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HS Code |
634209 |
| Cas Number | 446-19-5 |
| Molecular Formula | C7H6FNO2 |
| Molecular Weight | 155.13 g/mol |
| Appearance | Yellow to brown liquid |
| Density | 1.316 g/cm3 |
| Boiling Point | 216-218 °C |
| Purity | Typically ≥98% |
| Flash Point | 94 °C |
| Solubility | Insoluble in water |
| Refractive Index | 1.537 |
| Storage Conditions | Store at room temperature, away from light and moisture |
As an accredited 3-Fluoro-5-Nitrotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 g, with secure screw cap, chemical label displaying hazard symbols, product name, CAS number, and supplier details. |
| Shipping | **Shipping Description for 3-Fluoro-5-Nitrotoluene:** 3-Fluoro-5-Nitrotoluene is shipped in tightly sealed containers, compliant with UN regulations. Store and transport in a cool, well-ventilated area, away from heat and incompatible substances. Proper labeling and documentation are required to ensure safety. Handle as a hazardous chemical (possible flammable/irritant risks); consult SDS before shipping. |
| Storage | 3-Fluoro-5-Nitrotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and heat. It should be kept away from incompatible substances such as strong oxidizers and acids. Proper chemical labeling and secondary containment are recommended to prevent leaks or spills. Store according to local chemical safety regulations. |
Applications of 3-Fluoro-5-Nitrotoluene in Industrial ManufacturingAs a specialized manufacturer supplying 3-Fluoro-5-Nitrotoluene, we focus on delivering consistent grade, traceable batches, and precise specification controls to downstream industries. Our material supports diverse chemical synthesis requirements in key industrial sectors, serving as a critical intermediate for value-added products. 1. Agrochemical Active Ingredient Synthesis3-Fluoro-5-Nitrotoluene is a preferred halogenated aromatic intermediate used directly in the synthesis of certain herbicide and fungicide active molecules. Its electron-withdrawing fluoro and nitro substituents promote targeted substitution and coupling reactions during core construction in agricultural chemical plants. Process engineers select this material during the multi-step build-up of fluorinated agrochemicals, integrating it post-coupling and before reduction or cyclization to drive molecule specificity and increase downstream yields for patented products. Quality departments monitor contaminant profiles closely because downstream purification stages are optimized based on this input grade. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingPharmaceutical API plants use 3-Fluoro-5-Nitrotoluene in the synthesis of select fluorinated heterocycles and benzene derivatives present in active pharmaceutical ingredients. Chemists incorporate this compound during key Grignard or nucleophilic aromatic substitution reactions where the fluoro and nitro groups guide regioselective transformations. Input grade documentation is required for audit trails, and manufacturing submits full lot traceability during ICH Q7 GMP compliance. Quality control performs high-purity batch analysis to ensure low residual solvent levels before use in regulated environments. Industry compliance standards
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3. Specialty Dye and Pigment ProductionManufacturers of specialty dyes integrate 3-Fluoro-5-Nitrotoluene when synthesizing high-performance fluorescent and colorfast aryl azo and nitro dyes. The compound’s unique substitution patterns influence bathochromic shift and increase molecule stability in aggressive processing. Dye chemists select this building block for controlled amination or reduction to corresponding amino-fluorotoluenes before coupling with diazonium salts in pigment synthesis. Analytical quality teams ensure minimal ortho/para isomer contamination to avoid batch color variation downstream. Industry compliance standards
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4. Advanced Polymer Additive SynthesisProducers of specialty polymers and fluorinated engineering plastics incorporate 3-Fluoro-5-Nitrotoluene as a functional aromatic monomer precursor. This molecule enables targeted fluorination and nitro introduction during the copolymer monomer construction phase. R&D and production teams use this intermediate in staged aromatic substitution, followed by reduction and functionalization to yield chain-initiating or end-capping units. Stringent input quality checks ensure batch consistency, minimizing downstream polymerization drift and guaranteeing final resin specifications. Industry compliance standards
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Our team has spent the better part of two decades refining the synthesis and purification of aromatic intermediates, and 3-Fluoro-5-Nitrotoluene quite naturally stands out among our key products. This compound (CAS No. 446-18-8) carries the molecular formula C7H6FNO2, with a carefully balanced structure that brings out both reactivity and stability. The real value of producing such a material at scale rests in understanding its behavior during downstream reactions and how it answers the needs of pharmaceutical, agrochemical, and specialty material R&D. Our experience in controlling impurities gives us confidence in sharing actual performance in the lab, helping research scale up to real platforms.
Crafting 3-Fluoro-5-Nitrotoluene consistently means more than matching paper specifications. Over the years, we learned purity can be just as important as yield for users who demand predictable results. Typical material coming from our reactors scores above 99% by GC, with NMR and HPLC used routinely as part of our QA protocols. In practical terms, we see the actual boiling point sit between 213°C and 215°C under atmospheric pressure, and the yellow-tinged liquid form remains stable under ordinary lab conditions. Water content often falls below 0.2% using KF analysis. Achieving this reproducibility means a combination of solvent purification, closed-system distillation, and a well-dialed filtration step — all monitored in real time rather than through end-point testing alone. This approach sustains trust from teams who specify input quality for pilot or validation runs and cannot afford failed syntheses from off-target lots.
Scaling up aromatic nitrations with regioselectivity takes real attention to material behavior at every stage. For 3-Fluoro-5-Nitrotoluene, that control begins with sourcing a reliable fluorotoluene and verifying halide positional purity prior to any electrophilic substitution. Our reactors are equipped for jacketed temperature control to avoid unwanted side reactions or over-nitration, and we use continuous monitoring for acid composition and pressure stabilization. Product isolation depends on careful quenching — improper handling leaves persistent impurities, especially in the dinitro fraction. Neutralization and extraction are routinely backed by pilot analytics to ensure downstream hydrogenations or further substitutions run smoothly for our customers. This upstream diligence eliminates troubleshooting efforts for users developing fluorinated heteroaromatics from our product line.
Many who request 3-Fluoro-5-Nitrotoluene work in settings where route scouting for bioactives and crop-protection agents leads to regular process revisions. One project we supported started with a screen for alternative fluoro-nitro building blocks during a scale-up for kinase inhibitor development. Synthetic success relied on the nitro group at the meta-position, while the fluoro-on-benzene substituted reactivity patterns to give cleaner coupling products during derivatization steps. Using genuine material with verified impurity profiles, rather than unqualified technical grade, trimmed several weeks off process debugging. We’ve seen similar gains for process chemists fabricating new phenylhydrazines or fluorinated benzoate derivatives, as reliable starting materials cut down on risk and rework.
It’s tempting to substitute any available fluoro-nitro toluene in screening, but we’ve observed what happens when structural analogs change reactivity or downstream processing. 2-Fluoro-4-nitrotoluene, for example, brings heightened ortho effects, leading to steric congestion in Suzuki or Buchwald couplings. On the other hand, 3-Fluoro-5-Nitrotoluene offers both accessibility at the meta-position for directed ortho metalation (DoM) and clean electron-withdrawing influence for nucleophilic aromatic substitutions (SNAr). Out of several projects using the 3,5-positional isomer, we repeatedly saw lower by-product loads during reductions and aminations, which directly relates to the position of functional groups on the ring. This change translates to easier purification, consistent assay yields, and reduced waste handling downstream.
Working with nitro aromatics means giving proper respect to both toxicity and reactivity. From our own line experience, we recommend closed transfer operations, effective ventilation, and judicious use of personal protective equipment. Liquid handling remains straightforward, as 3-Fluoro-5-Nitrotoluene shows stable vapor pressure under typical plant temperatures; volatility issues rarely interrupt bulk storage or local transfer. Since material doesn’t pose the same explosive risk as more heavily nitrated aromatics, scaling up plant volumes comes down to maintaining discipline with acid and solvent recovery systems. Safe waste management means tracking all by-products off distillation and using granular adsorbents during cleanup — never assuming full conversion in a batch.
Often, our clients ask about specific impurity profiles and how we keep cross-contaminants out of finished product. Our QA process involves more than standard GC checks; we routinely apply mass spectrometry to rule out poly-nitro and halogenated contaminants, especially where downstream hydrogenations risk producing unwanted anilines. We implement regular instrument qualification and chemometric checks to track peak drift or carryover from other manufacturing lines. While many suppliers offer only basic technical grades, our working relationship with developers demands we show both main spot purity and verify absence of critical interferences below 0.1%. This sort of certificate detail wins repeat orders, as it removes doubts for those taking new chemistry out of the lab and up into kilo scale pilot runs.
Synthetic chemists frequently cite unwanted rework caused by input variability in specialty compounds. Over the years, collaborating on troubleshooting revealed where genuine 3-Fluoro-5-Nitrotoluene delivers time savings and process reliability. In one case involving the preparation of fluorinated pyrazoles, access to a fully characterized starting material avoided side product formation at the ring closure stage. Since product features strong electron-withdrawing power from the nitro and fluoro groups in defined positions, nucleophilic substitutions proceed with higher conversion at lower temperature. Chemists reported easier control over reaction exotherms, and saw fewer halide scrambling incidents that can affect less well-defined isomers. This insight led to a shift in route planning, moving from non-selective mixed isomers toward our dedicated 3,5-isomer, driving both time and cost performance in ongoing production.
Managing nitro compound waste streams places steady pressure on fine chemical producers. From our end, investing in solvent reclamation and acid recovery systems keeps both effluent and raw material losses to a minimum. Every reactor batch runs against a checklist for responsible neutralization, minimizing generation of nitrate/nitrite by-products with batchwise pH checks. We continue to engineer our waste extraction tanks to trap volatile organics, and push for energy-efficient reactor cycles where possible. We encourage downstream partners to mesh their spent solvent handling with the reclamation strategies we use in-house. This teamwork has trimmed both transportation needs and disposal expenses over multi-year collaborations.
Scaling up from bench synthesis to commercial output is never as linear as the reaction equation might promise. Running a semi-batch versus a continuous flow setup for nitration sometimes triggers batch-to-batch variation or temperature lags. Through process optimization trials in partnership with active pharmaceutical ingredient (API) makers, we standardized on temperature and quench controls that stabilize isomer ratios even at barrel scale. New jacketed glass and lined steel reactors delivered tighter oversight of exotherm events and ensured consistent stirring, preventing local overheating and fouling. Ongoing training for operations staff, including regular audits from third-party inspectors, remains central to upholding batch reproducibility and plant safety. Product registration for regulated pharmaceutical markets runs in parallel, emphasizing full traceability on each delivered lot.
Purchasing directly from a producer with in-house technical support makes a tangible difference for process teams. Unlike bulk chemical dealers or repackers, direct manufacturers like us maintain full control of supply chain raw materials, processing equipment, and analytical oversight. This traceability means users receive product with a known origin and can request feedback on synthesis, rework, or custom modifications with short turnaround. Our experience supporting custom synthesis for medicinal chemistry groups routinely leads to process improvement suggestions, such as adjusting solvent ratios or exploring alternative protecting groups to boost downstream coupling efficiency. Sourcing locally, instead of from international container consolidators, also reduces transit risk and allows adjustment of lot sizes to match customer pilot deadlines.
Our plant team often fields requests from university and industrial research groups looking to modify, derivatize, or scale up work based on 3-Fluoro-5-Nitrotoluene. We pay close attention to detail in technical documentation, shipping test samples, and supporting new application notes. Researchers in fluorine chemistry or nitroarene cross-couplings have driven development in customized applications, including ligand building, advanced probe design, and agrochemical lead optimization. Maintaining a robust dialogue around synthesis challenges and performance testing positions us well to serve new sectors developing advanced materials and next-generation pharmaceuticals. Stories from project leaders using our intermediates to push patent filings or unlock new molecular scaffolds inspire both process upgrades and continuous improvement on our production floor.
Staying ahead in fine chemical supply involves keeping up with both region-specific safety and toxicity updates. Recent years brought closer scrutiny to aromatic nitro compounds in several jurisdictions, prompting data-sharing on impurity controls and batch-specific traceability. Our on-site lab maintains regulatory tracking for major target markets, pre-empting customer needs for new dossier updates or updated safety data sheets. Material supply for regulated applications means a clear record of both testing and full lot traceability stretching back to raw materials. Prioritizing compliance before demand spikes can head off project delays, and our collaborations with compliance teams from several leading pharmaceutical companies have led to ongoing upgrades of our hazard assessments and waste minimization protocols. These partnerships ultimately foster sustained trust and comfort for those carrying new chemistry through regulatory submissions.
Some buyers focus purely on price per kilogram, yet for specialty building blocks like 3-Fluoro-5-Nitrotoluene quality and dependability outweigh short-term cost savings. In our experience, subtle differences in impurity profile, analytical transparency, and willingness to support customer troubleshooting matter far more in the long run. Speedy response times and ability to share technical application insight separate established producers from commodity chemical middlemen. Each major product launch in the pharmaceutical or crop science sector that relied on our material for route scouting confirmed the value in sustained technical dialogue and product support — plus peace of mind knowing the chemistry will behave as expected every time.
Over the years, close work with process chemists and project teams led us to develop a responsive technical service approach. Fielding questions about solvent compatibility, reactivity under new coupling partners, and custom packaging, our technical team stands ready with real-world process insights rather than generic MSDS references. Customers request modifications — changed container sizes, single-source documentation, alternative purity grades — and our plant responds with both flexibility and speed. In several instances, this willingness to adapt matched material supply directly to the needs of discovery, pilot, and early manufacturing groups, reducing both downtime and cost.
As new green chemistry methods and selective-catalysis routes emerge, demand grows for aromatic intermediates with defined electronic and steric features. Our production technology is evolving too, with investments in in-line analytics, digital batch records, and automated impurity tracking. This progress helps users push the boundaries in pharmaceuticals, crop protection, material science, and specialty polymer development. The foundational reliability of our 3-Fluoro-5-Nitrotoluene gives users the freedom to scale up with less risk, explore novel reactivity windows, and deliver results where performance matters.
Success stories shared back from research chemists help refine not just the product, but the process and service behind each ton shipped. Knowing our focus on actual production—rather than trading or reselling—removes layers of uncertainty and puts customer teams in direct touch with hands-on manufacturing expertise. Whether the end goal involves high throughput screening, scale up to regulatory submission, or continuous process optimization, we support innovation through steady supply, rigorous QA, and a partnership philosophy grounding every aspect of 3-Fluoro-5-Nitrotoluene manufacture.