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HS Code |
258893 |
| Cas Number | 102587-95-5 |
| Molecular Formula | C6H2BrClN2 |
| Molecular Weight | 217.46 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 74-78°C |
| Density | 1.81 g/cm³ (approximate, estimated) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=C(C(=NC=C1Cl)C#N)Br |
| Inchi | InChI=1S/C6H2BrClN2/c7-5-1-4(3-9)10-2-6(5)8/h1-2H |
As an accredited 5-Bromo-3-chloropyridine-2-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams of 5-Bromo-3-chloropyridine-2-carbonitrile, labeled with hazard pictograms, lot number, and CAS information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Bromo-3-chloropyridine-2-carbonitrile involves securely packing 10–12 metric tons using 25kg fiber drums. |
| Shipping | 5-Bromo-3-chloropyridine-2-carbonitrile is shipped in tightly sealed containers, protected from moisture and light. It is transported under applicable hazardous material regulations, typically with full labeling for chemical hazard, and handled by trained personnel. Ensure compliance with local and international shipping guidelines for toxic and environmentally hazardous substances. |
| Storage | 5-Bromo-3-chloropyridine-2-carbonitrile should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances, such as strong oxidizing agents. Use chemical-resistant containers and avoid exposure to moisture. Ensure proper containment to prevent environmental contamination. |
| Shelf Life | 5-Bromo-3-chloropyridine-2-carbonitrile is stable for at least 2 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 5-Bromo-3-chloropyridine-2-carbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures consistent reaction yields and reduced by-product formation. Melting Point 114°C: 5-Bromo-3-chloropyridine-2-carbonitrile with melting point 114°C is used in high-throughput organic synthesis, where it provides optimal crystallization for solid-phase processes. Molecular Weight 219.45 g/mol: 5-Bromo-3-chloropyridine-2-carbonitrile with molecular weight 219.45 g/mol is used in agrochemical research, where it enables accurate dosage formulation. Particle Size <50 microns: 5-Bromo-3-chloropyridine-2-carbonitrile with particle size less than 50 microns is used in formulation development, where it promotes rapid and uniform dissolution in solvents. Stability Temperature up to 40°C: 5-Bromo-3-chloropyridine-2-carbonitrile with stability temperature up to 40°C is used in long-term storage applications, where it maintains chemical integrity over extended periods. Water Content ≤0.2%: 5-Bromo-3-chloropyridine-2-carbonitrile with water content less than or equal to 0.2% is used in moisture-sensitive reactions, where it minimizes hydrolysis and degradation. Assay ≥98.5% (HPLC): 5-Bromo-3-chloropyridine-2-carbonitrile with assay ≥98.5% by HPLC is used in custom synthesis, where it provides reliable analytical qualification for batch release. Residual Solvent <500 ppm: 5-Bromo-3-chloropyridine-2-carbonitrile with residual solvent content less than 500 ppm is used in GMP manufacturing, where it meets stringent regulatory safety and quality standards. |
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Every chemical factory has a few products that serve as the backbone for intricate syntheses. 5-Bromo-3-chloropyridine-2-carbonitrile falls into that category for us and, increasingly, for many researchers and formulators worldwide. After years of producing this compound, we’ve seen it play several key roles—most often as a trusted intermediate for advanced pharmaceuticals and specialty agrochemicals.
We know well the constraints chemists face at the bench and in plant-scale productions. Whenever scale-up demands repeatable purity and consistent reactivity, the fine details of a building block matter. Through our in-house process, we’ve honed 5-Bromo-3-chloropyridine-2-carbonitrile to offer sharp batch-to-batch consistency. Many in the market tout high-purity or streamlined synthesis; from our experience, real reliability comes through control at every stage—starting with the raw halopyridine feedstock and moving through each chlorination, bromination, and cyanation step with strict monitoring.
Typical finished product emerges as a pale crystalline solid, handled in kilogram to multi-ton quantities. By running persistent in-process analytics, we maintain the specifications our partners need: purity touching or topping 99%, with water content and residual solvents well beneath industry thresholds. Melting points stay within tight limits. We always monitor heavy metal content, since even traces can sabotage a downstream catalyst or shift product color—details that shape real-world performance, not just paperwork compliance.
The chemical structure delivers more than its formula suggests. The bromine at the five-position, chlorine at three, and cyano group at two give this pyridine carboxamide more than a simple substitution pattern. These groups control reactivity in cross-coupling, nucleophilic attack, and functional group transformation. We’ve followed our product into Suzuki, Buchwald–Hartwig, and other palladium-catalyzed systems. Its electron-deficient ring pushes the reactivity envelope in these stages, making it a reliable scaffold for complexity-building—a key reason why pharmaceutical teams select it repeatedly.
Organic synthesis is never just about chemicals in a jar. Our customers, ranging from pharmaceutical development to crop science innovators, value how this compound accelerates route scouting and optimization. More than a new scaffold, it bridges the gap between creative molecular design and manufacturing scale viability.
Pharmaceutical research teams often add the cyano and halogen functionalities to streamline the creation of heterocyclic drug cores, kinase inhibitors, and antiviral agents. The unique arrangement of substituents reduces synthetic steps compared to isomers or less functionalized pyridines. This matters in process research, where a single extra transformation means weeks in a pilot plant or substantial extra solvent expense.
Outside pharma, agricultural chemistry leverages 5-Bromo-3-chloropyridine-2-carbonitrile as a starting point for potent crop protection agents. Its ability to direct further selective functionalization—such as in C–N and C–C bond-forming strategies—lets scientists design compounds that resist degradation and target specific pests, while bypassing less selective, less persistent options that depend on older halopyridines.
It might be tempting to lump all pyridine derivatives together, but side-by-side work tells another story. Compared to 3,5-dibromopyridine, for example, 5-Bromo-3-chloropyridine-2-carbonitrile offers both increased versatility and a distinct reactivity window thanks to the dual halide and nitrile grouping. Colleagues at several major pharmaceutical firms have told us they see higher selectivity in coupling reactions, and purifications come easier thanks to reduced by-product profiles.
We’ve witnessed that the distribution of bromine and chlorine around the ring, paired with the electron-withdrawing cyano group, changes the kinetic profile in palladium catalysis and sulfur-based cross-couplings. Our internal tests confirm higher yields compared to using closely related structures, with less need for costly deprotection or ring activation steps. Years of direct feedback from scale-up engineers remind us that such efficiencies make a real dent in plant economics and waste treatment budgets.
Looking up and down the supply chain, the distinction isn’t technical residue; it touches everything from waste stream simplification to energy cost management. Where some intermediates can be difficult to solubilize or demand noxious activation conditions, our crystalline product integrates into most polar organic solvents without surprise polymerization or hydrolysis events. This reliability in handling saves hours in both bench work and process validation.
Anyone who manufactures fine chemicals learns early that lab-scale elegance can quickly unravel under production stress. For 5-Bromo-3-chloropyridine-2-carbonitrile, we invest as much in the consistency of upstream processing as we do in the specs of the final solid. Precise control over the initial halopyridine feed and careful reaction temperature management set the stage. Synthetic route tweaks, such as catalyst loading and careful distillation parameters, ensure clean halogen introduction and minimal side-product formation.
Raw materials quality serves as a cornerstone—low-metal content in the pyridine backbone, quality-controlled bromine and chlorinating agents—since any impurity travels through every subsequent transformation. Time and again, we have seen customers drawn to our batches after previous experiences elsewhere, sometimes driven by trace metal contamination leading to erratic catalysis in their own processes. By taking impurity mapping seriously upfront, we shield downstream users from costly troubleshooting, and long-term relationships have grown from such trust.
Every finished batch reflects lessons captured from the shop floor. Our plant engineers record temperature, pressure, and product quality daily. By investing in in-line monitoring and rapid feedback loops, we keep yields high and impurity drift low. Fast intervention—switching feedstocks, adjusting solvent polarity, or altering crystallization times—means finished product stays within spec, reducing rework cycles and pilot plant downtime.
Customers working toward regulatory filings regularly send us requests for detailed impurity profiles—not just headline purity numbers. We respond with historical batch data, trend analysis, and practical guidance on solvent selection or purification tweaks. Especially for later-stage pharmaceutical projects or scalable pesticide actives, clarity about minor by-products helps prevent late-stage surprises.
One process chemist shared that switching from less reproducible suppliers to our product line shaved weeks off their API route optimization, cutting analytical troubleshooting almost in half. Our ability to maintain those specs at scale comes down to prioritizing data, responsiveness, and an open line between production and R&D engineers, rather than rigid adherence to legacy batch records.
The regulatory world grows more demanding every year. Auditors want more than a Certificate of Analysis—they want traceability, impurity justification, and robust supply chain documentation. We support this mindset, not just as a box to check, but because clear provenance means safety, repeatability, and durability in every downstream product.
We support every major stage of compliance: REACH registration, ISO processes, audit accommodation. Our technical managers work directly with QA teams at pharmaceutical plants to map our impurity cascades so every stakeholder, from purchasing to QA/QC, knows what arrives at their loading dock. Transparency about batch genealogy avoids headaches for both sides. Along the way, we skip the shortcuts that lead to inconsistencies or regulatory gray areas. Investments in real-time analytics and lot-level documentation ensure every outgoing kilogram leaves a traceable trail. Customers’ questions have shifted from “Can you supply?” to “Can you share validation protocols and historical data?” We maintain a regularly updated QMS that stands up to these deeper dives.
Today’s chemical industry cannot dismiss the environmental consequences of fine chemicals manufacture. From the start, we look for process options that minimize halogenated solvent usage and restrict waste acid formation. Process engineers collaborate with environmental managers to pre-treat bromide and chloride streams before disposal, rather than send them into municipal or on-site treatment in less managed form. Monitoring emissions, capturing solvent for reuse, and exploring lower-impact oxidants shift the sustainability footprint downward with every campaign.
We partnered with local regulators during plant upgrades to ensure emissions meet or outperform legal limits, and we reinvest GHG savings into continuous process improvement. Beyond just emissions, energy and raw material use stay under steady review—process intensification efforts and automation continue to push our yields per liter, letting each kilo of starting pyridine go further with less waste.
We engage monthly with process chemists, pharmaceutical R&D teams, and agricultural innovation centers. Real-world feedback—how 5-Bromo-3-chloropyridine-2-carbonitrile performs across different catalysts or solvents, how scalability aligns with pilot plant targets—feeds straight back into process tweaks. Our approach favors direct engagement over isolated lab work; results on our site matter most when they translate into your plant’s success.
This real-world linking shows up in unlikely places. A customer in Europe experienced persistent batch-to-batch reactivity swings using generic intermediates; our product’s handling properties and reactivity regularity boosted their pilot success rate, which allowed them to file regulatory dossiers ahead of schedule. Stories like this reinforce our belief that tight integration between manufacturer and user pays off. Adjustments to crystal size or drying protocols sometimes change not just our own downstream handling but influence the work-up steps in a partner’s synthetic route.
We take pride in helping streamline those steps, as shaving even a single chromatographic refinement or filtration saves days in commercial settings. Maintaining that responsiveness is only possible with active dialogue and shared data.
Supply risks loom large in specialty chemistry, especially as demand ebbs and flows with innovation cycles or regulatory updates. We work with redundant processes and qualified suppliers to lock in our access to core raw materials and reagents. Feedback from multinational customers alerted us early to the need for adaptive logistics and warehousing, so we maintain enough inventory to bridge temporary disruptions. Rigorous testing before each outbound shipment locks in confidence for new and established partners alike.
Our teams regularly stress-test production and logistics arrangements to anticipate changes—whether market-driven, regulatory, or equipment-based. By conducting detailed risk mapping and staying agile, we have delivered reliable supply throughout global volatility, and that steadiness draws in customers seeking more than a commodity transaction. They value the assurance that production delays at their own end will not be mirrored by lapses in intermediate availability on ours.
We hear several recurring themes from chemists starting work with halopyridine nitriles:
Drawing on years in production and close user partnership, we share not only our validated routes but knowledge of how process drift, temperature fluctuation, or raw material choice can impact practical performance. We offer technical discussions as part of supply partnerships, recognizing that success in practice depends as much on shared insight as it does on specification sheets.
The chemical landscape is awash in new reagents and synthetic ‘shortcuts’. What we see in the field is that process reliability, well-documented impurity control, and ease of handling ultimately beat novelty for customers building long-term product lines. While novel pyridine analogs periodically spark interest, mature intermediates like 5-Bromo-3-chloropyridine-2-carbonitrile keep their value through documented performance, transparency, and process stability.
Our role as manufacturer creates responsibility to meet, not just claim, these standards every time. We back our process insights with repeatable outcomes, a willingness to adapt, and a practical recognition of how each campaign will be used. Every order reflects not merely successful synthesis, but successful partnership.
Looking back over years of production, the ongoing journey with 5-Bromo-3-chloropyridine-2-carbonitrile has offered a clear lesson: shared trust, not simply technical compliance, drives progress from concept to commercial realisation. Chemical manufacturing succeeds at its best when built not only on technical rigor, but on honest collaboration and a persistent drive to refine—batch after batch, order after order.
Feedback from customers continues to refine our practice. These insights shape not only how we produce, but also how we grow with the industry’s changing needs. Our experience with this intermediate underlines the value of clear communication, robust technical support, and adaptive approaches to scale and regulation. By staying focused on practical results and shared progress, we help unlock new pathways and efficiencies for all those relying on fine chemical innovation.