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HS Code |
264374 |
| Product Name | 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol |
| Cas Number | 329-89-5 |
| Molecular Formula | C8H6ClF3O |
| Molecular Weight | 210.58 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 51-54°C |
| Density | 1.41 g/cm³ |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C=C1CO)Cl)C(F)(F)F |
| Inchi Key | GWXVZLDWXLHLQP-UHFFFAOYSA-N |
As an accredited 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Chloro-3-(trifluoromethyl)benzyl alcohol, labeled with chemical name, CAS number, and hazard symbols. |
| Shipping | 4-Chloro-3-(trifluoromethyl)benzyl alcohol is shipped in tightly sealed, chemically compatible containers under ambient temperature. Packaging complies with all relevant hazardous material regulations, and containers are clearly labeled for chemical identification and handling precautions. Shipping documentation includes safety data sheets, and transportation is conducted by certified carriers to ensure safe and compliant delivery. |
| Storage | 4-Chloro-3-(trifluoromethyl)benzyl alcohol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from light and moisture. Ensure the storage area is equipped with proper spill containment and is clearly labeled. Use personal protective equipment when handling this chemical. |
Applications of 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol in Industrial ManufacturingAs a specialized manufacturer of 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol, we supply this intermediate for key production processes in several industrial sectors. Below, we outline primary application fields, providing specific detail on compliance, formulation, process placement, and the types of downstream finished goods our customers manufacture with this raw material. 1. Pharmaceutical Intermediate for Active Ingredient SynthesisThis compound serves as a building block for selective active pharmaceutical ingredient (API) synthesis, especially in manufacturing anti-inflammatory and central nervous system agents. Pharmaceutical producers integrate it early in multi-step syntheses due to its functionalized aromatic structure, which enables precise molecular modification. Production consistency hinges on raw material purity, and our material undergoes strict quality controls to meet industry requirements for medicinal chemistry. Industry compliance standards
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2. Agrochemical Synthesis IntermediateMany agrochemical manufacturers rely on this material to build new generation herbicide and fungicide molecules with advanced efficacy profiles. It introduces electron-withdrawing and halogen functionalities necessary for tuned biological activity and environmental persistence. Precise handling and validated process control are routine to avoid cross-contamination and ensure compliance with international agrochemical regulations. Industry compliance standards
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3. Specialty Polymer PrecursorsProducers of specialty polymers incorporate this benzyl alcohol derivative into the synthesis of high-performance resin systems, especially fluorinated polyaromatic and heterocyclic polymers. Its aromatic ring with trifluoromethyl and chloro substituents provides unique thermal and chemical stability to downstream polymer matrices. Customers require high batch-to-batch consistency to meet performance guarantees for engineering thermoplastics and specialty coatings. Industry compliance standards
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4. Aromatic Compound Derivatization in Fine Chemical SynthesisProducers of fine chemicals and custom intermediates introduce this raw material as a starting point for synthesizing a range of substituted aromatic structures—particularly where strong electron-withdrawing capabilities are desired. The defined placement of chloro and trifluoromethyl groups allows for subsequent targeted transformations in research, development, and scale-up pipelines. Detailed traceability and documentation accompany each supply to meet strict customer and regulatory audit requirements. Industry compliance standards
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Crafting 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol draws on decades of hands-on synthesis. In our facility, every batch passes through rigorous steps, balancing the needs for purity and consistency. The journey begins with precision sourcing of halogenated aromatic compounds, followed by controlled stagewise reaction with trifluoromethylating agents. Nothing gets rushed. The safety measures and routine analytical checkpoints minimize impurities such as dichlorinated or over-oxidized byproducts. Experience has taught us to monitor not only the main reaction profile but also trace residuals from starting materials. Careful storage and prompt sequestration stand as key details—not just chemical reactions, but real-world, practical lab work.
We’ve seen how poorly handled raw materials or old glassware can introduce moisture and lead to unwanted hydrolysis, contaminating the final product. With every run, our chemists keep an eye on actual in-process data and not just theoretical projections. Reproducibility matters more than chasing a theoretical maximum yield. The goal is not only quantity, but tight control over physical and analytical characteristics. When quality assurance inspects each lot, they look for color, odor, melting point, and specific chromatographic profiles. A repeatable fingerprint emerges, batch after batch.
Our standard product consists of 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol with an assay above 99%. Only carefully screened solvents support its synthesis, and purification steps have grown more efficient each year. Typical raw material specs always receive a direct audit before introduction to production lines. Batches show clear pale-yellow color, refractive index in a narrow range, and GC purity specification matches, not only in our instruments but at third-party reviewed labs as well.
Water content always falls below 0.1%, limiting risk for hydrolytic side reactions. Each shipment carries clear lot traceability so downstream users in pharma, agrochemicals, or specialty materials never face ambiguity about the material’s origin or handling. We maintain a digital record of every step—from receipt of intermediates to packaging in high-density polyethylene drums (or amber glass for sensitive customers).
Over years of supplying this compound, we’ve observed that research labs treat it as a reliable substrate for a variety of downstream transformations. Benzyl alcohols carrying halogen and trifluoromethyl groups find roles in selectivity tuning for medicinal chemistry. Process chemists appreciate the electron-withdrawing capacity of both chlorine and trifluoromethyl, opening new routes for nucleophilic substitution without tedious protecting-group strategies.
As a manufacturer, we’ve received detailed feedback from teams developing active pharmaceutical ingredients. One project, back in 2021, involved a mid-stage scale-up for a fluorinated antiviral precursor. Their synthetic route depended on smooth oxidation to the benzaldehyde stage, and work-up would stumble if side-products crept above 1% content. They reported cleaner reaction profiles using our material than with a global supplier where up to 3% contaminant levels once disrupted downstream crystallization.
In crop science, a number of customers utilize 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol during synthesis of selective herbicides. Halogenated benzyl alcohols allow more predictable conversion to chlorinated acid derivatives, and careful selection of starting alcohol ensures fewer process bottlenecks. The alcohol itself possesses good shelf stability when kept in cool, dark storage. Over the years, we’ve adjusted packaging and order fulfillment to address field complaints—moving away from metal drums and introducing specialty plastic liners after a case of minor metal contamination turned up in 2019.
Scientists in polymer and materials chemistry use this compound to introduce fluorinated and chlorinated aryl groups into resin matrices. The structure promotes hydrophobicity and chemical resistance, which proves attractive for coatings and specialty film applications. Every now and then, we receive a request for upscaled quantities beyond research scale. Internal engineers co-design new tank farms that minimize cross-contamination, always with a view on maintaining reproducibility from kilo to multi-ton orders.
Day-to-day plant experience has revealed that benzyl alcohol derivatives thrive under stable, inert conditions. Fresh synthesis runs move quickly to drying and packaging, limiting air and light exposure that can spur color changes or subtle decomposition. Our standard logistics routes take into account not only shipping times but also warehouse climate—uncontrolled temperature swings carry a real risk of polymerisation or bottle swelling.
Shipping partners ask for up-to-date safety data, but the reality in the warehouse is more about preventing condensation buildup and safeguarding drums from accidental impacts. We have invested in temperature monitoring and air filtration systems after learning that even short interruptions or leaky dock doors can introduce enough humidity to trigger product degradation. Each delivery now moves with tamper-proof seals and randomized lot inspections.
Chemical plants investing in this compound want predictability, not just a nameplate specification. Anomalies in color, minor off-odors, or analytical outliers have cost research groups days or weeks of troubleshooting. We understand the real-world impact: a single off-run can force an entire series of process revalidations or risk project timelines. Our technical team maintains open channels with customer chemists and often advises on in-process checks during their scale-up stages.
We watched a major pharmaceutical partner struggle through a raw-material quality crisis with a trader-supplied batch that failed to oxidize cleanly—heaps of organic layer emulsions, haze, and downstream yield falls. Our experience in batch documentation, tracked reference samples, and retention of analytical profiles allowed them to quickly trace issues and resume development with minimal downtime.
Chemicals carrying both trifluoromethyl and chloro functionalities form a niche arena. This molecule specifically stands apart for a few key reasons. Its structure combines strong electron withdrawal (from both Cl and CF3) with a manageable primary alcohol handle. Many close analogs—such as 4-Chlorobenzyl Alcohol or 3-(Trifluoromethyl)Benzyl Alcohol—offer only a portion of the desired reactivity.
We’ve tested comparative runs with other benzyl alcohols in pharmaceutical intermediates and seen sizable yield and selectivity swings. Both the ortho and para effects of substituents play a role not only in synthetic reactivity but in by-product profile during scale-up. For some oxidations, the presence of CF3 at the meta position along with Cl at the para position helps steer chemoselectivity, lowering formation of unwanted over-oxidized species. Process chemists regularly request spectra and data not only for our main product but also close congeners, looking for small tweaks that bring advantages in scale-up.
We also see significant differences in downstream performance between high-purity material produced in-house and nominal equivalents purchased from bulk traders. Common complaints about third-party material point to variable odor, brown coloration, and persistent traces of starting trifluorotoluene. By refining our own processes and holding strict retesting standards, we’ve minimized these concerns. Repeat business and open project notes from partners underline that difference.
Working in fine chemicals, we’ve seen the regulatory burden grow. APIs and crop-protection intermediates now fall under increasingly exacting standards for residual solvents, identified impurities, and even trace metals. Our plant has aligned with both Good Manufacturing Practice (GMP) and ISO quality management. Routine audits keep us sharp. Documentation of our analytical records, complaint logs, and operator training processes ensure any unusual result gets flagged and addressed with root-cause analysis. This reduces the risk for downstream users facing regulatory submission hurdles.
We never underestimate the value of support to innovation. Synthetic chemists constantly seek faster, cleaner, and safer methods. With active lines of communication open—from our own R&D group to their teams in pharma, agchem, or materials—we help troubleshoot isolation, suggest alternate purification options, or recommend alternate reaction conditions. If a customer’s route stalls due to an impurity, our lab team supports parallel testing for custom purification or alternate production routes.
We do not shy away from the industry’s real challenges. Environmental concerns around halogenated and fluorinated compounds grow louder each year. Handling waste and ensuring environmental compliance forms as much of our day as process optimization does. Our facility pursues solvent recapture, energy-efficient reaction setups, and containment of all process streams. Engineers work to optimize reaction temperatures, reduce solvent volumes, and wherever possible replace legacy materials with greener alternatives—without ever compromising final quality.
Wastewater streams receive both internal monitoring and third-party validation before discharge. Employees receive extensive training not only on safety but also waste segregation and reporting of process anomalies. For example, in 2022, a small release of halogenated solvent from an unexpected line breach triggered immediate process review, fresh containment measures, and a protocol update to prevent any recurrence.
Supply chain resilience remains another core focus. COVID-19 and subsequent disruptions forced us to rethink raw material storage, multi-sourcing for critical components, and in a few cases, reengineering routes to avoid vulnerable intermediates. We learned the hard way that even a week-long shipping delay of just one precursor could force tough customer conversations. Long-term partnerships and local supply contracts now anchor our approach, supported by real-time inventory systems and safety-stock buffers for key products.
Manufacturing specialty benzyl alcohols isn’t static. Every year, we refine our protocols. Recent changes have reduced process residues by 30% and improved overall yield by several percentage points. Constant engagement with our users informs each improvement. If a recurring feedback trend appears—such as a request for colorless grade or finer particle size—our process development team pushes for viable solutions, balancing feasibility and safety.
Our on-site analytical team keeps adding new equipment: ultra-high resolution LC-MS and better chromatography columns allow us to pick up trace impurities earlier. Batch-to-batch consistency, not theoretical “best case,” takes priority. Feedback loops between users, QA, and production keep us honest and responsive. Over time, we’ve built a real track record of failures, fixes, and new baseline standards—not just a set of numbers on paper.
We favor hands-on benchmarking. In 2023, our team ran a long-term study comparing stability and ease of use between 4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol and several mono-substituted analogs stored under varying temperature and humidity conditions. Data backed up what we’d heard anecdotally: Our in-house product not only held up better against yellowing and pH drift but also yielded higher conversion rates in both benzylic oxidation and etherification reactions.
A few years ago, customer labs reported odd discrepancies in melting point across different shipments. Pulling together archived process notes, operator logs, and retained sample libraries, we pinpointed minor deviations in drying protocols as the root cause. We responded by tightening every SOP and retraining shift leaders. Since then, variation has dropped sharply. Lessons learned translate into reliability for everyone along the chain.
Relationships with customers run deeper than just technical data sheets. We keep lines open, debating new applications and troubleshooting old problems. Any deviation from norm triggers immediate review—sometimes leading to batch rework, sometimes to a simple heads-up and corrective action. When unique requests arise—such as custom impurity thresholds or dual-container packaging—our operations team directly partners with the user, mapping out feasible ways forward.
End users occasionally seek custom modifications or develop novel reactions relying on this niche substrate. Compound screening, joint analytical sessions, and after-action reviews are all part of the service. With every interaction, we aim to ground decisions in laboratory evidence, real-world plant experience, and deep respect for user innovation. Open dialogue fosters resilience on both sides, especially when facing difficult process challenges or regulatory hurdles.
Trust grows one interaction at a time—not through marketing language but by meeting needs and standing behind every shipment. Our lab and customer support desks handle requests not as isolated tickets, but as connections with repeat scientists and process engineers solving problems in real time.
4-Chloro-3-(Trifluoromethyl)Benzyl Alcohol stands as a testament to what deep manufacturing experience delivers. Every gram leaving our plant carries with it the benefit of both historical learning and ongoing, hands-on refinement. We support users not only with a quality product but with expert guidance, rapid troubleshooting, and a willingness to adapt. As demand for precision chemistry grows—in life science, agriculture, and advanced materials—having a manufacturer partner who values real feedback, practical improvement, and open communication makes all the difference. Experience shapes quality, and quality shapes breakthrough chemistry.