2,5-Pyridinediamine, N2-(4-aminophenyl)-

    • Product Name: 2,5-Pyridinediamine, N2-(4-aminophenyl)-
    • Chemical Name (IUPAC): N1-(4-aminophenyl)pyridine-2,5-diamine
    • CAS No.: 5307-14-2
    • Chemical Formula: C11H11N5
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    145581

    Cas Number 5309-02-2
    Molecular Formula C11H11N5
    Molecular Weight 213.24 g/mol
    Iupac Name N1-(4-aminophenyl)pyridine-2,5-diamine
    Appearance Solid
    Melting Point Approximately 220-224°C
    Boiling Point Decomposes before boiling
    Solubility Slightly soluble in water
    Purity Typically >98%
    Synonyms N2-(4-Aminophenyl)pyridine-2,5-diamine
    Smiles c1cc(N)cc(n1)Nc2ccc(N)cc2
    Inchi InChI=1S/C11H11N5/c12-8-1-3-9(4-2-8)16-11-7-10(14)6-5-13-11/h1-7H,12,14H2,(H,13,16)
    Storage Conditions Store at room temperature, protected from light and moisture
    Hazard Statements May cause skin and eye irritation

    As an accredited 2,5-Pyridinediamine, N2-(4-aminophenyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,5-Pyridinediamine, N2-(4-aminophenyl)- is supplied in a 25g amber glass bottle, clearly labeled with safety and handling instructions.
    Container Loading (20′ FCL) Container Loading (20′ FCL): The chemical is securely packed in drums, efficiently loaded into a 20′ full container load for safe shipping.
    Shipping 2,5-Pyridinediamine, N2-(4-aminophenyl)- is shipped in tightly sealed containers, protected from light and moisture to prevent degradation. It should be handled under standard chemical safety protocols, including proper labeling and documentation. Shipping may require compliance with relevant hazardous material regulations depending on quantity and destination. Transport temperature should be controlled if specified.
    Storage 2,5-Pyridinediamine, N2-(4-aminophenyl)- should be stored in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Ensure proper labeling and use secondary containment to prevent leaks or spills. Handle using appropriate personal protective equipment and follow all safety guidelines.
    Shelf Life 2,5-Pyridinediamine, N2-(4-aminophenyl)- typically has a shelf life of 2 years when stored in a cool, dry, airtight container.
    Application of 2,5-Pyridinediamine, N2-(4-aminophenyl)-

    Purity 98%: 2,5-Pyridinediamine, N2-(4-aminophenyl)- with purity 98% is used in high-performance polymer synthesis, where it enables enhanced mechanical strength and durability.

    Molecular weight 198.22 g/mol: 2,5-Pyridinediamine, N2-(4-aminophenyl)- with molecular weight 198.22 g/mol is used in pharmaceutical intermediate production, where it ensures controlled pharmacokinetic properties.

    Melting point 165°C: 2,5-Pyridinediamine, N2-(4-aminophenyl)- with melting point 165°C is used in advanced dye manufacturing, where it provides superior thermal stability during processing.

    Particle size <10 µm: 2,5-Pyridinediamine, N2-(4-aminophenyl)- with particle size less than 10 micrometers is used in organic semiconductor fabrication, where it offers improved dispersibility and uniform thin-film formation.

    Stability temperature up to 120°C: 2,5-Pyridinediamine, N2-(4-aminophenyl)- with stability temperature up to 120°C is used in epoxy resin modification, where it maintains chemical integrity under processing conditions.

    Solubility in ethanol >50 g/L: 2,5-Pyridinediamine, N2-(4-aminophenyl)- with solubility in ethanol greater than 50 g/L is used in specialty ink formulations, where it facilitates homogenous solution preparation and consistent coloration.

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    Certification & Compliance
    More Introduction

    2,5-Pyridinediamine, N2-(4-aminophenyl)-: A Closer Look at a High-Purity Intermediate

    Practical Insights from the Manufacturer's Floor

    Producing advanced intermediates begins with recognizing each molecule’s unique structure and behavior. 2,5-Pyridinediamine, N2-(4-aminophenyl)-, often referenced by its CAS number 698-45-7, stands out in our manufacturing portfolio because of its finely tuned reactivity profile and selectivity in targeted applications. From years on the plant floor, we know quality in specialty pyridine derivatives comes from scrupulous attention not just to synthesis routes but to every step after — crystallization, purity adjustments, and packaging. This compound’s structure, integrating both a pyridine and a substituted aniline with dual amino functionalities, gives it utility where nuanced molecular frameworks matter most. Our batches draw on practical improvements earned through continuous in-house testing and feedback from downstream formulators who depend on consistent performance batch after batch.

    Model and Specifications That Make a Difference

    We supply 2,5-Pyridinediamine, N2-(4-aminophenyl)- as an off-white to light yellow crystalline powder. Rigorous attention is paid to elemental and spectroscopic purity, not just because regulatory standards demand it, but because chemists downstream tell us how even minor impurities can sabotage cyclization or cross-linking yields. Typical purity grades exceed 98%, consistently supported with HPLC and LC-MS data logged under each lot. Moisture control is not an afterthought: residual water can undermine both storage life and coupling efficiency, so we maintain Karl Fischer readings well within tight thresholds. Finished material arrives in moisture-barrier lined drums — not just as a packaging convenience, but because experience taught us what repeated cycles of warehouse heat and humidity can do to open or loosely bagged material.

    Our internal specifications don’t just stop at chemical purity. Particle size and morphology, though seemingly minor details, shape the reproducibility of certain reactions. We tune grinding and sieving operations to address customers’ insistence on a reliable powder flow, whether fed into glass reactors or steel kettles. During scale-up, we tackle agglomeration risk and minimize static-induced particle fines that can gum up feed hoppers — a problem any worker in production has cursed at one time or another. As a manufacturer, our metrics borrow as much from the realities of handling as from digital certificates of analysis.

    Where 2,5-Pyridinediamine, N2-(4-aminophenyl)- Finds Its Role

    Research and industrial teams reach for this compound where multifunctional building blocks are required for organic synthesis, particularly as a precursor to specialty heterocycles, or as an intermediate in pharmaceutical and advanced material sectors. Its structure brings both electron-donating and aromatic stabilization into synthetic plans — a feature that’s hard to duplicate if one slides in pyridine or phenylene diamines piecemeal.

    In one line of application, the dual amino groups at defined positions enable regioselective substitution, simplifying routes for active pharmaceutical ingredients or their analytical probes. Chemists synthesizing kinase inhibitors or developing complex ligands look for starting materials that will carry through multiple protection/deprotection or cyclization steps without introducing stubborn byproducts. We have received feedback from API producers who value the way our product’s stability under mild conditions helps maintain overall process economy — reducing the time spent on rework or byproduct separation.

    On the materials side, polymer chemists notice the impact of this molecule in forming robust, thermally stable resins and rigid aromatic frameworks. Some users adapt it towards manufacturing advanced coatings or diagnostic reagents, where clear spectral signatures and controlled reactivity are essential. Each order comes not just with a piece of paper, but with concrete practical support: if a user finds incompatibility with a planned synthetic sequence, we work alongside their R&D chemists to either resolve the route or adapt our process conditions.

    Comparing with Other Pyridinediamines and Substituted Arylamines

    Decades in chemical manufacturing have taught us that similar-sounding names on a catalog page mean little until one lives with a molecule in process. Compared to other pyridinediamines — such as 2,6- or 3,5-diaminopyridines — 2,5-Pyridinediamine, N2-(4-aminophenyl)- brings more than a shift in the nitrogen positions. The presence of the para-aminophenyl group extends its conjugation and permits specific downstream transformations that those other isomers can’t support.

    The handling profile is also different. For example, simple pyridinediamines might dissolve evenly across a range of polar solvents, but this extended molecule sometimes demands more nuanced solvent selection, especially at higher concentrations. We have had partners recount how they wasted valuable trial time before consulting us for practical guidance on achieving clean solutions or avoiding precipitate formation. Differences also emerge in reactivity towards alkylating agents or acylating conditions; more than once, a switch from a common diamine to this compound enabled access to substituted macrocycles or fused polyaromatics with fewer protection steps.

    Compared with plain aniline or para-phenylenediamine derivatives, our product stands out with the added reactivity and aromatic resonance from the pyridine ring. This isn’t merely a trivial substitution. The behavior in diazotization, oxidative coupling, and coupling with isocyanates or acid chlorides proves distinct. We’ve noticed how certain color-forming reactions in analytical chemistry, or in creating chromophores, benefit from the way this molecule bridges electron density between its rings. These properties are hard-won for researchers trying to push performance boundaries in their dyes or ligand scaffolds.

    Real Production Challenges and Solutions

    Experience in the plant teaches resolve. During the synthesis of 2,5-Pyridinediamine, N2-(4-aminophenyl)-, temperature and pH control write the difference between clean product and intractable tars. We built and refined stepwise addition protocols to moderate exotherms not just because vendors suggested it, but in response to our own batch failures and operator observations. Our records show reduced impurity levels after incorporating in-line monitoring and feedback adjustment of reactant feed.

    Waste management isn’t an afterthought. As our efficiency has grown, we found closed-loop solvent recovery indispensable. The synthesis generates a recognizable profile of side-streams, and over the years, our team developed treatment and recycling routines that allow us to reach recovery rates above industry averages. By minimizing impact on local water and reducing liabilities, we color our operational decisions with sustainability, not just regulatory compliance. This results in less solvent needed per ton synthesized over multi-year contracts, saving cost and reducing overall environmental risk.

    Shipping and storage require practical thinking. This compound, though stable under the right conditions, absorbs moisture and degrades if left exposed — a fact learned the hard way before moisture-barrier packaging became our rule. After rare but memorable customer complaints about off-color material, we devoted resources to better humidity monitoring, desiccant inclusion, and faster container turnover. There’s no substitute for seeing the real-life impact of a packaging shortcut on customer trust.

    Why Consistency and Traceability Matter

    From our own operations and customer audits, we know process traceability and documentation make the difference between routine supply and regulatory headaches. Each drum is traceable back through every production variable: batch number, reactor used, sequence of reagent additions, cleaning procedures, and the raw material sources. During line audits from major pharmaceutical partners, this transparency has prevented cascading project delays.

    Counterfeit and substituted intermediates have occasionally flooded the market. Few things damage process efficiency and quality assurance faster than unverified supply lines. Our system locks down every shipment with documented origin, in-plant analysis files, and test data unlinked from external brokers. New customers often tell us about reliability issues they faced from third-party resellers — fluctuating melting points, unidentified TLC spots, inconsistent color or lumping. That led them back to a manufacturer who stands behind the product from start to finish.

    Listening and Learning from Application Feedback

    Real-world results shape continuous improvement. We’ve had NMR analysts call with questions about minor peak shifts and GC-MS specialists requesting batches with tighter impurity controls. These conversations lead directly to process refinement, not just polite reassurances. One customer’s trouble with C-N cross-coupling reaction inhibition led us to test different recrystallization protocols, finding conditions that minimized a stubborn side impurity. Another’s need for particularly fine powder initiated a 6-month evaluation of milling techniques. Both cases resulted in process overrides for specific runs, now reflected in the main batch cycle.

    Our collaboration with polymer innovators opened new directions, especially in the design of rigid backbones for high-performance materials. Joint studies have illuminated where subtle impurities could impact polymer chain integrity — details only revealed by close, ongoing technical dialogue. Such partnerships have reaffirmed the value of direct technical support and transparent process adaptation, an advantage hard to match when dealing through distant supply chains.

    Challenges and Solutions in Secure, Sustained Supply

    Supply chain stability for starting materials and intermediates stands as a top concern. Raw materials for 2,5-Pyridinediamine, N2-(4-aminophenyl)- sometimes fluctuate in price and availability, especially when upstream demand in electronics or fine chemicals spikes. Having multiple pre-qualified sources and maintaining an inventory buffer, even when market pressure tempts otherwise, has kept our regular customers insulated from disruption. This policy did not stem from a corporate directive, but from previous order backlogs and missed delivery dates no manufacturer wants to repeat.

    Periodic technical reviews with our procurement and production teams identify speculative changes, such as alternate catalyst use or shifts in solvent grades, and test them extensively before any production scale-up. We’ve learned not to gamble with process reliability just to save on reagent cost, as the extra help requests from struggling end-users quickly outpace any imagined savings. That vigilance protects our entire downstream supply chain.

    Why Investing in Continuous Manufacturing Pays Off

    Batch production has its merits, but years of direct process control revealed opportunities in continuous manufacturing for specialty intermediates like this one. Steady-state operations have trimmed batch-to-batch variability, allowed prompt impurity correction in real time, and reduced the manual adjustments that once led to inconsistencies.

    Investing in inline analytical controls and data logging contributed more than smoother internal audits. It shortened lead times and allowed us to promise and deliver faster turnaround — a real differentiator for customers aiming for short development timelines. In recent years, these process improvements have allowed us to anticipate bottleneck risks and ramp up capacity on weeks’ notice, even as demand cycles shift.

    Summary of Lessons from Direct Manufacturing Experience

    Years of direct experience producing and supporting 2,5-Pyridinediamine, N2-(4-aminophenyl)- have made us cautious about promising shortcuts, but confident in delivering reliability. This intermediate brings clear advantages for synthetic complexity and process efficiency beyond its catalog descriptors. Our attention to control from raw material intake through packaging and logistics has been shaped as much by troubleshooting real production problems as by formal quality control policies. The result: a dependable, high-purity product whose behavior in the field we know first-hand — details not caught in standard technical literature.

    Users looking for more than a simple commodity will find in this compound a useful platform for both established applications and emerging needs. We remain open to technical dialogue, knowing each new downstream use provides feedback that can bring the next iteration of improvement. This two-way street between manufacturing plant and R&D laboratory sits at the core of producing not just a molecule, but a tool for real innovation.