Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

5-Chloro-2,3-Diaminopyridine

    • Product Name 5-Chloro-2,3-Diaminopyridine
    • Alias 5-Chloro-2,3-pyridinediamine
    • Einecs 636-044-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    131728

    Product Name 5-Chloro-2,3-Diaminopyridine
    Cas Number 23056-74-2
    Molecular Formula C5H6ClN3
    Molecular Weight 143.57
    Appearance Off-white to light brown solid
    Melting Point 135-139°C
    Purity Typically ≥98%
    Solubility Soluble in water, DMSO, and methanol
    Synonyms 5-Chloro-2,3-pyridinediamine
    Smiles C1=CC(=NC(=C1Cl)N)N
    Storage Conditions Store at 2-8°C
    Safety Phrase Irritant; avoid contact with skin and eyes
    Ec Number 245-718-7

    As an accredited 5-Chloro-2,3-Diaminopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle sealed with a tamper-evident cap, labeled "5-Chloro-2,3-Diaminopyridine, analytical grade, 25g."
    Shipping 5-Chloro-2,3-Diaminopyridine is shipped in tightly sealed containers to prevent moisture and contamination. Packaging complies with relevant regulations, ensuring safe handling and transit. It is typically transported at ambient temperature, with proper labeling for hazardous materials, and accompanied by safety data sheets for safe storage, use, and emergency procedures.
    Storage 5-Chloro-2,3-diaminopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances (such as strong oxidizing agents). Keep away from moisture and sources of ignition. Store at room temperature or as otherwise specified on the material safety data sheet (MSDS). Proper labeling and secondary containment are recommended.
    Application of 5-Chloro-2,3-Diaminopyridine

    Applications of 5-Chloro-2,3-Diaminopyridine in Industrial Manufacturing

    As an established manufacturer, we supply 5-Chloro-2,3-diaminopyridine for specialized industrial applications where precise chemical performance, compliance, and formulation transparency are required. This section outlines its principal uses in downstream processes, highlighting relevant standards, formulation ratios, manufacturing process stages, and end-product types in which this material plays a critical role.

    1. Pharmaceutical Intermediate for API Synthesis

    5-Chloro-2,3-diaminopyridine serves as an essential building block in the synthesis of selected active pharmaceutical ingredients, particularly those derived from pyridine scaffolds. Its controlled reactivity preserves the required substitution patterns during heterocyclic assembly, making it integral for guaranteed product quality. Downstream pharmaceutical manufacturers integrate it into multi-step syntheses, carefully managing traceability and residual compliance at each stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP Requirements)
    • Ph. Eur. (European Pharmacopoeia) monographs for final APIs
    • USP/NF where relevant for pyridine-based APIs

    Typical usage ratio

    • 0.1–0.6 molar equivalent, depending on desired substitution in target API core; optimization aligns with stepwise reaction yield and purity requirements

    Downstream process integration

    • Added to solution-phase synthesis during coupling or ring construction steps; typically enters after initial framework assembly to achieve selective diamino chlorination

    Final product types

    • Antiviral drug intermediates
    • Anti-inflammatory agents based on pyridine motifs
    • Analgesic active pharmaceutical ingredients
    • Other specialized APIs requiring aminopyridine derivatives

    2. Dye and Pigment Intermediate

    Chemical producers value 5-Chloro-2,3-diaminopyridine for its function as a core reactant in azo and metal-complex dye production. Its specific substitution pattern imparts necessary chromophore precursors when integrated during dye manufacture, impacting hue stability and fabric compatibility for downstream textile and ink applications. Compliance scrutiny emphasizes restricted impurity content and batch traceability.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for regulated dye intermediates)
    • REACH Regulation (EC) 1907/2006 for chemical substances
    • ZDHC MRSL for restricted chemical lists in textile processing

    Typical usage ratio

    • 5–18% by weight relative to total aromatic amine basis; adjusted to control color depth and reactivity with diazotized components

    Downstream process integration

    • Charged into batch reactors following diazotization of aromatics, enabling coupling to form stable dye intermediates, then further processed for metal-complex or direct dyes

    Final product types

    • Metal-complex dyes for textile and leather finishing
    • Azo functional dyes for printing inks
    • Direct dyes for cellulosic fibers
    • Colorant dispersions for industrial coatings

    3. Agrochemical Synthesis Building Block

    Many downstream agrochemical companies adopt this material as a definitive intermediate in the formulation of pyridine-based crop protection agents. Precision in addition sequence ensures no unwanted side-reactions, supporting the consistent synthesis of fungicide and herbicide cores under strictly regulated environmental and worker safety norms.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management (for agrochemical production)
    • Directive 2009/128/EC (Sustainable Use of Pesticides in the EU)

    Typical usage ratio

    • 0.2–1.1 molar equivalents, modified based on targeted heterocycle in active molecule and desired conversion rate; precise ratio determined via pilot synthesis

    Downstream process integration

    • Introduced after initial halogenation or amidation to construct the diamino-substituted pyridine ring central to the active ingredient structure

    Final product types

    • Pyridine-based herbicide intermediates
    • Fungicide methylpyridine derivatives
    • Seed treatment actives
    • Soil protection additive intermediates

    4. Specialty Polymer Modification

    Polymer and advanced materials manufacturers rely on 5-Chloro-2,3-diaminopyridine to impart specific amine/chloro branching sites in specialty polyamide and polyimide production. Its incorporation improves solubility profiles and customization for application-driven properties such as heat resistance and electrical insulation. Ratio and timing of addition are governed by proprietary R&D and process qualification requirements.

    Industry compliance standards

    • ISO 9001:2015 (Quality Systems for advanced polymers)
    • RoHS Directive 2011/65/EU (for electronic-grade polymers)
    • UL 94 flammability classification (for electrical insulation applications)

    Typical usage ratio

    • 0.5–3.0% by weight in final monomer charge, adapted to achieve desired cross-linking density or thermal property modification; balance depends on end-use performance targets

    Downstream process integration

    • Dosed during monomer blending or copolymerization to introduce functional amine and halogen groups before polymer chain extension and finishing

    Final product types

    • Heat-resistant polyamides
    • Engineered thermosetting polyimides
    • High-performance coatings for electronics
    • Insulating films and molded polymer parts

    5. Chemical Reagent for Analytical Chemistry

    Analytical laboratories and specialty reagent producers integrate 5-Chloro-2,3-diaminopyridine in standardized colorimetric assays and trace metal analysis, leveraging its unique reactivity for high selectivity in spectrophotometric readings. Downstream users require tight purity specifications and validation under regulated laboratory quality frameworks.

    Industry compliance standards

    • ISO/IEC 17025 accreditation (for analytical laboratories)
    • Sigma and ACS reagent grade qualification
    • REACH Annex XVII (laboratory chemical restrictions)

    Typical usage ratio

    • 0.02–0.1% in working analytical mixtures based on calibration range and sample matrix; adjusted to minimize matrix interference while maintaining sensitivity

    Downstream process integration

    • Prepared into standard solutions for batch colorimetric testing or as starting reagent in trace analysis kits requiring selective derivatization

    Final product types

    • Chemical reagent kits for metal ion detection
    • Analytical standards for laboratory QC
    • Custom reference solutions for environmental monitoring
    • In-house operational solutions for industrial process analytics
    Free Quote

    Competitive 5-Chloro-2,3-Diaminopyridine 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 5-Chloro-2,3-Diaminopyridine: Developed and Delivered by the Manufacturer

    Our Long-Term Commitment to Chemical Precision

    For over two decades, our daily work in chemical synthesis has brought a wide range of fine chemicals and building blocks into research and industry labs around the world. Among the thousands of compounds we handle each year, 5-Chloro-2,3-Diaminopyridine frequently stands out as a critical choice for advanced pharmaceutical intermediates and heterocyclic compound synthesis. Unlike most third-party outlets, our approach begins at raw materials, continues through every stage of synthesis, and ends with in-house analysis before the product reaches your facility. The value of this vertical integration becomes clear to anyone who has pushed a reaction to scale, faced batch-to-batch variances, or needed a reliable partner to troubleshoot a fussy step in pyridine functionalization.

    Understanding 5-Chloro-2,3-Diaminopyridine

    5-Chloro-2,3-Diaminopyridine, often referenced by researchers under the model DAP-C5, occupies a prominent place among the substituted pyridines because of the way its structure couples electronic effects with practical reactivity. This molecule, with a chloro substituent at the 5-position on a pyridine ring and amino groups at the 2 and 3 positions, brings a desirable combination of reactivity and selectivity to the table. Years of working hands-on in this field taught us that small changes in the positions or substitutions of the ring can mean a world of difference in lab performance or scalability. Where other halogenated diamino derivatives sometimes stall progress with inconsistent supply or uncertain purity, our process allows us full visibility into every stage: from selection of starting chloropyridine stock to final analytical verification.

    Why 5-Chloro-2,3-Diaminopyridine Serves Key Industry Needs

    What gets overlooked in the conversation about fine chemicals is the true cost of downtime or rework when a batch fails. In medicinal chemistry, especially, the pressure to move quickly from library design to lead identification never lets up. Delays in the supply of a critical intermediate can ripple through entire projects. Working directly from manufacturing, we see demands change in real time. One month, the emphasis might fall on compound library expansion. Next, a particular substitution pattern—like 5-chloro with ortho diamino groups—suddenly becomes the scaffold everyone needs. Because we handle the synthesis start-to-finish, our technical staff tracks the entire development timeline alongside our customers. If a research team encounters solubility trouble or a tricky reactivity profile in their downstream steps, we regularly consult with them, sometimes adapting purification or amination methods to bring a custom solution closer to their specific workflow.

    The backbone of this molecule serves not only pharmaceutical and agrochemical R&D, but also advanced materials science. Experienced chemists reach for 5-Chloro-2,3-Diaminopyridine to create diverse ligands, functionalized heterocycles, and novel catalyst precursors. Its structure gives distinct synthetic handles—chloro for cross-coupling or aromatic substitution, amino groups for condensation and derivatization. Over and over, it demonstrates versatility not just as a static reagent, but as an engine for new research pathways.

    Physical and Chemical Profile Backed by Experience

    We manufacture 5-Chloro-2,3-Diaminopyridine in crystalline form. After repeated batch trials and customer feedback, we standardized our offering as a free-flowing light brown to tan crystalline solid. Melting point and identity checks are performed on every run, using HPLC, NMR, and elemental analysis protocols refined in our own labs. Unlike generic suppliers who might offer similar molecules but with variable methods, every kilogram that leaves our production site comes with a data set built from the very same analytical machines our chemists use for process monitoring and problem-solving.

    Long before a drum or an ampoule is packed, our technicians confirm the absence of unwanted isomers, verify the moisture content, and confirm process reproducibility. Our drying steps—proprietary but rooted in fundamentals—help extend shelf-life under ambient storage. Avoiding excess humidity or unknown residual solvents appears trivial, but it has made the difference for customers who need a clean baseline for crystallizations or further modifications. From years of feedback, we’ve trimmed our specification range to what synthetic chemists actually need for reliable scaling and trouble-free handling, rather than just matching abstract regulatory demands.

    Comparing 5-Chloro-2,3-Diaminopyridine to Other Relevant Pyridines

    A lot of organizations focus only on “what’s available now” inventory. Direct involvement in development chemistry teaches us to anticipate future needs as well. Many researchers come to us after trying similar molecules—say, 2,6-diaminopyridine or 3,4-diaminopyridine—with mixed success. In our experience, 5-Chloro-2,3-Diaminopyridine’s balance of reactivity, steric availability, and moderate electron withdrawal makes it work where other diamino derivatives do not. The position and presence of the chloro group also change how substitution or ring transformation reactions proceed.

    We have tested the difference on multiple preparations: Some halogenated diamines show unpredictable behavior in Suzuki or Buchwald cross-couplings, reacting sluggishly or giving unwanted byproducts. Our in-house teams kept detailed records of how our DAP-C5 model handles these reactions. Under controlled laboratory conditions, we see better control of site selectivity, and isolation of intermediates comes easier. The lack of uncontrolled moisture and microimpurities—a common issue with older commercial stocks—means fewer unwanted side reactions or colored residues.

    Common Applications in Synthesis and Beyond

    Work in intermediate-scale production highlights just how many companies now adopt the molecule for targeted synthesis of pharmaceuticals and agrochemicals. Contract research teams rely on it for creating new pyridine-based kinase inhibitors or as a scaffold for anti-infective programs. Its role in making high-affinity ligands and specialty dye precursors continues to grow. Our pharmaceutical partners use it for both bolt-on amide formation and as a precursor for heterocyclic ring systems that form the backbone of promising new APIs. We see requests not only for standard bulk supply but also for kilo-lab support, pilot trials, and special purity or particle size batches aimed at unique demands.

    In advanced materials, the molecule offers robust potential for surface modification, ligand-directed assembly, and the development of functional films. Having manufactured its relatives—like 2,3-diaminopyridine, 5-bromo-diaminopyridine, and others—we routinely compare data to steer our customers toward the compound best mapped to each application, rather than simply selling what is at hand. Our technical team builds custom records on each of these jobs, accumulating not just analytical data but process narratives our customers can access for troubleshooting or planning new experiments.

    Manufacturing Practice: More than an Assembly Line

    Automated plants and high-output facilities often lose sight of the problems researchers meet in small-scale reactions. Working directly with chemists reveals the impact of tiny differences. Sometimes, our lots ran unexpectedly due to a shift in an upstream intermediate’s impurity profile, and we caught it only because our lab staff still personally reviews each NMR spectrum. The hands-on culture we built rewards vigilance—once, we caught a trace contaminant that hadn’t even shown in a standard QC protocol, all because one of us noticed a faint off-color during crystallization. That level of scrutiny remains one of our strongest contributions to everyone relying on our product for critical projects.

    Lessons learned from production scale translate directly to service. During a scale-up collaboration with a leading R&D outfit, we assisted in adjusting reaction solvents and crystallization steps to line up batch yields and purity targets. On another occasion, after a partner encountered blockage in downstream amination, we investigated the fine structure via LC-MS, identified a hidden impurity, and tuned our process accordingly. Our lines stay open to customer suggestions, and we keep development flexible—sometimes making subtle shifts in our protocol to cater for unusual or high-spec requirements. What gives us confidence is knowing every fix or improvement tested on our own line, before we recommend it.

    Storage, Handling, and Ongoing Support

    Beyond chemical and physical benchmarks, storage and consistency affect everyone’s project clock. From our experience, uncoated storage vessels and temperature fluctuations degrade certain pyridine derivatives. Our facilities keep temperature and humidity under strict control. Each lot undergoes stability trials, so we know and can advise on optimal storage. Simple practices—airtight jars, minimal handling, protection from excessive light—have allowed customers to keep stocks active for extended periods, sometimes outlasting typical supplier guarantees by several months. Customers often seek our input on handling after experiencing clumping or discoloration with other sources. We guide them on best practices earned from years of handling these bench-top challenges ourselves.

    For labs working up scale, material safety, and waste-handling advice sometimes means the difference between a clean process and a logistical bottleneck. Our on-call application scientists have run the same reactions on the bench, so they avoid abstract answers and can walk customers through solvent choices, waste neutralization, and even tips on filtration and drying. Our documentation notes real-world troubleshooting and observations that only come from repeat hands-on experience with 5-Chloro-2,3-Diaminopyridine.

    Building Trust through Responsible Sourcing and Analysis

    As direct manufacturers, we control each precursor’s quality and investigate the supply chain end-to-end. There have been times when a supplier batch of 5-chloropyridine didn’t meet our standards. Rather than passing those risks down the line, we rejected the batch at the intake stage. The better the control at each step, the less risk for everyone testing a new synthetic route. Regulatory and environmental requirements keep shifting; our team keeps pace by updating our processes to meet compliance, monitor residues, and document trace elements more stringently than typical market practice.

    During every campaign, in-process samples get retained for future analysis. This helps us respond to any questions that arise months or even years after initial delivery. In one memorable case, a partner faced unexpected side products in a long-term clinical-scale program, and by going back to archive samples, we isolated the root source in a surrogate byproduct, tracing all variables from years before. This isn’t about hitting targets in a spec sheet; it’s about knowing the batch story from synthesis through use, and building a relationship of reliability with every firm we supply.

    Preparing for Tomorrow’s Research Directions

    The world of chemical development changes with new academic discoveries, emerging therapeutic targets, and the shifting emphasis of the bioeconomy. Staying involved from the level of research discussions up through plant operation keeps us ahead of trends. Whether it’s rising interest in bidentate ligands for catalysis, expansion of pyridine libraries for fragment screening, or new uses in dyes and photonics, 5-Chloro-2,3-Diaminopyridine stays relevant in our catalog for a reason. Experience showed us that keeping the channel open between lab work and scaled production benefits everyone downstream.

    Our staff joins roundtable discussions, participates in scientific partnerships, and stays informed about both failed and successful applications. Over the years, we have contributed insight at symposia on heterocyclic chemistry, shared case studies from partnering with pharma and agrochemical projects, and taken feedback all the way back to our pilot reactors. This enables us to anticipate demand, plan supply, and offer guidance to new ventures as they scale up their chemistry.

    Collaboration, Not Just Supply

    No two projects are identical. A standard product offering might serve most applications, but sometimes an extra level of purity, or a tuned physical form, gives a commercial advantage. Through years of developing 5-Chloro-2,3-Diaminopyridine alongside diverse customers, we learned the value of working as partners rather than arms-length vendors. Our chemists answer technical queries directly, with answers based on running similar reactions in our own labs, and are prepared to dig into the details, whether the issue involves analytical data, stability, or reaction optimization.

    Many clients appreciate our willingness to handle requests for custom quantities, modified crystallinity, or blended batches for high-throughput screening. We don’t outsource these requests, preferring to build the solution internally and keep knowledge among our core group. Over time, this approach has led to improved formulas, fewer surprises, and a track record of practical, incremental innovation. Instead of just moving product, we aim to move the work forward for everyone who partners with us.

    Continuous Improvement Driven by Real-World Challenges

    No process reaches perfection, and each year brings new lessons. Feedback on filtration rates, appearance, or solubility often comes from customers in the middle of a deadline. By taking every comment seriously—and connecting back to earlier pilot runs or side experiments—we’ve incrementally improved everything from drying methods to purification solvents. Generics suppliers might settle for “good enough,” but hands-on production teams know that a single recurring impurity can haunt a reaction cascade for months. Our own scale-ups informed minor tweaks. One request for a finer particle size batch led us to review and customize our milling protocols until we met the target, which then became standard practice for that application range.

    Analytical improvements don’t stop at batch release. We’ve invested in up-to-date chromatographs and direct hands-on training. This commitment shows itself in the clarity of our certificates and the confidence customers express when troubleshooting with us. Problems don’t always stop at the supplier’s door, and by sharing our full analysis history and batch notes, we help our partners manage unexpected outcomes in their work.

    The Manufacturer’s Perspective: Value Beyond the Batch

    Providing 5-Chloro-2,3-Diaminopyridine is more than a transaction. From acquiring well-documented starting materials, through systematic synthesis and purification, on to real technical support and repeat partnership, we have learned that true value lies in transparent manufacturing and practical support. Our experience proves that controlling every step—rather than relying on brokers or hidden subcontractors—leads to more consistent outcomes for everyone downstream. Every jar holds not just a reagent, but the work, care, and expertise built up over years focused on quality chemistry.

    For any team preparing to launch a new synthesis, scale up a program, or troubleshoot a hard-to-control reaction, working with a manufacturer that invests in knowledge, not just inventory, makes a measurable difference. We remain dedicated to raising the standards for production, analytics, and partnership, so that every batch of 5-Chloro-2,3-Diaminopyridine supports ambitious, innovative, and successful science. Our doors are always open to the feedback and collaboration that keep us moving forward with every project we support.