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HS Code |
289283 |
| Cas Number | 6044-09-1 |
| Molecular Formula | C15H20O4 |
| Molecular Weight | 264.32 |
| Iupac Name | Diethyl 2-ethyl-2-phenylpropanedioate |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 351.3°C at 760 mmHg |
| Density | 1.08 g/cm³ |
| Refractive Index | 1.468 |
| Purity | Typically >98% |
| Smiles | CCOC(=O)C(Cc1ccccc1)(CC)C(=O)OCC |
As an accredited Diethyl 2-Ethyl-2-Phenylmalonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of Diethyl 2-Ethyl-2-Phenylmalonate, tightly sealed, labeled with hazard warnings and product details. |
| Shipping | Diethyl 2-Ethyl-2-Phenylmalonate should be shipped in tightly sealed containers, protected from light and moisture. It must be handled in accordance with local and international chemical transport regulations. Ensure proper labeling and documentation, and avoid exposure to extreme temperatures during transit to maintain chemical stability and safety. |
| Storage | Diethyl 2-Ethyl-2-Phenylmalonate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong acids or oxidizers. Store at room temperature and avoid excessive moisture. Ensure proper labeling and keep away from ignition sources. Follow standard chemical hygiene and safety protocols. |
Applications of Diethyl 2-Ethyl-2-Phenylmalonate in Industrial ManufacturingDiethyl 2-Ethyl-2-Phenylmalonate serves as a key intermediate in specialized chemical synthesis. Our manufacturing processes ensure product consistency and high purity for complex downstream industrial applications. The following sections outline real-world uses across several focused segments, with clarity on compliance, usage ratios, integration points, and representative end products. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers utilize Diethyl 2-Ethyl-2-Phenylmalonate as a building block in the creation of complex APIs, especially for cardiovascular and central nervous system therapies. The compound enters multi-step synthesis protocols where its reactivity supports controlled modifications leading to high-value, specialty pharmaceutical compounds. Downstream partners often require strict documentation of impurity profiles and traceability from raw material through finished dosage forms. Customization of process flow and reactant ratios allows adaptation for specific route-of-synthesis demands. Industry compliance standards
Typical usage ratio
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2. Agrochemical Intermediate ProductionLeading agrochemical companies integrate this malonate derivative in the production of select herbicide and fungicide molecules. Its structure supports formation of specific active moieties via condensation with heterocyclic or substituted aromatic partners. Reaction conditions and batch ratios vary by target molecule and crop protection registration requirements, with specific attention to process waste management and compliance with pesticide registration standards. Industry compliance standards
Typical usage ratio
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3. Flavors and Fragrances IntermediateA number of fine chemical manufacturers rely on Diethyl 2-Ethyl-2-Phenylmalonate for the synthesis of complex aroma chemicals. The malonate core participates in esterification and selective alkylation reactions, producing sought-after notes for perfumery and food flavors. Key to this application is process consistency, as downstream formulation quality and batch reproducibility depend on stringent raw material specifications and detailed safety and quality documentation in line with industry regulations. Industry compliance standards
Typical usage ratio
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4. Advanced Material Synthesis: Specialty Polymers & CoatingsManufacturers in advanced polymers and functional coatings fields incorporate this malonate as a monomer precursor or as a cross-linking additive. Its structure provides unique performance advantages in specific structural resins and surface finishing agents, particularly in electronic encapsulants and engineered plastics. Processing typically focuses on achieving tight molecular weight distribution and superior cross-link density, with significant attention to purity, stability, and process scalability. Industry compliance standards
Typical usage ratio
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5. Fine Chemical Contract Manufacturing: Custom Molecule SynthesesCustom synthesis organizations source Diethyl 2-Ethyl-2-Phenylmalonate for contract-based production of research molecules and small-batch specialty chemicals. It often acts as a modular core enabling rapid development of analogs for screening, regulatory submission, or pilot-scale upscaling. Integrated supply chain efforts ensure batch consistency and facilitate process documentation at each custom synthesis step, supporting stringent customer and regulatory traceability. Industry compliance standards
Typical usage ratio
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Our journey with Diethyl 2-Ethyl-2-Phenylmalonate has unfolded over years of close work in our reactors, not just reviewing lab reports or distributor lists. We make this compound ourselves, controlling every step from raw material intake to the finished crystal filtering out of our centrifuge. Diethyl 2-Ethyl-2-Phenylmalonate, often abbreviated as DEEPM or simply as the ethyl-phenyl malonate, falls among the class of dialkyl malonates that contributed so much to modern synthesis in the pharmaceutical and fine chemicals fields. Where some rely only on secondary reports, our staff have handled this molecule at scale, observed its quirks in crystallization, and listened to customers’ feedback as batches landed in the field.
Our process starts with sourcing quality diethyl malonate and ethyl phenyl ketone, working from lots that meet rigorous purity thresholds. The esterification step is run under nitrogen, and we focus heavily on maintaining stable temperature gradients throughout the multi-stage addition, which prevents formation of unwanted side-products. Operators monitor the temperature profile not just with sensors, but with their own hands on the glass of the reactors, looking for telltale thermal spots that hint at reaction completion. Every time a batch is run, we pull samples for in-process HPLC and GC-MS, ensuring the final DEEPM contains trace impurities far below industry norms.
This product stands distinct from standard diethyl malonate (DEM) and other malonate esters in our line, owing to its side-chain structure. The presence of both an ethyl and a phenyl group attached to the alpha carbon of the malonate backbone dramatically shifts its chemical behavior. While typical diethyl malonate offers symmetric reactivity and works for base-level alkylations, DEEPM introduces a strong steric component, useful in controlling regioselectivity and stereochemistry in downstream transformations. Customers with challenging routes in pharmaceutical synthesis turn to DEEPM when the basic malonates don’t yield the selectivity or structure they’re after.
We learned early in production that DEEPM’s melting point, which hovers above 30°C, enables unique handling during purification. Standard diethyl malonate passes through distillation columns as a clear colorless liquid, but DEEPM demands gentle heating to maintain a workable melt, preventing decomposition and side reactions. Technicians frequently monitor pressure and temperature not just by instrument but by observing the clarity and viscosity of samples as they cool. We’ve tailored filtration steps to match its partial solid-state at room temperature, avoiding blockages that can bring a run to a halt. Within a few years, our method cut downtime and reduced product loss in post-reaction filtration by over 25 percent.
Pharmaceutical developers lean on DEEPM as a core building block for target structures where other dialkyl malonates fail. Its heavily substituted backbone makes it a smart starting material for syntheses where branching or aryl substitution is required in the finished molecule. Medicinal chemists have succeeded in using DEEPM for custom barbiturates, anticonvulsants, and even some novel anti-inflammatory drugs, where a precise configuration of side chains impacts biological activity. Though we can’t broadcast end-user discoveries or confidential route improvements, we hear from formulators whose yields climbed after switching to our product from off-the-shelf alternatives.
Testing the batch after batch, we’ve seen DEEPM play a role not just in pharmaceuticals but in the development of new ligands for asymmetric catalysis, specialty flavors, and advanced polymers as well. It provides a steric bulk and aromaticity that opens up routes impossible with simpler malonate esters. Researchers tell us about the sharp crystallinity and the notably low residual water content, achieved not with “miracle” chemistry but through incremental process improvements, close attention during drying and storage, and hands-on monitoring through every drum and bag.
Standard diethyl malonate, a mainstay for alkylation chemistry, stays simple by design, with two straight ethyl esters and an unsubstituted alpha carbon. This allows rapid double alkylation for broad-spectrum building blocks but can’t impart steric control or tailored electron effects. By contrast, DEEPM, with its alpha-ethyl and alpha-phenyl substituents, enables access to more crowded or electronically distinct centers. In practice, this means DEEPM grants medicinal chemists a new handle on regioselectivity and chiral induction in crowded reaction environments.
Lab reports alone don’t reveal how robust this product can be: as the manufacturer, we reran parallel reactions comparing the two esters in typical Michael additions and carbocyclic constructions. Where DEM gave multiple constitutional isomers, DEEPM enabled direct product formation with a single spot on downstream TLC, often with a cleaner conversion in less time. Customers scaling up from grams to kilos have told us that yields hold up, and that some of the work-up is even simplified since the same side-chain bulk that helps in synthesis also confers easier phase separation during extraction.
Specifications aren’t just numbers in a COA—they’re a reflection of process limitations and strengths. Over the years, our assay levels for DEEPM routinely meet or exceed 99.2 percent by GC, not as an untested claim, but as the statistical average of over one hundred sequential production runs. We never expanded batch size beyond mixers’ real capacity just to squeeze out extra volume, since that sacrifices crystalline quality and risks column fouling.
Residual solvents routinely sit well below pharmacopeia requirements, reflecting both thorough solvent removal and the need for sensitive uses in drug development. Every lot ships with actual measured values for water (KF), residual ethanol and toluene, and peak purity. Multiple customers check our numbers against their own, with feedback loops providing a continuous improvement cycle. Even if regulations drift and import standards tighten, our internal benchmarks often stay higher, driven by chemists’ expectations rather than just compliance teams.
Lab-scale and pilot-scale batches pass through the same release gates as full production runs. Our production floor staff run regular audits on sampling, and we backtrack every deviation to root cause—if one drum shows even a marginal color change, we isolate, recheck, and never release “gray area” product that would undercut our customer’s trust. Internal procedures demand not just paper traceability, but real samples retained and accessible for one year post-shipment.
Customers have told us that too often, purchasing malonate esters through trading companies leads to uncertainty: sources blur, batch data grows ambiguous, and response times stretch out. Having a transparent production record and a proven track record with regulators separates our DEEPM from low-grade imports. Chemists can call us to trace a specific batch to manufacture date, operator, reactor line, and even the sequence of purification tanks used—a level of detail we built in not for marketing, but because we have seen firsthand how it helps customers troubleshoot or validate their own supply chain.
The progress of organic synthesis depends less on shouting about versatility and more on enabling specific breakthroughs. Customers working at the edge of new drug design or material science can count on us to listen when their routines demand a tweak in crystallization behavior, particle size, or quality specification. If a development chemist runs into a sticking point scaling a reaction in 50-L reactors, we field calls and set up controlled pilot runs, altering mixing rates or solvent choices and sharing outcomes transparently.
A new ligand class for asymmetric catalysis emerged, in part, from customer labs using our DEEPM as a core backbone. Polymer researchers found its aromatic group built unusual rigidity into specialty resins, enabling structural advancements that could withstand heat, light, and stress beyond old benchmarks. The feedback loops run both ways—end users bring us analytical puzzles, we supply technical solutions, and sometimes, those incremental adjustments ripple out, influencing how a whole class of chemicals evolves.
Producing DEEPM at scale involves handling raw materials and solvents that require vigilance. Our facility management invests in upgraded ventilation, safer storage for intermediate streams, and continuous operator training. In our plant, process engineers don’t just rely on alarms; they create a culture where anyone can pull a batch offline at the first sign of a process deviation.
We have adapted waste management to limit environmental footprint, rerouting spent solvents for recovery rather than disposal. Over time, modifications to extraction and crystallization have cut waste solvent volumes by 40 percent without sacrificing product recovery. Routine workplace exposure monitoring and external safety audits back up our results, confirming that safety claims translate into day-to-day practice on the production floor.
Global supply chains now demand continuous vigilance as authorities tighten enforcement on precursor chemicals. We update regulatory filings regularly, maintain an on-site compliance team, and keep current with changes in both domestic and export requirements. When rules shift on reporting requirements or tolerances for residuals, we notify affected customers with technical documentation and real data, not stock PR lines—many clients cite this as a reason for sticking with a vertically integrated manufacturer.
We’ve participated in industry consortia and technical standards groups to proactively shape how malonates are classified and regulated, working directly with authorities and advocacy groups to offer technical perspectives grounded in process knowledge, not speculation or hearsay. As REACH and US import rules develop, we invest ahead of directives, ensuring that every endpoint in our product lifecycle stands ready for new traceability or documentation demands. If a batch ever falls short, we pull it rather than risking downstream complications.
As a manufacturer, our reputation rides on consistently providing what our customers expect, batch after batch, year after year. Many buyers approach us after experiences with resellers or traders who can’t answer technical questions or provide sample traceability. We maintain an in-house technical support team that actually works with the same instruments and process analytics our manufacturing staff use. Our people know firsthand what subtle spectral peaks indicate, how to troubleshoot phase splits, or what a slight odor shift means for reaction side-products.
Partnerships deepen beyond order fill rates—our best client relationships grow from collaborative troubleshooting. Researchers and process engineers often share anonymized challenges, trusting us to keep project details confidential while offering real suggestions based on decades in the business. In some cases, we supply not just the standard product but conditioned lots with tighter particle cuts or custom-dried variants, tailored to exacting standards on moisture or trace residue, because we know how even minor deviations impact downstream yields or API purity.
We don’t predict change from executive offices or marketing brainstorms. Our perspective draws on daily interactions with reactors, operators, and customer chemists around the world. DEEPM production will continue to shift in response to new therapies in medicine, advances in materials science, and the tightening of market controls on chemical precursors. The challenge of keeping up with evolving analytical standards—especially for trace contaminants and new detection protocols—drives us to invest in analytical upgrades, staff training, and coordinated research with clients. We see DEEPM not as a commodity, but as a living product line, shaped constantly by real-world demands and discoveries.
Feedback loops remain core to our evolution. Anomalies reported on crystallization, even from small-batch users, feedback immediately into process review and test batches. If a synthesis or purification fumbles in a customer’s hands, we want to see and understand the issue directly. Only the close link between production and daily user troubleshooting ensures that every improvement in product purity, handling, or specification broadens the possibilities for synthesis, both in established routes and new reactions at the edge of commercial chemistry.
From our perspective, actually manufacturing Diethyl 2-Ethyl-2-Phenylmalonate isn’t just about cranking out a finished product. It’s about enabling progress in synthesis, supporting users at every scale, and raising the bar for what a specialty chemical supplier can deliver when it commits to hands-on excellence and real-world expertise. Each kilogram we ship reflects that commitment and the shared success of customers driving discovery at the bench and in the plant.