|
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 | 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. |
Applications of 5,6-Dimethoxy-2-Phenylindole in Industrial ManufacturingAs 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
Typical usage ratio
Downstream process integration
Final product types
2. Reference Standard and Control Material in Pharmaceutical Quality Control LabsRegulated 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
Typical usage ratio
Downstream process integration
Final product types
3. Research Intermediate for Novel Heterocyclic Compound LibrariesChemical 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
Typical usage ratio
Downstream process integration
Final product types
4. Diagnostic Reagent Precursor for Immunohistochemical ApplicationsBiomedical 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
Typical usage ratio
Downstream process integration
Final product types
5. Specialty Ligand Synthesis for Coordination Chemistry ResearchAdvanced 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 5,6-Dimethoxy-2-Phenylindole prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.