|
HS Code |
588461 |
| Chemical Name | Malonic Acid |
| Iupac Name | Propanedioic acid |
| Molecular Formula | C3H4O4 |
| Molar Mass | 104.06 g/mol |
| Cas Number | 141-82-2 |
| Appearance | White crystalline solid |
| Melting Point | 135-137 °C |
| Density | 1.619 g/cm³ |
| Solubility In Water | Very soluble |
| Pka1 | 2.83 |
| Pka2 | 5.69 |
| Odor | Odorless |
| Flash Point | None (non-flammable) |
| Ec Number | 205-503-0 |
As an accredited Malonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, tightly sealed plastic bottle with hazard labeling; contains 500 grams of Malonic Acid, chemical grade, for laboratory use only. |
| Shipping | Malonic Acid is shipped in tightly sealed containers made of compatible materials to prevent moisture absorption and contamination. It is classified as a non-hazardous material but should be handled with care. The packaging must comply with local and international regulations, and the product is usually transported at ambient temperature, away from incompatible substances. |
| Storage | Malonic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from moisture, heat, and incompatible substances such as oxidizing agents and strong bases. Protect it from direct sunlight and humidity. It should be clearly labeled and kept away from sources of ignition. Follow all relevant safety guidelines and local regulations for chemical storage. |
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Purity 99%: Malonic Acid 99% Purity is used in pharmaceutical synthesis, where high purity ensures optimal yield and minimal impurities. Melting Point 135°C: Malonic Acid 135°C Melting Point is used in agrochemical manufacturing, where consistent melting behavior supports precise reaction control. Molecular Weight 104.06 g/mol: Malonic Acid 104.06 g/mol is used in polymer industry formulations, where accurate molecular weight enables reproducible polymerization reactions. Particle Size <50 μm: Malonic Acid Particle Size <50 μm is used in fine chemical processing, where small particle size enhances dissolution and reaction rate. Stability Temperature up to 120°C: Malonic Acid Stability up to 120°C is used in cosmetic ingredient development, where thermal stability maintains product quality during processing. Aqueous Solubility 140 g/L: Malonic Acid Aqueous Solubility 140 g/L is used in buffer solution preparation, where high solubility enables effective pH adjustment. Low Volatility: Malonic Acid Low Volatility is used in flavor and fragrance intermediates, where reduced evaporation losses improve process safety and yield. Assay by titration ≥99.5%: Malonic Acid Assay ≥99.5% is used in analytical chemistry applications, where high assay guarantees consistent analytical results. |
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One look at malonic acid, and you might see just another fine, crystalline solid. But dig a little deeper, and you discover a chemical that has quietly supported both researchers and factories for decades. I came across malonic acid during an organic chemistry lab, surrounded by beakers, flasks, and a handful of overconfident students who learned quickly that pure theory falls short the moment you handle real materials. The white crystals didn’t just melt—they shifted our results when we adjusted the smallest things. This hands-on introduction, shared with anyone who has worked with the stuff, reveals what datasheets rarely cover: malonic acid matters because it works, and the results show up day in and day out.
A product’s reputation is built on reliability and transparency. Malonic acid—C3H4O4—stands out for its purity and consistent performance. Most users gravitate toward the technical and reagent grades, both offering more than 99% purity. These forms come in free-flowing powders, with granules fine enough to dissolve smoothly in solvents like water and ethanol. Focused efforts in manufacturing give today’s material a steady, near-neutral pH in solution, low ash content, and almost no heavy metal contamination. This all means you can trust results at the bench, in the classroom, or at scale.
For folks who are detail-oriented, it boils down to measurements that make a difference. Melting points hover around 135 degrees Celsius, solubility in water pushes close to 140 g/L at room temperature, and the product ships with moisture levels well below 0.5%. This is not just trivia; running a reaction where unexpected water content ruins the yield has a way of teaching you the importance of these numbers. My own trial-and-error approach, like those who tried to cut corners, found results much smoother with a batch that held tight to these standards.
Malonic acid finds its way into labs and plants with a sort of understated power. Its main claim to fame, especially among synthetic chemists, is simple: it lays the groundwork for countless reactions. Students spend hours learning about malonic ester synthesis, and for good reason—the flexibility it offers in creating new carbon bonds still drives the field today. The carboxylic groups at both ends open doors to condensed products, used in pharmaceuticals, food additives, and specialty polymers.
Pharmaceutical research leans on malonic acid for building complex ring structures. Several antihypertensive agents, barbiturates, and vitamin B1 analogs trace their origins back to malonic acid’s small but mighty frame. It sits at the start of a long chain of transformations that, with a steady hand and good technique, lead to target molecules that help people in practical, visible ways.
Malonic acid also marks its territory in flavors and fragrances. Some of the tartness and smoothness you recognize in commercial flavor enhancers depend on the clean, sharp acidity that malonic acid provides. I recall a project with food application specialists who leaned on it to tweak a beverage blend, balancing sweetness with just enough acidic punch to call it refreshing. That touch of acidity is not just theory—it shapes real products, shelf to shelf.
Too many buyers thread the maze of acids—succinic, oxalic, acetic—wondering if they can swap one for another. The differences show up quickly once it lands on the workbench. Starting with chemistry, malonic acid’s two carboxyl groups are spaced by just one carbon, giving it a unique combination of reactivity and mildness when compared to its cousins. Succinic acid, sitting next to it on the periodic shelf, carries an extra carbon, stretching the backbone, and changing acidity and solubility in ways that matter for catalysis and synthesis.
Where oxalic acid swings hard as a strong acid and cleaning agent, malonic acid’s moderate touch fits the subtle needs of organic synthesis. It offers the right balance needed for controlling stepwise reactions. This balance can make or break an experiment: in my own hands, swapping malonic for a similar dicarboxylic acid derailed a promising esterification, turning an expected crystal yield into a sticky mess.
Environmental health stands even taller as a distinguishing mark. Malonic acid breaks down easily—no stubborn byproducts or toxicity stacking up in waste streams. Compared to many complex synthetic acids, malonic acid gives producers breathing room when it comes to disposal and compliance, cutting out some of the headaches common to other carbon-based acids.
The flexibility of malonic acid means a single container can support an entire teaching unit and, with scale, support a pilot plant’s trial run. Research and development teams use it in pilot batches of specialty plastics, like those needed for advanced 3D printing resins or next-generation biodegradable polymers. It plays a quiet but crucial part in the quality assurance labs of major manufacturers, acting as a reference standard for calibration thanks to its predictable stoichiometry.
Technical colleges and university labs depend on malonic acid in their curriculum. Undergraduate synthesis labs teach core organic chemistry using real reactions that start with this compound. My own instructors insisted on hands-on learning, knowing that working with solid malonic acid built not only understanding of theory but respect for practical skills—measuring, drying, and dissolving with care. Watching students connect theory to visible, reliable results proved more effective than any textbook.
Companies talk a lot about green chemistry, but execution matters. Malonic acid supports sustainability because its manufacture taps into feedstocks from renewable crops like corn. Modern routes steer away from older methods tied to fossil resources, pivoting to bio-based fermentation. This approach shrinks the carbon footprint and lowers energy intensity. Waste treatment also gets simpler, since malonic acid dilutes to low-impact waste or transforms into CO2 and water through standard biological systems. Not all chemicals can make this claim.
In daily factory practice, workers see fewer safety headaches, and logistics managers face less red tape for shipping and storage. A modest label—“readily biodegradable”—marks a notable shift from dealing with stubborn residues or tough-to-treat effluents typical of other organic acids. This tangibly reduces both compliance costs and environmental risk, answering a growing demand from regulators, customers, and communities.
Pulling from published sources, malonic acid’s advantages draw consistent mention. Technical bulletins describe its steady melting point, strong acidity, and ease of purification. Academic articles highlight its crucial role as an enolate precursor. Global production volume may not match that of bulk acids like citric or tartaric, but the specialized demand holds steady. Several industry surveys underscore its utility in pharma and flavor production, contributing to a market where reliability trumps volume.
Leading chemical databases list negligible toxicity in aquatic tests—often a sticking point for process safety audits. Regulatory reviews from both the EPA and the European Chemicals Agency clear it for broad use, marking it as a substance with low potential for cumulative harm. This echoes what percolates through factories and labs: working with malonic acid lowers back-end costs, reduces risk, and supports tighter environmental stewardship.
Despite its strengths, malonic acid is not a one-size-fits-all solution. Crystalline handling requires a dry, cool environment—humidity quickly turns a bottle of free-flowing powder into a stubborn lump. Storage close to basic or alkaline materials risks unwanted neutralization, cutting into effectiveness and value. Scale-up for industrial batches sometimes faces price pressure, especially as commodity acid prices swing with crop cycles or shifts in feedstock availability.
Every professional dealing with procurement learns the dance between price and performance. A few years back, the spike in corn prices sent ripples through the malonic market, pushing buyers to weigh the merits of alternative acids. Switching away, only to switch back once results dropped, reminded many teams—including mine—that malonic acid earns its place through results, not just cost per kilo.
Addressing practical hurdles starts at the supply chain. Secure, climate-controlled storage preserves product usability—small investments in dehumidification or sealed containers prevent most spoilage. Purchasing managers see value in regular shipments rather than bulk stocking, lowering risk from long-term storage hiccups. I learned, after losing half a drum to caking, that a tighter delivery schedule outpaces big, occasional orders.
Process engineers often suggest pairing malonic acid with precise metering equipment to maintain dosage accuracy. Dosing by hand in small labs works fine, but in larger batch operations, automation improves both safety and reproducibility. Cross-checks with robust moisture and pH testing give early warning signs if material begins to drift.
Many users blend malonic acid with stabilizers during scale-up. Simple calcium or sodium salts often provide easier handling and can expand the acid’s reach to different reactions, where reactivity or solubility shift the equation just enough to match process needs. These tweaks, pioneered by both university teams and industry veterans, reflect deep experience rather than mere theory.
Malonic acid’s journey from lab curiosity to industrial workhorse follows a clear trail—adoption wasn’t forced by marketing but by performance and reliability. This story repeats as scientific understanding grows: materials that work, in real hands and across shifting priorities, earn their place. By sticking to solid chemistry, careful storage, and regular quality assurance, teams can tap into the benefits while sidestepping practical pitfalls.
My own work—running small test syntheses, scaling product trials, troubleshooting flavor formulations—leans on malonic acid’s predictability. Walking through plant floors, watching techs measure out powder for a blend or a batch, brings the significance home: every step, traced back, depends on a raw material trusted to deliver again and again.
Looking forward, as sustainability becomes more than just a buzzword, malonic acid sets an example of merging classic chemistry with modern priorities. Transparent supply lines, bio-based feedstocks, and honest limits—all factor in to keep malonic acid not just relevant but vital. Listening to both lab voices and plant veterans, the message is clear: reliability and real-world results count, no matter what the future brings.