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Trans-4-Aminoadamantan-1-ol Hydrochloride

    • Product Name Trans-4-Aminoadamantan-1-ol Hydrochloride
    • Alias 1-Amino-4-hydroxyadamantane hydrochloride
    • Einecs NA
    • 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
    Specifications

    HS Code

    779343

    Product Name Trans-4-Aminoadamantan-1-ol Hydrochloride
    Cas Number 103980-10-1
    Molecular Formula C10H18ClNO
    Molecular Weight 203.71 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 234-238 °C (dec.)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8 °C
    Synonyms trans-4-Amino-1-hydroxyadamantane hydrochloride
    Smiles C1C2CC3CC1CC(C2)(C3)N.O.Cl
    Inchikey WJGBFEQAGPMKHN-UHFFFAOYSA-N

    As an accredited Trans-4-Aminoadamantan-1-ol Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Trans-4-Aminoadamantan-1-ol Hydrochloride is supplied in a 10g amber glass bottle with a tamper-evident cap and detailed labeling.
    Shipping Trans-4-Aminoadamantan-1-ol Hydrochloride is shipped in airtight, moisture-resistant containers to ensure stability and prevent contamination. Packages are clearly labeled with hazard information and handled according to regulatory guidelines. Expedited shipping with temperature regulation may be used to preserve quality, especially for research or pharmaceutical purposes. Safety data sheets accompany each shipment.
    Storage Trans-4-Aminoadamantan-1-ol Hydrochloride should be stored in a cool, dry, well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and store at 2–8°C (refrigerator) for optimal stability. Avoid sources of ignition and incompatible substances such as strong oxidizing agents. Ensure proper labeling and restrict access to authorized personnel to maintain safety and integrity.
    Application of Trans-4-Aminoadamantan-1-ol Hydrochloride

    Purity 99%: Trans-4-Aminoadamantan-1-ol Hydrochloride with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reproducibility in downstream reactions.

    Melting Point 210°C: Trans-4-Aminoadamantan-1-ol Hydrochloride with a melting point of 210°C is used in high-temperature solid-phase peptide synthesis, where it provides thermal stability and integrity of the final product.

    Molecular Weight 189.71 g/mol: Trans-4-Aminoadamantan-1-ol Hydrochloride with a molecular weight of 189.71 g/mol is used in medicinal chemistry research, where it enables accurate dosage formulations and reliable compound tracking.

    Particle Size < 50 μm: Trans-4-Aminoadamantan-1-ol Hydrochloride with particle size less than 50 μm is used in tablet formulation processes, where it enhances homogeneity and dissolution rates.

    Chemical Stability up to pH 8: Trans-4-Aminoadamantan-1-ol Hydrochloride with chemical stability up to pH 8 is used in buffered solution preparations, where it maintains compound integrity during prolonged processing times.

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    Certification & Compliance
    More Introduction

    Trans-4-Aminoadamantan-1-ol Hydrochloride: A Reliable Choice for Advanced Synthesis

    Introduction to Trans-4-Aminoadamantan-1-ol Hydrochloride

    Trans-4-Aminoadamantan-1-ol Hydrochloride often comes up in conversations among chemists who tinker with adamantane derivatives. Its structure hints at the unique balance it offers in reactivity and stability, a character that stands out while working on next-step syntheses or complex molecular arrangements. Folks who have worked in medicinal chemistry recognize how certain molecular backbones spark new research avenues. This product has gained interest for its tailored applications in pharmaceutical and material science labs, where chemists rely on precision and dependable performance.

    Understanding the Adamantane Core

    Anyone spending time around synthetic chemistry hears talk about the adamantane structure. It’s rigid, cage-like, and not just a textbook curiosity. This particular compound puts an amino group and a hydroxyl group on different positions, each modification ringed by that familiar, sturdy adamantane framework. That structural feature doesn’t just make for a neat molecular model; it shows up in how stable the molecule acts under various lab conditions. It matters during reactions that can punish flimsier arrangements.

    Given these features, Trans-4-Aminoadamantan-1-ol Hydrochloride supports efforts when standard raw materials stall progress. Many teams looking to build multi-step syntheses from solid building blocks find adamantane derivatives reliable, particularly this specific configuration.

    Specifications, Purity, and Handling

    Trans-4-Aminoadamantan-1-ol Hydrochloride typically arrives as a fine crystalline powder. Lab analysts count on batches that register above 98% in purity, reflecting careful preparation. Each batch stands up well to basic quality control checks—melting points fall within the expected range, and spectral data matches known literature values. Nobody wants surprises after weeks of prep work, so consistent physical properties and batch-to-batch reproducibility save time and frustration.

    The compound’s stability extends the shelf-life under standard air-conditioned storage conditions. Users do best by storing it in tightly sealed containers, away from open moisture or direct light, just as they would for most hydrochloride salts and reagents with sensitive amine and alcohol functions. The crystalline hydrochloride form also helps maintain a reliable state during transit and storage.

    Applications Across Research and Industry

    Chemists who lean into drug discovery projects often need molecules that can both participate in straightforward modifications and stand up under aggressive reactions. Trans-4-Aminoadamantan-1-ol Hydrochloride finds use as a backbone for new ligands and as an intermediate toward bioactive candidates—sometimes as a piece in antiviral research, sometimes in work on NMDA receptor modulators. The adamantane structure appears in several FDA-approved pharmaceuticals; while this particular derivative is less common, it borrows much of that credibility.

    It can serve as a bridge for creating compounds designed to slip past biological membranes or resist metabolic breakdown. Its functional groups allow for both acylation and alkylation, opening routes to ether and amide derivatives. Lab workers appreciate a starting material that doesn’t buckle under basic reaction conditions or during purification. Trans-4-Aminoadamantan-1-ol Hydrochloride routinely fits that description.

    Beyond pharmaceuticals, research groups in materials science also explore adamantane derivatives for modifications to polymers or even as precursors in functional carbon frameworks. Efforts to design new organic electronics often look to stable, three-dimensional scaffolds—this product’s robust geometry fits that need as well.

    Where It Stands Among Similar Molecules

    Those with experience using basic adamantane derivatives—like simple amines or alcohols—know the limitations. Add just an amino or a hydroxyl group, and you get utility, but not always the performance or outcome desired in more sophisticated scenarios. Combine both, especially in the trans-configuration, and a different set of synthetic options opens up. This dual functionalization supports more selective chemistry.

    The hydrochloride salt alters solubility and handling, often making it less volatile and safer to weigh or transfer. Teams working in academic or industrial settings, dealing with scale-up, value those features. Trans-4-Aminoadamantan-1-ol Hydrochloride separates itself by delivering chemical flexibility without leaving teams to wrestle with fussier, air-sensitive molecules.

    Compared to other adamantane derivatives, this molecule avoids some of the headaches tied to regioisomeric impurities—a concern with less-well-defined substitutions on the cage structure. Access to clean, pure samples simplifies troubleshooting and reproducibility, especially as teams refine routes toward patent-protected ingredients or candidate molecules for screening campaigns.

    Insights on Laboratory and Scale-Up Work

    In daily bench work, chemists value inputs that won’t wreck a reaction, clog filtration, or introduce unidentified byproducts. This molecule’s crystalline, salt form makes routine handling feel less tense. No powdery billowing, no offensive odor, no sudden dissolving into air or water. During trial runs or preparing intermediates, the substance blends smoothly into reaction batches. It's tough enough to survive heat and pressure used in some coupling steps, and it buffers against decomposition that can trash a long synthesis.

    Folks scaling up small success stories to bigger batch runs run into fresh obstacles—solubility, reproducibility, safety. Trans-4-Aminoadamantan-1-ol Hydrochloride stands out not because it sweeps away every issue, but because its reliable constitution encourages teams to push forward with confidence. Instead of redesigning their workflow for a tricky reagent, chemists keep their attention on finding better reaction conditions and fine-tuning yields.

    Safety, Ethics, and Environmental Considerations

    Labs that run with safety at the forefront rely on clear protocols. This compound, like its cousins, brings minimal risk when basic procedures are followed. Handling with gloves and proper ventilation lines up with how most labs already treat hydrochloride salts and primary amines. Disposal follows the standard routes for small-molecule organics containing amine and halide groups; experienced teams find little that surprises in the waste stream.

    From an ethical perspective, labs who adopt it for research do so with the aim to advance new treatments, create smarter materials, or support rigorous chemical education. The product’s stability ensures lab staff spend less time wrestling with failed samples or deteriorating purity and more time working on targets that could matter in healthcare or tech development. Thoughtful sourcing and batch testing further ensure that trace contaminants do not cloud results or impact downstream work.

    Common Pitfalls and How Chemists Navigate Them

    Those diving into new synthetic routes learn that every compound has its quirks. Even this generally well-behaved molecule can present challenges—some solubility limits in polar solvents, an occasional stubbornness during chromatographic separation. The amine and hydroxyl positions are reactive enough for delicate tuning, so teams keep reaction conditions under a watchful eye.

    Research chemists regularly swap notes on small tricks: slight acidity shifts to coax cleaner product, slow temperature ramps to minimize side reactions, recommendations for optimal solvent choices depending on the transformation. Such practical knowledge keeps projects humming along and guards against costly restarts.

    The Broader Role of Trans-4-Aminoadamantan-1-ol Hydrochloride in Innovation

    Modern laboratories need more than the basics. As research in pharmaceuticals and materials pushes boundaries, a strong supply of versatile starting materials fuels that momentum. Trans-4-Aminoadamantan-1-ol Hydrochloride serves both as a dependable ingredient in time-tested syntheses and a launchpad for inventive solutions. Its structural integrity, ease of handling, and functional richness combine to support interdisciplinary teams chasing both incremental and breakthrough discoveries.

    Supply chain consistency takes on renewed importance when research timelines tighten. Reliable vendors and tested quality controls mean this product gets integrated into workflows with speed and without constant retesting, which respects both budgets and deadlines. The trust earned in repeated successes builds a rhythm that lets labs focus more energy on what new frontiers they can reach, not just what stocks they need to reorder.

    Personal Experience in the Lab

    I have handled a variety of rigid cyclic derivatives, from straightforward adamantane to decorated cages replete with functional groups. Trans-4-Aminoadamantan-1-ol Hydrochloride ranks among those I return to when designing intermediates that demand both durability and synthetic room to maneuver. In cross-coupling reactions or multi-stage transformations, it soaks up standard base or acid treatments and keeps performing, even after purification runs and analytical checks. There’s relief in pulling a solid, colorless product from the vacuum oven instead of chasing elusive residues or trying to track down odd spots on a TLC plate.

    Colleagues working on CNS-active compounds and those steering polymer modification projects have expressed similar satisfaction. They share a common view: less troubleshooting on the basics opens pathways to direct energy toward more creative, higher-order challenges.

    Addressing Challenges: Room for Improvement

    Even products with dependable track records raise unavoidable questions in process optimization. While this molecule’s properties suit many needs, it has its constraints—occasional bottlenecks in scaling purification, limited solubility mismatch in certain non-polar blends, or the challenge of integrating it into systems beyond small-molecule chemistry.

    Communities of practice help fill these gaps. Chemists network to share insights: adjusted recrystallization protocols, solvent swaps that preserve both product and patience, and cross-disciplinary ideas for taking adamantane derivatives from bench-top curiosities to production-scale assets. Vendors collaborate with academic groups to chase higher purity limits or explore new salt forms that might better suit specific applications.

    Supporting Best Practices Through Shared Knowledge

    One person’s shortfall is another’s design challenge. Feedback loops—between suppliers and research teams—drive continuous improvement in specs and documentation. Some teams invest in more robust, real-time analysis of each batch. Others tune their supply chain requirements to guarantee both chemical and paperwork traceability, reflecting an increasing commitment to transparency and reproducibility. All this elevates the product’s role from a single-use reagent to a trusted foundation in a repeatable workflow.

    From where I sit, supporting mutual learning transforms even established molecules like Trans-4-Aminoadamantan-1-ol Hydrochloride into crucial enablers. With more public sharing of methods and troubleshooting guides, tomorrow’s researchers start farther ahead.

    Future Use Cases and Responsible Growth

    Emerging technologies continue to ask more from their molecular building blocks. Advanced drug delivery systems and targeted therapeutics need adaptable, robust intermediates. Organic electronics, where three-dimensional rigidity carries real performance benefits, can draw from the same characteristics highlighted in this molecule. Researchers probe new chemical space by modifying known scaffolds; the adamantane core’s record in stability and bio-compatibility suggests this product is more than just another specialty chemical.

    As demand spreads beyond traditional pharmaceutical research—into fields like smart materials and sensor design—supplier networks grow more conscious about responsible sourcing, safe transport, and strong verification procedures. The professional networks behind these developments prove vital. They ensure that every sample matches its certificate and that labs counting on repeat orders can access precisely what their protocols demand.

    Collaborative Solutions for Persistent Issues

    Nobody in the business of molecular innovation expects unbroken workflow or trouble-free deliveries. Where gaps appear—in process reproducibility, data transparency, or even regulatory reporting—open communication and industry cooperation set solutions in motion. Chemists, supply chain specialists, and technical support teams build informal alliances, solve bottlenecks, and refine compound documentation. Even if a single compound cannot transform a field, the cooperative approach to handling, testing, and deploying it strengthens the larger community.

    Solutions often arise from simple exchanges: a better drying technique, flagging a recurring impurity, or negotiating minor composition changes to fit unique experimental plans. Quality grows from practice, attention to detail, and the willingness of labs and suppliers to correct course quickly. Trust builds with each successful run and each honest conversation about what works—and what needs work.

    Meeting New Research Demands Through Thoughtful Adaptation

    Trans-4-Aminoadamantan-1-ol Hydrochloride demonstrates that chemistry’s building blocks do more than support individual reactions. They allow teams to dream up new molecules, evaluate previously unexplored biology, or strengthen materials for future technologies. The community developing, refining, and using these compounds adapts by keeping discussions open, searching for cost-effective advances and greener approaches without undercutting reliability or safety. These efforts often have deep, direct impact in shaping tomorrow’s research landscape.

    Incremental improvements—long shelf-life, easier purification, confident verification—might not draw headlines, but in any research-driven environment, they add up. That sustained progress lets new ideas flourish and lets labs tackle big problems without unnecessary roadblocks tripping them up at the most basic level.

    Final Thoughts

    Trans-4-Aminoadamantan-1-ol Hydrochloride stands as a practical, proven asset for chemists in the lab and teams scaling up for broader trials. Every feature, from its robust adamantane skeleton to careful dual functionalization, underpins its reputation. Experienced hands appreciate materials that combine reliability with flexibility. This compound delivers both and shows the tangible benefits of a strong research culture—one grounded in sharing know-how, pushing for higher standards, and remaining open to continuous improvement.

    The growing connections between research groups, suppliers, and quality assurance teams form the real foundation that lets compounds like this make a difference at the lab bench and beyond. Those shared efforts ensure that every order supports not just an experiment but the broader pursuit of new medicines, smarter materials, and creative technologies. From my perspective, that’s worth building on.