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Epiandrosterone

    • Product Name Epiandrosterone
    • Alias 3β-hydroxy-5α-androstan-17-one
    • Einecs 208-256-1
    • 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
    VTB
    Specifications

    HS Code

    883881

    Name Epiandrosterone
    Iupac Name 5α-androstan-3β-ol-17-one
    Molecular Formula C19H30O2
    Molar Mass 290.44 g/mol
    Cas Number 481-29-8
    Appearance White crystalline powder
    Melting Point 176-178 °C
    Solubility Slightly soluble in water
    Synonyms isoandrosterone, 3β-hydroxy-5α-androstan-17-one
    Origin Naturally occurring steroid hormone
    Biological Activity Weak androgenic activity
    Metabolism Metabolite of DHEA and androstanediol
    Usage Research chemical, bodybuilding supplement
    Legal Status Varies by country

    As an accredited Epiandrosterone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle labeled "Epiandrosterone, 25 grams." Features chemical structure, hazard warnings, lot number, and manufacturer's logo in blue text.
    Shipping Epiandrosterone is shipped in compliance with chemical safety regulations, typically in securely sealed, labeled containers to prevent contamination or leakage. Packaging ensures protection from light, moisture, and physical damage. Material Safety Data Sheets (MSDS) accompany each shipment. The process adheres to international and local transport standards for non-hazardous chemicals.
    Storage Epiandrosterone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and direct sunlight. Keep it at room temperature, typically between 2–8°C (36–46°F). Ensure the storage area is secure and access is restricted to authorized personnel. Avoid strong oxidizing agents and incompatible substances.
    Application of Epiandrosterone

    Applications of Epiandrosterone in Industrial Manufacturing

    Epiandrosterone functions as a crucial intermediate and additive within targeted chemical industries due to its androgenic profile and molecular structure. Our production lines supply high-purity material directly to industrial manufacturers for use in quality-controlled downstream processing. This section details essential application areas, with specificity in compliance, usage ratios, process integration points, and types of end products.

    1. Pharmaceutical Steroid Synthesis

    Pharmaceutical companies use Epiandrosterone as a core starting material for synthesizing clinical and veterinary steroidal drugs. Formulation chemists precisely control purity and process conditions according to strict industry regulation, driving demand for high-grade material. It participates in multi-step organic synthesis, serving as a precursor for active ingredients in regulated formulations, including corticosteroids and anabolic products which require certified traceability and batch consistency.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP Guidelines
    • United States Pharmacopeia (USP) monographs
    • Chinese Pharmacopoeia (ChP) applicable sections

    Typical usage ratio

    • Used as 1–10% by mass in initial reaction charge, scalable with target yield and reaction chain length
    • Direct ratio adjustment subject to product purity requirements and downstream derivatization targets

    Downstream process integration

    • Entry at first condensation or hydrogenation step of multi-stage synthesis
    • Intermediate purification after selectivity-limiting reactions
    • Final conversion and crystallization steps before formulation

    Final product types

    • Testosterone and anabolic steroid APIs
    • Corticosteroid pharmaceutical intermediates
    • Steroid-based anti-inflammatory tablets
    • Veterinary reproductive hormonals

    2. Sports Nutrition and Prohormone Preparations

    Epiandrosterone undergoes precise blending and encapsulation within nutraceutical manufacturing environments for the production of sport supplement products aimed at adult populations. Processing teams monitor dosages and excipient integration under FSMA and cGMP controls, using validated filling and inspection systems. Labeling and trace compliance require verified raw material certificates and declared batch origins.

    Industry compliance standards

    • US FDA cGMP for Dietary Supplements (21 CFR 111)
    • Food Safety Modernization Act (FSMA)
    • European Food Safety Authority (EFSA) Novel Foods regulations
    • NSF International Certified for Sport® where applicable

    Typical usage ratio

    • Commonly 25–100 mg per finished serving, not exceeding 2% total capsule weight
    • Adjusted downwards based on regional supplement legislation

    Downstream process integration

    • Blending with flow agents and excipients before granulation
    • Capsule or tablet compression and coating with in-line QC sampling
    • Batch-level traceability locked during final packing

    Final product types

    • Prohormone capsules for bodybuilding nutrition
    • Enhancement tablets for sports markets
    • Pill or softgel SKUs for specialized fitness retailers
    • Bulk supplement powders for contract packagers

    3. Endocrine Research and Analytical Standards

    Laboratory and analytical reagent suppliers demand Epiandrosterone as a standard for hormone profiling, calibration, and validation of clinical or veterinary endocrine assay platforms. High chemical purity ensures trace analytical accuracy. Material batches support immunoassay kits, GC-MS reference standardization, and are documented according to scientific catalog requirements.

    Industry compliance standards

    • ISO 17034 General Requirements for Reference Material Producers
    • ISO/IEC 17025 Testing and Calibration Laboratories
    • OECD Guidelines for the Testing of Chemicals
    • US EPA Analytical Methods relevant to hormone detection

    Typical usage ratio

    • Employed as neat standards or diluted to 1–20 μg/mL within assay protocols
    • Usage rates depend on assay sensitivity and manufacturer kit instruction

    Downstream process integration

    • Stock preparation for calibration curves in diagnostic laboratory processes
    • Working standard blending for LC-MS and GC-MS hormone quantification
    • End-use in immunoassay kit filling and expiration-controlled storage

    Final product types

    • Ready-to-use laboratory reference standards
    • Immunoassay calibration controls
    • Diagnostic kits for hormone analysis
    • Research chemical reference vials

    4. Cosmetic and Personal Care Formulations

    Cosmetic formulators apply Epiandrosterone in hormonal cosmetic lines and specialist anti-aging solutions under close regulatory oversight. Blending occurs at microdosing levels in creams and serums, aligning to international cosmetic regulations for ingredient safety and permitted claims. Stability tests and allergen assessments are carried out at every stage.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • US FDA Voluntary Cosmetic Registration Program (VCRP)
    • ASEAN Cosmetic Directive (ACD) for Southeast Asia
    • Cosmetic Ingredient Review (CIR) safety substantiation

    Typical usage ratio

    • Integrated at 0.01–0.1% of formula mass for cosmetic creams and serums
    • Level determined by product category (face vs. body) and local authority clearance

    Downstream process integration

    • Emulsification phase addition with strict homogenization control
    • Pre-mixing in non-aqueous media for targeted delivery formulations
    • Final fill-line microfiltration and preservative addition

    Final product types

    • Anti-aging serums and lotions
    • Specialist endocrine-based cosmetic creams
    • Dermatological topical preparations
    • Premium skin enhancement products for clinic and retail

    5. Veterinary Pharmaceutical Manufacturing

    Veterinary health product producers introduce Epiandrosterone as a synthetic intermediate or direct additive in reproductive and growth promotion formulations. Process teams ensure batch segregation to avoid cross-contamination, adhering to animal-specific GMP and veterinary drug registration protocols. Purity documentation and identity verification are mandatory at multiple stages to comply with regional regulation.

    Industry compliance standards

    • VICH GL guidelines for veterinary APIs
    • US FDA Center for Veterinary Medicine (CVM) standards
    • EU Regulation (EU) 2019/6 on veterinary medicinal products
    • China Ministry of Agriculture Veterinary Drug GMP

    Typical usage ratio

    • Variable: 0.1–3% in premix, adjusted for species, breed, and weight target
    • Dosing flexibility based on formulation species (cattle, swine, poultry) and end-use authorization

    Downstream process integration

    • Bulk blending stage for premix or injectable concentrate
    • Microbial filtration and in-process QC in solution manufacturing
    • Final batch assembly with tamper-proof veterinary packaging

    Final product types

    • Veterinary reproductive health injectables
    • Animal growth regulation feed additives
    • Oral suspensions for livestock breeding
    • Specialist hormonal therapy products for veterinary practice
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    Certification & Compliance
    More Introduction

    Epiandrosterone: Perspective from the Chemical Bench

    Introduction to Epiandrosterone

    Producing Epiandrosterone in our facility takes us deep into the world of steroid chemistry where details matter at every step. We work with C19H30O2 in its purest, crystalline form. In the lab, we see epiandrosterone as a white, odorless powder, usually packed and shipped by the kilogram to clients who demand consistently high purity. Every batch tells a story about the skill, control, and process discipline needed to meet project needs, whether for research or synthesis in varied applications.

    Understanding Epiandrosterone Properties

    Epiandrosterone stands apart from typical androgens. This 3β-hydroxy-5α-androstan-17-one presents a relatively mild androgenic profile. What feels unique in our production is its stability through standard storage and handling. Melting occurs within a narrow window near 177–181°C, which guides us during purification and analysis. Packing the powder, we notice its texture and flow—the fine details that suggest purity and batch consistency. Each API order starts with a commitment to that repeatability.

    How Epiandrosterone Moves Through Our Process

    In producing Epiandrosterone, we begin with either phytosterols or cholesterol, then move through multistep synthesis under strict control. Non-toxic solvents matter, both for worker safety and end-user trust. We filter, dry, and then verify identity using HPLC, NMR, and sometimes GC-MS when customers require further assurance. We often support partners from the planning phase, discussing whether epiandrosterone, as a weak androgen and metabolic intermediate, provides a better starting point than alternatives like DHEA or androstenedione for their intended research. Each lot is traced and managed to eliminate surprises—unexpected impurities or failings in stability quickly surface with transparent controls and robust documentation.

    Epiandrosterone in Industry and Research

    Colleagues requesting Epiandrosterone most often come from pharmaceutical R&D departments or academic groups probing steroidal pathways. A core reason for choosing epiandrosterone lies in its mild biological activity. Researchers can test hypotheses about androgenic modulation, metabolic cascades, or precursor manipulation without the intense biological impact seen with stronger androgens. This gives room for more precise dose-response relationships and reduced risks for cell culture or animal studies.

    From my time in commercial manufacturing, I see companies drawn to Epiandrosterone because it enables them to explore synthetic conversions with fewer complications. Its chemical backbone often serves as a controlled intermediate for preparing other androgens or specialized analogs. Compared to DHEA, epiandrosterone displays less conversion into estrogenic hormones and only moderate androgenic signaling. It lets formulators and chemists build endpoint molecules for new therapies or analytical standards.

    Specifications That Matter in Production

    We hold every batch of epiandrosterone to a minimum purity of 98%. Experienced analysts rely on validated HPLC methods as our primary confirmation, with strict retesting intervals for shelf-life verification. Microbial and heavy metal screenings follow protocols aligned with international norms for API-grade material. Moisture content never exceeds 0.5%, an important measure to prevent caking and guarantee proper weighing in laboratory scales. We package Epiandrosterone in double-sealed, opaque drums to shield it from light and moisture—a necessity, since long-term exposure, even in warehouse conditions, can influence assay results. Every container carries its unique lot code for traceability.

    Practical Differences from Other Steroids

    In our work, differences between epiandrosterone and related steroids matter. Epiandrosterone comes as a 5α-reduced product, possessing only weak androgenic effects compared to testosterone, which is more potent and can quickly overwhelm experimental systems. DHEA, its upstream metabolic cousin, acts both as a precursor and as a hormone, resulting in a complex interplay when used in biological tests. Androstenedione, another relative, leads more directly to potent androgens or estrogens depending on context. Epiandrosterone, by contrast, offers limited downstream biological conversion in mammalian cells. For this reason, many biologists prefer it in mechanistic assays where refined control over pathway dynamics is needed.

    Our experience shows that Epiandrosterone’s metabolic inertness within short-term studies leads to clearer results. Stronger androgens like methyltestosterone create background responses that clutter up readouts. Epiandrosterone stays more predictable, allowing data that is easier to interpret and less prone to confounding variables in the hands of skilled researchers.

    Broader Role in Chemical Supply and Research

    Many clients ask about epiandrosterone’s regulatory footprint. As a substance with limited direct physiological effects, requirements for licenses are less stringent than those for anabolic agents. This streamlines logistics, cutting down on paperwork and reducing lead times for regular academic and pharmaceutical buyers. But regulations evolve, and every shipping document passes through compliance review before leaving our plant.

    We also field questions from analytical labs on reference standard requests. Epiandrosterone often finds a place as an internal standard or calibration material in steroid panels. Certifying identity and purity becomes a daily task for technical staff, whose records ensure trust in every gram delivered.

    Usage Situations Drawn from Manufacturing Experience

    Staff here talk to university labs using epiandrosterone to explore its role in metabolic mapping or in drug screening for enzyme inhibition studies. Its mild profile allows these projects to step into unknown territory with less risk of severe cytotoxicity or pharmacological disruption. Industrial producers of fine chemicals sometimes order bulk Epiandrosterone as a precursor for further functional group manipulation, moving towards designer androgens or unique intermediates for proprietary synthetic programs.

    Our history with this compound stretches back to projects examining 5α-reductase activity. Providing both Epiandrosterone and its 3α-epimer lets scientists compare pathways directly. The relative ease of separation using modern chromatographic techniques lets us maintain parallel stocks, cutting lead times for research teams targeting comprehensive pathway analysis.

    Insights from Direct Production

    Day after day, our chemists scrutinize feedback from partners to adapt synthesis and purification. We have observed a gradual shift from classic extraction-based procedures to greener, enzyme-catalyzed synthesis routes. These newer methods reduce waste and cut energy demands, improving environmental profiles for bulk shipments. The market still values traditional routes for reliability, but our engineering teams continue pilot-scale trials to push sustainable production.

    Bulk buyers in Asia have requested certifications on origin and method of manufacture. Responsible sourcing and detailed method documentation improve client trust, and in recent years, our facility applied to extend our ISO certifications to cover green chemistry advancements—a step driven by growing demand for low-impact processes. These developments, in part inspired by user requests, continue to shape the way Epiandrosterone moves from concept to product.

    Supporting Better Outcomes

    Questions often arise about stability and shelf life. We store Epiandrosterone under nitrogen where possible. In standard industrial packaging, our shelf-life studies support holding at room temperature for extended periods without significant loss in assay value. Proper handling always surfaces in training: rapid weighing and transfer, capped containers, and operation away from strong light all contribute to product integrity. These seem like minor operational points, but over the years, we have tracked finished batch results and noted that client consistency improves when these basic steps are followed.

    Nothing replaces technical dialogue. Our analysts sometimes walk clients through the impact of trace water or unexpected oxidative factors during downstream processing. Even a few percent deviation in moisture content can throw off scaling in sensitive synthesis steps. This technical exchange, built on years of hands-on experience, keeps feedback loops short and batch results exactly where they should be, even as scale increases tenfold over the life of a project.

    Potential Solutions to Key Issues

    Scaling up always brings a few pain points. Epiandrosterone, despite its chemical stability, presents handling challenges at certain volumes. Early on, we identified that powder compaction can complicate weighing bulk lots. In response, our engineering team adapted packaging to include internal liners treated for static control, reducing product loss and facilitating cleaner transfers. Another technical lesson involved batch moisture: racetracks in the production line led to the installation of a dedicated desiccant-charged airlock for sensitive steps. With feedback from both internal and client teams, fresh ideas have pushed us towards higher output and more reliable batch release every year.

    International shipping created another learning curve. Since Epiandrosterone can intersect with regulatory frameworks in different regions, our team tracks a regularly updated set of logistics documents and legal opinions. What looks like a simple white powder transforms into a compliance project requiring customs review, export licenses, and sometimes notification to local authorities along the shipping route. Our packers work hand in hand with logistics partners to get cleared product to clients without avoidable delay.

    Why Purity and Control Matter

    Some competitors claim near-theoretical purity, but our own NMR and LC-MS checks occasionally flag trace impurities missed by standard HPLC. We believe in aggressive batch release criteria. Staff trained directly by experienced chemists apply spectral and chromatographic analysis to confirm every parameter. No aspect of testing gets overlooked, whether it concerns isomeric purity, residual solvents, or trace metals. New team members learn the ropes through close mentorship, which keeps both product quality and company reputation steady.

    Insights from Customer Feedback

    Every batch release brings honest conversations. Clients involved in downstream modifications often relay results back, especially when unexpected chromatograms or low recovery rates surface. We troubleshoot not only with analytical support, but sometimes with changes to drying cycles or re-crystallization steps during production. Epiandrosterone’s relatively simple molecular structure means that small process tweaks can yield large gains in yield and appearance, improving both lab and production outcomes. Some clients have required bespoke particle size grading; we responded with new sieving steps, adding flexibility without compromising purity.

    Supporting Education and Transparency

    Academic researchers count on transparency—open, technical dialogue on how each gram of Epiandrosterone was produced, tested, and delivered. In our quality review meetings, any recurring themes from user queries get added to our process documentation and distributed as bulletins to our regular buyers. We support lab partners with detailed spectral data, impurity profiles, and advice on storage or solution preparation based on real-world outcomes, not just regulatory minimums. These regular touchpoints add extra trust in each working relationship.

    Looking Ahead: Innovation in Epiandrosterone Production

    Interest in epiandrosterone expands as new applications emerge beyond classic androgen research. Teams in cosmetic development look at it as a bench compound for precursor studies. Analytical labs continue to find novel calibration strategies involving epiandrosterone due to its stability under a range of conditions. We see a responsibility to keep pace. Process innovation, sustainability efforts, and more responsive analytical support improve project satisfaction and batch reproducibility. We tie every improvement to field experience—measurements, data, and conversations that shape the direction of next year’s production goals.

    Final Thoughts from the Manufacturer’s Floor

    Working with epiandrosterone day in and day out has given us a direct sense of what researchers and formulators face. Whether the objective is basic science, product development, or analytic calibration, the margin for error shrinks when every gram entering a reaction or experiment is counted on for predictable performance. We recognize that what leaves our plant isn’t just a chemical; it’s the starting point for new knowledge, better products, or improved testing reliability. Managing every detail—raw material quality, process controls, analytical review, documentation, and logistics—keeps that product ready for whatever challenge the next user brings.