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2-Methyl-5-Nitroindole

    • Product Name 2-Methyl-5-Nitroindole
    • Alias 2-Methyl-5-nitroindole
    • Einecs 629-099-0
    • 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
    VTB
    Specifications

    HS Code

    701580

    Chemical Name 2-Methyl-5-Nitroindole
    Cas Number 15862-15-8
    Molecular Formula C9H8N2O2
    Molecular Weight 176.17
    Appearance Yellow to orange crystalline powder
    Melting Point 170-174°C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents, insoluble in water
    Storage Temperature Store at 2-8°C
    Synonyms 5-Nitro-2-methyl-1H-indole
    Smiles CC1=CC2=C(C=C1)[N](=O)C=CN2
    Inchi Key IQPDNQZFJIRCNI-UHFFFAOYSA-N
    Hazard Statements May cause irritation to skin and eyes

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

    Packing & Storage
    Packing 2-Methyl-5-Nitroindole is packaged in a 5-gram amber glass bottle, clearly labeled with chemical name, quantity, and hazard warnings.
    Shipping 2-Methyl-5-Nitroindole is shipped in tightly sealed containers to prevent moisture and light exposure. Packaged according to standard chemical safety regulations, it is clearly labeled and may be shipped as a non-hazardous material unless specified otherwise by local guidelines. Temperature and handling instructions are provided to ensure safe delivery.
    Storage 2-Methyl-5-Nitroindole should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials like strong oxidizers or acids. Keep the container tightly closed to prevent moisture absorption. Store at room temperature, away from ignition sources. Ensure proper labeling and utilize secondary containment to minimize the risk of spills or contamination.
    Application of 2-Methyl-5-Nitroindole

    Applications of 2-Methyl-5-Nitroindole in Industrial Manufacturing

    2-Methyl-5-Nitroindole provides reliable performance as a pharmaceutical intermediate and in other specialty chemical production segments. Our manufacturing integrates strict QC and advanced batch control, meeting the demands of regulated downstream sectors. Below, we outline key industrial manufacturing applications based on actual market usage and technical collaborations.

    1. API Intermediate for Antiviral Drug Synthesis

    Manufacturers use 2-Methyl-5-Nitroindole as a critical intermediate in the synthesis route of certain novel antiviral ingredients. The compound participates in indole ring construction and nitro group transformations, enabling formation of pharmacologically active scaffolds. Synthetic chemists introduce it during multi-step coupling and reduction sequences. The material's physicochemical stability supports robust scale-up, maintaining batch reliability for final API registration.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF monographs for process intermediates
    • 21 CFR Part 211 – US FDA GMP for Finished Pharmaceuticals
    • EU Guidelines for GMP (EudraLex Volume 4)

    Typical usage ratio

    • Batch input levels range from 100 to 250 g per kg of finished API, adjusted based on target synthesis yield and desired impurity profile

    Downstream process integration

    • Added during the key indole core elaboration step in gram-scale and pilot cGMP synthesis lines
    • Subjected to catalytic hydrogenation or nucleophilic substitution for downstream structural modifications
    • Feeds directly into isolation and purification units prior to final conversion into active ingredients
    • Integrated into validated multi-step batch records for DMF/CEP support filings

    Final product types

    • Antiviral API (e.g., experimental non-nucleoside inhibitors)
    • Intermediates for small-molecule drug candidates
    • Pharmaceutical analytical reference standards
    • Bulk APIs supplied to formulation plants

    2. Fine Chemicals for Dye Intermediate Production

    Chemical manufacturers incorporate 2-Methyl-5-Nitroindole as a nitroindole base in specialty dye intermediate syntheses. Its electron-rich structure enhances aromatic substitution, facilitating downstream azo coupling and oxidative processes. High-purity inputs are critical to delivering consistent color intensity and minimizing by-product formation. Downstream blending requires close monitoring of input impurity levels to secure reproducibility in extended batch manufacturing.

    Industry compliance standards

    • EN 71-3:2019 for safety of toy dyes (breakdown contaminants)
    • ISO 9001:2015-certified internal QC for colorant precursors
    • REACH pre-registration for chemical intermediates in Europe
    • Restricted substances lists per customers

    Typical usage ratio

    • Use level typically spans between 25 and 60 g per kg of final dye intermediate, modulated depending on required chromophore loading and color depth

    Downstream process integration

    • Charged during initial indole ring derivatization in closed-loop reactors
    • Reacted with sulfonation agents for solubility improvement
    • Further processed through diazo coupling lines for formation of complex dye molecules
    • Strict in-process controls for impurity cuts in batch-wise or continuous systems

    Final product types

    • Azo dye intermediates for textile, leather dyes
    • Synthetic colorants for printing inks
    • Precursor compounds for specialty organic pigments
    • Analytical dye markers

    3. Building Block in Research and Development for Heterocyclic Libraries

    Chemical R&D divisions employ 2-Methyl-5-Nitroindole for assembling diverse heterocyclic libraries, enabling drug discovery and agrochemical screening campaigns. Its functional scaffold supports diverse functionalization, including Suzuki-Miyaura cross-coupling and nitro-to-amino transformations. Researchers value its ability to yield unique indole-based analogs, accelerating lead optimization. Laboratories track lot numbers and maintain analytical monitoring to ensure result reproducibility across chemical libraries and screening plates.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for chemical and biological screening
    • Institutes’ internal QA systems for reference compound synthesis
    • ISO/IEC 17025 accreditation for analytical testing labs
    • OECD principles for chemical test substances

    Typical usage ratio

    • Used at 1–10 mmol scale per individual library compound synthesis, with quantity adjusted based on specific target structure complexity

    Downstream process integration

    • Introduced as core structure in initial stages of high-throughput solid phase synthesis
    • Functionalized via palladium-catalyzed coupling or reduction for scaffold diversification
    • Purified through preparative HPLC and submitted to screening campaigns
    • Recorded in laboratory information management systems for compound tracking

    Final product types

    • Small-molecule compound libraries for pharmaceutical and agrochemical screening
    • Lead-like indole scaffolds for SAR optimization
    • Analytical standards for MS/NMR calibration
    • DNA-encoded chemical libraries

    4. Precursor in Advanced Material Additive Synthesis

    Producers of specialty polymers and electronic materials utilize 2-Methyl-5-Nitroindole for introducing indole-based units into advanced additive frameworks. The structural element improves charge transport, UV stability, or adhesion properties within end-use materials. Precise molar inputs ensure targeted molecular weight and desired end-group content. Manufacturers run closed-system reactions to manage NG handling, minimize off-gassing, and control particle size distribution in final blends.

    Industry compliance standards

    • ISO 9001:2015 quality management for specialty additives
    • RoHS compliance for materials in electronics
    • IEC 62676 series for additive safety alignment in components
    • Customer-specific material safety sheets for end-use approvals

    Typical usage ratio

    • 0.5–3.0% by weight relative to total additive load in specialty polymer or coating batches, with ratio tailored to blend compatibility and functional performance

    Downstream process integration

    • Fed into monomer blend prior to polymerization in solvent or melt systems
    • Reacted during main-chain assembly on continuous production lines with viscosity and conversion monitoring
    • Subjected to downstream compounding or masterbatch preparation
    • Implementation in post-polymerization blending for property enhancement

    Final product types

    • Polymer additives for LED encapsulation
    • High-performance adhesives in electronics
    • Functional coatings for optoelectronic devices
    • Stabilizer blends for specialty materials
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    Certification & Compliance
    More Introduction

    2-Methyl-5-Nitroindole: Raising the Bar in Specialty Fine Chemicals

    Our Experience Bringing 2-Methyl-5-Nitroindole to Market

    In chemical manufacturing, reliability often means the difference between success and failure at the bench or on the plant floor. After decades of hands-on work producing indole series intermediates, 2-Methyl-5-Nitroindole has proven itself as a building block best handled by those who know indole chemistry inside out. Unlike third parties or resellers that simply relay catalog numbers, we balance purity targets and stability based on honest feedback from the end-users in pharmaceuticals, diagnostics, and specialty materials.

    2-Methyl-5-Nitroindole serves as a trusted scaffold for researchers and process chemists, especially for its ability to unlock pathways not always accessible with other indole derivatives. Introducing a methyl group at the 2-position and a nitro group at the 5-position brings notable changes in electronic properties. Fine-tuning reactivity in this way opens up substitutions and transformations impossible with unsubstituted indole or with simple nitroindole variants. The subtlety of electron-donating and withdrawing effects at these positions isn’t just academic—our partners report that yields, selectivity, or bioactivity can change sharply with a single shift in substitution. We work closely with R&D teams that demand not just another indole, but one with targeted reactivity and stability profiles.

    Quality Through In-House Process Control

    Achieving consistent quality for 2-Methyl-5-Nitroindole takes more than careful analytical measurements. Everything starts with solid, reproducible raw materials and tight control over every batch—something only the original manufacturer can guarantee. We have observed firsthand the impact of impurities or minor byproduct isomers on downstream process steps. From our synthesis route to purification, we track every variable so that each lot stands up under scrutiny—not just the first time, but every time. Workers at every stage have internalized the stakes for those on the receiving end, whether they are scaling up a key intermediate or performing structure–activity relationship work on a tight deadline.

    Melting point and purity, confirmed by TLC, NMR, and HPLC, remain critical in each Q.C. iteration, but practical knowledge also guides us: How does the compound respond to light, air, or long-term storage? What bulk handling techniques keep losses at a minimum? Our team learned early that reports of “unexpected” decomposition often stem from overlooked micro-environmental variables. As a manufacturer, we track these in real time, not only for compliance but also for the practical benefit of our customers’ projects. Our direct experience frequently leads to protocol tweaks that make life easier for chemists downstream.

    Why 2-Methyl-5-Nitroindole Offers Something Unique

    Indole chemistry covers a vast class of compounds, but the addition of a methyl at the 2-position shifts the entire molecular profile: The steric and electronic effects tune both chemical and biological behavior in ways that standard indole or 5-nitroindole cannot mimic. Over the years, users report that this specific substitution facilitates cross-couplings and alkylations resistant to more basic indole nuclei. In pharmaceutical research, these modifications impact cell permeability or binding profiles, giving rise to new leads impossible to reach from unmodified indoles. We have seen biologists depend on these nuanced properties to probe enzyme binding sites or to modulate metabolic stability in drug discovery screens.

    From a synthetic viewpoint, reactivity often changes course due to the nitro’s electron-withdrawing influence at position 5. This activation supports selective further functionalization, yielding complex analogs off the main indole backbone. Research into DNA probes and oligonucleotide modifications continues to mine 2-Methyl-5-Nitroindole for its ability to serve as a platform for labeling and unique recognition units. Direct feedback from application teams has confirmed that cheaper imitations or related structures miss the mark on stability, signal strength, or reactivity, costing valuable time in troubleshooting or repeat synthesis.

    We manufacture to specification, but also refine our process as new needs appear—solubility, particle size, or batch homogeneity—all balanced according to feedback from collaborators in laboratory or industry. Our R&D group bridges the gap between large-scale output and targeted requirements for niche application fields, so the result matches both innovation goals and regulatory compliance.

    Batch Consistency: Delivering on More Than Paper Specifications

    Consistency isn’t just about hitting a number on a certificate of analysis. As manufacturers, we routinely challenge our batches under variety of conditions: how it dissolves in the actual solvents used on site, how micro-scale impurities impact crystallization, and how compounds behave under storage. Procurement teams and end-users have told us where copycat batches have failed in pilot lines—even though “on paper” specs looked the same. That’s why every delivery from our facility includes the real-world lessons learned over years of scale-up, drying, and finishing, including transport and long-term storage stability.

    Close partnerships with clients helped us improve both handling and shelf life. Users running assays for genomics, diagnostics, or medicinal chemistry regularly consult us over technical details—shipping without temperature excursions, minimizing product exposure, and ensuring batch-to-batch consistency. Our feedback loop with downstream users forms the backbone of how we tune drying, milling, or formulation steps.

    Usage in Modern Research and Industry

    2-Methyl-5-Nitroindole fills multiple critical roles across research fields. Among nucleic acid chemists, it enables the construction of modified bases for DNA and RNA probes and expanded genetic alphabets. Our clients say it’s a preferred choice for constructing molecular scaffolds in FRET probe systems, where background signal must be minimized. Bioconjugation chemists exploit its unique placement of electron-donating and withdrawing groups to fine-tune reactivity, attaching fluorophores or other molecular tags in targeted diagnostics.

    Pharmaceutical teams favor 2-Methyl-5-Nitroindole for its adaptability: the structure acts as an effective intermediate for heterocycle construction, kinase inhibitor design, or as a precursor to pyrrolo[2,3-b]indole frameworks central to antitumor and antiviral compounds. Small modifications in the indole ring system link directly to the bioactivity and PK profiles in discovery programs—showing how the arrangement of a methyl and nitro group influences far more than just chemical reactivity. Our close coordination between production and chemists looking for specific scaffold modifications means we often build to requirements far more rigorous than generic catalogs typically supply.

    Scalability and Process Know-how

    Producing this compound at gram, kilo, and even ton scale brings lessons impossible to gain from bench-scale synthesis alone. Over the years, we’ve tested multiple routes, optimizing yields, safety, and byproduct control. The 2-methyl group, though seemingly minor, alters reaction course during nitration and downstream isolation; only by running pilot and production batches do those details come out. As manufacturing chemists, we adjust everything from solvent choice to recrystallization methods based on real-time data, knowledge gained from both successful and problematic runs.

    Temperature control in nitrating a methyl-substituted ring, purification following heterocycle closure, and handling of mixed isomer populations can all challenge even seasoned chemists. Labs working from third-party or resold materials have reported trouble replicating yields or achieving expected potency in bioassays due to minor yet impactful impurity profiles. Our role starts early—helping customers adapt their own process protocols to the quirks of real-world material. Partner feedback results in improved filtration techniques, optimized shipping containers, and advice on handling electrostatic characteristics inherent to dry powdered indoles.

    Differences from Other Indole Derivatives

    There’s no substitute for direct experience comparing close analogs side-by-side across a variety of applications. Standard indole or even just 5-nitroindole lack the nuanced electronics brought by the methyl group at the 2-position—affecting binding, solubility, and stability in both organic and aqueous environments. Some researchers attempt to substitute with lower-cost indole sources, but side reactions or shifts in chemical profile can send entire R&D campaigns back to the drawing board. The nitro group at position 5, coupled with the bulk and modulation of the 2-methyl, steers both reactivity and biological properties in ways no other indole framework does.

    We have observed differences in speeds of substitution, ease of ring closure in advanced heterocycle synthesis, and uptake in small molecule probe development. Teams have let us know about batch failures with alternate products that stemmed from subtle differences in starting material. Our experience includes troubleshooting at the process level—a service often unavailable from mere resellers or catalog houses. This hands-on technical partnership enables us to pre-empt issues, ensuring every lot truly meets end-use specifications beyond just chemical purity.

    Those working in pharma or biotech most commonly report sharper structure-activity trends and better in vivo stability when using 2-Methyl-5-Nitroindole compared to related compounds. For chemists developing oligonucleotide tools, the distinct substitution pattern aids in duplex stability and labeling efficiency, critical for both research reagent supply and IVD development.

    Real-World Challenges in Shipping and Handling

    Supplying indoles isn’t just about making a pure chemical and printing a certificate. After years of moving 2-Methyl-5-Nitroindole from synthesis kettle to packed drum, we’ve seen anything that can happen, will happen: caking due to humidity uptake, minor solvent residue impacting downstream analytics, or batch variability due to in-batch segregation during grinding. Customers in northern or southern climates see differences in self-life and ease of re-dissolution due to local shipping and warehousing conditions. We heard early on that enabling project success further downstream means factoring in all those technical logistics.

    Our packaging and storage protocols now reflect these experiences: all material undergoes thorough drying before packing, moisture-protective liners guard against atmospheric effects, and packaging options scale according to user need. We regularly work with users to arrange smaller aliquots or short-run custom pack sizes, reducing risk of spoilage and simplifying transfer in the client’s facility.

    Training and technical support don’t stop at the shipping dock. New customers gain from our accumulated expertise—not just how to store or dissolve the product, but also tricks for achieving the best yield in key reactions using our own real-world test results.

    Meeting Regulatory and Documentation Demands

    Manufacturing and supplying specialty chemicals like 2-Methyl-5-Nitroindole means engaging with an evolving landscape of quality standards and regulatory requirements. GMP expectations filter down even to smaller-scale research supply, and our documentation, tracking, and lot control match these demands. Users, especially in regulated environments, need validated traceability and batch histories. Our Q.A. documentation—backed by decades on the production floor—has regularly supported our customer’s own filings, audits, or due diligence checks.

    Beyond documentation, our role as manufacturer means standing behind every batch: if a question comes up, the people who made it handle the inquiry, not a third-party sales office. This direct line proves invaluable for rapid troubleshooting, supporting new method development, or submitting material for regulatory review.

    Feedback-Driven Improvements: Learning from Our Customers

    Working with 2-Methyl-5-Nitroindole means listening as much as making. Direct, unfiltered feedback from users has shaped countless process refinements—from analytical protocols to milling and packaging. Teams working in pharma discovery programs challenged us to improve fine-grained purity levels to match new bioassay needs. Synthetic chemists needed larger particle size distributions to ease filtration, so we adjusted our grinding and sieving routines. Environmental chemists evaluating fate and transport parameters sought extra stability data to model their systems appropriately.

    Many improvements came not through formal requests but through informal consultations between application specialists and our process chemists. The result isn’t catalog sameness, but real partnership that improves quality, utility, and project outcomes for all involved.

    Supporting Next-Generation Research and Diagnostics

    The demands from genomics, personalized medicine, and molecular diagnostics have grown in complexity and precision in the last decade. 2-Methyl-5-Nitroindole now serves as one link in the broader chain supporting molecular tool development. Our colleagues in oligonucleotide synthesis hone in on this molecule’s properties for amplified signal generation and sequence specificity. Diagnostics developers building probe-based detection platforms require absolute consistency and background-free results—expectations we meet by running custom analytical checks and shelf-life projections in parallel with manufacturing.

    As new uses emerge—be it for labeling, covalent bio-conjugation, or advanced material scaffolds—our investment in technology transfer and analytical training continues. The future market for such customizable, specialized indole derivatives depends on the depth of manufacturer support, something we’ve delivered through both decades of technical know-how and a willingness to improve alongside our customers.

    Looking Ahead: Commitment to Innovation in Indole Chemistry

    The indole class delivers building blocks sought after in both time-tested and next-generation chemistry. Through our work with 2-Methyl-5-Nitroindole, we’ve seen how even small changes—like the right substitution on the ring—unlock entire new families of useful compounds. Today’s industry demands manufacturers combine technical insight, flexible production, and hands-on support. Consistency in every batch, backed by direct communication and willingness to address new project demands, sets apart a true chemical producer from a generic supplier.

    We look forward to continuing our role in pushing the field forward, not only by supplying high-quality 2-Methyl-5-Nitroindole but by building lasting technical partnerships with the researchers, engineers, and process chemists charting new scientific territory. Our plant team and application scientists welcome inquiries—big or small—about sourcing, processing, or applying this key specialty chemical across the full spectrum of innovation.