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3,4-Dimethoxybenzyl Chloride

    • Product Name 3,4-Dimethoxybenzyl Chloride
    • Alias Veratryl chloride
    • Einecs 212-222-1
    • 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
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    Specifications

    HS Code

    805029

    Product Name 3,4-Dimethoxybenzyl Chloride
    Cas Number 102-88-5
    Molecular Formula C9H11ClO2
    Molecular Weight 186.64 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 151-153°C at 13 mmHg
    Density 1.165 g/cm3 at 25°C
    Refractive Index 1.561
    Solubility Insoluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Synonyms Veratryl chloride, 3,4-Dimethoxybenzylchloride
    Storage Conditions Store in a cool, dry, well-ventilated place; keep container tightly closed

    As an accredited 3,4-Dimethoxybenzyl Chloride 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 secure screw cap, labeled "3,4-Dimethoxybenzyl Chloride, 25g," includes hazard symbols and handling instructions.
    Shipping 3,4-Dimethoxybenzyl chloride is shipped in tightly sealed containers, typically made of glass or compatible plastic, to prevent moisture and air exposure. Packages are clearly labeled as hazardous, with appropriate UN numbers and handling instructions. Shipping is conducted in compliance with international regulations for toxic and irritant chemicals, ensuring safe transport.
    Storage 3,4-Dimethoxybenzyl chloride should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong bases and oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Store in a chemical-resistant container, clearly labeled, and limit access to trained personnel. Follow appropriate safety and regulatory guidelines.
    Application of 3,4-Dimethoxybenzyl Chloride

    Applications of 3,4-Dimethoxybenzyl Chloride in Industrial Manufacturing

    Used as a critical intermediate in fine chemical synthesis, 3,4-Dimethoxybenzyl Chloride plays a role in several established downstream sectors. As a direct manufacturer, we supply leading producers who demand consistency, controlled impurity profiles, and full transparency on compliance for their regulated markets. Below are key industrial fields where this material delivers unique functional benefits, processing compatibility, and regulatory alignment.

    1. Pharmaceutical Synthesis: Active Pharmaceutical Ingredient (API) Intermediates

    This material is primarily utilized as an alkylating agent for constructing arylmethane structures in the synthesis of several regulated pharmaceutical intermediates, especially in the development of anti-hypertensive, anti-arrhythmic, and CNS-active molecules. Its application requires tight quality control to comply with international pharmacopoeial standards and Good Manufacturing Practice (GMP) mandates, with addition rates adjusted based on the specific target compound’s synthetic pathway.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia Monographs (where applicable)
    • Chinese Pharmacopoeia ChP (when exporting to China)

    Typical usage ratio

    • 0.8–1.1 molar equivalents relative to the precursor amine or alcohol, adjusted to optimize conversion in batch or continuous flow synthesis
    • Excess quantities may be used to drive reaction completion, typically not exceeding 1.2 equivalents to control costs and downstream purification

    Downstream process integration

    • Introduced in the nucleophilic substitution or alkylation stage to form protected or functionalized benzyl motifs
    • Charged directly to dedicated reactors equipped for controlled temperature and inert atmosphere to prevent hydrolysis

    Final product types

    • Antiarrhythmic precursors (e.g., intermediates for verapamil synthesis)
    • Antihypertensive intermediates (construction of specialty amines and ethers)
    • CNS-active API intermediates used in R&D pipelines

    2. Agrochemical Intermediates for Selective Herbicide Manufacture

    Leading agrochemical firms use this raw material to build key protected aromatic scaffolds in complex herbicidal synthesis. The consistency and traceability of the input directly influence downstream batch reliability, while careful adjustment of input ratios minimizes processing residues and side reactions during the multi-step production of selective weed control agents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC 1907/2006) registration for EU-bound materials
    • Globally Harmonized System (GHS) for labelling and SDS
    • ISO 9001:2015 QMS for traceability and change control

    Typical usage ratio

    • 0.9–1.15 molar equivalents, optimized per batch based on residue analysis
    • Input amount adjusted for target compound yield and minimization of byproducts

    Downstream process integration

    • Fed into intermediate alkylation or etherification stages using solvent- or catalyst-assisted methods
    • Purified through multi-stage distillation or chromatography before final product coupling

    Final product types

    • Selective herbicide intermediates (e.g., substituted benzylic ethers/sulfonamides)
    • Precursor components for triazine-based weed control formulations
    • Active ingredient scaffolds for experimental crop protection products

    3. Flavor & Fragrance Ingredient Manufacturing

    Flavor and fragrance compound producers rely on controlled batches of this ingredient for the synthesis of specialty aromatic aldehydes and alcohols, deployed in high-purity formulations for consumer goods. Exact dosing is vital for meeting IFRA and food-grade thresholds, as residual chloride or methoxy contaminants can alter olfactory and food safety properties.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredients
    • US FDA 21 CFR 172.515 (Food Additives Permitted for Direct Addition to Food for Human Consumption)
    • FEMA GRAS certification for the resulting flavor compound
    • ISO 22000 Food Safety Management for downstream applications

    Typical usage ratio

    • 0.75–1.0 molar equivalents (relative to nucleophile), with real-time adjustment based on product purity targets
    • Minimized excess to improve downstream product isolation and limit waste

    Downstream process integration

    • Incorporated in controlled batch reactions for synthesis of specialty benzaldehydes and benzylic alcohols via Grignard or reduction pathways
    • Reaction mixture is subject to multi-step purification to isolate food- or fragrance-grade finished aromatic compounds

    Final product types

    • Aromatic aldehydes for premium fragrance blends
    • Flavor-active benzylic alcohols for beverage and confectionery applications
    • Precursors for natural-identical vanillin derivatives and related aroma chemicals

    4. Dye and Pigment Additive Synthesis

    Leading dye manufacturers employ this chemical intermediate in the production of specialty methoxy-substituted azo and anthraquinone dyes, where functionalizing the aromatic ring structure enables tailored lightfastness and solubility profiles. Precise formulation and input monitoring underpin regulatory filing for textiles and food packaging applications, especially to ensure compliance with EU REACH and restricted substance directives.

    Industry compliance standards

    • EU REACH Regulation (Annex XVII and SVHC)
    • OEKO-TEX® Standard 100 (for textile application)
    • ISO 14001 Environmental Management for pigment production
    • US FDA CFR 178.3297 (colorant use in food-contact plastics, where applicable)

    Typical usage ratio

    • 1.0–1.25 molar equivalents in the diazotization or coupling stage, depending on chromophore complexity and desired color strength
    • Input often trimmed with in-process analytics to avoid overfunctionalization and minimize waste streams

    Downstream process integration

    • Added at early step to introduce methoxybenzyl functionality on core aromatic rings during coupling or acylation reactions
    • Post-reaction product subjected to chromatographic or crystallization purification for stability and hue control

    Final product types

    • Methoxy-substituted azo and anthraquinone dyes for synthetic fiber coloring
    • Functional pigments for technical plastics with high UV resistance
    • Food-contact-compliant colorants for specialty packaging inks
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    Certification & Compliance
    More Introduction

    Introducing 3,4-Dimethoxybenzyl Chloride: Precision in Aromatic Synthesis

    Our Approach in Manufacturing Aromatic Chlorides

    Over the years, our team has seen firsthand the shifts in demand for specialty benzyl halides, and 3,4-Dimethoxybenzyl Chloride stands out in our product lineup. This compound, sometimes referred to as veratryl chloride, carries a distinct methoxy substitution pattern on the aromatic ring, making it more versatile than its simpler analogs. As a manufacturer, consistency in purity—often at or above 99%—makes a tangible difference for clients downstream, especially those working in the pharmaceutical and fine chemicals arenas. We control every part of the process, right from raw material sourcing to meticulous closed-system chlorination, to obtain a crystal-clear, slightly yellow liquid known for reliability.

    Physical Characteristics Shaped by Authentic Process Control

    Handling veratryl chloride reveals a spectrum of character traits. In the production hall, batches go through rigorous distillation under reduced pressure. The resulting product consistently boils between 136 and 138°C at reduced pressure and pours smoothly at room temperature. This attention to physical stability translates to better shelf life and safer handling for formulators and researchers. We design our storage protocols around these properties, since natural light and air can trigger unwanted side reactions. Glass-lined vessels, oxygen scrubbing, and careful packing practices come from years of refining the logistics behind aromatic halides. These steps set high-quality material apart from commodity versions seen in the open market.

    Applications Where Each Molecule Matters

    Our clients use 3,4-Dimethoxybenzyl Chloride as a core intermediate in crafting complex active pharmaceutical ingredients, fragrant aldehydes, and specialty agrochemicals. Unlike unsubstituted benzyl chloride, which primarily finds use as an alkylating agent in relatively simple transformations, the dimethoxy variant enables more targeted chemistry. In laboratory-scale research, our material has helped advance the synthesis of potential anti-cancer scaffolds and neuroprotective agents. During scale-up, the precise control over batch purity has allowed multistep syntheses to move forward without costly chromatographic scrubbing.

    In our experience, downstream yields suffer dramatically if residual impurities creep in during the initial stages. To avoid this, we fine-tune our distillation based on both GC and NMR fingerprinting. Some clients have shared stories about trialing third-party material, only to find later that batch-to-batch inconsistency—especially trace chlorinated byproducts—can sabotage a whole route. By contrast, careful process control and batch certification help streamline regulatory filings for pharmaceutical partners. It’s not just about molecular weight and boiling point reports; it’s about eliminating weeks of troubleshooting for chemists relying on clean feeds for their reactions.

    Distinct Advantages Over Other Benzyl Halides

    Where 3,4-Dimethoxybenzyl Chloride really shows its value is in regioselective synthesis. The electron-rich nature of the methoxy groups at positions 3 and 4 activates the aromatic ring, allowing smoother nucleophilic substitution and higher selectivity in Friedel-Crafts reactions compared to simple benzyl chloride. This remains critical for flavor and fragrance chemists aiming to build scaffold diversity without excessive protection and deprotection steps.

    We’ve witnessed clients compare it side by side with 2,4-dimethoxybenzyl chloride and even 4-methoxybenzyl chloride, discovering that small changes in substitution dramatically alter both reaction rates and byproduct profiles. The ortho-positioned methoxy group shifts electron density and changes reactivity profile in couplings, a subtlety often overlooked. Our team works hand in hand with formulation scientists to troubleshoot these effects, providing spectral data and reaction condition advice based on our direct production experience. There’s no substitute for granular feedback straight from the synthesis reactors, especially when minor differences translate to major process bottlenecks at larger scale.

    Balancing Cost, Quality, and Scale for Industrial Demands

    Running high-purity aromatic halide lines carries its own set of challenges, especially as raw material cost fluctuations bite into operating margins. Instead of pushing the pressure onto customers, our internal R&D program searches for smarter ways to recover solvents and optimize chlorination yields, aiming to keep both pricing reasonable and purity uncompromised. Over the years, we’ve adopted continuous flow chlorination for critical intermediates to cut down on waste and minimize the environmental impact, with all emission and discharge levels closely monitored.

    Bulk shipping comes with its own set of headaches. Overexposure to anything but inert-atmosphere packaging can mean losses from hydrolysis or slow polymerization. We’ve designed custom drum linings for export and offer tailored packaging for scale-ups, either in UV-blocked drums or small ampoules for sensitive applications. Clients in Europe and North America often need additional documentation to meet changing regulatory standards, so our batch reports include everything from heavy metal assay results to residual solvent analysis.

    Regulatory Considerations and Process Transparency

    Over the past decade, careful tracking and disclosure have become non-negotiable in specialty chemical production. Every lot of 3,4-Dimethoxybenzyl Chloride carries a full production history, right down to the personnel assigned to blending and batch release. This approach allows strict traceability. With regulations tightening on chlorinated aromatics, we register new synthesis methods as appropriate and report impurity thresholds in line with international guidelines. Clients working on GMP or near-GMP lines frequently request supporting evidence for ICH Q3A and Q3C compliance, and we’re equipped to deliver those datasets from our in-house analytics.

    Our lab data supports product safety, but field feedback informs every improvement. During a recent review, a pharmaceutical partner flagged the need for lower residual chloroanisole levels in feedstock. Our team went back to the reactor, adjusted reflux profiles, and cut impurity tails by an additional 30%, boosting client confidence. Such continuous feedback loops, only possible in direct manufacturer-client relationships, ensure standards stay ahead of regulatory trends.

    Safety, Storage, and Handling: Realities from the Floor

    3,4-Dimethoxybenzyl Chloride demands respect throughout storage and handling. Chlorinated aromatic liquids bring risks both from acute vapor exposure and from possible formation of lachrymatory agents. Many safety plans rely on theoretical recommendations, but practical experience teaches the real lessons. Valve failures during charging or delays in inert purging have the potential to cause downtime or injury. Our production teams wear positive-pressure suits and monitor real-time air levels, ensuring no batch leaves unless it meets strict internal and customer safety profiles.

    Unlike simple benzyl chloride, the dimethoxy variant offers slightly improved volatility management, but we never grow complacent. Decades of hands-on chemical manufacturing have taught us that regular storage checks, drum rotation, and periodic retesting are more valuable than overloading with extra preservatives. For logistics staff, regular refresher training on drum handling and spill containment is standard practice, reflecting the lessons of past incidents.

    Supply Chain Challenges and Practical Solutions

    Unpredictable supply shocks over the past years have highlighted the importance of reliable local and regional production. Rather than stretching global supply networks thin, we invest in redundancy—both through additional reactors and backup raw material sourcing. Our material rarely sits idle ahead of shipment, cutting lead times for urgent custom synthesis needs in pharma and R&D.

    We have felt the ripple effects of port congestion, customs delays, and regulatory red tape. To address this, we maintain strong relationships with regional freight handlers and offer flexible shipment sizes. Our production scheduling allows for batch reservation, enabling partners to synchronize their own supply chains without scrambling for late replacements. Having seen the cost of a missed opportunity or delayed clinical trial, we prioritize proactive communication, from advance notice on requalification batches to batch stability reports before shipment. These steps do more than promise consistency; they deliver it through transparent, proven process controls.

    Research and Development Insights

    In-house development forms the backbone of our operations. Every year, our chemists run dozens of experiments to explore subtle improvements in yield and impurity profile. Some of the most valuable advances have come from scaling up pilot runs to multi-ton reactors, revealing how small variables at bench scale can become major levers or stumbling blocks in production. Open collaboration with academic partners has shed light on new uses for 3,4-Dimethoxybenzyl Chloride, such as in the preparation of specialized dye intermediates or corrosion inhibitors.

    Each research partnership offers a chance to explore novel protection strategies or greener synthetic alternatives. Commitment to environmental stewardship spurs us to trial new catalysts and solvent recycling protocols. Decades ago, chlorinated aryls were made in batch glassware without much regard to waste; evolving industry standards now demand careful lifecycle analysis. Our team meets these challenges with a combination of veteran process engineers and young talent, running simulations before changing production lines. We learn from each other, and the resulting process flexibility pays dividends in cost control and rapid adaptation to emerging customer needs.

    Commitment to Ongoing Quality and Technical Support

    Technical support is just as important as product quality. Each client requirement carries its own challenges—some want analytical support to suit a new synthetic route, others need help troubleshooting crystallization or purification issues. Long-term partners rely on our rapid response to certificate requests or technical data questions. Our in-house technical team stays close to production, ensuring customer queries never sit in limbo or get lost in translation.

    Transparency matters most during critical troubleshooting. We offer side-by-side comparison data from alternate lots, and schedule conference calls with senior production chemists as needed. Having walked through these issues ourselves, our advice reflects real-world know-how, not just textbook answers. Some clients are scaling up for the first time; others have spent decades battling the complexities of multi-step aromatic synthesis. Whatever the challenge, we combine hands-on experience with state-of-the-art analytic capability to help them succeed.

    Product Evolution and Future Perspectives

    The specialty chemical sector never stops evolving. As new reaction pathways emerge and clients look to synthesize ever more complex targets, we evolve in parallel—updating process maps, investing in cleaner technologies, and cataloging lessons learned. Years of manufacturing 3,4-Dimethoxybenzyl Chloride have given us deep insights into what works and what can be improved. This ongoing learning fuels our product development and informs the advice we share with our partners.

    Though 3,4-Dimethoxybenzyl Chloride seems like a small cog in the machinery of modern synthesis, its reliability powers countless innovations in health care, fragrance, and green chemistry. Strong partnerships with end users, direct engagement on technical hurdles, and relentless process optimization form the backbone of our success. With every shipment, we aim to not just meet a specification, but to be a dependable partner in pushing the boundaries of modern chemical science.