|
HS Code |
670591 |
| Productname | 3,5-Difluorocinnamic Acid |
| Casnumber | 153504-70-2 |
| Molecularformula | C9H6F2O2 |
| Molecularweight | 184.14 |
| Appearance | White to off-white powder |
| Meltingpoint | 182-186°C |
| Boilingpoint | 347.4°C at 760 mmHg |
| Solubility | Slightly soluble in water; soluble in organic solvents such as methanol, ethanol, DMSO |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=CC(=C1)F)C=CC(=O)O |
| Inchi | InChI=1S/C9H6F2O2/c10-7-3-6(4-8(11)5-7)2-1-9(12)13/h1-5H,(H,12,13) |
| Refractiveindex | 1.570 (est.) |
| Density | 1.364 g/cm3 |
| Storage | Store at room temperature, in a tightly sealed container |
As an accredited 3,5-Difluorocinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3,5-Difluorocinnamic Acid is packaged in a 25g amber glass bottle, sealed with a screw cap, and labeled for laboratory use. |
| Shipping | 3,5-Difluorocinnamic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically transported at ambient temperature under dry, ventilated conditions, and labeled according to chemical safety regulations. Ensure compliance with local, national, and international shipping regulations for chemical substances. Proper documentation accompanies each shipment. |
| Storage | 3,5-Difluorocinnamic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of moisture, heat, and ignition. Protect from light and incompatible substances such as strong oxidizing agents. Properly label the container and store at room temperature unless otherwise specified, following all relevant safety and regulatory guidelines. |
Applications of 3,5-Difluorocinnamic Acid in Industrial Manufacturing3,5-Difluorocinnamic Acid supports critical synthesis routes in advanced chemical production. Our factory supplies this specialty intermediate to established sectors that require dependable quality, regulatory transparency, and consistent batch performance. 1. Pharmaceutical Intermediate for Fluorinated Drug SynthesisPharmaceutical manufacturers employ 3,5-Difluorocinnamic Acid to build fluorinated scaffolds in next-generation therapeutic molecules, particularly for anti-tumor and central nervous system drug candidates. Customers integrate this building block within multi-step GMP syntheses where positional fluorine substitution modulates potency, bioavailability, and metabolic stability. We supply substance with verifiable traceability, batch purity documentation, and process control data for regulated substance development and early-phase manufacturing. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis for Selective HerbicidesPesticide formulators utilize 3,5-Difluorocinnamic Acid as a precursor for aromatic ring modifications in selective herbicide development. The molecule’s difluoro substituents influence herbicidal mode-of-action profiles and soil degradation rates, supporting R&D and commercial production application. Formulation plants strictly monitor impurities and by-product content as per agrochemical safety requirements, integrating our input material after incoming QC clearance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemicals for Organic Semiconductor MaterialsSemiconductor and display manufacturers require 3,5-Difluorocinnamic Acid for synthesis of specialty organic semiconductors, such as fluorinated oligomers and polymers for OFET and OLED components. Its molecular structure supports electronic device miniaturization, charge mobility, and stability under thermal and light stress. In this class, the input must meet stringent trace metal content and particle size controls, fulfilling the high purity demands for both pilot-scale innovation and mass production environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemicals for UV-Curable Adhesive FormulationsIndustrial adhesive manufacturers utilize 3,5-Difluorocinnamic Acid as a reactive modifier in UV-curable and thermal-setting adhesives. Its introduction enables tuning of viscosity, cross-link density, and optical properties in transparent and colored adhesive systems. Suppliers process the material under ISO-controlled blending and in-line mixing, and monitor batch-to-batch consistency for integration with initiated acrylate polymerization processes. Documentation supports compliance audits and downstream labeling needs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3,5-Difluorocinnamic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Every chemist working on developing pharmaceuticals, advanced materials, or agrochemical agents has run up against the issue of purity and consistency. Years of manufacturing fine chemicals have taught us that trace impurities become real problems during scale-up. When we produce 3,5-difluorocinnamic acid (CAS: 84371-65-3), our focus remains fixed on supplying a material that lets researchers and process chemists make reliable progress, not waste time troubleshooting off-spec inputs.
This compound features the cinnamic acid backbone modified with two fluorine atoms at the 3 and 5 positions. This substitution pattern can sound academic, but it influences reactivity in unmistakable ways. In our plant, demand for 3,5-difluorocinnamic acid comes largely from pharmaceutical innovators who require defined aromatic substitution to impart desired biological activity or to serve as a precursor for more complex molecules. Working at full scale, our production batches routinely exceed 99% HPLC purity—achieved through rigorous chromatography, multiple crystallizations, and ongoing internal audit of batch records.
Our experience shows that moisture content undermines long-term stability. We use sealed glass or fluoropolymer containers, protect the product from excess humidity, and monitor each lot with Karl Fischer titration. Trace amounts of halogenated byproducts or starting materials get flagged in routine QC analysis. Any detected levels over 0.2% trigger a repetition of the purification process; customers never see these failed lots. Through this attention to process detail, we enable downstream users to spend less time performing their own purification.
Some customers ask about the value of adding two fluorines to the molecule, compared to the standard cinnamic acid or the mono-fluorinated variants. In my experience, fluorine atoms at the meta (3,5) positions make the aromatic ring less susceptible to oxidative degradation. This improves shelf life and offers resistance to metabolic breakdown—qualities that make this derivative especially valuable in active pharmaceutical ingredient (API) research.
Packing two electron-withdrawing atoms onto the ring modifies the acidity of the carboxylic acid group. Reaction conditions that work for unsubstituted cinnamic acid may need adjustment; esterification or amidation, for instance, proceeds with altered rates and can require more potent catalysts. Over years of customer feedback, we have seen researchers achieve higher selectivity in functional group interconversions with this di-fluorinated product compared to its non-fluorinated relatives.
No two cinnamic acids behave quite the same in synthetic schemes. 3,5-difluorocinnamic acid occupies a unique middle ground: it displays higher chemical resilience than the regular compound—without the extreme deactivation that shows up with heavier halogenation or additional electron-withdrawing substituents. This aspect supports its use in iterative cross-couplings and in the generation of bespoke conjugates. Where the non-fluorinated version might undergo rapid side-reactions, this product lets process chemists control transformations with greater predictability.
3,5-Difluorocinnamic acid finds utility far outside the academic bench. We have established partnerships with drug discovery groups that use it as a scaffold for optimizing potential treatments. Upon derivatization, it often appears in proprietary small-molecule inhibitors, imaging probes, and even experimental herbicides. Strong demand comes from medicinal chemists who need to expand chemical diversity in a targeted way without sacrificing physicochemical stability.
Some contract research teams apply the acid directly in Suzuki-Miyaura couplings, where the fluorine atoms modulate electronic properties of the aromatic core, supporting synthesis of more complex biphenyls and styryl systems. Here, batch homogeneity becomes critical; modest variation in the degree and position of fluorination leads to different reactivity patterns or yields unpredictable side-products. The feedback we get from pilot and full-scale users consistently identifies our lot traceability and tight control over isomeric purity as essential to meeting project milestones. Sub-par material, in their hands, translates to weeks of wasted effort amid costly project delays.
Polymer chemists have also found this molecule valuable as a building block for specialty polymers, where its unique physiochemical profile can alter the properties of the resulting materials. This doesn’t just mean a subtle shift in melting point or solubility; in one instance, a customer in electronics development achieved markedly greater resistance to hydrolysis and solvent exposure by incorporating the 3,5-difluorinated moiety, far outperforming non-fluorinated controls. These practical wins matter more than any theoretical feature set.
Our process doesn’t revolve around a generic spec sheet. Every parameter we monitor comes from observing where things go wrong in the lab and in the field. HPLC purity targets the 99% mark as a baseline, and we screen each batch for fluorine content using NMR and ion-selective electrodes to prevent cross-contamination with closely related analogues. Melting point sits reliably in the narrow 165-170 °C range, a signal that crystallization completed as intended. We routinely document particle size and surface area, as variation here changes handling and integration into downstream operations—in a pilot plant setting, flowability and filtration rates hinge on this data.
Our customers tell us repeatability from lot to lot counts for more than hitting a single analytic metric on paper. To back that up, we tie every kilo of 3,5-difluorocinnamic acid to a certificate that details not just the batch data, but notes on storage, recommended shelf-life under real-world conditions, and observed stability in simulated process streams.
Producing fluorinated aromatics can pose significant safety risks and process barriers not encountered with their non-halogenated counterparts. Using reagents like Selectfluor or DAST requires specialized containment and environmental controls, which add complexity to both cost and scale-up. The biggest lesson here has been the significance of reaction time and temperature control—overexposure or overheating invites degradation and the formation of hazardous byproducts like HF, which demand careful abatement and monitoring. We deploy both on-line GC-MS and off-gas capture systems in the process area, reducing potential workplace exposures and helping protect both operators and downstream users from unwanted contaminants.
This isn’t just about production safety. Global demand for fluorinated building blocks has increased, leading to tight raw material supplies and volatile prices for fluorinating agents. Anticipating supply chain hiccups, we’ve expanded secondary sourcing from multiple vetted suppliers and established buffer inventories. The value here shows up not in spreadsheets but in customer testimony: regular buyers report minimal schedule disturbances, despite global disruptions.
Another challenge relates to international regulatory differences concerning fluorinated compounds. Some regions require extensive data on toxicity and environmental persistence before approving shipments. Our technical support team remains engaged with regulatory agencies and client QSAR modelers to proactively document each batch, including any new observations for degradant or impurity profiles. That relationship with the end users and regulatory authorities minimizes clearance times and reduces the likelihood of import hold-ups or recalls.
Scaling from grams to hundreds of kilos per year brought unique learning curves. Flask chemistry doesn’t always translate smoothly; solvent selection, agitation speed, and crystallization conditions interact in subtle ways as equipment volume rises. Early on, we carried over lessons from dozens of parallel reactions, learning which solvents best promote nucleation and which filtration steps allow for full isolation without carryover of amorphous crud. Not every manufacturing run makes the cut for pharmaceutical customers; the margin for error narrows with grams of active etched onto vials destined for clinical work. We reroute off-spec batches to non-pharma applications, making use of the material without compromising the standards our main clients require.
Our engineers traced problems in one sub-optimal campaign to minute changes in solvent evaporation rate caused by seasonal humidity. Losing a single point in purity forced us to recall and reprocess the entire lot—a costly lesson, and one we teach every new staff member. Since then, we’ve implemented fully automated atmospheric controls in our drying and isolation suites, and switched to real-time monitoring of key process parameters like solvent pressure and filter cake temperature. Staying obsessive in the small details produces better, more consistent product that stands up in both research and manufacturing settings.
Production of fluorinated aromatics like 3,5-difluorocinnamic acid rightly raises environmental and health questions. The global conversation about per- and polyfluoroalkyl substances (PFAS) has brought scrutiny to any process that introduces persistent fluorinated organics. The difference here comes from product design and waste management. We have moved away from older fluorination reagents that generate difficult-to-treat byproducts, and now employ closed-loop systems that capture and treat exhaust gases instead of venting them. Solvent recovery units recycle more than 70% of process solvents, and rigorous tracking of waste streams ensures compliant, traceable disposal.
On the worker safety side, continuous review of process hazards, supplemented by real-time air monitoring and regular training, keeps accident rates low. Our approach centers on transparency: all users of 3,5-difluorocinnamic acid receive up-to-date information on any observed safety, health, or environmental hazards, straight from our own experience, not just copied from regulatory databases. Customers often remark that our MSDS packages and handling guidance outmatch typical suppliers, which sources tell us reduces their own risk management workload down the line.
Success in specialty chemical manufacturing rarely comes from flashy marketing. In our experience, buyers keep coming back to suppliers they trust to deliver the right material the first time. We trace each lot of 3,5-difluorocinnamic acid from raw material to final drum, logging every analytic check, process adjustment, and transport step. On rare occasions when a question arises about a previous shipment, we can pull that data in minutes, not days, and work directly with technical teams to resolve the issue before it turns into a disruption.
Our involvement doesn’t end when drums leave the plant. We keep open lines with both R&D and production chemists on the customer side, fielding queries about downstream processing, solubility, or analytical troubleshooting. Many customers report that the interplay of strong technical support and reliable product availability has helped them accelerate development timelines for their small-molecule drug or new material. For some, avoiding a single delayed delivery or failed batch has justified their switch from a lower-cost supplier with spotty support.
Perhaps the hardest challenge faced in the fluorinated intermediates sector remains cost fluctuation. Feedstock prices wobble with every regulatory change or trade disruption. We maintain transparency about these realities: for returning buyers, we lock in advance commitments when possible, and offer insights into upcoming market trends—supported by data from global chemical exchange platforms. For new users, we break down pricing structures and detail what goes into each euro, dollar, or yen, including specific cost drivers like purification time or increased safety requirements. We find buyers value this candor over price wars that ignore the realities of fine chemical production.
Looking at the industry shift toward specialized, functionalized building blocks, we see growing numbers of small startups, university spinoffs, and process development teams adding 3,5-difluorocinnamic acid to their arsenals. For those new to its chemistry, we recommend starting with small scale reaction screens before committing precious process time to kilo quantities—experience shows subtle changes in substitution can change not just yields, but stereochemistry or downstream process robustness. We support this approach with detailed application notes and real-world case studies, many developed in partnership with customers who faced and overcame practical roadblocks at scale.
For pharmacological innovators, the value in using this precisely substituted cinnamic acid relates not just to chemical reactivity, but to improved metabolic resistance and pharmacokinetics compared to less substituted analogues. Users in the polymer and advanced materials sectors, on the other hand, gain functional diversity without losing the workflow compatibility afforded by the simple cinnamic acid core—meaning insertion into existing process chains without rewriting established protocols.
The field doesn’t stand still. As more ambitious chemistries arrive—heteroatom variation, complex cross-couplings, continuous flow reactions—the requirements for tailored building blocks like 3,5-difluorocinnamic acid continue to evolve. We actively collaborate with academic and industrial partners to improve process yields, lower waste, and reduce energy usage without eroding the purity customers demand. Selected R&D campaigns have even shifted production from older batch reactors to flow chemistry units, reducing footprint and allowing for safer, quicker scale transitions.
One thing has become crystal clear through supplying this material: today’s advances come from the intersection of tight process control, total supply chain visibility, and lived-on-the-floor production know-how. We continue to invest in both new plant technologies and in the technical training of our staff, betting that the next breakthrough our product supports will be made possible by the details we sweat today—so that chemists and engineers worldwide can keep forging ahead, undistracted by doubts about raw material quality.
Stepping back, 3,5-difluorocinnamic acid might seem like just one more entry in the roster of fine chemical intermediates. The difference lies in hands-on commitment taken from every kilo we produce, every drum we ship, every customer we support through every phase of their development journey. As demand for reliable, high-purity fluorinated intermediates accelerates, we know the future will bring both unknown challenges and new opportunities—and based on experience, thoughtful investment in people, process, and partnership will keep this essential material in the hands of those pushing the boundaries of chemistry forward.