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19-Norandrost-5(10)-Ene-3,17-Dione

    • Product Name 19-Norandrost-5(10)-Ene-3,17-Dione
    • Alias 19-Norandrostenedione
    • Einecs 216-245-3
    • 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

    745517

    Iupac Name 19-norandrost-5(10)-ene-3,17-dione
    Molecular Formula C18H24O2
    Molar Mass 272.38 g/mol
    Cas Number 862-89-5
    Pubchem Cid 12530
    Appearance White to off-white crystalline powder
    Melting Point 139-142°C
    Solubility In Water Insoluble
    Density Approx. 1.14 g/cm³
    Synonyms 19-Nor-5(10)-androstene-3,17-dione
    Chemical Class Steroid
    Logp 3.4 (estimated)
    Smiles O=C4CCC1CC2CCC3=CC(=O)CC[C@]3(C)[C@H]2CC1C4

    As an accredited 19-Norandrost-5(10)-Ene-3,17-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass vial containing 5 grams of 19-Norandrost-5(10)-Ene-3,17-Dione; labeled with product name, purity, and safety warnings.
    Shipping The chemical **19-Norandrost-5(10)-Ene-3,17-Dione** is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to standard hazardous material regulations, typically in UN-approved bottles within cushioned, labeled outer cartons. Transport follows all local and international guidelines for safe handling and delivery of research chemicals.
    Storage 19-Norandrost-5(10)-ene-3,17-dione should be stored in a tightly sealed container, away from moisture, direct sunlight, and sources of heat. Keep it in a cool, dry, and well-ventilated area, ideally at controlled room temperature (about 20–25°C). Store separately from incompatible substances and ensure proper labeling to prevent accidental misuse. Use appropriate chemical storage protocols.
    Application of 19-Norandrost-5(10)-Ene-3,17-Dione

    Applications of 19-Norandrost-5(10)-Ene-3,17-Dione in Industrial Manufacturing

    As a direct manufacturer with extensive experience in steroidal intermediate production and purification, we supply 19-Norandrost-5(10)-Ene-3,17-Dione for specialized downstream sectors that rely on stringent process controls, regulatory compliance, and consistent material performance. The following detailed application scenarios summarize real industrial usage, formulation parameters, typical process integration, and relevant finished products in regulated markets.

    1. Pharmaceutical Intermediate for Progestin Synthesis

    This dione serves as a critical intermediate in the pharmaceutical synthesis of several progestin compounds, especially those formulated for oral contraceptives and hormone replacement therapy. Facilities in this sector require precise control over impurity profiles and strict adherence to pharmacopoeial monographs to support the downstream conversion into active pharmaceutical ingredients suitable for regulated medicine manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) for intermediate purity criteria
    • EU Pharmacopoeia standards for 19-nor steroid intermediates
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Used at 1.0–1.3 molar equivalents relative to target progestin synthesis; exact mass calculated by stoichiometric requirements for each API.

    Downstream process integration

    • Introduced during core intermediate block assembly; serves as a precursor for selective reduction and functionalization to yield norethisterone and derivatives.
    • Reacted by hydrogenation and acetylation routes in cGMP pilot plants or commercial API lines.

    Final product types

    • Norethisterone
    • Norgestrel
    • Lynestrenol
    • Standardized API for hormonal pharmaceuticals

    2. Steroidal Intermediate in Veterinary Drug Manufacture

    Inevitably, several veterinary pharmaceutical producers employ this intermediate during the synthesis of steroidal hormone analogues for use in livestock reproductive management. The production lines focus on process traceability and compliance with veterinary drug registration standards in both domestic and export markets to assure hormone integrity and the absence of restricted by-products.

    Industry compliance standards

    • VICH GL24 Good Manufacturing Practice for active veterinary substance production
    • Pharmacopoeia of the People's Republic of China (ChP) for veterinary actives
    • EU Regulation (EC) No 470/2009 for residues in food-producing animals
    • FDA CVM Guidance for Industry #61

    Typical usage ratio

    • Applied at 1.1–1.4 molar equivalents per batch, adjusted according to target molecule and overall reaction yield optimization studies.

    Downstream process integration

    • Fed into steroidal skeleton modification stages prior to side-chain introduction; processed by catalytic hydrogenation, isomerization, and side group esterification in GMP veterinary active plants.

    Final product types

    • Synthetic progestins for veterinary applications
    • Hormonal implants for livestock
    • Oral tablets or feed additives containing veterinary hormone analogues

    3. Building Block in Industrial Steroid Chemistry Research

    Chemical research institutes and dedicated process development laboratories value this material as a starting point for the exploration and optimization of novel steroid scaffolds. Its reactivity profile allows researchers to tailor molecular modifications, leading to patented derivatives or custom intermediates for non-commercial pilot studies and technical evaluations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for R&D laboratories
    • OECD Good Laboratory Practice (GLP) principles for technical development
    • Institutional Chemical Hygiene Plans (CHP) for controlled substance handling

    Typical usage ratio

    • Employed at up to 30% of solid substrate input in test batch syntheses; ratios vary according to target molecular backbone and functionalization scheme.

    Downstream process integration

    • Used as the fundamental substrate introduced at the outset of synthetic routes; typical reactions include oxidation, reduction, halogenation, or ring modification in bench-scale reactors.

    Final product types

    • Small molecule steroid analogues for patent filing
    • Custom research intermediates
    • Analytical standards for process validation

    4. Precursor in Anabolic Steroid Production for Regulated Therapeutics

    This compound is incorporated by licensed pharmaceutical manufacturers to synthesize anabolic steroid APIs indicated for the treatment of specific medical conditions, including muscle wasting disorders. These operations focus on robust documentation for chain of custody and batch traceability, fulfilling regulatory protocols for finished dosage formulation approval.

    Industry compliance standards

    • WHO Good Manufacturing Practice (GMP) for pharmaceutical production
    • USP monographs for anabolic steroid APIs
    • DEA 21 CFR Part 1301 Controlled Substances
    • Pharmacopoeia of Japan (JP) as applicable

    Typical usage ratio

    • Typically loaded at 0.9–1.2 molar equivalents per batch depending on target conversion rate and impurity threshold acceptance limits for final API specification.

    Downstream process integration

    • Enters synthesis during the initial stage as the core norsteroid precursor; undergoes catalytic reduction and subsequent esterification and purification steps prior to formulation as API powder or injectable concentrate.

    Final product types

    • Nandrolone decanoate API
    • Nandrolone phenylpropionate API
    • Bulk anabolic steroid intermediates for further downstream fill/finish
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    Certification & Compliance
    More Introduction

    19-Norandrost-5(10)-Ene-3,17-Dione: Deep Dive into a Crucial Intermediate

    Working day in, day out with complex organic intermediates, our technical crew knows a thing or two about the real nuts and bolts of producing 19-Norandrost-5(10)-Ene-3,17-Dione. This compound has become a mainstay in our plant, recognized by those in the pharmaceutical and synthesis fields for its critical role as a hormone precursor. Over years of refining batches and scaling up tonnage, certain truths about its properties, applications, and key distinctions from related molecules have become clear.

    Getting to Know the Compound

    We usually refer to 19-Norandrost-5(10)-Ene-3,17-Dione by its short name, Norandrostenedione. Its structure features the norandrostene backbone, with ketone functionalities at the 3 and 17 positions. This arrangement gives the molecule a specific reactivity pattern that our chemists have learned to leverage in follow-up reactions or conversion cascades. When comparing Norandrostenedione to its close relatives like Androst-4-ene-3,17-dione or testosterone derivatives, this particular placement of double bonds and functional groups often leads to substantial changes in downstream synthesis behavior.

    The molecule’s physical appearance reflects a lot about its purity. A fine, off-white crystalline powder is standard. Clumping, off-colors, or persistent odor hint at problems in crystallization or contamination. Operators here learn to recognize subtle cues during filtration and drying steps: the way the powder settles says plenty about the success of upstream reactions. Minor shifts in temperature control during hydroxylation or dehydrogenation can show up in final product texture, influencing consistency in later synthesis tasks.

    Consistency, Scale, and Specifications

    We see robust demand for Norandrostenedione with purity upward of 98%, as even minor contamination in intermediates propagates unpredictably in downstream synthesis. Analytical runs—HPLC, FTIR, NMR—verify batch quality. We maintain a tight particle size range to benefit handling. Over years, our QC techs have narrowed in on an efficient filtration and drying protocol to deliver that desired powder, with easy re-dissolution into organic solvents. Particulate uniformity supports predictability for anyone charting long synthesis routes downstream.

    Moisture stays below 0.5%, managed by controlled vacuum drying rather than shortcuts like forced convection. Stability over long storage periods requires careful wrapping, oxygen-excluding packaging, and controlled warehouse conditions. Improper storage, even for a short period, invites degradation; our records show this most commonly impacts color and initial melting point.

    Where Norandrostenedione Matters Most

    Those operating in the pharmaceutical sector recognize Norandrostenedione immediately as a critical building block for steroid hormone synthesis. This non-methylated intermediate allows for precise introduction of further functional groups at key positions, setting the stage for a variety of custom hormones or modified steroids for research and therapy. The pharmaceutical pathway favors Norandrostenedione over 4-androstenedione in some scenarios due to its less reactive double bond system, which provides unique flexibility for specific functionalizations.

    We’ve witnessed increased interest in this molecule among teams specializing in synthesis of less common hormones—especially where estrogenic side activities must be minimized. The compound’s structure permits downstream transformations that steer clear of unwanted aromatization. Many clients working on designer steroids or exploring prohormone alternatives lean toward Norandrostenedione as a starting point for its straightforward adaptability.

    Key Differences: What Separates Norandrostenedione from the Rest?

    Direct comparison with well-known intermediates such as Androstenedione or Dehydroepiandrosterone (DHEA) usually returns to talking about double bond placement and biological reactivity. Androstenedione has a 4-ene structure, while Norandrostenedione features a 5(10)-ene configuration lacking a 19-methyl group. The absence of that methyl changes both chemical reactivity and subsequent enzymatic behavior. Synthesis teams ask for this compound by name when they want to avoid side reactions common with the 4-ene series.

    DHEA finds use in more mainstream applications and dietary supplements, where its presence in the final formulation is actually desired. Norandrostenedione, by contrast, rarely makes it to the shelf on its own. It is a true intermediate, serving as a controlled fork in the steroid synthesis roadmap. We regularly discuss this distinction with R&D customers—choosing Norandrostenedione for multi-step custom hormone syntheses where the parent molecule’s neutral characteristics simplify structure-activity studies or reduce regulatory scrutiny related to anabolics.

    We’ve found Norandrostenedione creates fewer headaches for scale-up thanks to its solubility profile. It dissolves readily in standard polar organic solvents at moderate temperatures, allowing for easy transfer and processing. Some close relatives present problems—forming emulsions, clumping, or requiring repeated solvent exchanges. The saved hours in filtration and fewer loss points help both large and small syntheses run smoother in our experience.

    Safe Handling and Operational Wisdom

    On the plant floor, Norandrostenedione doesn’t present extraordinary risks beyond standard operational care. Our safety teams reinforce correct PPE and handling protocols, but seasoned workers know that dust management is more critical than outright toxicity. The powder’s fine nature can produce airborne concentrations if handled aggressively, so slow tipping and closed containment systems pay dividends in both yield and workplace hygiene. Occasional lessons—usually triggered by a minor dust event—remind all of us why dust collection and air quality controls deserve steady attention during charging and packaging.

    Packing involves double-layered polyethylene liners, followed by rigid containers that resist impact and limit intrusion of atmospheric moisture. Older methods—single bags or non-rigid drums—proved inferior, inviting clumping in high humidity or slow degradation if exposed even a short time. Documentation and barcode tracking ensure material tracing from reactor to drum, simplifying quality complaints and troubleshooting mishaps if they emerge months later in the chain.

    Supplying for Both Routine and Niche Synthesis Needs

    Some customers require only a small lot for research and feasibility runs. Others gear up for routine manufacturing of advanced intermediates or semi-synthetic APIs. Norandrostenedione consistently turns up at the intersection of hormone research, semi-synthesis, and the pursuit of analogues where classic routes from cholesterol or plant sterols run into dead ends, excessive costs, or regulatory waits. By manufacturing at a scale that keeps pricing stable, and maintaining tight control over incoming raw materials and reaction conditions, we help both well-established drug groups and nimble start-ups keep processes predictable and cost-effective.

    One lesson stands out after years in this trade: research teams often iterate quickly, pivoting projects to follow exploratory results. Providing Norandrostenedione from a manufacturer’s capacity, not relying on distant traders or stockists, keeps lead times short and documentation reliable. Rapid support for growing projects brings teams back for subsequent lots, and keeps open the possibility of custom synthesis or adjustments to batch characteristics—such as tighter purity specs or extended post-processing steps.

    Confronting Regulatory and Supply Chain Challenges

    Over the past decade, pathways for controlled intermediates tightened across a range of countries. Spot audits, batch documentation, and full transparency on origin now form standard elements of our shipping and compliance routines. On our end, these measures mean more paperwork and longer record-keeping, yet have proven essential to maintain uninterrupted global supply. It also drives collaboration with reputable logistics providers, as noncompliance can lead to detentions or even outright loss of shipment.

    We’ve fielded increasing queries as regulatory scrutiny around performance-enhancing chemicals picks up globally. Our team responds with certified COA, full batch records, and verifiable chain of custody—both to satisfy authorities and to reassure our downstream partners. By offering this transparency routinely, trust develops, and buyers spend less time verifying what’s actually in the drum or reacting to unwelcome surprises mid-project.

    Environmental and Efficiency Commitment

    As a chemical manufacturer, reducing solvent use, energy consumption, and batch scrap has become more than a talking point. Recent years brought plant investment in more efficient condensing, solvent recovery, and closed-system drying. Our new reactor lines achieve higher conversion per cycle, reducing waste in both feed and finished good. The specific Norandrostenedione process was one of the first in our facility to benefit from vacuum ovens, slashing drying times and minimizing energy footprint. Recovery rates on our process solvents now consistently top 90%—a tangible difference that brings both bottom-line and sustainability gains.

    The plant recycles rinse and wash waters, routing any steroidal residues to a recovery system that concentrates these wastes for secure disposal or managed re-use in non-crucial applications. Given the sensitivity of hormone compounds to environmental release, all effluent receives multi-stage treatment, exceeding local standards on hormone content and organic load. Plant visitors often ask whether these investments pay off. Consistent operational cost reduction and positive inspection results suggest the answer is yes.

    Serving Evolving R&D Needs

    Synthesis teams continue to demand new levels of purity, alternative grades, or even matched batches to explore subtle differences in biological response. We’ve worked with a wide range of researchers to supply Norandrostenedione in quantities from kilos to tons, always with a mind to how a change in impurity profile or a tweak to crystal form might affect their pathway. Collaborations with university groups or early-stage biotechs have led to iterative improvements in both process and knowledge sharing—what begins as a technical run often sparks further dialogue on alternate feedstocks or custom isolation procedures.

    The compound regularly features in exploratory programs on hormone analog development, such as non-aromatizable anabolic candidates or therapeutic targets with altered side effect profiles. The flexible double bond position and lack of 19-methyl group assist in scoping out new biological profiles that diverge from classic anabolic/androgenic pathways. These real-world explorations regularly feed back into our plant as requests for tighter impurity control or options on crystalline morphology, supporting an ecosystem where the manufacturer does more than just deliver the drum. Our technical staff holds regular cross-talks with end-users, sharing both historical wisdom and new observations gathered at scale.

    Building Partnership Through Reliability and Experience

    Buyers and development teams have dozens of choices for hormone intermediates. Through decades refining the Norandrostenedione process, we’ve learned that consistency matters as much as formal specification. Customers lean on our batch-to-batch reproducibility, which hinges upon tight control of raw steroid feedstock, careful handling of oxidizing agents, and strong operator training programs. No amount of paperwork or automation can substitute for well-trained plant crews watching real-time indicators—changes in reaction color, subtle shifts in crystallization, or the smell at the filter cake.

    We invest in keeping those hands-on skills alive, even as upstream automation grows. The possibility of equipment fouling, unexpected color changes, or moisture pickup keeps real-world experience essential to guaranteeing each batch meets strict requirements. End-users value predictability when building multi-step syntheses, and it’s this attention to detail through all stages—from raw material acceptance to final QA release—that earns long-term trust.

    Looking Forward: Responding to Market and Technological Change

    Norandrostenedione sits at an intersection of proven process chemistry and rapid innovation in hormone research. Its role as a platform for next-generation steroid targets means process and regulatory environments must evolve in parallel. We keep a close eye on new analytical methods, automation controls, and feedback from customer labs testing alternative conversions. Occasionally, market volatility around steroid precursors challenges global supply chains. Long-term relationships with reliable raw material partners hedge against sudden shortages or cost spikes, ensuring continuity for our partners. Technical service teams remain accessible to troubleshoot, answer route-specific questions, or join speculative R&D efforts on novel functionalization pathways.

    Recent years have also seen strength in custom synthesis—projects that start with Norandrostenedione as a base but venture into modified esters, ring rearrangements, or field-specific analogues. These efforts draw on both plant-scale manufacturing and fine-tuning at kilo scale, blending reliable execution with a willingness to meet unique technical requests. Not every synthesis project succeeds, yet those that push boundaries lead to the new tools, adjusted processes, or enhanced documentation that improve capabilities for all our partners. The cycle makes the manufacturer an extension of the R&D ecosystem, offering insight, flexibility, and robust documentation rather than just finished goods.

    Final Perspective from the Production Line

    Our daily work with Norandrostenedione testifies to its unique spot among hormone intermediates. Knowing which factors—the right solvent, fine-tuned drying, clean packaging—truly matter turns what could be a commodity into a strategic resource for pharmaceutical and R&D ventures. Standardized batch control underpins fast and flexible response to shifts in technical requirements, project timelines, or regulatory climates. Over years, the drum of Norandrostenedione that leaves our plant carries with it not just a specification, but a legacy of chemical expertise, operational rigor, and ongoing collaboration with those pushing at the edge of hormone synthesis. It’s this grounded, real-world experience that keeps both our process and our partnership valuable to the ever-evolving landscape of modern chemistry.