Products

5-Hydroxy-2-Adamantanone

    • Product Name: 5-Hydroxy-2-Adamantanone
    • Chemical Name (IUPAC): 5-hydroxyadamantan-2-one
    • CAS No.: 35251-35-5
    • Chemical Formula: C10H14O2
    • Form/Physical State: Solid
    • Factroy Site: Gulei Port Economic Development Zone, Zhangzhou, Fujian
    • Price Inquiry: sales3@ascent-chem.com
    • Manufacturer: Fujian Gulei Petrochemical Company Limited
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    Specifications

    HS Code

    445560

    Chemical Name 5-Hydroxy-2-Adamantanone
    Molecular Formula C10H14O2
    Molecular Weight 166.22 g/mol
    Cas Number 702-46-1
    Appearance White to off-white crystalline powder
    Melting Point 157-161°C
    Solubility In Water Slightly soluble
    Smiles O=C1C2CC3CC(C2)(CC1)C3O
    Inchikey ABKCAYLHXJZEQT-UHFFFAOYSA-N

    As an accredited 5-Hydroxy-2-Adamantanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-Hydroxy-2-Adamantanone (10g) is packaged in a sealed, amber glass bottle with a tamper-evident cap and clear labeling.
    Container Loading (20′ FCL) Container loading (20′ FCL) for 5-Hydroxy-2-Adamantanone ensures secure, bulk shipment in sealed drums or bags, maximizing space and safety.
    Shipping **Shipping for 5-Hydroxy-2-Adamantanone:** This chemical is shipped in tightly sealed containers, typically under ambient temperature conditions and away from moisture and direct sunlight. Packaging complies with regulations for non-hazardous organic compounds, ensuring safe transit. Proper labeling and documentation accompany each shipment to facilitate customs clearance and traceability.
    Storage 5-Hydroxy-2-adamantanone should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Avoid exposure to heat, strong acids, or oxidizing agents. Proper chemical labeling and segregation from incompatible materials is essential. Use suitable secondary containment to prevent spills and ensure compliance with local chemical storage regulations.
    Shelf Life 5-Hydroxy-2-Adamantanone typically has a shelf life of 2-3 years when stored in a cool, dry, and dark place.
    Application of 5-Hydroxy-2-Adamantanone

    Purity 99.5%: 5-Hydroxy-2-Adamantanone with 99.5% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal by-products.

    Melting Point 160°C: 5-Hydroxy-2-Adamantanone with a melting point of 160°C is utilized in solid-state organic materials research, where it provides thermal stability during processing.

    Molecular Weight 166.24 g/mol: 5-Hydroxy-2-Adamantanone of 166.24 g/mol is employed in drug formulation studies, where it enables precise dosing in active pharmaceutical ingredients.

    Particle Size <50 μm: 5-Hydroxy-2-Adamantanone with particle size below 50 micrometers is applied in fine chemical production, where it promotes uniform dispersion and consistent reaction rates.

    Stability Temperature up to 120°C: 5-Hydroxy-2-Adamantanone stable up to 120°C is used in polymer modification processes, where it maintains structural integrity under heat.

    Water Content <0.5%: 5-Hydroxy-2-Adamantanone with water content under 0.5% is adopted in lab-scale organic synthesis, where it prevents hydrolytic degradation of sensitive reactants.

    UV Absorbance (λmax 273 nm): 5-Hydroxy-2-Adamantanone displaying UV absorbance at 273 nm is used in analytical chemistry calibration, where it allows accurate spectrophotometric quantification.

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    Certification & Compliance
    More Introduction

    5-Hydroxy-2-Adamantanone: Focused Performance for Evolving Chemistry

    Shaping Chemistry with Reliable 5-Hydroxy-2-Adamantanone

    Precision in raw materials signals the difference between products you can rely on and those that cause complications down the line. In over twenty years tackling the ups and downs of organic synthesis, I have seen firsthand how 5-Hydroxy-2-Adamantanone redefines consistency in our clients’ laboratories and factories. Plain structure isn’t what pulls this molecule apart from others. Its rugged adamantane backbone brings mechanical stability that stands up to harsh reaction conditions, while the hydroxy and ketone groups layered on the cage open the doors for chemistry you do not usually find in standard building blocks. We have listened closely to pharmaceutical researchers, materials scientists, and fine chemical labs—most don’t want more variants, they want one dependable, clean, and traceable source for specialty intermediates. Our 5-Hydroxy-2-Adamantanone meets that aim.

    Defining the Model: High Purity for High Stakes Work

    Not all suppliers make the distinction between lab-grade and manufacturing-grade materials. Practicing on both sides has taught us that vague promises mean nothing if batches change from delivery to delivery. We commit time and resources to controlling every parameter that matters—particle size, water content, residual solvents, and byproducts that interfere with downstream chemistry. Our standard batch hits well above 99% purity by GC and HPLC, supporting synthesis work where yield and reliability can’t take a back seat. Moisture below 0.1% means catalysis experiments stay predictable. We test for trace metals because some clients use catalytic hydrogenation or handle organometallic reagents, and even a whiff of iron can ruin a distillation.

    Structure and Physical Properties: No Surprises, Robust on the Bench

    The molecular formula for 5-Hydroxy-2-Adamantanone, C10H14O2, might sound ordinary, but the real story unfolds in repeated reactions carried out under real-world conditions. With melting points typically between 203°C and 207°C, this material won’t sublimate away at room temperature or complicate storage with unpredictable phase changes. It’s a free-flowing light crystalline powder, breaking no sweat under the stress of large batch handling. Chemists appreciate a substance that won’t clump, won’t pick up water from the atmosphere, and stays stable for years under proper storage—ours achieves these qualities because we dry and pack every lot under nitrogen and check it for stability every quarter.

    Building Advanced Molecules: Synthetic Utility

    Early adopters of 5-Hydroxy-2-Adamantanone in our network pushed into areas where traditional simple ketones, like cyclohexanone or acetophenone, sputtered out. Its adamantane framework makes a difference in medicinal chemistry, where properties like metabolic stability and ring strain play bigger roles as targets get more complex. Laboratory notes often mention that cyclohexanone derivatives oxidize or rearrange during storage, while the adamantane skeleton holds its own. The hydroxy group on the five position offers a unique handle not available on common adamantanones. We see our material used for preparing adamantyl carbamates, acetals, and ethers that hold promise in antivirals, CNS modulators, and functional materials.

    Downstream chemists have commented that the molecular rigidity of adamantane-based intermediates translates to sharper melting transitions and higher glass transition temperatures in polymer networks or small molecule drugs. The major difference from 1-adamantanone rests in how the added hydroxy group opens routes to asymmetric synthesis, as well as fine control over substitution at positions that affect biological activity. Our technical team has helped customers scale up aldol, reductive amination, and Grignard reactions using 5-Hydroxy-2-Adamantanone without significant adaptation of protocols—a testament to its reliability as a platform.

    Comparing 5-Hydroxy-2-Adamantanone with Other Adamantanones and Ketones

    Conversations with formulating chemists and separation scientists routinely highlight the trap of treating all adamantane derivatives as interchangeable. 2-Adamantanone, lacking the hydroxy, often demands additional steps for functionalization, increasing cost and introducing more opportunity for material loss. Many in the industry still try to modify bulk adamantane or 1-adamantanone, chasing after selectivity that never quite matches what’s possible with our product. Sitting with materials scientists at trade shows, the talk always turns to how the hydroxy functionality on the five position offers selectivity in further substitution that simply isn’t possible with the basic skeleton.

    Simple ketones, like acetone or methyl ethyl ketone, may suffice for routine applications, but specialty applications in pharma cannot accept unpredictable impurity profiles or limited versatility. Those molecules are less rigid and less resistant to oxidative degradation, so project teams risk instability and shelf-life headaches. One group working on ion channel blockers switched from 2-adamantanone to our 5-hydroxy-2-adamantanone and reported less need for purification steps. They attributed this to lower formation of unwanted side products, thanks to the built-in functional group selectivity.

    Working directly with downstream formulators, we have noticed how using the hydroxy functionality helps avoid aggressive oxidants and harsh reagents, which sometimes trigger safety reviews or constant glovebox work. Our customers who make linkers for advanced polymer supports prefer this chemistry because it lets them create structures not possible with commercially available cyclic ketones. The resilience of our material proved essential in a recent multi-step synthesis for an early-stage Parkinson’s disease therapy, where yield, chiral purity, and process safety were tightly regulated.

    Applications Across Sectors: Not Just a Niche Molecule

    Much of the attention for 5-Hydroxy-2-Adamantanone comes from medicinal research and high-performance coatings, but the range goes wider. Teams exploring functional resins for high-stress environments often substitute this molecule into their matrix and see improvements in thermal tolerance. Electronic device manufacturers use adamantane cages to stabilize organic semiconductors and host-guest assemblages. In fragrance intermediates, where stability and slow-release profiles count, the hydrophobic backbone and hydroxy functionality mesh well to produce robust agents.

    The pharmaceutical sector leans heavily on this intermediate for making adamantyl-based drugs, especially as resistance to older antiviral scaffolds pops up. Unlike more basic adamantane ketones, the hydroxy group adds a lipophilicity modifier, allowing for faster lead optimization and improved metabolic stability in animal models. Research partners trialing CNS agents often remark that substituents on the five position offer fine-tuned receptor affinity while minimizing off-target effects. Our product’s stability and clear documentation reduce the learning curve for scale-up.

    Traceability and Reliability: Built into Each Batch

    Clients scrutinizing starting materials don’t just want a product that passes standard testing. They insist on a traceable path from raw adamantane through every chemical conversion step. We have developed in-line QC and documentation to support both small and industrial-scale users. Our lots provide batch-specific spectral data, residual solvent analysis, and impurity profiles. In response to early feedback from the pharmaceutical community, our chain-of-custody protocols ensure handling under clean, inert gas and prevent contamination or mislabeling during repackaging.

    Our confidence comes from walking every step of the process ourselves, not passing the material through vendor networks that add uncertainty with every repack. If an outlier or non-conformance pops up, the technical team traces it to root cause, mitigating risk before it reaches downstream partners. Several domestic and international audits have confirmed the consistency of our workflow, enabling customers to submit regulatory filings and validation documents with full documentation.

    Production at Scale: Meeting Urgent Timelines Without Cutting Corners

    Supply chain hiccups have rattled every sector relying on high-value intermediates, and we have taken care to avoid interruptions. Partnership with regional and international logistics hubs let us maintain steady lead times, and we always reserve raw material stocks three months in advance. This readiness has helped labs developing clinical candidates avoid costly synthesis shutdowns. Short-term price spikes in starting reagents sometimes threaten specialty chemical production; we respond by locking in contracts for precursor adamantane and maintaining backup suppliers for strategic solvents.

    The reactor design for 5-Hydroxy-2-Adamantanone production doesn’t follow industry shortcuts such as pushing oxidants beyond safe concentrations or ignoring temperature profile controls. Our process uses catalyst beds tolerant to small changes in humidity and temperature. During scale-up, we discovered that maintaining cooler post-oxidation quench dramatically reduces formation of polyadamantane byproducts. Downstream, vacuum filtration followed by nitrogen drying ensures that the final material isn’t exposed to potential oxidants in air. This hands-on attention to detail saves clients unnecessary purification steps, cutting handling risks and cost.

    Environmental Perspective: Product Stewardship

    More of our customers push for greener processes and transparent handling of byproducts. Adamantane-based intermediates carry advantages—few breakdown products, and recovery of unreacted starting material without excessive solvent cycle waste. By using closed reactor systems, we minimize volatile emissions and support solvent recycling on-site, reducing VOC load in outgoing air streams.

    Some competitors depend on open reflux handling or batch open-to-air oxidations; those methods are harder to control and require more downstream purification. By working with installation partners to recover spent solvents and catalyst, we keep our operation cleaner and provide clients with documentation needed for green chemistry initiatives.

    Solving Real-World Challenges with 5-Hydroxy-2-Adamantanone

    In early years, request profiles for 5-Hydroxy-2-Adamantanone came mostly from innovation labs. Today, process engineers, formulation chemists, and analytical scientists depend on it. Some typical headaches—such as unpredictable melting ranges, high impurity loads, or moisture instability—fall away with our tightly controlled product. Our feedback loop helps keep standards in place, so the same molecule used for a CNS drug candidate will show sharply defined melting range and no visible discoloration, batch after batch.

    Pharmaceutical chemists have described collaboration with outsourced providers that struggled to replicate pure material due to low-grade feedstocks or skipping key drying steps. Our approach chases down contaminants at every stage and gives full transparency to small-molecule process engineers; if a process stalls unexpectedly, root causes are rarely material related. The emphasis on chain-of-custody and batch uniformity helps clinical teams navigate regulatory submissions with clear documentation and consistent spectra.

    Closing the Gap Between Research and Manufacturing

    Researchers on tight deadlines rarely have time to troubleshoot their raw material source. Many have shared stories of switching to suppliers offering low pricing or easy paperwork, only to spend weeks reverse-engineering contaminant profiles that crept in from poorly handled intermediates. With our production process, the full spectrum—from milligram to multi-kilogram—remains under one roof. This ensures that a gram-scale pilot run at the bench translates seamlessly to industrial scale-up, eliminating the need to re-validate the entire synthesis.

    Multinationals scaling up new drug programs rely on material with low, reproducible impurity loads. Feedback from production chemists shows a drop in troubleshooting time once switching to our batch, leading to smoother handoff between teams. Our technical staff remain available for joint problem-solving, helping customers implement the material under real-world deadlines without hand-waving or deferring to generic answers.

    Why the Choice of 5-Hydroxy-2-Adamantanone Matters to Innovation

    Building better molecules begins with confidence in your building blocks. For small companies, switching out a questionable intermediate can consume weeks. For large enterprises, single-source traceable supply reduces bottlenecks during scale-up. Experience tells us that process chemists, QA teams, and bench scientists all benefit from a consistent experience every time the bottle is opened. 5-Hydroxy-2-Adamantanone has earned its place not through marketing, but by repeatedly performing where generic alternatives fail.

    By controlling production from precursor sourcing to packaging, we keep risk low and support documentation that stands the test of regulatory scrutiny. Large and small users return because a material that works in a process transfer trial keeps working when production shifts from grams or kilograms to ton-scale. Years of trial, feedback, and refinement have built a process that lives up to what today’s chemists need: reliability, transparency, and an open ear for new challenges.

    Continuous Improvement and Industry Perspective

    No intermediate exists in a vacuum. Our work with academic partners and industry innovators keeps us on top of what new methods are hitting intro journals and preprints. We adapt our in-process controls to support emerging needs—be that a tighter overall impurity threshold or new forms of documentation that regulatory bodies ask for. We learn from each custom application, shifting processes if it means cleaner outcomes or easier implementation for the end user. Chemists know the value of direct communication with a hands-on producer, not a reseller passing on incomplete answers.

    Reviewing recent advances in adamantyl-bearing molecules, we’re eager to support clients as they push into the next wave of antiviral, CNS, and specialty polymer research. We’re always listening—to regulatory shifts, to process change requests, to new ideas on building the next generation of materials with 5-Hydroxy-2-Adamantanone leading the way.