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11Α-Hydroxy-4-Androstenedione

    • Product Name 11Α-Hydroxy-4-Androstenedione
    • Alias 11α-OHA
    • Einecs 252-230-0
    • 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

    616992

    Chemical Name 11α-Hydroxy-4-androstenedione
    Molecular Formula C19H26O3
    Molar Mass 302.41 g/mol
    Iupac Name 11α-Hydroxyandrost-4-ene-3,17-dione
    Cas Number 911-37-7
    Appearance White to off-white crystalline powder
    Melting Point 208-210°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 11α-OH-4-androstenedione, 11α-hydroxyandrostenedione
    Biological Role Steroid hormone intermediate
    Origin Naturally occurring metabolite in steroid biosynthesis
    Stability Stable under recommended storage conditions
    Storage Conditions Store at 2-8°C, protected from light
    Application Used in research related to steroidogenesis

    As an accredited 11Α-Hydroxy-4-Androstenedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle labeled "11Α-Hydroxy-4-Androstenedione, 1g". Features batch number, storage instructions, and hazard symbols.
    Shipping **Shipping Description for 11Α-Hydroxy-4-Androstenedione:** Shipped in secure, chemical-resistant packaging, 11Α-Hydroxy-4-Androstenedione is transported under temperature-controlled conditions to ensure stability. Proper labeling, including hazard and handling instructions, is affixed. Shipping complies with all applicable regulations for chemical transport and includes documentation for safe and traceable delivery.
    Storage 11Α-Hydroxy-4-Androstenedione should be stored in a tightly sealed container, away from direct sunlight, moisture, and incompatible substances, such as strong oxidizers. It should be kept in a cool, dry, and well-ventilated area, ideally at temperatures of 2–8°C (refrigerated conditions) to maintain stability and prevent degradation. Proper labeling and secure storage are essential for safety.
    Application of 11Α-Hydroxy-4-Androstenedione

    Purity 98%: 11Α-Hydroxy-4-Androstenedione with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-efficiency precursor yield for corticosteroid production.

    Molecular weight 302.4 g/mol: 11Α-Hydroxy-4-Androstenedione with molecular weight 302.4 g/mol is utilized in medical research studies, where it provides reliable substrate consistency for enzyme pathway analysis.

    Melting point 220°C: 11Α-Hydroxy-4-Androstenedione with a melting point of 220°C is employed in chemical process optimization, where it guarantees thermal stability during compound formulation.

    Particle size <20 μm: 11Α-Hydroxy-4-Androstenedione with particle size less than 20 μm is applied in topical formulation development, where enhanced surface area supports better dissolution rates.

    Stability temperature up to 40°C: 11Α-Hydroxy-4-Androstenedione stable up to 40°C is used in storage and transport solutions, where it maintains compound integrity under controlled conditions.

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    Certification & Compliance
    More Introduction

    11Α-Hydroxy-4-Androstenedione: Advancing Options in Endocrine Chemistry

    An Honest Look at a Powerful Molecule

    Most people don’t think about hormone pathways or the chemistry behind medical compounds, but ask anyone dealing with hormone-sensitive conditions, and you’ll hear about the impact a single molecule can have. Among chemists and clinicians, 11Α-Hydroxy-4-Androstenedione signals something big. This steroid molecule adds new options for both research and therapeutic strategies, answering unanswered questions that have hovered over the fields of endocrinology and oncology for decades.

    The Model: Purity, Build, and Benchmarking

    Held up against more familiar compounds like androstenedione and 4-androstenedione, 11Α-Hydroxy-4-Androstenedione diverges in structure by a precise tweak—a hydroxyl group attached at the 11-alpha position. At first, it seems like splitting hairs. Yet, this subtle chemical difference transforms behavior in the body. The best commercial solutions deliver extremely high purity (over 98%) and controlled particle size, because anything less would undercut reliable results for researchers and clinicians alike.

    Lab testing puts this molecule through the wringer: mass spectrometry, infrared analysis, and chromatography lay bare what’s in the flask. That might sound technical or fussy, but anyone who’s worked in a bench lab knows how tiny impurities wreck good science. With 11Α-Hydroxy-4-Androstenedione, the right specification ensures scientists can build on facts, step by step, without second-guessing the sample.

    Real-World Usage: Research and Beyond

    The story of 11Α-Hydroxy-4-Androstenedione stretches beyond the test tube. Its most notable application lands in hormone-related cancer research. As an inhibitor of the aromatase enzyme, it blocks a critical step in estrogen production, which matters deeply for diseases like breast cancer. Steroid aromatase inhibitors first made waves in the 1970s and 1980s, and since then, newer versions have chipped away at side effects and increased specificity.

    Anyone who’s watched family or patients working through these illnesses knows how valuable even small pharmaceutical advances become. Instead of sledgehammer drugs that wipe out all hormone activity, researchers hope for targeted action — stopping disease without blitzing other pathways. 11Α-Hydroxy-4-Androstenedione, with its precise targeting and unique metabolic path, helps sharpen that focus.

    How It Sets Itself Apart: Tweaks That Matter

    It’s easy to lump all steroid compounds in one box, but the 11Α-hydroxy variation marks a genuine pivot. Standard androstenedione, a longstanding research tool and banned performance drug, acts as a precursor along the testosterone and estrogen pathways. The core difference comes from that extra hydroxyl group sitting at the 11α position — not just a chemical oddity, but a real game-changer in both function and metabolism.

    In the hands of scientists investigating adrenal steroidogenesis or the fine points of enzyme inhibition, this tweak determines whether a compound helps or confuses the narrative. For example, 11Α-Hydroxy-4-Androstenedione offers a unique route to inhibit aromatase compared to the classic options, meaning it might block estrogen buildup where traditional drugs struggle.

    If you’ve ever spent nights scanning through clinical study results, you know: specificity and selectivity keep coming up. There’s no shortage of broad-spectrum inhibitors. What matters now are molecules like this one, which offer some hope to shift research and patient care toward precision, not just brute force.

    What Draws Experts to 11Α-Hydroxy-4-Androstenedione?

    Ask a bench chemist, and you’ll hear about smooth solubility and sharp analytical profiles. Talk with clinical pharmacologists, and interest turns to oral bioavailability, speed of metabolism, and lower potential for toxic metabolites. This molecule isn’t a slick marketing reinvention, but a hard-earned product of decades sifting through structure-activity relationships in steroid chemistry.

    Because of its structure, the molecule interacts differently within key metabolic pathways. This creates research leads not just for hormone-dependent cancers, but also adrenal disorders. The increased hydroxylation at the 11-alpha site might sound esoteric, but it’s here where scientists track down why side effects get minimized or why some drugs show promise where others didn’t.

    From Theory to Practice: The Researcher’s Dilemma

    A big chunk of biomedical work boils down to the quality of what goes into your experiment or clinical trial. Too many studies have collapsed from off-the-shelf reagents that didn’t measure up — wrong isomer, unexpected side reactions, impurities causing noisy data. 11Α-Hydroxy-4-Androstenedione, in its high-purity and standardized versions, pushes back against those issues that often slip under the radar.

    Researchers appreciate the way it holds up during synthesis, storage, and repetitive dosing protocols. Stability isn’t just an add-on in laboratory work; it means months of storage without loss in activity, clarity in test results, and honest measurements you can report or publish without the nagging feeling something’s off.

    Some colleagues have relayed cases where inadequate starting materials sent months of post-doc work down the drain. By contrast, working with well-characterized compounds lets researchers keep attention where it belongs: interpretation, insight, and discovering what the molecule can actually do.

    Therapeutic Windows and Clinical Hopes

    Switch gears from basic science, and the clinical stakes grow heavier. Early-stage compounds always walk a tightrope between power and side effects. The search for new steroid-based inhibitors never stops at chemistry alone; the path bends through animal models, human testing, and anecdotal reports from practitioners at the front lines.

    What’s different about 11Α-Hydroxy-4-Androstenedione? Its altered metabolism and target specificity carry the promise of better control over hormone levels in real patients. The theory runs that by zeroing in on a precise step in the biosynthetic pathway — with minimal “collateral” effects downstream — doctors could steer hormone modulation with fewer unwanted effects. This is especially critical for women battling breast cancer, for whom estrogen plays so powerful and unpredictable a role.

    Oncology teams have plenty of storylines where the right molecule, combined with the right protocol, delivered a meaningful boost in survival or quality of life. While no single compound changes the face of cancer overnight, these incremental advances count in the trenches. For those who have watched friends or family face long-term hormone blockade, the search for gentler, swifter, or smarter options remains urgent.

    The Market: Trends and Transparency

    There’s a healthy shift underway among suppliers, too. Gone are the days of murky sourcing and vague documentation. Top-tier products today arrive with batch-specific analysis, traceable origin, and regulatory support for both research and clinical investigation. This isn’t an abstract improvement — it means that end-users, whether working under Good Manufacturing Practices (GMP) or investigative settings, maintain trust in the chain of custody and documented quality.

    I’ve seen the gradual move toward this kind of transparency in several labs, driven both by regulation and self-imposed standards. It reduces the margin for error, lessens the chance for surprise outcomes, and builds a foundation where collaboration between chemists, clinicians, and manufacturers feels possible, not adversarial.

    Differentiation From Other Products: Not Just a “New Flavor”

    The temptation to call each minor steroid variation a whole new class borders on marketing inflation in the biochemical supply industry. In the case of 11Α-Hydroxy-4-Androstenedione, the chemical modification hits right at a functional crossroads. It neither mimics previous compounds nor simply adds weight to an old idea.

    Comparisons often come up against 4-Androstenedione, a popular option in both research and athletic contexts. The 11Α-hydroxy version, though, avoids the direct conversion to testosterone, pushing instead toward more nuanced regulatory effects on enzymes like aromatase. While many prohormone products risk indiscriminate action, this adjustment helps minimize “off-target” impacts. It’s attractive to both cautious scientists and careful clinicians looking to avoid messy feedback effects or regulatory complications.

    Some may recall earlier troubles with poorly controlled steroid supplements pushed in the fitness world. 11Α-Hydroxy-4-Androstenedione steps outside that shadow, showing value in strictly controlled and documented research, with little overlap with that unregulated gray zone. Simply put, it’s become a “cleaner” choice for those who care about both scientific clarity and subject safety.

    Quality Control: A Non-Negotiable

    Even a promising molecule stumbles if quality control doesn’t keep pace with market growth. Major suppliers now prioritize traceable supply chains, clean synthetic protocols, and repeated lot-testing to confirm molecular weight, melting point, and impurity profile. Skipping corners at any stage defeats the whole value proposition of a compound like 11Α-Hydroxy-4-Androstenedione.

    Those in the field recognize how cost-saving measures can backfire. I’ve heard stories (and lived some myself) where a slightly cheaper supplier handed over substances riddled with side-products or incorrect stereochemistry. After months of troubleshooting, the realization hits: you can’t fake quality and expect results.

    Investment in up-to-date analytics and collaborative quality reviews is paying off. Today’s best labs publish not just a list of testing methods, but the actual results, fostering real trust and peer-to-peer accountability. Open communication with suppliers — something long overdue — encourages early problem detection and shared solutions.

    The Regulatory Landscape

    Steroid molecules attract intense regulatory attention, for good reason. The risk of diversion into unapproved use remains real. As a result, responsible suppliers keep strict records, follow all reporting requirements, and participate in audits. Researchers, too, benefit from knowing that what they receive won’t expose them to legal or safety risks.

    Legitimate products include proper documentation for border crossings, institutional review, and research integrity. These are more than bureaucratic hurdles; such safeguards protect human subjects and support long-term reputability of both products and publications. The extra paperwork can feel daunting, but anyone who’s dealt with lost research time over questionable sourcing quickly learns its value.

    Potential and Limitations

    No single molecule closes the book on complex disease states or intricate metabolic puzzles. 11Α-Hydroxy-4-Androstenedione opens new doors but doesn’t provide all the answers. The compound’s stability and target specificity offer opportunities in several subfields — for example, endocrinology, oncology, and metabolic syndrome research — but the full breadth of its clinical and commercial impact remains to be seen.

    Some researchers have already flagged the need for larger study populations and longer-term follow-up before moving from lab bench to clinical bedside. Concerns about rare side effects, off-target enzymatic action, and long-term metabolite profiles remain active areas for study. The track record of similar compounds teaches us that bold claims up front don’t always translate perfectly into lasting medical impact.

    For those thinking about research direction, it’s not just about jumping to the newest tool. Solid comparisons, both in vitro and in vivo, help balance optimism with grounded skepticism. Paying attention to the hard-won lessons from steroid pharmacology keeps the conversation realistic, if still optimistic.

    Why This Molecule, Why Now?

    The health environment continues to shift, shaped by advances in genetics, biochemical screening, and targeted therapy. Old one-size-fits-all models have given ground to highly individualized treatments, shaped by patient genetics and disease specifics. In this atmosphere, a molecule like 11Α-Hydroxy-4-Androstenedione — with its differentiated profile — fits into a toolkit built for targeted intervention and lower unwanted effects.

    Patients and practitioners expect more than generic suppressants or risky “biohacks.” Instead, the search focuses on compounds with clear mechanisms, responsive dosing, and fewer complications. The challenge: to advance knowledge and therapy without letting hype outstrip what data and experience can genuinely support.

    Gaps in the Field and the Need for Collaboration

    Progress comes slow in the tangled world of steroid chemistry and hormone regulation. Far too often, small companies and research groups work in silos, reinventing answers already known elsewhere. The rise of standardized, well-characterized compounds like 11Α-Hydroxy-4-Androstenedione makes broader collaboration possible. Shared samples, open protocols, and published datasets let breakthroughs move from bench to real world faster.

    Some seasoned researchers still remember early days of stonewalling and secrecy in the field — missed opportunities, duplicated mistakes, and slow translations into clinical benefit. Now, with improved access to reproducible molecular tools, researchers and clinicians find they can speak the same language and solve bigger, more complex challenges together.

    Pushing the Industry Forward

    The emergence of 11Α-Hydroxy-4-Androstenedione reflects a slow, stubborn progress toward better science and patient care. The molecule brings not splashy marketing, but a quiet sense of possibility for anyone trying to understand, treat, or manage hormone-driven illness. By demanding honest analysis, supporting regulated access, and insisting on cross-disciplinary collaboration, those in the field have nudged the entire sector a step ahead.

    It would be a mistake to call this compound the final word. But it is, in many ways, a strong statement about what’s possible when scientific curiosity, technical know-how, and patient need all line up. For anyone moving research forward — or simply looking for more sophisticated options in hormone modulation — 11Α-Hydroxy-4-Androstenedione stands as a tool that rewards effort, transparency, and an open mind.