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2,6-Dimethylbenzyl Chloride

    • Product Name 2,6-Dimethylbenzyl Chloride
    • Alias alpha,alpha,2,6-Tetramethyltoluene
    • Einecs 210-616-1
    • 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
    VTB
    Specifications

    HS Code

    536842

    Cas Number 87-24-1
    Molecular Formula C9H11Cl
    Molar Mass 154.64 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 222-224 °C
    Melting Point -30 °C
    Density 1.05 g/cm³ at 20 °C
    Refractive Index 1.546
    Flash Point 101 °C
    Solubility In Water Insoluble
    Vapor Pressure 0.09 mmHg at 25 °C
    Ec Number 201-734-5

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

    Packing & Storage
    Packing 2,6-Dimethylbenzyl Chloride is supplied in a sealed 500 mL amber glass bottle, with safety labeling and tamper-evident cap.
    Shipping 2,6-Dimethylbenzyl Chloride is shipped in tightly sealed, corrosion-resistant containers to prevent leakage and moisture exposure. Packages are clearly labeled according to hazardous material regulations and handled with care. Transport is arranged via ground or air freight, following all safety guidelines to ensure proper containment, ventilation, and protection from heat or open flame.
    Storage 2,6-Dimethylbenzyl chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat sources, sparks, and open flames. Keep away from strong oxidizers, acids, and bases. Protect from moisture and direct sunlight. Use proper labeling and store in a designated chemical storage area, preferably in a corrosive-resistant cabinet.
    Application of 2,6-Dimethylbenzyl Chloride

    Applications of 2,6-Dimethylbenzyl Chloride in Industrial Manufacturing

    As a direct manufacturer of 2,6-dimethylbenzyl chloride, we supply this high-purity intermediate to a focused range of downstream sectors where consistent performance, traceability, and compliance are demanded throughout production. The application scenarios below detail how industry leaders integrate this material within specialized operations, supporting high-value end products through controlled formulation and well-defined processing stages.

    1. Pharmaceutical Intermediate Synthesis

    Leading API manufacturers incorporate this compound as an essential alkylating agent in multi-step syntheses, enabling the construction of specific aromatic side chains and core pharmaceutical scaffolds. Its use typically occurs in early or intermediate stages, where precise functionalization is necessary for downstream medicinal chemistry workflows, with demand driven by ongoing patent, regulatory, and process optimization cycles in regulated environments.

    Industry compliance standards

    • ICH Q7 “Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients”
    • US FDA 21 CFR Part 210/211
    • EU GMP EudraLex Vol 4, Annex 8 (Sourcing and Use of Starting Materials)
    • Chinese Pharmacopoeia (relevant monographs on impurities, residual solvents, and heavy metals)

    Typical usage ratio

    • 0.5%–2.5% w/w relative to total reaction mass, adjusted according to target molecule yield and process stoichiometry

    Downstream process integration

    • Added during the controlled benzylation or selective alkylation steps under inert conditions, followed by quenching and washing to reduce unreacted material and byproducts

    Final product types

    • Synthesized intermediates for antihypertensive agents
    • Custom aromatic building blocks for CNS drugs
    • Precursors to nonsteroidal anti-inflammatory compounds

    2. Agrochemical Active Ingredient Manufacturing

    Major crop protection formulators utilize this chemical as a critical intermediate or blocking group in synthesis routes for select fungicides and herbicides, where it contributes to molecular stability and enhances subsequent functionalization. Integrating the compound into agrochemical production enables controlled reaction pathways and facilitates scalable conversion required for bulk field-grade products.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China GB/T 1604-2018 (Technical Specification of Pesticide Active Substances)
    • US EPA Product Chemistry/Data Requirements (CFR Title 40, Part 158)
    • REACH Registration (EC 1907/2006) for production and downstream usage within Europe

    Typical usage ratio

    • 1.0%–3.5% w/w of total batch input, tuned to accommodate the specific active ingredient route and seed ratio in continuous or batch synthesis

    Downstream process integration

    • Dosed directly in closed-system reactors as the alkyl source during condensation or coupling reactions before purification and formulation

    Final product types

    • Key intermediates for triazole or strobilurin fungicides
    • Herbicidal actives for rice and grain crops
    • Custom-protected building blocks for patent-protected agrochemicals

    3. Specialty Fragrance and Aroma Chemical Synthesis

    Aroma chemical producers invest in high-grade chlorinated precursors to achieve targeted molecular profiles and stability in fragrance ingredients for use in global consumer products. 2,6-dimethylbenzyl chloride undergoes specific reactions to form stable intermediates or advanced synthetic musks, serving as a controlled structural motif for long-lasting aromatic properties in perfumery compositions and fine fragrances.

    Industry compliance standards

    • IFRA Code of Practice & Prohibitions
    • ISO 9235:2013 (Aromatic Raw Materials for Perfume Industry)
    • US FDA 21 CFR 172.515 for food-contact aroma chemicals
    • EU Regulation (EC) No 1223/2009 for cosmetic use

    Typical usage ratio

    • 0.2%–1.25% w/w based on batch scale, adjusted in synthesis according to yield optimization and odor concentration targets

    Downstream process integration

    • Introduced as a benzylating reagent during core formation of musk intermediates, with sequential distillation and odor testing to meet olfactory quality parameters

    Final product types

    • Synthetic musk base chemicals (e.g., polycyclic musks)
    • Aroma intermediates for perfumery and household products
    • Specialty scent compounds for detergents and fabric softeners

    4. Polymer and Resin Additive Synthesis

    Producers of specialty polymers and thermosetting resins integrate this intermediate in controlled alkylation and crosslinking steps, customizing resin backbone structures to improve thermal, chemical, or mechanical properties critical for end-use applications in coatings, laminates, and electrical encapsulation. Its use supports innovations in tailored curing speeds, adhesion, and environmental resistance profiles.

    Industry compliance standards

    • UL 94 Flammability Testing for plastics used in electronics
    • RoHS Directive 2011/65/EU for hazardous substance limitation
    • ISO 9001:2015 Quality Management System for chemical manufacturing
    • JIS K 6911 for synthetic resin modifier evaluation in Japan

    Typical usage ratio

    • 0.35%–1.8% w/w of resin or prepolymer blend, with dosage optimized for molecular weight, crosslink density, and curing characteristics

    Downstream process integration

    • Dosed during in-situ alkylation of monomer or prepolymer before polymerization or curing (e.g., in a two-stage batch reactor or continuous manufacturing line)

    Final product types

    • High-performance epoxy resins for electronics
    • Modified phenolic resins for automotive brake pads
    • Thermoset-dedicated coatings for industrial floors

    5. UV-Absorber and Stabilizer Intermediate Manufacturing

    Producers in the plastics and coatings industries employ this compound as a precursor for light stabilizer and UV-absorber additives, which protect polymers and coatings from photodegradation and discoloration. Precision in formulation ensures additive activity and compliance with product and food-contact safety regulations in high-visibility consumer and infrastructure applications.

    Industry compliance standards

    • US FDA 21 CFR 177.1520 for polymers in food contact
    • EU Regulation (EU) No 10/2011 for plastic materials in food packaging
    • ISO 4892-2 Artificial Weathering Tests
    • GMP for Additive Production (ISO 22000, where food packaging is involved)

    Typical usage ratio

    • 0.07%–0.26% w/w in masterbatch or polymer compound; varied according to end-use exposure intensity and target UV resistance strength

    Downstream process integration

    • Introduced as a key reagent during the synthesis of benzotriazole or benzophenone-based UV-stabilizer intermediates before compounding into polymer matrices

    Final product types

    • UV-stabilizer masterbatches for polyolefins and polycarbonates
    • Coating additives for automotive and outdoor infrastructure
    • High-clarity films and packaging materials resistant to UV-induced yellowing
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    Certification & Compliance
    More Introduction

    2,6-Dimethylbenzyl Chloride: A Straightforward Introduction From the Manufacturer

    Getting to the Heart of 2,6-Dimethylbenzyl Chloride

    2,6-Dimethylbenzyl chloride is one of those specialty intermediates that pushes forward a lot of innovation in both the chemical and pharmaceutical industries. You won’t find this molecule sitting on a shelf collecting dust; it sees daily use in real production lines. From the moment our line starts converting xylenes, the goal remains steadfast: deliver a consistent, high-purity benzyl chloride that supports synthesis and process efficiency downstream, without causing headaches in the plant or research lab.

    The Specifics: Model, Purity, and Physical State Matter

    Chemists recognize 2,6-dimethylbenzyl chloride by its CAS number, but what really matters in the field is how the material performs batch after batch. In practice, we manufacture it to achieve a purity above 99%—with gas chromatography verifications to back those numbers. Customers always want to know about residues, unreacted starting material, and organic impurities. It pays to mention our approach: we monitor organochlorine byproducts and the usual suspects like 2,6-xylene so that none of them creep above acceptable values—especially since small impurities can complicate downstream reactions.

    Our production method gives a colorless to light yellow liquid, slightly heavier than water, with a sharp and recognizable aromatic odor. Chemists handling this product value the viscosity and the way it responds to temperature swings—2,6-dimethylbenzyl chloride remains stable in standard indoor conditions but should stay away from bright sunlight or high humidity, which could ramp up decomposition or byproduct formation. Transport and storage both hinge on this. We use lined containers specifically proven to prevent leaching of metals or plastics that would mess with analytical work or reactivity.

    Into the Field: Real Uses and What Sets This Chloride Apart

    Whether you’re making biocides, specialty polymers, or intermediates for pharma, 2,6-dimethylbenzyl chloride plays a unique role. Its two methyl groups positioned at the ortho sites lend a particular reactivity not seen in plain benzyl chloride or the more common para-substituted versions. Our customers in fine chemicals synthesis use this molecule as an alkylating agent, especially where steric hindrance can suppress unwanted side reactions.

    Much of the demand stems from its clean reactivity in nucleophilic substitution. Formulators notice that with this structure, getting selectivity in the introduction of the benzyl group to target molecules becomes a manageable task—which isn’t always true with other chlorinated aromatics. For some of our long-term buyers developing synthetic building blocks, this difference determines yield, which in turn cuts costs and time in scale-up operations.

    Comparing to Other Benzylic and Aromatic Chlorides

    2,6-Dimethylbenzyl chloride is a close cousin to several other chlorinated aromatics. Manufacturers get asked about this a lot; customers want to know why they’d use this, and not just another benzylic chloride. The answer always comes down to reactivity and selectivity. Take benzyl chloride: reactive, but less selective. The extra methyl groups in the 2 and 6 positions block unwanted substitutions on the ring and guide the molecule to react in the right places. This helps when a chemist wants clean downstream material, especially in multistep syntheses or pharmaceutical work, where byproducts can derail expensive processes.

    Compare this to o-chlorotoluene or other monochlorinated derivatives. Those have their uses but lack the spatial arrangement that 2,6-dimethylbenzyl chloride brings to the table. That structure, with just enough bulk near the reactive site, reduces over-alkylation and suppresses side product generation. You see fewer headaches in purification and higher yields in controlled alkylations, which matters at kilo and ton scales.

    Manufacturing Challenges and Solutions On the Ground

    Sourcing high-purity 2,6-dimethylbenzyl chloride keeps us on our toes. The process starts by selecting clean xylene streams—impurities here can echo through every subsequent batch. Control of chlorination conditions is everything; over-chlorination or uneven mixing can drive up byproduct levels. Our reactor operators watch temperature, chlorine feed rate, and solvent ratios with an eye on reproducibility because small shifts alter selectivity and waste fractions.

    Waste management can’t be an afterthought. Chlorinated byproducts have strict regulations around them, and venting or disposal costs increase fast if scrubbing or distillation isn’t done correctly. Years of producing this benzyl chloride have made it clear: containment, continuous monitoring, and planned maintenance reduce both environmental impact and line downtime. We recover solvents and run closed-loop systems to keep emissions well below compliance targets, because fines and forced shutdowns help no one.

    Why Consistency Remains Vital

    One customer may use hundreds of kilos per campaign making biocides, another might scale up for a specialty adhesive or a pharma intermediate. Both agree on one thing: unreliable batches throw off entire syntheses and eat into margins. Consistency doesn’t come from luck but from hands-on process control, from raw materials all the way through to blending and packing—the shop floor stories about tracing a yield issue back to minute shifts in raw material are real.

    Monitoring each lot and logging every tweak to the process keeps this product behaving the same from batch to batch and year to year. We perform not just endpoint tests but in-process analytics, comparing current runs with historical data and tweaking feedstocks or processing windows to stay within a tight spec. That mindset saves headaches down the line for both us and our customers.

    Serving Innovation, Not Just Orders

    Research labs working on new biocidal compounds choose this chloride when searching for selectivity not afforded by common alkylating agents. Its particular structure impacts activity profiles for molecules destined for use in fungicides or antimicrobial coatings. Our team keeps in contact with these groups, sometimes producing small custom lots with even lower impurity profiles for exploratory synthesis or pilot scale-up. The feedback loops between manufacturer and user here change both the product and the chemistry—improvements don’t happen stuck at the desk, but out testing real samples on actual problems.

    Development of performance polymers sometimes draws on 2,6-dimethylbenzyl derivatives to impart resistance or flexibility to the end material. That’s not just ‘adding chlorine’; what matters are sterics, ease of downstream functionalization, and making sure copolymerization runs without unexpected fouling or waste. Our records show that batches tailored for these applications reduce in-plant troubleshooting and line shutdowns for the compounders who buy from us directly. It’s only through repeated feedback—both positive and critical—that we’ve tuned our processes to avoid common faults and keep the lines moving.

    Lessons From Scale-Up: What Really Goes Wrong, and How to Stay Ahead

    Scale-up can go off the rails for simple reasons: solvent switch, a slightly different catalyst batch, or a new piece of plant piping that leaches trace metals. Years ago, a change in the feedwater supply altered a single minor ion, and trace formation of a sticky byproduct spiked almost overnight. We caught it in the in-process analytics, tweaked the neutralization steps, and got back on track, but it illustrates the reality: what looks trivial on paper often changes everything at the scale of tons.

    Documentation and repeatable process flows reduce surprises. We build hold points into every campaign, where samples get checked against retention standards kept for years. Plant operators with hands-on experience, not just digital instruments, catch and solve upsets before they scale into real problems. Training and retention of these skilled workers matter as much as any sensor or software upgrade.

    Looking Ahead: Demand, Sustainability, and Product Development

    Demand projections make it clear: as molecular complexity in fine chemicals and pharmaceuticals increases, specialty intermediates like 2,6-dimethylbenzyl chloride gain importance. Companies push for higher purity starting materials to improve downstream yields and reduce purification costs. Our focus keeps shifting not only to meet current specs but to anticipate next-generation requirements; we watch emerging regulations on organochlorines, anticipate new target impurity levels, and adjust production flows long before external pressure forces a change.

    Sustainability pushes don’t get ignored. Chlorinated aromatics face a lot of scrutiny, so we invest in emissions capture and waste recycle technology. The best results we’ve seen come by working together with downstream users, sharing not just material but also data on fate and disposal of residuals. We piloted solvent recycling with a major customer, cutting both parties’ waste handling costs, and turned those results into plant SOPs. In an environment of tightening regulations and global competition, agility and openness help everyone hold the line on both compliance and cost.

    The Human Side at the Manufacturer: Day-to-Day Work and Building Trust

    Nobody who works at the plant sees themselves as just pushing product out the door. Most of the crew can recognize a tank of 2,6-dimethylbenzyl chloride by sight and smell, but it’s the details—clear labeling, sharp monitoring, and real record-keeping—that make the difference for plant and end user. Early each shift, operators check batch logs against customer specs, test color and acid content, and confirm tanks are sealed right to avoid contamination.

    Supply chains don’t always flow smoothly. A labor dispute, an uptick in regulatory checks at the port, or even a sudden cold snap that affects raw material transport can cause holdups. Over decades, direct partnerships built out of repeated troubleshooting and steady communication have carried us through these interruptions. This direct line to customers—engineers and chemists, often on their own manufacturing or research floor—means problems get solved fast, miscommunications stay rare, and specs stay tight.

    Final Thoughts on 2,6-Dimethylbenzyl Chloride in the Industry

    Years of direct manufacturing experience shape how we view 2,6-dimethylbenzyl chloride. Customers need more than paperwork or safety data; they need transparency, support during process changes, and candor about problems when they arise. The reason this product continues to find wide use comes down to a persistent focus on quality, predictability, and the ability to adapt to specific technical challenges. Working with 2,6-dimethylbenzyl chloride—with all the quirks and requirements it brings—reminds us that chemical manufacturing isn’t a theoretical exercise, it’s a practical, hands-on job that shapes real outcomes from plant floor to finished goods.

    Those new to using this intermediate sometimes expect off-the-shelf performance, but the reality of specialty chemicals demands collaboration from both sides. We’ve seen poorly controlled inputs or casual storage sabotage entire projects; on the other hand, strict but practical adherence to best practices, informed by field experience, leads to safer, cheaper, and more reliable operations. We remain committed to continuous improvement—because in chemical manufacturing, standing still is the fastest way to fall behind.