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HS Code |
301394 |
| Product Name | 2-Chloro-4-Fluorobenzylamine |
| Cas Number | 261953-36-4 |
| Molecular Formula | C7H7ClFN |
| Molecular Weight | 159.59 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Boiling Point | 229-230°C (estimated) |
| Density | 1.25 g/cm³ (approximate) |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Smiles | Clc1cc(F)ccc1CN |
| Inchi | InChI=1S/C7H7ClFN/c8-6-3-5(1-2-10)4-7(9)8/h3-4H,1-2,10H2 |
| Refractive Index | 1.583 (approximate) |
| Storage Conditions | Store at 2-8°C, tightly closed |
As an accredited 2-Chloro-4-Fluorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2-Chloro-4-Fluorobenzylamine is supplied in a sealed amber glass bottle with a tamper-evident cap and label. |
| Shipping | 2-Chloro-4-Fluorobenzylamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is usually transported as a hazardous chemical, following regulations for packaging and labeling. Ensure shipment complies with regional and international transport guidelines, including appropriate documentation and hazard classification. Handle with care during transit. |
| Storage | 2-Chloro-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 oxidizers). Protect from light and moisture. Keep the storage area clearly labeled and access restricted to trained personnel. Use proper chemical safety practices, including secondary containment and spill control measures. |
Applications of 2-Chloro-4-Fluorobenzylamine in Industrial Manufacturing2-Chloro-4-Fluorobenzylamine is a key intermediate applied by leading chemical manufacturers in advanced synthesis workflows across several regulated sectors. As a producer, we support downstream industries by offering consistent quality and technical guidance tailored to properly integrate this ingredient into complex multi-step manufacturing protocols. Below are the principal industry applications with relevant technical specifications and compliance requirements. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical producers incorporate this compound during multi-step syntheses for APIs focused on central nervous system and anti-infective therapeutics. It typically functions as a protected amine building block or as a nucleophile in couplings for selective amide or urea bond formation. Downstream partners operate under strict control regimes, employing validated GMP-lot processes and full traceability from raw material through API release. Production may involve downstream catalytic hydrogenation, acylation, or protected group transformation, requiring predictable purity and impurity profiles. Industry compliance standards
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2. Agrochemical Synthesis for Select Herbicides and InsecticidesMajor agrochemical companies rely on 2-Chloro-4-Fluorobenzylamine as a crucial intermediate for producing active materials with high selectivity against specific weed and pest targets. The compound’s functionalized aromatic backbone enables direct incorporation into amide, triazine, or urea herbicide classes, where electronic and steric influences fine-tune bioavailability and environmental stability. Batch records and chain-of-custody tracking must conform to regional agrochemical registration requirements, including impurity thresholds relevant to field safety. Industry compliance standards
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3. Specialty Chemical Building Block for Dyes and PigmentsLeading dye and pigment makers integrate this compound into production of specialty colorants with high lightfastness, solvent resistance, and stability under process temperatures exceeding 150°C. Its substituted aniline core becomes the chromophore anchor, often through nucleophilic aromatic substitution, coupling or condensation with phosgene derivatives, formaldehydes, or diazo intermediates. All raw material lots demand stringent assessment for halogen impurity carryover to meet downstream textile, plastic, and ink sector regulatory limits. Industry compliance standards
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4. Fine Chemical Intermediate for Electronic and Functional Material Synthesis2-Chloro-4-Fluorobenzylamine supports manufacturers of advanced electronic chemicals, including precursors for liquid crystal materials and functional polymers. The aromatic amine enables precision tuning of dielectric, anchoring, and polarity properties in display- and sensor-class formulation. Entry into multi-step syntheses for LC material blends or specialty resins mandates trace metal and halogen control, and batch records must fulfill detailed customer QM system audits and RoHS/REACH requirements. Industry compliance standards
Typical usage ratio
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Handling the daily challenges of manufacturing specialty amines like 2-Chloro-4-fluorobenzylamine brings both responsibility and pride. We focus on detail because consistency in every batch means reliability for chemists and formulators who rely on this intermediate to create advanced molecules. 2-Chloro-4-fluorobenzylamine, with the model code 2944-10-5, doesn’t just appear at a standard of purity; it comes from a chain of decisions, careful material selection, and extensive monitoring throughout the process to ensure its quality, which matters far beyond the manufacturing floor.
We see firsthand how 2-Chloro-4-fluorobenzylamine supports development in fine chemicals, pharmaceuticals, and agrochemicals. The presence of both chloro and fluoro substituents, specifically on the benzene ring, isn’t a quirk of nomenclature. These functional groups shape how the compound reacts, how it links to other molecular fragments, and how it influences biological activity down the synthesis chain. Customers in advanced R&D settings seek this amine when more common benzylamines can’t deliver the selectivity or physical properties their projects demand.
Precision is essential with aromatic amines that give formulators versatile starting points for targeted synthesis. We keep a tight grip on reaction conditions, purification, and waste controls because even slight deviations can introduce unpredictable byproducts that slow downstream processing. Years spent running kilo-lot and metric ton-scale batches have taught us that reproducibility enables customers to repeat results confidently, which shortens their development timelines. When product runs meet our tight specifications batch after batch, it keeps costs down for both sides and builds trust that’s earned, not advertised.
Chemists notice instantly when a shipment doesn’t fit expected benchmarks. We supply 2-Chloro-4-fluorobenzylamine as a colorless to pale yellow liquid or low-melting solid, depending on storage temperature. Purity typically exceeds 98% by GC, reflecting careful controls over reagents and vigilant exclusion of oxygen and water at every stage. HPLC and NMR fingerprinting back up those results and give end-users confidence when they start new formulation runs. Moisture and residual solvent content both stay within market-driven specifications, handled by vacuum drying and closed-system transfer from reactor to packaging.
We don’t rely purely on blanket testing after the fact; we integrate process analytical technology so we catch off-spec batches before they advance. Sulfated ash, heavy metals, and related impurities never leave our facility above internationally recognized limits. The attention to these details comes from years of adjusting equipment and training operators in what to watch for—any variability reflects on the team’s skill and commitment, and impacts customer relationships that stretch across decades, not transactions.
This molecule’s uniqueness comes from balancing reactivity against stability. The chloro and fluoro substituents on the aromatic ring influence how nucleophilic amines behave in condensation and coupling reactions. For medicinal and agrochemical research, this means developers can create derivatives with more selective biological activity or improved pharmacokinetics. Compared to standard benzylamine or mono-halogenated analogs, the dual substitution adds steric and electronic effects that make downstream functionalization more controlled.
Through our feedback with researchers, we hear that 2-Chloro-4-fluorobenzylamine often unlocks pathways for compounds that wouldn’t be accessible from traditional benzyl precursors. The modifications on the ring help modulate activity during SAR studies, letting discovery chemists generate analog libraries faster and fine-tune properties along the way. This isn’t theory—customers bring us challenging targets and trace their progress using starting materials produced in our reactors.
We’ve worked with project leaders who value having an uninterrupted supply chain for reagents such as 2-Chloro-4-fluorobenzylamine. That support shows up in anti-infective research, where amino-benzyl motifs are a late-stage installation step; in crop protection, where subtle shifts in halogen presence change potency or selectivity; and in specialty polymers, where the electron distribution supports more robust network formation. The track record comes from seeing these needs play out in production facilities and the labs of customers who report back on performance—not just from books or isolated suggestions.
On the ground, feedback often focuses on scalability. Small-lot users at bench scale appreciate knowing the starting amine won’t shift properties when they scale up to pilot or production volumes. Project managers in multistep syntheses value low impurity levels and the short lead times our team can turn around, minimizing inventory pressures and preventing delays. This dual focus leads us to keep finished goods inventory ready and maintain close relationships with suppliers of upstream intermediates so we’re not scrambling on key steps.
Synthetic routes to substituted benzylamines run across a spectrum of safety and cost considerations. Over the years, we’ve refined our processes in response to evolving regulations, changing feedstock markets, and real-time changes in customer requirements. Using hazardous chlorinating or fluorinating agents requires strict controls and diligent training. We’ve never had the luxury of treating environmental, health, or safety obligations as side issues. Strings of incidents—rare as they are—shape equipment investment and monitor strategy, aiming to preempt problems before they cost someone time or health.
Waste management means more than financial cost. Halogen-containing residues, even at low concentrations, shape how we select scrubbers, distillation, and recovery technology. Routine monitoring, not guesswork, minimizes environmental impact. Community expectations and regulatory inspections force us to improve, not just maintain, compliance—so every kilo produced has a traceable history, and our operators know what’s at stake if corners get cut.
We learn as much from the after-sales discussions as from R&D trials. Quality complaints, rare as they are now, push us to retrain supervisors and audit our protocols. In some cases, an impurity profile that passed internal tests appeared months later in a customer’s analytics, prompting us to trace back every handling and equipment touchpoint. Lessons drawn out of these experiences are turned into updated SOPs, smarter batch records, and better training modules.
Adaptability marks the difference between routine output and genuine partnership. Markets evolve—restrictions on some halogenated aromatics get introduced, new patents shift demand, and academic collaborators discover synthesis strategies that weren’t in play even a year back. Staying engaged with how the field moves lets us keep 2-Chloro-4-fluorobenzylamine relevant, not just available. This means tracking published research and patents, helping troubleshoot new reactivity, and even reformulating for solubility or purity as real projects require.
Competitors often conflate 2-Chloro-4-fluorobenzylamine with single-halogen analogs or substitute with commercially simpler benzylamines. Years in business have shown these substitutions often produce unpredictable yields or diminished final activity. That difference isn’t always visible on a spec sheet, but it plays out in pilot work and late-stage API campaigns. The dual halogen profile supports both the electron-rich and electron-deficient conditions, unlike unmodified analogs, which stall under certain reaction regimes.
Standard benzylamines can appear interchangeable at first glance, but end-users working with hydrogenation, reductive amination, or palladium-catalyzed cross-couplings report more reliable outcomes using the carefully substituted form we provide. The improved selectivity and higher overall conversion rates—especially when downstream steps demand clean, predictable transformations—offset the sometimes steeper upfront reagent price.
Traceability forms the backbone of all specialty chemical manufacturing, and that holds doubly true for sensitive building blocks like 2-Chloro-4-fluorobenzylamine. We log all precursor sources, with batchwise certificates and real-time inventory management feeding into audit trails. Customers facing regulatory and internal compliance checks reference these #s to assure auditors every bottle came from the expected synthetic lineage, free from forbidden residuals or mislabeling risks. This kind of transparent workflow gives purchasing teams and supply chain managers the leverage to focus on new project launches, not supply gaps.
Price fluctuation and regulatory bottlenecks happen, and nobody wins if a project gets stalled midstream due to export licensing or customs. We proactively monitor global regulatory changes on halogenated intermediates and hold reserve quantities so project managers can commit with confidence. Sometimes, this means rapid turnarounds for orders that land outside normal forecast—and our in-house logistics team, knowing the procedures, gets those shipments out without drama.
Manufacturing halogenated aromatics carries environmental responsibility, whether for air, water, or solid waste streams. We invested early in best-practice solvent recovery and emission control, adopting closed-loop reactors where possible. Solvents are recycled batchwise, and our in-plant testing stations let us tweak purification and minimize losses. This investment reflects both compliance and commitment—the local community knows our history, and we meet regularly with environmental auditors to review controls and update practices.
Product stewardship doesn’t stop once the amine ships. We spend time with downstream users to guide waste-neutralization protocols when their own processes generate halogenated byproducts, based on what we’ve found effective. This two-way knowledge stream, between our operations and those of our customers, helps set higher norms for safe handling and responsible outlet management up and down the value chain.
Every year brings new applications for 2-Chloro-4-fluorobenzylamine. Our role isn’t only to keep up a reliable supply—it’s also to exchange ideas on how the molecule slots into evolving R&D directions. Sometimes a team approaches us during early lead optimization when structural variation makes the difference between a lead and a failure. We’ve supported teams in process optimization when a residue from a cheaper amine threw off catalytic cycles, and shifting to our dual-substituted form led to a straightforward purification and higher yield.
People come to us with feedback, and it shapes every aspect of manufacturing. From product packaging and hazardous labeling to flexible sizing (offering both small bottles for R&D and drums for scale-up), we keep the listening lines open. Decades of partnership build trust more than any sales pitch. Our technical support team, made up of process chemists and engineers, stays available to help both in pre-purchase consultation and in post-sale troubleshooting, reflecting the reality that novel syntheses sometimes run into the unexpected.
End-users expect clear documentation. We ship each order of 2-Chloro-4-fluorobenzylamine with a comprehensive COA, detailing lot numbers, actual analytical values, and chromatographic traces as requested. Upon request, trace impurity data provide further clarity, especially for those running downstream syntheses where a part-per-million difference in impurity shifts results. We’ve found that direct dialogue with customer QA teams up front prevents friction later, especially when moving from kilo-lab to manufacturing scale.
Supporting documentation has expanded over the years as customer expectations evolve. Customers often require both legacy test protocols and more current multi-method confirmation on fluorine and chlorine content, including by IC and MS where relevant. This willingness to adapt our support infrastructure means fewer regulatory headaches and more seamless project launches downstream.
The world of pharmaceutical and specialty chemical development isn’t static. We regularly reevaluate both process chemistry and supporting analytics for 2-Chloro-4-fluorobenzylamine, investing in pilot runs with greener reagents or newer purification resins as they become viable. Ongoing investment in plant upgrades and operator education keeps safety and process repeatability at the forefront. An open feedback loop with customers brings early warnings about shifting regulations or new analytical norms, letting us re-qualify intermediates and avoid surprises during audits or customer launches.
Across all these efforts, one thread remains constant: reliability stems from the skill and judgment of people monitoring the process, not from automation alone. Each operator, analyst, and support specialist plays a part in delivering a molecule whose quality quietly enables the science and industry of others. 2-Chloro-4-fluorobenzylamine has a specific molecular identity, but the background manufacturing story—the decades of learning, improvement, and customer engagement—ensures it remains valuable far beyond the confines of a bottling line.