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HS Code |
843572 |
| Chemical Name | Tert-Butyl Ethyl Malonate |
| Cas Number | 867-13-0 |
| Molecular Formula | C9H16O4 |
| Molecular Weight | 188.22 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 78-80°C at 10 mmHg |
| Density | 1.03 g/cm3 at 20°C |
| Refractive Index | 1.4166 to 1.4186 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Flash Point | 82°C (179.6°F) |
| Smiles | CCOC(=O)CC(=O)OC(C)(C)C |
As an accredited Tert-Butyl Ethyl Malonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 250 g bottle of Tert-Butyl Ethyl Malonate is securely sealed in an amber glass container with a tamper-evident cap. |
| Shipping | Tert-Butyl Ethyl Malonate should be shipped in tightly sealed containers, protected from moisture and sources of ignition. Transport under ambient temperature, avoiding extreme heat. Ensure compliance with all local, national, and international regulations for chemical transport. Proper labeling and documentation are required. Handle with appropriate personal protective equipment during handling and transit. |
| Storage | Tert-Butyl Ethyl Malonate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure proper labeling and keep chemical storage areas secure to prevent unauthorized access. Follow standard laboratory safety protocols when handling. |
Applications of Tert-Butyl Ethyl Malonate in Industrial ManufacturingAs a manufacturer with direct experience supplying tert-butyl ethyl malonate, we focus on established downstream segments that depend on this compound for advanced molecular construction and controlled reactivity in specialty chemicals. Across pharmaceutical, agrochemical, materials, and flavors industries, its role as a C3 building block and protected diester intermediate secures predictable outcomes in targeted synthesis steps. Our applications support process engineers and product formulators who require both regulatory assurance and reproducibility. 1. Pharmaceutical Intermediates for Active Ingredient SynthesisIn pharmaceutical manufacturing, our product functions as a core alkylating agent and malonate synthon for early-stage active ingredient development, especially in β-ketoester pathways and diester modifications for prodrug strategies. Its steric bulk and ethyl/t-butyl protecting groups enable precisely timed deprotection in stepwise routes, with direct integration into nucleophilic substitution or condensation reactions under inert atmospheres. Controlled addition supports scale-up of unique intermediates for central nervous system and cardiovascular drugs, while batch record traceability aligns with multi-site GMP demands. Industry compliance standards
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2. Agrochemical Synthesis—Pyrazole and Triazole PrecursorsAgrochemical producers utilize this diester in constructing pyrazole and triazole skeletons, pivotal in crop protection actives such as herbicides, fungicides, and insecticides. Its structure enables consecutive alkylation and cyclization under controlled temperature and pressure, supporting process flexibility for divergent intermediate manufacture. Reactivity tuning via t-butyl deprotection ensures residue limits remain within regulatory thresholds crucial for agroenvironmental compliance and raw material traceability in global supply chains. Industry compliance standards
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3. Synthesis of Advanced Specialty Monomers for PolymersIn the specialty polymer sector, chemical plants leverage the t-butyl and ethyl functionalities of this compound to introduce tailored branching and crosslinking sites in high-performance acrylics and copolymers. Its malonate core offers hydrolytic lability for subsequent crosslinker generation, while controlling chain propagation and preventing premature gelation. Batch-to-batch purity control reaches critical importance in resin synthesis where mechanical performance and heat resistance specifications are contractually defined for advanced coatings and adhesives. Industry compliance standards
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4. Flavors and Fragrance Intermediate—Ester SynthesisFlavor and fragrance compound producers select this malonate derivative as a key ester precursor in fruit, sweet, and complex aroma development. Its reactivity provides avenues to synthesize protected or branched esters under mild conditions. Regulatory compliance with purity, trace solvent removal, and flavor safety is strictly enforced, especially when producing intermediates destined for direct food contact or human consumption under global food safety statutes. Quality assurance extends from raw material consent to batch GNCP documentation. Industry compliance standards
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Work in the laboratory gives a close-up view of what reliable intermediates mean for researchers. Tert-Butyl Ethyl Malonate is not just another malonic ester. Years of hands-on synthesis, batch consistency optimization, and collaborative feedback from process chemists have shaped our approach to delivering this compound. As primary manufacturers, we oversee every step — from sourcing raw diethyl malonate to the final purification. Every time we scale a batch, evidence of attention to detail shows up in the purity, color, and stability; deviations rarely happen, but even small anomalies lead to immediate re-examination of our process. Decisions in the plant aren’t abstract: they are based on experiences gained from years of filling orders for precision-demanding pharmaceutical and fine chemical applications.
Tert-Butyl Ethyl Malonate carries the molecular formula C9H16O4 and a CAS number widely referenced by procurement specialists. Its structure features a tert-butyl group substituting one ester function. Over successive pilot runs, our analytical teams worked to pin down key markers — reducing traces of diethyl malonate residuals, controlling tert-butyl alcohol carryover, and hitting an assay target above 99%. Each new lot gets a unique internal reference code, but we release under standardized parameters set by both client feedback and our regulatory updates.
We specify Tert-Butyl Ethyl Malonate by purity, water content, and color (as judged visually and by spectral baseline). It consistently shows a clear, pale liquid form. High-Performance Liquid Chromatography remains our daily checkpoint: results from years of practice show less than 0.5% total impurities, with batch-to-batch reproducibility monitored down to 5-10 ppm for critical contaminants. Regular feedback from medicinal chemistry teams tells us trace impure compounds in this malonate can disrupt clean reactions. This pushes us to keep side products low — and, when necessary, run an extra fractional distillation. Every batch shipped out sees a rapid GC-MS scan to screen for unexpected peaks. Our hands-on approach drives us to validate each shipment internally, not just to meet a loosely defined COA.
Chemists ask for Tert-Butyl Ethyl Malonate because of its predictable behavior in carbon–carbon bond formation. Over the last decade, our own development staff have used it for alkylation, Michael addition, and condensation reactions. The tert-butyl substituent gives certain advantages over the symmetric diethyl malonate — a more selective reactivity, better control in stepwise syntheses, and simplified deprotection. After routine scale-ups targeting active pharmaceutical ingredients (APIs) and specialty esters, practical feedback rolled in: this malonate handles well under standard lab conditions, and residues clean up with straightforward workups.
We see Tert-Butyl Ethyl Malonate mainly used for preparing α-substituted malonic esters and as a masked dicarbonyl building block. When working with partners in agrochemical research, we notice the preferred role of tert-butyl for smooth removal under gentle acid. Over the years, in-house teams report strong yields when using it for selective monoalkylation — less tendency to dialkylate compared to simple diesters. The tert-butyl protection actually offers a route to asymmetric syntheses, which gives process chemists a flexibility edge during scale-up campaigns.
One repeated customer observation involves the minimized number of protection or deprotection steps required — less solvent, fewer unit operations. Tert-Butyl Ethyl Malonate can let users advance targets without needing harsh base or elevated temperature, which directly impacts cost and throughput. This isn’t based on speculation: it stems from monitoring project outcomes, batch closeouts, and actual campaign retrospectives where raw material choice made or broke the planned schedule.
Long-term users often ask why prefer the tert-butyl ethyl species. It comes down to selectivity and versatility. The diethyl and dimethyl malonates remain familiar, but the tert-butyl group makes all the difference for downstream synthetic utility. This group cleaves more cleanly under acidic conditions; the need for harsh hydrolyses drops away, which means sensitive functional groups or chiral centers survive the process. Up in process development, when reaction reliability matters most, we never underestimate the ease of removing tert-butyl over methyl or ethyl esters. Fewer side reactions and lower levels of volatile byproducts enter the workup stream, so purity climbs with less post-processing.
On a practical level, solvent compatibility and volatility behavior make tert-butyl ethyl derivatives safer and easier to handle — our solvents team measured vapor pressure and observed that the compound doesn’t volatilize out as rapidly at ambient as the dimethyl variant. Chemical engineers overseeing pilot reactors highlight this difference, given the tighter temperature control and less loss to vent during distillation. In the plant, less evaporation means improved material balance and reduced odor complaints.
Direct production brings accountability. Starting from raw diesters, our process runs through base-catalyzed transesterification with tert-butyl alcohol. The challenge: suppress unwanted self-condensation and securely vent the evolved ethanol. We scale the operation batch-wise, adjusting timing by onsite GC snapshot testing. Any trace water left in the system gets vacuumed out in our finishing tanks, as we found even minor moisture spikes can promote hydrolysis down the line.
Testing each lot includes more than a glance at the analytics slip. Full IR confirmation, detailed HPLC reports overlaid with internal reference standards, and cross-checks against archived “gold standard” runs (withdrawn from lots that performed especially well in customer campaigns). Our confidence isn’t built on assumption but on experience troubleshooting issues for pharmaceutical companies needing precise enolate chemistry. We trace anomalies — even a slight drift in boiling point or a faint yellow tint — back to their origin. Interventions happened: sometimes a column repacking, sometimes tweaking distillation rate, sometimes investigating new grades of starting materials. Every adjustment comes from actual observed issues, not protocol dogma.
Our R&D partners send us feedback from medicinal, crop protection, and specialty chemical programs every season. They report the benefits of using a malonate that’s less prone to hydrolysis and easier to recover in workup, especially in programs where functional group compatibility is at a premium. Every note on yield, product color, and isolated purity when using our Tert-Butyl Ethyl Malonate translates to plant-level process refinements here.
Few customers notice the labor behind hitting consistent color and clarity, but it matters. Residual color often hints at low-level byproducts — and years of joint troubleshooting proved that such byproducts sometimes carry downstream and complicate crystallization or distillation. Our process team built extra clarification steps to deal with these real results. We’ve seen improvement in reaction outcomes and consistently cleaner spectra just from this attention to detail. These are changes born out of practical necessity, not broad marketing claims.
Every kilogram shipped comes from our site, tracked from raw incoming malonate through to the drum that leaves our loading dock. Regulatory compliance is never left to chance: we keep internal and external audits rigorous, using traceability and reporting standards recommended by industry associations and major pharmaceutical audit teams. All temperature and lot records are stored directly in our LIMS, so recalls or back-traces are evidence-driven. We have lived through ingredient shortages, and ramped our approach to risk mitigation — not just for show, but to keep contractual timelines real for every customer anticipating their next synthesis run.
Lab technicians at our facility handle open drums, sample splits, and micro-scale evaporations. Direct handling experience informs our storage and safety recommendations. Reactions proceed without excessive exotherm, and we learned early to store away from acid-sensitive agents and moisture sources. From a safety training angle, onsite debriefs after rare incidents shaped most of the instructions on our containers and transfer logs. Real-life use is reflected in our labeling and communication — lessons learned the hard way, not just restating static hazard statements.
We adopted closed transfer systems after seeing exposure peaks during drum-to-drum transfer. Investing in additional gaskets and sealed fittings improved the environment for operators and reduced air loadings from a chemical hygiene perspective. These aren’t glamor initiatives; they came straight out of repeated operational experiences.
Regulatory expectations grow every season; our plant meets expectations through solvent recycling, closed-loop wash systems, and responsible waste handling. Every lot can be traced for source solvent, inbound raw material, and process aids — we built this loop because we observed regulatory tightening from environmental authorities and evolving customer documentation requirements. In our sector, plant-based compliance exceeds abstract checklists — we maintain these practices to deliver both product quality and operational sustainability. Surge planning, buffer stock, and inbound QA on each chemical have become simply part of the job.
Tert-Butyl Ethyl Malonate differs from others not just on paper. Where symmetrical diesters ask for more protection or deprotection steps, this malonate lets most users skip those phases, focusing instead on creating the carbon–carbon bonds that get new molecules built. Users have sent us NMR data mid-campaign, showing cleaner spectra after switching to tert-butyl ethyl. This comes from fewer mixed byproducts and the stability of the tert-butyl group under assorted conditions. These are not marketing lines — we see the raw data, and customers back it up with their internal notes.
Over years of working directly with users, the stories that stick involve lab teams saving time, avoiding caustic waste, and getting more usable crude from their reaction pot. Competent suppliers should build on these observations, adjusting their process to match what the end use actually needs, not just what the textbook says.
Inefficiency often lurks in repeated workups, incomplete conversions, or handling unpredictable side-products. We directed root-cause investigations into failed syntheses only to find that out-of-spec malonate — too much residual acid or unreacted starting ester — cascaded into process delays. In response, we strengthened our internal QA review. Operators added additional in-process sampling, validated by a direct comparison to retained samples from “good” batches flagged by positive end-user reports.
Another issue comes up in scale-up: thermal instability and volatility. When a customer flagged early loss of compound under vacuum, we responded by tightening controls on distillation end-points, integrating lower-pressure purges, and sampling back-distilled fractions. This halted volatility loss and cut raw cost losses on the customer’s end. Simple as it sounds, these zero-in steps make a difference in reliable long-term supply.
We confront environmental and safety challenges by investing in better storage systems, in-house vapor recovery, and enhanced staff safety training. These are not marketing gestures; every time an operator flags a transfer issue or an odor spike, new engineering controls get consideration. Plant managers work to keep staff in the loop on safe practices, and every incident — even minor ones — feeds back into standard operating procedures.
Stepwise API synthesis often runs more efficiently by choosing the right malonate ester at the outset. We’re working with partners on pilot programs where selective functionalization at one remaining ester simplifies further synthetic steps. Scalable, robust results rely on this foundation. R&D teams tell us up-to-date supply and minimal lot-to-lot variability keep their developmental chemistry on schedule.
Process chemists looking for reductions in hazardous waste found that using Tert-Butyl Ethyl Malonate cut exposure to harsh acids and bases for ester cleavage. These changes produce direct time savings and shorter post-reaction cleanups — less solvent need, less waste to manage, safer workspaces. Our technical support line draws feedback from teams who report reductions in unit operations, which means greater time to focus on chemistry, less spent on non-value-adding steps.
As end-users ourselves, we do not rely on theoretical benefits alone. Regular fielding of questions, solving real-life synthetic bottlenecks, and participating in customer pilot studies shape both our batch methods and technical recommendations. If a campaign fails, it rarely comes down to an isolated variable. Process learning teaches not only how to eliminate known pitfalls, but also how to tweak parameters in response to evolving routes. This breeds a practical, collaborative approach, helping keep our product line in step with where pharmaceutical and fine chemical innovation trends move.
Sourcing Tert-Butyl Ethyl Malonate directly from a manufacturer who understands both the technical and operational nuances changes how efficiently synthetic chemists can work. Our on-the-ground experience means we are as invested in the outcome of a catalytic alkylation as the plant chemist overseeing a multi-ton batch. That experience becomes embedded in every shipment: minimum impurity levels, thorough analysis, process-driven feedback, and transparent communication.
Through years of batch production, customer dialogue, and refining process detail, we continue to see how high-purity specialty esters like Tert-Butyl Ethyl Malonate underpin success from discovery to scale-up. Consistent supply, aligned with honest feedback from those at the bench and in the plant, remains our benchmark for doing business. It’s this perspective — that of a working manufacturer tied to the outcomes in labs and processing plants — that we bring to every lot leaving our site.