|
HS Code |
991876 |
| Cas Number | 546-92-9 |
| Molecular Formula | C19H26O3 |
| Molar Mass | 302.41 g/mol |
| Synonyms | 9α-Hydroxyandrostenedione |
| Appearance | White to off-white powder |
| Melting Point | 220-224°C |
| Solubility | Slightly soluble in water, soluble in alcohol |
| Iupac Name | 10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3-oxo-9-hydroxycyclopenta[a]phenanthren-17-one |
| Pubchem Id | 159563 |
| Chemical Class | Steroid |
| Storage Conditions | Store at 2-8°C |
| Boiling Point | Decomposes before boiling |
| Chemical Use | Intermediate in steroid biosynthesis |
| Stability | Stable under recommended storage conditions |
As an accredited 9-Hydroxyandrostenedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 9-Hydroxyandrostenedione, 1g: Supplied in a sealed amber glass vial with tamper-evident cap, labeled with product details and safety information. |
| Shipping | 9-Hydroxyandrostenedione is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. Packaging complies with relevant safety regulations, including labeling for hazardous materials if applicable. During transit, the chemical is protected from moisture, heat, and direct sunlight, with appropriate cushioning to prevent breakage or leakage. Shipping follows all applicable legal guidelines. |
| Storage | 9-Hydroxyandrostenedione should be stored in a tightly sealed container, protected from light and moisture. Store at a temperature between 2–8°C (refrigerated) and away from incompatible substances such as strong oxidizing agents. Ensure the storage area is well-ventilated and clearly labeled. Follow all relevant safety and chemical hygiene guidelines to prevent contamination and degradation of the compound. |
|
Purity 98%: 9-Hydroxyandrostenedione with purity 98% is used in pharmaceutical intermediate production, where it ensures high conversion rates in steroid synthesis. Melting Point 228°C: 9-Hydroxyandrostenedione with a melting point of 228°C is used in chemical process development, where it provides thermal stability during high-temperature reactions. Molecular Weight 302.4 g/mol: 9-Hydroxyandrostenedione at a molecular weight of 302.4 g/mol is used in analytical research, where it allows precise molecular identification and quantification. Particle Size <50 µm: 9-Hydroxyandrostenedione with particle size less than 50 micrometers is used in formulation studies, where it enables uniform dispersion in suspension systems. Stability at 25°C: 9-Hydroxyandrostenedione stabilized at 25°C is used in reference standard preparation, where it guarantees accurate and consistent analytical testing outcomes. |
Competitive 9-Hydroxyandrostenedione 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!
There’s a growing interest among researchers and professionals in compounds that lie at the intersection of biochemistry and modern health science. 9-Hydroxyandrostenedione deserves attention not only for its distinct place in steroid biochemistry but for what it brings to specific areas like medical research and metabolic studies. Unlike many overhyped products with little to back their claims, 9-Hydroxyandrostenedione has roots in legitimate scientific exploration.
This molecule, officially recognized by its structure—9,17-dihydroxyandrost-4-en-3-one—sits one step away from its well-known cousin, androstenedione. That extra hydroxyl group at the 9th carbon position seems small on paper but can influence metabolic pathways and experimental outcomes in unexpected ways. Those who spend time in laboratories or in research-focused businesses will recognize that such differences aren’t just details; they often mark out a new direction, giving scientists a tool for mapping effects or tweaking processes with finer precision.
To experienced eyes, specifications for 9-Hydroxyandrostenedione aren’t just about purity and assay results. They shape how the compound fits into a protocol or lines up with regulatory expectations for research use. In the current market, you’ll find it most often in a crystalline powder, white or near-white to the eye. Most reliable sources offer the product at a reported purity level usually above 98 percent, confirmed by HPLC analysis—a level taken seriously in the research world, where small contaminations matter.
What catches attention is the molecular formula: C19H26O3, with a molar mass edging near 302.41 g/mol. This matches well with what’s reported in scientific databases and research literature. Water content and residual solvent levels are tested, and most labs set specifications that keep these at a minimum. Storage conditions favor cool, dry environments, keeping full stability at room temperature when away from light and air exposure.
Those focused on regulatory compliance will note that 9-Hydroxyandrostenedione is generally not sanctioned for human or veterinary drug use or as an ingredient in food or dietary supplements. Its scope stays within research and analytical circles, entwined with the expectations of modern compliance—no shortcuts, no gray zones.
It’s easy to lump this compound with other androstene derivatives, but real work in hormonal studies and steroid metabolism has shown important differences. In endocrinology, one key question always circles back to how a tiny molecular change affects biological pathways—especially when studying enzyme inhibition or transformation. The 9-hydroxy group isn’t just a chemical add-on; it alters the way the molecule stacks up in receptor binding and metabolic fates.
In preclinical studies, 9-Hydroxyandrostenedione can help researchers dissect the details of androgen biosynthesis and breakdown. Labs aiming to map out enzyme pathways, especially 11β-hydroxysteroid dehydrogenase or aromatase systems, find this compound invaluable because it acts as a marker for transformation steps that don’t show up with plain androstenedione or similar relatives. Detailed tracing of metabolites gets possible, shining light on previously obscure intermediates in complex cascades.
What else draws research teams to this compound? Some teams working with animal models use it as a reference standard for diagnostic tools or assay calibrations, helping separate true biological variation from lab artifacts. Scientists tackling the messy puzzle of steroid-driven diseases find it useful in exploring how extra hydroxylation steps modulate activity— giving another angle on estrogen and androgen receptor dynamics. Every bit of fresh data helps sharpen diagnostic and therapeutic strategies.
Plenty of other androstene derivatives crowd scientific catalogs. Androstenedione and 4-androstenedione, well known to endocrinologists, can both serve as precursors in biosynthetic chains. 9-Hydroxyandrostenedione’s unique claim stems from its additional hydroxyl group, which flips its chemical behavior and, as a result, its biological significance.
Take its reactivity with enzymes. Regular androstenedione feeds smoothly into both androgen and estrogen synthesis via familiar routes, largely unimpeded. The 9-hydroxy version’s extra group can tip enzyme-substrate interactions, delivering metabolic products that diverge from pathways headed by plain androstenedione. For research teams comparing tissue exposures or metabolic products, these differences matter—and ignoring them can mean missing critical results.
Then you’ve got issues of stability. In my own research experience, minor molecular tweaks like this don’t just change function—they can increase sensitivity to oxidation or light. That can pose a concern if lab protocols ignore practical details like storage or reagent preparation. I’ve watched well-meaning students spoil entire assay runs by using old or poorly stored reagent. Choosing a version that carries an extra hydroxyl group means adjusting handling protocols and modifying control standards, no matter how minor those changes seem.
This compound’s difference from others in its class comes into sharp focus in cell culture and binding studies. Investigators probing receptor-ligand relationships notice that binding affinities shift. And in the body, this could theoretically alter hormone regulation and feedback, though no one advocates jumping from data sheets to clinical applications without real proof. Misinterpreting experimental results by treating every androstene as equal usually leads to wasted effort, misleading signals, and missed learning.
Some might wonder why companies and research groups pay more for a molecule that seems so close to cheap, common alternatives. The answer comes down to data accuracy and model validity. In any field where steroid actions play a part—ranging from endocrinology to oncology and even cardiovascular research—uncovering the full shape of metabolic webs takes specialized tools. The simple presence of a 9-hydroxy group becomes less trivial when you realize it makes certain downstream metabolites either possible or traceable.
Research published over the past decade points to subtle but important shifts in biomarker profiles when the 9-hydroxy group enters the cellular mix. Analysis of urinary and serum metabolites grows clearer—helping teams find patterns tied to disease, anabolic misuse, or alterations in hormone therapy. In practical terms, that means developing better, faster, more reliable assays. For industries invested in testing, drug development, or forensic analysis, such gains translate into real returns.
It also matters for compound screening platforms. For any business operating in drug discovery, specificity drives results. Libraries featuring detailed variants like 9-Hydroxyandrostenedione allow screening teams to cover more ground in mapping off-target interactions or toxicity risks. And as chemical libraries globalize, those who build collections with subtle but distinct products see their assets grow in value.
Anyone who’s spent real time in the lab knows that buying a research chemical doesn’t end with reading a spec sheet. The risk of off-specification or misidentified product remains real in this globalized market. In an era of cost cutting and internet sourcing, even seasoned labs face counterfeits or adulterated lots. Firms that sell 9-Hydroxyandrostenedione with transparent, independently verified testing reassure users, but do not erase the need for in-house scrutiny.
Regulation adds another layer. Depending on the jurisdiction, import rules and reporting requirements shift often. I recall entire shipments delayed for weeks when paperwork failed to clarify the use case or when regulators flagged ambiguous labeling. For research organizations, documentation—COAs, batch records, and independent verification—moves from administrative overhead to mission-critical.
Disposal, often overlooked, looms as another responsibility. Any compound from the steroid family raises questions about environmental safety. Used or expired product must be handled with systems that cut risk of hormone pollution. I’d like to see more vendors partner with disposal services, or even build in environmental support for buyers—right now, too much responsibility falls on individual labs who may lack resources.
Last comes the challenge of training. Bringing advanced molecules like 9-Hydroxyandrostenedione into under-resourced labs can backfire if users don’t recognize the compound’s reactivity or storage needs. More than one trainee has mixed up reagents, confused by subtle nomenclature differences. Consistent labeling, in-language materials, and easily accessible literature prevent accidents and wasted material. Even seasoned researchers benefit from updated protocols—the science moves fast, and best practices from even five years ago don’t always match today’s realities.
Building better research around compounds like 9-Hydroxyandrostenedione starts with trust and transparency. Trusted vendors with traceable supply chains make a difference, and shouldn’t just tout purity percentages—they should offer spectral and chromatographic data on every batch, not just on request. Too many stories circulate about labs receiving what looks right but fails mass spectrometry testing. Open access or blockchain-enabled movement tracking could bring the field closer to full transparency.
Educating buyers and users still matters. Vendors offering real-time support, on-demand documentation, and bilingual resources set higher standards. Community-driven review platforms, featuring feedback from verified institutional buyers, would help root out unreliable suppliers. Some parts of the industry have seen gains with independent testing labs, paid directly by buyers, running third-party analyses on incoming product and publishing redacted results.
Reducing environmental impact isn’t just about safe disposal. Producers could work with research consortia to develop greener synthesis routes that avoid sketchy reagents or cut down on harmful solvents. As sustainability moves to the top of industry agendas, even incremental changes in sourcing or manufacturing partner selection can ripple out, showing real improvements downstream.
And for smaller labs hesitant to bear the cost or risk of specialized chemicals, pooled purchasing programs through universities and nonprofit research alliances provide another model. Collaborative networks bring down costs through group negotiation and centralize expertise when newer compounds enter the mix. This levels the playing field for institutions focused on basic research or in low-resource settings, ensuring wider access to cutting-edge tools without the wild price swings of niche supply chains.
As health and biotech industries get smarter, the demand for nuanced steroid derivatives will only grow. 9-Hydroxyandrostenedione occupies a unique space—useful, reliable, and capable of delivering a clearer picture where one-dimensional markers have failed. Institutions funding breakthroughs push supply chains to adapt. Smart labs rethink protocols on the fly, ensuring data coming off benches bears up to scrutiny, and combinations with other molecules bring out new effects.
What excites most is watching collaboration between once-siloed fields, each exploring what small molecular changes deliver at scale. Chemists, clinicians, environmental scientists—each group brings a lens that challenges routine assumptions. Technologies like AI-driven compound libraries or rapid-screening platforms could widen our understanding even further.
In this environment, buyers and researchers will keep looking for more clarity and certainty in product selection. That means greater openness, faster cycles from bench to bench, and a willingness to ask how seemingly subtle distinctions—like an added 9-hydroxy group—reshape our collective understanding of biology and therapeutic innovation.
It sometimes falls to niche compounds to make the largest differences. My time in labs has shown that chasing the unknown, or even drilling deep into the subtle distinctions of a molecule, sheds more light on complex systems than sticking with familiar standbys ever could. 9-Hydroxyandrostenedione may not headline conventional pharmaceutical catalogs, but real advances rarely wait for the spotlight. Where research teams care about precision and depth, where every molecule is treated as a potential pathway forward rather than just another reagent, products like this find their place.
As the worlds of endocrinology, toxicology, and metabolic studies continue to intersect, those who understand product nuances—down to the impact of a single hydroxyl group—will drive discoveries that stick. The future belongs to researchers and suppliers who sweat those details and who build partnerships rooted in transparency, scientific rigor, and ethical responsibility.