|
HS Code |
963391 |
| name | Nitrofuran |
| chemical_formula | C4H4N2O2 |
| molecular_weight | 112.09 g/mol |
| appearance | Yellow to orange crystalline powder |
| odor | Odorless |
| melting_point | 124-127°C |
| solubility_in_water | Slightly soluble |
| boiling_point | Decomposes on heating |
| CAS_number | 497-23-4 |
| pH | Neutral (in water) |
| storage_conditions | Store in a cool, dry place |
| uses | Antibacterial agent |
| stability | Stable under recommended storage conditions |
| toxicity | Potentially toxic if ingested or inhaled |
As an accredited Nitrofuran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Nitrofuran is packaged in a sealed amber glass bottle, labeled clearly, containing 100 grams, with hazard warnings and safety instructions. |
| Shipping | Nitrofuran should be shipped in tightly sealed containers, protected from light and moisture. It must comply with regulatory requirements for hazardous materials, including proper labeling and documentation. During transportation, ensure compatibility with other chemicals, and avoid exposure to extreme temperatures. Follow all applicable safety guidelines, including handling instructions and emergency procedures. |
| Storage | **Nitrofuran** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat or ignition. Keep it separated from incompatible substances such as strong oxidizers and acids. The storage area should be clearly labeled and access limited to trained personnel to ensure safe handling and prevent contamination. |
Applications of Nitrofuran in Industrial ManufacturingNitrofuran compounds serve as key functional intermediates in a limited number of specialized industrial applications, each governed by strict regulatory controls and process requirements. As an established chemical manufacturer, we supply nitrofuran derivatives customized to specification for critical downstream sectors, ensuring adherence to compliance standards, tailored formulation dosage, and precise integration into customer production processes. 1. Veterinary Active Pharmaceutical Ingredient (API) SynthesisVeterinary pharmaceutical manufacturers use nitrofuran derivatives—including furazolidone and nitrofurantoin—as essential building blocks in the synthesis of antimicrobial agents for livestock and aquaculture medicines. The integration of these intermediates requires close compliance with global and regional veterinary drug regulations, as well as formulation according to the finalized API’s target profile for animal health protection. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Industrial Dye ManufacturingNitrofuran intermediates provide indispensable core structures for specific dye molecules in the textile and leather dyeing industries. The downstream production of acid and disperse dyes requires nitrofuran moieties for the targeted shade, tinctorial strength, and fastness properties, with compliance controlled by environmental standards and end-use specifications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Polymer ModificationCertain engineering plastics manufacturers incorporate nitrofuran-based reactive groups to modify polymer backbones for electrical insulation and high-performance coating materials. These applications demand rigorous control over raw materials and finished product consistency to meet international material and electronic safety standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Agrochemical Intermediate ProductionAgrochemical formulators utilize nitrofuran derivatives as key intermediates during the synthesis of certain crop protection agents. Stringent regulation covers both the process and final use, demanding meticulous control through all production stages to ensure residue levels in food chains remain below stipulated safety thresholds. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Nitrofuran prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In over thirty years of hands-on chemical manufacturing, we have guided Nitrofuran production through every step, from raw material procurement to the precise, tightly controlled synthesis stages. In simple terms, Nitrofuran stands apart from many other specialty organics due to its rigid synthesis requirements and unique chemical backbone, featuring a furan ring bound to a nitro group. This structure determines both its reactivity and the tough quality demands needed in critical-use sectors.
Nitrofuran has earned its reputation largely through its role in specialty syntheses, particularly in the pharmaceutical, veterinary, and research fields. Our plant runs several Nitrofuran models, each tailored for defined applications: from high-purity crystalline for pharmaceutical research to technical-grade material used in intermediate synthesis. Meeting these needs never results from generic, off-the-shelf processes. It calls for steady process refinement, sharp analytical controls, and a deep understanding of how minor profile differences affect downstream results.
Processing Nitrofuran always reminds our team just how important predictable behavior is throughout a molecule's life. Its nitro functionality delivers selective reactivity, a property that unlocks a range of transformations in medicinal chemistry and advanced material development. Our pharmaceutical partners often highlight the difference our process consistency makes: one batch of Nitrofuran, run to strict analytical specifications, often determines not just the yield but also whether the subsequent synthesis meets purity criteria demanded by international regulators.
Animal health applications in particular draw heavily from reliable Nitrofuran sources. For years, we have worked with regulatory agencies to pin down and adhere to stringent impurity profiles. This level of regular scrutiny means our in-process checks, batch documentation, and shipment controls need to hold up to regular, surprise audits. Chemical manufacturers rarely get a second chance to correct contamination in these supply chains. One deviation in melting point, color index, or residual solvent content, and the resulting recall costs far outstrip the price of tight upstream controls.
Standard Nitrofuran from our reactors usually offers assay values above 98% on a dry basis, measured against strict chromatographic standards. Moisture content sits below 0.5%, and trace impurities routinely undergo both instrumental and classical chemical evaluation. These parameters emerged from years of working alongside both regulatory chemists and internal troubleshooters. Nitrofuran’s sensitivity to storage—particularly with regard to light and air—drives handling upgrades across our facilities, from closed-system loading to UV-blocked packaging lines.
Packing often sparks debate among end users, but through hard-won experience, we switched from metal drums to certified high-density polymer packaging to squash both the risk of contamination and unwanted catalytic interactions. This shift came only after several extensive storage trials, with samples monitored for both physical and chemical drift over long-distance shipments. Each adjustment we make reflects feedback from the field and our own internal tests, instead of theoretical best practices drawn from secondary literature.
Nitrofuran occupies a distinct chemical space compared to other heterocyclic nitro compounds. Its reactivity and solubility characteristics give it an edge in specific cross-coupling and amide-forming reactions. When compared to nitrobenzene or nitropyridine derivatives, Nitrofuran’s electron distribution and ring stability frequently lower activation barriers in target syntheses. This means it can deliver higher selectivity, sparing chemists the headaches of multiple purification steps downstream. It’s no surprise our most demanding customers—those building advanced intermediates for patented drugs—often specify Nitrofuran over alternatives, citing both cost-of-use and reduced batch failures.
At our facility, no batch leaves the synthesis block unless it matches the referenced chromatographic profile for Nitrofuran derivatives, including peak ratios and response factors tailored to our in-house reagents. As one production manager quipped after a recent troubleshooting episode: “No two nitroaromatic molecules behave alike when pushed to scale. But Nitrofuran, handled with care, doesn’t pull nasty surprises.” This field-derived knowledge stands in contrast to what catalog suppliers might advertise, as our work has shown—time and again—the subtle but critical differences between fresh, carefully monitored Nitrofuran and the variable, sometimes degraded stocks found through less direct routes.
Customers facing regulatory hurdles or working on time-sensitive production windows consistently report fewer delays and compliance headaches with our Nitrofuran. In pharmaceutical and specialty chemical manufacturing, late-stage surprises often trace back to impurity drift or lot-to-lot inconsistency. Years back, a client developing a new veterinary active experienced cascading process failures due to off-spec Nitrofuran they had sourced from a distributor. Tracing the problem back, it became clear the supply chain had ignored light and oxygen protocols, leading to degraded product. After they switched to material sourced directly from our controlled environment, their yields stabilized, and the risk of batch rejections dropped sharply.
Some may argue chemical equivalency from different suppliers should be just that—equivalent. But seasoned formulators and lab leaders point out the subtle differences that don't show up on a basic COA. For example, our active management of microtrace impurities, including those below regulatory concern, emerged from partnership-driven troubleshooting. This policy did not arise from external push but from close study of customer bottlenecks and sustained feedback loops. As a result, many of our repeat clients have integrated audits of specific Nitrofuran criteria into their vendor qualification, building a trust chain wider than a paper trail.
Handling and storing Nitrofuran at scale never counts as routine work. Nitrofuran’s susceptibility to light-triggered breakdown and air-driven oxidation requires robust closed container systems, regular storage zone audits, and direct oversight by experienced staff. We learned, often the hard way, that generic SOPs lifted from commodity chemical operations fail to capture the reality of how sensitive this compound can act. Instead of off-the-shelf procedures, we implemented dedicated storage modules with ongoing training to catch any slip-up before it leads to quality dips or safety incidents.
Compliance pressure—especially for pharmaceutical applications—runs high in finished Nitrofuran markets. Besides standard regulatory frameworks like REACH and FDA registrations, many end-use cases demand real-time analytics and visible traceability all the way from source raw materials to the packaged flask. We’ve responded by upgrading both our paper and digital trace systems, running proactive batch certification, and collaborating directly with auditors—internal and external—to ensure that every shipment aligns with both legal and customer-driven requirements.
New applications for Nitrofuran continue to open up, driven largely by academic collaboration and development in synthetic organic chemistry. Recent focus areas include advanced polymer materials and targeted antimicrobial research, both of which seek out clean and well-characterized Nitrofuran intermediates as starting blocks. Several research groups highlight the compound’s utility as a scaffold for building more complex ring systems. Our process control team works closely with R&D chemists to adjust production parameters as they explore derivative molecules, testing hypotheses and refining both analytical and physical handling strategies.
We have found that direct collaboration with universities and research partners brings unexpected insight. For instance, a modification to our condenser temperature profile, introduced during a pilot project with a synthetic chemist developing new Nitrofuran derivatives, produced tighter control over side-product formation. These kinds of improvements rarely appear in trade literature and only emerge through fieldwork—matching practical problems with tangible factory adjustments.
Every manufacturer faces disruptions, particularly in raw material sourcing and logistics. The Nitrofuran chain presents its own special risks, including limited sources for high-purity nitrofuran precursors and tight timelines for shipping under light-protected, temperature-controlled conditions. We saw firsthand during major market swings how pivotal it becomes to lock down both primary and secondary sourcing agreements for essential reagents. Our procurement team keeps a standing list of alternate sources, periodically testing sample performance all the way through finished Nitrofuran, so that even during raw market volatility, consistency in output does not falter.
On the logistics side, stable Nitrofuran delivery depends on more than just speed. It requires complete chain-of-custody control, double-wrapped packaging, and real-time shipment tracking. We partner directly with freight teams to ensure the shortest possible exposure to damaging conditions. This proactive role reduces stock write-offs for our customers and keeps our own operation lean and responsive. During the early pandemic period, we learned hard lessons about what happens when third-party carriers mishandle specialty shipments. After a full review, our supply team brought key cold chain delivery in-house, investing in both new containers and continuous monitoring devices. The days of hoping third-party partners understood our standards are largely over.
Nitrofuran buyers who transition from marketplace vendors to direct-from-manufacturer supply often report critical differences in both experience and outcomes. Our quality-assurance teams see fewer customer complaints and technical requests from direct buyers, as shared process parameters and open technical communication help resolve questions before they become problems. Transparency—both on analytical specifications and on changes to process or packaging—lets end users adapt faster and trust the supply more. By contrast, reseller models often lack this tight, real-time feedback and can introduce avoidable variability.
Manufacturing leads, especially those operating under GMP, know that direct engagement means faster troubleshooting and problem-solving. For Nitrofuran, this could mean real-assay verification pre-shipment, custom impurity testing, or order-sensitive scale-up. In some cases, after a complex synthesis failed on the customer side using material from various sources, we co-processed reference samples and ran side-by-side analytical and pilot synthesis to identify and root out the issue—a level of problem-solving simply not possible through non-manufacturing intermediaries.
Each batch of Nitrofuran gives us another chance to refine, adjust, and test our understanding of fine organic chemical manufacture. On-the-ground learning has taught us to value real-time analytical control and prompt response to even minor process deviations. Every recall on the global stage tells us that tight, proactive collaboration beats retroactive blame. For Nitrofuran, this focus brings more reliable manufacturing runs, stronger end-user results, and lower process risk.
Our experience says end users in key industries—pharmaceutical, veterinary, and advanced chemical research—stand at greatest risk from commodity approaches to such a specialized material. Not all Nitrofuran deliveries should look alike, either, as very tight impurity allowances or specific physical forms can drive completely different results in a downstream synthesis. We invest both time and capital in custom solutions drawn directly from customer pilot experience, not just specification lists.
Uninterrupted dialogue between manufacturing and customer labs often highlights both success stories and future improvement paths. Over time, this two-way flow of technical details and field feedback turns what began as a commodity chemical into a high-value partner molecule—one that responds to practical, real-world needs.
Nearly every major success with Nitrofuran in our history came through close listening—field problem, lab test, plant trial, analysis, then back again. What starts as a minor tweak for one customer often evolves into broader process improvements that benefit all users. Every change builds on the lessons of the last batch, the last shipment, the last research trial. With Nitrofuran, real trust and technical progress grow by rejecting a one-size-fits-all mentality and focusing instead on field-derived, factory-proven solutions.
Our work with Nitrofuran combines veteran factory know-how with a commitment to collaborative manufacturing and improvement. Each order strengthens a cycle: feedback from application, analysis of process, transparent communication, and continuous refinement. Customers trust our process not because of polished marketing or layered intermediaries, but because long-term, lived experience delivers on quality, consistency, and support, shipment after shipment. Nitrofuran’s reliability, in our hands, reflects decades of deliberate manufacturing, careful sourcing, and everyday partnership with the world’s most demanding chemical users.