|
HS Code |
215004 |
| Cas Number | 3160-89-0 |
| Molecular Formula | C8H12N2 |
| Molecular Weight | 136.20 g/mol |
| Iupac Name | 2,6-dimethylphenylhydrazine |
| Appearance | Yellow to brown liquid or solid |
| Melting Point | 38-42°C |
| Boiling Point | Unknown |
| Density | Unknown |
| Solubility In Water | Slightly soluble |
| Flash Point | Unknown |
| Smiles | CC1=CC=CC(C)=C1NN |
| Inchi | InChI=1S/C8H12N2/c1-6-4-3-5-7(2)8(6)10-9/h3-5,10H,9H2,1-2H3 |
As an accredited (2,6-Dimethyl-Phenyl)-Hydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a red cap, labeled with chemical name, hazard symbols, and safety instructions. |
| Shipping | (2,6-Dimethyl-Phenyl)-Hydrazine should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must comply with relevant hazardous material regulations, such as DOT, IATA, or IMDG. Proper labeling, documentation, and use of secondary containment are required to prevent accidental leakage or exposure during transit. |
| Storage | (2,6-Dimethyl-Phenyl)-Hydrazine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight. Keep it segregated from oxidizing agents, acids, and sources of ignition. Use secondary containment to prevent leaks. Always clearly label the container, and avoid storage in areas prone to temperature fluctuations or moisture. |
Applications of (2,6-Dimethyl-Phenyl)-Hydrazine in Industrial ManufacturingAs an experienced producer of (2,6-Dimethyl-Phenyl)-Hydrazine, we supply this high-purity intermediate to specialized downstream sectors that demand strict specification adherence, consistent batch performance, and comprehensive regulatory compliance. Below, we outline the established industry segments where our material serves a critical purpose, providing clear information on operational standards, suitable formulation concentrations, integration steps, and the commercial end-products resulting from its use. 1. Agrochemical Active Ingredient SynthesisMajor agrochemical manufacturers employ (2,6-Dimethyl-Phenyl)-Hydrazine as a key hydrazine derivative in the multi-step synthesis of phenylhydrazone-based herbicide actives. Its role centers on the formation of the hydrazone functional group, driving target molecular selectivity and stability for application-specific crop protection agents. Producers precisely monitor intermediate purity and conversion rates to ensure downstream activity and regulatory conformity in finished goods. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingSpecialty pharma producers utilize (2,6-Dimethyl-Phenyl)-Hydrazine in the controlled synthesis of specific APIs or API intermediates, notably where its steric and electronic properties are crucial for constructing N-arylhydrazone motifs. Process optimization focuses on maintaining strict impurity profiles and phase separation efficiency to meet stringent GMP-mandated purity standards in downstream synthesis steps. Industry compliance standards
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3. Colorant and Azo Dye Precursor SynthesisEfficient colorant manufacturers use (2,6-Dimethyl-Phenyl)-Hydrazine in synthesizing specific arylhydrazone coupler units as intermediates for high-performance azo dyes. Its chemical reactivity enables the development of shades with customized absorption ranges and enhanced lightfastness, critical for textiles, plastics, and specialty inks demanding lasting visual performance under exposure to various environmental conditions. Industry compliance standards
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4. Specialty Polymer Additive FormulationPolymer compounders in the high-value plastic modification sector rely on (2,6-Dimethyl-Phenyl)-Hydrazine as a chain-terminating modifier and crosslinking agent in synthesizing functionalized polymers. Its introduction assists with controlling molecular weight, enhancing thermal resistance, and improving chemical stability in engineering thermoplastics adapted for advanced industrial uses. Industry compliance standards
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At our manufacturing plant, (2,6-Dimethyl-Phenyl)-Hydrazine emerges from careful design choices and an ongoing commitment to quality. Colloquially, some chemists refer to it as 2,6-xylyl hydrazine, highlighting its dimethylated aromatic ring and a hydrazine group attached at the first carbon. We batch-produce material matching industry typical purity benchmarks, keeping water content and organic impurities low. Our attention to detail at every reaction and purification step preserves consistency, providing predictable quality for specialized users who value reproducible results.
Our final product presents as a solid at standard temperature, typically a white or slightly off-white powder depending on the batch’s moisture and storage conditions. Years spent optimizing our process have especially reduced the lot-to-lot variability customers sometimes experience elsewhere. We focus on delivering material with high assay, limiting residual solvents and minimizing colored byproducts that might interfere with downstream use. Packaging uses durable, airtight containers, preventing contact with air and light, since the compound can oxidize over time.
We built our production route on reliable chemistry: starting from 2,6-dimethylaniline, we developed a streamlined diazotization followed by controlled reduction. Operators monitor every run for temperature swings and mixing rates; a stable process means fewer surprises in the finished product. After the reaction completes, we follow with a sequence of washes, crystallization, and a final drying under vacuum. This careful approach avoids unwanted isomers or polymeric byproducts, which can sneak in without close oversight. We avoid shortcuts, recognizing every step shapes the compound’s long-term usability.
Chemists who know their aryl hydrazines often mention (2,6-Dimethyl-Phenyl)-Hydrazine by name for its balance of reactivity and selectivity. The two methyl groups at ortho positions slow down oxidation compared to unsubstituted phenylhydrazine, improving shelf life and handling safety. At the bench, researchers handling diazonium chemistry, and certain heterocyclic syntheses, call out this material where less hindered hydrazines can undergo unwanted side reactions or prove too unstable in solution. Its slightly higher melting point gives users a little more flexibility for storage and transportation, reducing loss from degradation.
Colleagues in custom synthesis, pharmaceuticals, and specialty pigments reach out for (2,6-Dimethyl-Phenyl)-Hydrazine whenever they face targets that demand cleaner transformations. The compound acts as a nucleophile, participates in hydrazone formation, and fits into libraries of intermediates for screening campaigns. The methyl substituents render the aryl ring less prone to electrophilic attack, often decreasing side product formation in multi-step syntheses. In our own collaborations, we have sometimes seen this hydrazine outperform its simpler cousins, facilitating step-economical routes that trim weeks off development timelines. Across decades, we’ve seen it deliver robust yields in preparations of azaheterocycles or in Suzuki coupling reactions conducted under challenging conditions.
Every hydrazine asks for respect due to its potential hazard profile. Regular training keeps our team alert to the compound’s toxicity and reactivity, reinforcing the importance of careful handling and rigorous quality control. By maintaining exacting purity standards, the risk of dangerous decomposition diminishes. Large-scale users, particularly those with automated lines, value the batch reliability our QA protocols guarantee, as problematic runs cost time and safety. On the other hand, the methyl groups that make the molecule robust can also limit its use in settings that demand highly activated hydrazines. We do not ignore these trade-offs, and our R&D group invests in alternative catalyst systems and procedures to broaden its utility where possible.
The aromatic hydrazine family spans a range of reactivity and stability. Classic phenylhydrazine—without methyl substituents—remains more sensitive to air, with a tendency to darken and degrade faster than most analogues. Our dimethylated variant resists this action, with the ortho positions shielding the hydrazine group from stray electrophiles and radicals. Side-by-side, this means less color development during storage and transport, reduced need for inert atmosphere operations, and longer shelf life. At the same time, this protection comes with a measured drop in reactivity, which can be beneficial for selectivity in target-oriented synthesis. Our experience tells us that for sensitive transformations, especially where the hydrazine group should avoid untimely oxidation or condensation, the 2,6-dimethyl substitution justifies itself in both lab-scale and industrial contexts.
Large-scale manufacture of (2,6-Dimethyl-Phenyl)-Hydrazine rewards careful calibration. We monitor starting material quality and watch batch records for anomalies. Our plant runs a closed system for much of the process, collecting off-gas for scrubber treatment to minimize release of volatile fractions. Trace metal levels tracked over the years have remained below detection, thanks to rigorous supplier vetting and equipment maintenance. The crystalline final product spends as little time in open air as possible, moving from dryer to packing under nitrogen. Each container receives a unique lot label, letting users source full traceability from our records. Losses at the final packing stage dropped by more than half after we tightened protocols and installed additional glovebox capabilities.
Many customers return, not only for chemical properties but for peace of mind. We stake our name on every shipment; shortchanging on process hygiene has no place in our company. Incidents where other sources shipped out-of-spec material have reached us through feedback forums and direct calls for help. Downtime and loss pile up when a supplier cannot guarantee reproducible assay, minimal water content, and low color bodies. The reputation we built comes from recognizing these financial and technical consequences, and retooling our plant repeatedly to meet higher expectations. Customers with complex projects trust us for a reason—we are transparent about our process, welcoming audits and site visits.
Our operation integrates best practices from years of environmental audits and regulator input. Hydrazine derivatives require careful containment by their very nature. In our plant, spent solvent collects in segregated tanks, and organics pass through in-factory incineration when possible, or ship securely to certified waste handlers. Safety drills address release contingencies, and every operator wears personal monitoring during task execution. Our team’s experience with old-style open batch regimes drives improvements—double-layered seals, reduced manual transfers, and real-time reaction monitoring all cut risk. The community and our own staff both expect upgrades every year. Feedback loops from actual incidents—not just desk-based hazard analyses—let us spot weak points and fix them ahead of regulation.
Interest swings in aryl hydrazines trace closely to developments in pharmaceuticals, materials science, and specialty dyes. Over the past five years, we observed peaks in orders following new published catalytic transformations—especially where selectivity or thermal stability matter. Movement into biomolecule conjugation and high-performance polymer components introduced new demand, forcing us to adapt our QC to more exacting standards set by downstream users. Custom orders for tailored purities and packaging have increased as a fraction of total volume. Our close relationship with users at the research and pilot scale brings in early signals of changes in formulation and application, letting us adjust batch sizes and delivery timing to real-world shifts, not just historic trends.
Customers weighing options face more than just price. Unsubstituted phenylhydrazine, while cheaper, brings headaches with storage and shelf-life; uncontrolled oxidation generates tarry byproducts, forcing frequent repurchases and rework. Para-substituted or bulky hydrazines often introduce too much steric hindrance, shutting down key reactivity for many pharmaceutical syntheses. Our 2,6-dimethyl version occupies a practical middle ground: robust enough to last months or longer under standard warehouse conditions, but reactive enough to deliver high conversion in cyclization or coupling steps. For those scaling up plant operations, this reduces waste and supports leaner inventory management—two concerns becoming ever more pressing as regulators and customers both expect sustainable practices.
Years of collaboration with users show where problems tend to crop up. Hydrazine-based intermediates can interfere with sensitive analytical techniques; trace impurities sometimes produce false peaks in chromatograms. Our hands-on experience running reference syntheses and supporting tech transfer means we anticipate these issues. To mitigate, we provide supporting batch data—sometimes even running extra columns for clients with GC-MS needs. Sometimes, adopting new solid handling gear solves dusting during weighing, improving both safety and dosing accuracy.
Old-timers in chemical manufacturing remember the days when production runs of aryl hydrazines floated on luck rather than control. Today, safety targets rule every aspect of our workflow. (2,6-Dimethyl-Phenyl)-Hydrazine brings a level of predictability only possible through modern process engineering. Start-up customers in academic spinoffs and established R&D groups alike speak to the importance of field-proven performance; they do not have time to wrestle with purity questions or unexplained delays. Our scale lets us draw lessons from pilot batches, pivoting quickly if we see yield drops or process upsets. Multi-tonne production no longer feels daunting; it has become routine with the right skills and equipment.
Feedback from production chemists provides our best learning. Batch failures, even rare ones, prompt deep dives into every variable. A hydrazine compound responds to tiny shifts—whether in agitation, pH, or even the trace acidity in cleaning solvents. Our engineering group reviews every troubleshooting report, tuning reactor setups and raw material specs. Trust grows not from marketing, but from the experience gained bouncing back from real setbacks; those lessons stick with us. Peer discussions at conferences and in industry forums point us to cutting-edge analytical protocols, which we add into our routine before market demand catches up. The culture of continuous improvement in the plant supports users who themselves work on the edge of chemical innovation.
Logistics departments play a crucial role in ensuring delivery worldwide. Our site sits within hours of major ports, and the packing rooms schedule shipments to limit product time out of controlled storage. Every operator recognizes that a delayed or compromised shipment can derail a synthesis program for weeks. We work closely with freight specialists to navigate regulations governing hazardous materials, updating paperwork and container design as rules evolve. We keep stock for regular clients, allowing faster turnaround when projects spike unexpectedly. Experience with customs documentation and compliance means smoother border crossings and fewer snags for end users.
As green chemistry takes a larger role in supply chain decisions, we’ve faced pressure to reduce waste and energy inputs. For (2,6-Dimethyl-Phenyl)-Hydrazine, we optimized the work-up stages to minimize solvent volumes and swap chlorinated carriers for safer alternatives. Our team tracks resource use with every campaign; even incremental savings translate to measurable reductions in environmental footprint when repeated over many tonnes of product. Conversations with end users show that more customers now care about upstream sustainability, not just price per kilogram. Aligning with environmental goals makes commercial sense, and every upgrade to manufacturing delivers dividends for our business and the broader community alike.
Change never stops in specialty chemical manufacture. Even a compound with decades of history, like (2,6-Dimethyl-Phenyl)-Hydrazine, sits at the intersection of changing needs and technology. Analytical tools advance every year—NMR, LC-MS, and online chromatography let us catch subtle shifts in profile that would have escaped notice in the past. We train operators on every new method, keeping skills relevant and responses quick when non-conformities occur. Collaboration with academic and industrial partners brings fresh eyes to long-standing procedures, sometimes delivering step-changes in safety or efficiency.
The value in (2,6-Dimethyl-Phenyl)-Hydrazine comes not just from molecular properties, but from the lived experience of producers and users alike—a community defined by attention to detail and a shared commitment to progress. Our story with this compound reflects decades of work, mistakes overcome, and improvements made not by chance, but by intent and persistence. Customers—from small startups to established multinationals—shape the direction of our R&D and quality assurance. Regular exchange builds mutual understanding and drives the level of product and service that advances new science.