5-Bromo-2-chloropyridine-4-carboxaldehyde

    • Product Name: 5-Bromo-2-chloropyridine-4-carboxaldehyde
    • Chemical Name (IUPAC): 5-bromo-2-chloropyridine-4-carbaldehyde
    • CAS No.: 356783-16-3
    • Chemical Formula: C6H3BrClNO
    • Form/Physical State: Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    638772

    Product Name 5-Bromo-2-chloropyridine-4-carboxaldehyde
    Cas Number 1054486-46-2
    Molecular Formula C6H3BrClNO
    Molecular Weight 220.45
    Appearance Light yellow to yellow solid
    Melting Point 67-71°C
    Purity ≥98%
    Boiling Point No data available
    Smiles C1=CN=C(C(=C1Br)C=O)Cl
    Solubility Soluble in organic solvents like DMSO and DMF
    Storage Temperature 2-8°C
    Synonyms 5-Bromo-2-chloro-4-pyridinecarboxaldehyde
    Inchi InChI=1S/C6H3BrClNO/c7-5-1-10-3-4(2-10)6(8)9/h2-3H,1H2
    Flash Point No data available
    Refractive Index No data available

    As an accredited 5-Bromo-2-chloropyridine-4-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 5-Bromo-2-chloropyridine-4-carboxaldehyde, sealed with tamper-evident cap and labeled for laboratory use.
    Container Loading (20′ FCL) 20′ FCL container loaded with 5-Bromo-2-chloropyridine-4-carboxaldehyde, securely packed in drums, adhering to safety and regulatory standards.
    Shipping 5-Bromo-2-chloropyridine-4-carboxaldehyde is shipped in secure, airtight containers to prevent contamination and moisture exposure. The packaging complies with chemical safety and transport regulations, including labeling and documentation. It is transported via ground or air as required, with appropriate hazard classifications, ensuring safe and prompt delivery to the recipient.
    Storage **5-Bromo-2-chloropyridine-4-carboxaldehyde** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials like strong oxidizing agents. Avoid moisture exposure. Store at room temperature unless otherwise specified by the manufacturer. Proper chemical labeling and secure storage are essential to ensure safety and maintain compound integrity.
    Shelf Life 5-Bromo-2-chloropyridine-4-carboxaldehyde should be stored tightly sealed, protected from light and moisture; shelf life is typically 2 years.
    Application of 5-Bromo-2-chloropyridine-4-carboxaldehyde

    Purity 98%: 5-Bromo-2-chloropyridine-4-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical yield and reduced by-product formation are achieved.

    Melting Point 105°C: 5-Bromo-2-chloropyridine-4-carboxaldehyde with a melting point of 105°C is used in solid-phase organic reactions, where consistent crystallinity ensures reproducible reaction conditions.

    Molecular Weight 236.45 g/mol: 5-Bromo-2-chloropyridine-4-carboxaldehyde with a molecular weight of 236.45 g/mol is used in medicinal chemistry research, where precise stoichiometric calculations enable accurate compound design.

    Particle Size <50 µm: 5-Bromo-2-chloropyridine-4-carboxaldehyde with particle size below 50 µm is used in heterogeneous catalysis, where increased surface area promotes higher reaction rates.

    Stability Temperature 25°C: 5-Bromo-2-chloropyridine-4-carboxaldehyde with a stability temperature of 25°C is used in ambient storage of research chemicals, where product integrity is maintained during extended storage.

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    Certification & Compliance
    More Introduction

    5-Bromo-2-chloropyridine-4-carboxaldehyde: Insights from the Manufacturing Floor

    An Introduction to the Chemistry Behind the Molecule

    At our plant, the story of 5-Bromo-2-chloropyridine-4-carboxaldehyde begins long before it lands in a customer’s flask. For years, our team has handled the multi-step synthesis and the delicate purification of this aromatic heterocycle. This compound, with its bromine and chlorine atoms positioned on the pyridine ring and an aldehyde group at the 4-spot, stands out as a key intermediate in many organic synthesis routes. We have observed its value grow along with advances in pharmaceutical building blocks, specialty material design, and agricultural research. The structure alone—by fusing electron-withdrawing halogens and a reactive formyl group—invites a range of transformations in the lab, and over time we’ve come to appreciate just how many downstream targets depend on its precise makeup.

    Colleagues from both academia and industry frequently remark on the consistent reactivity of our batches. Maintaining high-purity 5-Bromo-2-chloropyridine-4-carboxaldehyde requires hands-on experience and a genuine grasp of the compound’s quirks during crystallization. Even small changes in pH or solvent system shape its final form, sometimes shifting color, other times toughening filtration. Over the years, we have adjusted protocols—not by intuition alone, but by tracking how each adjustment ripples across the final product’s yield, melting point, and spectral clarity. This hands-on, incremental approach separates manufacturers with true in-house control from those simply repackaging stock.

    Model and Consistency Across Batches

    We produce 5-Bromo-2-chloropyridine-4-carboxaldehyde under a dedicated model, with dedicated glass-lined vessels held within set temperature and humidity windows. The batch model is not an off-the-shelf recipe—it reflects a stream of practical adjustments after years of scaling from bench to pilot. The aromatics division keeps every production step under one roof, from charging raw pyridine through to final HPLC analysis.

    Over repeated cycles, our plant’s data shows that moisture in the input pyridine often shifts aldehyde formation rates and final assay. An extra degree of evaporation, an extra rinse between steps—each detail guides the outcome. Repeated batch records, along with full spectral data, fill our log books. This practice lifts what might appear as routine synthesis to a science of tight process control, and our customers notice the difference in both yield and in downstream product uniformity.

    Specifications That Matter on the Shop Floor

    Assay, melting range, color, and moisture content form the backbone of our internal specifications. These numbers don’t get drawn up in the air; they have been refined report by report, year over year, by tracking real impact on customers’ reactions and their own purification hassles. Most batches of 5-Bromo-2-chloropyridine-4-carboxaldehyde leave our door at greater than 98% purity, measured by both GC and HPLC against trusted standards.

    From the production side, color alone tells much about a batch. An off-yellow or tan hue sometimes signals side-product formation, likely from over-bromination or oxidation at uncontrolled stages. The experienced eye of a plant technician picks up these signals before the first sample even reaches the QC bench. From there, we pair organoleptics with hard data—melting range usually falls tightly around the mid-100°C mark. If it drifts lower, decomposition or unreacted material may have crept in. Only after these tests do batches move to the warehouse, and no customer gets “near-miss” product as filler.

    Each lot comes with its own moisture data, as water influences both shipping stability and success in subsequent reactions. Our in-house team relies on Karl Fischer titration independently of outside labs. Whether the downstream step is a Grignard or a coupling, less background water sets our customers up for cleaner runs. These are lessons earned by troubleshooting not in the abstract but with hands dipped in real glassware.

    The Uses We’ve Seen and Supported

    At its core, 5-Bromo-2-chloropyridine-4-carboxaldehyde connects several worlds: pharmaceuticals, agrochemistry, and specialty polymers. In medicinal chemistry, the dual halogens on the pyridine ring open doors for selective cross-coupling and further derivatization. Our regular clients often transform this molecule into complex heteroaromatics, foundation stones for anti-infective or oncology drugs. The aldehyde at the para-position reacts freely in Knoevenagel, reductive amination, and Wittig transformations—a feature we’ve watched drive discovery projects at more than one large R&D center.

    On the crop science side, this compound serves as a backbone for micronutrient ligands and as a starting point for herbicide and fungicide development. Scale-up partners often cite its clean reactivity profile as the main reason they return to us batch after batch. A single extra impurity in this substrate can upend a whole combinatorial synthesis platform down the road, which puts pressure on our end to maintain lot-by-lot documentation.

    We have fielded requests from both research labs and scale-up centers who want consistent batches so that screening data holds up over months and across continents. Our know-how with solvent washes and careful temperature ramps feeds into this confidence. By tuning the process at the kilo scale, we’ve seen fewer headaches in product reactivity consistency compared to off-the-shelf or brokered alternatives. That, in turn, keeps customers focused on their own inventions instead of wrangling failed reactions caused by bad raw material.

    Differences Compared to Other Pyridine or Carboxaldehyde Products

    Working hands-on with pyridine derivatives highlights differences that often only show up in day-to-day chemistry, not on paper. 5-Bromo-2-chloropyridine-4-carboxaldehyde separates itself from simpler pyridine carboxaldehydes by its pattern of halogenation—both in reactivity and in handling. These substituents don’t just raise the molecular weight; they tune the electron density of the pyridine ring and the formyl carbon, making selective functionalization in later steps both achievable and robust.

    Other carboxaldehyde reagents often lack the dual halogen balance or fall short in terms of purity at multi-kilo volumes. While 2-chloropyridine-4-carboxaldehyde on its own can serve as a building block, adding bromine in the 5-position opens broader possibilities for Suzuki or Stille cross-coupling reactions. We have worked side by side with chemists who moved away from mono-halogenated pyridines after their projects stalled at C–C bond-forming steps that demanded greater selectivity and yield.

    In daily plant operations, product stability comes up often. Mono-halogenated analogues sometimes show accelerated decomposition—especially under light or in the presence of trace metals—leading to storage and shipping challenges. Our double-halogenated aldehyde product holds up better under standard warehouse conditions, backed up by our real-time and accelerated stability observations over the past decade.

    From a safety angle, this compound also offers a more predictable risk profile compared with related nitro- or amino-substituted pyridine aldehydes, which have a higher tendency toward uncontrolled exotherms during downstream chemistry. By keeping hazards lower, both we and our customers operate with a greater margin of safety. That fact shaped our line’s original design, as reduced incidents translate directly into reliability in the supply chain.

    On the Ground: Manufacturing Realities and the Importance of Traceability

    Day-to-day running of the synthesis line for 5-Bromo-2-chloropyridine-4-carboxaldehyde gives a fresh look at what reliability means in chemical supply. Many requests hit us from customers blindsided by substitution or purity shifts from brokers sourcing from obscure or unknown facilities. These stories shape our own insistence on sourcing raw materials only from audited suppliers. The downstream cost of an off-spec aldehyde is far greater than anything saved by cutting corners upstream.

    We maintain full records for every batch—starting material lots, reaction conditions, waste management logs, spectral archives, and shipment tracking. Chemists and procurement officers can trace each container all the way back to its raw inputs. Several times, this attention to detail has helped a product developer identify an unforeseen side-product, or clarify a batch-to-batch difference in synthesis outcomes. While some in the market view traceability as box-ticking, we treat it as insurance and as a signal of our plant’s DNA.

    We hear motivation in simple, practical terms from customers. Labs value knowing the exact impurity profile expected in a kilo lot, since this shapes both their separation columns and their safety assessments. Production teams—especially those scaling promising routes—look for predictable melting and color characteristics, minimizing requalification work. This feedback returns directly into our SOPs and quality review meetings at shift change, where no process tweak is too minor to get a hearing, since traceability makes everything visible.

    Regulatory, Health, and Environmental Considerations in Manufacture and Use

    Manufacturing halogenated pyridine aldehydes carries a practical burden: waste management and environmental compliance cannot be afterthoughts. Our responsibility starts with choosing raw materials from reputable sources, and extends to capturing and treating all spent reagents, solvents, and vented organics. Our effluent streams pass through dedicated treatment, and both air and water are routinely monitored for halides and VOCs.

    Downstream customers ask frequently about residual solvents such as DMF, DCM, and THF. We address this up front with independent analysis and full reporting of residuals. Teams in regulated sectors—API synthesis, in particular—build their filings around our documented levels. Night shift operators clean and purge reaction vessels with the same care as any new charge, knowing the next run depends on today’s discipline.

    During our own occupational monitoring, we’ve adapted process enclosures and dust control systems. Aldehyde-containing dusts present an inhalation risk in large volumes, so we outfit techs with proper PPE, and we refresh training anytime a process or protocol changes. Both government auditors and internal safety teams have responded well to our focus on open reporting and real-life observations from the production floor, not just written plans.

    Looking Forward: Balancing Innovation with Production Know-How

    Day by day, the business of chemical manufacturing stays rooted in details. Small improvements—better solvent recycling, tighter batch tracking, faster product cooldown—show their value across thousands of liters and hundreds of shipments. As more customers build complexity into their end products, large intermediates like 5-Bromo-2-chloropyridine-4-carboxaldehyde gain prominence. We stay alert to both customer feedback and shifts in synthetic approaches, since today’s standard protocol often gets reimagined by tomorrow’s chemistry.

    Our teams keep close contact with leading-edge research, both in terms of greener process development and in the shifting landscape of pharmaceutical, crop science, and material science targets. Customers bringing new projects often push us to explore further process miniaturization, milder reaction conditions, or non-traditional solvent systems. Years of piloting flow chemistry has shown us that some transformations long considered batch-only now give higher selectivity in microreactors. We weigh these options based on practical tradeoffs seen in our own operations: raw material compatibility, product isolation, final crystallinity, and—practically—equipment fatigue and cleaning turnarounds.

    Traceable, high-purity intermediates remain a central demand, and experience gives us the tools to deliver. Our approach never stops at reaching a passing assay; we follow each batch’s journey from raw pyridine drum to final aldehyde shipment, learning from every anomaly and every customer report along the way. The combined experience of every operator, shift supervisor, and analyst finds its way into today’s protocols.

    5-Bromo-2-chloropyridine-4-carboxaldehyde isn’t just another point on a catalog sheet. It represents both the challenges and the rewards of hands-on specialty chemical manufacture. As new applications and stricter regulatory regimes take hold, we meet those changes with technical depth, operational transparency, and a commitment to keeping our word batch after batch, drum after drum.