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HS Code |
588634 |
| Cas Number | 345-69-1 |
| Molecular Formula | C8H10FN |
| Molecular Weight | 139.17 |
| Iupac Name | 4-Fluoro-N,N-dimethylaniline |
| Synonyms | p-Fluoro-N,N-dimethylaniline; N,N-Dimethyl-4-fluoroaniline |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 202-204°C |
| Melting Point | -13°C |
| Density | 1.059 g/mL at 25°C |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CN(C)C1=CC=C(C=C1)F |
| Inchi | InChI=1S/C8H10FN/c1-10(2)7-3-5-8(9)6-4-7/h3-6H,1-2H3 |
As an accredited 4-Fluoro-N,N-Dimethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "4-Fluoro-N,N-Dimethylaniline, 100g," features hazard symbols, CAS number, lot number, and supplier information. |
| Shipping | 4-Fluoro-N,N-Dimethylaniline is shipped as a hazardous material in tightly sealed containers, protected from light and moisture. It must comply with regulations for flammable and toxic substances, including appropriate labeling and documentation. Transport should be by authorized carriers, ensuring secure handling and storage to prevent leaks, spills, or environmental contamination. |
| Storage | 4-Fluoro-N,N-Dimethylaniline should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials such as oxidizing agents. Protect from light and moisture. Use appropriate chemical storage cabinets, and ensure the area is clearly labeled and access is restricted to trained personnel. |
Applications of 4-Fluoro-N,N-Dimethylaniline in Industrial ManufacturingAs a specialized manufacturer, we supply 4-Fluoro-N,N-Dimethylaniline that supports several authentic, value-driven industrial sectors. This section highlights verified applications in which our product directly contributes to precision synthesis, formulation integrity, and regulatory-compliant output. Each scenario below details actual market requirements and operational roles based on industry-accepted standards. 1. Pharmaceutical Intermediate SynthesisDownstream pharmaceutical producers utilize this compound as a key intermediate in the synthesis of fluorinated active pharmaceutical ingredients (APIs), particularly those requiring substituted aniline cores. Its specific reactivity supports nucleophilic aromatic substitution reactions and targeted alkylation steps, serving as a reliable building block for drug substances such as selective serotonin reuptake inhibitors and certain oncology medications. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionIndustrial pesticide and herbicide formulators integrate this compound in the fine synthesis of fluorinated phenylamine derivatives, which form the basis of modern selective herbicides and fungicidal agents. Downstream usage supports high-performance products with targeted biological profiles, relying on precise aromatic fluorination for enhanced efficacy and stability in active molecules. Industry compliance standards
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3. Dye and Pigment ManufacturingProducers of specialty dyes for textiles and advanced plastics select this material to synthesize fluorinated azo and anthraquinone colorants. Fluoroalkyl substitution imparts increased photostability and chemical resistance to the final dyes, making them preferred for demanding industrial coloration, especially where exposure to UV or aggressive processing chemicals prevails. Industry compliance standards
Typical usage ratio
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4. Liquid Crystal and Electronic Material SynthesisAdvanced electronic material manufacturers, particularly those in the liquid crystal display (LCD) sector, employ this compound during molecular engineering of fluorinated aromatics. Its role centers on constructing mesogenic intermediates, where precise fluorine and methyl group placement tune dielectric anisotropy and viscosity, which is critical for display performance and electro-optical response characteristics. Industry compliance standards
Typical usage ratio
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Working in specialty chemicals for over twenty years, we have watched the demand for substituted anilines shape everything from pharmaceuticals to modern solvents. 4-Fluoro-N,N-Dimethylaniline, with its formula C8H10FN, regularly comes off our reactors because our clients in research, pharma, dyes, and advanced materials keep pushing synthetic boundaries, and this molecule gives them a head start. Unlike generic anilines, the addition of a fluorine atom at the fourth position amplifies reactivity, enabling chemists to design molecules that tackle selectivity challenges in synthesis. The methyl groups at the nitrogen not only affect solubility, but also support downstream alkylation and acylation reactions. We find that clients care about these details—not just purity percentages.
In our plant, every batch of 4-Fluoro-N,N-Dimethylaniline begins with precise controls over temperature, stir rate, and feedstock quality. Over the years, we learned that minor adjustments in the methylation stage or fluorination sequence can change product characteristics. Lab-scale research can tolerate these fluctuations, but industrial synthesis cannot. Our team stresses repeatedly that batch uniformity prevents headaches down the line. Those producing active pharmaceutical intermediates, specialty dyes, or liquid crystals depend on consistency. Our technicians keep each run within tight GC limits for major and trace impurities, and pyridine byproduct removal receives special attention as it can sabotage catalytic steps. Too many stories circulate about lost batches when a supplier dropped the ball on this point.
Veteran medicinal chemists say that placing fluorine on an aromatic ring isn’t just a trend—it shifts electronic properties and boosts metabolic stability in drug candidates. We have supplied both 4-fluoro and non-fluorinated N,N-dimethylanilines, and from our vantage point, the difference in biological and physical properties is noticeable. Fluorine, small but highly electronegative, not only increases the arene's resistance to metabolic oxidation, but also changes pKa and solubility. That means you gain new options in designing pharmaceuticals with slower clearance or more precise activity. We listen to chemists looking for improved CNS penetrance or more robust performance in dyes and find that 4-fluoro substitutions answer these calls far more often than non-fluoro analogues.
Nothing demonstrates this like feedback from clients working on agrochemical development. One of our regular customers reported that their crop protection candidates survived enzymatic degradation much longer after adding fluorine to the aniline scaffold. Another, in advanced polymer materials, pointed to improved thermal stability and subtle changes to dielectric constants when using our product versus traditional anilines. Repeatedly, side-by-side tests reveal that small molecular tweaks lead to big operational differences.
Lab documentation and specification sheets can only say so much. Years of manufacturing 4-Fluoro-N,N-Dimethylaniline have taught us that certain characteristics matter more than the numbers might reveal. Color and odor, for example, are more than aesthetic qualities—they are tip-offs for batch integrity. Our technical team monitors these features closely along with water content and trace halides. Colorless to pale yellow and a faint, amine-like odor mark a clean, well-produced material. Anything off—a brown tinge or a pungent rank—suggests that something got through our purification routine and needs another pass.
Because our product often ships in drums or intermediate bulk containers, we monitor peroxide formation and air sensitivity, especially during summer transports. 4-Fluoro-N,N-Dimethylaniline does not brown or thicken as easily as some analogues, which means clients spend less time checking degradation when opening containers. Shelf life has proven reliable, which matters for organizations that buy in bulk and might not use everything right away.
Academic researchers dig deeper into reaction mechanisms using 4-Fluoro-N,N-Dimethylaniline as a probe or model substrate. In scale-up, these insights turn into better couplings or substitutions. In pharmaceutical laboratories, this compound frequently goes into synthetic pathways as an intermediate for APIs targeting the central nervous system, pain management, and certain anti-infectives. Our pharma partners prefer the fluorinated version not for novelty, but because animal studies repeatedly show longer half-lives and better oral bioavailability compared to non-fluorinated options.
Dye and pigment manufacturers use its stability and vivid chromatic profile for development of lightfast, high-color-strength products. Many of our clients in dye synthesis appreciate our ability to keep metal impurities low, preventing adverse reactivity during azo coupling and condensation. They have shared that even slight differences in metal traces impact shade or batch-to-batch replication, leading to headaches in textile applications. We take their trust seriously and adjust our purification steps accordingly.
Material scientists are pushing 4-Fluoro-N,N-Dimethylaniline into polymer electronics, particularly in designing hole-transport layers for organic LEDs and field-effect transistors. They cite the structural rigidity fluorine imparts, supporting device stability. In these newer markets, rapid iteration calls for reliable supply, so keeping up with shifting production schedules has meant rolling out flexibility in our own operations.
On the shop floor, safe handling means more than ticking boxes on a safety data sheet. 4-Fluoro-N,N-Dimethylaniline may not have the acute toxicity of nitrobenzenes, but repeated inhalation or skin exposure can add up, especially in poorly ventilated spaces. Our workers use gloves and goggles, and we run localized extraction over reaction tanks. Taking shortcuts might save a few minutes, but rarely pays off in the long run. Over the years, we have responded to more than one inquiry about lingering odors in storerooms. Storing the material in sealed, inert-lined drums in a cool, shaded area stops evaporative loss and discoloration.
Workers loading or decanting the product rely on our detailed transfer protocols—grounding containers to prevent static sparks and confirming seals to block vapor leaks. These processes take diligence, but we find they keep both our product quality and our colleagues safe.
Choosing between 4-Fluoro-N,N-Dimethylaniline and its close relatives depends on more than raw price or purity numbers. Fluorine substitutions often demand specialized feedstocks and processing steps, which drive up costs slightly. In return, customers receive a product that offers not only greater stability but also opens new synthetic possibilities. We have watched formulators shift from using basic N,N-Dimethylaniline to the 4-fluoro version when developing compounds for more challenging regulatory environments where standards around persistence and metabolic breakdown are tightening. Our analytical feedback confirms this edge—GC, NMR, and mass spectrometry profiles show a sharper, more predictable performance than non-fluorinated samples, particularly under stress tests.
While lower-cost, generic dimethylanilines handle routine dye and pharma work, the fluorinated variant finds its niche among innovators confronting tougher demands: superior stability, precise bioactivity, and compatibility with high-performance matrices. By sticking with our refined process control and customer feedback loop, we help clients move beyond "good enough" toward genuinely differentiated products.
Those who have been sourcing chemicals for a while know that regulatory landscapes shift fast. The global reach of our product means we frequently field detailed questions about trace impurities, potential byproducts, and environmental impact. Our largest clients—especially in pharma—often audit us in person, and these visits reinforce the importance of robust quality management. We make sure to maintain detailed batch histories, not just for compliance, but as a learning tool. When regulatory agencies tighten oversight on trace contaminants or process waste, our in-line data recording gives us the confidence to make adjustments quickly without disrupting supply chains.
The fluorine atom in 4-Fluoro-N,N-Dimethylaniline often triggers heightened examination due to concerns around persistence and bioaccumulation. Although this compound does not belong to the notorious PFAS class, we have found that being transparent about our processes and encouraging downstream stewardship—safe waste handling, targeted synthesis—satisfies our partners and keeps us ahead of possible future rules. By sticking to closed-loop water systems and minimizing halogen leaks, we reduce environmental load and set new benchmarks for responsible manufacturing. Many experts believe that chemical suppliers who ignore local and global moves toward sustainability only invite trouble later. We prefer to work on these issues now—with client collaboration—before mandates force changes.
Many of our clients began by ordering standard lots but soon returned with questions about new reactions or special requests. We treat these questions as the best kind of feedback. Process chemists in pharma crowded our phones last year asking for advice on transitioning from lab-scale to kilo-lab production using our 4-Fluoro-N,N-Dimethylaniline. Rather than just shipping more material, we walked through their reaction schemes, offering insights on solvent choice or how to handle off-gassing under scale-up. These conversations often uncover pain points—solubility limits, reaction times, batch workup—the little things that so often crop up during actual manufacturing.
Dye makers experimenting with new fastness additives or shifting from sulfonation to halogenation approaches sometimes struggle with side-product control. By sharing what we have seen work on our own lines—solvent choices, temperature ramps, or in-process pH checks—we contribute solutions that go beyond the commodity mindset. We document these field fixes, bringing them back to our own development team to tweak future batches. Over the years, this feedback loop has made our 4-Fluoro-N,N-Dimethylaniline more reliable for emerging applications like OLEDs and advanced sensors.
Producing specialty fluorinated anilines brings its own hurdles. Raw material sourcing keeps procurement teams on their toes, as suppliers of high-purity fluorobenzene or methylating agents raise prices or tweak specs without notice. We have sharpened our qualification process for alternative suppliers, ensuring flame-ionization detection data and impurity scans match our primary lots. Process-scale methylation stages create fouling risks or exotherms. On days when amine odors linger, the maintenance crew knows to inspect condensers and vent systems, not just mask the problem with scrubber fluid. Long-term, these routines prevent residues from working their way into finished product.
Temperature and agitation control also matter. Overheating or under-stirring transforms the product's color and increases byproduct formation, especially tert-amine or ring-substituted impurities. We maintain digital logs, not for show, but to correct trends before they cascade into rejects. Even packaging must adapt. Our shift to lined steel drums years ago reduced customer complaints about oxidation and leakage. It took trial, error, and frank talks with end users before we found what really worked on this front.
Clients at various stages—researchers, production chemists, and QA/QC specialists—honestly contribute as much to our understanding as our own process engineers. Their tolerance for variability is lower than ever, especially in regulated industries. Batch-to-batch feedback, both praise and complaints, has shaped our approach. A medicinal chemistry start-up contacted us after their first few syntheses stalled out, puzzled by small output shifts. Reviewing their procedure and supply chain, we discovered their glassware wasn’t properly dried and minor differences in the amine base they used contributed to the outcome. Fixing this didn’t just save them time; it helped us spot where better product literature is genuinely useful.
Pharma partners in bioactive screening know that micro-scale changes in product trace profile translate to real changes downstream—unexpected peaks in HPLC, color changes, or byproducts that escape routine checks. They aren’t shy about sharing this, and we keep open lines with their QC.
Dye synthesis scientists taught us the importance of amending our own trace analysis, especially looking beyond just halides or amines. Their needs for high purity meant we invested in GC-MS tuning and better pre-packing checks.
The future for 4-Fluoro-N,N-Dimethylaniline doesn’t sit in data sheets or marketing slogans, but in how it unlocks the next generation of fine chemical and pharmaceutical breakthroughs. The growth of green chemistry drives specialists to examine halogenated intermediates for both benefits and risks, which we take seriously. We continue working with customers who see this compound not as a static ingredient, but as a living part of evolving science. Trends in medicinal chemistry and smart materials might specify even tighter impurity profiles or push for greener routes. By tracking new analytical tools and adjusting process setups on our own lines, we anticipate and meet these changes.
In our practice, making this molecule is less about formulaic repetition and more about problem-solving—each run shaped by chemistry, feedback, and regulatory pressure. Our aim remains the same: to offer a fluorinated aniline that keeps up with demanding research and manufacturing needs, while making incremental, concrete improvements every year. Experience has taught us that real trust gets built over time, one reliable shipment at a time.