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HS Code |
460834 |
| Chemical Name | Ethylformamide |
| CAS Number | 627-45-2 |
| Molecular Formula | C3H7NO |
| Molar Mass | 73.09 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 192 °C |
| Melting Point | -40 °C |
| Density | 0.945 g/cm³ |
| Solubility in Water | Miscible |
| Flash Point | 85 °C |
| Refractive Index | 1.418 |
| Vapor Pressure | 0.4 mmHg (25 °C) |
As an accredited Ethylformamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethylformamide, 500 mL: Clear glass bottle with secure screw cap, labeled with chemical details, hazard symbols, and handling instructions. |
| Shipping | **Shipping Description for Ethylformamide:** Ethylformamide should be shipped in tightly sealed containers, protected from heat, sparks, and open flames. Store and transport in a cool, well-ventilated area. Comply with all relevant regulations regarding flammable and potentially hazardous liquids. Ensure proper labeling and documentation. Handle with appropriate personal protective equipment (PPE). |
| Storage | Ethylformamide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of heat, sparks, or open flame. Keep it separate from oxidizing agents, acids, and bases. Use appropriate precautions to avoid inhalation or skin contact, and ensure emergency spill cleanup materials are available nearby. Store at recommended temperatures indicated on the safety datasheet. |
Applications of Ethylformamide in Industrial ManufacturingEthylformamide plays a specialized role in several chemical manufacturing sectors, supporting unique processing requirements and acting as a dedicated intermediate for advanced synthesis. As a direct producer, we continuously refine our specifications to align with downstream customer processes and stringent industry compliance. 1. Pharmaceutical Intermediate SynthesisProducers in the pharmaceutical sector frequently incorporate ethylformamide as a key building block during the synthesis of heterocyclic compounds and active pharmaceutical ingredients (APIs). Its chemical properties enable selectivity and improved yields in condensation and alkylation steps required for drug precursor construction, particularly in the formulation of anticonvulsant and anti-inflammatory medications. Batch QC teams monitor traceability from raw material batch intake into the active ingredient synthesis lines in compliance with qualification requirements. Industry compliance standards
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2. Agrochemical Active Ingredient ManufactureChemical companies manufacturing crop protection agents use ethylformamide as a specialty reactant to introduce formamide groups during the multi-step production of herbicide and fungicide intermediates. The material supports the functionalization and fine-tuning of molecular structures key to selectivity and bioactivity in extensive field trials, and is subject to agricultural chemical GMP and food safety directives, from piloting through to bulk campaigns. Industry compliance standards
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3. Specialty Organic Synthesis for Dyes and PigmentsManufacturers engaged in the synthesis of high-performance dyes and pigment intermediates include ethylformamide as a functionalizing agent, particularly in the modification of aromatic rings and amide formation for azo and phthalocyanine pigment backbones. Pigment production relies on the controlled introduction of ethylformamide to achieve specific chromatic and solubility profiles required for applications in textiles, inks, and plastics. Industry compliance standards
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4. Solvent and Additive in Electrolyte FormulationsIn the field of high-purity electrolyte manufacturing for lithium-ion batteries and electrochemical devices, ethylformamide is sometimes introduced in specific low-level proportions to modify solvation properties or assist in the dissolution of advanced electrolyte salts. Battery R&D teams leverage the compound's tailored polarity to optimize conductive salt solubility, viscosity management, and to mitigate side reactions during cell cycling, with tight traceability and quality surveillance in pilot and commercial production lines. Industry compliance standards
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Years of experience in chemical manufacturing have shown us that pure, consistent ethylformamide makes all the difference—especially for customers who value reliability and technical precision. Among amides, ethylformamide (C3H7NO) earns its spot for its stable properties and straightforward behavior under varying factory and laboratory conditions. We manufacture ethylformamide using controlled processes to keep impurities low, as even minor contaminations can create headaches downstream or impair synthesis quality. Current demand reflects its clear role in supporting organic synthesis, solvent formulations, advanced polymer research, and specialized pharma intermediates.
Ethylformamide doesn’t try to do the job of a commodity solvent. Unlike acetone or ethanol, it brings a specific chemical structure—an amide backbone with an ethyl and formyl group—that makes it valuable for chemists targeting certain bonds or reactions. Over time, we have refined our product to balance volatility and solvency, letting researchers run repeated assays or scale up plant batches without fighting inconsistent batches.
Traditional solvents run into limits under harsh reaction conditions. Ethylformamide handles a mix of temperatures and aggressive reagents that generic solvents can’t always manage. Its moderate boiling point supports distillation work, while its polarity allows for solubilizing tricky reactants that often resist standard approaches. When customers report tight yields or need a component for precision pharmaceutical intermediates, ethylformamide often features in their solution set.
Purity isn’t just a checklist for us; it’s a daily grind. We constantly analyze our ethylformamide production for water content, trace amides, unreacted ethylamine, and residual solvents. Moisture ruins batch reliability. We run Karl Fischer titrations as routine, double-checking content before shipping barrels or drums. Our technicians also watch color, as off-spec batches can indicate side reactions or storage issues. Even though it seems basic, that extra visual check has prevented wasted time and money for downstream users.
Density, refractive index, and boiling point readings get cross-checked before release. These figures aren’t marketing gold—just day-to-day realities for our team and for end users. Overlooking these details leads to unpredictable reactions and lower yield. Spec sheets only matter if the numbers match what actually arrives at the customer dock, and we back up any claims with independent test certificates.
Ethylformamide’s significance comes alive on the ground floor. In pharma intermediates, chemists prefer it for clean formyl transfers, acylation, and amidation reactions. The formation of certain heterocycles—a backbone structure in many advanced molecules—relies on a solvent that won’t interfere with ring closure or rearrangement. We’ve worked with niche drug makers who value the product for its gentle, predictable reactivity, avoiding byproduct headaches or costly post-reaction purifications. Its small size and polarity let it access active sites in multi-step syntheses where larger or bulkier solvents complicate purification.
Industrial customers use ethylformamide as a co-solvent in resin formation. It dissolves highly functionalized monomers that won’t go into solution with standard chemistry. Our team supports coatings producers looking for a robust alternative to higher-boiling amides which slow down their processes or increase energy bills. Instead, ethylformamide comes off easily with less input and lower overhead—especially important as energy prices climb.
For select agrochemical producers, the amide group in ethylformamide allows for low-toxicity formulations—achieving active ingredient delivery without risking solvent drag or environmental buildup. We’ve engaged with these manufacturers through pilot scale runs and provided full disclosure on residuals and breakdown products, so they can file local environmental paperwork confident in what they’re reporting.
Working in chemical manufacturing long enough, you get to test just about every similar material on the market. N,N-dimethylformamide (DMF) often comes up in customer requests. We remind clients that DMF’s methyl groups lead to higher volatility and greater regulatory scrutiny due to its propensity for forming carcinogenic breakdown products in certain industrial conditions. Ethylformamide runs safer in many settings while still handling high-solubility needs.
N-methylpyrrolidone (NMP) offers high polarity, but its cyclic structure and persistence in the environment make it an emerging regulatory headache. Ethylformamide won’t hold up as long under extreme alkaline conditions, but most polymer synthesis and solvent extraction work steer clear of those regimes anyway. If a customer needs a non-cyclic, rapidly biodegradable solvent with solid polar compatibility, ethylformamide stands up to the job.
Acetamides and propionamides find some applications across laboratory and production environments, yet they lack the exact balance of boiling point and reactivity needed for many specialty syntheses. Research chemists tend to prefer a compound that provides consistent intermediate polarity—a window where neither the reaction partners nor the product suffer from side reactions. This is a space where ethylformamide consistently performs.
Our plant runs on accuracy and transparency. Each batch we send comes with lot-level data, not generic pass/fail sheets. Customers have rigorous audits, and they expect us to make certificates of analysis available for traceability. The production line samples both start and end-point material, logging every deviation. In rare instances where a load falls short of spec, we hold it back and notify every scheduled recipient.
Customers in regulated industries demand disclosure on even tiny contaminants. We use gas chromatography and specific amide trace assays—not just bulk methods or general analysis—to reassure buyers that their incoming stock won’t cause downstream regulatory issues. Transport companies need to know the flashpoint and storage hazards up front. On our end, strict adherence to local workplace health and safety guidelines reduces accident rates and keeps insurance costs manageable.
Our approach involves open feedback with users who encounter bottlenecks or inconsistent performance. Over the years, we have adjusted drying cycles and storage protocols based on customer root cause analyses—not only relying on textbook or regulatory guidance. That perspective directly improves repeatability and minimizes time lost to troubleshooting at the user’s site.
It’s one thing to deliver a lab bottle with perfect results and another to hit spec in bulk containers, shipment after shipment. We keep reactor and storage materials compatible with amides, avoiding contamination from previous runs of aldehydes or acids—otherwise, customers see product yellowing or delayed crystallization. With repeated scale-up experience, we have found that even minor process changes—like valve swaps or new transfer lines—impact material consistency, so checks and cross-contamination logs stay non-negotiable.
Our larger volume customers, such as polymer houses and contract pharma plants, require steady logistics support. Supply interruptions due to raw material hiccups or transportation delays can lead to hours or days of plant downtime. We’ve invested in local warehousing and direct distribution networks to hedge against broader supply chain instabilities. Relationships with logistics providers also allow us to offer flexible delivery, tailored to critical run cycles and paced against buffer inventory.
Ethylformamide often comes up as a relatively obscure amide, bridging the gap between lower molecular weight solvents and more strongly interacting specialty reagents. In recent years, demand has spiked among advanced research groups working on new reaction mechanisms. Organic researchers consult with us on using ethylformamide for selective formylations or in emerging catalytic transformations where more reactive, less selective solvents break down end products.
We keep up with the shifting landscape by investing in joint development projects and custom batch runs for researchers. If prototyping shows benefit from modified solvent blends or stricter impurity cutoffs, we collaborate to deliver ready-to-use lots. No off-the-shelf approach suffices for all users, so our technical support stays on-hand for direct troubleshooting. With some long-term partnerships, we adjust our reactor profiles or introduce precision drying protocols to address specific bottlenecks surfaced by R&D teams.
Many customers today face tightening environmental standards. Ethylformamide, as with most amides, lands in a balanced spot between performance and environmental persistence. Disposal profiles and breakdown products affect not just factory operations, but also how users report emissions and compliance on a wider scale. We supply handling documentation and breakdown data that reflect current best practice for wastewater treatment. For customers moving toward zero-discharge or closed-system plants, the predictable carry of ethylformamide through standard purification cycles represents a key advantage over more complex solvent mixes.
Emission controls, especially in the EU and North America, mean that solvents can’t simply evaporate unchecked. Our storage and filling equipment capture vapors, and we provide returnable drums to reduce downstream waste. Some regions require additional labeling or trace impurity disclosure; our team routinely updates documentation to keep customers ahead of regulations without last-minute compliance scrambles.
Direct supplies from the manufacturer mean end-users get access to all plant know-how. Our technical staff has solved issues ranging from batch haze due to microscopic metal pickup, to fine-tuning drying cycles in order to meet one-off pharmaceutical synthesis purity needs. The most frequent calls concern product compatibility with particular catalysts or process conditions. Our plant chemists deliver practical troubleshooting rather than just quoting textbook figures.
Torching hours on inconsistency ties up time and resources. In working directly with major production houses, we help limit downtime with swift troubleshooting—sometimes shipping at odd hours or opening lab space for customer side-by-side trials. Our experience with various reactor materials and transfer systems means we understand how subtle system changes ripple through quality outcomes.
Real improvements in production quality come from end-user feedback. Large pharmaceutical plants want strict, narrow impurity ranges. Smaller R&D groups often look for adaptability: for example, more granular lot reports or quick turnaround for custom drying cycles. We adjust packaging and logistics to customer batch size—drum, tote, or tanker—without compromising product integrity. Listening close to bottleneck reports, whether it’s haze, color variation, or reaction stalling, keeps our product responsive rather than static.
A number of our recurring customers once tried ethylformamide from resellers or generic traders, only to switch back to direct supply due to unpredictability. Batch-level documentation, technical access, and uninterrupted support draw the line between smooth production and repeated delays.
Amides as a class continue to evolve in relevance, as high-purity applications drive up expectations for solvents and reaction aids. Ethylformamide, once considered just a supporting actor in chemical synthesis, now drives its own demand among those who prioritize repeatability. Scarcity or quality swings force extra investment in synthesis troubleshooting, so we double down on process control.
Organic electronics, specialty coatings, and API makers all cite the same requirement: batches should copy the same performance year over year. We leverage both historical process knowledge and new instrumentation, investing in upgraded reactors and real-time monitoring to guard against subtle drift. Even as broader feedstock markets fluctuate, experience underscores that quality control counts more than volume.
Recent years have seen a slow but steady shift toward tighter chemical regulations across solvents and specialty organics. Customers report rising paperwork, more stringent emission tracking, and closer oversight on trace amide reporting. With new research into greener solvents and shifting pharmaceutical requirements, ethylformamide’s relatively straightforward breakdown pathway keeps it relevant—especially in markets that penalize persistent pollutants.
Some sectors, such as advanced composites or electronics, have begun experimenting with alternative amides and low-boiling ethers. Yet, for every speculative project, dozens of producers still rely on ethylformamide’s manageable volatility, access to formyl chemistry, and moderate toxicity. Looking ahead, we invest in supporting documentation for both evolving customer projects and compliance regimes. We stay tuned to application pivots—for example, new formulations in battery chemistry or industrial extraction, where ethylformamide’s unique behavior stands apart.
Producing ethylformamide in-house, our value comes from direct connection to all parts of the supply chain. Technical documentation, real-time support, and willingness to adjust production fit into the reality that users don’t just want a liquid—they need a working, dependable part of their process. Nobody sees the day-to-day issues of inconsistent product as closely as we do. It teaches us that hands-on support and continued investment in people, plant, and process win trust over brochures or generic promises.
Whether for long-running plant lines or early-stage research, ethylformamide continues to carve its own space. With exacting process controls, honest reporting, and user-focused responsiveness, we back up not just every barrel, but also every batch behind it.