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HS Code |
193597 |
| Chemical Name | 2,3-Dimethoxybenzyl Chloride |
| Cas Number | 4460-86-6 |
| Molecular Formula | C9H11ClO2 |
| Molecular Weight | 186.64 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 133-135°C at 13 mmHg |
| Density | 1.18 g/cm3 at 25°C |
| Refractive Index | 1.547 (25°C) |
| Solubility | Insoluble in water; soluble in organic solvents |
| Purity | Typically ≥ 97% |
| Smiles | COC1=CC=CC(OC)=C1CCl |
| Flash Point | 121°C |
| Storage Temperature | Store at 2-8°C |
| Hazard Class | Irritant |
As an accredited 2,3-Dimethoxybenzyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, securely sealed with a screw cap, labeled clearly. Contains 100 grams of 2,3-Dimethoxybenzyl Chloride. |
| Shipping | 2,3-Dimethoxybenzyl chloride is shipped in tightly sealed containers, protected from moisture and light. It must be clearly labeled as a hazardous material and handled according to local and international regulations. Proper ventilation, temperature control, and appropriate documentation are required to ensure safety during storage and transport. |
| Storage | 2,3-Dimethoxybenzyl chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Protect it from moisture and incompatible materials such as strong oxidizers and bases. Properly label the storage container, and keep it in a chemical storage cabinet, preferably one designated for corrosive or reactive substances. |
Applications of 2,3-Dimethoxybenzyl Chloride in Industrial Manufacturing2,3-Dimethoxybenzyl Chloride supports a wide range of downstream synthetic processes. Our facility works closely with manufacturers across multiple sectors, ensuring reliable supply and consistent quality for advanced intermediates. Below are principal industrial applications in which this raw material forms a critical building block. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) SynthesisMainstream API manufacturers use 2,3-dimethoxybenzyl chloride as a protected benzylating agent during the synthesis of select antihypertensive drugs and central nervous system agents. Its function in N-alkylation and O-alkylation reactions enables precise structural modification of complex pharmaceutical intermediates. Downstream QC departments require strict traceability and process validation for each batch. Industry compliance standards
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2. Agrochemical Synthesis – Herbicide and Fungicide IntermediatesLeading crop protection chemical companies employ this compound for controlled benzylation in the production of selective herbicide intermediates and custom fungicide building blocks. The raw material participates in side-chain introduction and ring-protection reactions under tightly monitored batch conditions. All downstream processes demand traceability in compliance with agricultural chemical regulations and site-specific environmental controls. Industry compliance standards
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3. Fragrance and Aroma Chemical ManufacturingAromatics and perfumery manufacturers utilize this chemical for introducing methoxybenzyl motifs into musk and floral fragrance intermediates. The reactivity under Friedel-Crafts alkylation conditions supports synthesis of complex odor-active molecules, which undergo further functional group transformations before blending into master fragrances. Downstream customers require strict olfactory profile consistency and compliance with international fragrance regulations. Industry compliance standards
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4. Fine Chemical Synthesis for Liquid Crystal and Electronic Material IntermediatesProducers in the electronic and display materials sector rely on this chemical for precision alkylation of functional monomers used in liquid crystal formulations and advanced organic electronics. The introduction of methoxybenzyl groups imparts performance modification, required for downstream coupling and polymerization steps. Documentation and batch processing are validated under advanced QC protocols to meet electronics industry tolerances. Industry compliance standards
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5. Dye and Pigment Intermediate ManufacturingColorant producers incorporate our raw material during the synthesis of methoxy-substituted aromatic intermediates for dyes and organic pigments. This step enables color nuance control and enhances dye fastness properties. Manufacturing sites implement dedicated safety and containment due to the reactivity of chlorinated benzyl derivatives and maintain batch-specific analytical documentation. Industry compliance standards
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Every day in our plant, we see requests for specialty intermediates that can carry both reliability and flexibility through complicated processes. 2,3-Dimethoxybenzyl Chloride stands out in our catalog for this particular reason. It doesn’t just get ordered on paper—we see batches scrutinized in the lab, monitored for consistency, and trusted by our clients who need clarity in yield and processability. Our engineers and technical staff keep this compound front-of-mind because they know it solves problems chemists actually face on the bench, not just what looks good in brochures.
This compound belongs in the group of aromatic benzyl chlorides, but the dual methoxy substitutions in the ortho and meta positions create a unique reactivity profile that pushes it into a category beyond basic building blocks. You can tell just from its light yellow to pale appearance before purification that you’re looking at something with a particular purpose, not a generic commodity.
To talk about our 2,3-Dimethoxybenzyl Chloride is to talk about the rhythms of our own reactors. We keep a close hand on specifications—most batches run in the purity range above 98% by GC, and we stick with a moisture control protocol that manages trace water down to levels that safeguard shelf life during extended transit. Chloride content, residual solvents, and byproduct profiles shape every lot. Our quality team pulls samples directly from final vessels, never from pooled drums, to avoid batch-to-batch skew when reporting data. These details matter because our clients work with strict validation standards and regulatory expectations.
Some clients request lot-specific impurity certificates, especially for pharmaceutical development or higher-value agri intermediates. We respond by running parallel analytics, often matching NMR and GC-MS results against literature references. There are downstream reactions, like nucleophilic substitutions or reductive couplings, which can go off-track with even slight contamination or over-chlorination. On more than one occasion, we've held back material to further purify and recheck, rather than risk a customer's process run.
We notice a lot of attention around the volatility and slightly lachrymatory nature of this compound. Handling routines in our shop start with triple-sealed containers and vented storage away from heat sources. This isn’t a chemical that ‘sits on the shelf’; the best results come from rotating inventory to maintain freshness and prevent subtle decomposition.
2,3-Dimethoxybenzyl Chloride gets called up again and again in synthetic routes where the aromatic ring needs selective activation, especially in pharmaceutical R&D and agricultural chemistry. We’ve shipped this compound for projects involving antihypertensive intermediates or fungicidal leads, but discovery teams have told us they look for the balance of electron-donating methoxy stability and a leaving group that opens transformation doors without clogging up side-product pools.
In our feedback pipeline, several academic groups mention it as a preferred protecting group source for nitrogen or oxygen nucleophile protection steps in multi-stage sequences. Its performance in benzylation reactions is clean—minimal tar, manageable exotherms—and our production logbooks tell us the average crude yields hold up even when scale-up jumps from kilogram lab benches to full-reactor campaigns.
We also know it’s not a universal fix. Certain process screens favor para- over ortho-methoxy substitution, or demand non-chlorinated analogues to sidestep regulatory or waste-handling complications abroad. Still, 2,3-Dimethoxybenzyl Chloride keeps a loyal audience among those who appreciate its niche: those wanting reactivity without sacrificing robustness.
Processors regularly cite the clean, single-step conversion to the corresponding alcohol or amine derivatives. The methoxy groups resist harsh reaction conditions, meaning the parent structure survives in multi-step processes, only releasing the protecting group after the final transformation. That makes it valuable to those who can't afford a late-stage failure due to group migration or uncontrolled hydrolysis.
We’ve engineered our systems with an eye for both throughput and precision. Batch records show the effects of slight deviations in chloromethylating agent quality, or what happens when winter water temperatures slow down exotherm control. We’ve logged times where trace iron contamination or even atmospheric moisture led to observable shifts in purity—these learnings get baked back into SOPs, rather than being ignored or glossed over.
Nothing replaces the experience of actually running crude through to distillation. For years, we relied on classical distillation to separate out main fractions, but recent upgrades to packed columns and precise reflux control have let us cut down on byproduct tails and collect a more uniform product fraction. These aren’t just lab improvements—but shifts we see reflected in customer process reproducibility. We don’t see a perfect run every single time, but keeping error logs and acting on root cause analysis delivers smaller variation lot-to-lot.
The day-to-day realities of manufacturing also mean solving bottlenecks on the fly. Sometimes, demand swings fast—from a baseline hundreds of kilograms for routine campaigns to urgent inquiries in the low tons due to market spikes. We keep an active raw material sourcing network to avoid interruption, even at the cost of lead time flexibility for our standard clients. Our plant crews know that finding the right coupling agents, maintaining catalyst inventory, or replacing worn seals in a pinch means uninterrupted deliveries for end users who have little margin for mistakes.
We get a lot of questions comparing 2,3-Dimethoxybenzyl Chloride to ortho- or para- monochlorinated analogues, or plain benzylic chlorides without methoxy substitution. The presence of two methoxy groups in adjacent positions doesn’t just nudge the electron density: it drives selectivity in subsequent steps that standard 4-methoxy or plain benzyl chloride can’t match. This isn’t just a textbook matter—real-world batch logs from our customers confirm higher selectivity in Friedel-Crafts and SN2 conditions, and easier purification compared to more basic benzyl chlorides, where side reactions or over-chlorination often muddies the final product.
In practice, chemists looking for a ‘catch-all’ might start with unsubstituted benzyl chloride out of habit, but we see experienced teams switch after screening—especially if they’re chasing unique scaffold derivatizations, or need to minimize tar and insoluble crud in their filtrates. Those working on process scale-up value the dual-methoxy effect, not just academically but for its stabilizing impact on the molecule under moderate heat and pressure.
Regulatory compliance has become another separation point. In regions where environmental restrictions around halogenated organics have tightened, we respond with support for proper waste stream tracking and documented handling. The dual-methoxy structure doesn’t automatically simplify global regulations—so part of our job means keeping solvent-use documentation and impurity reporting up-to-date to back customers during import-export checks.
During process transfers or technology scale-outs, clients often share with us that 2,3-Dimethoxybenzyl Chloride offers easier analytical fingerprints, especially in HPLC or NMR verification, since the dual-methoxy protons behave more predictably than the multifaceted signatures in multi-halo products. This shaves significant time off QC round-tripping, letting production teams get to full-scale releases more quickly and with fewer headaches.
There’s a practical side beyond chemistry. Storage stability, resistance to ambient decomposition, and handling safety all improve with the added electron density from the methoxy groups. Accidents tied to volatile emissions and slow degradation trouble far fewer shipments compared to less substituted analogues, especially in long-haul containers where heat spikes can otherwise trigger slow polymerization.
As a manufacturer, we’ve always treated customer process feedback as ground truth. Early on, we stuck to fairly basic purification regimes—believing that end-users would purify further downstream. Over time, more clients started conducting intensive trace metal and solvent tests as part of their acceptance protocols. Listening to this, we invested in downstream carbon treatment and fine-filtration upgrades right at the end of our production chain, not after a failed delivery.
Our records tell stories where overlooked micro-impurities led to failed hydrogenation or unwanted resin formation at a pilot scale. It reminds us that what matters isn’t always obvious from macro analytics—sometimes it’s those trace contaminants that throw a wrench in an otherwise robust synthesis. By integrating this feedback across departments—from the people drawing samples to the engineers tuning column loads—we close the loop between the lab and the shop floor.
We’ve also learned that repeatability beats theoretical yield every time. A slightly lower yield reproducibly achieved with stable, clean product outweighs a theoretical maximum that falls apart in a scaled reactor. Our process validation reflects this: stress testing each batch, then rerunning QC analytics with client-supplied samples, helps us meet demands for both flexibility and reliability.
Every new protocol or technology we bring in comes after dozens of comparative batch runs—real shipments, split and sent to customers who kick the tires and send us back real-world handling notes. Charge orders in the plant include details from these trials, so every operator understands where a run succeeded or failed outside our plant. This iterative approach has let us carve out a reputation for not just meeting specs, but for backing up our claims with documented, repeatable outcomes.
In our industry, sustainability isn’t just a buzzword—regulators, clients, and internal teams all push for cleaner runs, less waste, and traceability along the entire supply chain. For a specialty intermediate like 2,3-Dimethoxybenzyl Chloride, this goes beyond just solvent recycling. We’ve introduced steps that reclaim chlorination media, upgraded vent scrubbers, and brought in continuous monitoring for effluent streams—choices inspired by both regulation and our own crew’s drive to leave the plant cleaner at the end of each shift.
Supply chain transparency has become a code we live by. Sourcing key raw materials from firms with their own documentation builds confidence that our batches don’t carry legacy contamination. We’ve moved away from gray-market intermediates by directly auditing upstream providers, even partnering with some for co-processing to lock in quality from the first step. This practice doesn’t always save money, but it guarantees real accountability if problems ever hit a downstream product.
Our warehouse logs track every container movement, so tracing a lot from reactor to truck—down to the crew signing off—lets us answer questions quickly during audits. This is not an abstract exercise. Regulators now demand genuine chain-of-custody records, and clients running GMP protocols expect nothing less. This level of documentation isn’t always appreciated until something goes off in the middle of a filing or a late-stage tech transfer. When that happens, our records become their insurance policy.
The move to greener chlorination agents and use of energy-efficient distillation setups across our lines reflects this push. We don’t see sustainability as subtractive—cutting corners or restricting tools—but as a driver for plant upgrades. Our crews feel proud bringing new containment systems online or automating emissions capture, and this pride translates directly to cleaner chemistry for our clients.
Behind every shipment of 2,3-Dimethoxybenzyl Chloride stands a supply team that understands the chemical is only as good as the process behind it. Regular meetings between shift supervisors, engineers, and QC keep our focus sharp. If a test result falls short, it triggers action—not a paper shuffle. We understand that the slightest drift in process parameters can snowball downstream. That is why so many long-term customers keep coming back for more, not out of habit but because they know we listen—and act—on the smallest process hiccups before they become bigger problems.
This attitude grew from years in the trenches. We’ve gone from half-ton glass-lined setups in cramped spaces to modern, automated lines that scale without missing detail. Every piece of feedback from a failed lab trial, a shipping hiccup, or a certification demand has shaped not just our product, but the way we operate. We see the task not as delivering a bottle, but as supporting the researcher or processor who has put their own reputation on the line.
There are easier chemicals to make, and certainly easier ones to move. Yet each lot of 2,3-Dimethoxybenzyl Chloride carries the weight of all those lessons—failures, improvements, and successful runs—made visible in clean, sharp NMRs, tidy GC traces, and customer batches that work the way they're supposed to. That's why supply partners and R&D leads who value real results, not just compliance boxes, still make this compound a cornerstone in discovery and production pipelines.
Our crew believes every drum or bottle shipped out matters for much more than this quarter’s numbers. Behind the scenes, it’s about building trust where chemistry meets real-world complexity. We’re not just supplying a tool; we’re shaping the outcomes that come from teams betting big on their next breakthrough. For us, that’s worth every ounce of effort.