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HS Code |
442506 |
| Chemical Name | 3-Chlorobenzyl Alcohol |
| Synonyms | m-Chlorobenzyl alcohol; m-Chlorophenylmethanol |
| Molecular Formula | C7H7ClO |
| Molecular Weight | 142.58 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 243-245 °C |
| Melting Point | 26-30 °C |
| Density | 1.24 g/cm³ |
| Refractive Index | 1.556 |
| Cas Number | 1825-61-2 |
| Solubility In Water | Slightly soluble |
| Flash Point | 114 °C (237 °F) |
As an accredited 3-Chlorobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 500 mL, sealed with a tamper-evident cap, labeled with chemical name, hazard symbols, and handling instructions. |
| Shipping | 3-Chlorobenzyl Alcohol is typically shipped in tightly sealed containers to prevent leaks and contamination. It should be packaged according to chemical safety regulations, labeled as a hazardous material, and handled with care to avoid exposure. Transportation must comply with local, national, and international regulations for the shipment of hazardous chemicals. |
| Storage | 3-Chlorobenzyl Alcohol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents and strong acids. Keep it in tightly sealed containers made of compatible material, clearly labeled, and protected from physical damage. Minimize exposure to moisture and light, and ensure appropriate spill containment measures are in place. |
Applications of 3-Chlorobenzyl Alcohol in Industrial ManufacturingOur production of 3-Chlorobenzyl Alcohol supports key sectors that demand stringent compliance and formulation precision. On this page, we outline the actual industrial applications recognized across global manufacturing, specifying regulatory standards, dosage considerations, pharmaceutical technology, and ultimate end-product uses for each scenario. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers use this compound in the synthesis of APIs targeting specific therapeutic classes, such as antihypertensives and antifungals. Production sites depend on the chlorinated benzyl alcohol group to achieve precise molecular modifications, influencing both reaction selectivity and yield during key medicinal chemistry transformations. Dosage within multi-step syntheses requires optimization based on molecular conversion and impurity profile constraints, evaluated during scale-up and QA validation. Industry compliance standards
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2. Agrochemical Synthesis IntermediatesAgrichemical facilities employ our product as a core intermediate in the structural modification of herbicide and fungicide actives, especially for molecules relying on chlorinated aromatic alcohol scaffolds. This integration facilitates the construction of active moieties conferring crop protection specificity and environmental persistence properties, aligned with evolving regulatory residue thresholds. Industry compliance standards
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3. UV-Curable Resin Modifier for Specialty CoatingsManufacturers of performance coatings exploit the aromatic reactivity of this compound within UV-curable resin formulations to adjust surface hardness and chemical resistance. Downstream users select this additive when tailoring crosslinker chemistry for advanced protective coatings employed in electronics, optical fibers, or automotive parts, where durability and chemical compatibility are mandatory. Industry compliance standards
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4. Fragrance and Flavour Building Block in Fine Chemical SynthesisProducers of aroma chemicals adopt this specialty alcohol as a structural agent in the multi-step synthesis of bespoke fragrance molecules, especially for intermediates requiring halogen-substituted aromatic motifs. Reactivity and purity allow for integration into GMP- or IFRA-compliant processes, controlling off-note generation and conforming to strict residue standards in finished perfumery or food flavors. Industry compliance standards
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5. Intermediate in Dye and Pigment SynthesisSpecialty dye manufacturers integrate this compound to generate halogenated aryl moieties required in certain solvent-stable and high-chroma colorants. This enables competitive coloration properties in industrial and textile markets, addressing both resistance to photobleaching and requirements for precise shade consistency across large-batch production. Industry compliance standards
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6. Fine Chemical Intermediate for Polymer Stabilizer ProductionChemical companies specializing in advanced polymer additives deploy this aromatic alcohol as a building block to develop polymer stabilizers, especially UV and thermal stabilizers used in high-performance plastics. The chloro-substituted aromatic core supports reactivity in constructing hindered phenol derivatives and benzotriazole stabilizer frameworks, meeting durability demands in critical engineering applications. Industry compliance standards
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In the world of specialty chemicals, 3-chlorobenzyl alcohol has found its place as a reliable intermediate for many sectors. Our team has managed each link of its production for over a decade, from raw material sourcing to final quality checks. This hands-on experience allows us to talk with confidence about its nature, capabilities, and practical differences from other benzyl alcohol derivatives.
3-Chlorobenzyl alcohol appears as a clear to slightly pale liquid at room temperature, with a faint aromatic scent—a subtle reminder of its benzene ring structure. The molecular formula C7H7ClO positions a chlorine atom at the meta position on the benzene ring, a structural detail that quietly but distinctly shapes both its reactivity and application range compared to its ortho and para counterparts.
Behind every drum leaving the plant, our production lines support strict in-process monitoring. We use high-purity benzyl alcohol and maintain a standardized chlorination reaction under controlled conditions. Over years, this process control approach has helped maintain a typical assay for 3-chlorobenzyl alcohol near or above 99%. Moisture, color, and trace impurity content get checked batch by batch, not because it’s in a spec sheet, but because downstream chemistry demands it.
Such constant attention to detail prevents surprises in later reactions, particularly for our largest customers working in the synthesis of pharmaceutical intermediates or specialty agrochemicals. They rely on this predictable quality, as even subtle impurities can impact reaction yields or product purity downstream.
3-Chlorobenzyl alcohol doesn’t end up on a shelf or in a package you’ll see in a store. Its job happens quietly, often as a trusted intermediate in a synthesis pathway. For our pharmaceutical customers, it serves in the stepwise construction of more complex molecules—such as antihistamines, antimicrobials, or even some central nervous system drugs. The meta-chloro substitution brings a level of electronic control that lets synthetic chemists steer reactions with better selectivity.
For others, the alcohol group in this molecule offers a good hook for esterification or etherification. We see it in the manufacture of certain dyes, in fragrance chemistry, and in crop protection research. Like the other benzyl alcohol isomers, 3-chlorobenzyl alcohol dissolves well in organic solvents but stays limited in water solubility, which can be helpful or limiting depending on the process.
We’re often asked about the difference between 3-chlorobenzyl alcohol and the closely related 2- or 4-chlorobenzyl alcohols. From our plant operations to customer feedback, we’ve seen subtle but important distinctions. The meta (3-) substitution on the ring adjusts both reactivity and the final molecular properties of derivative substances.
For chemists seeking electronic effects that moderate reaction speed but enable better regioselectivity, the 3-chloro placement delivers a sweet spot. Ortho substitution, in contrast, can introduce steric hindrance, complicating further functionalization or influencing physical properties like melting point and solubility. The para isomer sometimes offers alternative reactivity and can be easier to synthesize at high purity, but often yields downstream intermediates with a different performance profile.
From our production side, purification steps for 3-chlorobenzyl alcohol demand more rigorous process control than the para version. Crystallization, filtration, and distillation are tweaked for each batch, informed by analytical data and years of process improvements. This extra care pays off in consistent supply and fewer issues for customers scaling up their reactions.
Our teams regularly visit customer plants to help with bulk handling or quality investigations. Through these experiences, practical advice emerges. 3-Chlorobenzyl alcohol remains stable in ambient conditions if sealed and kept away from strong oxidizers or acids. In larger operations, we recommend stainless steel or HDPE drums with tight closures. Leakage—not common but possible with poorly maintained seals—deserves quick attention, as spills are slippery and traces of the compound linger unless cleaned with suitable organic solvents.
Some customers request guidance on safe metering, especially for processes that dose the alcohol automatically. Based on our own in-plant and customer-site trials, gentle heating to just above room temperature sometimes helps to lower viscosity for easier transfer—though high temperatures should be avoided to prevent degradation.
Nobody who produces 3-chlorobenzyl alcohol regularly will claim the process is effortless. Chlorination reactions call for controlled conditions—temperature spikes or poor mixing can lead to by-products, including di- or tri-chlorinated materials. Our approach uses incremental dosing of chlorine, supported by real-time monitoring of reaction progress with in-line spectroscopy.
Factory teams know that every change in upstream raw material quality or reaction environment impacts yield and purity. In some years, tighter regulatory limits on benzene derivatives have pushed suppliers to innovate. We found value in investing in better waste capture and purification systems. By recovering and recycling solvents within the plant, we have reduced emissions and improved purity—responding directly to customer and regulatory requirements without hiking up costs.
Feedback from partners in the pharmaceutical and agrochemical industries remains the most valuable part of our product development cycle. Synthetic chemists often share reaction yield data, impurity profiles, or downstream challenges with us. Sometimes, a new impurity shows up under specific storage or transport conditions. A few years back, one customer reported trace by-products during a scale-up for a late-stage pharmaceutical intermediate, traced to changes in their plant’s ambient humidity. Working together, we tweaked our drying and packaging protocols—not just for them, but for every shipment since.
This spirit of collaboration guides both our production philosophy and our troubleshooting efforts for 3-chlorobenzyl alcohol. We’ve added real-time analytics, bulk sample archiving, and tailored technical support to make sure every drum matches not just paperwork but real application requirements.
Production of chlorinated chemicals brings environmental responsibility. Over the years, stricter regional and global regulations have influenced plant design and emissions management. Our approach is direct: capture, treat, and minimize wastes at source. Effluent monitoring and scrubber upgrades run alongside process optimization projects. Sometimes these efforts have forced us to overhaul entire process segments, but the reduction in off-gas and chlorinated waste has been worth every investment.
3-Chlorobenzyl alcohol itself does not persist in the environment under normal use scenarios, as it breaks down by biological and chemical pathways. Still, we educate customers on proper handling and waste disposal, especially during washouts or cleaning of tanks used to store or transport this product. Our teams run periodic training and produce guidance not just for compliance, but to ensure safety and proper stewardship in every link of the supply chain.
Through countless technical service calls, we see how downstream uses for 3-chlorobenzyl alcohol hinge on reliability in physical and chemical consistency. For complex multi-step syntheses—whether a pharma block or agrochemical precursor—a single “off” drum can disrupt days or weeks of work. Our customers rely on both fast response and technical advice for troubleshooting.
Over time, we’ve tackled everything from unexpected trace peaks in GC chromatograms to advice on in-situ protection of the alcohol group. Sometimes, substituents on the benzene ring of downstream products influence bioactivity or stability of the final active ingredient. The meta-chloro brings different electronic effects compared to para—something synthetic teams appreciate for fine-tuning molecule performance. We partner with R&D groups to share data and even customize purification for projects with tighter-than-standard impurity requirements.
Bulk users care about more than purity and profile. Handling efficiency matters, as does security of supply and predictable delivery timings. In response, our plant maintains a buffer stock and forward schedules multi-ton batches during peak demand windows tied to the agricultural or pharmaceutical calendar. Each container—whether a drum or an IBC—comes with a full suite of analytical reports, including chromatographic purity, moisture content, and checks for critical trace contaminants.
We’ve moved to tamper-evident closures, barcoded tracking, and provide transparent batch history for every shipment. Over time, these steps have reduced logistics issues, ensured product integrity in transit, and built a predictable link between our own manufacturing and customer operations.
People on production lines face the risks up close. We provide them with detailed safety guidance and equipment. Direct contact with 3-chlorobenzyl alcohol can lead to irritation, making personal protective gear non-negotiable. Automated transfer systems help reduce exposure. Our own workers’ feedback matter, so we regularly review procedures based on their experience.
We pass this experience on to our industrial users. Points like localized ventilation, use of closed systems for transfer and blending, and immediate cleanup of small spills are highlighted not simply as regulatory boxes to check, but as real ways to keep people safe. This hands-on culture has driven down the number of incidents and reinforced a safety mindset with every new production batch.
Chemical manufacturing doesn’t happen in a vacuum. Over the years, shifts in raw material supply and tightening transport rules have forced agile planning. Chlorinated intermediates, in particular, draw scrutiny during transport and storage. We have built relationships with specialized carriers who understand these materials, audit their facilities, and share shipment tracking data in real time.
Stock-outs on upstream precursors led us to establish local and international supplier networks. As costs and lead times have gone through unpredictable swings, being present in every negotiation and staying transparent with customers about timelines has earned trust even during challenging market periods.
A growing portion of our 3-chlorobenzyl alcohol goes to customers with custom-process needs—high-purity requirements, special particle size, or alternative solvent systems for supply. Customization begins at our R&D bench, progresses through pilot scale, and ends with hands-on support during their first full-scale production. We document every modification and incorporate lessons learned into our standard production.
Longer-term, these collaborations often yield new process improvements. A customized drying step, for instance, might uncover better impurity control, which can then benefit the broader product line. This feedback loop keeps the product line both stable and adaptable in the face of evolving market and regulatory demands.
We’ve watched the demand for 3-chlorobenzyl alcohol evolve, especially as pharma and crop-protection companies focus on more specialized or sustainable chemistries. Research groups sometimes approach us with requests for non-standard packaging, analytical support, or batch reservation for time-sensitive projects. In response, our teams meet regularly to review trends in application, regulation, and customer feedback, then plan production and support accordingly.
We regularly evaluate potential improvements: adopting new analytical techniques for faster impurity identification, upgrading packaging to address transportation challenges, and fostering direct communication channels between plant chemists and customer R&D teams.
Our story with 3-chlorobenzyl alcohol is one of steady, experience-driven progress. This product serves as a reminder that behind every kilogram lies a web of decisions—on quality, safety, environmental care, and partnership. We see its main value not in a spec sheet, but in its reliable application in complex organic synthesis, tight manufacturing deadlines, and the day-to-day realities of chemical operations.
Every plant run, customer visit, troubleshooting call, and process tweak adds another layer of insight. While the basic structure of 3-chlorobenzyl alcohol hasn’t changed, the way we make, handle, and deliver it keeps evolving. In this way, we aim to support partners across the chemical industry with a product shaped by more than structure—one shaped by real-world experience and constant learning.