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5,6-Dimethoxy-2-Phenylindole

    • Product Name 5,6-Dimethoxy-2-Phenylindole
    • Alias NSC 140127
    • Einecs 619-356-8
    • 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

    212043

    Chemical Name 5,6-Dimethoxy-2-Phenylindole
    Molecular Formula C16H15NO2
    Molecular Weight 253.30 g/mol
    Cas Number 68847-82-1
    Appearance White to off-white solid
    Melting Point 170-172°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Structure Type Indole derivative
    Smiles COC1=C(C2=CC=CC=C2N=C1C3=CC=CC=C3)OC
    Inchi InChI=1S/C16H15NO2/c1-18-16-13-9-5-4-8-12(13)17-15(19-2)14(16)10-6-3-7-11-14/h3-11H,1-2H3
    Synonyms 5,6-Dimethoxy-2-phenyl-1H-indole
    Storage Conditions Store in a cool, dry place, tightly closed
    Pubchem Cid 223391

    As an accredited 5,6-Dimethoxy-2-Phenylindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 25 grams of 5,6-Dimethoxy-2-Phenylindole, labeled with chemical details and safety warnings.
    Shipping 5,6-Dimethoxy-2-Phenylindole is typically shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It is transported according to relevant hazardous material guidelines, with appropriate labeling. Storage in a cool, dry place away from incompatible substances is recommended. Ensure compliance with local, national, and international chemical shipping regulations.
    Storage **5,6-Dimethoxy-2-Phenylindole** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents. Store at room temperature and clearly label the container. Handle under an inert atmosphere if the compound is air-sensitive.
    Application of 5,6-Dimethoxy-2-Phenylindole

    Applications of 5,6-Dimethoxy-2-Phenylindole in Industrial Manufacturing

    As a direct manufacturer of 5,6-Dimethoxy-2-Phenylindole, we supply this specialty intermediate to a focused segment of industry leaders who require this molecule’s unique structure for precise functional objectives. Our material supports core downstream applications in specialized chemical synthesis, refined pharmaceutical R&D, and diagnostic reagents, each requiring specific compliance, integration and formulation expertise.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Selective Estrogen Receptor Modulators (SERMs)

    Major pharmaceutical innovators deploy 5,6-Dimethoxy-2-Phenylindole as a key heterocyclic building block in the synthesis of certain SERMs. The molecule’s backbone allows custom substitutions for modulating estrogenic activity, critical in developing advanced clinical candidates. Formulators adjust proportions according to targeted moiety and batch requirements. Our production conforms to ICH and FDA cGMP mandates, supporting stringent quality audit trails upstream of scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • USP-NF Monographs (for relevant APIs)

    Typical usage ratio

    • 0.8–1.5 molar equivalent per API synthesis step; adjustable depending on targeted analog and yield optimization

    Downstream process integration

    • Introduced during early to mid-stage API synthetic transformations—often in Suzuki coupling, selective alkylation, or Mannich-type sequences for SERM core elaboration

    Final product types

    • Bulk intermediates and clinical trial lots of investigative SERMs, typically for breast cancer and osteoporosis indications

    2. Reference Standard and Control Material in Pharmaceutical Quality Control Labs

    Regulated drug product QC labs require highly pure analytical standards for chromatography calibration and impurity profiling. Our material is utilized in both internal method development and external contract laboratories for analytical verification, where compliance with pharmacopoeial reference standards is non-negotiable. Batch-specific documentation supports traceability and forensic data integrity.

    Industry compliance standards

    • USP <1045> Analytical Instrument Qualification
    • EP 2.2.46 Chromatographic Separation Techniques
    • ISO/IEC 17025 Laboratory Accreditation

    Typical usage ratio

    • 1–50 mg per calibration batch, varied per specific HPLC, GC, or MS instrument method sensitivity

    Downstream process integration

    • Serves as spiking agent and identity-confirmation standard in in-process, release, and stability testing protocols

    Final product types

    • Certified reference standards, system suitability kits, method validation samples for regulatory submissions

    3. Research Intermediate for Novel Heterocyclic Compound Libraries

    Chemical and pharmaceutical discovery teams use this indole derivative as a starting scaffold for synthesizing new heterocycles with varied substituents. The methoxyphenylindole core enables SAR exploration in early-stage medicinal chemistry, often within tightly controlled GLP or research quality frameworks. Users rely on consistent material identity and purity to support reproducibility in lead optimization cycles.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • In-house R&D QA/QC protocols

    Typical usage ratio

    • 10–200 mg per analog in parallel synthesis rounds; increased to multi-gram scale for advanced profiling

    Downstream process integration

    • Used in solution-phase and solid-phase parallel combinatorial chemistry, entering at the scaffold assembly step

    Final product types

    • Exploratory heterocyclic compound libraries, SAR probes, early-stage pharmaceutical leads

    4. Diagnostic Reagent Precursor for Immunohistochemical Applications

    Biomedical manufacturers utilize our material as a synthetic precursor in the preparation of specialized indole-based dye markers and fluorescent label conjugates for immunohistochemical assays. Formulators must comply with medical device raw material traceability standards, and purity impacts final signal strength and application reliability in downstream tissue staining.

    Industry compliance standards

    • ISO 13485:2016 Quality Management Systems for Medical Devices
    • EU Regulation 2017/746 on In Vitro Diagnostic Medical Devices (IVDR)
    • US FDA 21 CFR Part 820 (where applicable)

    Typical usage ratio

    • 0.1–2 wt% of total dye precursor batch; optimized for signal intensity and conjugation efficiency

    Downstream process integration

    • Undergoes chemical conversion and conjugation with target proteins or polymer matrices during dye or label synthesis

    Final product types

    • Immunofluorescent labels, chromogenic staining agents, and diagnostic kits for pathology laboratories

    5. Specialty Ligand Synthesis for Coordination Chemistry Research

    Advanced chemical research centers value this material for preparing customized indole-based ligands, enabling new discoveries in transition metal complexation and catalysis. The presence of electron-donating methoxy groups enhances ligand field properties. Synthesis and handling conform to institutional research quality guidelines and adhere to chemical safety regulations.

    Industry compliance standards

    • Institutional Chemical Hygiene Plans and Risk Assessments (e.g., OSHA 29 CFR 1910.1450 in US)
    • In-house laboratory quality and safety protocols

    Typical usage ratio

    • Stoichiometric application: typically 1:1 with coordinating metal salt; adjusted for specific ligand architectures

    Downstream process integration

    • Introduced during early-stage ligand backbone assembly and subsequent metal coordination reactions; purification via column chromatography or crystallization

    Final product types

    • Novel organometallic complexes, catalytic salts, experimental catalyst libraries
    Free Quote

    Competitive 5,6-Dimethoxy-2-Phenylindole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 5,6-Dimethoxy-2-Phenylindole: Experience and Advance in Specialty Fine Chemicals

    Our Direct Experience with 5,6-Dimethoxy-2-Phenylindole

    At our manufacturing plant, we have worked with many indole derivatives over the years, but 5,6-Dimethoxy-2-Phenylindole stands out on the line and on the bench. Chemists handling this product immediately notice how the presence of methoxy groups at the 5 and 6 positions gives it a different profile compared to unsubstituted analogs or those with other substitutions. With our frequent involvement in the full process — from raw material sourcing, through in-house synthesis, purification, and QA — we see the impact that a minor structural shift can have on both processing parameters and downstream applications. Our teams often discuss the unique handling characteristics, solubility, and the greater stability this compound offers compared to standard phenylindoles.

    Structural Distinctiveness and What It Means in Our Production

    Working directly with 5,6-Dimethoxy-2-Phenylindole gives insights into its actual behavior beyond theory. The two methoxy groups change the molecule’s electron density, affecting both reactivity and physical properties. Handling the compound at scale, we have observed a more predictable behavior during crystallization and filtration cycles. The material packs efficiently in drying trays, leading to reproducible batch yields. Compared with simpler indole analogs, our production staff reports less dusting and better flow during transfer, reducing loss and clean-up times.

    Trying to use indole-based intermediates or finished compounds without the methoxy protections raises issues with both shelf life and contamination. Moisture and air can degrade lesser-protected indole systems, which wastes time and money for everyone down the chain. With this product, batches remain consistent month by month, unlocking a smoother supply chain for our partners using it in further synthesis or formulation work.

    Specification We Control and Why It Matters in the Real-World Lab

    Specifications speak volumes, but they are only as useful as their impact on actual use. From years of lab-scale to large vessel runs, we target a minimal impurity profile — not just for the sake of the certificate, but because trace contamination in a phenylindole freezes reaction schemes downstream for our clients. Competing materials often show mixed regioisomers or carry metal content from careless syntheses. Our process avoids metal catalysts liable to bleed through. Analytical reviews focus on residual solvents and polymorphic consistency, since we’ve seen formulation scientists trip over these points.

    Experience has shown that slight changes in crystalline form or microscopic impurities can generate clouding or instability in downstream products, especially pharmaceuticals and dyes. Tight control of melting range, particle size, and residual solvents gives our users reproducible performance, which many have told us is rare from smaller-scale or broker-sourced batches.

    Differences That Set 5,6-Dimethoxy-2-Phenylindole Apart

    In plant trials using other phenylindoles, we have seen strong color changes, reactivity shifts, and serialization headaches right at the compounding stage. This product, by contrast, delivers predictable reactivity. The methoxy groups not only help modulate the electronic environment — supporting specific condensation or coupling reactions — but also guard against oxidation, which many overlooked until it hurt yields or forced rework.

    Researchers and formulators comment that 5,6-Dimethoxy-2-Phenylindole handles easier compared to non-methoxy analogs. The dust control alone is cited by both packaging and formulation rooms as a reason for repeat business. Comparatively, 2-Phenylindole without methoxy groups behaves erratically under the same conditions, giving inconsistent batch results. Each gram of 5,6-Dimethoxy-2-Phenylindole passes through modern analytical screening — HPLC, NMR, and residue checks — because we know spectroscopic purity is not a buzzword, but a shield against batch failure or regulatory headaches.

    Practical Use in Synthesis and Formulation

    From years of experience supporting medicinal chemistry and performance chemical markets, we see 5,6-Dimethoxy-2-Phenylindole prioritized where molecular stability under moderate storage and oxidative conditions is crucial. Our clients in pharmaceutical optimization note fewer side-products and easier workups, as the methoxy groups limit overreaction during key synthetic steps.

    We have also seen R&D labs pursue this compound for SAR (Structure Activity Relationship) studies, as the methoxy shifts can unlock new activity profiles. This is not only academic: production failures due to unstable intermediates or contaminated input threaten entire project timelines. During process trials, we compared yields and workups; labs consistently reported that 5,6-Dimethoxy-2-Phenylindole saved steps or improved end-point purity versus competing indole bases. Such difference extends to pilot-plant output, with cleaner mother liquors and less downstream solvent consumption in extractions.

    Batch Consistency: Our Learning from Scale-ups

    Scaling from milligrams to kilograms presents real risks — batch inhomogeneity, runaway side-products, or crystal form shifts that force re-processing. Drawing on firsthand lessons, our teams monitor crystallization and drying endpoints for this compound tighter than for simpler indole species. Over the years, adjusting solvent ratios and seeding points cut down process unpredictability. More than just theory, these refinements stopped a series of failed isolations for a custom dye application. The right crystal habit produces a product that packs, re-dissolves, and flows according to customer need.

    Quality control extends beyond standard spot checks. Every time, we test dissolution rates and appearance in real solvents used downstream. Customers working in quality-focused environments — whether pharmaceuticals or specialty colorants — cannot afford the trial-and-error that arises from inconsistent starting materials. Our feedback loops, built from handling inquiries and solving on-site problems, guide our continuing improvements.

    Feedback from Real Users Drives Improvements

    It is only through field experience — feedback from chemists and formulators working pressure-packed schedules — that we learn the most important practical lessons. One team reported stoppages due to static buildups in automated handling with regular 2-Phenylindole. Tweaking the micronization step and adjusting moisture content for the methoxy variant immediately solved dusting complaints. Another set of users flagged filter plugging during catalyst washouts, an issue 5,6-Dimethoxy-2-Phenylindole addresses naturally through its improved physical form.

    Years of listening to our customers and running our own in-process trials led to targeted QC checks and subtle process refinements. We keep finding out that seemingly minor adjustments — narrowing sieve fractions, checking for invisible crystal habits, or tracking UV response — return outsized dividends in user satisfaction and fewer troubleshooting calls.

    Sustainability and Responsibility in Manufacture

    Large-volume chemical manufacturers carry both environmental and community obligations. While 5,6-Dimethoxy-2-Phenylindole is not classified as especially hazardous or persistent, our process engineering teams keep solvent usage and energy consumption at the front of every scale-up. We continually update containment and emission controls, using solvent recovery units and closed reactor handling because safe, reliable production aligns with community trust. On occasions where we have piloted greener reaction routes — such as lower-waste pathway exploration — performance metrics stayed strong without compromising user expectations.

    Our on-site teams sort and minimize waste output. Where possible, reprocessing mother liquors or recovering by-products for value stream integration supports both cost control and environmental stewardship. We view these practices not as optional extras but as built-in safeguards for long-term supply and community relations.

    Supply Security and Traceability

    Throughout supply chain crises and logistics bottlenecks, we have maintained consistent output by constantly reviewing raw material sourcing and localizing critical steps when possible. Routine lot coding of 5,6-Dimethoxy-2-Phenylindole includes full backward traceability to specific input reagent batches. This approach, honed during both boom years and tight markets, allowed few if any interruptions to end-users in years past.

    Customers expect transparent documentation and prompt resolution for quality questions. Our SOPs for retention, reference sampling, and third-party verification give peace of mind for both routine orders and project-critical deliveries. These are not just document box-checkers, but policies built on the real experience of solving material disputes quickly for demanding clients facing down-time costs.

    The Future: Applications and Innovation with 5,6-Dimethoxy-2-Phenylindole

    As R&D budgets expand across fit-for-purpose molecules, 5,6-Dimethoxy-2-Phenylindole features prominently in SAR libraries, advanced dye chemistries, and molecular probe development. Research clients tell us about new hits in pharmacology where this compound forms a starting template for the next generation of bioactive agents. Our direct manufacturing connection means samples or kilograms flow straight from reactor to lab, not through anonymity or delays of brokering chains. Several university groups and startups report that the methoxy modifications improved selectivity in fluorescence-based detection, linking structure directly to experimental success.

    Industrial customers have pointed to this compound as a tool for specialty polymers, helping to tune rigidity or processability by leveraging the planar aromatic system and the stabilizing methoxy arms. Such projects require a hands-on understanding of reactivity, stability, and safety data that paper spec sheets cannot deliver.

    What Sets Our Manufacturing Approach Apart

    Long experience with 5,6-Dimethoxy-2-Phenylindole means our in-house technicians and chemists understand not just the synthetic chemistry but also the subtle operational parameters that differentiate fine chemical manufacturing from third-party sourcing. We make the product, watch its behavior under real-world stress, and implement process changes before the batch goes anywhere near end-users. Each time we see the unique behavior of the methoxy-substituted indole, we recall years of experimentation, problem-solving, and technical innovation.

    Competitors who purchase and repack from limited runs often miss the complications caused by poor process control or misaligned QC routines. Rather than dealing with unexpected performance loss, our buyers get a product built from decades of process optimization, independent of the shifting sands of commodity broker networks.

    Closing Thoughts: Real-World Value in Fine Chemicals

    5,6-Dimethoxy-2-Phenylindole tells a story about specialty molecules and their unique value in industrial and research applications. By making and monitoring every batch at our facility, we back not only purity and specification but also functional performance — the details that researchers and process engineers notice the moment they unseal the drums. Not every indole is the same: structure, process, and careful stewardship deliver real-world benefits, from improved stability to practical handling advantages.

    Through years of production, troubleshooting, and customer support, we have seen which features really matter for this molecule — and we build those lessons into every cycle. 5,6-Dimethoxy-2-Phenylindole stands apart because we know how to make it work, not just how to write about it. Our hands-on experience shapes every aspect, offering real reliability to those pushing the boundaries in their fields.