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3-Methoxybenzyl Chloride

    • Product Name 3-Methoxybenzyl Chloride
    • Alias m-Anisyl chloride
    • Einecs 218-436-4
    • 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

    309601

    Product Name 3-Methoxybenzyl Chloride
    Cas Number 824-98-6
    Molecular Formula C8H9ClO
    Molecular Weight 156.61 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 238-240 °C
    Melting Point -6 °C
    Density 1.17 g/mL at 25 °C
    Refractive Index n20/D 1.547
    Flash Point 104 °C
    Solubility Insoluble in water, soluble in organic solvents
    Synonyms m-Anisyl chloride
    Smiles COC1=CC=CC(=C1)CCl
    Pubchem Cid 13600
    Ec Number 212-532-3

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

    Packing & Storage
    Packing 250g of 3-Methoxybenzyl Chloride is sealed in an amber glass bottle with a secure cap, labeled with safety and chemical information.
    Shipping 3-Methoxybenzyl chloride is shipped in tightly sealed, chemical-resistant containers to prevent leaks and exposure. Transport must comply with local and international hazardous materials regulations. The packaging is clearly labeled with hazard warnings, and shipments are handled by trained personnel to ensure safety and environmental protection throughout transit.
    Storage 3-Methoxybenzyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep it separate from oxidizing agents and strong bases. Use appropriate chemical storage cabinets, and clearly label the container. Ensure proper safety measures, including secondary containment, to prevent accidental spillage or exposure.
    Application of 3-Methoxybenzyl Chloride

    Applications of 3-Methoxybenzyl Chloride in Industrial Manufacturing

    3-Methoxybenzyl Chloride serves as a core intermediate for several specialty chemical industries, supporting the production of advanced molecules across pharmaceutical, agrochemical, and material sectors. As a direct manufacturer, we supply this raw material to downstream partners who rely on its specific reactivity for precise synthesis and large-scale batch processing. The following application sectors reflect actual, traceable industrial demand for this compound, highlighting its integration into formula development and critical process steps.

    1. Pharmaceutical Active Ingredient Synthesis

    Large-scale pharmaceutical plants utilize 3-Methoxybenzyl Chloride during the construction of key intermediates for active drug molecules, including non-steroidal anti-inflammatory drugs (NSAIDs) and central nervous system (CNS) compounds. Chemists exploit its benzyl group for protecting strategies and subsequent alkylation during multi-step synthesis pathways, with strict traceability and impurity profiling required to meet international pharmacopoeial requirements. Material addition proportions align with process specifications, adjusted according to target molecular weights, downstream yield targets, and reaction scalability in pilot and commercial setups.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.8–1.05 molar equivalents relative to nucleophilic intermediates; adjustments made per API synthesis route and required protecting group deprotection step

    Downstream process integration

    • Charged in Step 2 or 3 of custom multi-step batch synthesis for benzylation
    • Utilized in protection/deprotection cycles to safeguard or modify amine and phenol functional groups
    • Monitored by in-process HPLC and GC for purity and impurity control

    Final product types

    • Naproxen intermediates
    • CNS pharmaceutical intermediates (e.g., anticonvulsant API intermediates)
    • Other specialty aromatic drug scaffolds

    2. Crop Protection Intermediate Production

    Agrochemical manufacturers utilize this benzyl chloride derivative as a key building block for constructing selective herbicide and fungicide intermediates, where controlled reactivity permits selective functionalization on aromatic rings. Material handling and usage rates depend on downstream synthesis targets, which often involve multi-stage acylation and etherification. Compliance with agricultural and chemical manufacturing standards ensures material traceability, low residual impurity levels, and environmental safety data reporting. Production teams tailor addition amounts to the conversion rate and desired yield, tracked via batch logs and QC data.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU)
    • Global GAP for raw material traceability in agrochemical supply chains
    • FAO/WHO specification for technical active ingredients

    Typical usage ratio

    • 1.0–1.2 molar equivalents in nucleophilic aromatic substitution or etherification step; proportion set by target intermediate and permissible process loss rate

    Downstream process integration

    • Added to initial condensation step for benzyl-protected phenol or amine substrates
    • Employed in controlled temperature and agitation batches to suppress by-product formation
    • Batch release after in-process HPLC and yield verification

    Final product types

    • Triazole fungicide intermediates
    • Aromatic-selective pre-emergent herbicide precursors
    • Pyridine-carboxylate ester intermediates

    3. Aroma and Fragrance Compound Manufacturing

    Specialty fragrance producers incorporate this compound during the synthesis of high-purity benzyl derivatives that impart “anisic” and fresh-floral aroma notes. It enters precisely controlled alkylation and etherification reactions where the placement and reactivity of the methoxy group dictate the resulting olfactory profile. This intermediacy supports proprietary formulations for perfumery products where low residual chloride and process consistency must fulfill industry guidelines on impurities, toxicity data, and batch reproducibility.

    Industry compliance standards

    • IFRA (International Fragrance Association) Conformity Criteria
    • Cosmetic Ingredient Review (CIR) safety assessment
    • ISO 9235:2013 (Aromatic Natural Raw Materials — Vocabulary)
    • EU Cosmetic Regulation 1223/2009 for finished perfumes

    Typical usage ratio

    • 0.5–1.0 eq. as a limiting reactant in specific fragrance-building alkylations; ratio tailored per olfactory impact intensity and process efficiency

    Downstream process integration

    • Participates in aromatic etherification to create long-chain anisic fragrance bases
    • Subject to distillation and vacuum-stripping to minimize off-odors
    • Final QC by GC-MS for aroma profile and residual impurity quantification

    Final product types

    • Anisic benzyl-derived aroma molecules
    • Complex fragrance building blocks for luxury perfumes
    • Functional fragrances for soaps, detergents, and personal care bases

    4. Dye and Pigment Intermediate Synthesis

    Colorant factories utilize this material to enable selective aromatic substitution, supporting the preparation of complex dye intermediates for advanced textile and specialty printing inks. The compound's chemical architecture allows tailored electron-donating substitution patterns, influencing color-fastness and solubility in downstream pigment applications. Process engineers control its addition based on the desired chromophore and manage all production inputs to conform to textile, safety, and environmental protocols, often backed by extensive batch analytical documentation.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • ZDHC (Zero Discharge Hazardous Chemicals) Roadmap to Zero Programme
    • ISO 9001 Quality Management for colorant production
    • REACH registration for pigment intermediates

    Typical usage ratio

    • 0.7–0.95 molar equivalents in nucleophilic substitution on functional aromatic substrates; adjusted per desired hue intensity and process mass balance

    Downstream process integration

    • Dosed in batch or semi-continuous reactors targeting azo or anthraquinone dye intermediate build-up
    • Color adjustment controlled via in-process spectrophotometry
    • Filtration and purification downstream to remove residual chloride and unreacted material

    Final product types

    • Azo dye precursors for synthetic fibers
    • Anisidine-based pigment intermediates for ink and textile printing
    • Specialty chromophore components in photoresist colorant synthesis
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    Certification & Compliance
    More Introduction

    Introducing 3-Methoxybenzyl Chloride: Reliability Through Precision

    Description and Practical Significance

    3-Methoxybenzyl Chloride holds a unique place among benzyl chloride derivatives. Its molecular structure—C8H9ClO, CAS Number 824-98-6—features a methoxy group attached to the aromatic ring, offering more than just another chlorinated benzene. Over years of hands-on manufacturing, we have fine-tuned our synthesis pathways to ensure every batch responds to the demands of both research and large-scale production.

    This compound comes as a colorless to pale yellow liquid. Workers accustomed to handling specialty organochlorines notice right away that 3-Methoxybenzyl Chloride creates less harsh fumes than unsubstituted benzyl chloride, which makes it a better choice for operators at the bench or in pilot vessels. The odor is less pungent, less likely to linger in workspaces, and safer for those who handle it over long shifts.

    With a boiling point near 230°C and consistently low chloride contamination, our batches display strong chemical stability—even under ambient shipping conditions. We keep moisture levels below 0.1%. The chlorinated side chain gives it high reactivity, especially towards nucleophilic substitution reactions and Grignard chemistry. This lets process chemists pursue routes where unmodified benzyl chloride would either lag in selectivity or create more hazardous byproducts.

    Why Product Purity and Trace Consistency Matter

    Years in the chemical industry have shown us that even tiny contaminants can throw entire syntheses off course. Our purification systems, built after rigorous optimization, deliver a product with at least 99% purity (GC area normalization). Drums, carboys, or flasks are flushed and sealed using methods drawn from real-life GMP lessons—cross-contamination costs time, money, and credibility.

    Repeated testing on incoming raw materials proved that only certain grades of methoxybenzyl alcohol translate into pure 3-Methoxybenzyl Chloride. Reaction kinetics shift if trace aldehydes or ethers remain in the feedstock, leading to poor selectivity or color formation. By tracking each batch through its entire manufacturing log, and keeping turnaround time between synthesis and dispatch short, we maintain those color and odor profiles our customers expect—a pale liquid you can trust in both mass balance and chromatogram results.

    Analytical protocols matter as much as synthetic skill. We use both GC-MS and HPLC to check each production batch—not only looking for the main peak, but for the low-level side products chemists often overlook. Spotting satellite peaks at 0.03% area might seem excessive, but clients in pharmaceutical and agrochemical routes have to predict long-term impurity profiles. The work that goes into keeping these specs tight pays off most for projects running for months rather than days.

    How 3-Methoxybenzyl Chloride Gets Used in Industry

    Experienced chemists gravitate toward 3-Methoxybenzyl Chloride for a reason. The electron-rich aromatic ring, courtesy of the methoxy substituent, changes its reactivity in both expected and unexpected ways. It serves as an essential intermediate in the preparation of functionalized benzylamines, ethers, and esters. Our clients most often use it to build alkylating agents for active pharmaceutical ingredients, flavors, and odorants. High reliability translates to fewer reaction failures downstream, saving both raw materials and engineering time.

    In some of the more challenging total syntheses, such as those required for plant growth regulators or advanced pesticides, the methoxy substitution helps guide reactivity to the correct position on the ring. A shift in electron density can make or break the outcome of an alkylation step. Our field teams keep up with the latest synthetic methodologies, collaborating with customers to adapt production in line with evolving synthetic strategies—if a specific route requires lower water content or a particular isomeric profile, we can make those adjustments batch after batch.

    Beyond core organic synthesis, this compound enables late-stage diversification in medicinal chemistry. The methoxy group acts as a handle for further transformations—lithiation, cross-coupling, or halogen substitution steps benefit from both the starting material’s purity and its clever electron distribution. Formulators in the fragrance and flavor sectors rely on our chlorides to develop both base notes and masking agents that require tight color and odor control.

    Setting Expectations by Differentiating from Other Benzyl Chlorides

    It’s common for inexperienced buyers to bundle 3-Methoxybenzyl Chloride with more basic benzyl chloride offerings, but such generalization underestimates how strongly the methoxy group shifts physical and chemical behavior. Pure benzyl chloride is notoriously aggressive and prone to hydrolysis under moist air. Many producers simply relabel generic chlorinated toluene without accounting for contaminant migration or isomeric drift. We separate batches carefully, so cross-contamination from 2- or 4-methoxy analogs never confuses downstream yields.

    Compared to unsubstituted benzyl chloride, our 3-Methoxybenzyl Chloride features increased solubility in polar organic media, facilitating more direct workups in pharmaceutical synthesis—no lengthy phase separations or excessive washing needed. In addition, we keep the aromatic purity high, so side-reactivity never sabotages an advanced step in the customer’s process. We have seen poorly differentiated products lead to batch failures and customer complaints across markets from India to the US. Using analytical evidence, we have built systems to assure our customers of batch-to-batch uniformity, eliminating the risk of costly reruns.

    3-Methoxybenzyl Chloride stands apart from dichlorinated or trichlorinated analogs because those compounds react too quickly and lose selectivity. Such overchlorinated benzenes trigger side reactions that modern green chemistry strictly avoids. By targeting a single, pure chloro group ortho to the methoxy substituent, we provide both performance and environmental compliance. The synthetic pathways avoid large-scale halogen waste, and our containment and recovery procedures keep our work both safe and sustainable.

    Manufacturing Experience and Industry-Driven Problem Solving

    Over years of scale-up, we’ve seen too many “almost pure” lots that looked clear but contained trace halides or phenolic byproducts. Having built our own reactors, automated distillation units, and in-house analytics, our team responds quickly to subtle feedback—a faint yellow hue or an unexpected whiff points to issues others might ignore. Line workers train to recognize these cues and signal maintenance or analytic review right away.

    Several customers in the fine chemical space encountered off-site material that seemed correct until end-use testing. Their teams would report inconsistent reaction kinetics, variable color, or even failed crystalizations. We invited them to audit our process, from the alcohol feedstock’s acceptance through to the final barrel. By operating a closed-cycle chlorination unit, we block off-site moisture, airborne particulates, and migration of environmental chlorine, and our own control systems keep static pressures consistent throughout the batch run.

    Bottlenecks used to crop up around purification and isolation; distillation columns fouled with residue demanded more downtime than anyone wanted. By redesigning column packing and stripping routines, we cut maintenance stoppages in half. At scale, saving an hour per batch adds up quickly, especially during high-output periods like seasonal demand spikes. Long-serving operators worked with us to design sample ports for more frequent but minimal-loss sample collection, making our data more granular and batch predictions more accurate.

    Safety and Environmental Responsibility

    Handling alkyl chlorides always brings health and safety challenges. We learned through direct experience where ordinary precautions fall short—in older facilities, vapor management systems struggled to keep room concentrations safe. After several cycles of testing, our newer exhaust scrubbers capture over 99% of fugitive emissions. PPE standards rise and evolve—lab staff rely on both respiratory and chemical gloves reviewed annually by third-party consultants. We’ve invested in both air quality monitoring and fume hood upgrades, meaning staff can handle kilograms per shift without exposure incidents.

    Runoff and waste handling follow strict protocols, but that’s just the start. Chlorinated organics often get flagged for environmental risk, and years back our effluent streams occasionally registered trace contamination. By switching to closed-loop collection and on-site thermal destruction for spent solvent, we meet discharge targets and cut the regulatory paperwork. Regular third-party audits confirm we’re staying ahead of local, regional, and international guidelines, and customers audited our system during their own risk reviews—so far, none have found noncompliance.

    Last year, our product stewardship team worked with a packaging supplier to design drums with best-available liners and vent caps, preventing both leaks and tampering. Shipping routes are mapped and tracked, and hazardous goods paperwork always accompanies shipments. Warehousing partners know to segregate this material and cycle stock fast—no one wants an old, unexplained residue causing headaches months later.

    Customization Based on Real Technical Feedback

    Over the past decade, we’ve seen the needs of synthesis chemists shift. Teams used to request larger, single-batch volumes, but now mid-sized, high-purity lots are more common. Some customers require smaller packaging to avoid repeated exposure and vapor loss, while others want larger, drum-sized deliveries to keep pace with pilot plant trials. By building our internal logistics operations around demand spikes and seasonal forecasting, we keep lead times short—no three-month waits, no guesswork on stock levels.

    Not all processes tolerate even the normal low ppm of acid residue. Our process engineers designed custom post-chlorination washing steps based on feedback from a production partner’s pilot run. By monitoring alkalinity and wash water pH per batch, we eliminated catalyst quenching problems and kept downstream purity high. The industry moves fast, and waiting two weeks for a fix is not acceptable. We prioritize keeping customers informed, sharing early batch samples and revision logs whenever process tweaks lead to meaningful improvements.

    Polymer chemists, for example, sometimes need extremely low ROS (residual organic solvent), requiring distillation through new-generation wiped-film evaporators. We invested in these after direct collaboration with pharmaceutical developers, finding that high mechanical shearing not only stripped extra solvent but also prevented formation of discolored byproducts. Costly up front, but worth it after three rounds of customer pilot runs demonstrated cleaner end products and zero failed lots.

    Staying Ready for Emerging Industry Demands

    Regulatory changes hit faster than anyone expects. We learned this lesson years ago through tighter controls on chloroaromatic emissions and evolving requirements for REACH and TSCA compliance. Our regulatory compliance staff keep documentation up to date, and frequent training ensures we’re always ready for the next audit. Customers have called us directly after seeing new global regulatory bulletins and want answers about our chemical’s origin, control processes, and recordkeeping. Because our records are thorough and stored digitally, we can provide paper trails without delay.

    Newer synthetic methods sometimes need smaller lots with specific impurity profiles, not just the highest possible purity. Medicinal chemists working on targeted therapies contact us for specialized grades, often with unique specifications for residual water, halide, or hydrocarbon content. We manufacture tailored lots for these orders, monitoring them with both established protocols and cutting-edge spectroscopy. By listening to the front-line users, we master production challenges that spreadsheet-driven competitors overlook.

    Younger chemists—especially those in startup biotech companies—sometimes underestimate the care needed to manage chlorinated materials. We provide technical bulletins and direct consultation to keep their operations efficient and safe. If a project calls for a new synthetic route or an unusual solvent system, we share both what works and what failed for other teams, saving our customers wasted time and materials.

    Conclusion: Experience Translates Into Reliability

    From our earliest days working with pilot reactors through today’s automated process lines, the real story of 3-Methoxybenzyl Chloride involves more than just numbers. Persistent quality control, fast response to technical or regulatory demands, and direct feedback from hundreds of live projects have shaped our product and our culture. We don’t just rest on a production formula—we adapt, measure, and improve, because real-world chemistry depends on consistency as much as reactivity.

    Every bottle or drum we ship marks a handshake between experienced manufacturing and practical problem-solving. If your synthesis demands consistent, high-purity 3-Methoxybenzyl Chloride, then real-world lessons, not just specs, determine the outcome—both in the lab and on the production floor. Years of relentless attention mean we offer peace of mind along with every shipment.