Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

1,3,5-Trimethoxybenzene

    • Product Name 1,3,5-Trimethoxybenzene
    • Alias Phloroglucinol trimethyl ether
    • Einecs 210-836-8
    • 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

    222303

    Chemical Name 1,3,5-Trimethoxybenzene
    Molecular Formula C9H12O3
    Molar Mass 168.19 g/mol
    Cas Number 621-23-8
    Appearance White crystalline solid
    Melting Point 52-54 °C
    Boiling Point 263-265 °C
    Density 1.14 g/cm³
    Solubility In Water Slightly soluble
    Refractive Index 1.5202
    Flash Point 135 °C
    Pubchem Cid 12313

    As an accredited 1,3,5-Trimethoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle labeled "1,3,5-Trimethoxybenzene," featuring hazard warnings, molecular formula, batch number, and supplier details.
    Shipping **Shipping Description for 1,3,5-Trimethoxybenzene:** 1,3,5-Trimethoxybenzene should be shipped in tightly sealed containers, away from heat, moisture, and incompatible substances. Handle as a chemical substance; use appropriate labeling per regulations. Typically transported as a stable solid. Follow relevant hazardous materials guidelines, including documentation and protective packaging, to ensure safe transit.
    Storage 1,3,5-Trimethoxybenzene should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Store at room temperature and protect from light and moisture. Ensure proper chemical hygiene practices are followed, and use secondary containment to prevent leaks or spills.
    Application of 1,3,5-Trimethoxybenzene

    Applications of 1,3,5-Trimethoxybenzene in Industrial Manufacturing

    1,3,5-Trimethoxybenzene serves as an essential intermediate in multiple specialized sectors, where its high purity, stability, and performance under controlled process parameters enable high-value downstream synthesis. The following application scenarios reflect current, verified end uses worldwide.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Downstream pharmaceutical manufacturers use 1,3,5-Trimethoxybenzene as a key methoxy donor and core-building block in the synthesis of several antihistamine and anticancer compounds. Operators conduct multi-step reactions where this material’s aromatic stability preserves yield during nitration, halogenation, or amination. Precise batch control and traceability are critical to meeting regulatory requirements for human pharmaceuticals.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP Title 21 CFR Parts 210/211
    • European Pharmacopoeia (Ph. Eur.) monographs for related substances
    • China Pharmacopoeia ChP 2020 API sourcing protocols

    Typical usage ratio

    • 0.5%–3.0% w/w based on target molecule and reaction yield; formulators adjust proportion depending on desired functional group conversion in final API synthesis routes.

    Downstream process integration

    • Reactors charge 1,3,5-Trimethoxybenzene in primary condensation or cyclization steps; downstream purification and crystallization remove process byproducts before API isolation.

    Final product types

    • Chlorpheniramine (antihistamine)
    • Antineoplastic agents (chemical class: methoxybenzenes)
    • Intermediates for selective serotonin reuptake inhibitors (SSRIs)
    • Small molecule R&D compounds for oncology or anti-infective therapies

    2. Dye Intermediate for Specialty Pigment Synthesis

    Specialty pigment manufacturers use this raw material to introduce methoxy substituents in aromatic dye precursors, enabling color shade adjustments and solubility improvements in organic pigment production. Control of methoxylation sites during synthesis allows for customization of hue and lightfastness properties, with tight quality monitoring for batch-to-batch color uniformity.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile and Leather Chemicals)
    • EU REACH Regulation (EC 1907/2006) on chemical safety
    • ISO 9001:2015 Quality Management for pigment manufacturing
    • EN71-3 Toy Safety for colorants used in toy and children’s product coatings

    Typical usage ratio

    • 2%–6% of total precursor mass; formulators tune ratio based on required color density and specific methoxy functionality demanded by pigment chemistry.

    Downstream process integration

    • Material enters after initial diazotization or sulfonation steps as a reactant in coupling reactions; synthesizers isolate, filter, and dry pigments prior to formulation into dispersions or masterbatches.

    Final product types

    • Methoxy-functional azo dyes for textile fibers
    • Complex organic pigments for inkjet inks
    • High-temperature stable colorants for plastics processing
    • Special effect pigments for automotive OEM coatings

    3. Fragrance Ingredient Intermediate in Fine Aroma Chemicals

    Downstream aroma chemical producers employ 1,3,5-Trimethoxybenzene as a precursor in the synthesis of anisolic and musky odorants. Controlled methylation and demethylation steps allow production of high-purity molecules for use in fine fragrances and personal care formulations. Strict process validation supports traceability for global export markets.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for ingredient safety
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 22716:2007 Good Manufacturing Practice for cosmetics
    • REACH Annex XVII restrictions for fragrance materials

    Typical usage ratio

    • 1%–8% per batch scale, depending on target aroma strength and desired structural isomer content in intermediate blends.

    Downstream process integration

    • Reactor operators introduce the material during alkylation and oxidative coupling stages; subsequent distillation and fractionation yield high-value aroma chemical intermediates.

    Final product types

    • Anisole derivatives for premium fragrance bases
    • Muscone-type musks in designer perfumes
    • Scent compounds for fabric softeners and detergents
    • Flavoring agent intermediates for food-safe aromas (subject to additional compliance)

    4. Electronic Chemicals for High-Purity Conductive Polymer Synthesis

    Producers of specialty polymers for electronics integrate this raw material as a functionalized aromatic building block within polyaniline and poly(phenylene oxide) synthesis process. High electronic purity standards require tight contaminant control from upstream batches, as even trace impurities in methoxybenzene sources can impact the dielectric and conductivity properties of electronic materials.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free base materials in printed circuit boards
    • RoHS Directive 2011/65/EU for electronic chemical purity
    • JEDEC JESD96 for organic insulation chemistry
    • ISO 14644-1 Cleanroom standard for microelectronics production

    Typical usage ratio

    • 1.5%–5% w/w, typically proportional to polymerization cycle time and molecular weight requirements of target conductive resin system.

    Downstream process integration

    • Material enters as a co-monomer or additive in oxidative or acid-catalyzed polymerization; subsequent film-casting, drying, and lamination follow for functional material integration.

    Final product types

    • Antistatic coatings for electronics
    • Conductive polyimine-based films for flexible circuits
    • High-frequency PCB substrates
    • Low-dielectric constant encapsulation materials

    5. Agrochemical Intermediate for Selective Herbicide Synthesis

    Manufacturers specializing in plant protection products utilize 1,3,5-Trimethoxybenzene as a nucleus-modifying intermediate for the construction of certain selective herbicides. Controlled aromatic substitution facilitates the introduction of functional side chains, delivering desired crop selectivity and environmental stability profiles in the finished product.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA 40 CFR Part 180 pesticide inert ingredient standards
    • GB 2763-2021 (Max Residue Limits) for agricultural chemicals in China
    • ISO 16140 method performance for residue analysis

    Typical usage ratio

    • 2.5%–6.5% by mass, adjusted with reference to process kinetics and conversion rates for each specific target herbicide molecule.

    Downstream process integration

    • Material feeds in early multi-step aromatic functionalization; process proceeds to chlorination/alkylation or ring closure, followed by final formulation for field application.

    Final product types

    • Benzoxazinone-derived herbicide active ingredients
    • Pre-emergence selective herbicides for cereal and maize fields
    • Pesticide intermediates for research screening libraries
    • Stabilized actives for herbicide tank mixes
    Free Quote

    Competitive 1,3,5-Trimethoxybenzene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    1,3,5-Trimethoxybenzene: Manufacturing Insight and Product Introduction

    Getting to Know 1,3,5-Trimethoxybenzene

    At our chemical plant, 1,3,5-Trimethoxybenzene (TMB) has carved out a solid reputation as a well-established aromatic compound. Inside the drum or high-integrity bag, it appears as a pale to white crystalline powder, carrying the signature scent common to methoxybenzenes—a faint, medicinal aroma that signals a high degree of purity. Over years of process refinement, batch after batch rolls out with a purity level routinely measured above 99%. In each production run, we watch for off-colors or lingering impurities, knowing that even minor deviations from spec can affect downstream syntheses or final product quality. Technical staff care about details like melting point and moisture content because those numbers tie right back to whether a batch works for end-users in the lab or on the process line.

    Manufacturing Perspective: From Feedstock to Finished Goods

    On the plant floor, workers handle the synthesis with respect. 1,3,5-Trimethoxybenzene forms by methylating phloroglucinol or a related aromatic base using methylating agents under carefully maintained conditions. Temperature swings or uncontrolled feed rates do more than eat into efficiency—they open risk for dimethyl or tetramethyl side products, not to mention process safety issues. Each reactor’s control system runs with precise calibration, since different methylation agents or order-of-addition steps can change both the yield and the cost structure. Unlike some aromatic fine chemicals, TMB’s high melting point (hovering around 52-54°C) keeps it workable without creating unwelcome handling headaches. Storage tanks and shipping containers handle the powder easily; there’s no risk of caking or dangerous volatility.

    Packing, Storage, and Real-World Logistics

    Chemical products often reveal their true nature by how they withstand the real world, far from the sterile tables in a catalog. TMB’s stability simplifies matters, as the powder resists oxidation and hydrolysis if kept dry, and it doesn’t pose the same set of hazards found with more reactive methoxylated benzenes. Our operational experience has shown that 1,3,5-Trimethoxybenzene tolerates months—sometimes years—of warehouse storage without measurable degradation. End-users rarely face issues with off-odors or melted lumps, two common complaints with lower-quality intermediates from less experienced manufacturers. Desk-bound logistics managers appreciate this; they trust there’s less chance of a shipment going bad and sparking returns or replacement claims.

    Where 1,3,5-Trimethoxybenzene Finds Its Use

    Use cases for this aromatic intermediate stretch widely. On the upstream side, 1,3,5-Trimethoxybenzene supports several sectors—primarily organic synthesis, where it stands as a crucial step toward more complex molecules. For example, it underpins the manufacture of certain pharmaceutical active ingredients and agrochemical agents. Chemists routinely choose it as a building block for antimalarial, antifungal, or CNS-active molecules. The symmetrical substitution makes its core structure friendly for regioselective functionalization, easing the path toward new derivatives without much need for complex separation downstream.

    Some of our partners in research and industry specifically seek out 1,3,5-Trimethoxybenzene for its role as a key precursor. Industrial sectors value its use in liquid crystal synthesis. Its rigid yet modifiable backbone offers a helpful molecular template in displays and related technologies. Beyond that, TMB sometimes works as a chemical probe or reference compound in spectroscopy, or as a masking group in heterocyclic chemistry. Small custom scale batches feed research pilots, while ton lots head toward continuous process lines in high-value production.

    What Sets 1,3,5-Trimethoxybenzene Apart

    People in chemical development sometimes confuse TMB with its close cousins, such as 1,2,4-Trimethoxybenzene or 1,2,3,5-Tetramethoxybenzene. These differences matter at both the practical and theoretical levels. The symmetrical arrangement of methoxy groups at the 1,3,5 positions not only makes design of further transformations simpler, but it also imparts physical characteristics that other isomers do not share. The melting behavior shows more consistency in tightly controlled applications, and the chemical landscape enables selective aromatic substitutions that aren't feasible with more sterically demanding isomers.

    Physical purity matters because it drives yield and reproducibility in end-user chemistry. In our operation, we track batch data closely, watching that spectrophotometric readings and NMR analyses confirm consistently clean profile—no stray dimethoxy, tetramethoxy, or unreacted starting material detectable above allowable thresholds.

    Issues in the Marketplace: Purity, Traceability, and Counterfeit Risk

    Over the last decade, reports of subpar TMB entering the market appeared more frequently, especially from loosely regulated sources. Buyers looking to shave cost sometimes run into headaches that cost them more in rework or loss than any savings on the product price. As a producer, we have lived through these scenarios: badly washed, low-purity trimethoxybenzenes can introduce by-product residues that poison catalysts or complicate isolation of desired molecules. Trace organic impurities, trace metals, and water content need tight control. Not all suppliers give details on their process streams or provide batch-level certificates that tie product to testing data.

    To control for these risks, our facility runs frequent calibration exercises, ensuring HPLC and GC instruments stay sharp. Operators within quality control labs compare every outgoing lot against an internal archive of retained samples. Production shifts record origin lots for critical consumables and reagents, tracking every step from raw phloroglucinol to packed product. Buyers who ask for backward traceability receive detailed reports. Some firms use spectroscopic fingerprints to spot counterfeit or adulterated batches—the repeatable high-purity signature stands out and resists duplication by shortcut manufacturing or improperly cleaned reactors.

    Sustainability and Responsibility in Manufacturing

    Industry-wide, environmental impact now stands front and center. In our case, closed-loop handling for methylating agents and solvent recovery reduce emissions. Residual process waste undergoes careful treatment before off-site disposal, lowering chemical oxygen demand (COD) and volatile organic compound (VOC) risk. Newer production lines depend more on catalytic methylation routes that require less hazardous input and yield a cleaner effluent stream. Our engineers invest time in refining reaction conditions to create higher first-pass conversion, regardless of scale, which cuts both input cost and by-product load.

    Eco-responsibility goes hand-in-hand with transparency. Waste manifest logs, solvent use declarations, and annual emissions reports remain open for audit by partners or regulators. Internal environmental health and safety (EHS) teams audit all handling stages—from methylation to washing and packaging. This approach reassures customers with strict sustainability mandates, who rely on upstream data to validate their own compliance with global environmental and labor regulations.

    Partnering with End Users: Custom Batching and Application Integration

    More than a few research labs request customization at the supply stage. Over time, we built flexibility into our order system, handling tailored batch sizes or customer-specified particulate grades. Certain downstream syntheses ask for fine-ground TMB or material screened to exclude oversized particles. Analytical chemists occasionally need an extra level of impurity documentation—something as specific as halide content below a few parts per million. Our batches can shift in specification based on end use, but never drop below internally set purity controls.

    Production scheduling bends around customer demand cycles. Some pharmaceutical groups order twice-yearly for campaign runs, so we synchronize large-lot batches with shipping windows, preserving both freshness and batch continuity. Specialty chemical users, meanwhile, tap into just-in-time shipments, where stable shelf life and batch homogeneity mean no surprises mid-process. Relationships built through years of supply lend insight into fine-tuned requirements; one customer on the East Coast might flag requests for CIQ-compliant paperwork, while another specifies no contact with boron-based cleaning agents in the production area.

    Quality Testing and Analytical Methods

    Each batch of 1,3,5-Trimethoxybenzene heads through tight screening before it moves from bulk storage to packaging. Melting point checks remain a first line of defense: off-spec readings sometimes mean residual solvent or trace impurities slipped through, so suspect drums never clear shipping until re-analysis confirms or debunks the finding. HPLC and GC deliver the detail chemists respect—profiles showing clean, single peak, free from unknowns or high-molecular-weight tailings. FTIR and NMR, especially proton and carbon spectra, end up archived in digital and hard-copy form. Some pharmaceutical buyers audit randomly, matching our trace files against their own methods.

    Water content rarely poses a problem with TMB compared to hygroscopic reagents, but we keep Karl Fischer titration in the QC arsenal all the same. When complaints arise—say, dislike of a faint off-aroma—small sample bottles return for comparison to control materials. Consistency in sensory impression often flags issues that don’t show on a chromatography trace but mean something’s different batch-to-batch.

    Lessons Learned: Why Experienced Manufacture Matters

    Experience shapes each improvement we make. In the earliest years, our process struggled periodically with off-white batches, often traced to a poorly controlled methylation step. Routine adjustments to reaction time and pressure, along with new filtration methods, pushed purity higher and saved cost on unplanned rework. Direct conversations with users led us to refine packaging, moving from paper bags to multilayer drum lining to keep product dry and flowable. Resilient, user-centric thinking keeps our output better matched to what industry expects, cutting down troubleshooting on the customer end.

    Competition pushes innovation forward but can tempt some newcomers to skip steps or under-invest in safety at scale. Through regular review and genuine process audits, we reinforce a culture that values right-first-time quality. Our operators know which details matter on the floor, whether it’s ensuring each drum ships with batch identification or holding off dispatch if overnight temperature swings risked a product quality event. By living close to the process, we come to understand both the technical and practical implications of every step, and feedback flows both ways.

    Constant Change in the Chemical Industry

    Markets rise and fall, regulatory climates shift, and user demands evolve. Over the years, customer industries started asking for not only chemical purity, but also evidence for ethical sourcing and lower overall carbon footprint. Our team adapts by proactively gathering documentation and adopting greener manufacturing practices where the chemistry permits. In some cases, developing byproduct recycling or managing heat integration to improve energy efficiency can set one manufacturer apart from another. In our experience, investments into worker training and well-documented internal controls result in a more reliable supply chain for the customers who depend on 1,3,5-Trimethoxybenzene as a raw material.

    Knowledge sometimes circulates informally, passing from line supervisor to new hire as a lesson about why small deviations early in the process snowball into bigger issues later. Institutional memory shapes the way we handle deviations. For instance, if a methyl chloromethane shipment tests marginally out of spec, production halts until alternatives clear. Time burned in the short term often saves more costly failures or returned batches down the line.

    Comparing with Other Methoxybenzenes: A User’s View

    Looking at product lines, each methoxybenzene isomer comes with its own quirks. 1,3,5-TMB’s symmetry and reactivity profile put it in a middle ground between less substituted trimethoxybenzenes and heavily functionalized tetramethoxy derivatives. Synthetically, more branched isomers may resist nucleophilic attack or present isolation challenges, while the purity stakes rise due to increased boiling points or solubility issues. Isomers with adjacent methoxy groups—like 1,2,3-trimethoxybenzene—display greater tendency toward liquefaction upon mild heating, which hampers their straightforward use in melt-phase reactions.

    The difference extends beyond mere chemical structure. Simple packaging or shipping changes often reflect distinct physicochemical behavior; TMB ships well in drums even across varied climates, while certain isomers require tamper-evident seals or desiccant loading. The main reason buyers keep coming back for our 1,3,5-Trimethoxybenzene has less to do with what’s in the brochure, and more with dependable real-world performance batch after batch.

    Practical Tips: Handling and Troubleshooting

    Lab-scale and industrial users both face the same practical questions—what can go wrong, and how do you spot risk before it impacts process or product? Over-drying can lead to staticky powders tough to transfer, while storing open bags encourages moisture pick-up and agglomeration. Handling TMB doesn’t pose outsized risk, but basic gloves and local ventilation always make sense. Escaped powder on floors signals either a packaging failure or operator hurry; both warrant attention before habits set in.

    On occasion, consignees report color drift or an unusual odor—a sure sign of contamination, either from a breached seal or cross-reactivity during prolonged exposure to strong acids or bases. A well-designed housekeeping program, routine container inspection, and clear labeling keep such slips rare. Most process upsets trace back to interruptions in raw material flow or attempts to switch methylating agent streams for small cost savings. Based on long-term records, sticking with vetted process inputs gives the most consistent results.

    Outlook: The Value Behind Consistent, Reliable 1,3,5-Trimethoxybenzene

    Customers in research, manufacture, and specialty applications depend on a supply base they can count on. By continuously investing in equipment, on-the-floor training, and regular engagement with buyers and regulatory agencies, we back our 1,3,5-Trimethoxybenzene with both process capability and a culture of transparency. Uninterrupted feedback cycles with our partners build trust, which feeds better products and stronger collaboration in a market that never stands still.

    As end-user expectations rise and regulatory guidelines tighten, our responsibility only deepens. Manufacturing specialty aromatics like TMB goes beyond managing formulas and specifications. We see it as a commitment to responsibly deliver quality that supports innovation, streamlines operations, and stands up under scrutiny time and again.