|
HS Code |
580967 |
| CAS_Number | 565-69-5 |
| Molecular_Formula | C7H14O |
| Molecular_Weight | 114.19 g/mol |
| IUPAC_Name | 2,4-Dimethylpentan-3-one |
| Appearance | Colorless liquid |
| Boiling_Point | 117-118 °C |
| Melting_Point | -48 °C |
| Density | 0.801 g/cm³ (20 °C) |
| Flash_Point | 25 °C (closed cup) |
| Solubility_in_Water | Slightly soluble |
| Vapor_Pressure | 30 mmHg (25 °C) |
| Refractive_Index | 1.406 (20 °C) |
| PubChem_CID | 11540 |
As an accredited 2,4-Dimethyl-3-Pentanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 500 mL of 2,4-Dimethyl-3-pentanone, tightly sealed with a screw cap and hazard labeling. |
| Shipping | **Shipping Description for 2,4-Dimethyl-3-Pentanone:** This chemical should be shipped in tightly sealed containers under cool, dry conditions, away from sources of ignition and strong oxidizers. Proper Hazardous Materials labeling is required. Ensure compliance with local, national, and international shipping regulations for flammable liquids. Wear appropriate personal protective equipment during handling and transport. |
| Storage | 2,4-Dimethyl-3-pentanone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of heat, sparks, or open flames. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature and protect from direct sunlight. Ensure appropriate labeling and follow all relevant chemical storage regulations and guidelines. |
Applications of 2,4-Dimethyl-3-Pentanone in Industrial Manufacturing2,4-Dimethyl-3-pentanone serves as a key intermediate in multiple industrial sectors by supporting specialized downstream production processes. As an experienced manufacturer, we ensure consistent product quality and reliable delivery to meet the rigorous requirements of global partners in regulated environments. Our technical team assists customers with compliance, formulation tuning, and process optimization for real-world applications described below. 1. Agrochemical Intermediate for Herbicide SynthesisLeading agrochemical manufacturers use 2,4-dimethyl-3-pentanone to synthesize specific branched-chain herbicides, especially those relying on ketone intermediates for ring formation during active ingredient construction. Production facilities require traceable quality, precise dosing control, and prequalified raw material batches to maintain efficacy and regulatory approval in final pesticide formulations. Industry compliance standards
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2. Pharmaceutical Intermediate for Local Anesthetic ManufactureThe pharmaceutical industry employs this ketone in the synthesis of intermediate structures during the multi-step production of select local anesthetics. Integration follows strict GMP and pharmacopoeial documentation including full traceability, impurity tracking, and comprehensive batch validation. Downstream operations validate each raw batch to comply with regulated active pharmaceutical ingredient (API) workflow demands. Industry compliance standards
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3. Fragrance Ingredient Precursor for Fine Aroma ChemicalsFragrance compound producers utilize this ketone as a building block for high-purity aroma ingredients through aldol condensation and subsequent hydrogenation pathways. Strict batch characterization and impurity control enable its use in fragrance bases requiring consistent olfactory profiles for downstream blending into premium consumer perfumery and hygiene products. Industry compliance standards
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4. Solvent and Extraction Agent in Laboratory and Fine Chemical ProcessingLaboratories and fine chemical plants select 2,4-dimethyl-3-pentanone for its solvent properties and selective extraction capability in specific chromatographic and crystallization workflows. The material enables purification of mixtures where high selectivity and low water miscibility are critical, supporting both R&D and scaled-up pilot plant separation units. Industry compliance standards
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5. Catalyst and Additive Carrier in Polymer ModificationPolymer modification facilities incorporate this ketone as either a reactive carrier for catalysts or a chain-terminating additive in polymer blending and specialty resin synthesis for automotive and electronics applications. The raw material’s controlled volatility ensures precise dosing during reactive extrusion and in-situ catalyst delivery steps. Industry compliance standards
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Every year, we see a steady interest in mid-chain ketones, and 2,4-Dimethyl-3-pentanone continues to carry its weight in niche but essential roles. Producing this compound starts with carefully selected raw materials, controlling each batch from reaction to distillation — no shortcuts. The end result offers purity and consistency that chemists and downstream users rely upon. At the core, this isn’t just another aliphatic ketone. The methyl groups in the 2 and 4 positions give the molecule unique features, affecting not just reactivity but physical performance in real-world applications.
We supply the 2,4-Dimethyl-3-pentanone in a standard technical grade with a typical purity above 98%. For specialty projects that are more demanding, we monitor by GC and can push for higher purity upon early request. Our customers buy it because the molecule isn’t just a commodity— it’s an enabler. When users come to us with demands for specific assay ranges, we don’t run off a spec sheet; we run batches that meet realistic laboratory and industrial settings. This comes from direct experience: if a ketone doesn’t measure up, downstream operations grind to a halt, affecting coatings performance or causing headaches during org syn workups.
Handling 2,4-Dimethyl-3-pentanone doesn’t throw surprises — if you’ve spent time with low-molecular-weight ketones before, the drill feels familiar. You’ll notice it has a distinct, sweet acetone-like odor, but slightly more robust than your standard methyl ethyl ketone. Experienced hands run processes under extraction, maintain tight container closure, and focus on static dissipation in volatile atmospheres. The boiling point lands near 120°C. Such properties reward a production team that knows how to minimize evaporative losses and avoid product decomposition.
This molecule rarely appears on the glossy covers of industry trade magazines, but over the years, its value speaks for itself. The main uses revolve around organic synthesis. Skilled chemists pick it as a building block for specialty intermediates: fragrances, pharmaceutical synthons, and various fine chemicals. Folks in research appreciate its moderate polarity and compact structure, which foster selectivity in condensation and alkylation reactions. Paint and coatings formulators know it as a solvent with strong dissolving power, lower tendency to leave reside, and a manageable evaporation profile. Other ketones like 2-pentanone or 2,4-dimethyl-2-pentanone may serve in similar slots, but subtle reactivity differences shift process design and outcomes. Choosing 2,4-dimethyl-3-pentanone means opting for a balance of boiling range, miscibility, and lower steric hindrance.
One aspect that often comes up: downstream safety and compatibility. In projects with strict residue limits or cosmetic intermediates, the absence of certain side impurities makes a difference. Our in-house labs do more than tick boxes — we continually run spectrum and chromatography checks because we’ve witnessed how small trace contaminations turn into big headaches in multi-step synthesis. Customers in API-related sectors keep coming back for this reason; they need confidence, not just a COA.
Comparisons get more interesting when you go beyond surface similarities. On paper, a string of aliphatic ketones looks interchangeable, but time and again, customers share that little tweaks in molecular structure lead to big differences in use. For instance, 2-pentanone, while close in molecular weight, flashes off much more quickly, requiring different venting protocols and limiting its use for slower-drying coatings. In contrast, 2,4-Dimethyl-3-pentanone’s higher boiling point and increased hydrophobicity keep formulations stable under heat, making it fit where others fail.
Compared to 2,4-dimethyl-2-pentanone, the 3-pentanone isomer shows a different reactivity; it’s less hindered and often exhibits cleaner conversions when used as a precursor in Grignard additions or oxime production. Years of running head-to-head pilot trials taught us that switching between isomers isn’t just a matter of adjusting reaction temperature; entire work-up routines may need redesigning.
Value shows up in the end-use results. We’ve seen customers who switched to 2,4-dimethyl-3-pentanone for polymer research cite not just improved solubility of monomers, but also easier product isolation. Paint labs have reported that it provides more controlled drying curves without tacky residue on specialty surfaces. Researchers also value the comparatively mild volatility in bench settings, especially if scale-up runs last longer than anticipated.
Staying ahead in the chemical industry demands more than sticking to a recipe. The real-world challenge often roots itself in keeping impurities in check. In our plant, minor system leaks or unnoted distillation tails from unrelated processes can introduce byproducts that, at parts-per-million levels, throw off a sensitive synthesis. That’s why we commit to ongoing in-process monitoring; trusting a final check alone isn’t good enough. Our operators constantly measure and record distillation fractions, cross-checking against reference standards, so that downstream users get what their protocols expect, not just what the paperwork promises.
Transportation comes with its own set of concerns. 2,4-Dimethyl-3-pentanone isn’t classified as particularly hazardous, but vapor build-up in transport tanks, especially during hot months, requires us to retrofit vented closures and liner upgrades. Neglecting these details can lead to product losses, or in rare cases, unsafe handling at the customer’s site. Insisting on batch traceability isn’t just regulatory — it’s what allows quick troubleshooting if an anomaly pops up two months down the line.
Over the years, long-term customers taught us that trust gets built on handling the details others might treat as an afterthought. We don’t ask users to chase down fine print — our technical team stays ready to discuss the process, the analytical data, or peculiarities about reagent interactions. Each customer application presents its own set of variables: some want high-purity for a plant-scale intermediate, others just need robust, reliable solvent for an ongoing series of coatings batches. We can adjust collection intervals or perform extra QA rounds at customer request. We keep batch records open, because transparency is part of producing chemicals that end up in critical workflows or high-value final applications.
Having produced thousands of kilos over the years, we know that little details change the outcome. For instance, this ketone’s specific gravity and moderate viscosity make it easier to handle in pneumatic filling systems. Operators prefer it in re-circulating loop setups, where its low tendency to gum or polymerize even after several days of storage at ambient temperatures reduces unplanned maintenance. Controlling headspace pressure, especially in semi-bulk drums, also means losses stay minimal — an important consideration for sites without on-site purification.
Downstream labs appreciate tight control over side impurities. That’s not just a QC concern — it impacts overall reaction times, yield, and sometimes even regulatory filing, when users submit documentation on residual solvents. For those in R&D, a predictable boiling profile helps avoid issues with unplanned azeotrope formation or contamination of distillation columns used for multiple solvent runs.
Direct feedback loops between our technical teams and field users shape ongoing improvements. In synthetic work-ups where 2,4-dimethyl-3-pentanone acts as the main solvent or reagent, researchers appreciate the low tendency for peroxide formation compared to some other mid-weight ketones. This small safety margin becomes vital when working in facilities with limited peroxide controls.
Our coatings and lacquer clients notice fewer issues with gloss retention in their finished products compared to similar ketones. One technician reported that a problematic streaking issue vanished after switching, tracing the improvement down to the slightly slower evaporation rate and narrower volatility window.
R&D teams working in custom synthesis highlighted improved purity of acid chlorides when using freshly supplied 2,4-dimethyl-3-pentanone instead of mass-batch alternatives. The reaction profiles tracked more closely to literature, saving time otherwise spent troubleshooting side-reactions.
We’ve witnessed the issues that pop up when buyers chase the cheapest offer. Aging or poorly stored stock can smell off, and small amounts of moisture or stabilizer residues often get overlooked by middlemen. Chemists running delicate reactions pick up on these inconsistencies right away — performance drops, repeated filtrations, and more time wasted clarifying the source of a bottleneck. When you source direct, you’re not left questioning how many times a drum has been repackaged, or whether the “production batch” listed on a label means last month or last year.
Investing in direct relationships means more efficient troubleshooting if unexpected results show up on a test run. Our technical staff don’t just recite catalog numbers. We dive into the process, pull archived analytical data, and help users establish whether an off-spec reaction owes to product, process, or unanticipated contaminants from elsewhere in their workflow.
Whether formulating an ink requiring a defined evaporation rate or synthesizing novel intermediates, users count on consistent performance batch over batch. We stay flexible, knowing that new projects sometimes push boundaries and demand tighter parameter ranges than generic industry norms. Our on-site analytics, deep inventory tracking, and willingness to adjust process steps based on open customer feedback underpin this reliability.
We remain ready to engage, answer questions, and troubleshoot, not only during major projects but also for experimental inquiries and one-off challenges in the customers’ hands. The most successful applications often stem from open dialogue, where a problem is caught and solved at the root, not papered over with vague assurances.
Expectations in the specialty ketone market continue to evolve. Some users increasingly demand documentation about raw material sources, or seek assurances that secondary feedstocks do not bring in problematic trace metals or halides. We’ve invested in improved raw material qualification and in tracking each incoming batch through our ERP systems, because we’ve seen even small upstream changes cascade into substantial production adjustments.
With greater scrutiny from downstream regulators, especially in the pharma and food additive spaces, documentation on batch histories, reprocessing events, and handling practices matters now more than ever. Buyers want evidence, not generalities, about procedures on minimizing contamination, handling cross-contact, and retention policies for retained samples. We keep these files open for technical review, audit, and compliance filing.
Years in this field demonstrate that every molecule brings its own quirks, and 2,4-Dimethyl-3-pentanone is no exception. Supplying this product means more than moving containers from one site to another. It’s about understanding application context, providing flexibility, and backing claims with real-world data. Our commitment remains steady: direct, evidence-based communication and persistent attention to the operational realities that end-users face.
If your team is ready for deeper technical dialogue, needs batch-specific performance data, or wants to troubleshoot a lab bottleneck, reach out to us. We believe good chemistry starts with good conversation backed by years of hands-on experience.