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HS Code |
790745 |
| Chemical Name | 3-Fluoro-4-Methylbenzyl Alcohol |
| Molecular Formula | C8H9FO |
| Molecular Weight | 140.16 g/mol |
| Cas Number | 144806-05-5 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 231-233 °C |
| Density | 1.16 g/cm³ |
| Purity | Typically >98% |
| Smiles | CC1=CC(=CC(=C1)F)CO |
| Inchi | InChI=1S/C8H9FO/c1-6-2-3-8(10)7(9)5-6/h2-3,5,10H,4H2,1H3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Refractive Index | 1.520-1.530 |
| Storage Temperature | Store at 2-8 °C |
| Synonyms | α-(3-Fluoro-4-methylphenyl)methanol |
As an accredited 3-Fluoro-4-Methylbenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 3-Fluoro-4-Methylbenzyl Alcohol, labeled with chemical name, CAS number, and hazard warnings. |
| Shipping | **Shipping Description:** 3-Fluoro-4-Methylbenzyl Alcohol should be shipped in tightly sealed containers, protected from light and moisture. It is typically regarded as a non-hazardous substance for standard ground and air shipping, but proper labeling and compliance with local, national, and international transport regulations are required to ensure safety during transit. |
| Storage | 3-Fluoro-4-Methylbenzyl Alcohol should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Store it separately from strong oxidizing agents and acids. Ensure all containers are clearly labeled and handled with appropriate personal protective equipment to prevent accidental exposure or contamination. |
Applications of 3-Fluoro-4-Methylbenzyl Alcohol in Industrial Manufacturing3-Fluoro-4-Methylbenzyl Alcohol supports the synthesis and formulation needs of multiple specialty chemical segments. Our clients in both specialty and fine chemicals rely on this intermediate for building advanced molecular structures. The following industrial application fields represent key downstream integrations with compliance, mixing, process, and end product details. 1. Pharmaceutical Intermediate SynthesisLeading pharmaceutical manufacturers use this material to construct complex active pharmaceutical ingredient (API) side chains, especially in the preparation of fluorinated drug molecules. The hydroxyl and fluorine functional groups enable selective modification during multi-step organic syntheses, supporting scale-up for proprietary molecules under stringent process validation. Its role as an intermediate requires high batch consistency and traceable quality for registration with authorities in regulated markets. Our continuous reactors enable precise control of purity standards demanded by global pharma partners. Industry compliance standards
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2. Agrochemical Building BlockAgrochemical formulators select this benzyl alcohol for its fluorinated aromatic core, which functions as a crucial structural element in the synthesis of new generation herbicides and fungicides. The derivative forms participate in etherification, reduction, and alkylation reactions vital for the construction of active crop protection ingredients. Delivering consistent purity avoids batch variation risks during scale-up and field trials for global registration. Dedicated cleanroom lines ensure contamination control for agricultural downstream partners. Industry compliance standards
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3. Flavours and Fragrances SynthesisFlavour and fragrance houses integrate this fluorinated benzyl alcohol as a tailored precursor for synthesizing specialty aromatic aldehydes and ketones. The unique substitution pattern allows creation of performance boosters for perfume and flavor blends in strict accordance with food and cosmetic legislation. In-house batch certification guarantees trace-level analysis for non-listed impurities as required by international formulation standards. Our traceability system supports customers with documentation for export and brand assurance audits. Industry compliance standards
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4. Advanced Polymer Additive DevelopmentPolymer compounders use this benzyl alcohol derivative as a monofunctional co-monomer or end-group modifier for engineering polymers and fluorinated resins. The structure provides improved chain mobility and weather resistance, critical for coatings and films in demanding sectors. With consistent purity and low water content, our material supports polymerization processes where batch reproducibility is paramount. Technical support covers specifications for thermal stability, residual solvent, and trace metal content matching application needs. Industry compliance standards
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5. Specialty Chemical Synthesis for Electronic MaterialsElectronic material suppliers incorporate this aromatic alcohol as a building block for the synthesis of intermediates required in the production of photoresists, dielectrics, and specialized solvents for the semiconductor industry. The fluorinated ring structure improves resistance to degradation under UV and plasma conditions. Tight in-process controls at our manufacturing site achieve the low ionic impurity levels demanded by downstream semiconductor customers. We provide full batch documentation to support audits and long-term supply chain assurance. Industry compliance standards
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Decades in this industry have taught us that quality hinges on the finer points—the starting material, the process conditions, the finishing steps. As a chemical manufacturer focused on aromatics and fine intermediates, we see 3-Fluoro-4-Methylbenzyl Alcohol emerge as an essential intermediate for many modern synthesis projects. This compound, with the structure of a fluorinated benzyl alcohol (CAS 456-49-5), bridges demand between sophisticated pharmaceutical building blocks, custom agrochemical actives, and smart material syntheses.
This product, known with the model code 3F4MBA in our portfolio, carries a methyl group at the para position and a fluorine atom at the meta position of the benzene ring, relative to the benzylic alcohol side chain. The precise positioning shapes reactivity and opens up distinct downstream routes. Analytical work performed daily on our batches shows consistent results—high purity, typically 99% GC-assay and above, with trace moisture and no residual solvents thanks to effective vacuum distillation. Our internal QC standards rely on both NMR and HPLC profiles, which consistently prove the absence of critical side products, especially those that might interfere during scale-up or synthesis of more valuable downstream molecules.
The molecular formula C8H9FO, paired with a molecular weight around 140.16 g/mol, tells a part of the story. In terms of appearance, 3-Fluoro-4-Methylbenzyl Alcohol presents as a colorless to pale yellow liquid, which holds stability through storage at ambient conditions, provided it’s shielded from direct light and moisture. Every time our technical team releases material from warehouse storage, we independently recheck the sample to guarantee no hydrolysis or oxidation has occurred, because our research customers cannot afford surprises in their synthetic steps.
The main reason chemists request this compound comes down to selective functionalization at the aromatic ring. Our pharmaceutical partners use 3-Fluoro-4-Methylbenzyl Alcohol as a handle to build complex molecules, especially for late-stage fluorination in lead molecules. Many proprietary kinase inhibitors, anti-infectives under development, and several API side chains trace some of their origin to this trusted intermediate. The fluoro-methyl-benzyl core offers a unique combination—a metabolically stable aromatic system and a benzylic alcohol that can be easily converted into other functional groups such as aldehydes, acids, or even more complex heterocycles.
The agrochemical segment also makes consistent use of this alcohol. Newer generation fungicides, herbicides, and insecticides often incorporate both fluorine and methyl at the benzyl position to modulate biological activity, improve field stability, and steer selectivity in target organism interaction. This material acts as a reliable stepping stone in those synthetic schemes.
Academic labs and innovation-driven materials researchers find further uses—tracking isotope exchange, employing the molecule as a probe for substitution patterns, creating polymer side chains, or even integrating the aromatic ring into new liquid crystals. Requests from these groups often come with custom quantities and speculation about novel transformations to push functional chemistry boundaries. We listen closely because the smallest batch today maybe scales to a kilogram or ton years down the line. That’s the path many of our now-established products have taken since pilot production began in our original plant.
Every chemist knows that swapping one atom for another—methyl for ethyl, fluorine for chlorine—can alter how a molecule behaves in both simple reactions and living systems. 3-Fluoro-4-Methylbenzyl Alcohol offers a unique profile not found in its close relatives. Benzyl alcohol itself presents high reactivity and low selectivity, and plain 4-methylbenzyl alcohol offers greater steric hindrance but without increased metabolic stability. Adding the fluorine at the 3-position changes both electronic and steric parameters, giving downstream chemists a differentiated approach. For instance, compared with 3-chloro-4-methylbenzyl alcohol, the fluoro compound maintains better oxidative resilience while staying compatible with organometallic transformations and selective halogenations. We’ve seen customers bounce between substrates for a project, before returning to the fluoro-methyl variant because of a cleaner reaction profile or higher final yield. The synthetic difference between a 65%-yield end product and one repeatedly hitting the 85% mark spells the difference between a successful process and recurring troubleshooting. Every substitution brings trade-offs, but this particular configuration strikes a balance few alternatives can match.
As a direct manufacturer, control over raw input matters most. Our sourcing of primary raw materials draws on longstanding relationships within Asia and Europe, with plenty of experience shielding critical supply chains from volatility and purity drift. Each precursor undergoes triple filtration and quantitative GC analysis before entering batch production—no exceptions. We’ve established a dedicated fluoro-organic line, minimizing cross-contamination risk and meeting the unique demands of fluorinated aromatics, which react unpredictably in equipment gouged by other chemistries.
Only a handful of companies run reactors specifically lined for this class of molecules. Our internal glass-lined and PTFE-lined reactors, sized from pilot to full-scale, have made all the difference in batch reproducibility. Monitoring the reaction through in-situ IR, we track endpoint with greater accuracy, avoid overreduction during benzylic alcohol formation, and capture intermediate sampling to prevent runaway exotherms. In any industry, speed wins, but in fluorochemical manufacturing, caution delivers superior products. Extra time invested in tailoring the workup—fine-tuning extraction steps, vacuum controls, and phase separation—lets us suppress off-flavors and byproduct taints. This brings real value to partners running long-step syntheses, who notice even 0.5% impurities cascading through later synthesis or regulatory filings.
Years working with high-purity benzyl alcohol derivatives confirmed that packaging and logistics matter as much as any reaction yield. Our team has developed a system for storing and shipping 3-Fluoro-4-Methylbenzyl Alcohol based on the requirements of various industries—glass bottles for sample quantities, sealed aluminum containers for bigger batches, and lined steel drums for multi-ton deals. Internal nitrogen blanketing and tamper-evident seals preserve product quality through customs, ocean transit, and final delivery. No matter where the destination—labs in Switzerland, reactors in the South of France, or formulation hubs in Singapore—we track every delivery down to batch number and date code. Feedback from customers sometimes reveals small details: how a leaky cap can introduce trace moisture, or how a mishandled drum rolls a sediment layer. These firsthand accounts push us to keep troubleshooting, leading us to revise seals, coatings, and even shipping routes whenever risk emerges. It’s a cycle of learning—careful monitoring on our end, practical adjustment in each logistics cycle, and a blend of humility and perfectionism few outside manufacturers understand. The real difference often comes down to these details, not what’s printed in any brochure.
Quality and regulatory expectations grow tighter each year. Our plant labs run every batch of 3-Fluoro-4-Methylbenzyl Alcohol through a multistep evaluation protocol. Technicians begin with spectroscopic identity confirmation (NMR and FT-IR), followed by GC-MS profile, then Karl Fischer moisture check, and end with heavy metals screening by atomic absorption. We have built a history of robust documentation: material traceability, retained sample archives, and up-to-date safety datasheets reflecting ongoing regulatory and toxicology findings.
Handling fluorinated aromatics carries its share of challenges. Over the years, our safety protocols have evolved alongside the science. Dedicated containment zones, local exhaust, and glovebox stations anchor our main plant safety program. Routine training cycles reinforce the basics, and our incident logs feed weekly risk reviews. It’s not just about keeping the chemistry safe; it’s about building long-term trust—and meeting every commitment—to those who depend on our products. When a research or production line relies on our batch, we shoulder a direct responsibility to perform every time, not just in bulk specs, but in the subtleties that separate one source from another. This discipline flows from accumulated experience in isolating, neutralizing, and, if any challenge arises, directly supporting users in addressing small usage issues or scaling questions. Our technical support channel keeps those lines of communication personal and practical, not buried in forms or redirected by third parties.
One hard lesson in chemical manufacturing: no process ever really stands still. Over the years, synthetic pathways have shifted with raw-material trends, environmental stewardship programs, and new regulatory expectations. Our R&D staff spend substantial time in optimizing existing runs of 3-Fluoro-4-Methylbenzyl Alcohol. They continually test catalysts that suppress unwanted overreactions, search for greener solvents matching reactivity needs, and monitor energy/water consumption. In-house, recycling solvents and streamlining byproduct disposal pays off both for the bottom line and our operational footprint.
Occasionally, customers approach with process-transfer challenges: material from a previous supplier showing slight color changes, altered reactivity, or low-end boiling residue. Our years of in-house batch records, pilot plant runs, and analytical archives put us in a strong position to diagnose these issues. By rearranging workup procedures, introducing stepwise purification, or tweaking reagent addition schedules, we regularly help customers over technical hurdles. Some improvements may appear minor—a better method to dry the final product, a tailored filtration step, or a change in anti-oxidant load—but the end result often secures a multi-year partnership. Real-world problem-solving, beyond the datasheets and technical bulletins, creates the dual story of strong chemistry and reliable commercial partnership. This is not available from traders or brokers who lack the visibility into plant operations and direct technical experience dealing with batch-to-batch deviations.
The environmental footprint of manufacturing fine chemicals like 3-Fluoro-4-Methylbenzyl Alcohol weighs heavily on our decisions. Direct exposure to regulatory audits and shifts in local wastewater rules means that process improvement isn’t just a buzzword. Dealing with halogenated waste, controlling emissions, and managing solvent recycling are live issues—solved not on paper, but batch by batch. Our upgrades toward closed-loop distillation, improved scrubbers, and in-line solvent reuse didn’t happen overnight. They arose from close cooperation with plant staff, regulatory authorities, and, honestly, the watchdog eyes of global customers tracking every environmental trend. Adapting real processes and retooling for stricter requirements delivers better outcomes for our workers, the surrounding communities, and the business overall. Pressures for transparency and sustainability have forced the entire sector to rethink, update, and take nothing for granted. Our ongoing investments here reflect both responsibility and practical foresight.
Every run of 3-Fluoro-4-Methylbenzyl Alcohol looks straightforward on paper: warm up the reactor, charge reagents, stir, monitor, then workup and distill. Reality brings mixed feeds, equipment maintenance, and inevitable surprises. Our operators carry a wealth of practical know-how—recognizing a slight change in reaction exotherm, a pump pulling air, or a valve with minor drip. These signals matter and cannot be flagged by distant oversight or outsourced quality checks. Weekly team roundtables focus on sharing in-plant observations, troubleshooting together, and adjusting SOPs based on the last run’s learnings.
Direct feedback flows up the chain. Plant engineers who notice a trace impurity in overhead samples can flag it for isolation lab staff, who can then run impurity profiles and decipher cause—raw impurity, equipment, or process hiccup. Fielding such problems as a cohesive, technically-minded crew gives us an advantage. Every bottle or drum that leaves our facility carries not just material, but the sum of this experience. We maintain internal batch records, logbook traceability, and a clear correction protocol. This, more than any abstract quality badge or external endorsement, defines what sets a manufacturer apart. It’s the knowledge that each bottle headed offsite has passed through hands and eyes that know what trouble looks like—and how to catch and fix it fast.
Working directly with end-users and formulation teams—rather than through layers of brokers or middlemen—lets us stay close to shifting technical demands. When a pharmaceutical team requests microbially-tested material, or an agrochemical user identifies a new impurity threshold, we can discuss, adjust, and implement right at source. No round of back-and-forth waiting for upstream translation, no broken communication as information hops between traders. Years of these collaborations show that such direct relationships breed breakthroughs in both performance and risk control. Trade customers trust us during critical troubleshooting phases—lasting improvements rooted in real process knowledge, not just on-paper certificate tweaking.
Cross-industry experience also smooths troubleshooting, especially for those scaling a lab-scale transformation to ton-scale operations. A formulation may proceed flawlessly with lab-grade material, then stumble on a new impurity or handling quirk at production scale. Our involvement in these troubleshooting cycles—sharing data, adjusting run conditions, even sending technical advisors for onsite support—unlocks solutions and shortens development timelines. This cycle of learning and adaptation feeds back into our own processes, creating a virtuous spiral: improved product on our end, more predictable syntheses on the customer’s, and a pattern of mutual trust that outlasts every contract or technical note.
Many plants operate on the same floor plans and equipment for decades, but staffing and culture define every outcome. As a manufacturer steeped in generations of chemical production, each senior engineer, process chemist, and operator brings tribal knowledge into our operations. That experience—often unrecorded but always discussed on the plant floor—finds its way into lot-to-lot consistency, subtle process adjustments, and rapid response if the unexpected flares up in batchwork or QC checks.
Fresh graduates working alongside seasoned hands absorb details no textbook offers—the particular odor of incomplete workup, the reaction rate giving away micro-impurity, the sound of a healthy solvent boil, or the tactile sense for clean product separation. We don’t take such depth for granted. Our bottom-up approach relies on constant cross-talk between lab development, plant processing, and sales—a perpetual loop designed to surface problems early, tackle them with practical measures, and document results for continuous improvement. This attention to the human element in manufacturing shapes every drum of 3-Fluoro-4-Methylbenzyl Alcohol we ship.
Our experience as a bonded manufacturer tells us fine chemicals are not commodities. Each intermediate carries a story of scientific challenge, regulatory scrutiny, and commercial partnership. 3-Fluoro-4-Methylbenzyl Alcohol occupies a distinctive niche, valued by medicinal and agrochemical scientists for the properties only its molecular layout offers. Through investments in equipment, process, and people, we ensure this product meets expectations every time.
We never take our partnerships—be it with a lone research chemist or a multinational’s R&D team—for granted. Ongoing communication, willingness to adapt, and steady technical improvement reflect the ethos of a true manufacturer, not just a supplier. Our doors remain open to user feedback and cooperation, believing that the next advancements in this field will come from collaboration as much as from chemistry itself. Each batch of 3-Fluoro-4-Methylbenzyl Alcohol embodies this commitment to quality, knowledge, and long-term partnership—the hallmarks of genuine excellence crafted in the lab and proven in the plant.