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2,3-Dichloroquinoxaline

    • Product Name 2,3-Dichloroquinoxaline
    • Alias 2,3-DCQ
    • Einecs 249-118-7
    • 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

    241712

    Product Name 2,3-Dichloroquinoxaline
    Chemical Formula C8H4Cl2N2
    Molecular Weight 199.04 g/mol
    Cas Number 3445-89-8
    Appearance White to off-white solid
    Melting Point 142-146 °C
    Density 1.51 g/cm³ (estimated)
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed
    Smiles Clc1nc2ccccc2nc1Cl
    Inchi InChI=1S/C8H4Cl2N2/c9-7-11-5-3-1-2-4-6(5)12-8(7)10
    Hazard Statements Irritant

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled "2,3-Dichloroquinoxaline, 25g", featuring hazard warnings and chemical identification details.
    Shipping 2,3-Dichloroquinoxaline is shipped in tightly sealed containers, compliant with safety regulations for hazardous chemicals. Packaging ensures protection against moisture, light, and physical damage. The shipment includes proper hazard labeling, documentation, and handling instructions. Transport is arranged via authorized carriers, following relevant local and international chemical transport guidelines to ensure safe delivery.
    Storage 2,3-Dichloroquinoxaline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it protected from moisture and direct sunlight. Store the chemical away from heat and ignition sources, and ensure that it is clearly labeled. Use appropriate personal protective equipment (PPE) when handling.
    Application of 2,3-Dichloroquinoxaline

    Applications of 2,3-Dichloroquinoxaline in Industrial Manufacturing

    2,3-Dichloroquinoxaline serves key roles across multiple chemical manufacturing sectors, contributing critical functional groups and structural motifs. Its performance and handling characteristics suit rigorous industrial synthesis workflows, supporting reliable scale-up and downstream integration.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers employ 2,3-Dichloroquinoxaline as a key intermediate for quinoxaline-based API scaffolds, especially in synthetic routes targeting anticancer, antimicrobial, and antiviral compounds. The compound’s dichloro substitution introduces valuable reactivity for selective nucleophilic substitutions and palladium-catalyzed coupling reactions. Controlled handling ensures impurity profile management and compliance with stringent drug master file documentation throughout multistep batch synthesis.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals (U.S. FDA)
    • European Pharmacopeia monograph requirements for relevant API intermediates
    • Chinese Pharmacopoeia standards for chemical raw materials

    Typical usage ratio

    • Used at 0.8–2.5 molar equivalents depending on target API; ratio adjusted according to substrate reactivity and impurity limits

    Downstream process integration

    • Fed into the early or mid-stage condensation, cyclization, or cross-coupling reactions
    • Undergoes purification prior to advanced intermediate transformations
    • Strict in-process sampling for trace residuals in line with regulatory filings
    • Sits in closed-setup reactors to minimize operator exposure

    Final product types

    • Anticancer small-molecule APIs (e.g., kinase inhibitors with quinoxaline cores)
    • Antimicrobial drug entities
    • Biosimilar active pharmaceutical ingredients incorporating nitrogen-containing ring systems

    2. Agrochemical Synthesis: Herbicide and Fungicide Precursors

    Within agrochemical plants, 2,3-Dichloroquinoxaline acts as a chlorinated heterocycle for the development of quinoxaline-based herbicides and fungicides. Its reactivity profile enables nucleophilic aromatic substitution and stepwise cross-coupling with tailored agroactive sidechains. Manufacturing attention focuses on scale-appropriate batch control, trace chlorinated byproduct limits, and downstream residue risk in accordance with agricultural sector regulations.

    Industry compliance standards

    • FAO/WHO Specification Guidelines for Pesticide Technical Material
    • EU REACH Regulation (EC) No 1907/2006 for plant protection product intermediates
    • China GB 2763 Maximum Residue Limits for Pesticides in Food
    • ISO 9001:2015 (Quality Management Systems - Agriculture Sector)

    Typical usage ratio

    • Introduced at 1.0–1.7 molar equivalents in multi-step syntheses depending on target herbicide/fungicide structure; process development determines substitution excess to minimize side chain loss

    Downstream process integration

    • Primary chlorinated heterocycle insertion via etherification or amination
    • Subject to residue testing prior to formulation blending
    • Inline QC sampling synchronized with batch campaign records
    • Integrated with process water and waste solvent capture systems

    Final product types

    • Selective post-emergence herbicides based on quinoxaline chemistry
    • Wheat and rice-field fungicides with chlorinated quinoxaline rings
    • Active concentrate intermediates for export formulation plants

    3. Specialty Dye and Pigment Synthesis

    Dye manufacturers use 2,3-Dichloroquinoxaline to introduce electron-withdrawing chlorine substituents or fund the quinoxaline core in high-stability pigment molecules. This compound supports selective functionalization for vivid, photostable pigments required in advanced coatings, printing inks, and polymer coloration. Process controls focus on consistent chromophore formation, lightfastness, and regulated impurity traceability from raw material through to finished batch testing.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textiles dyes
    • EN 71-3:2019 (Safety of Toys – Migration of Certain Elements) for coloring agents
    • ISO 13320 for particle size analysis in pigment formulations
    • Regulation (EC) No 1223/2009 (EU Cosmetic Regulation) when pigment used in personal care products

    Typical usage ratio

    • Utilized at 5–30% w/w basis in dye molecule synthesis, depending on pigment intensity and solubility requirements

    Downstream process integration

    • Acts in the first condensation or ring closure step with aromatic amines
    • Enters high-temperature reactors for pigment backbone formation
    • Follows with dispersion and milling prior to final product blending
    • Batch traceability maintained from raw material lot to final pigment coil

    Final product types

    • High-stability industrial coatings (metal, automotive, engineering plastics)
    • Inkjet printing pigments for packaging and commercial labels
    • Textile dyes for synthetic fiber coloration

    4. Advanced Material Monomer and Polymer Modification

    Producers of specialty resins and functional polymers introduce 2,3-Dichloroquinoxaline to create modified polymer backbones with nitrogen-heterocyclic functionality, improving thermal properties and stability. The dichloro substitution provides reactive sites for subsequent amination, etherification, or cross-linking, customizing the macromolecule for high-performance coatings and specialty composite materials. Continuous-polymerization lines employ strict feedstock purity and controlled addition protocols to manage molecular weight distribution and finished product consistency.

    Industry compliance standards

    • ISO 9001:2015 for process and quality system requirements in polymer manufacturing
    • EU RoHS Directive 2011/65/EU for electrical and electronic material composition
    • ASTM D638 for tensile properties of plastics
    • UL 94 Flammability Standard for plastic materials used in devices and appliances

    Typical usage ratio

    • Incorporated in the range 2–15% by monomer mole fraction, based on polymer application and property targets

    Downstream process integration

    • Charged directly into the monomer mix for batch or continuous polymerization
    • Feeds into pre-polymer preparation for chain extension or copolymer crosslinking
    • Allotment documented by in-process QC samples and retained reference batches
    • Follows with post-polymerization functionalization in specialty grades

    Final product types

    • High-performance engineering plastics used in automotive, electronics, and aerospace
    • Thermally stable coatings for industrial equipment
    • Specialty composite matrix resins for structural applications
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    Certification & Compliance
    More Introduction

    2,3-Dichloroquinoxaline: A Signature Intermediate in Advanced Synthesis

    A Closer Look at 2,3-Dichloroquinoxaline

    In the demanding field of specialty chemicals, producing consistent, well-characterized intermediates shapes the reliability of downstream applications. 2,3-Dichloroquinoxaline, with its chemical structure based on a dichlorinated quinoxaline ring, stands out in this respect. Several years on the manufacturing floor have shown me that every batch tells a story—one told by raw material quality, reaction control, and thorough purification.

    Produced in our reactors under tightly controlled parameters, 2,3-Dichloroquinoxaline emerges as a solid crystalline compound. The typical product batch achieves a purity of 98% or higher, judged by HPLC and elemental analysis. Consistency across lots matters so much in pharmacological and agrochemical syntheses that even a fraction of a percent difference shows up downstream—sometimes wrecking entire research cycles. We never lose sight of how much faith formulators and researchers place in these numbers.

    Why 2,3-Dichloroquinoxaline Earns its Place in Research and Production

    Many chemists look at dichloroquinoxalines for their unique reactivity, especially in nucleophilic substitutions. The electron-withdrawing effect of chlorine at the 2 and 3 positions brings about these reactivity changes. We’ve seen the compound play a backbone role in the fabrication of substituted quinoxalinyl pharmaceuticals, pesticides, and advanced materials. Over the years, demand for this molecule has only increased with the appetite for fine-tuned heterocyclic scaffolds.

    Let’s talk practical process. A synthetic chemist approaches our product looking for a robust, reliable starting material—one that doesn’t bring along byproducts, contaminants, or unexpected reactivity. 2,3-Dichloroquinoxaline fits that bill thanks to careful choice of feedstocks and close monitoring of reaction endpoints. Our technicians conduct GC and NMR sampling through each stage; not just as a box-ticking exercise, but because we know how much every impurity profile can shift outcomes further down the chain.

    Real-World Applications: Beyond the Laboratory

    While the lab may be the first stop, this compound has a reach that goes well beyond academic benches. In pharmaceutical synthesis, derivatives of 2,3-Dichloroquinoxaline find their way into kinase inhibitor research, antitumor candidates, and a growing envelope of central nervous system agents. Several AGRO majors select this compound when building new pesticide families. It’s also showing promise as a precursor for specialty dyes and optical brightening agents.

    Experience has shown us that success depends on reliability. A research group on a tight timeline cannot afford downtime caused by variable intermediates. Commercial-scale processes demand not only chemical purity, but consistent handling properties: flowability, particle size, and low moisture. In our manufacturing, careful tray drying, sieving, and sealed transportation remain non-negotiable steps. This helps downstream customers avoid caked-up material or sluggish dissolving, both of which can stall multi-ton syntheses. The pressure for speed and scale is nothing new, so avoiding such operational friction is a principle that’s ingrained in how we produce each batch.

    How 2,3-Dichloroquinoxaline Sets Itself Apart

    Not every quinoxaline or chlorinated heterocycle offers the same promise. Over the years, we’ve had requests from process chemists and R&D groups for material comparison runs. Take, for example, 6,7-dichloroquinoxaline or 2-chloroquinoxaline. They exhibit different regioselectivity during substitution and ring-opening, often limiting their utility for certain targets. 2,3-Dichloroquinoxaline has earned its reputation thanks to the accessibility of both chlorine atoms in substitution reactions, opening doors for precise introduction of amino, alkoxy, or aryloxy groups.

    From a process perspective, the crystalline product form and melting point of 2,3-Dichloroquinoxaline offers easier handling compared with more oily or waxy intermediates. Solid material is less prone to volatility and loss during weighing or transfer. The distinct pale yellow coloration also aids visual inspection for process operators: any variation from batch to batch signals potential impurities. Having spent days tracking down why a certain shipment shifted shades, my respect for physical inspection matches my faith in chromatography.

    Pain Points and Solutions from the Plant Floor

    Scaling dichloroquinoxalines remains demanding. Early on, physical hazards from exothermic halogenation taught us the value of reaction calorimeters. Monitoring temperature climbs during chlorination, especially beyond lab scale, is essential to avoid runaway reactions. Using continuous-feed addition and real-time cooling, we’ve reached a point where accidental hot spots simply do not occur. These investments, though significant, have paid back in uninterrupted supply and worker safety.

    Moisture sensitivity presents another challenge. Heterocyclic compounds, especially those with electron-deficient rings, tend to pick up water when handled in humid climates. Tight sealing, desiccant-lined drums, and climate-controlled storage cut spoilage to near zero, even during long ocean shipments. Our team learned this the hard way early in export, but now batch retention samples, stored at each production run, let us verify the integrity of every order over time.

    Efforts to minimize byproduct load also matter. Unwanted chlorinated side-products or residual starting materials can wreak havoc on yield calculations downstream. On our line, high-purity feedstocks, double-stage crystallization, and cross-lot analytical tracking close the gap between small-scale runs and full plant output. It’s a game of continual upgrades—a mindset of improvement that draws from every feedback call and customer complaint. No standard lasts forever, so the push for cleaner, safer, and more reproducible batches shapes every upgrade we fund.

    Supporting Data from Long-Term Production

    We track analytical trends across years, not just quarters. For 2,3-Dichloroquinoxaline, compiled data has shown that as purity climbs above 98%, yields in downstream synthesis also generally rise by several percent. Failure rates for pilot plant conversions dropped, leading to two fewer maintenance stoppages per year on one of our customer’s plants. Maintaining a low total impurity profile (less than 1% area by HPLC) avoids costly reprocessing in regulated environments, especially for pharmaceutical building blocks.

    Process documentation, too, reflects evolving knowledge. After several shipments received feedback about handling caked solids, we invested in vacuum drying steps and adopted new drum linings. Not every fix appears in academic papers or sales brochures. Some get logged in handwritten notes, passed down between shifts, or in morning review meetings. Institutional knowledge, hard won over thousands of batches, stands shoulder to shoulder with our technical data.

    Why Specification Alone Doesn’t Tell the Whole Story

    Some buyers, usually pressed for time, ask only for assay and impurity numbers. But anyone on the manufacturing side knows specification sheets never tell the full story. Handling properties, reactivity in real-world reactions, and the feel of the material out of the drum all shape success. Over the years, we’ve received samples from new suppliers—sometimes they look fine on the paperwork, but gum up equipment or show unusual solubility in process solvents.

    Our own product’s specs include melting point, color, assay, moisture, and particle size—each tested every run. Yet it’s the day-to-day experience of warehouse staff, chemists, and process engineers that fills in the blanks. We always encourage process chemists or plant managers to share back how material performs in their own setups. Data from end use helps close the feedback loop, refining both specs and production methods.

    Building Trust in a Changing Regulatory Landscape

    Every chemical producer now faces tighter oversight, both at home and in global markets. For compounds like 2,3-Dichloroquinoxaline, traceability and data accountability have become key. We audit our own processes not out of compliance box-checking, but as a safeguard for our end users who themselves operate under strict validation. Electronic batch records, sample retention for every lot, and careful logging of critical parameters build a chain of trust for everyone downstream.

    Several clients, especially in life sciences, require access to analytical data packs covering multiple lots. We provide these as a standard, not an afterthought. Transparency builds relationships that last longer than individual sales: feedback over years has steered us toward less hazardous reagents, greener solvents, and gradually tighter impurity controls. Sharing our knowledge of how batches behave under real transport conditions and storage atmospheres adds value that shows up in less rework and more confidence in each delivery.

    Looking Forward: Industry Challenges and Continuous Improvement

    What comes next for 2,3-Dichloroquinoxaline production? Growing demand asks us to balance output with sustainability. Raw material volatility pushes ever closer attention to supplier audits—staying ahead with alternate sourcing and in-house quality checks. Process safety and emissions monitoring continue to lead our capital investments: closed systems and automated handling reduce both worker risk and product contamination. We benchmark against both the best of peer producers and rigorous internal audits.

    Manufacturing fine chemicals never stands still. Experience taught us the value of listening: to customer feedback, supplier innovations, and our own front-line staff. Every safety incident, raw material inconsistency, or unexpected yield shift shapes tomorrow’s solutions. As experienced as our current plant crew is, they pass lessons forward so each batch, each shipment, gets a little better, a little safer, and a little more consistent. That’s the cycle that keeps this field both challenging and rewarding.

    Summary: 2,3-Dichloroquinoxaline as More Than a Commodity

    This compound does not just fill a line on a catalog list. It represents years of plant engineering, chemical insight, and operational care. Pharmaceutical, agricultural, and advanced materials companies trust that solving the fine details at the intermediate stage frees their teams to focus on breakthrough ideas rather than process troubleshooting. The everyday work of making, testing, and shipping 2,3-Dichloroquinoxaline underlines the importance of reliability and open communication between manufacturer and user.

    Every tank batch comes with its own small challenges—weather, raw material batch variation, equipment tuning. Solving these, quietly and consistently, helps keep the wheels of industry turning at speed. Our focus on hands-on improvement, person-to-person support, and a continual feedback loop drives both product quality and customer trust. In a time when technical excellence and practical know-how are at a premium, compounds like 2,3-Dichloroquinoxaline prove that real progress comes from a combination of sharp chemistry and day-to-day dedication.