture levels are monitored—too much water interferes with hydrogenation and distillation, so target below 0.2%. We routinely verify residue on ignition under 0.1%. Our teams run GC/MS and HPLC checks to stay ahead of potential process drifts, controlling byproducts like o-xylene and p-xylene isomers. Getting this right takes integrated quality control, not shortcuts.

    Its distinctive trimethyl substitution pattern means it crystallizes out of solvents where some other anilines will not. That trait can make a big difference to downstream processes, from dye intermediate manufacture to coupling reactions in agrochemical synthesis. Handling requirements demand good ventilation, splash-resistant gloves, and—given the risk for methemoglobinemia—strict personal monitoring. Over the years, our shop-floor teams have helped institute regular training that goes beyond regulatory requirements because practical safety steps keep long-term expertise in-house.

    Key Roles in Modern Industry

    2,4,6-Trimethylaniline helps form the backbone of several commercial and industrial applications. The most established use involves production of specialty dyes, notably the azo, triarylmethane, and anthraquinone families. We see it as the preferred amine for certain fast dyes, where steric shielding from the three methyl groups imparts desirable resistance to photobleaching and washing, critical for fabrics and printing inks that meet textile specifications.

    In the pharmaceutical world, 2,4,6-Trimethylaniline serves as a key starting material and as a protected synthetic intermediate when making antihypertensive drugs, anaesthetics, or antineoplastic agents. Process chemists appreciate how its layout curbs side-reactions and can offer high yields with precise functionalization. Year after year, we’ve partnered with pharmaceutical companies shifting from lab scale to campaign manufacturing, sharing what we’ve learned with tough-to-handle reactions, hazardous waste management, and purification bottlenecks.

    Catalyst development also draws heavily on this compound—both as a ligand base or as a nucleophile in derivatizing metal complexes. Our dialogues with academic partners and industrial R&D teams focus on batch reproducibility and how trace impurity profiles can change a whole reaction outcome, whether in a pilot plant or a 3,000-liter hydrogenation reactor. This is not a job for random sourcing; small impurities from one supplier’s process can spell trouble where consistency determines success or failure.

    Differences from Similar Aromatic Amines

    Chemists sometimes ask why they can’t swap in toluene, xylidine, or plain aniline instead. The three methyl groups at ortho and para positions change the entire reactivity landscape. 2,4,6-Trimethylaniline resists nucleophilic attack at the ring carbon positions, which gives both stability and selectivity in subsequent transformations. That boost in steric hindrance pays off during N-acylation and sulfonation steps. Other isomers like 2,3,6-trimethylaniline do not yield the same product distribution, a phenomenon we’ve tracked through both mass spec and hands-on trial runs.

    Compared to aniline, which rapidly oxidizes and couples uncontrollably under many conditions, 2,4,6-Trimethylaniline keeps its identity even in harsh oxidative chemistry. That makes it the molecule of choice for electronic dye precursors and certain polymerization initiators where you cannot afford batch-to-batch drift. We learned early in our production that substituting with xylidines or lutidines changes viscosity and impacts filtration—small parameters that matter when scaling up to tonnes.

    Practical Considerations from Plant to Customer

    Packing this compound to suit real-world needs takes planning. The crystalline solid flows best when kept cool and dry—big humidity swings encourage lumping, while elevated temperature prompts discoloration. We secure shipments in high-density polyethylene drums lined with Mylar for projects that face long ocean transit and increased risk of moisture ingress. Customers seeking solutions for blocked feeders or caking in automated weighers have taught us to re-examine anti-caking agents and rethink our particle size specs, often leading to investments in milling and sieving support.

    Efficient loading onto vehicles or into containers becomes a routine focus as volumes grow. We monitor not just lot purity, but all the many things that can go wrong—broken liners, lost labels, secondary containment failures. In chemical manufacturing, it's rarely the chemistry itself but the logistics where trouble starts. By walking every order down the line ourselves, and reviewing past hitches, we help ensure our QC work keeps pace with order fulfillment.

    The Value of Process Integration

    Unlike brokers, we manufacture this product under one roof—from sourcing clean, methylated aromatics to hydrogenation, distillation, and final crystallization. We know where our methyl groups come from (often via isomerization technology from indigenous toluene). Deciding on kettle size, column height, and agitation—all these parameters matter more than what surface-level certifications show. Over the years, teams have shared hundreds of improvements, like better column packing to minimize hold-up or streamlining solvent swaps that cut batch cycle time.

    Every drum pulled off our line draws from a process informed by continuous feedback from analytical chemists, plant operators, and technical sales. We’ve come to trust experience, not just data sheets. When a chromatogram looks off or a purity trend shifts, the shift leader works alongside the lab head—sometimes at midnight, sometimes at shift change. We value consistent hands on deck and work to keep skills fresh, training new hires as hands-on partners, not as hands-off observers.

    Trends and Market Shifts

    Global shifts in regulation and market demand keep us on our toes. Some of our customers in Europe lean toward EcoVadis and other sustainability audits, and we’ve adapted. In-house, we reduce mother liquor waste, recover solvents aggressively, and reconsider steam trap layouts every fiscal year to minimize energy draw. Some raw material streams rise and fall in price according to global feedstock availability. In recent drought years, we've changed wash water recovery systems to keep net water use in check.

    Novel electronics and green energy projects have brought new uses to the material, especially for specialty polymers and photoresist components. These buyers bring new scrutiny: tighter specs and new impurity scans. Our customer support team fields questions not only about batch numbers or MSDS details but about trace metals, environmental impact, and potential for ultratrace leachable organics. Just delivering a drum is rarely the end—long-term accounts push for transparency, collaborative troubleshooting, and support through scale-ups.

    Solving Challenges in Application

    Our support doesn’t stop when an order leaves the dock. Textile dye manufacturers report that process water mineral content can shift color outcomes—so we collaborate to analyze local water and suggest optimal rinse stages. Pharmaceutical customers face issues with product oxidation during mid-reaction holds. Our engineers co-develop in-line filtration systems and propose antioxidants suited to their cGMP environment. We tune product granularity for downstream handling, preventing static charge build-up in pneumatic feed systems.

    For those moving from kilo lab work to full pilot plants, we lend our processing insights—choosing the right solvent for crystallization, troubleshooting filtration speed, and helping pin down storage practices. Years in the field have taught us to spot bottlenecks early. The best technical support starts with nuanced listening, then offering what has worked (and what hasn't) from our own lines. Customers bring new questions every month; finding real solutions means direct engagement, sustained learning, and turning feedback into better products for all.

    The Path Forward: Building Safety, Sustainability, and Trust

    Current debate over aromatic amines and potential carcinogenicity in some applications looms large. We face these concerns head on by adhering to best practices, staying out in front of regulatory requirements, and supporting customers with transparent documentation. Down in our plant, real people handle each drum, and their health always guides our operational priorities. Air monitoring, regular bloodwork, and PPE are standard, not optional; our improvement committees include seasoned operators and medical staff, not just managers and compliance officers.

    Developing greener processes gives us an active role in shaping the sustainability of chemical supply chains. Over the last few years, we’ve adapted continuous distillation where possible to trim energy use and waste. We shifted to lower-toxicity solvents for washing and adapted our scrubber design to catch fugitive emissions, taking lessons from both successes and stumbles. Customers sometimes request biobased or carbon-neutral options for upstream aromatics. We're honest about what can be achieved today, and we look for partners to develop next-generation sourcing together.

    Conclusion: Our Commitment to Quality and Partnership

    Supplying 2,4,6-Trimethylaniline means more than filling orders—it involves shared expertise, attention to every step, and an eye toward future challenges. Unlike bulk commodity trading, manufacturing this product well requires hands-on familiarity with the equipment, teamwork up and down the value chain, and a relentless focus on getting things right. We learn from every batch, every trial, and every conversation with the people who depend on our materials. That’s how we protect quality, innovate responsibly, and build relationships that last.

    Experience remains our most valuable raw material. By sharing what we've learned, acting on feedback from the factory floor to the R&D lab, and taking each client’s goals to heart, we keep raising the standard for 2,4,6-Trimethylaniline manufacturing. If you’re pushing for technical solutions, practical support, or honest discussions about what this molecule can do for your business, our doors—and our lines—remain open.