6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde

    • Product Name: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde
    • Chemical Name (IUPAC): 6-bromoimidazo[1,2-a]pyridine-3-carbaldehyde
    • CAS No.: 874288-13-0
    • Chemical Formula: C8H5BrN2O
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    438649

    Iupac Name 6-bromoimidazo[1,2-a]pyridine-3-carbaldehyde
    Molecular Formula C8H5BrN2O
    Molecular Weight 225.05 g/mol
    Cas Number 932443-27-9
    Appearance Light yellow to orange solid
    Melting Point 135-140 °C
    Purity >98%
    Solubility Soluble in DMSO and DMF
    Smiles C1=CN2C=NCC(=C2C=C1Br)C=O

    As an accredited 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, with tamper-evident cap; white label detailing chemical name, molecular formula, batch number, and hazard warnings.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde ensures secure, moisture-free bulk transport in sealed drums.
    Shipping **Shipping Description:** 6-BromoH-imidazo[1,2-a]pyridine-3-carbaldehyde is shipped in sealed, chemically compatible containers under ambient conditions. Packaging complies with safety regulations for laboratory chemicals. Handling includes protection from moisture, light, and extreme temperatures. Accompanied by a Safety Data Sheet (SDS) and relevant labeling, shipping follows national and international chemical transport guidelines.
    Storage 6-BromoH-imidazo[1,2-a]pyridine-3-carbaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Handle under an inert atmosphere, if necessary. Store at room temperature or as recommended by the manufacturer to maintain stability and prevent degradation.
    Shelf Life Shelf life: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde is stable for 2 years if stored in a cool, dry place.
    Application of 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde

    Purity 98%: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield formation of target molecules.

    Melting Point 145°C: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde with a melting point of 145°C is applied in solid-phase organic reactions, where thermal stability enhances reaction control.

    Molecular Weight 238.06 g/mol: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde at a molecular weight of 238.06 g/mol is utilized in structure-activity relationship studies, where it facilitates accurate dosage calculation.

    Stability Temperature up to 120°C: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde stable up to 120°C is used in medicinal chemistry workflows, where thermal resistance maintains compound integrity during reactions.

    Aldehyde Reactivity: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde with high aldehyde reactivity is employed in heterocyclic compound synthesis, where its functional group promotes efficient condensation reactions.

    Low Moisture Content (<0.5%): 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde with low moisture content is used in analytical assays, where it reduces side reactions and improves reproducibility.

    Particle Size <50 μm: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde at particle size below 50 μm is utilized in formulation development, where fine dispersion optimizes blend uniformity.

    Solubility in DMSO (≥10 mg/mL): 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde with solubility in DMSO at or above 10 mg/mL is applied in biochemical screening, where high solubility ensures consistent sample preparation.

    Assay by HPLC ≥99%: 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde characterized with HPLC assay of ≥99% is used in reference standard preparation, where analytical accuracy is critical for calibration.

    Free Quote

    Competitive 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@boxa-chem.com

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    6-BromoH-imidazo[1,2-a]pyridine-3-carbaldehyde: Technical Perspective from the Manufacturer

    Bringing 6-BromoH-imidazo[1,2-a]pyridine-3-carbaldehyde to the Lab Bench

    After decades of working directly with heterocyclic building blocks, experience has taught us to recognize the nuanced demands chemists face with each new synthetic target. Inside our facility, the process of producing 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde begins with a focus on controlling bromination at the 6-position without compromising the integrity of both the imidazo core and the formyl group at position 3. Achieving this, batch-to-batch, is a result of diligent process refinement — not just adherence to standard procedures, but years of bench-level learning from prior process yields, solvent choices, and the persistent problem-solving effort that chemistry requires.

    Our Approach in Synthesis: Consistency and Clarity

    This compound comes with a molecular formula suited for versatility in research settings. In laboratories, reproducibility of your final yields depends on the input material quality. We listen closely to the feedback from colleagues at research sites, who know a subtle impurity or even a trace of moisture can throw off a downstream transformation. Our direct synthesis routes are built on knowledge from purification bottlenecks and challenging crystallizations. We’ve learned that not all crystalline batches behave the same: achieving consistent melting points, clean spectroscopic profiles, and workable shelf-life becomes a constant pursuit rather than a checkbox on a manufacturing worksheet.

    What Sets 6-BromoH-imidazo[1,2-a]pyridine-3-carbaldehyde Apart?

    This compound isn’t just another halogenated azine. Over the years, we have handled dozens of imidazo[1,2-a]pyridine derivatives. Ajdusting bromo or aldehyde groups to different positions can lead to quite different reactivity and selectivity in later steps. The 6-bromo and 3-formyl combination opens doors often closed to its structural cousins. It offers synthetic handles for palladium-catalyzed coupling, further elaboration at the bromo site, and crucial introduction of side chains at the aldehyde. Colleagues working in medicinal chemistry continue to gravitate toward this product whenever they plan to access fused bicyclic targets that require site-selective modifications.

    While some related substances are more common in catalogues, not all provide the same synthetic flexibility. Simple pyridine derivatives lack the imidazo core, which is essential for reaching more diverse, drug-like architectures. Brominated imidazopyridines at other positions tend to limit further regioselective elaborations. Through hands-on evaluation, the 6-bromo substitution patterns have repeatedly shown utility in both methodology development and discovery pipelines, whether the field is oncology or CNS research.

    Specification Realities: The View from the Production Floor

    Years on the chemistry floor have proven that tight control over chemical purity pays off in customer results. Our batches routinely undergo NMR, HPLC, and mass spec analyses before ever seeing a shipping box. Purity levels generally meet the >97% mark by HPLC; sometimes the effort to push higher is balanced with diminishing synthetic returns downstream, depending on end-user needs. Analysts here have also observed that trace byproducts, which evade most catalogue supplier specs, become visible under detailed scrutiny of the full analytical suite — and we act on that, not just report it.

    The color and form may shift within a narrow range from off-white to faint yellow, but this does not indicate compromise in aldehyde reactivity or bromo fidelity. Moisture sensitivity is there, so we use desiccation and nitrogen-purged packing. Scale-up beyond research quantities follows the same in-house process — each larger batch starts from the same rigor as the first.

    Why Chemists Come Back to Us

    The main feedback from clients — the ones doing real work at the bench — is about reliability. Complicated library syntheses break down when the ligands or building blocks don’t behave as expected. We’ve lost count of how many calls we’ve fielded troubleshooting reaction issues that trace back to subtle impurities or polymorphic differences. Right from the first pilot runs, investing in robust isolation and validated analytical controls has cut down on surprises for both us and our colleagues in academic and pharma settings.

    Sourcing from traders or anonymous catalog houses often means accepting less clear background on production steps or solid support when things go wrong. We stay directly involved because it’s our own protocols, facility environment, and professional pride at stake. There’s a running list inside our team of customers who have needed rapid re-supply, shipment tracking, or even batch-specific data — and our direct manufacturing position lets us respond precisely, based on actual in-house knowledge.

    Application and Use: Real Research, Real Scale-Up

    In medicinal chemistry, 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde shows up everywhere from initial hit-to-lead efforts through to scale-up campaigns. Its dual functionality makes it a go-to for fragment-based elaboration or even just as a rapid entry point toward more complex fused scaffolds. On several occasions we’ve seen teams successfully adapt Suzuki coupling at the 6-position, right after reducing the aldehyde. Sometimes, the aldehyde gets the first modification — that’s another main pathway into secondary alcohols or as a step toward more complex C–C linking.

    Researchers keep sharing papers on new macrocycles and kinase inhibitors starting from this specific core. Being at the manufacturing end, we keep up with literature not out of idle curiosity, but because each new reaction or transformation teaches us whether minor changes to production can make life easier for people at the synthesis bench. Our experience with scale-up for clinical intermediates tells us that robustness of supply and consistent product lot-to-lot becomes far more important as a project moves from milligrams to kilograms.

    Risks and Reality: Common Pitfalls and How We Tackle Them

    Any synthetic chemist knows, introducing a bromo group at the wrong spot leads to wasted time and costs. Labs using bulk materials often learn this the hard way. From the production side, we maintain targeted reaction conditions, careful reagent selection, and rigorous product isolation — not just to “pass” a QC test, but to ensure no isomeric by-products sneak into the product stream.

    Another real-world issue: batch-to-batch reproducibility. We train our synthetic team to spot the subtle cues, such as an odd hue, minor shifts in TLC behavior, or peak splitting in NMR. If these show up, the lot does not progress. More than once, joint troubleshooting with partner labs has revealed that upstream solvent choices or even minor temperature deviations can ripple into product instability in later batches. These are not academic “what-ifs,” but recurring industry obstacles. So, our production management stays hands-on, keeping process logs detailed and responsive to every investigation.

    Environmental and Safety Commitment in Production

    Government compliance and regulatory expectations for halogenated intermediates such as this one await manufacturers at every turn. We invest heavily in solvent recovery, responsible effluent handling, and controlled emissions – not simply because of external requirements, but because most team members live near the site and want to avoid unnecessary hazards for neighbors and staff. Carrying out bromination chemistry safely involves equipment attention, maintenance, and a refusal to cut corners on ventilation or personal protective measures. Production crew, not just visitors or auditors, sign off on each safety drill and waste management review.

    Discussions with industry colleagues in both large- and small-scale manufacturing strengthen this approach — almost every incident that ever made the news started from either poor process transparency or undocumented shortcuts. The environment around a chemical production site does not forgive carelessness, something we teach each incoming technician on day one.

    Why In-House Manufacturing Matters for the End User

    Trading companies may offer apparent convenience, but without firsthand access to the process record, users risk encountering issues when they face an out-of-spec product or sudden change in quality. Our position as the manufacturer of 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde means there’s no ambiguity about formulation, storage, or historical synthetic changes. Chemists working within accelerated timelines or tight quality targets benefit from the direct line to those who synthesized, characterized, and packed the batch.

    Years of industry exposure shows most process failures start with a knowledge gap between product origin and end use. By retaining control over every synthesis variable — order of reagent addition, quenching temperature, even choice of recrystallization solvent — we deliver confidence along with every bottle. That’s not an abstract claim: our lab staff keep real-time production records, stay available for customer queries, and engage in ongoing dialogue about pain points in both analytical and preparative applications.

    How Feedback Shapes Our Future Batches

    We track every user inquiry, complaint, and success story about this compound. Our manufacturing team hosts regular meetings reviewing how specific feedback has prompted changes: sometimes to packaging, sometimes to storage, and often to purification runs. Every time a batch is flagged at the user end, the first response goes directly to production and QA. Unlike an outsourced supplier, our teams are invested in the hard lessons that come from real lab incidents, whether someone finds a packaging seal issue or a chromatographic impurity.

    Improvements don’t come just from internal brainstorming. Chemists worldwide, using 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde in unpredictable new reactions, come back with observations about solid handling, residual solvents, or even odd odors on opening. Each of these gets reviewed at the next lot production planning. Accountability runs throughout the supply chain, but it’s more than a slogan for us — each team member senses the stakes of losing a chemist’s trust.

    Supporting Discovery and Next-Generation Products

    Researchers need more than just a clean bottle; they need technical continuity for multi-step campaigns. This means documents, impurity profiles, and open responses about how even trace elements can affect yield or mechanistic outcome in the next step. Our in-house analytical chemists, process optimizers, and QC specialists remain accessible for direct technical discussion, ready to support not just routine deliveries but also pilot or clinical-scale scale-ups.

    Beyond the daily drive to produce a consistent intermediate, the bigger vision recognizes that users push this molecule into new directions: lead optimization, structure-activity studies, or novel heterocycle assembly. For years, we have supplied pilot campaigns that move from grams to tens of kilograms, and every transition from research to manufacturing scale teaches new lessons about batch quality, impurity fate, and efficient work-up.

    Summary of Differences from Other Market Products

    6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde offers more than comparable compounds, thanks to its dual-reactivity profile. Colleagues share that positional isomers don’t deliver the same downstream flexibility for further modification. Derivatives without the imidazo ring consistently show reduced biological “hit” rates and less favorable pharmacokinetic properties in preliminary screens. Other halogenated imidazopyridines, particularly those with the bromo group outside the 6-position or aldehyde moved elsewhere, frequently slow down subsequent steps due to less reliable C–H activation or incompatibility with their synthetic toolkit.

    Manufacturers that prioritize simple throughput or third-party packing lose track of analytical discipline and customer priorities. By placing emphasis on both the synthetic rigor and technical accessibility of our staff, we offer users more than a bottle of compound: research support, transparent technical data, and openness about each product’s limitations and best practices for use.

    Looking Ahead: How Manufacturing Insight Supports Scientific Growth

    As more scientists pivot toward new therapeutic targets, the value of well-characterized, reliably produced intermediates only grows. The long-term partnerships we’ve formed depend on real technical understanding, not just catalogue numbers or cost per kilo. Our view is shaped by years of hands-on batch manufacturing, process troubleshooting, and technical customer support that keeps translating experience into measurable progress for research programs.

    We recognize that every bottle of 6-bromoH-imidazo[1,2-a]pyridine-3-carbaldehyde shipped sets the stage for research, discovery, and the hard work of chemical innovation. That direct connection to science, through manufacturing, never gets taken for granted on our end.