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HS Code |
742781 |
| Product Name | Deuterated Acetone |
| Synonym | Acetone-d6 |
| Chemical Formula | C3D6O |
| Molecular Weight | 64.12 g/mol |
| Cas Number | 666-52-4 |
| Appearance | Colorless liquid |
| Boiling Point | 55.5°C |
| Melting Point | -94.9°C |
| Density | 0.872 g/mL at 25°C |
| Purity | Typically ≥99 atom % D |
| Solubility | Miscible with water |
| Refractive Index | 1.358 (20°C) |
| Odor | Characteristic acetone odor |
As an accredited Deuterated Acetone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Deuterated Acetone is packaged in a 100 mL amber glass bottle, sealed securely, and labeled with safety and chemical information. |
| Shipping | Deuterated Acetone (Acetone-d6) must be shipped as a hazardous material according to international and local regulations. It should be packed in leak-proof, chemically compatible containers, clearly labeled, and cushioned to prevent breakage. Shipments typically require UN certified packaging, Safety Data Sheet (SDS) inclusion, and appropriate labeling for flammable liquids. |
| Storage | Deuterated acetone (acetone-d6) should be stored in tightly sealed containers, preferably glass, to prevent moisture absorption and evaporation. Keep the container in a cool, dry, and well-ventilated area away from sources of ignition and direct sunlight. Clearly label the container and store it separately from incompatible materials such as strong oxidizers. Handle under inert atmosphere if long-term purity is required. |
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Purity 99.9%: Deuterated Acetone with 99.9% purity is used in high-resolution NMR spectroscopy, where it ensures minimal background signal for accurate spectral analysis. Isotopic Enrichment 99.96% D: Deuterated Acetone with 99.96% deuterium enrichment is used in deuterium labeling experiments, where it provides reliable isotopic tracking in reaction mechanisms. Boiling Point 56.2°C: Deuterated Acetone with a boiling point of 56.2°C is used in analytical chromatography, where it permits rapid solvent evaporation for efficient sample preparation. Stability Temperature up to 60°C: Deuterated Acetone stable up to 60°C is used in thermally controlled kinetic studies, where it maintains structural integrity during reaction monitoring. Low Residual Water <0.01%: Deuterated Acetone with residual water content below 0.01% is used in moisture-sensitive syntheses, where it reduces unwanted side reactions caused by water. Molecular Weight 60.11 g/mol: Deuterated Acetone with molecular weight 60.11 g/mol is used in mass spectrometric calibration, where it enables precise mass determination and calibration accuracy. UV Transparency: Deuterated Acetone with excellent UV transparency is used in UV-visible spectroscopy, where it minimizes baseline absorption for more reliable measurements. Low Viscosity: Deuterated Acetone exhibiting low viscosity is used in solvent exchange processes, where it enables efficient sample dissolution and uniform mixing. Freeze Point −94.7°C: Deuterated Acetone with a freeze point of −94.7°C is used in cryogenic NMR applications, where it maintains liquidity at low temperatures for stable sample environments. Volatility: Deuterated Acetone possessing high volatility is used in rapid sample drying protocols, where it accelerates evaporation without leaving residue. |
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Deuterated acetone, often called acetone-d6, brings something different to the laboratory table. Scientists in chemistry and biochemistry circles reach for it when regular acetone just can’t get the job done. This isn’t because of hype or marketing language; it’s because deuterated acetone actually contains heavier hydrogen isotopes, called deuterium, which change the way the molecule behaves in key experiments. I’ve seen researchers smile at the relief deuterated acetone gives during nuclear magnetic resonance (NMR) spectroscopy, an area where those subtle molecular tweaks make all the difference.
Researchers look for solvents that stay “invisible” on the NMR spectrum. Ordinary acetone just won’t do—the sharp hydrogen peaks cover everything else. Deuterated acetone solves that headache because the deuterium atoms barely register in the proton NMR window. The difference may sound minor unless you’ve spent hours chasing clean spectra, but the first time you see a sharp signal without messy background lines, you realize how important the right solvent can be.
Deuterated acetone stands out with its chemical formula (CD3)2CO. In simpler language, it replaces the standard hydrogens with deuterium. The vapor pressure, boiling point, and chemical stability largely match the familiar acetone, which means you don’t wrestle with a new learning curve every time you switch solvents in your routine. The isotopic purity often surpasses 99%, a critical level for those chasing even the faintest signals. Lab techs and graduate students appreciate that kind of reliability when every run matters and budgets stay tight.
I recall countless late nights in the NMR room, running experiments that depended on high-purity solvents. If the solvent carried even a small impurity or didn’t deliver on its isotopic promise, solid data might slip away. With deuterated acetone, samples dissolve cleanly, and unwanted solvent lines rarely show up in the spectra. For anyone trying to tease apart tiny details—such as protein folding, organic reaction intermediates, or drug compound conformation—this level of consistency is more than a luxury.
In NMR spectroscopy, regular solvents muddy the results. Skilled chemists know this gets in the way of seeing important molecular details. Deuterated acetone lets researchers focus on their molecules of interest without battling spectral interference. Its uses extend well beyond single applications. Anyone studying reaction kinetics, isotope effects, or the finer points of organic structure reaches for deuterated solvents at some point. I’ve seen groups working on pharmaceutical development use deuterated acetone to track how drugs interact with biological systems, because ambiguous data slows down progress and raises research costs.
Even those outside the research spotlight—quality control specialists in industrial labs—use deuterated acetone to check product consistency and purity during synthesis. For many, deuterated solvents sound niche, but in practice they bridge knowledge gaps between synthetic chemistry, life sciences, and analytical troubleshooting. With the push for innovation in drug discovery, cleaner environmental detection methods, and refined materials, deuterated acetone remains a staple tool for both experienced chemists and those just starting out.
Many people ask what sets deuterated acetone apart from the common form used in every art classroom and cleaning cupboard. The molecular tweak—swapping deuterium for hydrogen—gives it a heftier atomic signature and naturally raises the price. That might seem like a small change, but in NMR work, it translates to a silent solvent line, letting weak or complex signals emerge from the noise. Some think you can just dilute ordinary acetone, but in practice that rarely works for detailed study; spectral lines stay messy and critical information gets lost.
Another difference shows up in how the solvent interacts in certain experiments. Deuterated acetone isn’t consumed or changed in most chemical reactions, but its “heavy” hydrogen shifts the vibrational energy profile of connected molecules. For anyone tracking isotope effects—say, chemists measuring small shifts in chemical reaction rates—using deuterated acetone makes these changes measurable. Regular acetone can’t deliver the same clarity or reproducibility. In NMR practice, the cost of deuterated acetone is justified by the clear-cut results and fewer wasted sample runs. I’ve worked in groups that tried to pinch pennies with lower-quality solvents, only to lose weeks redoing experiments that standard acetone had muddied.
Choosing deuterated acetone often comes down to balancing budgets with scientific necessity. The higher cost points back to tricky production processes—involving the replacement of hydrogen through careful catalytic reactions and repeated distillations. This isn’t a small-scale craft affair; it’s an industrial effort, which means real world factors like energy use and waste management deserve a moment’s thought. Environmental safety stays front-of-mind in any modern lab. Storage and handling rules for deuterated acetone match those for the normal variant—avoid flames, keep the cap tight, check for fumes—but because labs use less per experiment, the risk profile shifts in manageable ways.
I’ve watched grant budgets stretch with careful solvent planning. Some research groups rotate between deuterated and non-deuterated solvents, tailoring the choice to each project stage. Early screening may use basic solvents, and then detailed structure work calls for deuterated versions. This strategy saves cost without sacrificing clarity where it matters. No tool suits every job, but for detailed NMR work, deuterated acetone proves its worth by reducing chaos and delivering precise results. It’s the “pay a little now, save a lot later” kind of purchase.
Ensuring deuterated acetone meets strict purity standards remains a key issue for buyers and suppliers alike. Unintended impurities—like residual water, trace organic material, or under-deuterated acetone—can wreck spectra or mask delicate signals. In my time working alongside analytical chemists, every shipment earned a quick screen by GC or NMR before hitting the sample prep queue. Lab stewardship isn’t just a formality; a contaminated batch can cost researchers months in lost effort. Reputable suppliers openly share batch certificates, isotopic enrichment percentages, and impurity profiles. This transparency helps scientists verify at a glance that what arrives in the bottle matches what’s required in the protocol.
With growing interest in sustainability, some labs ask about the origin of their deuterated solvents. Production facilities producing deuterium-enriched products rely on a supply chain rooted in heavy water, mainly sourced from energy or isotope separation projects. While not a central environmental concern like some hazardous chemicals, responsible labs stay mindful of procurement impacts and look for suppliers committed to reducing environmental footprints.
Even though deuterated acetone meets high scientific demands, labs often run up against predictable hurdles: cost, supply chain hiccups, and sometimes batch-to-batch variability. Every research manager faces the pressure to do more with less. As a workaround, many teams pool resources, sharing vials between groups, or recycle small amounts by distillation, though cost savings here usually stay modest. Digitizing solvent inventory systems and integrating purchasing with grant oversight help keep bottles available where and when they’re needed. Some universities now train students to use deuterated solvents efficiently—minimizing waste in pursuit of economic and ethical research practices.
A novel solution has been the development of miniaturized NMR equipment, which needs smaller solvent volumes. This not only stretches budgets but lowers long-term waste. Technological advances in NMR—stronger magnets and better signal processing—let scientists run sensitive experiments using less deuterated solvent per test. I remember the learning curve well: younger researchers trained on older machines had to adapt, measuring solvent to the last drop, while new schedules and automation systems helped track precisely who used what and where.
Pharmaceutical companies rely heavily on deuterated acetone during drug discovery. It provides clear protein-ligand binding spectra and helps map intricate biomolecular structures. They lean on its high isotopic purity to avoid regulatory headaches during research, since strong documentation sometimes makes the difference between patent approval and rejection. In the academic sphere, groups studying natural product synthesis or analytical method development turn to deuterated acetone to overcome noise and verify difficult structural assignments. For me, guiding students through critical experiments, the value of seeing a “clean” spectrum—no ambiguity, no do-overs—always outweighs the extra cost.
Though deuterated acetone has carved out its role in NMR, secondary applications surface frequently. Some groups use it as a reaction solvent for isotope labeling studies, where the goal is to trace molecule movement and transformation in living systems. Because it behaves nearly identically to standard acetone but delivers different NMR signals, researchers can run parallel experiments to unravel complex mixtures. This comparative approach continues to open new research fronts in analytical chemistry, forensics, and even environmental sciences.
Cost remains a real barrier for institutions in less wealthy regions or at smaller research sites. While some outreach programs and consortia negotiate better deals, the higher input cost for deuterium and the complex manufacture keep prices firm. Open-access academic partnerships and international collaborations sometimes unlock better pricing through collective bargaining. This breaks down one wall in the global research ecosystem, making frontier science accessible to more people. For those curious, open science initiatives sometimes share standardized spectra in digital libraries, helping labs without direct access to high-purity deuterated acetone gain the calibration and analysis experience, if not the physical solvent.
I remember early days in underfunded labs, where every microliter of deuterated solvent was tracked as closely as gold. Sharing protocols for solvent recovery—even something as simple as sealing unused NMR tubes for later runs—kicked off a culture of stewardship among junior staff and students. People also learned to optimize sample concentrations, run shorter tests, and analyze only what was truly necessary. These small-scale efficiencies do add up, both at the bench and for the institution’s bottom line.
Deuterated acetone carries flammability, volatility, and inhalation risks similar to standard acetone. Because researchers use smaller volumes, and because the price makes wanton use impractical, accidental spills rarely pose large environmental or health hazards in lab settings. Safety teams train newcomers to handle all organic solvents with respect: work in a fume hood, keep bottles sealed, label all aliquots. These basic steps, reinforced by regular lab audits and refresher sessions, protect both people and long-term research output.
Recent shifts toward green chemistry and minimization of solvent usage extend to deuterated varieties. Some organizations explore recycling programs or experiment with solvent-less workflows, especially for preliminary screening steps. As these ideas spread, the hope is for a new equilibrium—high-fidelity results with minimal environmental or health impact.
The story of deuterated acetone continues to evolve. As laboratory instrumentation gets more sophisticated and research questions grow complex, solvents like acetone-d6 stand out for their ability to unravel answers hidden just below the noise. I’ve watched younger colleagues build projects that a decade ago seemed out of reach—all because the tools, including high-quality deuterated solvents, became more available and affordable.
Some companies are pushing for “greener” production methods to reduce both the isotopic and carbon footprint. Newer catalytic processes target lower waste and higher yield from deuterium sources; some exploration even looks at recycling deuterium from byproducts or heavy water in nuclear reactors. These trends keep one eye on the science and another on stewardship.
Even as frontier fields like quantum computing and advanced materials science require new analytical techniques, the humble deuterated acetone bottle remains an everyday workhorse. Many emerging applications—solid-state NMR studies in polymers, high-throughput screening for nano-encapsulation technologies, trace impurity analyses in food chemistry—draw on the same clarity that seasoned researchers first recognized decades ago.
No single product makes or breaks scientific discovery, but deuterated acetone’s legacy comes from delivering reliable results where they matter most. From high school students glimpsing their first NMR spectrum, to senior researchers mapping new drug compounds, access to pure, well-characterized deuterated solvents shortens the road between question and answer. I have seen firsthand how good solvent choices translate into smoother workflows, clearer results, and a culture of quality in science. With steady growth in interdisciplinary research and global collaboration, deuterated acetone stands not as a luxury, but as a trusted tool that keeps advanced science moving forward.
For anyone working at the boundaries of traditional chemistry, opening a bottle of deuterated acetone hints at the kinds of discoveries that careful attention and the right materials can produce. That practical sense of precision, trust, and reliability is what sets this product apart.