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5-Bromo-3-Methyl-1H-Indazole

    • Product Name 5-Bromo-3-Methyl-1H-Indazole
    • Alias 5-Bromo-3-methylindazole
    • Einecs 629-326-6
    • 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
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    Specifications

    HS Code

    830227

    Product Name 5-Bromo-3-Methyl-1H-Indazole
    Cas Number 887593-52-2
    Molecular Formula C8H7BrN2
    Molecular Weight 211.06
    Appearance Off-white to light yellow solid
    Melting Point 140-144°C
    Purity ≥98%
    Solubility Soluble in DMSO, slightly soluble in methanol
    Smiles CC1=NN(C2=CC(Br)=CC=C12)
    Inchi InChI=1S/C8H7BrN2/c1-5-8-6(2-3-7(9)4-8)10-11-5/h2-4H,1H3,(H,10,11)

    As an accredited 5-Bromo-3-Methyl-1H-Indazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-3-Methyl-1H-Indazole

    Applications of 5-Bromo-3-Methyl-1H-Indazole in Industrial Manufacturing

    As the direct manufacturer of 5-Bromo-3-Methyl-1H-Indazole, we focus on its established roles in advanced chemical synthesis across multiple regulated industrial subsectors. Our product serves as a high-purity intermediate in specialized downstream manufacturing settings, where consistent compliance, predictable formulation integration, and traceable process control are key requirements for commercial scale-up and quality certification. Below, we detail major application fields with scenario-specific application details based on actual customer adoption and acknowledged standards.

    1. Pharmaceutical API Intermediate for Oncology Agents

    Pharmaceutical groups use this indazole derivative as a core building block in multistep syntheses for pyrazolyl indazole-based kinase inhibitors and emerging oncology APIs. The substance enters schemes where selectivity, reactivity of the brominated indazole nucleus, and stability under controlled conditions are critical to final yield and impurity management throughout the active pharmaceutical ingredient (API) lifecycle. Its predicable halogenation supports reproducible outcomes in pilot to commercial batchwork, with rigorous documentation of origin and in-process controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • 21 CFR Parts 210/211 (FDA, US cGMPs)
    • European Pharmacopoeia monographs for intermediates
    • Certificate of Suitability (CEP) traceability

    Typical usage ratio

    • 10–17% of total intermediate stage mass; ratio varies with target API scaffold and halogenation strategy, optimized by synthetic route and stepwise molar calculations.

    Downstream process integration

    • Introduced as a reagent during early or mid-stage condensation, cyclization, or substitution reactions in multi-step synthesis lines for indazole or indole-derived APIs.

    Final product types

    • Small-molecule antitumor drug substances (e.g., kinase inhibitors, immunomodulators)
    • Clinical-scale API advanced intermediates
    • Investigational new drug (IND) compounds for cancer R&D

    2. Agrochemical R&D: Herbicide Lead Compound Synthesis

    Major agrochemical manufacturers leverage this material in the design and scale-up of selective herbicidal compounds, particularly indazole or pyrazole analogs targeting specific enzyme systems in crops and weeds. The halogenated indazole moiety offers tunable reactivity for radical substitution or coupling modifications, allowing fine-tuned physiological activity in optimization campaigns. Adherence to environmental and worker safety regulations governs both experimental and pilot plant use, as process emissions and residues require documentation and validation prior to registration submissions.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for chemical synthesis
    • ISO 9001:2015 Quality Management Systems
    • EU Plant Protection Product Regulation (EC) No 1107/2009
    • EPA FIFRA standards for US pesticide intermediates

    Typical usage ratio

    • 6–12% of total synthetic batch; ratio further adjusted based on coupling partner stoichiometry and route screening outcome in discovery-to-pilot scale.

    Downstream process integration

    • Charged in the first or second step of route scouting for lead herbicide molecules, especially where indazole or pyridinylidene fragments form the pharmacophore of candidate actives.

    Final product types

    • Experimental pre-registration herbicide actives
    • Process development intermediates for patent-protected agrochemical families
    • Analytical standards for residue analysis programs

    3. Advanced Heterocyclic Materials for Electronic Chemicals

    Circuit board and display chemical manufacturers utilize indazole derivatives as controlled intermediates or precursors in the formulated production of specialty electronic materials. In such applications, the controlled electron-withdrawing effects from the bromo substituent are exploited to tailor ligand scaffolds or chelating agents for use in optical layer deposition, OLED emitters, or as controlled charge carriers. Given the strict demand for purity, batch reproducibility, and compatibility with high-throughput microfabrication protocols, all production records and analytical validation data must follow international electronic chemical manufacturing and occupational safety guidelines.

    Industry compliance standards

    • IEC 62474 Material Declaration for Electronic Products
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU) pre-registration or notification
    • RoHS Directive 2011/65/EU compliance for restricted substances
    • ISO 14001:2015 Environmental Management Systems

    Typical usage ratio

    • 2–7% per working formulation; varies based on composite target doping level and the electronic function of the layer produced.

    Downstream process integration

    • Used as a feedstock or complexation agent in the solution synthesis or vapor phase deposition of custom heterocycles for display backplanes, electron transport layers, or OLED emissive layers.

    Final product types

    • Active matrix display chemicals (TFT, OLED, QLED precursors)
    • Conductive or semiconductive organic electronic materials
    • Specialty coating additives for integrated circuit fabrication

    4. Fine Chemical Synthesis: Dye and Pigment Intermediate

    Dye, pigment, and specialty colorant companies employ the indazole core as a strategically functionalized intermediate to expand shade range and colorfastness in next-generation organic pigments. The presence of the methyl and bromine substituents enables access to novel chromophores with tailored spectral properties, especially for demanding textile, plastics, and printing ink applications. Stringent raw material identity tracking and end-use-specific compliance dominate procurement and in-process documentation, especially where customer industries require low residual impurity and reproducible lot-to-lot performance.

    Industry compliance standards

    • ISO 9001:2015 and 14001:2015 Certified Quality & Environmental Management
    • REACH Annex IV (EU) notification for pigment intermediates
    • Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers (ETAD) guidance
    • OEKO-TEX® chemical safety standards (when used for textile end-uses)

    Typical usage ratio

    • 5–18% by weight in the intermediate synthesis stage; optimal level determined by chromophore design and downstream colorant formulation demands.

    Downstream process integration

    • Employed during targeted N-alkylation, azo coupling, or condensation stages to introduce specific chromogenic moieties or to synthesize stabilized dye bases for further derivatization.

    Final product types

    • Performance pigments for plastics and synthetic fibers
    • Textile dyes with enhanced washfastness/lightfastness
    • High-stability printing ink colorants
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    Certification & Compliance
    More Introduction

    Exploring 5-Bromo-3-Methyl-1H-Indazole: Beyond the Basics

    The Path to Precision in Modern Chemistry

    Over the past decade in the chemical sciences, I’ve watched researchers dig deeper into the world of heterocycles. One compound that’s been gaining traction is 5-Bromo-3-Methyl-1H-Indazole. In any synthetic lab that explores new pharmaceutical or organic materials, this unique indazole derivative keeps popping up on order sheets and discussions. To someone outside the industry, the name might just sound technical, yet the value behind this compound requires a closer look. Its relevance isn’t just about adding a bromo or methyl group for the sake of novelty—it’s about enabling very targeted progress in some of the toughest areas of molecular design.

    The Structure and the Story Behind It

    I remember my first encounter with 5-Bromo-3-Methyl-1H-Indazole during a late night in graduate school, running a standard heterocycle synthesis route. The core structure—indazole—sits at a sweet spot of stability and reactivity. Add methyl at the third position and bromine at the fifth, and suddenly, you land on a molecule that offers interesting opportunities for functionalization and cross-coupling moves. This single tweak in the scaffold often sets the stage for constructing more complex frameworks. The compound typically appears as an off-white to light yellow solid, and laboratories are keen on its purity levels, usually demanding an HPLC purity upwards of 98%. Small differences in purity can seriously sway yields or final performance for target molecules down the line.

    Where Chemists Turn to 5-Bromo-3-Methyl-1H-Indazole

    Ask any medicinal chemist hustling under a grant deadline, and they will tell you that the push for new kinase inhibitors, antitumor candidates, and CNS drugs often revolves around modular synthesis. Here, this molecule becomes more than just a raw input. It plugs neatly into Suzuki, Buchwald-Hartwig, and other cross-coupling reactions, bringing a reliable bromo handle right to the ring. Unlike common starting materials that often drift through a sea of side-reactions or byproducts, 5-Bromo-3-Methyl-1H-Indazole allows teams to go after their target molecules with focus and fewer detours.

    The Methyl Group: Not Just a Decoration

    Anyone who’s tinkered with small molecule design knows a methyl group can change everything—from solubility in organic solvents to metabolic stability and binding affinity at a target enzyme. In this indazole derivative, the methyl at position three isn’t just an afterthought. When synthesizing more elaborate derivatives or designing drugs for tough protein pockets, that tiny change can make all the difference. Medicinal chemistry is filled with examples where seemingly minor modifications transform a mediocre lead into a viable candidate.

    Choosing the Model: Specs Backed by Real-World Lab Needs

    Specifications don’t just tick boxes on a SDS or certificate of analysis; they speak to the practical concerns in the lab. Here’s what usually matters to the people who use 5-Bromo-3-Methyl-1H-Indazole: chemical purity, water content, and a reliable melting range. Chemists are on the lookout for materials with minimal trace metals and remaining solvents, as even minor impurities can derail a reaction sequence or contaminate downstream products. In my own work, a compound that’s easy to handle, stable at room temperature, and ships well without strange odors or discoloration earns a quick spot among favorites.

    Standing Out from the Crowd: Not Just Another Indazole

    There’s a host of indazole derivatives out there, but not all are created equal. 5-Bromo-3-Methyl-1H-Indazole sits right at the intersection of reactivity and selectivity. The position and identity of substituents really do shape how a molecule interacts in the chemistry stack. For instance, compare it to 4-bromo analogues, and you’ll see vast differences in where subsequent reactions can take place—something any synthetic chemist notices quickly. Small, thoughtful substitutions allow for greater freedom in late-stage modifications or for attaching key pharmacophores.

    Beyond Synthesis: Real-World Impact in Drug Discovery

    Reflecting on project timelines where weeks hang in the balance, I’ve seen time and again how a well-chosen intermediate can tip the scales. Companies aiming to design next-generation pharmaceuticals need intermediates that offer both flexibility and reliability. With 5-Bromo-3-Methyl-1H-Indazole, teams can introduce aryl groups, alkyl chains, and even fluorinated motifs with greater confidence. Its predictable reactivity saves valuable time, letting researchers focus on optimization rather than troubleshooting. Anyone who has spent late hours tracking down reaction failures understands the value of consistency in building blocks.

    Quality and Trust: Why Source Matters

    Purchasing chemicals isn’t just a transaction. The supplier’s track record counts for a lot. Labs prioritizing reproducibility gravitate toward sources that provide batch-to-batch consistency and full transparency about their processes. Suppliers who offer detailed NMR, MS, and HPLC data give peace of mind and reduce the headaches from failed reactions or inconsistent yields. Years ago, a project I worked on was derailed by subpar starting material. Since then, I take sourcing decisions seriously, always steering toward products with robust analytical data and a reputation supported by peers.

    Reducing Risks in Scale-Up

    Shifting from the bench to pilot scale has its own set of risks. Handling batches of 5-Bromo-3-Methyl-1H-Indazole for a multi-kilogram synthesis brings up questions around dust, temperature stability, and safe disposal routes. Research-led companies are moving toward greener practices by selecting intermediates that allow for efficient, low-impact reactions. Many have incorporated real-time monitoring and automated purification to trim waste and control costs. In my time supporting process, attention to sections like solvent compatibility and low-temperature crystallization techniques paid off immensely in yield and purity.

    Solving Everyday Obstacles

    Smart researchers don’t just accept off-shelf solutions; they push suppliers for modifications or custom specifications. Higher purity, special particle sizes for improved suspension, or custom packaging for air- and moisture-sensitive work show real cooperation between production and R&D. Those of us improvising new synthetic routes have often asked for premade solutions tailored to our workflows, whether that’s outsized packaging to reduce transfer losses, or a pre-dried format. This kind of collaboration beats the “off-the-rack” mentality every time.

    Regulatory and Safety Footprint

    Every compound destined for pharmaceutical research has to come with a stack of paperwork. Regulatory pressure now means chemical suppliers provide evidence for GMP compliance and traceability, but it’s up to end users to follow through with responsible lab practices. Teams keep Material Safety Data Sheets on hand, making sure everyone’s familiar with the right storage conditions, PPE, and spill response procedures. I’ve seen research groups implement weekly check-ins just to keep safety and compliance front and center, especially as new chemicals enter the mix.

    Bridging Academic and Industry Needs

    Graduate students starting their journey often ask whether to search academic or industrial supply channels for new intermediates. My advice leans toward stable, traceable sources, even for small batch work, to reduce headaches later on. Direct interaction with technical support teams—often overlooked—can yield huge insights into storage, stability, and troubleshooting for tricky reactions. The technical support stories from real chemists who’ve run the same routes echo louder than any generic data sheet.

    Making Connections with Downstream Workflows

    Most molecules have lifespans far beyond their initial synthesis. In my experience, 5-Bromo-3-Methyl-1H-Indazole ends up as part of an intricate sequence—often destined for cross-coupling, N-alkylation, or other transformations leading to clinical candidates. It’s here that handling qualities—whether the compound clumps in storage, or takes up moisture, or suffers degradation from light—can have lasting effects. Getting the physical form right, and adjusting for physical or storage requirements, saves not just the month but the entire project.

    Encouraging Collaboration in the Supply Chain

    Supply chain breakdowns don’t just threaten timelines; they chip away at trust. Periods of short supply reveal which suppliers keep meaningful reserves, and which maintain regular analytical checks to guarantee product integrity. Open communication from sourcing to shipment keeps everyone in the loop if things veer off track. I’ve worked with teams that send periodic feedback on off-standard batches, driving iterative improvement not just in documentation but in finished goods themselves.

    Transparency: Earning Trust, Backed with Data

    Chemistry doesn’t advance without honest data. Companies and academics alike benefit from robust, up-to-date certificates of analysis and open reporting of batch inconsistencies. Detailed disclosures make life easier for R&D teams who stake their projects on each reaction. Last-minute surprises on impurity profiles, or poorly documented production changes, put more at risk than just materials cost—they can undo months of careful documentation. In my experience, open access to supplier data improves both scientific understanding and confidence.

    Fostering Sustainability in Advanced Intermediates

    Sustainability and price are rarely mutually exclusive. As green chemistry principles continue to sweep through the research landscape, many of us have transitioned to sourcing intermediates like 5-Bromo-3-Methyl-1H-Indazole from producers embracing renewable solvents, solvent recycling, and energy-efficient crystallization. Some teams even request full life-cycle analyses for key intermediates. While this wasn’t the norm a decade ago, today’s researchers recognize the broader ripple effects of these buying choices. The transformation isn’t just about public perception—it results in cleaner chemistry, improved lab safety, and lowered long-term costs.

    Sharing Lessons and Keeping Standards High

    Looking back over years in both academic and industrial labs, I’ve learned that the success of synthetic campaigns leans heavily on the right intermediates, and the lessons surrounding their use aren’t confined to textbooks. Process chemists swap stories about favorite batches, preferred packaging, and clever tricks to overcome solubility or mixing headaches. Open forums at conferences and practical workshops pile up best practices. R&D teams who invite ongoing feedback from synthetic chemists, process engineers, and end-user clients hold the advantage in both efficiency and product quality.

    Reducing Surprises Down the Line

    Consistent supply, dependable specs, and honest documentation make up the trifecta for reliable procurement. Scientists build entire drug discovery or material development pipelines on this foundation. Problems often arise from cutting corners or choosing a generic supplier that trims costs but skimps on quality checks. I’ve seen research slow to a crawl because of misidentified impurities or shipping mishaps. For a compound like 5-Bromo-3-Methyl-1H-Indazole, taking shortcuts often works out less favorably in the end.

    Driving Progress Means Choosing Wisely

    Every scientific milestone starts with dozens or hundreds of smaller, careful choices. Selecting the right starting materials or intermediates determines how smoothly a program can move from bench to clinic, or from test tube to pilot plant. My advice always follows experience—work with teams who back their materials with facts. Be relentless in testing new batches and don’t shy from pushing suppliers for better transparency and quality.

    Bringing it All Together

    In a market crowded with similar-sounding options, 5-Bromo-3-Methyl-1H-Indazole stands out for its chemical versatility, consistency from reputable sources, and adaptability to both standard and cutting-edge synthetic approaches. Chemists, process engineers, and project managers know the headaches that arise from unreliable or variable intermediates. Years of hands-on work have taught me to spot the qualities that make synthesis smoother: clear specifications, verified purity, transparent reporting, and reliable supply partners who listen and improve. As more researchers look for precision and reliability from their starting points, compounds of this kind aren’t just line items on a purchase order—they drive innovative science forward and shape what’s possible in the future of chemistry.