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R-Methyl 3-hydroxybutyrate

    • Product Name R-Methyl 3-hydroxybutyrate
    • 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
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    Specifications

    HS Code

    381976

    Chemical Name R-Methyl 3-hydroxybutyrate
    Cas Number 13893-53-3
    Molecular Formula C5H10O3
    Molecular Weight 118.13 g/mol
    Appearance Colorless liquid
    Boiling Point 66-68°C at 13 mmHg
    Density 1.053 g/cm3 at 25°C
    Optical Rotation [α]D20 +25° (c=1, CHCl3)
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ethanol and dichloromethane
    Smiles C[C@@H](C(=O)OC)CO
    Storage Conditions Store at 2-8°C, keep tightly closed

    As an accredited R-Methyl 3-hydroxybutyrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing R-Methyl 3-hydroxybutyrate is supplied in a 25g amber glass bottle with a secure screw cap and tamper-evident seal.
    Shipping R-Methyl 3-hydroxybutyrate should be shipped in tightly sealed containers, protected from moisture and light. It must be handled according to standard chemical safety regulations, with appropriate labeling and documentation. During transport, it should be kept at controlled room temperature and in compliance with local and international shipping regulations for chemicals.
    Storage R-Methyl 3-hydroxybutyrate should be stored in a cool, dry, and well-ventilated area, away from sources of heat and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong oxidizing agents. Use appropriate chemical storage cabinets, and ensure clearly labeled containers to prevent accidental mixing or misuse.
    Application of R-Methyl 3-hydroxybutyrate

    Purity 99%: R-Methyl 3-hydroxybutyrate with 99% purity is used in pharmaceutical synthesis, where it ensures high yield and selectivity for chiral intermediates.

    Optical Purity >98% ee: R-Methyl 3-hydroxybutyrate with optical purity >98% ee is used in asymmetric catalysis, where it provides excellent enantiomeric excess in final products.

    Molecular Weight 118.13 g/mol: R-Methyl 3-hydroxybutyrate with molecular weight 118.13 g/mol is used in biochemical research, where accurate mass facilitates precise metabolic flux analysis.

    Stability Temperature up to 40°C: R-Methyl 3-hydroxybutyrate stable up to 40°C is used in long-term storage of analytical standards, where it maintains structural integrity over extended periods.

    Boiling Point 164–166°C: R-Methyl 3-hydroxybutyrate with a boiling point of 164–166°C is used in fine chemical manufacturing, where controlled evaporation optimizes solvent recovery and process efficiency.

    Low Moisture Content <0.1%: R-Methyl 3-hydroxybutyrate with low moisture content (<0.1%) is used in peptide coupling reactions, where minimal water content prevents hydrolysis and increases reaction efficiency.

    Density 1.07 g/cm³: R-Methyl 3-hydroxybutyrate with density 1.07 g/cm³ is used in specialty solvent systems, where consistent density improves formulation accuracy and reproducibility.

    GC Assay ≥99.5%: R-Methyl 3-hydroxybutyrate verified by GC assay ≥99.5% is used in enantioselective drug synthesis, where high purity supports regulatory compliance and product safety.

    Melting Point -30°C: R-Methyl 3-hydroxybutyrate with melting point at -30°C is used in cryopreservation formulation, where low freezing point preserves biological activity during storage.

    Residual Solvent <50 ppm: R-Methyl 3-hydroxybutyrate with residual solvent content below 50 ppm is used in food-grade flavor synthesis, where minimal contaminants ensure product safety and flavor purity.

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    Certification & Compliance
    More Introduction

    R-Methyl 3-hydroxybutyrate: Taking a Closer Look at Its Place in Modern Science

    Every so often, a compound quietly changes the possibilities in a field, shifting how scientists, engineers, or medical professionals approach their work. R-Methyl 3-hydroxybutyrate stands among those. While the name might seem technical or distant at first glance, for someone who’s spent hours exploring biochemistry labs, it's immediately familiar as a molecule that’s earned respect by doing more than just fulfilling a chemical need. It plays a key role in studies of metabolism, energy pathways, and chiral chemistry. The fact that this compound shows up in academic journals and high-end research labs around the world signals its real-world value.

    A Compound Built for More Than the Basics

    R-Methyl 3-hydroxybutyrate comes as a clear, colorless liquid, typically with high purity, and is identified by a molecular structure that captures a specific chirality. That technical detail gives it a distinct profile compared to many other methylated hydroxybutyrate compounds. The importance of chirality shouldn’t be understated; a mirror-image version of this molecule just doesn't behave the same way in the body or a reaction vessel. Anyone who's handled both enantiomers in the lab knows it makes a world of difference. This is the type of detail researchers look for in experiments that demand accuracy — not just something that “works,” but something that works in a heightened, precise way.

    In my own experience, handling R-Methyl 3-hydroxybutyrate brought a few challenges at first. Working with it in metabolic flux studies, it became clear that purity made a real difference in outcomes. Small contaminants can throw off the whole result, especially if you're using sensitive detection equipment or running studies where low concentrations trigger biological responses. It was humbling, realizing that even slight deviations in chirality or purity levels could lead to misleading conclusions, so the assurance that you’re getting well-defined R-isomer can really save a lab from costly missteps.

    Why This Compound Matters in Research

    For metabolic research, R-Methyl 3-hydroxybutyrate acts as more than a reagent. It serves as a tool for tracing metabolic processes. In animal studies, researchers have used it for exploring alternate energy sources, particularly in the context of ketone bodies and how the body copes during times of carbohydrate restriction. It’s been at the center of growing discussions about therapeutic ketosis, brain energetics, and the search for ways to support neurological health under stress. Human metabolism is anything but straightforward, and using the right molecule gives clearer answers.

    Beyond biochemistry, there’s a solid interest in how R-Methyl 3-hydroxybutyrate performs in enantioselective synthesis. Specialty pharmaceuticals often require a single chiral form to ensure safety, potency, and reduced side effects. I’ve watched colleagues in organic chemistry focus on this molecule for building blocks where stereochemistry means everything. While the technical details can get deep, the practical message is simple: choosing the right chiral compound at the start streamlines downstream synthesis, avoids waste, and lowers risk of unwanted byproducts. That efficiency trickles down to both budget and time, always in short supply in any lab I’ve worked in.

    What Sets R-Methyl 3-hydroxybutyrate Apart

    Comparing this product to standard methyl 3-hydroxybutyrate or a racemic mixture, a few things immediately stand out. The R-isomer interacts differently in enzymatic processes, aligning more closely with the way natural ketone bodies work inside the body. This makes it more suitable for work that tries to model physiological pathways. In my view, this feature alone justifies its premium and the extra care companies put into making sure customers get the right version. It might sound mundane, but when you’re running sensitive cell models or synthesizing precise pharmaceuticals, these differences can make or break a project.

    Another big difference comes from the market’s push for traceability and consistency. I’ve worked with plenty of generic chemical suppliers, picking up reagents that fluctuated in quality or reliability, and the setbacks pile up—delays in publication, repeated experiments, and wasted resources. R-Methyl 3-hydroxybutyrate suppliers, responding to real-world demand, often back up their product with clear traceability, batch-to-batch consistency, and third-party analytical reports. With rising regulatory scrutiny and the need to comply with international standards, this transparency isn't just bureaucracy—it’s a best practice.

    Technical Focus: Model, Specifications, and Practical Use

    Digging deeper, the most reliable suppliers provide R-Methyl 3-hydroxybutyrate with purity levels often pushing above 98%. The chemical formula and structure confirm its identity, and sellers usually list essential analytical data, like optical rotation and chromatographic purity, right alongside it. It's a level of detail I appreciate on a practical level, since it spares hours of independent verification. Professional environments—be it a university lab or private sector R&D branch—have narrow margins for error, and the assurance that the product lives up to its label pays real dividends.

    The product normally ships in liquid form, packaged in amber glass to safeguard it from light and minimize the chances of breakdown. Storage recommendations keep things practical—refrigeration or cool, dry spaces to keep the molecule stable for longer periods. Anyone who's lost a batch to careless storage learns fast about the importance of following these guidelines.

    On the usage front, researchers most often dissolve it in aqueous or organic solvents, depending on their process. It proves compatible with a variety of downstream applications: metabolic tracing, enzyme studies, pharmaceutical intermediate synthesis, and even specialized nutritional research. Labs working with this compound appreciate consistency in solubility and reactivity, factors that spare researchers headaches and repeated troubleshooting.

    Impact in the Medical and Pharmaceutical Fields

    Many conversations around R-Methyl 3-hydroxybutyrate rightfully center on its role as a research chemical, but its potential stretches into medical innovation. Over the past decade, ketone body analogs and related compounds have found space in clinical trials for neurological disorders and rare metabolic diseases. In practice, using this particular chiral form reflects a careful approach to experimenting with how brains or muscles can adapt to alternate fuels. Cutting-edge projects have asked whether supplementing or increasing levels of this compound (or closely related ones) might provide neuroprotective effects or therapeutic benefit in conditions like epilepsy, Alzheimer’s, or rare mitochondrial diseases.

    As someone who’s spent time reviewing clinical trial registries and talking with clinicians at research hospitals, the skepticism is always present—a new molecule isn’t automatically an answer. But as evidence mounts, the conversation shifts toward careful, stepwise adoption. R-Methyl 3-hydroxybutyrate’s specific action profile, tied to its purity and stereochemistry, gives these studies a cleaner signal. Down the line, that means safer trials, clearer endpoints, and the potential to learn lessons that could eventually move into the pharmacy or even consumer supplement markets.

    Pharmaceutical companies see another benefit: regulatory comfort. With precise documentation and well-defined specifications, submitting an Investigational New Drug application or a patent claim for a new drug based on this compound becomes less of a bureaucratic slog. Precision at the chemical level translates to a smoother regulatory process and more confidence that what’s produced in batches matches what was studied in trials.

    What Needs to Change: Barriers and Solutions

    Moving from pure science to broader adoption brings its own set of hurdles. Not every lab can afford premium compounds, and sometimes that forces workarounds that cut into quality. I’ve witnessed researchers struggle with grants that barely cover basic operating expenses, never mind high-grade, specialty chemicals. Larger organizations and grantmakers should prioritize broader access to such crucial molecules, recognizing that advances in drug development or disease modeling often trace back to what happens in bench science.

    Then there’s the topic of global regulatory harmonization. Variance in chemical standards, documentation, and testing protocols slows everything down. Greater harmonization of acceptance criteria for research chemicals would not only spare duplicated effort but also foster trust in cross-border collaborations. In the case of R-Methyl 3-hydroxybutyrate, seeing shared standards for purity, chiral confirmation, and contaminant reporting ensures that what’s used in a lab in Tokyo means the same as what’s ordered in Paris or Boston.

    The demand for transparency and quality shouldn’t be seen as just another regulatory headache, but as an investment in credibility. Suppliers can support this by making independent analyses easily accessible and by staying open about where and how their products are synthesized. The payoff is more reliable science, smoother collaboration, and shared confidence in results.

    Looking Ahead: Sustainability Considerations

    One thing that comes up in any long-term discussion about specialty chemicals is how the supply chain adapts. Sourcing raw materials for chiral intermediates has a clear environmental footprint. Green chemistry trends push suppliers to develop routes that waste less, avoid problematic solvents, and recycle critical catalysts. The hope is that over time, companies shift more of their production lines to eco-friendlier methods, making it easier for labs to use these products with a clean conscience.

    Customers on the research side can help steer this shift by rewarding suppliers who disclose their process steps and highlight achievements in sustainability. As I’ve seen in the laboratory world, once a few prominent institutions commit to these standards, the rest of the market often follows, raised by a mix of competition and peer pressure. This kind of crowd movement carries real weight—far beyond what individual regulations might achieve.

    Real-World Stories: Applications in Practice

    In neuroscience, teams working on understanding energy metabolism sometimes use R-Methyl 3-hydroxybutyrate as a reference standard or investigational tool. A neurologist described to me how, in studies of head trauma, this compound provided a valuable model for how alternate substrates support brain function after injury. That insight, grounded in basic science, now trickles into medical debates about alternate feeding strategies for critically ill patients. 

    The organic chemistry world prizes control over molecules. I remember a colleague who built a complex molecule—destined for clinical testing—that hinged on an early-stage reaction using R-Methyl 3-hydroxybutyrate. Any misstep in chiral control at that stage, and the team faced weeks or months of tedious downstream purification. The story ended up as a win for both the science and the timeline, because the compound performed as expected and spared them the pain of repeated syntheses. These moments play out all the time—less as headline-grabbing stories and more as the quiet victories that keep research efforts moving forward.

    The Evolving Marketplace

    Transparency and customer service emerged as defining features in the specialty chemical business. In the past, ordering chiral compounds often meant taking a risk on what turned up, but today’s best suppliers commit to quality control and documentation at every stage. I see more companies posting Certificates of Analysis and full chromatographic reports as part of their standard offering, and the result is greater peace of mind for buyers. Those who cut corners get left behind as old stories of failed experiments and inconsistent results fuel the shift toward better practices.

    With the growing importance of specialty chemicals in everything from personalized medicine to advanced materials science, companies that invest in quality and transparency set themselves apart. This isn’t just good for the client; it raises the bar across the industry and contributes to the credibility of published research everywhere the product lands.

    Final Thoughts on Value and Impact

    Looking at R-Methyl 3-hydroxybutyrate from the vantage of someone who’s worked through its quirks and possibilities, it’s clear the compound offers more than technical benefits. It represents the intersection of scientific precision, practical research needs, and the ethical responsibility to produce tools that empower discovery without creating a mess. Its exacting standards reflect a broader cultural shift—toward rigor, transparency, and sustainability in the pursuit of knowledge and better therapeutics.

    Supporting products like this one means supporting a working culture where details matter, shortcuts have consequences, and real progress comes from caring about how every piece fits together. The labs—academic or industrial—that make space for this compound, demand documentation, and integrate its value into research pipelines become the proving grounds for new therapies, smarter diagnostics, and the next wave of molecular innovation. R-Methyl 3-hydroxybutyrate might seem like a niche investment now, but its impact ripples through every serious attempt to explore, explain, and improve the biochemical processes at the core of health and science.