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HS Code |
966794 |
| Chemical Name | 4-Chloro-2-(trifluoromethyl)aniline |
| Cas Number | 2349-25-7 |
| Molecular Formula | C7H5ClF3N |
| Molecular Weight | 195.57 |
| Appearance | Light yellow to brown crystalline solid |
| Melting Point | 44-47°C |
| Boiling Point | 218-220°C |
| Density | 1.42 g/cm3 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1Cl)N)C(F)(F)F |
| Inchi | InChI=1S/C7H5ClF3N/c8-5-2-1-4(7(9,10)11)6(12)3-5/h1-3H,12H2 |
| Pubchem Cid | 13526 |
As an accredited 4-Chloro-2-(trifluoromethyl)aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, tightly sealed, hazard-labeled for toxic and irritant properties, with chemical name, CAS number, and supplier details. |
| Container Loading (20′ FCL) | 20′ FCL: 160 drums (200 kg each), totaling 32 MT. Drum material: HDPE. Chemical kept dry, cool, and ventilated. |
| Shipping | 4-Chloro-2-(trifluoromethyl)aniline is shipped in tightly sealed containers, protected from moisture and light. It is packed according to chemical safety regulations, typically as a hazardous material. Proper labeling and documentation are required, and the package may be subject to transportation regulations for toxic or environmentally hazardous substances. |
| Storage | **4-Chloro-2-(trifluoromethyl)aniline** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Label the container clearly and avoid exposure to excessive heat. Personal protective equipment should be used when handling to prevent skin and eye contact. |
| Shelf Life | 4-Chloro-2-(trifluoromethyl)aniline is stable for at least 2 years when stored tightly sealed, cool, and protected from light. |
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Purity 99%: 4-Chloro-2-(trifluoromethyl)aniline with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurity formation. Melting point 59°C: 4-Chloro-2-(trifluoromethyl)aniline with a melting point of 59°C is used in agrochemical formulation, where its defined solid-state enhances handling and storage stability. Stability temperature 120°C: 4-Chloro-2-(trifluoromethyl)aniline with a stability temperature of 120°C is used in high-temperature organic synthesis, where it maintains structural integrity during reaction processes. Particle size <50 µm: 4-Chloro-2-(trifluoromethyl)aniline with particle size less than 50 µm is used in pigment manufacturing, where it promotes uniform dispersion in polymer matrices. Moisture content <0.5%: 4-Chloro-2-(trifluoromethyl)aniline with moisture content below 0.5% is used in electronics chemical production, where low water content prevents hydrolysis and ensures product reliability. Molecular weight 195.57 g/mol: 4-Chloro-2-(trifluoromethyl)aniline with molecular weight 195.57 g/mol is used in custom chemical synthesis, where precise molecular mass supports accurate formulation development. |
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We make 4-Chloro-2-(trifluoromethyl)aniline in large volumes every month, watching the pure, colorless-to-light-yellow crystals come off the drying line. Our experience with the compound goes way back—early on, we recognized that the combination of a chloro and a trifluoromethyl group on the same aromatic ring produced big changes in reactivity. Chemically, it answers to the formula C7H5ClF3N, with a molecular weight hovering just above 195. Over years of customer projects, we have shipped it to research teams, API manufacturers, agrochemical pilot lines, and dye intermediate developers who require high consistency in their raw materials.
Some see this molecule as just another substituted aniline. For us, the differences matter a lot in practice. The para-chlorine and ortho-trifluoromethyl groups throw the electron density off balance in the benzene ring, driving unique behavior. During nucleophilic aromatic substitutions, the position of the trifluoromethyl group next to the amino group makes it much less reactive toward unwanted side reactions than its isomers. Many find the meta isomer easier to source, but the ortho version performs better in pharmaceutical and agrochemical building block applications where regioselectivity matters.
For product consistency, our material maintains purity at 99% or above (as tested by GC and HPLC), but purity on paper only matters so much. We have learned to screen for ultratrace contaminants like ortho-positioned positional isomers and polyhalogenated leftovers from earlier steps. These fine controls earn trust from clients formulating advanced actives, where downstream hydrogenations or cross-couplings can magnify even tiny impurities.
Aniline intermediates with a similar structure—such as 2-chloro-4-(trifluoromethyl)aniline—often end up less selective under certain coupling conditions. Substitution patterns often dictate reactivity, and this compound’s unique pattern unlocks new synthesis routes not possible with the other variants. Many researchers come to us after discovering the limits of more common analogs; side products stack up, and no solvent swap fixes the bottleneck. Our manufacturing team revises downstream steps for these customers, using only 4-Chloro-2-(trifluoromethyl)aniline, for both pilot and scale-up batches, after sharing detailed technical feedback from actual plant trial data.
A molecule like this, with both a nonpolar trifluoromethyl punch and a reactive amine, calls for care during purification. Impurities hang tight to the product, especially if earlier stages yield polychlorinated anilines. We route our crude product through a precise acid-base extraction cycle, using ammonia inventories sourced in-house, and finish it with a short-path distillation to preserve sensitive functional groups. We track the total base (as aniline) and residual proto-dehalogenated aromatics to below 200 ppm before signing off.
We built our liquid-handling systems to minimize oxygen exposure—it is not just about oxidation, but also about preventing subtle color shifts that downstream customers flag as QA issues. For analytical routines, our in-plant GC/MS runs check for co-distilled solvent artifacts and degradation fragments before every packing job. While this limits throughput, it lets our team catch process drifts faster. When a batch tips toward the off-spec side, we pull the line and retrace every raw material order, solvent batch, and operator checklist—hard experience taught us that even a small mistake in the workup step can impact everything from reactivity to solid-state stability.
Many downstream uses for 4-Chloro-2-(trifluoromethyl)aniline shape our understanding of how the molecule behaves under different conditions. In pharmaceutical projects, clients often build amide or urea linkages from the aniline group. The unique substitution pattern increases activity for certain kinase inhibitor scaffolds, and toxicity profiles in preclinical animal models show the benefit of the added trifluoromethyl’s electron-withdrawing effect. Our material’s reliability in reactivity and minimal side reactions supports iterative SAR (structure-activity relationship) work, a key step as clients tweak molecule families before picking leads to advance.
We also receive requests from crop protection developers, seeking stable intermediates for herbicide or fungicide R&D. The trifluoromethyl boosts metabolic stability in plants, and its resilience under field conditions is backed up by years of data. From our plant, we ship drums directly to formulation labs where only trace residual metals or halogenates can make the difference between success and shelf-life failures. Precision in upstream purification keeps those levels where our toughest customers expect them.
Other customers use the product to modify dyes and specialty pigments. For these, color consistency and batch reproducibility outrank every other property, since a small charge of the amine can set the tone for hundreds of liters of finished dye solution. Our team works with pigment chemists to fine-tune process parameters, even adapting crystallization timing to match microstructure needs in dye synthesis.
We have seen a rising trend for this aniline’s use in new material science areas, including small-molecule OLED dopants and specialty polymer additives. Substituted anilines with a combination of chloro and trifluoromethyl groups unlock better charge transport characteristics. These projects taught us fresh lessons: attention to trace amine impurities does not just safeguard yield—it also affects the performance and color fade in demanding applications like displays or functional films.
Working as a chemical manufacturer means interacting with reality, not theory. Our team developed a habit of pulling samples at every step, instead of waiting until final QC. This practice reduces wasted time and material, since it is easier to correct a drift early in the workup than to rework a finished batch. Our approach has developed over years in the plant: we spot-check for free amine content, halogen balance, and melting point, tuning our final batch to sit in a narrow melting range for easier downstream processing.
We package our 4-Chloro-2-(trifluoromethyl)aniline in drums and kegs designed for chemical resistance. Internal lining and transfer lines get checked for compatibility, because reactive traces can leach, especially with aromatic amines. Many customers have strict contaminant limits, not just for process safety but because unplanned interactions during scale-up can cost weeks of lost time. Instead of risking a generic approach, we work directly with end users to select storage and transfer strategies fit for their regional climates and batch size.
As fluorinated aromatics draw more regulatory discussion, we invested in containment, local emission control, and closed-loop solvent recovery. Our experience brings a practical view—safe handling starts with training and real accountability. During audits, we show full traceability: each raw material lot ties back to supplier test data, and deviations in impurity patterns get logged with corrective actions.
Waste minimization is routine rather than an afterthought. Our team recycles non-contaminated solvents wherever feasible, and off-gas streams from our aniline reactors pass through activated-carbon abatement units. Following regulations is not about avoiding fines, but about keeping our community’s trust. Full batch logs, emissions records, and safety drill documentation stay ready for inspection.
Many labs think of aniline intermediates as interchangeable, but our experience says otherwise. The placement of the chloro and trifluoromethyl groups shifts both boiling point and solubility, which means process steps written for another isomer often do not translate smoothly. Even subtle shifts in recrystallization conditions or solvent polarity can alter the impurity profile.
Unlike unsubstituted aniline or chloroanilines lacking the trifluoromethyl, this version stands up much better to harsh reaction conditions. Strong bases and nucleophiles, common in coupling reactions, produce fewer decomposition products. We have seen routine synthetic steps run more cleanly, fewer byproducts get isolated, and less need for downstream purification. For process chemists, these workarounds lead to real savings on time, solvent, and raw material expenses.
Safety-conscious users notice one more advantage: the CF3 group dampens volatility and reduces the vapor pressure. While no aromatic amine should be considered benign, this intermediate produces fewer fumes than unsubstituted analogues, reducing the load on vapor handling and ventilation systems. Hands-on users appreciate lower odor in the final process suite, especially during solvent removal or open-transfer steps.
Every run through the plant teaches us something. Early batches surprised us with color drift and minor side product formation; close analysis traced this to a trace impurity in the aqueous workup, missed by less sensitive test methods. Revising our in-process controls taught us that hands-on monitoring—pH at each extraction, split-phase separation, and operator sampling—catches potential problems long before they show up as customer complaints.
Bigger differences came from modifying the cooling curve during post-reaction crystallization. Instead of a single, fast cool-down, we hold intermediate temperatures to promote exclusion of oily byproducts, allowing easier filtration and drier cakes on the first pass. Not every adjustment shows up in a spec sheet, but a few degrees or minutes at this stage can save hours of downstream cleanup and reduce solvent consumption for redissolution steps.
Even base material selection influences stability—switching to a higher-purity, in-house manufactured ammonia gave us better control of residual salts. The link between raw material quality assurance and finished-batch purity often gets overlooked. By documenting not just the end-point test results but the entire sequence, from sourcing to blending and filtration, we keep our standards high and our customers’ project development smooth.
Working alongside end users for years reshapes how we measure success. Short lead times and speedy shipments matter, but we focus on making each batch as predictable and fit for purpose as possible. Feedback after a failed test, or even just a minor agility tweak, triggers reflection on our side. If a customer’s reactor runs into slurry handling troubles, or they notice a color drift, our process team reviews the batch entries, compares against past runs, and works through possible adjustments.
Process optimization does not follow a one-size-fits-all path. We pay attention to how our product gets used, adjusting for scale—whether that means hundred-gram run-ups in an R&D hood, or drum-scale charging into pilot-scale reactors. Open reporting of lessons learned and transparent correction plans help build long-term relationships with both new and established clients.
Shipping aromatic amine intermediates has its unique challenges. Aromatic amines, especially those with halogens or fluorinated groups, tend to react with trace acid in barrels or with some rubber seals, which can compromise purity long before a batch makes it into a customer’s plant. Over years of trial, we learned to use chemically resistant containers, check for liner compatibility, and train crews to avoid cross-contamination during filling or loading.
Timing logistics with weather shifts taught us more—cool climates require insulation, as the product can tend to solidify at lower temperatures. Drum heaters are on standby in winter, as we learned the hard way that a solid mass in transit can add headaches days or weeks after dispatch. Pre-shipment testing in the warehouse and photographic documentation back up our claims; tracing each drum from fill to receipt means fewer surprises at customer sites.
Each region presents its quirks. Exporting to zones with longer shipping routes demands added attention: secondary containment, redundancy in labeling and documentation, and advance coordination on customs requirements. We routinely requalify containers and logistics providers, based on real-world performance and customer feedback. Only through direct involvement with each link in the chain can we guarantee that what leaves our plant is what arrives at the destination, unchanged and ready for use.
The technology and conditions for synthesizing 4-Chloro-2-(trifluoromethyl)aniline evolve each year, not just in theory but in day-to-day manufacturing. Advances in separation technology—better membrane filters, improved phase-separation tanks, and upgraded solvent recovery lines—allow us to squeeze out more efficiency and safety, all while keeping impurity levels low.
Staff training cycles expand and adapt with new findings. Hands-on drills for spills, test runs with new equipment, and routine review of process logs keep the team sharp and the plant responsive. Experienced operators recognize the telltale signs of off-spec material much earlier than any automation can: color shifts, odor, or even subtle change in reaction time point toward a root cause, and our system encourages speaking up and logging every anomaly.
Quality culture forms the backbone of our approach. Technical audits from long-term customers push us to document every procedural adjustment, from raw material inspection to drum cleaning protocols. We keep digital and hardcopy logs accessible and traceable for at least five years, building a habit of real-time error correction over cover-up or makeshift fixes.
Each batch of 4-Chloro-2-(trifluoromethyl)aniline that leaves our plant carries the weight of customer R&D efforts and the reputation we’ve built over decades. Real questions from partners and hands-on lessons drive our process decisions. We have seen projects pivot on small differences—melting range, reactivity with alkylating agents, color retention, or stability under storage conditions—reminding us that even standard catalog molecules take on added life in the hands of skilled chemists.
By keeping our focus on operational transparency, joint problem-solving, and methodical technical improvements, we make sure our product stands apart from generic offerings. While technology and regulation both continue to move, the logic of chemical manufacturing remains: listen to the lab’s needs, test everything, and learn from what each batch, and each customer, teach in practice.