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HS Code |
330719 |
| Chemicalname | 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile |
| Casnumber | 396-12-9 |
| Molecularformula | C9H5ClF3N |
| Molecularweight | 219.59 |
| Appearance | White to off-white solid |
| Meltingpoint | 61-64°C |
| Density | 1.40 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥97% |
| Smiles | N#CC1=CC(C(F)(F)F)=CC=C1Cl |
| Inchi | InChI=1S/C9H5ClF3N/c10-7-2-1-6(5-14)3-8(7)9(11,12)13/h1-3H,5H2 |
| Storagetemperature | Store at 2-8°C |
| Hazardclass | Irritant |
As an accredited 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, with tamper-evident cap, printed hazard labels, chemical name, CAS number, and supplier details clearly marked. |
| Shipping | **Shipping Description:** 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile should be shipped in tightly sealed containers, protected from moisture and light. Handle with care as it may be harmful if inhaled or absorbed through skin. Transport according to local regulations for hazardous chemicals, ideally under cool conditions. Ensure robust packaging to prevent leaks and contamination. |
| Storage | **Storage Description for 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile:** Store in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use only with proper ventilation and avoid prolonged exposure. Ensure proper labeling and restrict access to authorized personnel. Wear suitable personal protective equipment when handling. |
Applications of 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile in Industrial ManufacturingWe supply high-purity 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile to global manufacturers seeking specialized intermediates for advanced chemical synthesis. Below, we detail its main industrial application scenarios, regulatory framework, incorporation protocols, production integration points, and representative finished goods. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate ProductionLeading pharmaceutical manufacturers utilize this compound as a key chlorinated aromatic building block for the synthesis of specific APIs, notably in the class of central nervous system agents and selective receptor modulators. Its electron-withdrawing properties facilitate precise coupling and cyclization reactions in multistep routes. This intermediate typically appears in stages following the preparation of substituted benzene cores, especially where clean nitrile group introduction is essential for downstream specificity. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)Major agrochemical companies rely on this nitrile-bearing compound as a core intermediate in the construction of complex active molecules for crop protection products. Its unique trifluoromethyl and chloro functionalities support selective halogenation and enhance bioactivity through metabolic stability, positioning it as a preferred synthon in proprietary fungicide and post-emergence herbicide preparation. Industry compliance standards
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3. Specialty Chemical Manufacturing for Liquid Crystal CompoundsLarge producers of specialty fine chemicals integrate this material in their synthesis of advanced liquid crystal monomers. The electron-deficient aromatic ring, in tandem with trifluoromethyl substitution, imparts high dielectric anisotropy and thermal stability, supporting the production of performance-differentiated LC phases for flat-panel display components. Stringent purification and polymerization process control is maintained to achieve necessary alignment and viscosity specs. Industry compliance standards
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4. Advanced Polymer Additives for High-Performance FluoropolymersManufacturers producing high-performance engineering plastics employ this chemical as a functionalized chain modifier in the synthesis of specialty fluoropolymers and related copolymers. The presence of both chloro and trifluoromethyl groups provides unique reactivity for regulating polymer backbone architecture, heat resistance, and flame retardancy. Strict process control is essential to incorporate the material at specific conversion stages to avoid unwanted by-product formation. Industry compliance standards
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5. Crop Protection Fine Chemical Intermediates for Seed Coating AgentsSpecialty formulators for modern agro-seed coatings use this intermediate as a precursor for active agents that impart protection against fungal pathogens and insect larvae. Its chemical structure allows for the creation of highly selective, non-systemic actives with sustained release profiles, which can be embedded directly in polymeric seed coating matrices. Varying formulation requirements from global regulatory authorities influence its incorporation rate, necessitating batch-specific adjustments under controlled manufacturing conditions. Industry compliance standards
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Working as a chemical manufacturer comes with years of direct involvement—from synthesis design through to scaling production—so every product reflects both precise chemistry and practical experience. Among the lineup, 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile stands out with its firm spot in custom synthesis, pharmaceutical intermediates, agrochemical precursors, and specialty materials. In practice, it brings together a tricky substitution pattern on the aromatic ring with a reactive nitrile group, and that combination leads to real-world value across several sectors.
It’s always the details in structure that explain performance out in the lab or factory. The compound features a trifluoromethyl group at the 5-position and a chlorine atom at the 2-position on a phenylacetonitrile core. This layout does two things. First, it tunes the electronic nature of the ring, opening up distinct pathways for downstream functionalization—not just theoretical points, but actual differences when reacting with various electrophiles or nucleophiles. Second, fluorination increases the overall stability, especially thermally, and this shows up during higher-temperature steps in multi-step synthesis, where lesser analogs become unreliable or give unwanted side products.
Typical production delivers material as a white to off-white crystalline solid, often exhibiting sharp melting behavior matched to scientific references—key for repeatable reactions. Purity checks run via HPLC and NMR, with daily standards demanding 98% minimum purity, while residual solvents and water fall below 0.5%. Over the years, getting to these specs consistently has required dialing in every batch and running careful column purification. It’s never only paperwork for us; each drum and bottle reflects hands-on quality control and constant refinement.
Scaling up isn’t easy for multi-substituted aromatics, mostly thanks to regioselectivity concerns during both chlorination and trifluoromethylation. Over time, process tweaks—catalyst loadings, solvent choices, and temperature ramps—have brought down impurity levels with every metric logged and reviewed. Sometimes small shifts in reagent quality can throw off expected outcomes, so raw material sourcing goes through strict incoming testing. Our reactors are held to rigorous pressure and temperature standards. These factors come together to create a product that enables complex molecular assemblies to work reliably batch after batch—something our partners in R&D and manufacturing notice right away.
We’ve shipped 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile into both global and domestic markets, supporting diverse fields. In pharmaceuticals, it consistently turns up as a critical intermediate during heterocycle formation, especially triazole or pyrazole synthesis. The chlorinated and trifluoromethylated core helps block off undesired pathways, guiding selectivity, and can dramatically improve yields for partners working on active pharmaceutical ingredients. Agrochemical researchers routinely use it during development of fungicides and herbicide leads, leaning into the molecule’s electron-withdrawing nature to deliver selective binding and metabolic stability in crops. Specialty monomer manufacturers use it as a seed for fluorinated polymer projects. Our facility has even had inquiries for electronics materials, especially where stability, process-compatibility, and resistance to degradation matter.
From experience, switching from plain 2-chlorophenylacetonitrile or only trifluoromethyl-phenylacetonitrile analogs usually fails to offer the same outcomes. The presence of both chlorine and trifluoromethyl substituents enhances blocking efficiency during cross-coupling or nucleophilic aromatic substitution, which leads to fewer over-reactions and easier purification steps downstream. Also, the electronic tuning is just right for certain Suzuki–Miyaura or Buchwald–Hartwig type couplings, where other structures either stall out or give multiple products.
No two substitution patterns offer the exact same reactivity. After years of talking to medicinal chemists, it’s clear that the 2-chloro position in this molecule blocks ortho-metalation, which helps tailor later-stage functionalization. If only a trifluoromethyl group is present, the electron-deficiency rises to where some cross-couplings require over-aggressive catalysis—opening doors for unwanted side chemistry. The current pattern hits a sweet spot many chemists look for, keeping the right balance between reactivity and chemoselectivity. Our plant operators keep a close eye on product homogeneity, as polymorphic forms sometimes create problems for customers who need batch-to-batch reproducibility.
Years of hands-on work have taught us that process engineers and bench chemists alike care about more than just molecular structure. Packaging sees attention to details—solvent levels, residual acidity, solid handling flow, and dust minimization all show up on internal checklists. During storage, we recommend air-tight containers and low-humidity conditions, since the nitrile group, while stable, absorbs moisture if left exposed. Proper environmental controls maintain both purity and physical form.
We see fewer incidents with material clumping or degradation after moving away from generic warehouse setups toward temperature- and humidity-controlled spaces. Since scale-up often requires moving drums by forklift and repeated partial use, our packaging stands up to daily lab and factory work. Bench technicians appreciate it when a chemical dispenses cleanly and doesn’t require constant redrying or repurification—a reality frequently overlooked during product design elsewhere.
Decades in this industry have shown that synthetic efficiency goes well beyond reagent cost; engineers and chemists consistently value predictable behavior in every batch. Having seen poorly controlled intermediates trigger failed runs, project delays, or even dangerous exotherms, we double down on scale-up precision. Early on, our technical team worked side by side with customers to track the impacts of minor changes—solvent swaps, base choices, or heating rates—on overall productivity and waste generation. Consistent crystallinity, clear spectral signatures, and minimal trace contaminants translate to smoother synthesis, less downtimes, and more controllable yields.
As workflows have grown, we’ve invested in drum-to-vessel transfer solutions that cut down on contamination risks and off-spec stock. Documentation travels with every lot, giving full traceability and letting chemists know both what’s in the drum and what’s not. After years of shipping globally, we’ve also adapted to local regulations and requirements without compromising on shelf life or handling experience.
Every plant will have the occasional hiccup—yields drop, a new impurity sneaks in, or filtration slows down unexpectedly. Over the years, we’ve learned that tracing small issues back to raw input quality, equipment calibration, or minor shifts in reaction parameters can quickly bring a process back on track. Frequent batch reviews and close communication with end-users mean these problems rarely last long. Instead of blaming “lab variability,” we collaborate to find the root problem and resolve it quickly—whether that means improving drying steps, tightening up atmospheric controls, or revisiting our filtration choices. Knowing the compound inside and out means we can provide realistic troubleshooting advice informed by hands-on production, not just theory.
With each year that passes, the need for full documentation grows across regulated and advanced industries alike. Our site audits, GMP-compliant record-keeping, and digital databases put detailed synthesis and analysis data into our customers’ hands. This approach is built on feedback from teams who need to justify every input for regulatory filings or quality management systems. No black boxes, no shortcuts. If 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile batches show a one-off deviation—even if it looks minor—we flag it and work with the customer to assess potential impact.
Having stood on both sides of the quality question—for internal process development and as a supplier—we understand how overlooked differences between lots can ripple through demanding synthesis campaigns. Documentation matches up with both in-house reference spectra and external standards. We’ve remained open to third-party audits and side-by-side performance evaluations, learning from each to improve our practices and ensure the next batch fits customer needs even better.
Operating as a manufacturer goes hand-in-hand with stewardship. Waste byproduct reduction and responsible emissions management feature strongly in our process strategy, supported by routine audits and technical investments over the years. Operators receive regular updates and safety training that directly incorporate practical experience—spills, exposure, and waste neutralization all benefit from this hands-on approach and regular knowledge sharing.
In addition, our site maintains a strong alignment with evolving environmental standards: solvent recycling programs, on-site waste treatment, and energy-reduction measures built into the facility itself. Besides improving overall safety, these efforts keep material costs down for customers by keeping production more efficient. Teams are encouraged to propose improvements or flag issues—every worker has seen the difference a well-maintained facility and stringent chemical management policy makes, not only for compliance but collaborative working and product consistency.
Product development doesn’t stall with a working process. Over the years, customer input and internal review led us to try different synthesis methods, aiming for greener reagents, lower waste, and more gentle conditions. Alternative trifluoromethylation agents, stricter raw material vetting, and real-time purity checks during batch workups have all improved yield and reliability. We pay attention to shelf life requests and special handling needs, tweaking packaging and offering flexible pack sizes to keep users supplied according to project demand.
Each improvement feeds back into our primary goal: deliver material that works in the real world, whether in a kilo-lab or a multi-ton plant. The technical team keeps up with the literature and industry conferences, comparing notes on promising advances and making sure our process flexibility stays responsive to evolving sector needs. Internal training and regular cross-team updates help everyone on site stay aligned with industry direction and customer priorities.
The world market for intermediates featuring halogen and fluorine substitution has grown more competitive with every year. Offshore producers, short-lived trading houses, and sporadic brokers have all shifted market dynamics in different ways. Our position as an actual chemical manufacturer brings several advantages. The ability to control every synthesis detail remains critical for projects where reliability, traceability, and ongoing support matter. We’ve experienced firsthand the hidden costs of sourcing from fragmented supply chains—lost batches, uncertain reactivity, and documentation gaps all interfere with high-stakes work.
Focusing on direct communication and real-world feedback, we partner with R&D teams, process engineers, and procurement professionals to not just deliver product but help optimize its use. This collaborative approach emerges from many years of knowing what it takes to keep lines running smoothly, minimize downtime, and respond flexibly to evolving project timelines. We stand behind the chemistry, supporting partners long after a batch leaves our dock.
Looking back over years in fine chemical production, each success story and challenge underscores why a tailored, transparent approach matters. 2-Chloro-5-(Trifluoromethyl)Phenylacetonitrile, with its careful substitution profile and reliably measurable performance, keeps finding new roles in cutting-edge industries. From purification staff to process chemists and R&D leads, the compound’s adaptability, manufactured at consistent high quality, stands as a result of ongoing in-house learning and practical troubleshooting.
What sets our process apart isn’t just the underlying chemistry, but the commitment to every person who depends on our output—from the first small sample to large-scale shipments. By focusing on reliable daily operation, in-depth technical support, and full transparency on everything we do, we build the kind of working partnerships that last. As both techniques and customer needs move forward, our focus stays on delivering hands-on, performance-driven chemistry that stands up to real-world use—batch after batch, year after year.