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HS Code |
280225 |
| Productname | 2-Fluoro-4-Nitrobenzoic Acid |
| Casnumber | 403-15-6 |
| Molecularformula | C7H4FNO4 |
| Molecularweight | 185.11 |
| Appearance | Yellow solid |
| Meltingpoint | 188-192°C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.615 g/cm³ |
| Smiles | C1=CC(=C(C=C1C(=O)O)F)[N+](=O)[O-] |
| Inchi | InChI=1S/C7H4FNO4/c8-5-2-1-4(7(10)11)6(3-5)9(12)13/h1-3H,(H,10,11) |
| Storagetemp | Store at room temperature |
| Hazardstatements | Irritant |
As an accredited 2-Fluoro-4-Nitrobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, white printed label with hazard symbols, product name, chemical structure, batch number, and handling instructions. |
| Shipping | 2-Fluoro-4-Nitrobenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is typically transported as a solid at ambient temperature, labeled according to hazardous material regulations. Proper packaging ensures stability, safety, and compliance with chemical shipping standards, including documentation and tracking for laboratory or industrial delivery. |
| Storage | 2-Fluoro-4-Nitrobenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases or oxidizers. Protect it from light and moisture. Store at room temperature, avoiding excessive heat. Ensure proper labeling, and keep the chemical away from ignition sources and direct sunlight to maintain its stability and safety. |
Applications of 2-Fluoro-4-Nitrobenzoic Acid in Industrial ManufacturingAs a reliable manufacturer of 2-Fluoro-4-Nitrobenzoic Acid, we supply strict-quality batches to support specialty synthesis and downstream production in regulated industrial environments. Below, we outline the principal application sectors and technical specifics for established downstream use cases. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)Pharmaceutical manufacturers use this material as a key intermediate in multi-step syntheses for APIs, particularly in producing anti-inflammatory agents and niche oncology compounds. The molecule’s substituted aromatic structure handles functional group transformations under controlled reaction stages. Our customers adjust addition points based on required purity, yield, and regulatory track record for route selection. Industry compliance standards
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2. Agrochemical Synthesis AgentProducers in the crop protection sector use this compound to construct molecular backbones for triazole-based fungicides and novel herbicides. Operators select it for its compatibility in halogenation and nitration substitution patterns, flattening synthetic complexity and enabling stepwise modular assembly across several patented actives. Industry compliance standards
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3. Specialty Dyes and Pigment Manufacturing IntermediateDownstream manufacturers in colorant production utilize this compound for ring activation, crucial for introducing specific chromophore moieties in the synthesis of highly stable azo and anthraquinone dyes. Structural substitutions facilitate process-color fastness and adjust hue modulation required by the textile, inkjet, and automotive coatings industries. Industry compliance standards
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4. Advanced Polymer AdditivesManufacturers in advanced polymer materials incorporate 2-Fluoro-4-Nitrobenzoic Acid as a monomer modifier or chain stopper in synthesizing specialty high-temperature polyamides and engineering plastics. Its aromatic substitution delivers targeted polarity and rigidity, fine-tuning mechanical performance and chemical resistance for demanding electrical, automotive, and aerospace polymer systems. Industry compliance standards
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5. Fluorinated Fine Chemical Building BlockProducers of specialized fine chemical intermediates employ this molecule as a foundational core in developing fluorinated aromatic derivatives for liquid crystals and specialty solvents. The electron-withdrawing groups on the aromatic ring enable regioselective further modifications, crucial for downstream innovations in advanced material synthesis and display technology integration. Industry compliance standards
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Producing 2-Fluoro-4-Nitrobenzoic Acid for the global fine chemicals market, we follow a process engineered for reliability, transparency, and batch-to-batch traceability. The molecular structure brings together a fluorine atom at the ortho-position and a nitro group at the para-position on a benzoic acid backbone, resulting in both physical stability and reactivity suited for downstream transformations. From the shop floor to the laboratory, we give close attention to the needs driving the specialty chemical sector. The finished product emerges as a faint-yellow crystalline powder, carrying a molecular weight of 185.11 and a melting range that proves useful in multi-step synthesis. The purity levels exceed 99%, confirmed with in-house chromatographic and spectroscopic methods.
In our two decades of manufacturing, specialty benzoic acids like this have become indispensable in agro, pharma, and dye intermediate segments. The fluorinated nitrobenzoic acid family often attracts attention for two reasons: the electron-deficient aromatic ring allows selective coupling, and the fluorine atom enhances compound stability in harsh processing steps. We have shipped tons of this material to medicinal chemistry labs for constructing tailored inhibitors and imaging agents, and to pigment factories where precise halogenation steers color fastness. Researchers tend to call out the careful balance between substitution pattern and functionalization they get with 2-Fluoro-4-Nitrobenzoic Acid, especially compared to non-fluorinated or meta-substituted counterparts.
A benzoic acid intermediate is only as valuable as the consistency in its halogen and nitro placement. Even minor impurities—whether positional isomers, starting material carryover, or color bodies—can trigger unnecessary optimization rounds downstream. Our facility was designed with this pain point in mind. The modern synthetic route uses stable precursors and avoids reagents that introduce by-products challenging to remove at scale. Line clearance and closed-system filtration keep microbial and foreign contaminants out of crystallization zones.
Market talk often skips over the realities of hazard mitigation and downstream compatibility during manufacture. Fluorinated nitro compounds bring both rewards and unique hurdles. HF and nitro aromatic handling requires inert atmosphere controls, PPE routines, and exhaust treatment. We adopted inline fluorine monitoring well before it became common, logging each lot with QC chromatograms accessible on joint review with buyers. This supports better risk management for teams engaged in validated process scale-up or regulatory studies.
In practical terms, each raw material lot matches reference standards, and reactors never see mixing between campaigns for non-related chemistries. While this adds overhead, we decided early that avoiding batch contamination means less downtime. The idea is fewer surprises when the customer’s application enters the critical scale-up or regulatory phases.
Many labs reach for standard 4-nitrobenzoic acid or derivatives like 2-chloro-4-nitrobenzoic acid when drafting synthetic schemes—usually for library build-outs or intermediate scaffolds. Those compounds work well for basic derivatization, but the presence of fluorine on the ortho-position in our product does more than tweak electronics. It widens the substrate window for nucleophilic aromatic substitution and introduces greater metabolic stability, showing up as longer half-lives in drug metabolism studies and less rapid decomposition during dye or pigment processing.
Developers in pharmaceutical chemistry rely on 2-Fluoro-4-Nitrobenzoic Acid to construct advanced intermediates where both electron-withdrawing demand and steric hindrance are essential. Those in the pigment segment appreciate the diminished leuco-formation and blocking effects that fluorine imparts, giving colorants sharper definition and lower migration in vinyl or polyamide matrices. By contrast, non-fluorinated analogs tend to trigger more side-reactions in cross-coupling workflows or under strong nucleophiles.
Our chemists have tested these differences head-to-head by running parallel nitration and halogenation reactions, carefully titrating each reagent for reactivity and yield. These practical in-house comparisons inform our clients before scale-up—especially when variable feedstocks threaten project economics and delivery timelines.
Western markets expect trace-level impurity documentation, and it’s the downstream partners who pay the price when upstream neglect leads to incomplete removals. Over the years, we’ve worked to minimize dichloromethane residues and reduce the ethereal odor still present in some lots produced with legacy filtrations. Enthusiasts for “green” chemistry in the US and Europe requested reformulated crystallization solvents to streamline their effluent treatment, and we trialed several alternatives. The final protocol uses a less persistent organic composition while keeping recovery yields steady.
High-purity requirements do add costs, but the alternative—unplanned plant stops or costly purification at the user’s end—carries greater expense. Pharmaceutical customers share tales of high-throughput screens failing due to overlooked halogen scrambling or a color body causing UV interference in analytical runs. Our proactive quality intervention brought these issues down to below ICH Q3A guidelines.
Testing at every step has led to more than one late-night adjustment. For instance, a client using our product for a Suzuki-Miyaura coupling reported that an unexpected trace impurity was causing false positives in their ligand binding assays. That’s never pleasant to hear, but we now run impurity profiling with both mass spectrometry and NMR after each scale-up, not just for marketing’s sake but because fixing contamination post-delivery usually means lost time and cost for everyone.
Many outside the industry underestimate the logistic variables in handling 2-Fluoro-4-Nitrobenzoic Acid. The balance between product sensitivity and robustness in packaging presses us to constantly monitor temperature, shock, and ambient humidity at each hub. We no longer use single-ply liners, as we traced capillary leaks during export shipments in humid monsoon conditions. Now, all outbound drums get double seals and internal tamper-evident bands to prevent ingress. These hands-on changes emerged from extensive feedback, not hypothetical accident scenarios.
Partners working on JIT schedules reported that missed customs clearances and late arrivals from secondary ports became a critical choke point. In response, we coordinate clear packaging instructions, and regulatory paperwork stays attached on both the inside and outside of drum covers. We clear hazard certificates and ensure the right HS codes down to the kilo, which reduces time spent dealing with non-compliance penalties. In this way, we learned that documentation matters just as much as chemistry in helping partners avoid fines and avoidable delays.
End users keep us honest, and feedback loops start in their pilot labs. Agricultural research groups cited the improved reactivity fingerprints of 2-Fluoro-4-Nitrobenzoic Acid in select herbicide precursors, enabling site-specific activity without unintended cross-reaction. Medicinal chemists routinely report greater diversity in coupling options. At the same time, this compound’s low water-solubility has nudged a few downstream clients to invest in modified dissolution protocols, using co-solvents or surfactants to speed up reaction set-up.
One pharmaceutical client remarked that, for a kinase inhibitor program, switching from 2-chloro to 2-fluoro substitution in their benzoic acid starter not only lifted selectivity but also diminished toxicity concerns in preclinical ADMET screens. The real-world impact hid in metabolic pathway shifts, confirmed by their outsourced analytical service. The result: cleaner regulatory filings and more confident IP positions. On the pigment side, textile houses valued the stability of dye precursors in multi-bath dyeing, citing less back-staining and color drift.
Some users shared stories about high-throughput error rates driven by the presence of photolytic degradation products in their prior sources. In response, we improved storage and illumination controls both in our warehouse and along transit routes. External audits led to investments in climate-controlled racking, especially for contracts involving extended buffering. Here, practical tweaks came directly from hearing where previous sources fell short.
As manufacturers, our choices reflect where the most disruptions hit: batch purity, lot traceability, and supply predictability. On the purity front, moving away from open-kettle setups and into fully contained reactors made invasive, variable contamination virtually obsolete by the mid-2010s. We adopted integrated fluorine waste quarantine and improved nitric acid handling, lowering exposure for staff and improving environmental outcomes for neighbors. Downward pressure on environmental risk keeps all of us safer and keeps permits in place.
Our engineering team prioritizes not just tracking, but anticipating, regulatory changes affecting restricted substance export controls. Because fluorinated nitroaromatics attract attention from customs and compliance bodies, we keep digital batch records and chain of custody documents updated for each kilogram produced. Years ago, manual logs introduced error and confusion, a lesson we learned the hard way after a missing line on a bill delayed a pivotal ocean shipment. With cloud records, such mix-ups no longer cost teams their launch windows or regulatory incentives.
Customer support doesn’t run on scripts here. Each technical query or incident ticket receives review by those who worked on synthesis or packaging. A scale-up partner once caught a subtle impurity pattern when adapting our product to an enzymatic coupling, leading us to overhaul both wet and dry transfer containers for improved hygiene and fewer cross-contaminants. Instead of treating such findings as defensive moments, we treat each failure analysis as a way to improve upcoming runs. This attitude flows from seeing firsthand how mistakes on one batch can ripple through a downstream customer’s launch calendar and regulatory budget.
It’s not unusual for new requests to push us outside comfort zones. Academic inquiries drive some of our most challenging batches, where ppm differences in impurity or material handling cause meaningful shifts in research outcomes. We maintain a research access program, opening controlled lots in sub-kilo quantities for teams testing novel transformations, radiolabeling, or chiral center introductions. These partnerships exposed us to upcoming trends: green catalysis, more sustainable halogen substitutions, and in situ monitoring technology.
In exchange, we gain hands-on feedback about how 2-Fluoro-4-Nitrobenzoic Acid fits in catalytic cross-coupling with new ligand technologies, or how its properties influence ligand field strength and hydrogen bonding in medicinal analogues. This insight feeds back into both scale and process improvement, so subsequent lots meet the next wave of demand.
Direct handling of 2-Fluoro-4-Nitrobenzoic Acid brings standard challenges common to nitroaromatics, yet we’ve learned to avoid risks by tightly scripting hazard controls and PPE protocols. Nitric acid emissions, spent solvent generation, and powder dusting all require real vigilance. Plant operators perform daily checks, review data for anomaly flags, and rotate shifts so nobody grows inattentive after hours in a high-hazard zone.
Downstream, we provide full composition and residual solvent data along with every batch. Regulatory filings in both the EU and US draw on our data sets for risk assessment, so we put in the extra work upfront, making audits and sustainability reviews smoother for partners. Instead of overselling green credentials, we focus on the practical reduction in hazardous solvent use, reduced overall effluent, and measurable worker exposure improvements over the last decade.
On the ecological front, actual improvements mean less spent solvent shipped offsite and a smaller perimeter of chemical odor or airborne fugitive. Plant neighbors, both industrial and residential, have noticed these changes. We take these experiences as a reminder: quality for downstream applicants and stewardship upstream, extending from raw input through to final disposal or conversion by our partners.
Demand for high-purity 2-Fluoro-4-Nitrobenzoic Acid pulls stronger each year, especially with stricter guidelines for solvent carryover and impurity profiling in regulated sectors. More discovery labs focus on halogenated intermediates with increased downstream compatibility and reduced regulatory exposure. Manufacturer track record, not just a lowest-price bid, shapes most long-term supply agreements now. Our experience suggests that by keeping an open line with synthesis teams and logistics planners rather than masking real bottlenecks, customers receive the kind of predictability that supports on-time launches and minimal plant downtime.
In pigment and agrochemical fields, reliability beats minor price shifts. The value shows up most clearly when a critical intermediate like 2-Fluoro-4-Nitrobenzoic Acid forms the spine of a novel synthetic route, the type that determines IP defensibility or registration status. Reliable documentation and impurity profiling win more repeat business than standardized checklists or lowest-bid claims. We commit to supporting these demands by sharing real-world, operational lessons rather than market templating.
Today’s specialty chemical buyers want more than a line-item price or generic batch COA. Years of real-time process improvements, technical troubleshooting with clients, and in-person line audits have toughened our protocols and refined our product offering. Every kilogram of 2-Fluoro-4-Nitrobenzoic Acid entering the market comes with the direct involvement of teams who manage risk, anticipate supply pinch points, and balance efficiency with quality.
Customers—whether in pharmaceutical labs, pigment works, or catalyst houses—show us that the difference between disappointment and solution rests in details only a manufacturer gets to see. We respond by maintaining direct lines of communication, welcoming early intervention in process scale-up, and treating every technical problem as a potential future improvement both for us and end users.
By continually engaging in hands-on process refinement, open data reporting, and collaborative troubleshooting, we see progress that goes beyond raw numbers. This approach keeps 2-Fluoro-4-Nitrobenzoic Acid viable as both a key building block for innovation and as a platform for ongoing operational improvement.