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2-Amino-9H-Pyrido[2,3-B]Indole

    • Product Name 2-Amino-9H-Pyrido[2,3-B]Indole
    • Alias AαC
    • Einecs 208-760-7
    • 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

    393326

    Iupac Name 2-Amino-9H-pyrido[2,3-b]indole
    Molecular Formula C11H9N3
    Molecular Weight 183.21 g/mol
    Cas Number 25389-94-0
    Appearance Off-white to beige powder
    Melting Point 315-317 °C
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO
    Smiles C1=CC2=C3C(=C1)NC(=NC3=CC=C2)N
    Pubchem Cid 10474
    Inchi InChI=1S/C11H9N3/c12-11-13-7-3-1-2-8-9(7)14-10(11)6-5-4-8/h1-6,14H,(H2,12,13)
    Synonyms 2-Aminonorharmane

    As an accredited 2-Amino-9H-Pyrido[2,3-B]Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 5-gram amber glass bottle with a secure screw cap, labeled with hazard, purity, and identification details.
    Shipping 2-Amino-9H-Pyrido[2,3-b]indole is shipped in tightly sealed containers, compatible with its chemical properties, and protected from moisture and light. The shipment follows applicable regulations for laboratory chemicals, ensuring safe handling and transportation. Appropriate hazard labeling and documentation are included, and the package is handled only by authorized personnel during the shipping process.
    Storage 2-Amino-9H-Pyrido[2,3-b]indole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature or as specified by the supplier. Ensure proper labeling, and access should be restricted to trained personnel. Use appropriate secondary containment if required.
    Application of 2-Amino-9H-Pyrido[2,3-B]Indole

    Applications of 2-Amino-9H-Pyrido[2,3-B]Indole in Industrial Manufacturing

    2-Amino-9H-pyrido[2,3-b]indole serves as a crucial intermediate for advanced chemical synthesis in multiple specialized industrial sectors. Our manufacturing expertise ensures the material’s consistent performance in applications where molecular complexity and compliance are critical. Below we detail core downstream scenarios where direct industrial consumption is established, with application-specific technical requirements and process parameters.

    1. API Intermediate Synthesis for Oncology Pharmaceuticals

    This heterocyclic compound is a recognized building block in the synthesis of targeted anticancer pharmaceutical actives, particularly in pyridoindole-based kinase inhibitors. Leading pharmaceutical producers incorporate it during the construction of multi-ring scaffolds required for high-affinity molecular targeting, using its amine functionality in selective N-alkylation and amidation steps. The integration of this intermediate follows closely controlled cGMP batch protocols to ensure trace impurity limits and molecular consistency prior to final API purification stages.

    Industry compliance standards

    • ICH Q7, Q3A/B (Control of Impurities in Drug Substances)
    • EU GMP Part II (Active Substances)
    • US FDA 21 CFR 210/211
    • Pharmacopoeias: USP, EP—Reference to final API compliance

    Typical usage ratio

    • Range: 0.5–2.5 molar equivalents, adjusted per target molecular yield and impurity thresholds

    Downstream process integration

    • Charge to condensation or coupling step during API intermediate formation, prior to final cyclization and purification

    Final product types

    • Small molecule oncology APIs
    • Pyridoindole-derived kinase inhibitor drug substances
    • High-purity pharmaceutical intermediates for solid oral dosage forms

    2. Advanced Dyes and Fine Pigments Manufacturing

    Colorant manufacturers incorporate 2-amino-9H-pyrido[2,3-b]indole in the synthesis of specialty aromatic dyes, where the compound’s conjugated system enhances chromophore intensity and solubility characteristics. Its role as a diazo coupling partner supports the development of photostable, high-intensity dyes for industrial printing and textile applications. To ensure compliance, processors maintain traceability from raw material intake through oxidative coupling and sulfonation steps.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006—Annex XVII (Restrictions on certain aromatic amines)
    • OEKO-TEX Standard 100—Class I/II for finished textiles
    • ISO 9001 quality management for pigment processing

    Typical usage ratio

    • Content: 0.1–1.8% w/w of complete dye batch, fine-tuned for color intensity and reactivity

    Downstream process integration

    • Introduced at the diazo coupling stage for chromogenic framework extension before subsequent functionalization and spray-drying

    Final product types

    • Reactive dyes for cellulose fiber printing
    • High-persistence pigments for plastics and fibers
    • Photostable colorants for industrial ink formulations

    3. Analytical Chemistry Reference Standards Production

    Producers of certified reference materials utilize this indole derivative as a primary standard and matrix spike for carcinogen exposure analysis and genotoxicity testing protocols. Analytical laboratories demand precisely characterized batches with validated impurity profiles to calibrate LC-MS and GC-MS instruments, especially for monitoring mutagenic polycyclic compounds in environmental and food safety surveillance. Batch production under metrologically traceable systems ensures suitability for global proficiency testing schemes.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for reference material producers)
    • ISO/IEC 17025:2017 (Testing and calibration laboratories)
    • ILAC G12 and EURACHEM/CITAC guides

    Typical usage ratio

    • Spiking standard: 5–100 μg per calibration sample, as dictated by sensitivity range of target analytic system

    Downstream process integration

    • Direct formulation into volumetric standards and internal calibration solutions after gravimetric purity assessment

    Final product types

    • Certified reference standards for carcinogen quantitation
    • Traceability kits for method validation in environmental, food, and pharmaceutical labs

    4. Specialty Polymer and Resin Additives

    Resin and engineering plastics formulators integrate this pyridoindole compound to introduce specific nitrogen heterocycles as functional groups, contributing to improved crosslinking or UV absorption behavior in advanced polymer networks. Industrial users select batch grades based on critical factors such as amine content, trace metals, and moisture levels. Compound addition occurs during pre-polymer blending or in situ modification, under monitored thermal conditions to ensure incorporation efficiency before polymer shaping or casting steps.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 on plastic materials intended to come into contact with food—if food-contact applications
    • ASTM D256, D790 (Mechanical property testing)
    • ISO 9001—Polymer additive manufacturing

    Typical usage ratio

    • Formulation: 0.02–0.2 phr (parts per hundred resin) by weight, adjusted per polymer matrix reactivity and performance targets

    Downstream process integration

    • Dispersion at pre-polymerization or melt-blending stage, followed by curing or extrusion depending on the final material specifications

    Final product types

    • UV-absorbing engineering plastics and coatings
    • Specialty resin grades for electrical encapsulation
    • Polymeric materials for specialty optics or device housings
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    Certification & Compliance
    More Introduction

    2-Amino-9H-Pyrido[2,3-B]Indole: Our Experience Manufacturing a Key Synthetic Intermediate

    Building on Years of Fine Chemical Manufacturing

    As a chemical manufacturer with decades of hands-on experience, we have seen how 2-Amino-9H-Pyrido[2,3-b]indole has become increasingly valuable across research and development, especially in pharmaceutical, biochemical, and toxicological fields. Our own journey producing this compound grew out of a broader effort to offer high-quality heterocyclic building blocks, particularly those crucial for studying enzyme inhibitors and carcinogen metabolism. This compound, known in research circles for its structural features that mimic biologically active molecules, involves several non-trivial steps that require close process control.

    Understanding This Compound’s Structure and Use

    2-Amino-9H-Pyrido[2,3-b]indole stands out because of its fused indole and pyridine ring system, a structure seen among various biologically active alkaloids. Research into pharmaceutical and toxicological mechanisms often hinges on such scaffolds. What distinguishes this compound isn’t just the unique arrangement of nitrogen atoms in its core, but also the reactivity profile driven by the amino group. These features allow synthetic chemists to link it into larger molecules, leading to complex molecular libraries that support drug discovery or biochemical screening.

    Laboratories investigating mutagenicity, carcinogenicity, or metabolic pathways often turn to 2-Amino-9H-Pyrido[2,3-b]indole as both a research substrate and a reference standard. Our manufacturing expertise comes into play because this isn’t a commodity material; it requires tight handling of precursor purity and reaction conditions. Any deviation can lead to colored byproducts or loss of selectivity, complicating downstream use in analytical or biological studies.

    What Makes Our Production Approach Different

    Early in our own process development, we learned that the batch size, glassware configuration, and subtle heating gradients have outsized effects on yield and purity when making this compound. Grignard reagents, oxidants, and dehydration steps are finicky; control of water and oxygen is crucial during specific phases. We also noticed issues crop up if starting pyridine sources aren’t purified beforehand, so we invested in inline filtration and nitrogen blanketing systems. None of these choices happen in isolation — there’s always a knock-on effect on crystallization and isolation.

    Comparison with other indole-based compounds highlights the difficulties. For example, handling indole-3-carboxaldehyde seems straightforward after working with fused heterocyclics like 2-Amino-9H-Pyrido[2,3-b]indole. Our experience demonstrates that minor process tweaks, adopted only after diligent in-house trials, lead to improvements in yields above 90 percent with consistent melting point and color characteristics — essentials for researchers needing reliable analytical data. This constant refinement, rooted in repeated in-lab observations, sets the quality of our finished product apart from material produced using more formulaic or scaled-out processes.

    Specification and Analytical Consistency

    Most requests for this compound come with rigorous purity specifications. We meet analytical benchmarks for HPLC, NMR, and mass spectrometry, but experience tells us to focus first on the clarity of crystalline product and reproducibility between lots. Trace metal content and solvent residue pose real problems if left unaddressed; our team pre-emptively runs ICP-MS and GC checks on both intermediates and finished batches. Analysts in downstream applications have remarked on the consistency of our lots, a point that only comes from years spent correcting for real-world process drifts.

    For the customer, this transparency in quality standards means the finished 2-Amino-9H-Pyrido[2,3-b]indole performs predictably in synthesis or assay settings. We’ve seen customers come back after false starts with samples from brokers or laboratory resellers, who often haven’t tracked handling conditions after purchase from the factory. Freshness, homogeneity, and storage away from excess light and humidity keep the amine group from degrading or yellowing, which our controlled packaging approach reinforces.

    Application in Drug Discovery and Toxicological Research

    One of the main reasons researchers use this compound involves its bioactivity resemblance to key metabolites formed during the metabolic activation of food-borne or environmental aromatic amines. Testing these compounds, especially in mutation assays, calls for pure, freshly synthesized product with no degradation byproducts. It’s a responsibility we take seriously because inaccurate results can mislead studies on potential cancer risk or therapeutic activity.

    Medicinal chemists also value this compound’s indole-pyridine core as a platform for further modifications. Our close work with contract R&D labs revealed how acylation or alkylation of the amino group, using our material, leads to hundreds of new analogs for screening against enzyme targets. The highly conjugated system enables robust absorption properties, allowing for trace-level detection with minimal background, a factor that saves both time and resources for teams running dose-response or mechanistic assays.

    Manufacturing Reliability and Transparency Matter

    The sophistication in producing this compound comes from years of feedback loops: running the reactions, spotting the yellowing edge in a crystallization lot, tweaking solvent profiles, checking with the analytical team, then running another batch. We do not leave key steps to outside partners; our synthesis follows validated internal pathways developed by chemists who have actually handled this compound on the bench. Any out-of-spec observation gets flagged early, never after shipment. Infrequent but real hazards in some stages, such as exothermic intermediate formation, mean we bring in safety review and updated risk assessments, always improving on what earlier batches revealed.

    This degree of in-house control separates us from traders and brokers, who can’t always answer why a bad HPLC trace shows up, or whose material history looks murky under audit. We know exactly which materials ended up in each batch, when they were synthesized, and how long they sat in primary storage before shipment. These are minor details in isolation, but together, they build reliability.

    Comparing to Other Fused Indole or Pyridine Compounds

    Colleagues sometimes ask how 2-Amino-9H-Pyrido[2,3-b]indole differs from other polycyclic aromatic amines they use. Beyond the cosmetic distinctions, the main differences track to reactivity and impurity profiles. The fusion of indole and pyridine introduces more pronounced π-electron delocalization, which impacts its redox potential and how it behaves in enzymatic assays compared to monocyclic indole systems like 2-aminoindole or 2-aminoquinoline.

    We have tried to synthesize many similar looking scaffolds. Each introduces its own quirks: some suffer from fast oxidative dimerization; others attract hydrolysis or give troublesome side products during crystallization. In contrast, 2-Amino-9H-Pyrido[2,3-b]indole resists these pitfalls when protected from humidity and stored properly. Its physical handling — fine crystal flow, stable color, manageable dustiness — comes as much from process knowhow as from theoretical structure. We have built protocols around these findings, documenting them for in-plant training and QA audits, so each technician follows proven best practices.

    Challenges and Our Solutions

    Early batches never satisfied our standards. We saw unwanted isomers and color streaking, especially when precision on temperature or reaction time lapsed. Shortly after scale-up, routine QA showed certain solvents retained impurities that only careful solvent distillation eliminated. We invested in rotary evaporators and solvent purification columns that eliminated batch-to-batch surprises. Even now, we routinely track the sources and ages of every reagent that enters the process — old stock or impure base solvents show up as variations in yield and purity more often than published literature admits.

    Process safety sits at the root of reliable manufacturing. Some of the intermediates in synthesizing 2-Amino-9H-Pyrido[2,3-b]indole show sensitivity to air and light, requiring batchwise handling under inert gas and careful bottling. Technicians working with these systems undergo regular hazard communication training, because a single slip can produce reactive off-gassing or unexpected pressure buildup. These details rarely make it into sales or specification sheets, but they matter for consistent, safe material supply.

    Feedback Loops in Quality Improvement

    Direct conversations with researchers using our product drive changes in our workflow. We have seen cases where post-synthesis processing, like filtration or drying, introduced tiny but significant levels of silica or plasticizer contaminants. Responding to this, we moved to stainless steel and glass for all points of contact, removed all high-shed filter papers, and implemented final washes to guarantee a clean product. This led to reduced background noise for sensitive mass spectrometry and bioassay applications, particularly where parts-per-billion impurities can cloud results.

    We treat analytical transparency as an integral part of manufacturing rather than an afterthought. In the early years, some generic products sourced from third-party suppliers failed customer retesting, typically due to minor unidentified peaks or color instability. Returning to our own process and batch-by-batch validation, we created a more robust production record, giving confidence that every analytical certificate matches what sits in the bottle.

    Supporting Evolving Research Applications

    The landscape for research compounds continues to evolve rapidly. Scientists are now exploring not only mutagenicity and pharmacology, but also synthetic transformations, photochemistry, and even materials science applications of fused indole-pyridine systems. We have seen an uptick in requests linked to advanced screening techniques, such as LC-MS/MS platforms, which require even tighter purity controls and lower limits for specific contaminant groups.

    We stay ahead by routinely updating our production and analytical technologies. For instance, recent investments in HPLC–DAD and higher-field NMR have uncovered previously unseen side products at trace levels, prompting ever-stricter lot release criteria. While some distributors sell “good enough” lots with wider acceptance windows, our own standards reflect both regulator guidance, such as ICH impurity guidelines, and our experience with what end users actually see in day-to-day research.

    Real-World Lessons on Inventory Management

    Our warehouse practices evolved from past setbacks. Early on, ad-hoc stocking meant occasional exposure to heat or moisture, degrading sensitive products like 2-Amino-9H-Pyrido[2,3-b]indole. Now, batches move directly from production to controlled storage, never mingling with incompatible chemicals or lingering in uncontrolled transit. Material rotates through an inventory system set up for chemical traceability — not just a simple “first in, first out” model, but one that flags any anomalies in lot consistency or environmental exposure.

    Logistics can be overlooked by those who merely broker or resell. By controlling each phase — synthesis, in-process storage, final filling, shipment — we keep age and condition within spec. Direct feedback from researchers taught us that even a month too long on the shelf, or a week in a humid warehouse, can alter melting points or induce low-level decomposition. Maintaining product freshness and chemical stability, for us, means both rapid turnover and full documentation so users know exactly what arrives on their benchtop.

    What Researchers Can Expect from Our Batches

    Those who work with our 2-Amino-9H-Pyrido[2,3-b]indole find fine, off-white to pale yellow crystals that dissolve cleanly in standard solvents, without waxy residue or undissolved grit. This consistent appearance comes not just from careful monitoring, but from years of cumulative expertise — trial, correction, and applied learning. Every bottle includes a detailed batch certificate, showing chromatographic, spectroscopic, and moisture test results, with raw data always ready for audit or review.

    Researchers tell us purity matters most, but so does predictability in handling: scooping, weighing, dissolving, and combining with other reagents. We ship in amber glass, flush-sealed with low-leach closures. Each lot comes labeled with synthesis and QC dates, expiration guidance, and recommended handling — a result of feedback from both academic and industrial users who pointed out the practical challenges overlooked elsewhere.

    Looking Forward with Rigorous In-House Standards

    While automation and scale-up remain tempting, our experience producing 2-Amino-9H-Pyrido[2,3-b]indole suggests some manual oversight always wins out, especially for fine chemicals in dynamic research environments. Each batch not only supports important scientific advances — from mapping metabolic pathways to advancing synthetic medicinal chemistry — but also tests the limits of what careful manufacturing and process knowledge can achieve. Our focus remains on meeting or exceeding evolving analytical standards while delivering material that makes a difference at the bench.

    Conclusion

    Careful handling, regular feedback, and continual process adjustment have shaped how we produce and deliver 2-Amino-9H-Pyrido[2,3-b]indole. Years of dedication to manufacturing excellence, driven by a commitment to transparency and customer partnership, set our material apart. Every batch reflects the care and knowledge drawn from real-world chemical manufacturing, passed directly to the hands of today’s researchers.