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HS Code |
358168 |
| Chemical Name | 1,4-Difluoro-2-Methyl-5-Nitrobenzene |
| Molecular Formula | C7H5F2NO2 |
| Molecular Weight | 173.12 g/mol |
| Cas Number | 446-18-4 |
| Appearance | Yellow solid |
| Boiling Point | 225-227 °C |
| Melting Point | 38-40 °C |
| Density | 1.44 g/cm³ |
| Solubility | Insoluble in water |
| Smiles | CC1=CC(=C(C=C1F)[N+](=O)[O-])F |
| Refractive Index | 1.540 (predicted) |
As an accredited 1,4-Difluoro-2-Methyl-5-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 250 grams of 1,4-Difluoro-2-Methyl-5-Nitrobenzene; labeled with hazard information, batch number, and supplier details. |
| Shipping | **Shipping Description:** 1,4-Difluoro-2-Methyl-5-Nitrobenzene is shipped in tightly sealed containers to prevent leakage and exposure. It should be handled as a hazardous material, following all regulations for transport. Protect from heat, moisture, and physical damage. Ensure proper labeling, documentation, and use of suitable secondary containment during shipping. |
| Storage | 1,4-Difluoro-2-methyl-5-nitrobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep it separate from incompatible substances such as strong oxidizers and reducing agents. Ensure proper labeling and secondary containment, and store at a controlled room temperature to prevent decomposition or hazardous reactions. |
Applications of 1,4-Difluoro-2-Methyl-5-Nitrobenzene in Industrial Manufacturing1,4-Difluoro-2-Methyl-5-Nitrobenzene serves as a critical intermediate in several chemical manufacturing processes. Precise engineering and strict quality control ensure consistent performance across specialized downstream sectors. As a direct manufacturer, we provide this material for established applications where purity, consistency, and regulatory compliance remain essential for downstream integration. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical companies use this compound as a key fluorinated aromatic building block for regulated API syntheses, particularly in the production of selective kinase inhibitors and oncology drug candidates. It participates in nucleophilic aromatic substitution reactions, delivering high yields and selectivity required by pharmaceutical standards. Process engineers control input ratios based on reaction kinetics and purity to align with multistep GMP manufacturing protocols. Industry compliance standards
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2. Advanced Agrochemical SynthesisProducers of crop protection chemicals rely on 1,4-difluoro-2-methyl-5-nitrobenzene as a core intermediate for constructing pyridine and triazine herbicides. The compound undergoes controlled reduction and further functionalization under strict batch procedures to prepare lead structures for modern agrochemicals. Subsequent formulation steps require tight quality checks on residual by-products. Industry compliance standards
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3. Electronic Chemicals – Liquid Crystal Material SynthesisDisplay manufacturers and electronic chemical producers use this fluorinated compound in liquid crystal and specialty material synthesis. The molecule’s substitution pattern supports designing high-performance nematic and chiral liquid crystal variants needed for thin-film transistor (TFT) and high-end LCD panel production. Strict specifications on purity and metal-ion content are maintained for electronic grade requirements. Industry compliance standards
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4. Performance Polymer Monomer ManufacturingSpecialty polymer producers integrate this material as a monomer or functionalized intermediate for advanced fluorinated arylene polymers, where thermal stability and chemical resistance are critical. The manufacturing process incorporates the compound via electrophilic substitution and subsequent polymerization with co-monomers, supporting materials for high-end membrane, filtration, and engineering plastic products. Industry compliance standards
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In the world of fine chemicals, 1,4-difluoro-2-methyl-5-nitrobenzene offers a blend of utility and complexity. From our vantage point as a manufacturer who has seen this intermediate become a preferred building block, we've come to appreciate its unique chemistry and the practical challenges it both poses and solves. The process of making this compound takes you beyond bench-scale curiosity and requires an understanding of how each structural detail impacts applications downstream. Over the years, we've witnessed how demand from pharmaceutical, agrochemical, and specialty chemical companies shapes the way we approach both purity and scale. The nature of this molecule is rooted in its substituents: a pair of fluorine atoms, a nitro group, and a methyl group arranged on a benzene ring. This combination provides chemical stability, reactivity in selective transformations, and a pattern of compatibility that stands apart from similar nitrobenzenes.
Manufacturers like us recognize that 1,4-difluoro-2-methyl-5-nitrobenzene carves out a niche because its properties go beyond the ordinary. The two fluorine atoms occupy the para positions, limiting unwanted side-reactions during nucleophilic aromatic substitutions. This positional arrangement lets process chemists introduce functionality exactly where they want on the ring. The methyl group offers a touch of extra electron density, which can either speed up or temper reactions when you’re aiming for selectivity downstream. The nitro group defines the compound’s role as an electron-withdrawing anchor, which is vital when developing new agrochemical scaffolds or preparing pharmaceutical intermediates that rely on high-yield coupling steps.
Not every substitution pattern performs equally. Before shifting to scale, we ran comparison batches with related nitrobenzenes and saw that minor tweaks in substitution patterns would shift the reaction yield or even block subsequent modifications. In our hands, the 1,4-difluoro-2-methyl-5-nitrobenzene scaffold struck a balance. The arrangement supports both direct halogen exchange and subsequent reduction steps with minimal by-product formation. This all comes together when you’re targeting custom transformation or looking to feed a synthesis sequence with minimal fuss. We've seen this precise substitution become crucial for specialty intermediates, and that’s reflected in long-term demand from our downstream partners.
Making this compound at commercial scale doesn’t just involve scaling up a lab reaction. The precursor selection affects both cost-efficiency and quality. We use carefully sourced methyl-substituted fluoroanilines, because the alternate routes via direct fluorination bring in handling issues that only grow at big-batch scale. The nitro group introduction requires tight temperature control and carefully staged addition to minimize over-nitration or ring oxidation, a lesson learned after early trial runs produced colored impurities that complicated downstream purification. Recrystallization from specific solvents, combined with controlled pH adjustment, produces a solid that holds up under both storage and shipping—a seemingly small detail until end users comment on delayed recrystallization or off-spec melting points.
The process design takes into account not just speed or yield, but the realities of handling these compounds in a busy plant. Fluorinated aromatics carry their own risks: minor leaks can cause environmental headaches, and even traces of metallic impurities from reaction vessels can generate batch-to-batch variation that undermines analytical consistency. Over time, we redesigned equipment for better compatibility and enforced more stringent monitoring. Dedicated operators, trained not only in handling but in recognizing subtle color changes or viscosity shifts, have made all the difference to delivering product on-spec day after day. This investment in both infrastructure and people pays off every time a customer scales up their own process and calls out reduced downtime or unproblematic filtration in their follow-on reactions.
Customers approach us with a keen interest in specifications, but their actual questions always come down to “Will it work in my process?” We offer the compound in batches standardized for purity, usually in excess of 98% by HPLC, with residual solvent and inorganic contaminants brought below the detection threshold that would impact either reactivity or bioassay testing. We’ve learned through feedback that minimizing trace water is often just as important, since moisture can promote decomposition or interfere with sensitive coupling agents.
Color is not just cosmetic—it flags stability. Our in-process controls track for yellowing or darkening, letting us catch and remediate before packing for shipment. Particle size also matters, affecting both solubility and blending, so we offer limited sieving by request, always with documentation of the milling step. Each detail emerges from years of process optimization, conversation with chemists at the bench, and post-delivery troubleshooting. Specs in a document never convey the real-world impact the way weekly conversations with QC labs do.
The primary use cases fall under advanced intermediates. In pharmaceuticals, the substitution pattern frequently matches a protected site on a larger API scaffold. In agrochemical research, this compound enables rapid structure-activity studies by serving as a platform for introducing heterocycles or nitrogen-rich groups. Chemists often mention the ease of nucleophilic aromatic substitution at the ortho- or para- positions, especially compared to non-fluorinated relatives. By focusing on this substitution pattern, our formulation helps researchers avoid non-selective activation and improve stepwise yields in their target molecules.
We’ve supported customers who needed kilogram lots for evaluating antifungal actives, and others who pivoted their screening programs after seeing improved yields when compared to working with non-methylated analogs. The methyl group’s position not only tweaks electronic character but also physical solubility in organic solvents, which comes up in every kilo-scale batch someone dissolves for a column run or a critical crystallization step.
Despite a superficial similarity with 1,4-difluoro-5-nitrobenzene or dimethylated analogs, the chemistry shifts with even small changes in the ring. We have run pilot-scale tests with related difluoronitrobenzenes, only to find either unwelcome increases in by-products or difficulty in post-synthesis modifications. Customers returning to our product after testing competitor grades point to fewer side reactions when performing Buchwald-Hartwig aminations or Suzuki couplings—the regioselectivity improves, byproduct formation drops, and nobody misses extra purification steps.
A less obvious but impactful distinction turns up during waste treatment and safety assessments. The combination of methyl and fluorine atoms appears to reduce the formation of nitrophenolic byproducts under some reduction conditions. Safer handling and disposal are strong selling points for medium-scale production, and we’ve fielded more than a few regulatory compliance calls asking for documentation of those exact points. Lower volatility and controlled particle size also matter, as the molecule resists forming dust—a big plus for safety and convenience during open transfers in semi-automated lines.
Three years back, supply chain disruptions made both raw fluorinated aromatics and nitration agents harder to obtain or more expensive. We adjusted our purchasing and invested in strategic stockpiles so our customers would not feel the ripple effects. This included ramping up local sourcing of precursors and qualifying new suppliers who could demonstrate both reliability and documentation. The value of transparent, traceable supply chains has grown, not just for our peace of mind, but for regulatory filings by customers who need confidence in their starting materials.
Sustainability has shifted from a buzzword to an everyday benchmark. Most of our partners monitor waste generation, EHS reporting, and solvent recovery in their own synthesis work. We support these aims by publishing green chemistry data and continually seeking process tweaks that lower solvent use, reduce exothermic risk, and improve yield per run. After multiple cycles of process optimization, our updated protocol reduced nitration effluent by over 20 percent. Waste acidic streams undergo neutralization and analysis well before leaving our site, a point we emphasize in our material disclosures.
No matter how advanced the chemistry, consistent output is the product of skilled operators and hands-on management. Over time, our technicians have honed their sense for what a finished batch should look like. Regular cross-training between QC and production lets us spot small issues before they turn into bottlenecks. Every week, we huddle to discuss upcoming orders, review in-process controls, and swap notes on upcoming regulatory changes that might shape batch documentation or impurity thresholds.
Investment in on-site testing—GC, HPLC, and wet chemistry—brings rapid feedback, meaning less time spent investigating off-spec samples. From an E-E-A-T point of view, this translates into both trust and tangible results. We have shipped 1,4-difluoro-2-methyl-5-nitrobenzene worldwide, facing every conceivable customs or shipping scenario. Reliable packaging, accurate paperwork, and direct communication with the receiving labs all help keep business and research running, even across long supply chains. Over the last decade, these practices have resulted in low rejection rates and high customer retention.
Every batch teaches us something. During one campaign, a subtle shift in precursor quality led to an unexpected drop in the yield during nitration. Rather than pushing through, our team paused, re-examined the entire workflow, and traced the issue to a minor impurity from the new supplier. Quick decisions and long-term relationships mean we got the problem addressed, kept the batch in specification, and maintained the build schedule. A troubleshooting mindset—more about hands-on investigation than spreadsheet theory—keeps mistakes scarce and improvements on track.
Customers often ask for guidance on how their own use of our molecules can be streamlined. Whether it comes down to recommended solvents for dissolution, ways to avoid polymerization during downstream conversion, or tips on waste disposal, we treat these as two-way conversations. We respect that nobody knows your process better than you, but sharing tricky experience points—“don’t heat above this temperature in this solvent” or “filter while still warm to avoid clogging”—saves time and trouble for everyone.
Delivering high-quality 1,4-difluoro-2-methyl-5-nitrobenzene is about more than passing a certificate of analysis. Regulatory landscapes keep shifting, new use cases surface, and environmental scrutiny intensifies. We actively track international standards for purity, stability, and documentation. Up-to-date SDS and batch records are always available, and we routinely submit samples for independent validation. This transparent approach builds long-term trust with both long-standing clients and new entrants to the space.
We keep safety at the core of our process, for our team and for our clients. Every delivery includes full documentation, and our support line puts users in direct touch with process chemists familiar with handling and best practices. Any incident—no matter how minor—triggers an incident review and a process update. Investing in strong safety cultures, much like process controls, keeps everyone aligned and out of trouble.
From the factory floor to the end user’s bench, 1,4-difluoro-2-methyl-5-nitrobenzene delivers value through careful synthesis, tailored handling, and real-world support. Our ongoing commitment to quality, transparent communication, and process improvement continues to shape both how we make this product and how our customers succeed in their own projects. This product’s success is a testament to practical chemistry, skilled people, and open communication between everyone involved. Whether heading into the pharmaceutical lab, the agrochemical pilot plant, or any specialty project that draws on its unique profile, we’ll keep refining both our process and our partnership with the many teams who count on this molecule.