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3,4-Dimethoxytoluene

    • Product Name 3,4-Dimethoxytoluene
    • Alias Veratrole
    • Einecs 210-656-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    219709

    Name 3,4-Dimethoxytoluene
    Cas Number 13719-48-1
    Molecular Formula C9H12O2
    Molecular Weight 152.19
    Appearance Colorless to pale yellow liquid
    Boiling Point 216-218 °C
    Melting Point -24 °C
    Density 1.044 g/cm3 (at 25 °C)
    Refractive Index 1.521 (at 20 °C)
    Flash Point 89 °C
    Solubility In Water Insoluble
    Smiles COC1=CC(=C(C=C1)C)OC
    Pubchem Cid 18616

    As an accredited 3,4-Dimethoxytoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 mL of 3,4-Dimethoxytoluene, sealed with a screw cap and labeled with hazard and safety information.
    Shipping 3,4-Dimethoxytoluene is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported following regulations for flammable liquids, kept away from sources of ignition and oxidizing agents. Proper labeling and documentation are required, and handlers must use appropriate protective equipment during transport.
    Storage 3,4-Dimethoxytoluene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, or direct sunlight. Keep it separate from oxidizing agents, acids, and bases. Ensure appropriate labeling and secondary containment to prevent leaks or spills. Store at room temperature and handle using standard chemical storage protocols.
    Application of 3,4-Dimethoxytoluene

    Applications of 3,4-Dimethoxytoluene in Industrial Manufacturing

    3,4-Dimethoxytoluene serves as a key intermediate across various chemical synthesis routes, offering reliable performance in pharmaceutical, specialty chemical, agrochemical, and dye manufacturing. Developed and supplied in bulk by our facility, this compound meets demanding quality standards for critical downstream processes.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients

    Pharmaceutical manufacturers use 3,4-Dimethoxytoluene as an essential building block in synthesizing specific APIs, including selective monoamine oxidase inhibitors and antipsychotic agents. The compound participates in multi-step synthesis via demethylation, halogenation, and coupling reactions, primarily under GMP-controlled environments. It enables production of high-purity intermediates that undergo further transformation into regulated drug substances, meeting global market approval requirements.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Directive 2003/94/EC
    • US FDA 21 CFR Part 211
    • Ph. Eur., USP, JP monographs for finished APIs

    Typical usage ratio

    • Applied at 0.8 to 1.2 molar equivalents as a synthesis precursor relative to final API active moiety
    • Adjusted according to synthesis yield and impurity profiles as monitored by HPLC

    Downstream process integration

    • Introduced in Step 1 or 2 of multi-step pharmaceutical synthesis (e.g., O-demethylation followed by halogenation/amination)
    • QC performed after each critical step to monitor impurity carryover

    Final product types

    • Monomethylated benzene derivatives for CNS drug classes
    • Phenolic precursors for MAO inhibitor APIs
    • Finished tablet and injectable pharmaceutical forms

    2. Agrochemical Intermediate for Herbicide and Fungicide Synthesis

    Leading agrochemical producers integrate 3,4-Dimethoxytoluene to construct methoxy-substituted aromatic rings in selective herbicides and fungicides. The compound undergoes demethylation and condensation with amides or heterocycles, creating unique functional groups durable under field conditions. Used under strict process and environmental controls, it assists in producing stable actives with targeted crop protection profiles.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 for plant protection substances
    • ISO 9001 for agrochemical production
    • REACH registration where required within the EU

    Typical usage ratio

    • Utilized at 1.0 to 1.5 equivalents relative to downstream arylchloride or arylamide moieties
    • Adjusted for desired methoxy content and final product stoichiometry

    Downstream process integration

    • Added as the aromatic base for acylation prior to formulation of technical concentrates
    • QC includes GC-MS verification of methoxy group retention post-reaction

    Final product types

    • Herbicidal active ingredients (e.g., substituted phenylamides)
    • Fungicidal pre-mixes for seed and foliar treatment
    • Ready-to-use crop protection formulations

    3. Synthesis of Specialty Aromatic Chemicals

    Specialty chemical manufacturers use 3,4-Dimethoxytoluene as a precursor for synthesizing anisole-based flavor and fragrance compounds, antioxidants, and fine chemical intermediates. Through Friedel–Crafts alkylation, oxidative coupling, or reduction, the material is transformed into tailored molecules for consumer and industrial end-users. Its specific electron-donating profile supports high specificity during ring substitution, minimizing side reactions.

    Industry compliance standards

    • IFRA (International Fragrance Association) Safety Standards
    • ISO 9001 quality management for specialty chemical production
    • REACH registration and ECHA data for substances in Europe
    • Food Chemicals Codex (for flavor ingredients)

    Typical usage ratio

    • Usage ranges from 0.5 to 3.0 weight-% in multi-step syntheses, depending on target aromatic content
    • Adjusted for yield optimization and downstream purity constraints

    Downstream process integration

    • Incorporated during Step 1 aromatic core formation or Step 2 alkylation
    • Intermediate purification by distillation or crystallization prior to final derivatization

    Final product types

    • Food-safe flavor enhancers (e.g., vanillin derivatives)
    • Fragrance intermediates for perfumery
    • Antioxidant additives for polymers and consumer goods

    4. Dye and Pigment Processing

    Industrial dye manufacturers adopt 3,4-Dimethoxytoluene for producing methoxy-containing azo- and anthraquinone dyes. It provides the aromatic ring for diazotization and coupling, resulting in vivid, high-stability colorants for textile and plastics. Strict batch monitoring ensures color consistency and compliance with environmental discharge limits, especially in effluent-sensitive regions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile inputs
    • ZDHC MRSL (Manufacturing Restricted Substances List)
    • REACH Annex XVII for dye substances
    • ISO 14001 environmental management

    Typical usage ratio

    • Typically 0.7 to 1.5 equivalents relative to the diazonium component in multi-step dye synthesis
    • Load adjusted based on target chromophore and substrate binding requirements

    Downstream process integration

    • Introduced in early-stage aromatic feedstock blending prior to nitration or sulfonation
    • Product purified through sequential crystallization and solvent-extraction

    Final product types

    • Textile dyes with enhanced wash-fastness and light stability
    • Plastic colorants for specialty molding applications
    • Printing ink pigments for flexographic and gravure processes

    5. Electronic Chemicals and OLED Intermediates

    Producers of organic light-emitting diode (OLED) materials and other electronic chemicals rely on 3,4-Dimethoxytoluene for functionalizing aromatic cores. Its controlled substitution pattern supports precise electron-donating properties needed in synthesizing polyaromatic frameworks and charge transport materials. Handling occurs within cleanroom and high-purity environments to meet strict defect and trace metal requirements.

    Industry compliance standards

    • JEITA standards for electronic material purity
    • SEMI C93 purity specification for specialty organics
    • ISO 14644 cleanroom standards for production
    • IEC 61249-2-21 for halogen-free material labelling

    Typical usage ratio

    • Mixed at 0.1 to 1.0 equivalents based on target aromatic structure in small-molecule OLED synthesis
    • Ratio varies with end-use device requirements and batch scale

    Downstream process integration

    • Added during core arylation or methoxylation phases of host/guest molecule synthesis
    • Purification under reduced-pressure conditions to achieve ppm-level impurity profiles

    Final product types

    • Small-molecule organic semiconductor intermediates
    • Hole-transfer material precursors for OLEDs
    • Functionalized aryls for light-emitting display panels
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    Certification & Compliance
    More Introduction

    3,4-Dimethoxytoluene: Steady Quality Direct from the Manufacturer

    Reliable Sourcing for Chemical Synthesis

    Chemical production demands more than just base ingredients. We’ve been manufacturing 3,4-Dimethoxytoluene for over a decade, which means every drum or pail reflects not only the raw material itself, but also the rigorous process controls our technicians enforce daily. Our team emphasizes repeatability and traceability down to the lot. Quality starts at our reactors—never at a trader’s warehouse.

    Key Details for Bench and Bulk Users

    3,4-Dimethoxytoluene is an aromatic compound that features two methoxy groups at the 3 and 4 positions of a methylated benzene core. Its formula, C9H12O2, distinguishes it from similar toluene derivatives. We provide this product in clear, nearly colorless liquid form, verified by both GC and NMR to minimize uncertainty on purity. Our runs routinely reach 99%-plus purity, with moisture below 0.1%, since most downstream processes cannot tolerate higher content without effect on yield.

    We produce this compound in batch reactors set up for both research and commercial orders. Over time, process chemists have helped optimize reaction times and workup to reduce residual starting materials and minimize colored impurities. Many customers come to us after trying less consistent supplies and running into spectral outliers—our in-house lot data always travels with the shipment, so labs can check back if troubleshooting is required. The close integration between our QA team and production makes isolation and solutions far more direct than dealing through distributors.

    Consistent Performance in Fine Chemical Synthesis

    Most buyers of 3,4-Dimethoxytoluene put it to work as a substrate or intermediate in pharmaceutical and agrochemical synthesis. The two methoxy groups activate the benzene ring for further substitution, and a methyl group anchors position-specific transformations. Having run test reactions ourselves, we know selective formylation or halogenation works best when trace contaminants (especially phenolic or demethylated species) are controlled. Small impurities load up on columns and can degrade catalyst activity in downstream steps.

    Many advanced laboratories move from analytical grade to kilogram-scale orders only after test reactions succeed unambiguously—this step-up requires all lots to remain chemically identical. We use traceable, in-house spectra to confirm consistency, so synthetic chemists can rely on their process validity. Bulk producers working on APIs or fine flavors often comment that variable sources of aromatic intermediates spell trouble for batch reproducibility. Longstanding relationships with our partners arise from catching and resolving deviations long before they travel downstream.

    How It Stands Against Similar Compounds

    Some clients ask whether 2,5-Dimethoxytoluene or 2,4-Dimethoxytoluene can substitute for 3,4-Dimethoxytoluene. The difference lies not only in the substitution pattern on the benzene ring, but in resulting reactivity profiles. Electronic distribution shifts with each pattern, strongly influencing reaction efficacy in Suzuki coupling, Friedel-Crafts alkylation, and oxidative transformations. In our hands, isomers display marked differences when exposed to the same downstream chemistries: the 3,4-substitution often displays superior selectivity in certain palladium-catalyzed routes or in regioselective demethylation. Relying on a single isomer reduces purification hassles and improves yield calculation reliability.

    Process engineers appreciate that our lots come with confirmed isomeric ratios so that later product validation doesn’t require tracking down a technical supplier error. Labs pursuing natural product synthesis or preparing pharmaceutical scaffolds often deal with stringent regulatory validations, and having documentation that tracks every drum to its batch analysis makes compliance far easier. We understand that documentation headaches often start with ambiguous upstream sourcing. Unlike mixed-batch lots passed through large trading houses, direct-from-manufacturer sourcing maintains integrity.

    Practical Experience Shapes Quality Control

    Quality inspectors check each batch for main peak purity, but they also examine UV spectrum and evaluate color against an internal standard. We noticed early on that subtle colored byproducts sometimes affect sensitive downstream color reactions, so we established a double-filtration protocol and light-transmissivity checks. Water content is another critical point—toluene derivatives are hydrophobic, but trace water disrupts Grignard or alkyl lithium applications. Our facilities run vacuum distillation lines on-site to reduce and check for water before final containerization.

    We maintain a systematic cleaning process for reaction vessels and filling lines, with periodic cross-contamination checks. This diligence comes from direct experience: a single unflushed transfer hose once delayed a critical scale-up project by contaminating a batch with a previously run anisole-type intermediate. As a result, QA now mandates intermediate cleanouts between each product changeover. Lab teams document every run, and all routine test results ship with product.

    Applications that Depend on Manufacturer Integrity

    Downstream processes convert 3,4-Dimethoxytoluene into specialty building blocks—sometimes even into fragrance ingredients, antioxidants, or fine specialty chemicals. Pharmaceutical developers depend on reliable sourcing, as does anyone requiring independently reproducible results. The unpredictability of third-party resellers lies not just in their paperwork, but in delayed identification of offspec material. Direct feedback from process chemists, combined with robust record keeping, guides our continuous refinement cycle. Only a manufacturer taking direct responsibility can guarantee consistent fine-tuning and prompt correction in response to customer observations.

    Biotechnology firms and flavor houses benefit from our process transparency. Once, a client scaling up a new flavor synthesis flagged an unexpected trace impurity, which turned out to arise from a minor chromatography solvent residue. Our QA solved the issue by changing the column drying protocol, and kept the client updated through technical bulletins—even small changes may carry downstream. Process transparency helps partners audit and validate processes without friction.

    Batch Documentation: What Matters

    Every outgoing lot ships with the relevant analytical spectra, moisture analysis, and identification data. Unlike bulk traders breaking shipments and reblending from variable sources, we keep incoming raw materials, process steps, and outgoing product linked by internal batch codes. Analytical runs are saved for every shipment—if a customer sends back questions about reactivity, we pull up matching chromatograms to investigate. Regulatory paperwork can also trace steps from feedstock through to packed product. This batch-level transparency minimizes surprises and supports customer audits.

    On request, we provide technical follow-up on any unusual analytics, such as unexpected NMR peaks, minor UV shifts, or traces of unanticipated side-products. We know that method validation often relies on anticipated input properties. That’s why upstream consistency is more than a marketing line—it downshifts the risk of late-stage batch failures, especially in GMP settings or for flavor/fragrance registrants.

    Reducing Delivery Bottlenecks

    Producers accustomed to third-party channels often run into shipment variability and last-minute out-of-stock situations. Our in-house logistics team controls scheduling from manufacturing line to end-user dock, with on-site tracking rather than dispatching through intermediaries. Any supply interruptions get communicated immediately, so downstream producers can adapt their mixing or synthesis schedules in time. Predictability becomes more valuable as batch values rise. Our just-in-time scheduling works because we control the bottlenecks in-house—no dependency on outside approval or delayed restocking.

    We learned early from delays with external warehouses that direct delivery requires tailored packaging. 3,4-Dimethoxytoluene fills into polyethylene-lined steel drums for bulk delivery, with smaller glass containers used for bench-scale labs. Containers get pre-washed, weighed, and checked for suitable rinser agent residue, as some glass chemistry labs observed trace leaching from substandard containers. Our packaging process grows from chemists’ and process users’ actual observations—feedback cycles prompt regular updates.

    Managing Regulatory and Environmental Requirements

    As direct producers, we make compliance straightforward. Local and national standards see regular updates, and we regularly review both internal and external testing, so there are no late surprises for end users with shifting regulatory frameworks. Waste minimization has come to represent not just an environmental concern, but an input cost factor as solvent recoveries tighten worldwide. Our processes have reduced solvent use per batch by optimizing extraction steps and switching to higher-yield workups—these shifts do not occur by accident, but by direct observation and trial.

    Our environmental team tracks both air and liquid waste. Solvent recycling loops have increased, and spent aromatic streams are treated to minimize both local emissions and staff exposure. Experienced staff know that small spills or venting issues can disrupt operations for weeks and set back shipment schedules, so both training and infrastructure investments center on preventive action. We keep transparent records available so clients audit their own footprints as supply chain accountability evolves.

    Mistake Prevention: The Value of Direct Manufacturing

    Mistakes cost most when they show up late. Experienced chemists rely on trusted upstream sourcing because discrepancies—off-color, unusual smell, or invisible contaminants—can cripple a batch worth thousands. We respond to every feedback, and past improvements often trace back to client observations. Direct sourcing means the same group who makes, fills, and tests the material hears and implements process changes.

    We extend sampling flexibility for validation runs, allowing technical clients to test multiple lots side-by-side. Unpredictable origin or blended shipments, often the norm for non-direct sales, can turn up inconsistent spectral data that undermines expensive downstream validation. Our exposure comes from working side-by-side with customer process engineers to diagnose tricky outcomes, which has led to modifications in purification steps or additional optional drying cycles. This hands-on troubleshooting only works when the manufacturer can adjust production practices directly.

    Research, Development, and Customization

    We invest in research to refine every stage, from daily production to the last packaging adjustment. Our R&D supports custom volumes and specs under controlled, documented conditions. As new synthetic approaches or reactions develop, our team adapts purification, drying, and filtration to meet updated expectations. Research clients running exploratory reactions appreciate open dialogue, even post-purchase. Our tech group shares reaction tips, observed compatibilities or incompatibilities, and practical treatment or work-up suggestions. This communication not only resolves bottlenecks, but helps innovation move faster by anchoring experiments in reproducible upstream quality.

    Rooted in Experience, Ready for Your Next Project

    Over the years, we’ve learned that a single lot’s reliability can affect years of downstream research or production. Only a manufacturer, not a trader or reseller, sees both the process inputs and long-term results. We’ve grown with clients, adapted production steps for new industry standards, and tackled unexpected technical barriers because we hear about them first-hand. Reliable supply, transparent data, technical feedback, and consistently high purity—these stand out as the values only direct production delivers.

    Bringing 3,4-Dimethoxytoluene directly from reaction kettle to customer dock, we see the stakes both in broad-scale manufacturing and at the bench. If your lab or process depends on real transparency and technical collaboration with the producer, you’ll find decades of operational expertise built into every lot. For any application—pharmaceutical, chemical synthesis, or specialty development—partnership with an experienced, invested manufacturer pays off long after the drum is empty.