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HS Code |
619306 |
| Chemicalname | 3-Chloro-4-Fluorophenylacetonitrile |
| Casnumber | 41404-78-8 |
| Molecularformula | C8H5ClFN |
| Molecularweight | 169.58 |
| Appearance | White to off-white solid |
| Meltingpoint | 61-65°C |
| Density | 1.271 g/cm³ (estimated) |
| Solubility | Soluble in organic solvents like DMSO, DMF |
| Purity | Typically >98% |
| Smiles | N#CC1=CC(=C(C=C1)Cl)F |
| Inchi | InChI=1S/C8H5ClFN/c9-7-3-2-6(5-11)1-8(7)10/h1-3H,5H2 |
| Synonyms | 2-(3-Chloro-4-fluorophenyl)acetonitrile |
| Storagetemperature | Store at 2-8°C |
As an accredited 3-Chloro-4-Fluorophenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g amber glass bottle is securely sealed with a tamper-evident cap, labeled "3-Chloro-4-Fluorophenylacetonitrile, CAS 943113-79-1". |
| Shipping | 3-Chloro-4-Fluorophenylacetonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is transported as a hazardous chemical according to relevant regulations, requiring proper labeling and documentation. The shipment must ensure ventilation and temperature control, with handling by trained personnel using appropriate personal protective equipment to prevent exposure. |
| Storage | **3-Chloro-4-Fluorophenylacetonitrile** should be stored in a tightly sealed container, away from moisture and incompatible substances, such as strong oxidizers and acids. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Label the storage area clearly and ensure only authorized personnel have access. Follow all relevant safety and handling guidelines. |
Applications of 3-Chloro-4-Fluorophenylacetonitrile in Industrial ManufacturingAs a direct manufacturer, we supply 3-Chloro-4-Fluorophenylacetonitrile to downstream industries that require precise performance at a molecular level for their advanced synthesis needs. Our material plays a key role in several specialized segments, with each application scenario demonstrating specific compliance requirements, manufacturing integration stages, composition ratios, and resulting product types unique to its field. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical companies use this intermediate in the multi-step synthesis of various APIs, particularly in the psychiatric and anti-inflammatory drug segments where benzyl derivatives form essential structural elements. The compound enters the route as a halogenated acetonitrile, facilitating nucleophilic substitution that leads to more complex phenylacetic or phenylethyl cores found in final actives. Material traceability, impurity profile, and batch reproducibility receive continuous scrutiny to comply with international drug quality regulations. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisLeading agricultural chemical manufacturers employ this compound to construct advanced pre-emergent herbicide actives and novel insecticidal chemistries. Its dual halogen-functionalized aromatic profile allows formulation chemists to pursue competitive selectivity and environmental breakdown rates in the resultant actives. Bulk traceability and consistent bulk assay levels are maintained according to agricultural formulation standards. Industry compliance standards
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3. Fine Chemical and Custom Synthesis Building BlockProducers in the fine chemicals sector source this material as a halogenated acetonitrile scaffold to access libraries of fluorinated aromatic compounds for research, electronics, and material development pipelines. Batch homogeneity and consistent halogen patterning are prioritized as downstream clients require reliable reactivity and scale-up predictability in aromatic substitution and coupling pathways. Industry compliance standards
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4. Specialty Polymer Precursor ManufacturingChemical manufacturers in advanced polymer development leverage our material as a precisely substituted aromatic nitrile monomer for producing high-performance specialty resins. Its halogen configuration offers unique advantages in step-growth or chain-growth polymerizations, particularly for introducing site-specific functional groups that enhance solvent resistance, thermal stability, or fluorine content in the polymer backbone. Industry compliance standards
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In the world of chemical synthesis, every step matters. At our facility, the conversation around 3-chloro-4-fluorophenylacetonitrile isn’t about trends, it’s about function and impact. This compound stands out for its dual halogen substitution and reliable nitrile group, opening gates to efficient synthetic routes and new chemistries. The model most encountered in our manufacturing lines appears as a pale, solid crystalline mass, handled with respect in every batch. Trust in this intermediate springs from day-to-day observation—when a synthesis demands both resilience and manageable reactivity, we reach for this nitrile. The purity levels, often exceeding 98%, guide the outcome, so we check every drum before it moves another step.
Working with 3-chloro-4-fluorophenylacetonitrile never falls into a routine. Each batch runs through a controlled environment; temperature and humidity can shift the crystallization. Our chemists spend their days checking the melt point by hand, recording it, and double-checking spectra. Even a minor trace of impurity travels quickly through the process, and that affects downstream yields. It’s this everyday challenge that led us to refine our solvent systems and handling equipment. A faint chlorinated note hangs in the air during loading—noses trained over years know when something’s off. The specifications haven’t been shaped by generic expectations, but by hard-earned knowledge gained during scale-up and troubleshooting. Actual melting ranges, precise solubility in common organic solvents, and exact halogen content—these numbers aren’t just technical details, they set the practical limits of what can be done downstream.
Ask a hundred chemists why they’re reaching for this intermediate and you’ll get overlapping stories. Our experience centers around pharmaceutical and agrochemical pathways—processes that start simple and spiral into complexity. The compound’s structure—with both chlorine and fluorine atoms alongside the nitrile—offers unique opportunities. In medicinal chemistry, that halogenated pattern translates to metabolic stability. We’ve made plenty of alpha-aryl acetic acid derivatives, assembling cores for local drug development teams who rely on well-vetted raw materials. For crop protection and active ingredient discovery, leads often stem from quick functional group transformations involving this molecule. I remember one particular pilot batch where omitting this intermediate added six more steps to the route; the change threw our whole shift into overtime. So, the usage isn’t theoretical—it’s an answer to real limitations faced at the bench and in scale-up.
When we look at other phenylacetonitrile derivatives, the differences become real during reaction setup, not in an abstract spreadsheet. The 3-chloro-4-fluoro substitution brings stability that isn’t always present in similar compounds. For example, monohalogenated substrates tend to oxidize or hydrolyze in the drum, especially if storage stretches longer than planned. Here, the double substitution holds up better, giving us time and confidence between receipt and use. Handling echoes that difference: laboratory chemists feel a dry, dense powder, less clumpy, with better dispersion in the solvent. We’ve taken shipments from outside sources with single-substituted versions, only to see them start to degrade after a humid weekend. Switching back to our in-house batches, complaints stop. Technicians appreciate the predictability—fewer reruns, cleaner TLC plates, and higher GC purity after basic workup.
There’s no substitute for experience on the production floor. Nitriles can emit noxious fumes, especially under heat, so all batches here run with dedicated venting, and monitors get checked hourly. Controlling the acidity during final crystallization prevents decomposition, a lesson learned after too many failed runs under rushed schedules. Storage gets its own attention; after watching a series of shipments yellow from light exposure, we switched to opaque containers and log every lot’s shelf life. Initially, scale-up brought a slew of headaches: pressure surges during chlorination, unpredictable end-points, and erratic filtration times. The key improvements didn’t come from manuals—they came from onsite notes jotted during overnight shifts. Every tweak aimed to give the downstream chemists a more consistent compound.
Our team takes pride in internal monitoring—knowing each drum’s journey from raw materials to final warehouse storage. By managing every input, from halogenation agents to the potassium cyanide for nitrile installation, we avoid unwanted surprises. We don’t rely on third-party assurance. Once, inferior raw materials from a one-time supplier threatened the integrity of an entire month’s production; losing those hours forced us to double down on supply chain screening. Now, procurement works hand-in-hand with the floor staff, because a missed alert in the quality room translates to lost time and extra solvent use. Each shipment reflects our standards, and every deviation triggers a review—no batch leaves without full analysis, even when demand runs high. This diligence shows in customer feedback—complaints over mislabeling or variable color stopped years ago.
Reacting 3-chloro-4-fluorophenylacetonitrile with common reagents produces a family of useful molecules—each important for further synthesis. Process engineers sometimes call in with questions about unexpected impurity peaks, usually traced back to handling or subtle pH drift during dissolution. We keep direct lines open between our batch supervisors and partner labs, so minor issues get picked up before a hundred-liter vessel is compromised. It’s not just about purity at the start—it’s how a product like this behaves in real-world labs, not just in catalog descriptions.
After shipping hundreds of lots over the years, patterns emerge. Our product resists caking, flows well, and doesn’t gum up mixers—details that seem trivial until a plant run stalls. We learned this through reporting and revisiting every outlier batch. Equipment operators, often overlooked in the conversation, bring us feedback about how their tanks, pumps, and sieve assemblies handle new shipments. Some years back, a minor process change in the drying step improved bulk density and prevented bridging during pneumatic transfer; the improvement went straight into standard operating procedures. Reactions that call for slow addition or precise temperature ramps take well to the consistent thermal profile of our compound. The feedback loop from plant to packaging to R&D tightens year by year, resulting in a product shaped for the field, not the catalog.
Experience guides every safety protocol here. Chlorinated and fluorinated aromatics carry real risks—corrosive to skin, challenging to vent, and slow to break down in waste streams. Each operator moves through annual retraining, especially after incidents in the industry highlighted what goes wrong with inattentive procedures. As the team learned during a near-miss years ago, double-checking goggle seals and glove ratings isn’t bureaucracy—it’s essential survival in a hazardous setting. The fumes from a heated batch linger, so the exhaust system gets inspected before any large run. Spills get isolated, logged, and cleaned with specialized agents. Waste treatment includes multi-stage breakdown for the nitrile and aromatic residues, driven by on-site experience with environmental audits and strict local regulations.
Years of operation brought the environmental stakes front and center. 3-chloro-4-fluorophenylacetonitrile sits at a crucial intersection: it enables modern synthesis, but mishandling can persist in the environment or harm factory workers. Our commitment reached a new level after partnering with local waste authorities and installing regenerative incinerators. Every kilogram produced is tracked, and scrap quantities feed directly into process adjustments. Feedback from environmental review boards led us to tighten water discharge parameters; any trace contamination gets reprocessed, not diluted. Improvements in process yield mean more product with less waste, lowering the total burden on downstream treatment facilities. Nothing sharpens focus like a regulator’s visit—our practices now emphasize the same vigilance inside and out, reinforcing a cycle of accountability beyond the plant gate.
A product’s real value appears in its daily use, not just at point of sale. Chemists at the bench push for minor tweaks: finer powder for faster dissolution, reduced dust during transfer, or improved pourability for automated systems. These requests—built on years of start-and-stop lab work—get routed back to our production line, where every change carries risk and reward. We hold open discussions with users about batch variability and pain points. Sometimes a complaint about slow dissolution leads to a change in drying protocol; in other cases, process operators suggest better packaging to prevent static during winter transfers. Chemistry teams have grown to trust our responsiveness, shaped by shared language and mutual respect built over long-term collaboration.
Technically, the differences between 3-chloro-4-fluorophenylacetonitrile and close relatives like the monofluoro or monochloro analogues seem small—one atom’s change, a difference in substitution pattern. During real work, those differences accumulate. Double-halogenated versions hold up far better in the open air, with less tendency toward acid-catalyzed cleavage or background coloration. We see higher crude yields in alkylation and Grignard reactions. In trials with single-substituted nitriles, our QC staff found more by-product formation requiring extra chromatography. Our formulation staff reports that the mixed halogens enable unique selectivity, unlocking more diverse routes to tailored products. Over time, a clear preference for the 3-chloro-4-fluorophenylacetonitrile form has emerged across R&D, pilot, and manufacturing operations—not from habit, but from observation and outcome.
Successful production isn’t a fluke; it’s the result of systematic troubleshooting and adaptation. We analyze every production hitch, no matter how routine. During the hottest months, excess heat affected crystal form and handling—solved by incremental upgrades to cooling systems and by tightening humidity control in storage rooms. When dust levels triggered safety alerts, we installed improved fume extraction and adjusted granulation times. Batch-to-batch consistency matters as much to our customers as it does to us, so we draw from dozens of small process changes—switching filter cloths, recalibrating scales, and fine-tuning solvent recovery ratios. Our teams operate with an ongoing mandate: every adjustment pursues the reliable flow of good material, with no surprises waiting in the drum.
Our stake in 3-chloro-4-fluorophenylacetonitrile isn’t just about filling demand; it’s about fostering the research ecosystem that relies on our work. Local university projects and startup pharma ventures run on tight budgets and short timelines. They need intermediates that don’t add trouble. By tightening our controls and taking feedback seriously, we allow more scientists to reach their goals—whether that’s a new therapeutic pathway or a better herbicide structure. The benefit radiates out: fewer failed runs mean more productive labs, better project outcomes, and less waste sent to disposal. We see our work as both a technical challenge and a foundation for larger discovery.
Anyone can draw up a specification or list supplier details. Actual trust grows batch by batch, shipment by shipment, reinforced through feedback, adaptability, and a relentless attitude toward improvement. Stories from our customers stick—a project saved by a dependable intermediate, a headache avoided because a bad batch was caught before it left our warehouse, an urgent overnight request that was met because production flexed shifts. These stories don’t appear in the marketing copy, but they make up the substance of our reputation. We think about our product as a living part of someone else’s workflow—not a commodity checked off a catalog, but a tool that solves problems and enables creativity in a thousand ways.
Manufacturing never stands still. Regulatory expectations and customer demands evolve. Our R&D group stays close to the shop floor, and every incremental improvement makes its way into the production log. We experiment with greener reagents, shorter cycle times, and advanced impurity profiling. Sometimes, a flash of insight in the plant leads to a redesigned workup; other times, customer pressure drives a specific upgrade. Keeping 3-chloro-4-fluorophenylacetonitrile at its best means thinking about both the micro-scale details—a missed solvent swap, a sticky filter pad—and the bigger picture of responsible manufacturing. The product’s value grows with every improvement made, every risk managed, and every relationship strengthened.
From the shop floor to the customer’s lab bench, our connection to this compound runs deep. We care about every drum leaving the gate, every reaction run, every question from a chemist on the line. Open channels, rigorous checks, purposeful adaptation—these are words we live by, not just promises in a brochure. 3-chloro-4-fluorophenylacetonitrile has taught us the value of process, discipline, and shared understanding. Chemical manufacturing isn’t flashy. It’s hard, detail-driven work done by people who never settle for “good enough.” Our product carries that spirit from the first planning meeting to the last package shipped. That’s the difference experience—and dedication—makes.