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6-Ketocholestanol

    • Product Name 6-Ketocholestanol
    • Alias 6-Ketocholestane-3β,5α-diol
    • Einecs 212-682-2
    • 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
    VTB
    Specifications

    HS Code

    221210

    Name 6-Ketocholestanol
    Cas Number 3681-86-5
    Molecular Formula C27H46O2
    Molecular Weight 402.65 g/mol
    Appearance White to off-white solid
    Melting Point 161-163°C
    Solubility Insoluble in water, soluble in organic solvents
    Synonyms 5α-Cholestan-6-one-3β-ol
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Iupac Name 5α-cholestan-3β-ol-6-one

    As an accredited 6-Ketocholestanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 6-Ketocholestanol is packaged in a 250 mg amber glass vial with screw cap, labeled for laboratory use and chemical safety.
    Shipping 6-Ketocholestanol is shipped in secure, airtight containers to prevent contamination and degradation. The packaging ensures protection from light and moisture, maintaining product integrity during transit. Shipments comply with regulations for non-hazardous chemicals and include detailed labeling. Standard shipping methods with tracking are used to guarantee safe and timely delivery.
    Storage 6-Ketocholestanol should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated). Use proper personal protective equipment when handling. Store away from incompatible substances such as strong oxidizers and acids. Label containers clearly to avoid confusion and ensure safety during use and storage.
    Application of 6-Ketocholestanol

    Applications of 6-Ketocholestanol in Industrial Manufacturing

    We supply 6-Ketocholestanol to specialized industrial manufacturers who require traceable, stable raw materials for chemical synthesis in high-value, high-compliance downstream markets. The sections below illustrate its established industrial uses across several focused manufacturing contexts, grounded in real-world production workflows and regulatory requirements.

    1. Pharmaceutical Steroid Intermediate Synthesis

    6-Ketocholestanol serves as a cholesterol derivative intermediate for the synthesis of corticosteroid and bile acid drugs in active pharmaceutical ingredient (API) production facilities. Its rigid ring structure and functionalized ketone group enable downstream manufacturers to selectively produce highly pure steroid compounds required in regulated pharmaceuticals, especially for bile acid analogues and selected corticosteroid APIs with specific chiral attributes dictated by international pharmacopoeias and patent-protected synthesis routes.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) monographs on cholestane intermediates
    • US FDA cGMP (21 CFR Parts 210/211) API regulatory standards
    • Japanese Pharmacopoeia (JP) APIs Synthesis quality requirements

    Typical usage ratio

    • 0.8%–6% w/w relative to total batch mass, adjusted based on target API yield, desired purity, and downstream conversion efficiency in multi-step synthetic schemes

    Downstream process integration

    • Batch introduction during the early-stage cyclization and oxidative modification steps, post-extraction and crystallization as a precursor for key chiral core formation

    Final product types

    • Cholic acid and its semi-synthetic analogues for gallstone dissolution
    • Hydrocortisone precursor steroids
    • Bile acid-based pharmaceutical APIs
    • Patent-specific corticosteroid molecules and intermediates

    2. Research-Grade Lipid Membrane Analytical Standards

    In industrial and academic research, 6-Ketocholestanol is utilized for preparing analytical standards and calibration controls in lipidomics and biophysical membrane studies. Analytical chemistry labs and QC departments of biopharmaceutical firms require this sterol for highly specialized assays such as membrane fluidity measurement, protein-lipid interaction assays, and trace-level sterol profiling using NMR and LC-MS/MS. Accurate, certified purity and controlled batch reproducibility are essential for satisfying traceability and data integrity standards in GLP/GMP-regulated laboratory environments.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) principles
    • ISO 17025 accredited analytical lab procedures
    • USP General Chapter <800> for hazardous drug handling
    • QC documentation per FDA 21 CFR Part 58

    Typical usage ratio

    • 5–50 µg/mL in assay buffer or up to 0.2% w/w in reference matrix blends, dependent on the analytical method sensitivity and standard curve requirements

    Downstream process integration

    • Dissolution into organic solvents, followed by direct mixing into model membrane preparations, or as spike-in controls prior to sample extraction and chromatography

    Final product types

    • Lipid standard kits shipped to pharmaceutical QC labs
    • Internal and external QC calibration samples for analytical services providers
    • Research-use-only membrane models for pharmaceutical development
    • Commercial NMR and mass spectrometry calibration solutions

    3. Veterinary Drug Synthesis Focusing on Bile Acid Analogues

    Veterinary pharmaceutical manufacturers integrate 6-Ketocholestanol as a precursor in the semi-synthesis of tailored bile acid derivatives indicated for companion animal and livestock digestive therapies. These processes, subject to veterinary-only API production controls, require strict adherence to feed-additive GMP and specialized purity monitoring, as the end products are destined for animal health use under national and regional veterinary medicine frameworks.

    Industry compliance standards

    • VICH GL8 Good Manufacturing Practice for Veterinary Drugs
    • Regulation (EU) No 2019/6 on veterinary medicinal products
    • US FDA 21 CFR Part 226 (Current Good Manufacturing Practice for Type A Medicated Articles)
    • ISO 9001:2015 Quality Management Systems for feed additive production

    Typical usage ratio

    • 1.2%–8% w/w within bile acid derivative synthesis batches, tuned based on targeted conversion rates and batch yield objectives within semi-synthetic conversion routes

    Downstream process integration

    • Post-extraction, used as a direct input in chemical transformation reactions such as selective oxidation, lactonization, and side chain modifications prior to purification and granulation

    Final product types

    • Veterinary bile acid analogues for canine and bovine digestive applications
    • Feed premix additives containing semi-synthetic cholane derivatives
    • Oral veterinary tablets and boluses
    • Liquid veterinary formulations

    4. Biotechnological Enzyme Substrate Development

    Industrial and contract research organizations apply 6-Ketocholestanol as a selective substrate in enzyme characterization and kinetic screening for biocatalyst development. Downstream users incorporate the material into high-throughput screening workflows for enzymes catalyzing sterol oxidation or functional group modifications, under documented traceability protocols that align with emerging bio-manufacturing standards and ISO-accredited method validation requirements.

    Industry compliance standards

    • ISO 13485 for in vitro diagnostic device raw materials
    • OECD Test Guidelines for biotransformation studies
    • ISO 9001:2015 production and QC systems
    • REACH (EC 1907/2006) for biotechnological solvents and intermediates

    Typical usage ratio

    • 50–250 µM in enzyme assay buffer, or up to 0.5% w/w relative to total substrate mass when scaling up enzyme conversion reactions for product isolation

    Downstream process integration

    • Dispersion into buffered aqueous or biphasic systems as the primary or co-substrate in bioreactor-based enzyme activity profiling, followed by extraction and analysis of conversion products

    Final product types

    • Enzyme substrate kits for industrial biocatalyst contract research
    • Reference substrates for biochemical kinetic assay development
    • Enzyme-screening service deliverables for pharmaceutical and agrochemical clients
    • Semi-preparative-scale bio-transformed sterol derivatives
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    Certification & Compliance
    More Introduction

    Introducing 6-Ketocholestanol: A Practical Perspective from Manufacturing Experience

    Getting to the Heart of 6-Ketocholestanol Production

    Every batch of 6-Ketocholestanol that leaves our facility carries the mark of careful attention to detail and steady technical refinement. Over years in the lab and on the production floor, we have honed synthesis and purification steps to deliver a reliable, high-quality product. This sterol derivative starts its journey as cholesterol, which undergoes selective oxidation to reach the 6-keto stage. The process doesn’t run on autopilot – hands-on monitoring makes a difference at every phase, from picking reagents to controlling temperature and pressure. At the end, we obtain a crystalline powder that chemists and development teams can depend upon, with purity regularly touching 98% by HPLC analysis. Each run confirms that our quality control measures catch impurities early, keeping final product contamination low and reproducibility strong.

    Model, Form, and Typical Specifications

    We focus on a single main variant of 6-Ketocholestanol, distributed as a white to off-white crystalline powder. Target purity remains above 98 percent, meeting the demands of both research labs and development scientists who can’t risk a compromised assay or result. The melting point consistently measures in the neighborhood of 139-142°C, matching published literature values and confirming the right structure. Residual solvent checks meet strict targets, well below ICH guidelines. Moisture content rarely creeps beyond 0.5 percent, and we keep oxidative byproducts in check by storing finished goods under inert atmospheres and cool, dry conditions. All of these measures result from real issues encountered over years: single-degree shifts in melting point often tip off a failed run or an unscheduled interruption in temperature ramps. Samples from the middle and end of every lot go through extensive NMR and mass spectrometry assessments, and we compare spectra batch-to-batch to avoid surprises. Every container is traceable back to its batch, production date, raw material source, and even operator – transparency and accountability help maintain confidence in our process and finished goods.

    Usage – Lessons Sourced from Collaboration and Customer Feedback

    Our customers span multiple fields – cholesterol metabolism research, steroid biochemistry, lipid signaling pathway work, animal feeding studies, and more. In the basics, 6-Ketocholestanol serves as a mimic or metabolic intermediate for tracking cholesterol oxidation, serving as a substrate for nematode and insect sensor studies, and acting as a tool compound for receptor binding experiments. A surprising number of researchers have turned to this material for enzyme characterization; some use it as a standard for 6-oxo derivatives within analytical protocols. We’ve had university groups rely on our material for experimental validation, and industrial partners design it into screening kits and assay reagents. Animal health labs sometimes use 6-Ketocholestanol in dosing studies, observing physiological outcomes and enzymatic pathways activated by ketone-modified sterol derivatives. Every year brings a few new applications – this only emerges with a consistent, dependable compound at the foundation. Production tweaks and protocol changes in our facility nearly always stem from direct customer feedback. One group found downstream solvents left subtle traces that interfered with bioassays; we reformulated our washing system and now issue a cleaner, more biologically compatible end product. Real-world feedback pushes methodological improvements far more effectively than academic debate.

    Comparing 6-Ketocholestanol to Related Compounds

    For the uninitiated, the jump from cholesterol or other oxysterols to 6-Ketocholestanol isn’t just about an extra ketone group. Right at C-6, that carbonyl switch fundamentally changes the molecule’s behavior in cells and model systems. Regular cholestanol and cholesterol themselves might serve basic structural or energetic roles, and their derivatives usually have predictable effects on membrane models and enzymatic reactions. Add the 6-keto group, and binding affinity for enzyme active sites shifts; new metabolic routes open up, and the molecule can serve as a unique probe or block. Oxysterols like 7-Ketocholesterol or 25-Hydroxycholesterol see wide use, but those modifications direct the molecule’s fate down different biological paths. In our experience, 6-Ketocholestanol stands out for its stability during extended storage, limited ease of air oxidation when processed correctly, and unique utility as a substrate for 6β-hydroxylases and related enzyme systems. Where 7-Ketocholesterol tends to autoxidize and break down under light or air, 6-Ketocholestanol behaves more tamely, as long as we keep storage cold and dark. Analytical chemists we supply value this trait when storing reference standards for months between runs. The difference is practical – not just structural on paper but logistical in day-to-day lab life.

    Manufacturing Challenges and Real-World Resolutions

    Getting to high-purity 6-Ketocholestanol isn’t just a rote chemical process. Cholesterol as a starting raw material varies in quality based on its origin. Over time, we realized certain suppliers’ lots brought trace peroxide impurities, which cascaded into side reactions if unchecked. To head this off, we introduced tight incoming QC and set up a parallel peroxide-removal step for volatile starting material lots. In scaling, temperature control requires special attention – an exothermic blip in the oxidation phase can set off a runaway scenario. We installed automated watchdog sensors on our reactors, with hard-wired cutoffs and alarms, after a near-miss during an upscaling trial. One lesson: don’t skimp on old-fashioned operator vigilance, no matter how automated the line looks. Reproducibility, especially between scale-up and pilot runs, also posed challenges. We found the solution in tighter control over crystallization rates, using jacketed cooling vessels and in-line monitoring. Maintaining this vigilance keeps our product consistent across 10-gram and 5-kilogram lots. These process tweaks rarely appear in “ideal” literature syntheses. But the little operational details keep contamination low, yield regular, and the product suitable for demanding lab and industrial needs.

    Storage Stability – More Than a Footnote

    Storage conditions speak volumes in the sterol derivatives world. Fresh material straight off the line rarely causes problems, but leaving 6-Ketocholestanol sealed for months in warm, humid rooms led to visible yellowing and decreased solubility. We share storage guidance with every lot: dry, inert, and low-temperature environments preserve quality. With time, we upgraded packaging as well. Amber glass vials, nitrogen fills, and secondary packaging improved shelf life and actual working consistency years down the line. We track complaints and replaced subpar vials as soon as material changes hands – these lessons feed directly back into packing upgrades. Our best batches, kept under the right conditions, remain analytically indistinguishable from newly synthesized material for well over a year. Field feedback tells us which labs hold fast to these rules and which struggle with air or moisture exposure. In practice, integrity depends as much on downstream handling as anything done in the production hall.

    End-User Preparation and Handling Techniques

    Talking to researchers gives insight into real preparation challenges. Dissolving 6-Ketocholestanol for cell culture or assay work doesn’t always follow textbook guidelines. Some formulations need gentle heating, others benefit from pairing with an organic co-solvent. Early on, customers reported cloudiness and precipitate after routine mixing based on outdated solvent tables. This led us to conduct solubility analysis across a wider range of solvents – methanol, ethanol, DMSO, and propylene glycol each show practical strengths and limits. Sharing this data meant customers cut prep time and improved assay repeatability. Fine-tuning reconstitution protocols pays off in reproducibility and creates fewer callbacks or wasted samples. For high-throughput applications, we recommend aliquotting stock solutions immediately after prepping to limit batch variation as much as possible. The big takeaway: real-world use brings a host of laboratory surprises, and upstream insights shared from manufacturer to end-user make a daily difference.

    Downstream Impacts and Broader Applications

    While classic 6-Ketocholestanol applications lie mostly in academic and pharma research labs, we’ve observed its reputation grow in applied settings. Veterinary investigations use this sterol derivative in metabolic and toxicity studies, modeling how livestock and laboratory animals process oxidized sterols. Food safety scientists run the compound as a marker in packaged dairy and processed foods analysis, tracking levels and degradation during shelf lives. Regulatory labs, too, run standards on incoming and outgoing shipments to confirm ingredient claims. In drug discovery, synthetic chemists use 6-Ketocholestanol as a stepping stone, adding further modifications to probe new biochemical territory. Where other sterols can foul up mass spectrometry or create ambiguous results, our process delivers a cleaner, well-characterized analyte that stands up to scrutiny – an edge for investigators who need results they can trust in audits and formal validation work.

    Health and Environmental Footprint: A Manufacturer's Responsibility

    Producing oxysterols presents unique health and environmental considerations. We handle all process steps in closed containment, protecting not just operators but the local air and groundwater. Exhaust streams run through carbon filters, and spent solvents undergo solvent recovery. Waste is cataloged and shipped for destruction under national hazardous waste guidelines rather than simple landfill. Occasional small spills call for rapid lime or activated carbon cleanup, and protocols ensure all floor-level employees know emergency steps beyond what posters mandate. Water from process lines is analyzed weekly – anything amiss triggers shutdown and engineering review. This diligence isn’t optional, and regulatory inspectors don’t grade on a curve. Years of consistent audits and regular staff training matter more than any single batch out the door. Lessons learned from earlier, less-regulated decades drive a stricter approach now, with future adjustments drawn from ongoing risk assessments and evolving chemical safety literature.

    Cost and Economic Considerations from a Manufacturer's Viewpoint

    6-Ketocholestanol does not qualify as a commodity chemical by any stretch. Cholesterol raw materials can fluctuate in price, especially during disruptions in the animal byproduct supply chain or shifts in global tariffs. Increased demand from biotech sectors sometimes creates squeeze points. Each batch’s labor and infrastructure requirements run high because our processes never scale to the “bulk chemical” realm. Energy demands, especially in controlled low-temperature oxidation, only grow as supply chains face higher utility and regulatory costs. Some competitors chase higher yields through less-pure shortcuts, but we have learned that small savings in synthesis quickly turn into headaches down the line – failed analytical QC, costly recalls, and damaged lab relationships. Instead, our focus remains on maintaining reliable, repeatable output with minimum downtime. These invisible expenses rarely make sales sheets, yet we consider them essential for the long view.

    Tracing Origins: Batch Integrity and Full Transparency

    Customers increasingly request – and rightfully deserve – clarity about their material’s production lineage. Each 6-Ketocholestanol batch, from the initial weighed-out cholesterol to the dated finished product jar, gets logged and reviewed against physical and digital records. Problems trace back through stages with full accountability for materials, instruments, and handling. This level of traceability doesn’t come from a single tracking software but from persistent adherence to documentation best practices. Over time, this practice caught small mislabelings or overlooked equipment issues. Corrections get logged and addressed, never ignored. Our lab staff keep up with regular cross-training, so no process relies solely on one expert. Customer recalls remain low as a result, and quality audits seldom uncover repeat infractions.

    Supporting Ongoing Research – Open Communication and Collaboration

    Supplying 6-Ketocholestanol to researchers is more than just boxing up powder. We take calls, answer emails from students and postdocs, and collect feedback from seasoned scientists pushing into new applications. Candid feedback and sometimes critical questions have motivated more method development in our lab than any competitive pressure. These open lines of communication inform process improvement, unusual solvent compatibility, and even new batch size offerings. Earlier this year, two research teams requested custom purifications in pursuit of slight process improvements; we adapted quickly, returning with options and keeping both researchers in the loop about feasibility and cost. Building strong professional relationships makes innovation possible and builds trust throughout the supply chain. Every production run brings a chance to help others publish, file a patent, or unlock a new scientific direction. Lessons we draw from these exchanges ripple through production, technical documentation, and customer support.

    Future Prospects – Listening and Adjusting in an Evolving Field

    Progress in sterol chemistry rarely follows a straight line. Today’s “niche” compound becomes tomorrow’s mainstay, especially with rising interest in oxidized cholesterol metabolites and the health implications tied to them. As research pushes further into lipid signaling, cytoprotective pathways, and metabolic syndrome modeling, we anticipate more nuanced demands for 6-Ketocholestanol – possibly at new purity grades, tailored particle sizes, or alternative solvent-free forms. Being ready for these demands means keeping lines open with researchers, staying aware of regulatory developments, and staying invested in the stability and traceability of our process. Change rarely comes in a sudden wave; user feedback and real-time problem solving keep each step forward steady. Our commitment is to stick close to our customers, build incrementally on trust, and welcome new knowledge rather than holding fast to old protocols just because they worked yesterday. In sterol manufacturing as elsewhere, real progress comes from listening, learning, and moving forward with care and transparency.