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HS Code |
105789 |
| Cas Number | 13015-88-8 |
| Molecular Formula | C3Cl2N2 |
| Molar Mass | 134.96 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 74-76 °C |
| Boiling Point | 230-235 °C (decomposes) |
| Density | 1.56 g/cm³ |
| Solubility In Water | Reacts with water |
| Iupac Name | 2,2-dichloropropane-1,1-dinitrile |
| Synonyms | 2,2-Dichloromalononitrile |
| Pubchem Cid | 218699 |
As an accredited Dichloromalononitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 g of Dichloromalononitrile is supplied in a tightly sealed amber glass bottle with hazard labeling and chemical identification details. |
| Shipping | Dichloromalononitrile should be shipped as a hazardous chemical, in accordance with relevant regulations (such as DOT, IATA, or IMDG). It must be securely packed in airtight, labeled containers, protected from moisture and incompatible substances, and placed within appropriate secondary containment to prevent leaks. Shipping requires documentation and hazard labels indicating toxic, irritant, and environmental risks. |
| Storage | Dichloromalononitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases, oxidizing agents, and moisture. The storage space should be clearly labeled, secure, and equipped with proper containment to prevent accidental spills. Protective equipment should be readily available, and access restricted to authorized personnel. |
Applications of Dichloromalononitrile in Industrial ManufacturingDichloromalononitrile provides advanced reactivity in several industrial sectors. As the original manufacturer, we collaborate closely with downstream users in pharmaceuticals, agrochemicals, dyes and pigments, polymer intermediates, and advanced materials. We produce at high purity to support demanding synthesis and formulation requirements. 1. Pharmaceutical Intermediate for Pyrimidine SynthesisPharmaceutical manufacturers use dichloromalononitrile as a key precursor in synthesizing heterocyclic building blocks, especially for pyrimidine derivatives. The high electrophilicity of this compound enables selective condensation with amidines or ureas. Downstream facilities employ it in tightly controlled, anhydrous batch reactions, where it acts as a core fragment for antiviral, anticancer, and CNS drug scaffolds. Precision in process design maintains product quality and impurity profiles to comply with drug regulatory frameworks. Industry compliance standards
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2. Synthesis of Herbicidal and Pesticidal Building BlocksDichloromalononitrile is a core component in the agrochemical industry, providing chlorinated nitrile groups that enable downstream manufacturers to construct unique herbicidal backbones. It enters production as a key intermediate for selective synthesis of triazine and pyridazine derivatives. Strict handling protocols apply to manage exothermic profiles and ensure final product consistency. Users must adapt charge ratios based on crop-selectivity needs and regional regulatory tolerances. Industry compliance standards
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3. Chromophore Construction for Dyes and PigmentsColorant and pigment manufacturers employ dichloromalononitrile as a nucleophilic acceptor in condensation reactions forming key chromophore systems. Its dichloro-nitrile functionality allows for precision substitution, enabling the fabrication of high-performance pigments notable for thermal and solvent stability. Formulators monitor reaction kinetics and solvent profiles to achieve batch-to-batch consistency required for downstream textile, ink, and plastic coloration. Industry compliance standards
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4. Preparation of Functional Polymer IntermediatesPolymer manufacturers use dichloromalononitrile as a functional monomer or cross-linker precursor, especially in synthesizing high-density engineering plastics and specialty resins. Its dual nitrile groups allow for site-specific polymer backbone modifications. Downstream plants integrate it in reactive extrusion or bulk polymerization, often modifying the input ratios for targeted molecular architectures and cross-link densities. Finished polymer products benefit from improved chemical resistance and thermal stability. Industry compliance standards
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5. Advanced Material Synthesis for Organic ElectronicsManufacturers of organic semiconductors utilize dichloromalononitrile for introducing electron-withdrawing nitrile groups during the synthesis of organic field-effect transistor (OFET) or organic photovoltaic (OPV) materials. It plays a role in constructing conjugated electron acceptor moieties, facilitating bandgap tuning for advanced electronic devices. Precision in purification and reaction stoichiometry supports the fabrication of high-purity, low-defect electronic grade materials. Industry compliance standards
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Navigating the world of fine chemicals, we've seen firsthand how small molecules like dichloromalononitrile shape innovation across industries. Much more than just a commodity, each drum represents years of optimization, experimentation, and industrial discipline. From the first batch we produced at scale, we recognized that dichloromalononitrile needs careful handling and real experience to yield consistent results. Our chemists approach this compound with focus—both to maximize its quality in synthesis and to ensure its safety in every container that leaves our production site.
We offer dichloromalononitrile as a crystalline solid. Each batch rolls off the line with a typical purity above 98%. Our process tracks moisture, residual solvents, and traces of similar nitriles, maintaining integrity for demanding industrial applications. Years spent refining our crystallization and purification have trimmed undesirable byproducts. Batch-to-batch consistency isn’t a catchphrase in our facility—it is a guarantee, relying on tight instrumentation and the practiced eyes of our lab team. A bottle from last year matches a shipment from this morning: the same melting point, the same reactivity profile, the same crystal structure.
Dichloromalononitrile (CAS No. 628-45-7) doesn’t blend in among common nitriles. Its formula, C3Cl2N2, brings a unique double chlorination to the malononitrile backbone. This feature means extra electron-withdrawing power—something synthetic chemists leverage for selectivity and reactivity in organic transformations. Our own team first noticed how those chlorine atoms influence reaction rates using base-catalyzed condensations and cyclizations. You don’t find this degree of reactivity in run-of-the-mill malononitrile derivatives. Once customers understand the value dichloromalononitrile brings to heterocyclic and pharmaceutical synthesis, their feedback consistently underlines its role as a robust intermediate.
The crystalline powder ranges from white to slightly off-white, reflecting trace variances in feedstock, never in process purity. With a sharp, pungent odor, the compound warns workers if a seal fails. Boiling point measurements land just over 230°C, a property we’ve confirmed through thousands of small-scale and pilot runs. Hydrolysis and decomposition are key risks—something we constantly monitor, especially in long-term storage. More than a list of specifications, these figures anchor decisions from the warehouse to the reactor. We watch ambient humidity and container integrity as tightly as we log shipment weights.
Early on, most of our dichloromalononitrile went into bench-scale chemical experiments. Over the last decade, growing demand among pharmaceuticals and agrochemical developers shifted our focus to larger volumes. This compound’s strong electron-withdrawing nitrile and chloro groups make it a versatile intermediate for synthesizing heterocyclic scaffolds, especially for medicinal chemists seeking to introduce rigidity or point-functionalization in a target molecule. We’ve collaborated with teams optimizing new active ingredients who found that dichloromalononitrile’s enhanced reactivity reduces synthetic steps, cuts solvent use, and raises yields.
Our team once worked with a polymer innovator chasing novel cross-linking agents. Their design called for rapid, controlled reactivity with functional polymers—something our dichloromalononitrile delivered in spades compared to the mono-chloro or unsubstituted malononitrile analogs. In custom synthesis runs, our technical advisers helped fine-tune stoichiometry and timing for these large-scale applications. Feedback from their pilot lines confirmed what we observe: dichloromalononitrile provides a sharper, more efficient path toward activating challenging carbon backbones.
We see a second wave of customers in pigment and dye synthesis. Our product’s dual chloro sites introduce color stability and performance in pigment intermediates. Researchers cited improved light fastness and sharper color development using derivatives based on dichloromalononitrile. From field reports, these dyes outperform conventional alternatives in industrial textiles and coatings.
In our experience, malononitrile forms a familiar cornerstone in organic chemistry, yet its chlorinated versions open new synthetic frontiers. Some labs try to substitute mono-chloromalononitrile for dichloromalononitrile, thinking the two act interchangeably, only to notice significant activity changes in cyclization and condensation reactions. Dichloromalononitrile’s twin electron-withdrawing groups make it more reactive, especially where controlled, strong activation is essential. You won’t see the same selectivity or product distribution using simpler malononitrile or even mono-chloro analogs. This difference plays out on-process yield sheets, not just in academic papers.
We’ve tracked performance in various synthetic contexts: with dichloromalononitrile, reaction times drop, side-products fall, and isolated yields rise—provided the operator respects its reactive nature. The firmer electron pull brings cleaner transformations. Compare it to trichloromalononitrile derivatives, and you enter another territory: too much reactivity, too little control, higher risk of decomposition and poor material recovery. Through trial, feedback, and iterative quality improvements, we hit a sweet spot—high enough reactivity for modern synthesis, low enough background activity to avoid wasted starting materials and byproducts.
Our process starts with carefully sourced raw chemicals, vetted for contaminants and batch tested. Chlorination and dehydration proceed under tightly controlled pressures and temperatures–years of refining process conditions taught us how sensitive dichloromalononitrile formation can be. A temperature spike ruins not just a day’s run, but risks tank integrity. We’ve built our operations on the lessons from close calls and process deviations, adding redundant safeguards, skilled technicians, and detailed logs at every stage. Our maintenance crew knows the importance of precision valves and sensors, since slight leaks or back-pressure events can halt a batch in its tracks.
On leaving the reactor, every batch passes through several purification steps, including distillation and multiple crystallizations. Lab checks flag any trace of impurities—our staff uses chromatography, mass spectrometry, and wet chemical tests inline rather than relying solely on end-product snapshots. Inspection doesn’t stop at analytics: product managers keep tabs on color, scent, and even the tactile feel of the crystals. Long experience tells us that subtle textural shifts sometimes—before any formal test flags a problem—herald a slip in drying or solvent removal.
Working daily with dichloromalononitrile’s volatility forged new habits in our halls. Every operator receives in-depth hazard scenario training. We run regular drills for containment and exposure events. Storage practices mean separating incompatible materials, controlling access, and tracking inventory in real-time. The pungency, while inconvenient, provides a built-in warning. A cracked seal rarely goes unnoticed, and staff understand immediate action protects not just product, but health and business continuity.
Plant leaders enforce rigorous air handling, PPE, and monitoring. We keep neutralizing sprays and spill kits on every level. Our customer support team advises on safe transfer, labeling, and disposal, never defaulting to boilerplate manuals. Decades of accident-free operation count as a source of pride, but never as a reason to relax vigilance around dichloromalononitrile.
Our compliance team stays vigilant. Regional regulations governing the handling, transport, and disposal of hazardous organics change constantly. We work with compliance officers and outside auditors to keep quality systems sharp. Every batch comes with a full regulatory background. Meeting and exceeding local standards means more than ticking boxes: it builds trust with customers, regulators, and the communities around our production hubs.
Minimizing environmental impact is not a marketing gesture—it is a core tenet of our production philosophy. Diligence in waste stream management, solvent recovery, and gas scrubbing limits emissions and reduces hazardous waste. Production staff regularly suggest tweaks, and management listens. On several occasions, operators identified changes to cooling or venting systems that markedly cut byproduct output and energy use per ton produced. Transparency matters: every environmental report and compliance certificate is open to review.
Long after each drum leaves our gate, it’s customer feedback, troubleshooting calls, and application reports that shape the next phase. Innovation isn’t confined to R&D; it grows from listening. When early adopters pointed out handling issues with our packaging under high-humidity conditions, we retooled to triple-seal every pail. After one biotech group asked for custom particle sizing to optimize their continuous reactor setup, we designed a modular post-crystallization process. Now they run with fewer clogs and greater throughput. Each story means we’re not just supplying an off-the-shelf chemical. We’re working alongside our customers, helping fine-tune process parameters or troubleshoot anomalies over weekends and holidays.
Direct, real-world feedback means we learn from customer discoveries, too. Sometimes a pharmaceutical partner uncovers an unanticipated side reaction or handling detail. Our team logs these discoveries, building a knowledge base that doesn’t exist in standard references. We share lessons across departments. Recent changes in handling protocols—adopted after a customer alert about temperature-sensitive degradation on overseas shipments—became part of standard practice. These changes reduced transit loss and added shelf-life for our customers’ raw material stocks.
Dichloromalononitrile presents ongoing technical and ethical challenges. Balancing reactivity with stability is not a solved problem, especially as new downstream uses appear. Pharmaceutical innovators require even lower impurity thresholds, pushing us to improve purification tech and invest in faster analytics. Environmental expectations intensify every year. Authorities demand lower emissions, and downstream users face stricter effluent controls. Last year, we trialed an in-line scrubber that reduced volatile organic emissions by over 30%—now installed on all production lines. Each improvement traces back to emerging market and regulatory demands rather than academic abstracts.
Supply chain resilience and transparency keep us motivated. Sourcing precursors from stable and responsibly managed vendors takes priority over short-term savings. Cost and quality can’t sit at odds. We carry buffer stocks of sensitive materials, audit vendors for labor and environmental standards, and publish origin documentation for customers seeking to de-risk their own supply chains.
On the technical front, next-generation uses for dichloromalononitrile appear on the horizon. Peptide chemists explore new coupling strategies based on its unique properties. Materials scientists seek tougher, more heat-resistant polymers using its reactivity. We test these concepts on our pilot lines, reporting direct results back to the customers and research teams involved. As a manufacturer, nothing beats the sense of engagement from helping turn an academic idea into a scaled-up industrial reality.
Lab-synthesized dichloromalononitrile often fails to perform reliably on industrial scale. We’ve seen many attempts using off-brand or in-house materials bog down in failed condensations, excessive byproduct formation, or inconsistent crystallinity. Our process—built from decades of in-plant experience—yields material with predictable melting behavior, low residual moisture, and high reactivity batch after batch. Customers uncover time savings, less waste, and easier downstream purification when they swap unreliable material for ours.
Many buyers juggle price quotes from brokers or distributors. The real discriminator lies in after-sale reliability and responsive troubleshooting. Figures in a table never tell the whole story. Our commitment goes beyond just producing dichloromalononitrile: we stand by every drum, every certificate, and every technical inquiry. Our production documentation stands open for review, and our technical team remains available for customer consultations long after the initial delivery. Focusing on process stability, actual usability, and long-term relationships means fewer surprises and more productive work for our customers.
For us, dichloromalononitrile is not an anonymous white powder. Every batch embodies countless hours—early shift, late night, maintenance check, QA round, and safety drill. We know the stubbornness that comes from a cold start on a reactor. We’ve lived through raw material shortages, sudden spec changes, and the urgency of a customer’s late-night production call. In an industry where every kilogram matters, our pride sits in practical results: fewer failed syntheses, fewer safety incidents, more robust supply chains.
We walk into the plant every day focused on the real outcome—helping customers build better chemicals themselves. That’s why we produce dichloromalononitrile the way we do, and why each order reflects not only the chemistry but decades of lived expertise.