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4-Iodo-2,5-Dimethoxyphenethylamine

    • Product Name 4-Iodo-2,5-Dimethoxyphenethylamine
    • Alias 2C-I
    • Einecs 212-729-3
    • 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

    587820

    Chemical Name 4-Iodo-2,5-Dimethoxyphenethylamine
    Common Abbreviation 2C-I
    Molecular Formula C10H14INO2
    Molecular Weight 307.13 g/mol
    Chemical Class Phenethylamine
    Appearance White crystalline powder
    Cas Number 69587-11-7
    Melting Point 173-174°C
    Solubility Soluble in water and ethanol
    Iupac Name 2-(4-Iodo-2,5-dimethoxyphenyl)ethanamine

    As an accredited 4-Iodo-2,5-Dimethoxyphenethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque, sealed plastic vial labeled "4-Iodo-2,5-Dimethoxyphenethylamine, 10 grams" with hazard symbols and batch number.
    Shipping 4-Iodo-2,5-Dimethoxyphenethylamine is shipped in compliance with all applicable regulations. The chemical is securely packaged in airtight, labeled containers to ensure stability and safety during transit. Temperature control, hazardous material documentation, and tracking are provided as required. Shipping is restricted to authorized destinations and licensed recipients only.
    Storage 4-Iodo-2,5-dimethoxyphenethylamine should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it in a cool, dry, and well-ventilated area, preferably within a chemical storage cabinet designed for hazardous or sensitive materials. Clearly label the container and restrict access to authorized personnel only, following all relevant legal and safety regulations.
    Application of 4-Iodo-2,5-Dimethoxyphenethylamine

    Applications of 4-Iodo-2,5-Dimethoxyphenethylamine in Industrial Manufacturing

    As a specialized manufacturer of 4-Iodo-2,5-Dimethoxyphenethylamine, we supply this compound for advanced synthesis in regulated scientific, diagnostic, and chemical industries. Each application scenario detailed below reflects practical use cases in downstream industrial settings, with an emphasis on compliance, formulation ratios, process integration, and end-product examples.

    1. Pharmaceutical Reference Standards Synthesis

    Pharmaceutical QC laboratories use our product as a certified chemical reference standard for analytical method validation and calibration in regulated environments. Laboratories integrate it in traceable analytical runs to support forensic and toxicology testing, as well as for establishing validated protocols to monitor controlled substances. Standard preparation requires strict source documentation, traceability, and stability data as mandated by international regulations.

    Industry compliance standards

    • United States Pharmacopeia (USP) Reference Standards Program
    • European Pharmacopoeia (Ph. Eur.) guidelines on analytical reference substances
    • ISO/IEC 17025:2017 for test and calibration laboratories
    • Good Laboratory Practice (GLP, OECD No. 1)

    Typical usage ratio

    • 0.1–1 mg per analytical run in HPLC/GC-MS calibrations, depending on instrument sensitivity and linearity requirements
    • Batch preparation up to 50 mg per standard, adjusted for method validation scale

    Downstream process integration

    • Dissolution in solvent matrix as stock standard solution, followed by graded dilution for instrument calibration curves
    • Incorporation into proficiency test samples for internal/external lab audits

    Final product types

    • Certified calibration standards for analytical laboratories
    • QA/QC proficiency testing kits for toxicology screening
    • Internal reference controls for forensic sample analysis
    • Regulatory-grade method validation sets for drug testing

    2. Fine Chemicals Research Intermediates

    Chemical research facilities require our compound as a key building block for the design and synthesis of novel phenethylamine derivatives. Skilled chemists utilize it in multi-step organic syntheses to explore new chemical space and develop molecules for potential use in CNS receptor studies or for structure-activity relationship (SAR) mapping. All research protocols follow registered chemical safety and environmental controls.

    Industry compliance standards

    • Chemical Facility Anti-Terrorism Standards (CFATS, US)
    • REACH Regulation (EC) No 1907/2006 for laboratory chemicals in the EU
    • OECD Guidelines for the Testing of Chemicals
    • Lab-specific material handling SOPs and Material Safety Data Sheet (MSDS) compliance

    Typical usage ratio

    • 0.05–0.5 molar equivalents per target molecule batch, depending on synthetic scheme and step yield
    • Scale-up batches from 100 mg to multi-gram, adjusted according to target compound quantity

    Downstream process integration

    • Addition in protected or deprotected form to amination, alkylation, or condensation reactions
    • Purification by chromatography or crystallization prior to structural diversification

    Final product types

    • Novel phenethylamine derivatives for receptor binding assays
    • Customized analytical probes for neuroscience research
    • SAR libraries for pharmaceutical screening
    • Specialty fine chemical catalog standards

    3. Forensic Science Reference Material Production

    Forensic laboratories depend on our material for the preparation of controlled substance simulations and law enforcement training materials. Its documented purity and chemical characterization enable calibration of detection methods, support chain-of-custody, and assure authentic handling processes during criminal investigation or public health analysis. Production of these references adheres to international drug control conventions and laboratory accreditation.

    Industry compliance standards

    • United Nations Office on Drugs and Crime (UNODC) drug reference material guidelines
    • ISO/IEC 17043:2010 for proficiency testing in forensic labs
    • ISO 17034:2016 for reference material producers
    • National Forensic Laboratory Accreditation requirements (e.g. ASCLD/LAB-International)

    Typical usage ratio

    • 10–500 micrograms per proficiency test ampoule or simulated casework sample
    • Production scales determined by annual demand and inter-laboratory exchange needs

    Downstream process integration

    • Dilution and accurate dispensing into inert carrier matrices
    • Stability assessment protocol before release to end-users

    Final product types

    • Control set ampoules for forensic laboratories
    • Drug detection canine training kits
    • Blind testing samples for judicial proficiency programs
    • Law enforcement calibrator products

    4. Custom Synthesis for Bioanalytical Method Development

    CROs (contract research organizations) and bioanalytical labs order our compound for producing metabolite analogs, isotope-labeled standards, and reference materials used in clinical and preclinical studies. Formulation accuracy, chemical purity, and documentation of origin are critical for regulatory filing and compatibility with advanced LC-MS/MS or GC analytical platforms. These projects typically operate under strict quality frameworks such as GxP.

    Industry compliance standards

    • EMA Guideline on Bioanalytical Method Validation
    • US FDA Guidance for Industry: Bioanalytical Method Validation
    • Good Manufacturing Practice (21 CFR 210/211 and ICH Q7 for APIs)
    • GMP Certificate of Analysis (CoA) traceability

    Typical usage ratio

    • 10–250 mg per custom synthesis project, with adjustment based on metabolite complexity and assay design
    • Isotope-labeling efficiency influences precise amounts in radiolabel tracing applications

    Downstream process integration

    • Initiation of synthesis as starting substrate for stable isotope or analog production
    • Integration into multi-step purification and characterization procedures

    Final product types

    • Stable isotope-labeled reference standards
    • Custom metabolite analogs for clinical validation
    • Bioanalytical method validation kits for CROs
    • Pharma-sponsored clinical trial analytical controls

    5. Academic Chemical Education and Demonstration

    University and higher education chemistry departments utilize our high-purity intermediates for safe demonstration experiments, structure elucidation practicals, and development of analytical techniques in post-graduate instruction. Faculty and technical staff work with precise weighing, documentation, and waste handling as required by campus chemical hygiene and local legal frameworks.

    Industry compliance standards

    • American Chemical Society (ACS) chemical safety protocols
    • Federal and state university hazardous chemical regulations
    • Chemical Hygiene Plan (OSHA Standard 29 CFR 1910.1450)
    • Department of Transportation (DOT) rules for shipping laboratory chemicals

    Typical usage ratio

    • 1–20 mg per batch for instructional demonstration or laboratory exercise
    • Lab experiment size determined by class size and institutional approval

    Downstream process integration

    • Direct use in NMR, IR, and UV-Vis spectroscopy sample prep
    • Participation in micro-scale synthetic demonstrations for hands-on laboratory coursework

    Final product types

    • Demonstration batches for advanced organic chemistry instruction
    • Lab-prepared analytical teaching sets
    • Course-specific reaction outcome samples
    • Educational chromatography standards
    Free Quote

    Competitive 4-Iodo-2,5-Dimethoxyphenethylamine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding 4-Iodo-2,5-Dimethoxyphenethylamine: A Manufacturer’s Perspective

    Introduction to Our Compound

    4-Iodo-2,5-Dimethoxyphenethylamine, known in research circles for its precise structure and unique substitution pattern, has quietly shaped innovation in specialty chemicals. At our facility, we start with carefully sourced raw materials, putting each batch through rigorous checks to ensure consistent molecular weight and crystalline purity. Among its peers, this compound comes with a 4-iodo substitution, paired with two methoxy groups at the 2 and 5 positions of the phenethylamine backbone. This gives it several distinguishing features over other phenethylamines, both in terms of reactivity in synthesis and its role as a chemical intermediate.

    Molecular Structure and Model

    In the world of manufacturing fine chemicals, a clear understanding of molecular structure sets one product apart from another. 4-Iodo-2,5-Dimethoxyphenethylamine’s structure influences both synthetic routes and how it behaves under typical lab conditions. The phenethylamine skeleton serves as a backbone for a large group of related compounds. Iodination at the 4-position increases molecular weight compared with unsubstituted and other halogenated analogs, while the two methoxy groups influence solubility and mild basicity. In practical terms, we see these changes in melting points and solvent behavior during our quality checks, which we run with each lot.

    Our Manufacturing Approach

    We have spent years refining our route for producing this material. Our process favors yields without introducing by-products that could complicate downstream applications. By running the core steps at controlled temperatures and adjusting reagent ratios, we aim to cut down on potential side products that can crop up with less selective iodination. Our reactors and purification lines rely on hands-on oversight, where the team tracks each intermediate with modern analytical tools. This gives us full confidence in batch-to-batch reproducibility.

    For any chemical manufacturer, resource procurement and waste management are just as critical as synthesis. Sourcing reagents that meet our purity standards takes effort, especially for halogenation steps, where a less refined iodine source quickly introduces variability. Waste streams have to be managed with care because halogenated by-products present special disposal challenges under local and national regulations. As chemists on the frontline, we do not view these as afterthoughts but as core parts of our workflow, factored in from the very beginning.

    Specifications: What Sets Our Product Apart

    Beyond the molecular formula, specifications stem from hard-won experience in the plant. We set our minimum assay targets based on feedback from long-standing research partners who share their downstream synthesis needs. Typical material rolls out in crystalline form, and each lot is checked not only for purity by HPLC and NMR but also for key trace elements where our customers’ applications are sensitive. Iodinated phenethylamines tend to absorb moisture with time, so we learn from each shipment, carefully packaging to avoid clumping or breakdown during storage and transit.

    Our experience shows the value in keeping the particle size distribution consistent from lot to lot. Finer grains may help rapid dissolution in some reactions, but excessive fines cause dust issues and can hang up in handling equipment. Rather than taking a one-size-fits-all approach, our operations team stays in touch with end-users, adapting granulation techniques to keep reactivity and ease of handling balanced for their typical processes.

    Applications: How Researchers and Industry Put It to Use

    Direct customers, most often in advanced organic synthesis labs, turn to 4-Iodo-2,5-Dimethoxyphenethylamine as an intermediate for preparing more complex targets. This compound’s specific substitution opens doors to selective cross-coupling reactions, especially where introducing an iodine at the 4-position enables faster and cleaner transformations compared with less activated halides like bromide or chloride. Certain academic labs reach out to us with protocols involving Suzuki or Sonogashira couplings, where this iodo group brings clear kinetic advantages.

    In pharmaceutical development, the compound’s role often stays behind the scenes as a building block. While the phenethylamine scaffold itself has a long research history, introduction of both the iodine and the two methoxy groups gives researchers knobs to turn for tuning physical and biological properties in test compounds. Teams focusing on SAR (structure–activity relationship) studies report that the iodinated variant provides a useful contrast to otherwise similar derivatives where the halogen or methoxy positions differ. For those walking through the steps of new molecule design, having these options in hand sharpens the toolkit.

    We have also seen rising curiosity in analytical circles, using 4-Iodo-2,5-Dimethoxyphenethylamine as a standard for calibration or as a reference point in studying environmental breakdown products. Many of these requests stem from wider public health and analytical monitoring programs. Our feedback cycle with these groups lets us refine expected trace impurities or isotopic variation tolerance, which can be surprisingly important in high-sensitivity methods.

    Comparisons With Related Compounds

    No chemical exists in a vacuum. Over my years in the industry, I’ve noticed that end-users often need to decide between several phenethylamine derivatives for a particular project. 4-Iodo-2,5-Dimethoxyphenethylamine stands out among halogenated analogs for the size and nature of its iodine atom. Brominated or chlorinated analogs, though sometimes easier to source, often lag in performance in coupling reactions where heavy atom activation is desirable. Our product takes a little more work in the synthesis stage, given the higher cost and handling care with iodine, but consistently demonstrates better conversion rates for certain downstream chemistry. These real-world gains in lab utility have justified the extra time and cost for most partners working on innovative molecular scaffolds.

    We field regular questions comparing our product to unsubstituted 2,5-dimethoxyphenethylamine or those carrying substitutions at different ring locations. From experience, I know that shifting the halogen or modifying substituents leads to marked changes in reactivity, sometimes making or breaking a pathway’s viability. The 4-position offers the best of both worlds for many modern coupling strategies, giving a handle for functional group interconversions that’s not easily matched by the alternatives. Our own internal data supports this, as we see a clear preference for the iodo derivative once researchers are exposed to side-by-side comparisons in pilot runs.

    Real-World Challenges and Solutions

    Manufacturing specialized phenethylamines rarely follows a straight line. Occasionally, a run will deliver slightly off-spec product due to unplanned side reactions—this happens most often at the iodination stage, where even slight fluctuations in reaction temperature can lead to ortho- or para-iodinated byproducts. We combat this by constant instrumentation upgrades and human oversight, never relying on automation alone. Senior operators routinely review sample data in real time; if readings drift, intervention happens before a whole tank’s worth of material is affected. Process refinement comes from these lessons; it’s a never-ending cycle of improvement that has been part of our ethos since the first batches.

    Shipping iodo-organics also brings its issues. Some regions restrict the movement of iodine-containing materials based on local regulation. We handle documentation thoroughly so that customers aren’t hit with unexpected delays at customs or compliance checkpoints. Because halogenated compounds can carry extra regulatory baggage, our logistics chain stays up to date on evolving controls. Sometimes customers express concern about shelf life. Our shipping department invests in moisture-proof, light-shielding packaging, based on reports from researchers whose earlier purchases from other sources lost potency over time. Sending out compromised product reflects poorly on us, so every outgoing package receives a final sign-off from both warehouse and QA personnel.

    Feedback Loops and Ongoing Development

    Valuable insights rarely come from textbooks alone. Often, researchers bring us feedback about challenges they encountered with commercial sources purchased elsewhere—anything from discoloration that hints at trace degradation products to stubborn residues that complicate reaction workups. We treat every comment as motivation to scrutinize our own process, requesting additional aliquots for third-party analysis if needed. Sometimes, a new request will push us to tweak drying times, or pursue yet another round of recrystallization, even if it impacts total output for a few days. We approach this back-and-forth not as a burden but as the everyday reality of supplying a material where precision matters.

    Requests for modifications come in as well, especially from new fields venturing into advanced organic synthesis. Some labs may prefer a coarser or finer cut to match their existing protocols. Others want tighter limits on specific elements due to regulatory or functional needs. Working closely with these end-users, our process engineers translate ideas into practice, making real-time adjustments in the plant. Keeping the line of communication open avoids guesswork and helps avoid costly repeat batches due to misaligned expectations.

    Attention to Legal and Safety Concerns

    Iodinated phenethylamines command legitimate attention when it comes to safety and regulatory awareness. It’s no secret that some compounds in this family have been subject to patchworks of local regulations based on their chemical class. Our in-house regulatory team tracks relevant advisories and consultation requests so the production and shipping chains follow best practices. We invest time with customers at order placement, discussing use cases and guiding them through proper documentation steps. Our production crew also receives ongoing training. Handling iodine intermediates and ensuring proper ventilation, storage, and spill control are not just afterthoughts—they minimize risk for both our operation and our customers’ labs.

    Cost management remains an issue, too, as global price swings occasionally hit iodine and key solvent supplies. Our purchasing arm plans several quarters out, signing contracts to lock in prices where possible. Raw material variability can impact both price and the subtle chemistry that goes into our final product. Reducing supply chain disruptions isn’t about keeping shelves full, but about preventing sudden jumps in impurity profiles or unexpected delays. Customers count on us to deliver both reliability and integrity batch after batch.

    A Commitment to Continuous Improvement

    Experience has taught us that making an iodinated compound is as much about adaptability as chemistry. Each batch brings new insights. Over years, small improvements in process control or handling can make a visible impact downstream. Our teams look for these incremental wins, studying where bottlenecks creep in or where traditional purification steps might cause product loss. Many of our current workflow practices—careful titration of iodinating agents, staged crystallization, multilayer filtration—grew directly from mistakes or mishaps in past runs. It’s a tradition in this industry to learn early, adjust quickly, and share lessons company-wide.

    No manufacturer ever claims perfection, but a culture that welcomes feedback and works on each batch as if it’s the most important project earns long-term loyalty. We put our name on every shipment precisely because we know exactly what goes into each lot—from raw material to packaging tape. Researchers who rely on our compound get exactly what they expect: consistent, clean, well-characterized 4-Iodo-2,5-Dimethoxyphenethylamine designed for the work that matters most in their labs. In an evolving field, those standards rarely go out of style.

    Looking Ahead

    Trends in specialty chemicals are pointing toward even greater customization, often driven by the next wave of research demands. Molecules like 4-Iodo-2,5-Dimethoxyphenethylamine occupy an increasingly important spot in synthetic chemistry, both as stand-alone scaffolds and as launchpads for complex derivatives. Our production line adapts each year based on feedback, regulatory shifts, and advances in analytical instrumentation. Sometimes the hardest part is keeping up with new reaction schemes coming out of collaboration with academic labs and commercial R&D partners. Process documentation occasionally feels like a living document, updated as soon as a better step or control method is discovered.

    We have seen a broader range of inquiries beyond traditional organic synthesis. As chemical manufacturing moves forward, compounds with unique substitution patterns, like this one, have a bright future in unexplored research directions. That means ongoing investment in purification, analytical verification, and close coordination between our plant floor and every bench scientist down the line. Continued dialogue with users and regulatory bodies keeps our quality high and ensures all batches meet or surpass the current best practices.

    Standing behind every shipment, our experience in manufacturing 4-Iodo-2,5-Dimethoxyphenethylamine spans both successes and learning moments. Each run represents the intersection of chemistry, adjustable industrial process, and careful listening to the needs of modern researchers. Our mission continues: to raise the bar on specialty chemical craftsmanship and enable important discoveries, one carefully prepared batch at a time.