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HS Code |
272086 |
| Cas Number | 140-75-0 |
| Molecular Formula | C7H8FN |
| Molecular Weight | 125.15 |
| Iupac Name | 4-fluorobenzylamine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 195-197 °C |
| Melting Point | -9 °C |
| Density | 1.12 g/cm3 |
| Solubility In Water | Moderately soluble |
| Refractive Index | 1.538 |
| Flash Point | 75 °C |
| Purity | Typically ≥98% |
| Synonyms | p-Fluorobenzylamine |
As an accredited 4-Fluorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Fluorobenzylamine, 25g: Supplied in a sealed, amber glass bottle with a secure screw cap, labeled with hazard and identification details. |
| Shipping | 4-Fluorobenzylamine is shipped in secure, airtight containers compliant with hazardous material regulations. The packaging ensures protection from moisture, light, and physical damage. Handling and transport are conducted by licensed carriers, with safety labeling and documentation provided. Delivery is tracked to maintain regulatory compliance and ensure the chemical's integrity during transit. |
| Storage | 4-Fluorobenzylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents and acids. Keep the container protected from light and moisture. Properly label the storage area and ensure restricted access to qualified personnel only. Follow all applicable safety and regulatory guidelines for handling and storage. |
Applications of 4-Fluorobenzylamine in Industrial Manufacturing4-Fluorobenzylamine serves as a critical intermediate for industrial synthesis in several regulated downstream segments. As a manufacturer, we provide strict quality control and technical support to achieve efficient conversion and compliance in each specific scenario below. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis4-Fluorobenzylamine acts as a protected amine or direct coupling agent in the preparation of advanced pharmaceutical intermediates for fluoroaryl-containing APIs. It undergoes amide or urea formation, followed by further elaboration to deliver target molecules such as CNS-active compounds. Pharmaceutical manufacturers require precisely controlled input quality for subsequent crystallization, purification, and isolating trace impurities before formulation. Industry compliance standards
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2. Agrochemical Intermediates ProductionChemical crop protection manufacturers use 4-Fluorobenzylamine as a core building block during the multi-step synthesis of specific fluoroaromatic herbicides and fungicides. Precision in stoichiometry and impurity management remains vital to downstream selectivity and environmental compliance for finished pesticide actives. Industry compliance standards
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3. Fluorescent Dye ManufacturingAdvanced material producers incorporate 4-Fluorobenzylamine into the synthesis of fluorophore precursors, particularly in the creation of arylamine-functional dyes. These dyes demand rigorous control over the introduction of electron-withdrawing groups for optimal photostability and emission characteristics, with the amine present from initial coupling reactions onwards. Industry compliance standards
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4. Advanced Polymer ModificationPolymer and specialty plastics manufacturers incorporate 4-Fluorobenzylamine during the derivatization of fluorinated polymers. This step often aims to introduce amine functionality into the polymer backbone or side chains, enhancing material compatibility, reactivity, and durability for electronic and protective coatings. Industry compliance standards
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5. Fine Chemical and Custom SynthesisAt the fine chemical scale, contract synthesis operations leverage 4-Fluorobenzylamine for developing bespoke organic molecules. Here, specific project-based demands govern batch size, purity grade, and integration, as the amine supports the assembly of fluorinated benzyl moieties in custom ligands, catalysts, and functionalized building blocks. Industry compliance standards
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At our manufacturing site, the work with 4-Fluorobenzylamine starts from the molecule up. We know this compound by its CAS number, 140-75-0, and it remains on our daily list because it addresses practical needs for fine chemical producers, pharmaceutical research labs, and advanced material developers. This aromatic amine, built around a benzyl backbone with a fluorine atom in the para position, strikes a balance between reactivity and stability, which doesn't come by accident. Our production aims to make this intermediate as reliable as possible for customers whose work depends on each batch’s consistency.
Our batches of 4-Fluorobenzylamine are made to meet high purity standards, with GC showing regular results between 98% and 99.5%. The physical state is a clear, colorless to slightly pale yellow liquid under room conditions. Boiling point checks sit close to 190°C, which matches published literature. We do routine NMR, IR, and water content analysis, not just because protocols tell us to, but because customers in contract research or custom synthesis projects check these numbers themselves. If traces of related phenyl compounds or residual solvents creep above tiny percentiles, our QA picks it up before the drums ever leave shipping.
Common packaging options include 1kg bottles up to 25kg drums, all sealed tightly against moisture ingress. Our storage protocols allow the amine to maintain declared purity even after months on the shelf. Large volume shipments are filled to order directly from reactor to container, closely tracked with batch numbers for traceability, as demanded by compliance audits from global partners who need certainty about the source and handling of their materials.
Over decades, we have watched 4-Fluorobenzylamine shift from niche specialty to everyday use in several sectors. Pharmaceutical chemists in early discovery regularly order this amine for construction of fluorinated intermediates. The molecule’s fluoro group moderates electron density on the benzyl ring, which lets scientists direct reactivity in multi-step syntheses. In CNS-active small molecules, for instance, the compound often supports target structures that require both lipophilicity and chemical flexibility, something standard benzylamine doesn’t always provide.
Chemical engineers working in custom polymers alter monomer properties by stitching in a fluorine determinant. The 4-position on the ring ensures the molecule’s influence stays distal to the amine, preserving nucleophilicity for downstream reactions. This ability to both anchor a substituent and lengthen chains with desired polarity plays out in adhesives and coatings, which explains the steady orders we see from coating developers in both Asia and Europe.
Agrochemical research also values 4-Fluorobenzylamine as a building block for fungicides and herbicides under patent. Its unique fluorescence and electron-withdrawing attributes tweak metabolism profiles and environmental breakdown rates in a way that standard benzyl derivatives cannot guarantee. Research teams return to us not just for quality, but for supply continuity, since so much R&D time rides on the reliability of starting compounds.
Direct manufacturer experience has taught us that small molecular differences mean major shifts in both process design and end-product features. 4-Fluorobenzylamine sets itself apart from its close relatives. Ordinary benzylamine and ortho- or meta-fluorinated analogues bring different electronic and steric challenges into multistep synthesis.
Customers running hydrogenation, acylation, or reductive amination steps find the para-fluoro substitution lowers side reactions or unexpected rearrangements. Laboratory tests show that it tolerates catalytic systems used for the coupling of amines with acids or isocyanates, which often trip up less pure or inappropriately substituted amines. Replication of spectral properties across batches backs up the case for our focus on batch homogeneity. Our chemists run parallel reactions with non-fluorinated analogues, and impurities rise for those, with knock-on effects on isolation cost and time spent troubleshooting.
Working on milligram scale, people sometimes believe any source will suffice. Our plant has seen long-term project managers come back after failed scale-ups when other suppliers shipped variable quality. From pilot to full manufacturing campaigns, the para-fluoro isomer remains popular for those looking to avoid the handling headaches that meta- and ortho- isomers tend to introduce. Steric effects and electron tunneling change yield or force processes to run at higher temperatures. Our version of 4-Fluorobenzylamine stays liquid, easy to measure, and stores predictably, minimizing operational interruptions.
Unlike traders or resellers, we oversee every reaction step for 4-Fluorobenzylamine within our facilities. The experience stretches from glass-lined reactors for sensitive amination steps to large-scale distillation. By sticking to best-in-class process controls and validated utilities, we keep cross-contamination off the table, even during campaign shifts to other halogenated benzylic compounds. In our plant, engineers run regular checks on pH and reactant flow rates, watching for the pressure build-ups that could introduce impurities or unsafe conditions. The commitment to plant floor safety directly ties to batch purity.
We maintain a closed-loop feedback system through production, purification, and packaging. Wastewater streams get tested for any fluorinated residues, ensuring that the environment stays high up on our agenda even if no one asks for these numbers on the certificate of analysis. For international shipments, every container is labeled with a unique batch number that follows a digital trail back to original reactor records. Our QA department tracks customer feedback and periodically adapts our cleaning, flushing, and drying procedures. This detail in monitoring, more than any standard text, underpins why project chemists and buyers keep stable accounts with us.
Research teams choose 4-Fluorobenzylamine for its ability to enable new designs in medicinal chemistry, fine chemical engineering, and materials science. The presence of fluorine, just by itself, brings metabolic stability and altered polarity in target molecules. Our role is to support labs racing to complete first syntheses of next-generation pharmaceuticals, with the supply of this starting material often on the critical path. Query logs from scientists in North America and India show custom requests for analysis details and impurity profiles, which tells us real users value clear, truthful documentation far more than vague assurances.
Scale-ups introduce their own hurdles. On pilot lines, the compound moves from gram to multi-kilogram lots, and this is where purity and lot uniformity can make or break batch reliability. Our team helps scientists avoid costly rework by shipping extra analytical samples in advance and keeping pilot plant records on hand to resolve any batch-to-batch questions. From direct experience, we’ve seen both early-stage and seasoned buyers ask for historical data with spectral overlays, seeking confidence about lot interchangeability. Once they run into problems with inconsistent isomer ratios or unexpected solvent residues, switching suppliers seldom solves the issue without baseline QC data from the actual manufacturer.
Process chemists cite the consistent handling characteristics of our 4-Fluorobenzylamine—pourable at room temperature, sharply defined melting and boiling points, and the absence of mysterious residues after evaporation. All of these give teams the confidence to scale their work from milligrams to hundreds of kilograms, even if regulatory filings or patent applications remain years away.
Our site operates under an integrated safety management plan, which covers handling guidelines for all halogenated amines including 4-Fluorobenzylamine. Operators receive regular training on personal protective measures, spill response, and safe transfer—since aromatic amines sometimes cause allergic reactions in susceptible individuals. Ventilated workstations and containment valves reduce accidental exposure risks in formulation labs or packaging stations. By reducing off-gassing and packaging the amine in HDPE containers, we limit the risk of vapor formation during shipping and storage. We do not delegate safety or environmental control to third parties.
From early development to regular supply, we field regulatory questions around REACH compliance, restricted substances, and product stewardship. Every batch comes with traceable origin and processing documentation, a result of working in markets where authorities expect lifecycle transparency. Internal audits and customer reviews have pushed us to minimize legacy solvents and residual halide content, which often factor into import clearance delays. Over the past year, technical staff improved the flowchart and updated ECCN and HS code verification to match changes in international trade regulations. These aren’t marketing points—they prevent real headaches during customs inspection and ensure that researchers and process engineers don’t lose time to document shortfalls.
The growing attention on PFAS emissions and environmental loading of specialty amines prompts a regular review of our wastewater treatment and emissions. We set quarterly benchmarks for fluoride content downstream of our process, and this feeds into community reporting and auditing in the regions where we manufacture. For disposal, the product’s high solubility demands careful neutralization and controlled incineration managed on site. No drum leaves us without tracking and signed authorization, part of our standard operational discipline.
Disruptions in solvent supplies, halogenated precursors, and even drum manufacture have highlighted the importance of forward planning in the modern chemical business. We buy raw materials long before orders surge and put safety stock in climate-controlled storage, insulating repeated customers from last-minute delays. Market intelligence drives our procurement, gleaned from direct relationships with upstream suppliers, not just spot market alerts. The volatility in costs for fluorinated intermediates tests how we balance quality and value to end users tackling their own R&D deadlines.
Education also remains a daily concern. Many new clients, especially in start-up research, underestimate the handling nuances of aromatic amines. Even the basic difference between meta- and para-fluorination in reaction behavior can determine product success. We regularly run remote workshops, share handling videos, and publish notes on reaction trends seen with 4-Fluorobenzylamine under real manufacturing conditions. Technical support extends beyond sending a safety data sheet; our team of chemists answers specific questions about compatibility, work-up, and product isolation based on validated data sets, not speculation.
The last five years have seen rising demand for fluorinated building blocks, especially as new drug classes and coating technologies reach the market. 4-Fluorobenzylamine sits at a unique intersection where molecule design and large-scale feasibility actually overlap. Our R&D lab continues to investigate ways to improve atom economy in its synthesis, cutting down both waste and cycle time. The idea is to provide even cleaner product with a smaller environmental footprint, which meets future regulatory scrutiny as well as customer requests for greener options.
We see opportunities in automating further aspects of process control, monitoring pH drops and reaction exotherms in a way that preempts impurity spikes. Partnering with academic labs and industrial users, we gather feedback on new catalytic systems or reaction coupling techniques that favor para-fluorobenzyl cores. Each year’s development pipeline feeds back practical suggestions—tighter impurity thresholds, requests for non-standard pack sizes, or new application notes describing sector-specific behavior—not broad talk about possibilities, but actual working protocols.
Direct oversight of every production step forms the backbone of our approach. Our chemists know that end users don’t want guesses about substitution patterns, boiling points, or trace impurities; they want results that let their own experimental work succeed. Repeat business from global research institutions, advanced materials developers, and established pharmaceutical firms confirms that our product stands up to repeated scrutiny. Whether it’s a shelf-life evaluation at a Scandinavian biotech lab or a multi-tonne supply to an American contract manufacturer, the hallmark remains the same: predictable performance, clear communication, and delivery logistics grounded in years of doing the chemistry right.
For customers moving between benzylamines, experience shows that para-fluorination supplies a useful tool. The handling profile, purification ease, and chemical compatibility deliver bottom-line benefits for project and process leaders who cannot afford surprises caused by unstable or mismatched starting materials. We have seen engineers save weeks by trusting in the process controls and documentation that back every batch. No one makes perfection happen overnight, but practical, unbroken attention—from raw materials to filled drum—sets apart a chemical partner who knows both the small and large consequences for users.
From lab bench experiments to industrial campaigns, the importance of a dependable 4-Fluorobenzylamine source grows with each new technology wave. End users need the full story—real numbers, genuine experience, and honest communication that only dedicated manufacturers bring. Our commitment is to prove that experience is not marketing talk, but the basis for chemistry that supports the success of our customers time after time.