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HS Code |
506271 |
| Cas Number | 144689-63-4 |
| Chemical Formula | C7H7F2N |
| Molecular Weight | 143.13 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 70-72°C at 5 mmHg |
| Density | 1.154 g/mL at 25°C |
| Purity | Typically ≥98% |
| Solubility Water | Slightly soluble |
| Refractive Index | n20/D 1.536 |
| Flash Point | 81°C |
| Smiles | FC1=CC=CC(F)=C1CN |
| Synonyms | 2,6-Difluorobenzylamine; Benzylamine, 2,6-difluoro- |
As an accredited 2,6-Difluorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2,6-Difluorobenzylamine, sealed with a screw cap and labeled with safety information. |
| Shipping | 2,6-Difluorobenzylamine is shipped in securely sealed containers, typically under nitrogen or inert atmosphere to prevent moisture ingress. It should be packed in accordance with local and international regulations for hazardous chemicals, clearly labeled, and protected from heat and light. Safety documentation and appropriate hazard labels must accompany the shipment. |
| Storage | 2,6-Difluorobenzylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of heat and ignition. Protect from moisture and incompatible substances such as strong oxidizers and acids. Store under an inert atmosphere (e.g., nitrogen) if sensitive to air or moisture. Always label and handle in accordance with safety regulations. |
Applications of 2,6-Difluorobenzylamine in Industrial Manufacturing2,6-Difluorobenzylamine serves as a crucial intermediate in multiple specialized chemical manufacturing sectors. As a direct manufacturer, we support industries requiring consistent quality and regulatory-compliant material for advanced synthesis operations. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical companies incorporate this amine as a key building block in the synthesis of several fluorinated API candidates, including CNS-active compounds and antiviral molecules. The material’s unique substitution pattern aids selectivity and stability in medicinal chemistry. Its controlled integration during upstream intermediate formation is essential for maintaining pharmacological profile, batch reproducibility, and regulatory traceability throughout scale-up and validation stages. Industry compliance standards
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2. Agrochemical Intermediate ProductionProducers of advanced crop protection agents use 2,6-difluorobenzylamine as a precursor for synthesizing potent insecticide and herbicide active molecules. The material enters multi-step transformations such as acylation and cyclization, taking advantage of its double fluorine substitution for enhanced metabolic stability in the end-uses. Strict compliance with agrochemical standards and process documentation underpin all downstream manufacturing lines. Industry compliance standards
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3. Specialty Chemical Manufacturing for Electronic MaterialsManufacturers of electronic-grade specialty chemicals utilize our material to synthesize advanced monomers and ligands for semiconductor and display applications. The amine’s fluorinated structure enhances dielectric characteristics and compatibility in photoresist and OLED precursor batches. Tight process specification controls and materials traceability remain essential for downstream integration. Industry compliance standards
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4. Fine Chemical and Custom SynthesisChemical service providers and custom synthesis firms select this raw material to produce advanced fine chemicals, such as fluorinated aromatic amides and bespoke ligands. It enters contract synthesis projects where purity, enantiomeric excess, and project-based documentation are mandatory for regulated customers. Industrial users demand reliable supply and transparent quality assurance derived from direct manufacturer processes. Industry compliance standards
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Producers in the fine chemical sector, especially those with a focus on the building blocks needed for pharmaceuticals and advanced materials, keep coming back to 2,6-difluorobenzylamine. The straightforward structure—a benzylamine core with fluorines at the 2 and 6 positions—gives it a set of properties that match up with many cutting-edge applications in medicinal and agrochemical synthesis. Over years spent behind the scenes at the reactor and purification line, I've watched industries look for molecules like this to drive reproducibility and purity in complex projects. The switch from lab- to plant-scale production for this compound took patience and practical insight. Everyone in the trade knows lab successes mean little unless you can match output batch after batch for years on end.
For us, producing 2,6-difluorobenzylamine is not just batch chemistry. We consider consistency in titration endpoints and GC-HPLC profile checks as much as the origin of our starting benzylamines and fluoride sources. Over the years, we have learned how raw materials with even minor traces of certain metals or non-aromatic byproducts can complicate not just purification but downstream reactivity for customers pushing for clean transformations. Stable supply for this amine takes more than scale—it hinges on small decisions upstream, each one showing up in the purity, odor, and reactivity of each lot.
A typical product spec for our 2,6-difluorobenzylamine focuses on purity, moisture content, and residual impurities. We didn’t choose these numbers out of habit; they came from years of feedback when certain grades failed, leaving gaps in downstream yields or creating purification headaches. Purity above 98% is the starting line for our regular shipments, with available batches above 99%. The years have made it clear: a subpar grade full of byproducts may seem cheaper upfront, but costs hour after hour in fixing problems later. Moisture content, which some makers overlook, stays low under our protocols, often less than 0.3%, so it won’t trigger unwanted hydrolysis or side reactions.
On every analytics run, our lab checks for residual halogenated impurities and closely related amine homologues. Subtle contamination can change crystallization behavior or catalytic steps in a customer's next stage. Only by controlling the provenance and storage of all upstream reagents, from fluoride to benzyl chloride, do we get the results our users demand. Customers have sometimes tried switching between sources for this amine—usually price-chasing—and ended up calling us back. The difference often sits not in what’s labeled on the COA, but in those persistent unknowns under the curve, found only with a knowledgeable eye on the chromatogram.
Our long-term clients, both large and emerging, seek out 2,6-difluorobenzylamine not for flashy sales pitches, but because they know what it can do in real research and production. Medicinal chemistry groups reach for it early in a lead-optimization program, taking advantage of both the amine’s nucleophilicity and the unique electronic effects of the ortho-difluoro substitution. Bioactive compounds often call for precisely positioned fluorines, and this amine provides a direct way to introduce them on a scaffold. The electronic tweaks from the two ortho fluorines tune amide bond formation and keep byproduct formation to a minimum. We’ve seen specialty firms use it as a strategic feedstock to link up to more sophisticated protected fragments, as well as a cornerstone for wider spectrum agrochemicals.
Whether routing through reductive amination, amidation, or coupling to heterocycles, the point is always the same: every chemist on the end-user’s bench looks for reliability. High-purity 2,6-difluorobenzylamine provides predictable yields and manageable purification. Problems come fast when someone gambles on mystery amines, which might be diluted, colored, or off-odor—even tiny problems in a starting amine reverberate down a synthetic sequence, throwing scale-up off track. Years of producing this product have shown us that reports of “residual activity” from a raw material often link back to invisible trace byproducts. We track those, batch by batch, and adjust—not every supplier does.
Scale-up teams in both pharma and crop protection value this molecule for the versatility it gives in constructing small libraries of analogs. No surprise—it’s reactive, yet selectively so, and its low viscosity and volatility mean it handles smoothly with standard plant equipment. From the shop floor, I can tell you: operators rarely complain about 2,6-difluorobenzylamine blocking up valves or crusting pipes, unlike many sticky or high-polymerizing amines.
Let’s get practical about how 2,6-difluorobenzylamine compares to single-fluorinated, non-fluorinated, or differently substituted benzylamines. The double ortho-fluorine pattern changes everything. The electron-withdrawing effects of two ortho fluorines activate the amine toward acylation but reduce the likelihood of unwanted oxidation and overalkylation. This makes it a workhorse where selectivity is critical. For comparison, mono-fluorinated or unsubstituted benzylamines often yield broader, messier NMR and LC profiles in the hands of our clients—requiring more downstream scrubbing.
Colleagues in pharmaceutical R&D know the headaches caused by chain-transfer, oxidation, or problematic reactivity at benzylic spots. The difluoroaromatic ring helps block these issues, stabilizing the functional group against conditions that are tough on other amines. In some of our customers’ scale-up runs, switching from a mono-fluoro to the 2,6-difluoro version cut down both unwanted side products and costly column cleanup steps. The value, then, isn’t “increased yield per se”, but a practical drop in waste and downtime. That matters to managers balancing both time and cost.
From a sensory standpoint, 2,6-difluorobenzylamine also stands apart. Some benzylamines, especially unfluorinated ones, produce persistent amine odors or discolor faster, creating headaches in GMP and food-contact areas. Our product, kept under the right conditions, remains consistently colorless with only a faint, manageable odor. This goes back to quality control: I’ve seen first-hand how even a mild tinge in a bulk drum sparks concerns both at the plant and at QA review. We lean on decades of handling amines to keep product to spec, even through long shipping cycles.
A critical reality sets in for every major fine chemical—demand is cyclical, but quality demands never let up. Production isn’t simply a question of running the same recipe on repeat. Instead, every year brings slight shifts in raw material purity, sometimes prompted by upstream industrial changes you’d never see coming. We keep long relationships with our raw material sources and routinely insist on tighter specs than they set for general traders. Still, surprises happen: an upstream solvent plant changes a purification column, a byproduct spikes, an impurity appears. Test runs and parallel tracking let us spot quality drift before it blows up a batch. Investing in redundancy at the purification step adds cost, but it’s saved us from writing off far more expensive finished product.
I’ll say plainly, price pressures never go away, even with specialized amines like this. New entrants—in China, India, or Europe—try to push in on price by thinning out QA steps. The buyers who chase this route often circle back after discovering unexplained failures in product performance or analytic inconsistencies show up under heavy regulatory scrutiny. Experience teaches patience, both in maintaining in-house standards and in vetting suppliers for every raw material lot. It’s easier to prevent off-spec product than fix a stalled customer project in the field.
Markets for 2,6-difluorobenzylamine evolve in step with advances in combinatorial chemistry, medicinal chemistry, and green chemistry initiatives. Regulators and end-users both ask for lower impurity profiles and stronger traceability year after year. We’ve adapted over time by bringing in higher-resolution chromatography, digital batch records, and automated cleaning systems to minimize cross-contamination. By having experienced teams watch every lot through to shipment, we guard against the slow drift in quality that can dog other suppliers.
One misconception about specialty chemicals: that perfection is forever out of reach. Truth is, aiming for “zero deviation” in an interlocked production and testing framework gets closer than many expect, if you’ve got institutional memory on top of written SOPs. Those who stick with their formula, ignoring the quirks of new production campaigns, pay the price in recall costs and lost trust. Regularly involving frontline technicians in review meetings unearths problems no outside consultant could find—veteran eyes spot pattern shifts that slip by statistical process control alone. These details, from jar-lid torque to the replenishing rate of neutralization tanks, end up saving batches.
We haven’t always gotten it right on transparency. Early in our manufacturing story, customers asked for data we didn’t readily share; we changed, putting more comprehensive quality and traceability reports in the hands of those making critical decisions on the receiving end. Batch history, impurity trends, and microscopy images—such data, faced candidly, do more than reduce blame-shifting when problems arise. They ensure both sides can move forward in future campaigns, confident that process gaps will shrink over time.
Users testing new synthesis routes sometimes request custom modifications, adjusted grades, or coordinated joint stability studies. This isn’t just a service we offer, it’s the way innovation happens naturally between chemist and supplier. The need for open technical dialogue comes up often. A minor impurity that matters little in a bulk agricultural product could destroy the performance of a pharmaceutical active. Giving customers enough information to make the right call about grade and application paves the way for mutually beneficial relationships.
After years fielding technical calls—most frantic, a few routine—it gets clear how complex the afterlife of even a straightforward amine can be. Feedback from users isn’t only about whether a drum failed a reactivity test; it’s concerned with the long arc of storing, sampling, dosing, and blending these building blocks into final products. Issues over drum linings, sampling tubes, condensation, or evaporative loss show up in ways no desk-bound analyst could predict. Regular field audits and check-in visits teach us to design containers differently, choose cap linings that resist vapor migration, or adjust fill levels for haulage over long distances and shifting temperatures.
Some chemistries call for specialized shipment solutions—longer shelf-life, anti-static packaging, overfill warnings, real-time temperature logging, or even dedicated temperature-controlled storage. These are not “premium extras”, but responses to real-data and near-miss reports after decades of hands-on observation. Our own technicians taught us to log field data and act on trends, not just in the raw analytics from the drum, but from operator observations about off-gassing, slow material dispensing, or sequencing hiccups in batch loading. Making these changes has paid off multiple times.
The making and moving of any fluoroaromatic chemical isn’t just a question of quality; environmental and safety factors come built-in. The amination and fluorination steps that underpin 2,6-difluorobenzylamine synthesis challenge even experienced production managers. Choices about vent gas scrubbing, solvent recovery, and intermediate handling ripple forward—not just through the product, but through insurance, worker health, and community relations.
Our routine solvent recovery rates come from hundreds of small adjustments and relentless pressure to keep releases and overall waste below tough internal thresholds. Any fluoro compound needs careful vent monitoring and continuous checks for PFC content and trace residues. Our upstream technology allows us to minimize direct emissions, all while keeping final product uncontaminated by process byproducts. Waste minimization, especially the capturing and reusing of fluoride-containing side streams, has yielded cost as well as regulatory advantages. Failures may not trigger immediate fines, but they compound. Vigilant sites—audited both internally and by clients—make the long-term difference for stable supply and a clean reputation.
Most chemical manufacturers can point to certifications or audit reports. Those play a role, but what matters most for people on the floor and buyers at the loading dock is embodied experience. Customers return to us not because of sales language, but because they know if they call up with a problem during production, they’ll reach someone who’s worked with these materials both on paper and in the drum room. No single certificate can replace troubleshooting alongside a longtime client when they're up against a project delay. That’s why our internal training emphasizes not just GMP process, but judgment gained only from seeing it all break at least once.
We keep close ties with local emergency response units, internal environmental managers, and packaging experts, drawing insights back into our daily routines. That turns into fewer surprise audits, lower insurance claims, and a clearer path to process improvement. Customers pressed by evolving international standards know they can ask for documentation or justify claims in global regulatory systems, because our internal records go deeper than the “minimum viable” point. Our team has turned particulars about benzylamine storage, drum welding, or trace batch records into improved outcomes for users on every continent.
Markets that rely on building block chemicals like 2,6-difluorobenzylamine aren’t standing still. As green chemistry and sustainability initiatives force changes at every step—from solvent use to packaging non-returnable drums and tracking greenhouse gas emissions—we’re forced to keep innovating. We continue to invest in lower-impact fluorination options and participate in industry roundtables for better recycling of containers and byproducts. The challenge is real: running tight process controls on batch fluorination at commercial scale, all while keeping throughput and purity at a premium and waste below external targets.
We see, too, a shift in what customers expect. More end-users ask not only about price and purity, but about traceability, emissions profile, and product safety documentation for the full cradle-to-gate journey. This stretches back through every supplier and even further, to those extracting and refining each input. A responsible manufacturer balances both openness and protection of trade practice, always keeping an eye on pushing for lower impact, better transparency, and ever-higher reliability.
2,6-difluorobenzylamine remains a staple in the hands of chemists and technicians pushing projects from design all the way to finished goods. As a manufacturer with deep roots in daily process, my perspective connects not to some ideal version of chemical manufacturing, but to the actual needs and observed challenges of customers, colleagues, and supply chain partners. We continually refine not just the molecule itself, but the way we listen, adjust, and invest in safe, cleaner production. The story of this product is more than carbon, nitrogen, fluorine, and process steps; it’s the accumulated insight from every successful (or swiftly repaired) batch destined for real-world impact. For those who depend on specialty amines to power innovation, this practical depth is the real difference between commodity supply and trusted source.