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HS Code |
414126 |
| Chemical Name | 2,6-Difluorophenylhydrazine |
| Cas Number | 24319-56-8 |
| Molecular Formula | C6H6F2N2 |
| Molecular Weight | 144.12 g/mol |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 74-78°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Pubchem Cid | 219154 |
| Inchi Key | XXBINXDWNNVGTH-UHFFFAOYSA-N |
| Smiles | NNc1c(F)cccc1F |
| Storage Conditions | Store at 2-8°C in a tightly sealed container |
| Synonyms | 2,6-Difluorobenzenecarbohydrazide; 2,6-Difluorohydrazinobenzene |
| Hazard Statements | May be harmful if swallowed, causes skin and eye irritation |
As an accredited 2,6-Difluorophenylhydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Difluorophenylhydrazine is supplied in a 25g amber glass bottle, sealed with a screw cap, and labeled with hazard information. |
| Shipping | 2,6-Difluorophenylhydrazine is typically shipped in tightly sealed containers, protected from light, moisture, and heat, and labeled according to local and international hazardous material regulations. Handling and transport should comply with UN guidelines for chemicals, ensuring secure packaging to prevent leaks or exposure, and documentation of hazard classification is required. |
| Storage | 2,6-Difluorophenylhydrazine should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Protect from light and moisture. Store separately from oxidizing agents, acids, and strong bases. Use appropriate chemical-resistant containers and label clearly. Follow all applicable safety regulations and consult the MSDS for further guidance. |
Applications of 2,6-Difluorophenylhydrazine in Industrial Manufacturing2,6-Difluorophenylhydrazine supports several highly specialized downstream industries as a key intermediate in fine chemical and pharmaceutical syntheses. Its chemical structure enables precise functionalization, making it valuable in advanced manufacturing technologies. The following sections detail its main real-world industrial application scenarios, including regulatory requirements, formulation guidelines, integration into processes, and typical final products encountered in the commercial supply chain. 1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology DrugsAPI manufacturers use 2,6-difluorophenylhydrazine to construct hydrazone and heterocyclic frameworks during targeted anti-cancer drug production. This intermediate supports the design of molecules with enhanced metabolic stability and selectivity. It enters the synthetic route in the latter stages of API development, allowing controlled introduction of difluoro moieties essential for clinical effectiveness. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide Intermediate PreparationProducers in the agrochemical sector apply 2,6-difluorophenylhydrazine as a coupling agent for synthesizing selective herbicide scaffolds. Its use facilitates the construction of pyrazole and triazole derivatives, which are vital for activity enhancement and resistance management in crop protection compounds. The integration process occurs in the heterocyclization phase, ensuring regioselectivity and consistent batch quality. Industry compliance standards
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3. Dye and Pigment Intermediate for Textile and Specialty ColorantsThe specialty chemicals sector relies on 2,6-difluorophenylhydrazine as a key raw material in the synthesis of azo and hydrazone-based dye intermediates. It enables the precise introduction of electron-withdrawing difluorophenyl groups, boosting stability, lightfastness, and chromatic purity of advanced colorants demanded by high-performance textile and printing industries. Its use enhances downstream product fidelity, especially during coupling and color development stages. Industry compliance standards
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4. Fine Chemical Intermediates for Medicinal Chemistry ResearchChemical research organizations and custom synthesis labs utilize this hydrazine derivative for rapid lead optimization and novel molecule construction. The electron-deficient aromatic core enables functional tests in heterocycle synthesis and enzyme inhibitor development. Researchers introduce it during combinatorial library preparation to diversify chemical space, supporting medicinal chemistry and SAR (structure-activity relationship) exploration under stringent laboratory controls. Industry compliance standards
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5. Synthesis of Functional Polymers and High-Performance ResinsSpecialty resin and polymer manufacturers incorporate 2,6-difluorophenylhydrazine as a reactive monomer or chain-terminating agent. Its bifunctional character supports synthesis of advanced polyhydrazones and crosslinked network structures, improving chemical resistance and durability in electronics, coatings, and specialty adhesives. The integration point is post-polycondensation, where it forms part of the backbone or end-groups to tailor physicochemical properties. Industry compliance standards
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Working day in and day out as a producer of specialty chemicals, the importance of each stage in synthesis never escapes anyone. Our product, 2,6-Difluorophenylhydrazine, grew out of decades spent refining the methods and equipment necessary to support modern science and industry. Long before trends in pharmaceuticals and agrochemicals highlighted hydrazines like this one, industry veterans handled the real edge of process control, safety, and consistency. These lessons flow directly into our production, making each batch meet expectations not just on paper, but in real-world laboratories and manufacturing floors.
2,6-Difluorophenylhydrazine stakes out a unique spot among hydrazine derivatives. Its value shows up clearly during the synthesis of key intermediates for active pharmaceutical ingredients, crop science research, and high-end dyes. We produce this compound in a crystalline form, with a purity that consistently measures above the 98% mark verified by GC and HPLC analysis in our facility. The appearance is white to off-white crystals, reflecting tight control during purification and drying.
Every batch we produce follows a rigorous track record in both equipment design and analytical testing. We use reactors lined specifically for handling high-purity fluorinated compounds. Our in-process checks catch even minor contaminants. Moisture content stays well below competitor averages, based on regular Karl Fischer titration results. All the hydrazine values track close to theoretical yield—this low variability isn’t accidental. It comes from years of experience measuring the influence of temperature, agitation speed, and feedstock grade. No unused starting hydrazine lingers in the final product; analysts receiving our shipments gain the benefit of fewer surprises during their QC checks.
Many commercial labs first handle hydrazines on a gram scale. Tasks shift quickly once demand grows. We’ve scaled our 2,6-Difluorophenylhydrazine from synthesis in tens of grams to orders measured in tons. With each jump in volume, challenges appear—solubility limits, liquid transfer issues, workup efficiencies, safe venting for off-gassed hydrogen fluoride. Years ago, high-volume runs risked product discoloration and yield loss because of batch-to-batch variations in precursor lots. Tightening in-house purification steps for the 2,6-difluoronitrobenzene feedstock and tuning the reduction step allowed for consistent color and purity, even on the largest batches. These behind-the-scenes adjustments rarely show up in spec sheets, but customers with precision needs ask about them directly.
Every research chemist weighs cost against reactivity and selectivity. 2,6-Difluorophenylhydrazine offers a direct answer. The difluoro substitution at the 2 and 6 positions shifts both the electron density and steric profile relative to unsubstituted phenylhydrazine. This translates to different coupling behavior in azo dye preparation, reduced by-product formation in hydrazone synthesis, and a propensity for cleaner reductions in nitroaromatic conversion steps. In some pharmaceutical routes, switching from mono-fluoro- or unsubstituted hydrazines to the 2,6-difluoro version increases the yield of desired targets by as much as 10-15%. These gains do not come from theoretical speculation but from bench chemists logging results over countless runs. Academic groups have published related findings, but large-scale facilities confirm or overturn those claims only after hundreds of kilograms move through reactors.
Users often ask about differences between our compound and alternatives like unsubstituted phenylhydrazine or 4-chlorophenylhydrazine. The answer usually lies in three areas: stability, safety, and reactivity. The fluorinated positions in 2,6-Difluorophenylhydrazine raise the oxidative stability of the molecule. This matters in storage over several months and in reactions sensitive to autoxidation. Our synthesis layer builds into every shipment a guarantee of low trace metal content, since these can catalyze nonsense side reactions in hydrazine chemistry.
From a safety standpoint, 2,6-difluoro substitution lowers the vapor pressure relative to many lower molecular weight hydrazines. Workers handling drums in manufacturing plants report less odor, and incidents involving uncontrolled evaporation drop. These points might not change on a datasheet, but the practical difference shows in improved workplace air quality and easier compliance with health standards.
When we compare reactivity, strict substitution at both ortho positions distinguishes this product. Phenylhydrazine itself acts as a strong nucleophile and reducing agent, but chemists searching for enhanced selectivity and a different balance in SNAr or condensation reactions consistently migrate towards the difluorinated version. In competitive settings, users aiming for specific regioselective or chemoselective transformations rely on our 2,6-Difluorophenylhydrazine to offer cleaner conversion and fewer purification headaches at downstream steps.
Internal protocols have changed as we’ve grown from small-batch to bulk output. Early years saw frequent manual checks; these days, online sensors and automated feedback stabilize key reaction parameters. Operators still walk the lines, visually inspecting color and checking solubility against established standards. At the point of filtration and drying, long-serving technicians know exactly how long to hold a temperature or when to swap in fresh filtrate based on the feel of the material.
Even the final packaging reflects lab and end-user feedback. We package the product in materials tested for compatibility, avoiding reactions or absorption that might degrade quality during shipment or storage. Temperature data logs track ambient conditions so we can see if external handling introduced risks. This real-world attention to each stage produces fewer customer complaints and higher return-buy rates—a direct reflection of trust built batch by batch.
Pharmaceutical companies, agricultural researchers, and specialty dye houses continually need building blocks that balance stability and reactivity. 2,6-Difluorophenylhydrazine fits this demand by giving chemists control and predictability. A large research outfit in Europe found that switching to this compound cut down their purification steps by one-third during pilot runs, and finished product impurities dropped below their internal QC limits. Similar stories surface from early-stage drug startups who realize cost and time savings at the gram scale and maintain them when moving upwards to kilogram scale.
Collaboration also drives improvements. Customer technical feedback often leads to tweaks in our own process—sometimes as minor as a solvent swap, sometimes a more fundamental change in filtration techniques. These are not theoretical improvements; they grow out of hours spent on solving real production problems, validating new quality checks, and tracking how even minor lot-to-lot differences affect the science happening beyond our gates.
Industry headlines often highlight supply chain challenges, surges in demand, and regulatory changes. Experience tells us that reliable access to key intermediates makes or breaks R&D projects and manufacturing lines. We invested heavily in local sourcing of raw starting materials—2,6-difluoronitrobenzene, reducing agents, and solvents come from auditable, long-term partners. Contingency planning matters: backup reactor modules stand by for high-demand cycles, and we maintain buffer stock in climate-controlled warehouses.
Safety sits front and center. Our plant teams run regular drills and cross-train across handling, neutralization, and containment systems. Plant design grew out of learnings from earlier, less forgiving setups—now barriers, scrubbing systems, and real-time atmosphere monitors mitigate risk before issues escalate.
Handling hydrazine derivatives raises real questions about environmental impact and regulatory compliance. Decades of operation honed our waste stream management. All mother liquors and washings get treated in multiple containment steps. Analytical teams sample effluent daily, keeping trace organic compound levels below legal discharge benchmarks.
We have followed international regulatory developments to adjust production methods accordingly, minimizing any chance for incident or recall. Our audits from external inspectors provide clean marks—and, just as important, regular feedback guiding future process improvements.
Careful chemistry does not stop at the reactor door. Delivering 2,6-Difluorophenylhydrazine across borders or climates calls for more than standard packaging. Each drum or fiberboard carton contains a product certification printout drawn directly from our in-house QC records. Desiccant packs help maintain the low-moisture environment that preserves product for months if not years when kept under recommended conditions. Distribution partners rarely report handling incidents, but ongoing collaboration with their technical services team catches problems early. The result: high product integrity from our plant to customer benches and reactors worldwide.
Feedback shapes every improvement. Several small biotech firms came to us with reports that using cheaper, less pure hydrazines introduced batch failures and delayed project milestones. Transitioning to our 2,6-Difluorophenylhydrazine provided not only better yields but also records of shorter analysis cycles due to fewer unknowns in spectra. Agrochemical teams working with pesticide intermediates found that the higher oxidative stability led to much smoother scale-up and registration filings, since reproducibility checks cleared without extra rounds of cleanup.
Lab anecdotes echo this: synthetic chemists tell us that switching over cut time spent troubleshooting HPLC ghosts and unknown subpeaks. Time saved in the lab turns into faster publications, patent filings, and product launches. At the pilot plant, fewer rework orders and less downtime during batch processing translate to budget savings that make a difference at the year-end review.
The chemical landscape churns through waves of innovation in both process optimization and end applications. The feedback loop between advanced material demands and steady, reproducible supply continues to drive investments on our side. As newer synthetic routes push the limits of what hydrazine derivatives can accomplish, hours logged on both the factory floor and in tech support calls fuel ongoing refinement.
Cost pressures never let up. Producers sometimes cut corners or chase easy lower-cost wins at the price of reliability. Decades of seeing how minute failures ripple through a customer's production or research process push our teams to continually scan for hidden process variables and tighten troubleshooting playbooks. For those committed to the long game in specialty chemistry, this attention to quality and detail forms the backbone of real partnerships.
Longstanding commitment to 2,6-Difluorophenylhydrazine production did not arise from fleeting market spikes or isolated research breakthroughs. It developed from persistent follow-up, listening to end-users, and embedding those needs back into the factory workflow. Years of handling, adjusting, and scaling production built a wealth of knowledge that only direct manufacturing effort can provide.
Every order we ship carries the imprint of that experience, and every inquiry or customer report adds another layer. In real terms, this means we track and deliver product that saves downstream teams both time and effort, limits real-world production hiccups, and stands ready to adapt as science and industry push for what comes next.