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5Alpha-Androst-16-En-3-One

    • Product Name 5Alpha-Androst-16-En-3-One
    • Alias Androstene-3-one
    • Einecs 217-441-2
    • 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

    823310

    Chemical Name 5Alpha-Androst-16-En-3-One
    Molecular Formula C19H28O
    Molecular Weight 272.43 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 128-132°C
    Solubility Insoluble in water; soluble in organic solvents
    Cas Number 2206-96-6
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place away from light

    As an accredited 5Alpha-Androst-16-En-3-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 10 grams of 5Alpha-Androst-16-En-3-One; tamper-evident cap, clear labeling with hazard symbols.
    Shipping The chemical 5Alpha-Androst-16-En-3-One is shipped in sealed, chemically resistant containers to ensure safety and stability. Packaging complies with international regulations for hazardous materials. All shipments include proper labeling, documentation, and handling instructions. Expedited and temperature-controlled options are available upon request to maintain product integrity during transit.
    Storage 5Alpha-Androst-16-En-3-One should be stored in a tightly sealed container at controlled room temperature, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Ensure the storage area is dry, well-ventilated, and secure to prevent unauthorized access. Use appropriate chemical storage cabinets and clearly label the container. Handle with personal protective equipment, following relevant safety guidelines.
    Application of 5Alpha-Androst-16-En-3-One

    Applications of 5Alpha-Androst-16-En-3-One in Industrial Manufacturing

    Our producer-grade 5Alpha-Androst-16-En-3-One serves as a targeted synthetic building block for selected downstream sectors. Below, we specify practical industrial applications, with a breakdown by real industry use, dosage, regulatory demands, integration, and finished products.

    1. Pharmaceutical Steroid Intermediate Synthesis

    Pharmaceutical manufacturers use 5Alpha-Androst-16-En-3-One as a precursor in multi-step synthesis of anabolic and androgenic steroid active pharmaceutical ingredients (APIs). Its molecular configuration allows precise functionalization at the 3-keto and 16-ene positions, enabling robust conversion to derivatives such as trenbolone and related compounds under controlled reaction conditions. It enters designated reactors following strict validation for impurity profiling and traceability, following cGMP protocols to minimize contaminant risk during phosphorylation, reduction, and esterification steps. Downstream operators require consistent isomeric purity and controlled moisture content for successful conversion and high-yield batch processing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) for APIs (ICH Q7, US 21 CFR Part 210/211)
    • European Pharmacopoeia (Ph. Eur.) monographs for steroidal intermediates
    • USP General Chapters on Residual Solvents (USP <467>)
    • REACH Substance Registration for chemical intermediates

    Typical usage ratio

    • 0.10–0.25 molar equivalents per synthesis batch, depending on target derivative and conversion pathway. Scale and ratio adjusted based on intended API output and impurity control.

    Downstream process integration

    • Input to glass-lined or stainless steel synthesis vessel after specification approval and raw material QC.
    • Subjected to catalytic hydrogenation, oxidation, or acylation during API intermediate production.
    • Assayed by HPLC to confirm process control before downstream purification.

    Final product types

    • Active steroidal pharmaceutical ingredients (e.g., trenbolone, boldenone base)
    • Synthetic intermediates for corticosteroids
    • Raw materials for veterinary steroid formulations

    2. Veterinary Growth Promotant Synthesis

    Veterinary pharmaceutical processing plants employ 5Alpha-Androst-16-En-3-One to generate growth-promoting androgenic agents for livestock, including bovine and swine injectable or implant preparations. The raw material feeds directly into high-purity synthesis chains that require validated input for dosage consistency and residue safety. Operators must verify batch purity and confirm absence of unqualified impurities to satisfy residue control for edible animal tissues. The compound features in hydrogenation and coupling runs prior to microencapsulation or aseptic filling. Certificate of Analysis and full traceability documents accompany all deliveries for audit readiness.

    Industry compliance standards

    • Veterinary Drug GMP (China VICH/EU GMP)
    • FDA 21 CFR Part 226 for medicated feed manufacturing
    • European Medicines Agency (EMA) Maximum Residue Limits (MRLs)
    • ISO 9001:2015 (for chemical supply and batch records)

    Typical usage ratio

    • 0.05–0.22 grams per finished dose unit, controlled by target implant release profile; titrated based on in vivo residue limits and specific livestock applications.

    Downstream process integration

    • Metered to batch reactors for controlled synthesis or esterification.
    • Processed via filtration, RP-HPLC, and crystallization for injectable or implant-grade output.
    • Intermediate handled in Grade D cleanroom environments before finished dosage blending.

    Final product types

    • Bovine implant growth promotants (e.g., trenbolone acetate implants)
    • Swine anabolic feed additive APIs
    • Veterinary bulk actives for feedlot preparations

    3. Chemical Reference Standard Manufacturing

    Specialized analytical labs and reference material producers source 5Alpha-Androst-16-En-3-One to prepare certified reference standards and analytical controls for steroid screening in clinical, anti-doping, and forensic settings. The compound undergoes rigorous secondary purification, isotopic labeling, and stability testing to achieve required analytical purity. Manufacture requires trace organic analysis to confirm conformance with reference standard regulations, ensuring no cross-contamination for qualifying analytical protocols. All batches link to a certificate of analysis with spectroscopic and chromatographic validation.

    Industry compliance standards

    • ISO 17034:2016 (Competence of Reference Material Producers)
    • ISO/IEC 17025:2017 (Testing and calibration laboratory competence)
    • World Anti-Doping Agency (WADA) analytical protocols for steroid controls
    • Pharmacopoeial reference standard documentation (USP, EP)

    Typical usage ratio

    • Preparation bulk: 0.1–2.0 mg/mL stock solutions for analytical standardization; sub-milligram accuracy required.

    Downstream process integration

    • Dissolution in high-purity solvents for reference solution calibration.
    • Fine filtration, ampoule aliquoting, freeze-drying for sealed reference controls.
    • Spectroscopic fingerprinting (NMR, MS) post-purification for documentation.

    Final product types

    • Certified reference standards for LC/MS and GC/MS assays
    • Analytical grade steroid calibrators
    • Matrix-matched kit controls for laboratory proficiency testing

    4. Chemical Research and Discovery in Academic Synthesis

    University and institute research groups source 5Alpha-Androst-16-En-3-One for development of novel steroid analogues, receptor binding studies, and mechanistic biochemistry projects. The compound’s structural features make it an effective starting scaffold for side chain elongation, reduction, and halogenation. Labs require detailed impurity profiles and batch repeatability for reproducible results across reaction pathways. Input typically requires additional QA/QC steps such as 1H NMR, GC, and Karl Fischer titration for application in sensitive research assays. Material remains under research use only restrictions, with custom packaging in inert atmosphere vials to minimize degradation during storage and handling.

    Industry compliance standards

    • Institutional Chemical Hygiene Plans (OSHA 29 CFR 1910.1450)
    • REACH exemption provisions for research chemicals
    • Local/national chemical research licensing (e.g., DEA List I/II for controlled precursors where applicable)
    • GLP (Good Laboratory Practice) requirements in some regulated studies

    Typical usage ratio

    • Scale: 0.05–2.0 mmol per synthetic run, depending on target molecule and route optimization

    Downstream process integration

    • Dissolved in dry organic solvents for functional group modification
    • Reactive intermediate in target molecule mapping, for structure-activity relationship (SAR) studies
    • Direct input to parallel synthesis arrays or combinatorial libraries

    Final product types

    • Novel steroidal analogues for biochemical research
    • SAR probe molecules for receptor binding studies
    • Reference compounds for mechanistic pathway validation
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    Certification & Compliance
    More Introduction

    Understanding 5Alpha-Androst-16-En-3-One: Production Insights and Practical Experience

    What 5Alpha-Androst-16-En-3-One Means to Chemists in Production

    Chemical manufacturing asks for attention to detail, both in developing new processes and delivering consistent product. We’ve worked hands-on with 5Alpha-Androst-16-En-3-One for years and know it by its CAS number, structure, and the critical role it fills as a versatile intermediate in synthesis. Many in the industry refer to it simply as an “unsaturated ketone steroid,” but for us, it’s the outcome of painstaking refinements across years of pilot batches and full-scale runs. Whether it’s for laboratory research or specialty manufacturing, this compound earns its keep through reliability, purity, and the unique feature set that enables specific transformations, especially within hormone research, fragrance synthesis, and analytical standards.

    Model and Specifications: Manufacturing Standard Is Not Just a Number

    Over time, our mainstay has become the crystalline powder offering of 5Alpha-Androst-16-En-3-One, developed through a carefully controlled oxidation process. Every batch runs through a full set of chromatographic and spectroscopic verifications. Most scientists and R&D teams ask for 98% or higher purity; we typically exceed these expectations, with our routine production averaging 98.5-99.3%. The melting point, a handy indicator of purity, runs consistently within laboratory ranges and is checked regularly on both incoming and outgoing material. Visual inspection and IR/NMR fingerprinting have eliminated many headaches before compounds ever leave our facility.

    Contaminant control matters, especially since so much of this compound ends up in sensitive applications. We pay attention to both known byproducts and seasonal “unknowns” that crop up as process conditions shift, and our analytical team revalidates profiles every time any cleaning protocol or starting material changes. In practical terms, this means our clients rarely have to troubleshoot unexpected side products – something synthetic chemists always appreciate.

    With scaling, we’ve observed the impact of subtle changes: glassware that’s a bit older, or an operator’s twist on a crystallization. Trace water can shift yields downward, and even the grade of solvent might leave faint residues. These traditional manufacturing wrinkles shape the way each batch is planned and scheduled. We rely on physical samples and our own colorimetric and chromatographic tests before any shipment. More than once, we’ve caught sub-visible particles or micro-level color shifts that large distributors often miss.

    The Path from Raw Material to Finished 5Alpha-Androst-16-En-3-One

    Turning theory into product means grappling with real-world chemistry. Starting from pure plant-derived sterols, we run sequential modifications, with particular attention paid to temperature, reaction time, and exact reagent concentrations. Early steps, such as enzymatic and chemical dehydrogenations, set the precursor up for the targeted C16-enone functionality that makes this compound unique compared to its relatives. Successfully achieving the 16-en-3-one structure means controlling the harsh reaction environment without over-oxidation — easy to state, but any slip can tip the mixture toward unwanted isomers.

    Our experience has shown that oxidative cleavage works best in glass-lined reactors with precisely metered oxygen or ozone streams – not the makeshift setups seen in smaller niche factories. Each modification round undergoes purification through solvent extraction, careful recrystallization, and multi-stage filtration. Small details, like the surface area of stirring blades and reactor headspace, have caused fluctuations in yield before we optimized the hardware. By tracking these variables, we’ve kept our long-term yields steady, which keeps lot-to-lot consistency strong across years and process adjustments.

    Waste handling presents another part of the process few discuss. Saponified byproducts and spent acids receive full neutralization in-house. This not only meets regulations but also prevents trace contamination down the line. With every recurring synthesis, our technical team evaluates actual output against predicted models. Tweaks in temperature ramps or solvent exchange intervals pop up in our monthly process review, letting us track and eliminate drift.

    Usage: How 5Alpha-Androst-16-En-3-One Finds Its Applications

    Researchers have long worked with steroids bearing unique functional sites, but C16-en-3-one steroids carry special reactivity for synthesis routes in hormone analogs and selective fragrance precursors. In practical terms, biochemists appreciate the way the 16-ene double bond acts as a reactive site for further chemical transformations, such as selective reduction, epoxidation, and halogenation. We’ve talked to commercial labs who make full use of these reactivities, pushing toward rare or custom-modified steroids.

    Several clients approach us for the synthesis of intermediates destined for pharmaceutical research or specialty hormone mimics. Here, the consistency of our 5Alpha-Androst-16-En-3-One makes an impact, preventing re-synthesis or repeated column purification cycles. Time lost to cleaning up messy input multiplies down the chain — a lesson more than one contract lab learned the hard way before switching to higher-grade material.

    Fragrance houses seek this molecule for the animalic tonalities it introduces in musk synthesis, offering effect with a natural origin story compared to synthetic nitro-musks. The ability to orchestrate nuanced scents by functionalizing the enone system remains a topic of conversation among top perfumers. Chemical reactivity aside, repeatability drives business: slight deviation in the impurity profile or optical rotation shows up directly in product scent or reactivity downstream.

    For those in the analytical world, precise quantification of 5Alpha-Androst-16-En-3-One in biological samples means the difference between robust data and ambiguous results. Thus, we prepare analytical standards alongside bulk material, following the same trace impurity screens and documentation that bench chemists themselves trust. Our customers in university and industry labs have used our material as calibrants for assay development with LC/MS and GC/MS, reporting both dependable retention times and stable quantitation results.

    Seeing Past the Data Sheet: Differences from Other Steroid Intermediates

    The steroid market contains a variety of closely-related compounds: androstenedione, androst-4-en-3,17-dione, and their isomeric cousins. Yet not every intermediate offers the same chemistry, or behaves the same way in the lab. What we’ve found, working batch after batch, is that the presence of the 16-ene double bond in 5Alpha-Androst-16-En-3-One offers selectivity in transformations that would prove challenging, unpredictable, or even impossible on the more commonly available 4- or 5-ene steroids.

    Clients have described the frustration of side-product formation with more traditional intermediates, especially when pursuing modification at the D-ring. The 16-en-3-one structure resists typical rearrangements under mild conditions, opening the door to cleaner, more direct functionalization, whether adding new side chains or introducing halogens. This reduces costly downstream purification. In aroma compound synthesis, the shift to the 16-en structure brings out different musk tonalities and longevity. Our odor panels and technical partners have shared direct sensory contrast, comparing these materials not just in isolation, but in accord with other aromatic molecules.

    Another key observation comes from physical handling: crystal grain size, wettability during dissolution, and flow characteristics during weighing. Normal androstenedione or testosterone intermediates often clump, especially after storage in variable humidity. Our processed 5Alpha-Androst-16-En-3-One maintains crisp, easily pourable powder form, with minimal static or bridging. Raw material appearance may not occupy much mindshare in larger companies, but for lone bench chemists, every hour lost chipping compacted powder is a real cost.

    Comparing stability profiles, we subject 5Alpha-Androst-16-En-3-One to both accelerated and ambient stability checks. Across two-year spans, the compound holds up without significant hydrolysis, oxidation, or color change — performance that less refined intermediates often can’t match. Even at higher summer warehouse temperatures, the product maintains both spectral purity and physical properties, which helps downstream customers stick to their timelines without emergency re-orders or “mystery batch” investigations.

    Sourcing Directly from the Manufacturer: More Than a Supply Chain Relationship

    Having both R&D and commercial production on one factory site brings advantages less visible from an outside view. Issues or surprises get handled right away. Once, a customer in pharmaceutical development emailed about a faint nitrosamine impurity appearing in an LC scan; our team pulled up batch records in real time and traced the anomaly to a change in a minor acid supplier, rolled back the batch, shipped replacements, and requalified the process inside a week. These interventions happen because the chemists at the manufacturing level interact directly with what goes out the door, not through multiple reseller or distributor layers.

    Feedback leads to process improvement. One agricultural research team requested a variant with a custom melting point, so we ran a pilot with finer fractionation, eliminated early co-eluting isomers, and built a separate lot tailored to that project. Biomedical clients often require extra documentation — not just standard spectral data, but full traceability on solvent lots and glassware cleaning protocols. Our documentation and QC team build these trace packages in-house, reflecting actual hands-on labwork, not paperwork created for appearance.

    Batch size flexibility draws on real experience. Smaller runs (under 100 grams) benefit from quick batch switches in the kilo-lab, delivering research-scale material without the “last few grams” issues. For regular bulk users, drum-size (5-25 kg) output comes with calendar predictability — we synchronize reactor scheduling and logistics to customer production windows. Feedback from end-users on powder handling, solubility in various solvents, and odor has led us to optimize not just synthesis, but drying and packaging as well.

    Environmental Responsibility and Process Waste: Living with the Realities

    Any steroid intermediate brings environmental cost. Handling specialty solvents, acids, and oxidants calls for responsible capture and neutralization. Our plant remains vigilant about effluent control, with on-site analytics quantifying organic load before release. Reducing solvent usage without hurting product quality remains a regular target at process-improvement meetings. In recent years, solvent recycling initiatives recaptured more than 75% of all process acetonitrile and methanol, saving cost and shrinking ecological impact.

    We welcome audits from regulatory partners and contract researchers. Documentation reflects factual practices — not just what ought to happen, but the real, continuous attention that’s lived out in the plant. Reporting near-miss incidents gets rewarded, which lifts process transparency to a practical level. More than once, feedback from an auditor or bench worker has tightened up a process or flagged an unnecessary material stream for elimination. This feedback loop makes for cleaner, safer operation — not because regulators require it, but because it keeps our work, our people, and our material at consistently high standards.

    Supporting Rigorous Research and Manufacturing: What It Means for Users

    Our customers rely on truthful, practical information. Beyond product specs, direct communication about batch changes, process modifications, or unusual analytical findings makes all the difference. Our team keeps open doors with every lab, not only for regular feedback but also for out-of-cycle troubleshooting. Where other suppliers might simply swap in a substitute from back inventory, we handle concerns at the technical level, with chemists who know the process from reactant-to-reactant, not just from the paperwork. We recalibrate parameters when feedback emerges, sometimes after hearing about reaction yields, byproduct spectra, or even odor transfer issues in downstream manufacturing.

    We invest in technical support by supplying not only the compound but detailed historical data, reprocessed spectra, and cross-lab validation documents. When an unexpected analytical peak shows up in a customer’s GC trace, our technical team investigates with actual sample re-analysis, pooling in years of comparative runs. Our focus is not just authority in chemical manufacture, but practical, trustworthy guidance.

    Over the years, we have opened process tours for clients and research partners, offering firsthand view of synthesis, purification, analytics, and packing. Transparency helps everyone: internal feedback shapes better process, and external partners see for themselves the intact chain from raw starting materials to finished product.

    Continuous Improvement: Keeping 5Alpha-Androst-16-En-3-One Fit for Future Uses

    Chemical landscapes shift. Research groups develop new routes for hormone derivatives, fragrance blends become more intricate, and regulations around process contaminants evolve. Our response comes from actively learning what downstream users need, not holding tight to one process or market. Process analytical technology and in-line monitoring now catch batch drift the moment it starts, letting us keep purity and reactivity in the expected range.

    By holding both commercial and kilo-lab processes, we're positioned to test alternate raw material sources, trial new reagents, and fine-tune crystallization methods. Pilot work with greener oxidants and solvent-recycler technology has shown promise in tightening up economic and environmental margins. Our team circulates technical notes and informal bench data, making sure promising experiments turn into actual process upgrades.

    Through all of this, we rely on our hands-on team, whose lived experience ensures that each drum, bottle, or vial of 5Alpha-Androst-16-En-3-One represents not just a chemical entity, but a body of work and knowledge. For our clients, this means access to a product shaped by genuine manufacturing commitment, continuous learning, and respect for the realities faced on the research and production lines.