|
HS Code |
110226 |
| Cas Number | 403-21-0 |
| Molecular Formula | C7H2F4O |
| Molar Mass | 178.09 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 145-147 °C (at 15 mmHg) |
| Density | 1.447 g/cm3 (at 25 °C) |
| Refractive Index | 1.491 |
| Flash Point | 72.8 °C (closed cup) |
| Solubility In Water | Slightly soluble |
| Synonyms | 2,3,5,6-Tetrafluorobenzaldehyde; Benzaldehyde, 2,3,5,6-tetrafluoro- |
| Smiles | C1=C(C=C(C(=C1F)F)C=O)F |
| Inchi | InChI=1S/C7H2F4O/c8-4-1-6(10)5(9)2-7(4)3-12/h1-3H |
| Pubchem Cid | 24609756 |
As an accredited 2,3,5,6-Tetrafluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 250g 2,3,5,6-Tetrafluorobenzaldehyde is packaged in a sealed amber glass bottle with tamper-evident cap and label. |
| Shipping | 2,3,5,6-Tetrafluorobenzaldehyde should be shipped in tightly sealed containers, kept in cool, dry, and well-ventilated conditions. The chemical must be clearly labeled and protected from moisture and incompatible substances. Follow all applicable regulations for transporting hazardous chemicals, ensuring proper documentation and handling to prevent leaks, spills, or exposure during transit. |
| Storage | 2,3,5,6-Tetrafluorobenzaldehyde should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances, such as strong oxidizing agents. Keep the container tightly closed and protected from direct sunlight. Store in a chemical fume hood if possible, and ensure proper labeling. Avoid moisture and handle with gloves and protective eyewear. |
Applications of 2,3,5,6-Tetrafluorobenzaldehyde in Industrial Manufacturing2,3,5,6-Tetrafluorobenzaldehyde serves as a high-value building block in specialized chemical synthesis, providing fluorine-rich structural units favored in multiple advanced industrial fields. Our manufacturing experience supports downstream partners globally in integrating this compound into several key sectors that require stringent regulatory compliance and reliable supply stability. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ this compound during key steps of heterocyclic and aromatic API (active pharmaceutical ingredient) syntheses, especially for the generation of advanced fluorinated scaffolds in oncological, antiviral, and central nervous system (CNS) therapies. Its precise reactivity and low impurity profile support the high-purity demands of large-scale GMP production lines requiring batch-to-batch consistency throughout multiple synthesis stages, particularly in Grignard and condensation reactions. Industry compliance standards
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2. Agrochemical SynthesisProducers in crop protection utilize tetrafluorinated benzaldehyde as a core precursor for synthesizing new-generation herbicides and insecticides, prized for its ability to introduce multiple fluorine atoms that improve biological activity, environmental persistence, and selectivity in target species. Its reactive aldehyde function participates directly in formation of oxime ethers and fluorinated aromatic rings during formulation of selective agrochemicals. Industry compliance standards
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3. Functional Material Monomer PreparationDevelopers of specialty polymers and electronic materials consistently select this tetrafluorobenzaldehyde to introduce strong electron-withdrawing groups into monomer frameworks, essential for enhancing hydrophobicity, chemical resistance, and dielectric performance in advanced coatings, circuit board laminates, and optical films. Its high purity and well-defined substitution pattern guarantee reliable polymerization and material property reproducibility. Industry compliance standards
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4. Liquid Crystal Intermediate SynthesisManufacturers supplying the electronics sector integrate this fluorinated benzaldehyde as a critical intermediate in the custom synthesis of biphenyl and phenylpyrimidine derivatives, keys to the formulation of liquid crystal mixtures for high-performance displays. Its defined substitution enables precise molecular alignment, low birefringence, and heightened chemical stability, directly impacting the resolution and frequency response of LCD panels. Industry compliance standards
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After years of developing and perfecting the manufacture of aromatic fluorochemicals, our facility now produces 2,3,5,6-Tetrafluorobenzaldehyde with consistent purity and reliability. Through hundreds of reaction batches and purification cycles, we've seen how attention to each processing detail can make a visible difference in product performance. The small molecular tweaks—particularly the specific arrangement of fluorine atoms in the benzene ring—bring unique properties many chemists pursue for finely tuned downstream reactions.
Unlocking predictability in chemical feedstocks doesn’t come easy, especially with advanced aromatic fluoro-aldehydes. 2,3,5,6-Tetrafluorobenzaldehyde stands apart from other benzaldehyde derivatives. It owes that to the electron-withdrawing effect of four fluorine atoms symmetrically positioned around the ring. This configuration makes the compound substantially more reactive in certain electrophilic aromatic substitutions compared to mono-fluorinated or even di-fluorinated analogues. That level of fine-tuned reactivity translates to smoother process kinetics, tighter yields, and minimized by-product formation in industrial and lab workflows.
At each production run, we review analytical data from gas chromatography and NMR to ensure the aldehyde group stays crisp and intact, free from detectable over-oxidation or residual starting materials. By reinvesting in our reactor automation, we’ve managed to keep impurity levels at trace amounts and batch-to-batch variation minimal. No batch is scaled for shipment without running through both in-line and bench analyses, including GC-MS and moisture titration.
Experience shows that this compound prefers dryness. Moisture slows downstream nucleophilic additions or can trigger aldol condensation side-products if water sneaks in during storage or transfer. So, we've tailored our packaging protocols around dry, shielded vessels. Every drum or bottle out of the plant gets purged and sealed under inert gas. Cutting corners at this step leads to headaches for process chemists who rely on every molecule behaving the same, run after run.
One area we’ve seen strong adoption: synthesis of advanced fluoroaromatic building blocks. 2,3,5,6-Tetrafluorobenzaldehyde serves as a key intermediate for specialty ligands and biaryl pharmaceutical fragments. The regioselectivity from the four fluorine atoms changes the nucleophilicity and even the physical work-up characteristics compared to regular benzaldehyde. Process development teams regularly report that this unique reactivity profile allows for higher selectivity in condensation and Wittig reactions. That ultimately speeds up route screening for medicinal targets or agrochemical candidates.
Outside research labs, industrial-scale manufacturers appreciate the reproducibility. During scale-up, the performance remains steady—reactivity shifts only if storage instructions get ignored or if substitution patterns get swapped out for less stable isomers. Our technical support group has helped process chemists dial in the exact solvent, temperature, and catalyst conditions for high-throughput set-ups, showing in practical terms the value of producing this compound with consistent purity and controlled moisture content.
In our lab, new requests for obscure fluorinated compounds roll in every month. Many of those project plans rely on the specific properties of tetrafluorinated aromatics to build larger, functionally dense structures. Tetrafluorobenzaldehyde’s structure affects electron density and steric access at each site on the ring, steering extended condensation reactions or even directing meta- and para-substitutions during multi-step synthesis routes. This molecular architecture gives a leg up during fluorinated ligand housing design or while crafting more robust agrochemicals.
Compared to non-fluorinated benzaldehydes, the four-fluorine system resists unwanted oxidation. It’s less prone to ring-opening under harsh bases or oxidative halogenations. The added stability during protection-deprotection strategies in complex synthesis comes from experience—trials where competing aldehydes would degrade or scramble, this tetrafluoro variant stays intact.
Manufacturing at this level is not interchangeable with commodity chemical handling. Building the right infrastructure, selecting reactor linings, and calibrating for reliable heat transfer between runs required hands-on experimentation. Our crew routinely switches between glass-lined, PTFE, or Hastelloy reactors depending on upstream and downstream reagents. Over the years, investing in filtration technologies improved clarity far beyond basic cosmetic standards. Every decision, from raw material lots to storage temperature recommendations, stems from field experience over spreadsheet checklists.
Choosing this product over less-fluorinated or more randomly-substituted alternatives boils down to reliability. In routes where ortho or para-electron density manipulates the outcome, 2,3,5,6-Tetrafluorobenzaldehyde provides a set pattern. For applications demanding highly defined electronic environments—think photoresists, OLED intermediates, or next-generation fluorinated polymers—other forms of benzaldehyde can’t match its performance. The difference comes through in shorter purification times, less off-target reactivity, and greater selectivity in coupling reactions.
Years of packaging and shipping taught us the importance of practical safeguards. Even small temperature swings during transit can cause subtle changes in the aldehyde’s volatility. Sealed, inert-lined containers prevent cross-contamination or trace hydrolysis, which sometimes sneaks in if left overnight on a damp loading dock. The need for rapid, shielded transfer might sound excessive, but watching a shipment arrive compromised drives home how critical simple handling discipline becomes.
Some customers struggled with poor recovery rates after basic open-air weighing. We encourage inert gas environments whenever large-scale dispensing takes place. That precaution pays dividends in yield, even if it means a little extra up-front planning. Storage at stable conditions and minimal light exposure keeps every order ready for instant incorporation into multi-step campaigns, whether pumped into a flow reactor or staged for bulk batch chemistry.
Support for custom synthesis pushed us to refine even small details. Several pharmaceutical projects needed ultra-low-metal content in their fluorinated intermediates. By selecting all-fluoropolymer or ceramic process transfer lines, we brought typical metal levels down, avoiding catalyst poisoning or unwanted color formation in final API intermediates. Stories like this line our production notebooks and feed into monthly team reviews—it’s never just “make and ship,” but refine after each special order completes.
After troubleshooting alongside a customer, we reduced residual acids to nearly non-detect levels by slow-titrating reaction endpoints and drying under deep vacuum rather than using excess base. That let a downstream lithiation step proceed without clogging or foaming in microreactors. Process feedback loops like these changed shop practices. Every modification for one project built a playbook for future batches.
Feedback from partners drives us to rework purification steps for both yield and environmental benefit. Instead of relying on large-volume solvent washes, our team rotated in solid-phase extractions where possible, slashing both waste and cost on recurring orders. Dry distillation under reduced pressure has replaced several high-temperature purification steps. That approach improves yield and also protects the aldehyde function, especially when scaling for kilogram or slab shipments.
Waste reduction isn’t only a talking point. Quarterly audits map out where solvent usage spikes, or where energy and water consumption during chill cycles could be trimmed. Our operators tinker with smaller holding tanks, in-line temperature stabilization, and better recompression on coolant flows. These day-to-day changes allow regular supply to customers pushing for greener chemistry without compromising the sensitive nature of these complicated building blocks.
We don’t just ship drums and bottles; our technical team works through specific case studies with partners. By gathering post-run analyses and sharing real-world feedback, both sides learn faster. For emerging applications—enzyme-resistant coatings, battery electrolytes, or new-generation herbicide scaffolds—customers need not just a chemical, but one ready to withstand unpredictable processing and integration demands.
As new synthetic challenges appear, this product continually earns its place based on reliability in use—reproducible performance, batch after batch. Each refinement to our packaging, purification, or documentation comes out of discussion with end users, adapting day-to-day practices to fit practical requirements beyond theoretical standards.
Traceability improves confidence, especially for customers bound by increasing regulatory scrutiny. Detailed records lets us pinpoint root causes whenever anomalies pop up during a customer’s process. Connecting raw material lots, production dates, and reaction conditions creates a transparent history behind every order. This focus on traceability matters when high-value campaigns are on the line.
Our documentation remains as rigorous as practical. Not just quality certificates, but also batch chromatograms, usual moisture content, or notes on process tweaks help partners make smart decisions before charging the chemical into their own reactors. That openness limits surprises in both research and at production scale. Our operators get a full rundown of every change, learning from hiccups, smoothing out the next batch, and shipping documentation that reflects shop floor experience, not just digital forms.
Years of reaction development show where other benzaldehyde analogues underperform. In situations requiring extremely clean selectivity or unusual electron-demanding condensation, non-fluorinated or scattered-fluorine-substituted versions show higher rates of byproduct formation. The defined reactivity from this tetrafluorinated form streamlines work-ups, curtails column load, and eliminates much of the fiddly post-run cleaning. That becomes clear in both R&D routines and at scale.
In aromatic functionalizations with precise site-control, the predictable electronic effects of the 2,3,5,6-tetrafluorinated system lead to fewer surprises and smoother integration into growing synthetic chains. Colleagues experimenting with mono- or di-fluorinated versions consistently report more drag during purification and less consistency in desired product ratios. For technical chemists, these incremental pain points become a measurable drag on throughput.
Inside our plant, each order tells a story of continuous improvement. It might involve the fine-tuning of a single drying step or a customer who discovered an unexpected benefit using our product in a complex catalytic cycle. By keeping a constant feedback loop and making incremental upgrades to processes, we improve not only our product but also the experience of every lab and manufacturer depending on us.
In every way, 2,3,5,6-Tetrafluorobenzaldehyde embodies the lessons learned from years of manufacturing under tight demands. Every step, from raw material selection to the final seal on a drum, carries the imprint of countless production cycles and customer collaborations. Drawing on this experience, we strive to deliver more than a chemical; we deliver the knowledge that comes with crafting something well over time.