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HS Code |
902368 |
| Cas Number | 2947-61-7 |
| Molecular Formula | C7H6F2 |
| Molar Mass | 128.12 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 141-143 °C |
| Melting Point | -17 °C |
| Density | 1.15 g/cm3 |
| Refractive Index | 1.482 |
| Flash Point | 38 °C |
| Pubchem Cid | 19192 |
| Solubility In Water | Insoluble |
| Smiles | CC1=C(C=CC=C1F)F |
| Synonyms | 2,6-Difluoromethylbenzene |
| Vapor Pressure | 3.4 mmHg at 25 °C |
| Ec Number | 220-945-1 |
As an accredited 2,6-Difluorotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Difluorotoluene is supplied in a 100 mL amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2,6-Difluorotoluene is typically shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. The containers are clearly labeled with hazard and handling information. The chemical should be stored and transported in a cool, well-ventilated area, away from sources of ignition, and in compliance with local, national, and international regulations. |
| Storage | 2,6-Difluorotoluene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents. Keep it out of direct sunlight and protect it from moisture. Ensure proper labeling and restrict access to authorized personnel to maintain safety. |
Applications of 2,6-Difluorotoluene in Industrial Manufacturing2,6-Difluorotoluene serves as a critical intermediate in multiple chemical synthesis routes, contributing to high-value downstream products in strictly regulated industries. As a direct manufacturer, we understand its real industrial use ranging from agrochemical actives to pharmaceutical APIs and specialty electronic materials. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use 2,6-difluorotoluene as a precursor in the synthesis of fluorinated aromatic compounds integral to API development, particularly for anticancer and central nervous system (CNS) drugs. It enters multi-step organic synthesis for fluorinated phenyl building blocks, which increase metabolic stability and enhance drug molecule performance. Production lines implement tight process control to avoid contamination and guarantee traceability throughout the transformation steps. Industry compliance standards
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2. Agrochemical Active Ingredient PrecursorAgrochemical producers employ this material as a key intermediate in the manufacturing of highly active fluorinated herbicides and fungicides. The compound forms a structural basis for fine-tuning activity and environmental persistence. Downstream synthesis requires careful monitoring to avoid off-target reactivity, especially during aryl substitution and subsequent oxidation steps. Industry compliance standards
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3. Electronic Chemical MaterialsManufacturers of advanced electronic materials utilize this compound in fluorinated liquid crystals for display technologies and specialty monomers for photoresist resins. Its high chemical stability and electron-withdrawing fluorine atoms improve dielectric properties and UV resistance. Precise dosing and purity screening are essential due to the high sensitivity of downstream materials to trace impurities and side products. Industry compliance standards
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4. Fine Chemical and Specialty Resin IntermediateProducers of specialty resins and fine chemicals select this fluorinated tolulene for introducing specific electronic effects into polymer chains or thermoset materials. The controlled fluorination pattern improves final polymer surface energy and enhances solvent resistance. The compound typically enters etherification or polymerization reactions, where downstream users monitor feed ratios closely to avoid gel formation and ensure consistent product qualities. Industry compliance standards
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As an integrated producer of 2,6-difluorotoluene, we have witnessed firsthand how demand for this fluorinated aromatic compound keeps rising. The molecule itself—recognizable from its two fluoro groups attached to the toluene core at positions 2 and 6—carries more value than just a unique chemical structure. Its characteristics open doors for more efficient pharmaceutical syntheses, agrochemical advances, and materials with enhanced service life. Unlike traders or resellers, we work at the foundational level where purity and traceability can make or break end-use applications. Each batch draws from years of accumulated plant knowledge, refining practices for customers who require close control over impurity profiles.
We feature what specialists refer to as “industrial grade” purity, meeting consistently defined specification targets. The product typically aligns with a GC purity of 98% minimum. Moisture sits at trace levels, checked by Karl Fischer titration to prevent the introduction of hydrolytic sites in downstream chemistry. The residual toluene content falls well below actionable thresholds. Our team routinely tests for isomeric by-products, especially 3,5-difluorotoluene and monofluorotoluenes, ensuring robust selectivity at the reactor exit. Color measurement using APHA standards marks each lot: a pale, almost water-clear appearance signals that no excessive degradation or side-reactions occurred. We choose HDPE and steel drum packaging to guard against light-induced decomposition during storage or transport. Years of experience also taught us to monitor headspace gas composition for quality assurance.
Years ago, the predominant use for 2,6-difluorotoluene was as a research intermediate in university labs. That has shifted. Today, medicinal chemists recognize it for its role in synthesizing noncanonical nucleoside analogues. Swapping a regular thymine for this analog within DNA raises stability without disrupting reading function—a seemingly minor tweak with substantial benefits for diagnostic platforms and gene synthesis. Material scientists incorporate it as a monomer building block in specialty polymers, where the difluoro configuration imparts chemical resistance and rigidity. Crop science teams favor it when synthesizing halogenated benzyl compounds for advanced agrochemicals, using its straightforward substitution chemistry as a springboard to more elaborate targets.
Customers work with our product in Suzuki and Negishi coupling reactions without facing excessive by-product formation. The clean aromatic ring, activated by two ortho fluoro atoms, reacts predictably—even when scaled from gram to multi-tonne quantities. We’ve seen biotech customers leverage its hydrophobic and electronic properties to reduce background reactivity in enzyme assays, particularly when compared to mono-fluorinated analogs. Material producers often note that 2,6-difluorotoluene-based intermediates yield final products with higher glass transition points and greater UV stability compared to unsubstituted toluene derivatives.
Manufacturing 2,6-difluorotoluene presents a few challenges that separate genuine producers from surface-level suppliers. Sourcing starting fluorinated benzenes with reliably high assay on a fixed schedule tests vendor relationships every time market volatility hits. Any shortfall in precursor quality quickly cascades as yield loss downstream—details resellers can’t appreciate. During halogen exchange, we monitor exotherms tightly; unrestrained energy release invites tar and polychlorinated waste formation, jacking up both costs and environmental compliance burdens.
Real-world process control relies on in-line IR, chromatography, and robust operator training. No batch gets sign-off until it clears a full spectrum of impurity checks including halide, residual solvent, and thermal stability. The final hydrogenation step sounds routine, but nickel catalyst life depends on trace metals carried from earlier stages. Learning from catalytic failures has led us to design preventive maintenance routines and invest in upgraded filtration. These day-to-day realities don’t appear in slick commercial brochures, but they keep supply chains predictable for chemists and engineers counting on uninterrupted access.
The business of chemical manufacturing hinges on purity—not as a raw statistic but as daily deliverable. One customer shared their disappointment with off-spec shipments from importers, which created backlogs and analytical rework. Years ago, we faced similar frustrations. That led us to double our batchwise analytics and invest in custom in-process monitoring. Our experience taught us that the chemistry doesn’t end at reaction completion: it continues as soon as moisture, plastics, or trace oxygen touch the product. Frequent cGMP compliance checks and careful inventory rotation now keep our outgoing material squarely inside adopted standards. Buyers get what their methods and regulators expect, without the unpleasant surprise of drifting impurity levels upon retesting.
Supporting this level of reliability requires continuous sampling and statistical process control. Chromatograms from each campaign feed into long-term trend analyses, triggering corrective action before deviations reach the customer. Over the years, these efforts cut waste and reduced product recall risk while opening doors to partnerships with pharmaceutical companies whose audit teams routinely walk our floors.
Experienced chemists and purchasing agents compare 2,6-difluorotoluene against other positional isomers and richer fluorinated arenes. The double ortho-fluorine pattern sets it apart from both mono- and 3,5-difluorotoluene. Reactivity at the methyl group and on the ring positions follows a pattern not easily predicted from general rules. We have seen synthetic teams save both time and reagent load when shifting routes from the mono isomers to 2,6-difluorotoluene. The installation of fluoro groups at 2 and 6 suppresses unwanted side reactions—a result that often makes downstream steps more selective. These practical wins translate into higher yields and consistent product profiles, both in medicinal and polymer chemistry.
Comparing with heavier halogenated toluenes, such as chloro- or trifluorotoluene analogs, 2,6-difluorotoluene balances price, reactivity, and environmental impact. The dual fluorine setup improves bond strength, giving finished products higher oxidative and chemical resistance. Chloro variants, in our operational reality, create larger waste handling burdens and slower downstream transformations. Trifluoromethyl compounds sometimes outperform in high-end specialty materials, but they come at a steep raw material and process cost. For day-to-day lab and plant scale work, most customers prefer the predictable behavior and procurement economics of the difluorinated version.
As a chemical manufacturer, environmental planning matters as much as process yield. We have invested in on-site scrubbers designed for fluorinated organic emissions. By leveraging carbon adsorption and carefully titrated alkali wash systems, we keep air emissions well within permitted levels. Regulatory agencies focus sharply on organofluorine compounds due to their persistence in the environment. Over the past decade, we tracked tightening discharge guidelines and proactively upgraded effluent treatment. Having historic emissions data at our fingertips helped satisfy requests during site inspections. This forward-looking approach protects both our long-term business and the neighboring communities.
Waste minimization goes beyond just following the letter of the law. Our staff engineers collaborate with customers on closed-loop solvent systems, pushing both sides to swap out solvents with higher environmental impact for those compatible with our integrated waste stream. As recycling infrastructure matures, we now reclaim several co-product streams for secondary manufacturing. Our internal target: to divert a fixed percentage of process waste from incineration each year, closing the loop wherever technical feasibility allows.
Traceability shapes every step of 2,6-difluorotoluene production. Documented chain of custody starts with incoming raw materials. Each drum and tanker shipment tracking back to lot-level certificates. We regularly audit our suppliers for trace contaminants. Internal labeling, barcoding, and digital logs ensure that, should any issue surface months after delivery, we track each molecule back to its origin. This habit stemmed from a single incident when a minor impurity passed unnoticed and later triggered an adverse material review at a major account. The speed with which we pinpointed the issue—by leaning on our real-time batch data—restored customer trust and allowed us to prevent a repeat.
Regulatory scrutiny keeps increasing, and our traceability regime has helped navigate both domestic and international audits. Pharmaceutical and electronic material clients in particular rely on full documentation for their own compliance, and our focus streamlines their validation activities. We train staff routinely, not only on procedures but also on risk awareness and corrective action planning. Traceability isn’t just an IT system; it's part of the work culture.
Feedback from our user base keeps us tuned to shifting priorities. The molecule’s ability to fit into both routine and advanced synthetic sequences makes it more than just another commodity. Material scientists point to the strength of the carbon-fluorine bond for improving polymer weathering performance. Medicinal chemical teams like the way the difluorinated pattern improves metabolic stability in active drug candidates. Both sets of users value timely, high-purity supply. If a key batch arrives off-spec or delayed, their project suffers. These user voices confirm why we prioritize consistent output through plant upgrades and better staff training.
Over the past few years, rising energy and logistics costs put pressure on every link of the supply chain. We responded by tightening process integration, relocating some partner distribution points closer to customers, and updating inventory forecasting. While this adds internal complexity, it keeps fulfillment flowing in a market where sudden shortages often drive buyers toward riskier acronym-heavy traders. As direct manufacturers, we understand substitution risk. In our view, quality lapses from a broker or repackager rarely show up until a customer’s analytical checks catch the problem—by then, schedules slip and budgets strain. By handling precursor synthesis to finished batch under a single operational umbrella, we lower those risks for everyone involved.
Common challenges for 2,6-difluorotoluene users include upscaling from pilot to production, handling hazardous by-products, and managing the paperwork gauntlet that advanced sectors demand. We address these problems directly with open lines to our technical and regulatory teams. Our chemists routinely review customer reaction schemes, offering process adjustments or alternate formulations that cut waste or raise safety margins. Documentation headaches soften with our digital COA library and lot-specific historical data, all accessible for user audits. Ongoing collaborations with raw material vendors, utilities, and specialty carriers keep input variability to a minimum, buffering our output against short-term supply shocks. It’s one thing to ship a sample kilogram by courier; maintaining multi-tonne consistency over years takes hands-on perseverance.
We enjoy seeing our product spark new inventions, whether in therapeutic candidates or next-generation electronic films. Regular calls with research labs and process engineers shape our continuous improvement. Years ago, we labored over a sluggish Grignard step that capped yield at the grow-out phase. By tightening impurity control and advising a swap to a less-reactive base, our customer unlocked throughput without compromising critical impurity specifications. We keep documentation and support on pace, so startups and established firms alike can push their projects forward without slowdowns tied to missing analysis or shipping documentation.
We also carry experience in rapid response to regulatory changes. A sudden change in allowable residual solvent levels in a key market led us to speed up analysis validation and equip our production with real-time sensors. These steps didn’t just help us; they gave customers added breathing room as they navigated regulatory updates. We view these challenges as opportunities to set our bar higher and strengthen customer partnerships for tomorrow’s requirements.
Trust in chemical manufacturing grows over time. It starts by keeping batch records clear, deliveries prompt, and support lines open. When customers needed urgent updated documentation for a customs delay, we acted fast. A storm that slowed local logistics meant a temporary hand-off to an alternate port. Years of running operations “from the inside” reinforce why clear communication delivers mutual benefit. We offer application notes, troubleshoot on-the-ground issues, and engage in root-cause analysis if anything goes off-plan.
Our experience manufacturing 2,6-difluorotoluene from raw material to finished shipment taught us that every day, small decisions compound into big reputational milestones. Batch-to-batch repeatability, clear documentation, and integrity in communication drive long business relationships. These principles go beyond any datasheet—they become the backbone of a supply chain valued by innovators and producers who can’t afford downtime or supply risk.
Making and supplying 2,6-difluorotoluene since early in its commercial availability, we know the product as more than just a catalog listing. Its role in pushing technical boundaries in chemistry and industry stays closely tied to our ability to deliver it pure, on time, and with full traceability. Unlike middlemen, we can adapt processes, update documentation, and lend insight earned through practical experience. Every upgrade and improvement starts with a lived problem and a practical solution—experience that flows into every drum and delivery. For our customers, that’s the real value of working with a chemical manufacturer who sees the full picture.