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3,5-Dichloroisonicotinic Acid

    • Product Name 3,5-Dichloroisonicotinic Acid
    • Alias 3,5-DCINA
    • Einecs 619-043-2
    • 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

    643367

    Productname 3,5-Dichloroisonicotinic Acid
    Casnumber 61910-62-9
    Molecularformula C6H3Cl2NO2
    Molecularweight 192.00
    Appearance White to off-white solid
    Meltingpoint 222-226°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Storagetemperature Store at 2-8°C
    Smiles C1=CN=C(C=C1Cl)C(=O)O
    Inchikey UYXPSCSBDFKKFP-UHFFFAOYSA-N
    Synonyms 3,5-Dichloro-4-pyridinecarboxylic acid

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

    Packing & Storage
    Packing White, sealed HDPE bottle containing 100 grams of 3,5-Dichloroisonicotinic Acid, labeled with hazard symbols, lot number, and handling instructions.
    Shipping 3,5-Dichloroisonicotinic Acid is shipped in tightly sealed, chemically resistant containers to prevent contamination and moisture absorption. Packaging complies with relevant regulatory standards for hazardous chemicals. During transit, the product is protected from heat and physical damage. All shipments include appropriate labeling and documentation for safe handling and transportation.
    Storage 3,5-Dichloroisonicotinic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from moisture, heat, and sources of ignition. Store separately from incompatible materials such as strong oxidizers and bases. Properly label the container and follow standard laboratory chemical storage protocols to ensure safety and maintain product integrity.
    Application of 3,5-Dichloroisonicotinic Acid

    Applications of 3,5-Dichloroisonicotinic Acid in Industrial Manufacturing

    As a direct manufacturer specialized in 3,5-Dichloroisonicotinic Acid, we support major industrial segments with controlled, reliable supply tailored for key downstream applications. The following sections detail established end-use routes, including regulatory context, technical incorporation in complex formulations, and finished materials manufactured from this chemical building block.

    1. Agrochemical Intermediate for Herbicide Synthesis

    Global crop protection formulators integrate this compound as an advanced intermediate for synthesizing triazolopyrimidine-based herbicides. Its chlorinated pyridine structure provides a core scaffold for downstream transformations, supporting selective weed management agents that target specific plant enzymes. Our technical team works directly with agrochemical producers to standardize impurity levels and maintain traceability throughout multi-stage reaction sequences, which is critical for large-scale field application registrations.

    Industry compliance standards

    • FAO Specification 2021 (Pesticide Technical Grade Standards)
    • ISO 9001:2015 Quality Management Systems
    • REACH Registration for European chemical compliance
    • China GB 2763-2021 (Maximum Residue Limits for Pesticides in Food)

    Typical usage ratio

    • Usage as intermediate: 0.08–0.23 mole per mole of target herbicide active ingredient; process chemists determine the exact charge based on desired chlorination pattern and yield optimization in downstream synthesis.

    Downstream process integration

    • Charged to reactor in the first condensation/cyclization step to assemble the heterocyclic herbicide core; or introduced in halogen exchange sequences at gram-to-tonne scales during process intensification.

    Final product types

    • Triazolopyrimidine sulfonamide herbicides (technical concentrate and granule formulations)
    • Selective broadleaf weed control agents
    • Post-emergence crop protection products

    2. Pharmaceutical Intermediate in Antiviral Drug Manufacture

    API manufacturers employ our material as a coupling partner for constructing nucleoside and nucleotide analogs, especially those requiring selectively substituted isonicotinic acids in their backbone. It undergoes specific amide or ester formation under cGMP-compliant operations. Since regulatory filings demand low residual solvents and high chemical purity, our production maintains strict batch release protocols and collaborative documentation support during process validation and international DMF submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/EP/BP Pharmacopeial Monographs (for starting materials and impurities control)
    • FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4 GMP Guidelines

    Typical usage ratio

    • Integrated at 0.05–0.15 mole per mole of target API intermediate; process development scientists adjust charge ratios based on coupling efficiency and downstream conversion rates.

    Downstream process integration

    • Introduced during the amidation/esterification or Suzuki coupling stage to embed chlorinated isonicotinic motifs into the nucleoside building block; monitored for residual carryover into finished API.

    Final product types

    • Antiviral nucleoside analogues (bulk API)
    • Pharmaceutical intermediates for chronic hepatitis and HIV therapies
    • Clinical trial materials for novel antiviral candidates

    3. Advanced Material Precursor for Electronic Chemicals

    Downstream specialty chemical producers use 3,5-Dichloroisonicotinic Acid in synthesizing tailored ligands and monomers for advanced material applications, such as organic semiconductors and photoresist resins. Its rigid aromatic skeleton and multiple chloro substituents allow for precision tuning of dielectric and film-forming properties. Electronic-grade batches require metallic, organic, and particle contaminant controls, with production harmonized to microelectronics base material standards and traceability protocols for lot-to-lot consistency.

    Industry compliance standards

    • SEMI C3-1112 (Specifications for Electronic Chemicals)
    • RoHS Directive 2011/65/EU
    • JIS K 5600 (Japan Industrial Standard for Coating Materials)
    • ISO 14001:2015 Environmental Management Systems

    Typical usage ratio

    • Formulated between 0.5–6.0% w/w relative to the total reactive monomer mass, with electronic material developers calibrating addition rates based on intended polymer dielectric constant and molecular architecture.

    Downstream process integration

    • Co-condensation or polymerization feed to synthesis kettles for monomer derivatization; optionally converted into ligand complexes prior to thin film formation or UV-cured resist composition blending.

    Final product types

    • Organic TFT materials
    • UV-curable photoresist polymers (liquid and dry film)
    • High-purity specialty coatings for microelectronic devices

    4. Fine Chemical Raw Material for Fluorescent Dye Production

    Dye companies adopt this acid as a building block for synthesizing novel fluorescent pigments used in analytical stains and biological imaging. It serves as a starting point for functional group modification, enabling bathochromic shifts and tailored solubility in aqueous systems. Dyes manufactured with this precursor undergo stringent analytical testing for trace impurities, colorfastness, and heavy metal content, driven by global laboratory reagent and diagnostic material benchmarks.

    Industry compliance standards

    • EN 71-3:2019 (Safety of Toys – Migration of certain elements)
    • ISO 18330:2003 (Chemical analysis for dyestuff products)
    • China Pharmacopoeia (bio-imaging reagent purity)
    • REACH Candidate List (Colorant chemical registrations)

    Typical usage ratio

    • Deployed at 1.5–5.0% w/w of the final dye molecule input mass, with synthesis chemists modifying ratios based on optical density targets, emission profile, and solubility characteristics.

    Downstream process integration

    • Used as the initial aromatic acid feed or as a late-stage coupling partner during heterocycle assembly and diazotization stages, followed by purification for high-purity dye concentrate production.

    Final product types

    • Fluorescent and chromogenic dye standards
    • Live-cell imaging reagents
    • High-sensitivity analytical probes (HPLC, TLC, FISH applications)
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    Certification & Compliance
    More Introduction

    3,5-Dichloroisonicotinic Acid: Behind the Product

    Deep Roots in Chemistry, Real-World Needs

    Working as a manufacturer in the fine chemicals sector, we’ve seen demand for reliable pyridine derivatives climb steadily. 3,5-Dichloroisonicotinic acid (also known as 3,5-DCINA) has established a presence because it serves actual, specific needs in downstream chemical syntheses. Not all compounds with two chlorine substitutions are equal—placement on the ring, purity profile, and physical behavior make a measurable difference. This matters on the ground, where process chemists, R&D teams, and analysts look for more than a number in a catalogue.

    We manufacture 3,5-DCINA with the formula C6H3Cl2NO2 and a molar mass around 192. As the producer, we control the incoming materials, batch protocols, washing regimes, and drying methods. In our hands, that means white-to-off-white crystalline material, low residual solvent, and a melting point held at the high end of theoretical range. Most batches show purity above 99%, confirmed by HPLC and NMR, because end-users rarely tolerate ambiguities in highly regulated or scaled-up reactions. Results depend on details that stay invisible at the commodity level.

    Purity, Consistency, and Stability: What We’ve Learned

    Making this molecule is not just a “make-and-ship” task. We’ve spent years fine-tuning how temperature, pH control, and solvents affect not only the yield but also unwanted isomers or trace metal contaminants. Chemists downstream often direct batch feedback straight to us—one report of reduced crystallinity, a faint color, or changed reactivity always gets our attention. Keep melting point and IR spectra within narrow bands, and scale-up headaches disappear before they start.

    Our teams rely on a process designed to limit the carryover of 3-chloro or 2,6-dichloro isomers. The reason goes beyond meeting assay minimums. Even low-level isomer contamination knocks off the confidence synthetic chemists have in planning multi-step reactions. Certain applications, especially agrochemical intermediates, require different solvents, less dustiness, or larger crystal sizes. These aren’t nice-to-have details. Our job is tracking these variations from the first synthesis step all the way to shipment.

    Usage: Where Technical Precision Matters

    Most of the 3,5-dichloroisonicotinic acid flowing from our plant becomes an intermediate in pharmaceutical and crop protection syntheses. What gives 3,5-DCINA a preferred role over similar dichlorinated isonicotinic acids is its reactivity pattern on the pyridine ring. Substitution on the 3 and 5 positions avoids side-reactions that would arise with 2,6 or 2,4 substitutions, especially under basic or catalytic conditions. Custom manufacturing partners ask specifically for our material because they want to minimize over-reactions in the next synthetic step.

    The acid group at the para position gives a predictable anchor for amide or ester formation—critical for fine-tuning the reactivity in heterocyclic drug intermediates and novel herbicides. Sometimes a customer requests salt forms or custom particle sizes. We address these through in-process modifications rather than “add-ons”—and nearly every adjustment comes from a real-world request. Teams specializing in lithium battery R&D have also started trials with 3,5-DCINA for coordination chemistry, exploring new use cases for high-performance materials. These innovations usually begin with a technical dialogue about our product characteristics.

    How 3,5-DCINA Stands Out

    The chemical landscape has plenty of alternatives: isomeric dichloroisonicotinic acids, trichloro variants, chloronicotinic acids, or even unsubstituted isonicotinic acid. End users often ask why to invest in a product with such a specific substitution pattern. Our experience aligns with the regulatory and technical perspective: 3,5-DCINA’s structure influences downstream steps, safety profiles, and post-reaction purification. Customers working on regulated pharmaceutical routes have shared that changing even a single ring position during scale-up cascades into new impurity bulletins, altered API pathways, and demands for revalidation.

    We have tracked the difference DCT (dichloro-triazine) versus DCINA makes in multicomponent reactions. In our feedback meetings, pharmaceutical clients regularly report that 2,6-dichloroisonicotinic acids—while similar on paper—introduce more side-products that are hard to purge without lengthy chromatography. 3,5-DCINA’s substitution leaves the meta positions open and reactive, enabling nucleophilic aromatic substitution with fewer byproducts. In real-life kilo-lab operations, this shaves weeks off development timelines.

    Scaling, Documentation, and the Manufacturer’s Advantage

    One difference between buying from a manufacturer and selecting from a trader can be summed up with a single question: Who knows the batch from raw material all the way to packaging? Our QC team signs off exclusively on what came off our lines, not on pooled lots or “upgraded” warehouse blends. This attention grants us traceability from every drum or bag of sodium nitrite used in chlorination, through to the finished crystalline acid. Every certificate points back to lot-specific data, not rounded averages.

    Regulatory specialists and auditors frequently ask for full disclosure of synthesis history, handling methods, and solvent recovery protocols. We accommodate DSUR, DMF, or REACH dossiers by holding back original batch documents, chromatograms, and even thermal residue records. As direct producers, we document our exhaust scrubber readings, worker safety controls, and spent acid recycling. We are open to audits when a client requests. The steady climb of regulatory complexity means fewer hands in the chain translate into cleaner, more reliable paperwork.

    Managing Risks in Sourcing and Stability

    Raw material fluctuations and evolving environmental rules mean manufacturers who handle their own synthesis must plan for supply chain shocks and compliance upgrades. Over the last decade, restrictions on certain chlorinating agents have forced us to shift from traditional methods to safer, more sustainable processes. Our investments in closed-loop recovery for spent solvents reduce not only waste but operational costs, letting us keep price volatility lower even as market conditions swing.

    3,5-DCINA is stable under standard conditions but shows minor degradation with prolonged exposure to moist air. We handle all packaging in controlled environments; sealed fiber drums with double-liner bags cut down risk of hydrolysis and dusting. It’s easy to overlook environmental stress testing, but every instance of supply chain interruption—extended transport delays, hot warehouse storage, or cross-contamination reports—teaches us which factors deserve ongoing attention in both routine and exceptional circumstances.

    Taking Feedback Seriously, Not Just Collecting Data

    We rely on feedback from users who run kilo-scale pilot projects, troubleshoot analytical outliers, or see residue during formulation. Much of what makes our product distinctive comes from small adjustments grounded in customer insights—not quarterly review metrics. For instance, a client using a high-temperature esterification once reported off-color residue after prolonged reaction. Rather than blame their process, we re-examined our own final wash protocol, discovering a need for a drier solvent system. The next three campaigns saw no recurrence of their issue.

    Sometimes it’s as straightforward as particle sizing: A major agrochemical developer needed slurry filtration to work without repeated clogging. Our technical group invested a month adjusting crystallization regimes to produce material that met their requirement without compromising purity. It’s seldom about hitting a specification; more often, it’s about listening to actual problems, then changing the process to remove roadblocks. Close partnership speeds commercial launches on both ends.

    Beyond the Reaction: Sustainability and Compliance

    Producing chlorinated pyridines demands both technical skill and responsibility toward environmental and worker safety. By managing our own effluent treatment and adopting a zero-discharge policy on organic solvents, we cut downstream liability for our customers. Most partners in regulated industries now insist on sustainability audits as part of their onboarding, and we stay ready to demonstrate continuous improvement in our plant operations. Closed-loop solvent systems, energy recovery, and ongoing reduction of hazardous waste—these have become standard practices, changing the expectations for all manufacturers, not just ours.

    Sourcing regulations from Europe, North America, and East Asia differ, but compliance always boils down to detailed records and direct plant-level controls. Each year brings new impurity limits, process residue restrictions, or classification changes, and we adapt procedures quickly because we own the process from start to finish. Working directly with regulators has changed how we think about both product consistency and social responsibility. For many of our end users, knowing the origin and compliance of their starting material has become as important as price or lead time.

    Addressing Challenges: Keeping Production Reliable

    Every year brings its share of unexpected process hurdles. A batch may crystallize differently due to a minor shift in water content or agitation speed. Camera images from filtration lines help us spot early hints of agglomeration or solvation defects before they contaminate a full run. Comparing infrared spectra over time, we catch any drift in impurity profiles, letting us tweak conditions before material ever leaves the site.

    Our staff understand the pressure customers face from regulatory deadlines, pricing pressures, and tight project schedules. Open, fast communication about lead time adjustments or supply interruptions means fewer downstream headaches for all involved. Real transparency—about stability concerns, raw material availability, or small non-conformances—helps chemical companies run smoother campaigns. Our goal: discover issues before customers need to ask.

    Solutions Grounded in Experience

    Manufacturing 3,5-dichloroisonicotinic acid at scale is an ongoing learning process. Over time, we’ve developed alternatives for the most common process challenges: unstable intermediates, persistent isomer contamination, or transport risks across climates. Introducing in-line monitoring and staged solvent recovery, we drive down both waste and cost while improving consistency.

    Problems don’t go away by accident. One year, we struggled with a rise in batch coloration that appeared only in late summer runs. Root cause traced back to slightly altered cooling rates due to ambient temperature shifts. Upgrading to closed system cooling eliminated this flavor of seasonal variability. We publish technical summaries of such adaptations for our clients, building trust through openness.

    Customers sometimes worry about upstream supply disruptions or potential regulatory bans. We respond by sourcing from multiple approved raw material suppliers, running secondary syntheses, and maintaining excess inventory when needed. These safeguards matter especially to API producers or global agrochemical firms where every delay is costly. By controlling the full production chain, we give downstream users relief from the unpredictability of a multi-tiered, opaque supply network.

    What Others Miss: Human Elements in Chemistry

    While instrument readings and certificates of analysis fill binders, real quality reveals itself in how a manufacturer responds to something going wrong. A trader may ship a generic lot from wherever is cheapest at the moment, but only the producer understands which batch variable caused a blip in color, odor, or reactivity. We answer technical queries by consulting the engineers or operators who ran the batch, not by referencing a product brochure.

    Chemistry is as much about reliable partners as it is about measured values. We serve scientists who want predictability, not surprises, in their synthesis chain. By working directly with the people developing new drugs, crop protection agents, or advanced materials, we create a feedback loop that produces better outcomes for everyone along the line.

    The Manufacturer’s Perspective: Looking Ahead

    Market and regulatory shifts force us to adapt, but our long-standing relationships with major chemical producers, pharma R&D labs, and custom synthesis firms keep our process robust and responsive. 3,5-DCINA evolves with the requirements of its users; every adaptation adds another layer of reliability. Whether the project relates to greener synthesis protocols, more stringent impurity controls, or new regulatory landscapes, owning the entire production pipeline lets us move faster and with more certainty than distributors or generic suppliers.

    The story of 3,5-dichloroisonicotinic acid isn’t only in a chemical structure or a purity value—it’s in the sum of incremental improvements informed by end-use experience, continuity, and a commitment to practical problem solving. Manufacturing gives a unique vantage point; it places responsibility and opportunity together.

    We continue to invest in both plant upgrades and technical support for the clients shaping what comes next for this versatile intermediate. In the end, chemistry remains a relationship between solution-finders, whether in a lab, on a production floor, or across continents. That’s how progress happens—step by step, and with direct engagement between those who make and those who innovate.