|
HS Code |
292745 |
| Product Name | 2-Fluorobenzoyl Chloride |
| Cas Number | 394-45-8 |
| Molecular Formula | C7H4ClFO |
| Molecular Weight | 158.56 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 218-220°C |
| Melting Point | -2°C |
| Density | 1.355 g/mL at 25°C |
| Refractive Index | 1.552 |
| Purity | Typically ≥98% |
| Solubility | Reacts with water, soluble in organic solvents |
| Flash Point | 89°C (closed cup) |
| Chemical Structure | FC6H4COCl |
| Synonyms | o-Fluorobenzoyl Chloride |
| Smiles | O=C(Cl)C1=CC=CC=C1F |
As an accredited 2-Fluorobenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g, tightly sealed with a PTFE-lined cap; labeled with hazard symbols, product details, and safety information. |
| Shipping | 2-Fluorobenzoyl chloride is shipped as a hazardous material under strict regulations. It must be packaged in tightly sealed containers, clearly labeled, and transported in accordance with local and international guidelines for corrosive and toxic chemicals. Appropriate documentation and handling precautions are required to ensure safety during transit. |
| Storage | 2-Fluorobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as water, alcohols, and strong bases. It must be kept under inert atmosphere (like nitrogen) to prevent hydrolysis. Store in a chemical fume hood and label clearly as corrosive and moisture-sensitive. |
Applications of 2-Fluorobenzoyl Chloride in Industrial ManufacturingAs a direct manufacturer specializing in aromatic acyl chlorides, we supply 2-Fluorobenzoyl Chloride to advanced industrial sectors globally. Its precise reactivity supports multiple value-added downstream processes, particularly in pharmaceutical intermediates, agrochemical actives, and specialty materials. The following scenarios illustrate its established applications, manufacturing integration details, compliance focus, and formulation benchmarks in real industrial settings. 1. Pharmaceutical Intermediate for Fluorinated Benzamide APIsOur 2-Fluorobenzoyl Chloride is a key acylation agent in the synthesis of fluorinated benzamide intermediates, which serve as building blocks for antipsychotic, anticancer, and anti-inflammatory drugs. Customers typically conduct Friedel-Crafts acylation reactions using this material to introduce the 2-fluorobenzoyl group onto amine-containing scaffolds, enabling specific binding properties and metabolic profiles in the final APIs. Production environments require complete traceability and analytical assurance throughout every reagent stage. Industry compliance standards
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2. Synthesis of Agrochemical Active CompoundsMajor crop protection producers use our material for acyl chlorination during the synthesis of selective herbicide and fungicide actives featuring fluorinated benzoyl groups. These groups enhance agrochemical performance by optimizing lipophilicity and environmental persistence. 2-Fluorobenzoyl Chloride is commonly implemented in acylation steps to tailor active site specificity and application longevity in the end-use formulation. Industry compliance standards
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3. Fine Chemical Building Block for Aromatic Liquid Crystal Polymers (LCPs)Producers of advanced materials incorporate 2-Fluorobenzoyl Chloride during polymerization to introduce controlled fluorinated moieties into aromatic polyester chains. Such modification enhances thermal stability, chemical resistance, and dielectric properties of high-performance LCPs. Strict process and materials standards demand that our chlorinated intermediates maintain consistent purity and minimal residual moisture to avoid negative impact on final polymer properties. Industry compliance standards
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4. Custom Synthesis of Fluorinated Aromatic Reference StandardsSpecialty chemical laboratories and analytical standards suppliers use 2-Fluorobenzoyl Chloride to acylate selected amines and heterocyclic scaffolds, creating bespoke fluorinated aromatic standards for chromatographic and spectroscopic calibration. Our material supports ultra-high purity demads, with batch traceability and impurity profiling, ensuring suitability for regulated instrumental analysis in quality control and research environments. Industry compliance standards
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Standing directly at the reactor vessel, feeling the pulse of temperature controls and watching the conversion rate tick up on the monitor, the significance of products like 2-fluorobenzoyl chloride (often referenced by its CAS number, 394-45-8) becomes unmistakable. There’s a lot of talk in the market about chlorinated aromatic intermediates, but not enough discussion about what makes each one tick, and what that means for the end user on the factory floor. Our production team sees firsthand the difference that a tailored fluorobenzoyl chloride can make in downstream efficiency, purification, and overall product performance.
Years in the manufacture of benzoic acid derivatives have taught us that not all customizing happens in a laboratory notebook—much comes down to the conditions within the reactor, the purity of hydrogen fluoride, and how fast you bring down the process temperature after chlorination. Minor deviations can shift impurity profiles, especially for halogenated benzoyl chlorides like this one. The market often treats 2-fluorobenzoyl chloride as a simple intermediate, but the story doesn’t end with a molecule on a spec sheet. Consistent melting point, reliable assay, and a physical appearance free from residual color or oligomeric impurities—these all reflect the discipline of the production line, not just the job of QC at the endpoint.
We don’t rely on generic suppliers for raw ingredients. Years ago, variations in the electronic grade of fluorinated toluene fed into unwanted side reactions, especially during large-batch operations. The industry often sees fluctuations in product clarity and pungency, which end users only discover after mixing into amide or ester synthesis. To address this, we refined both feedstock selection and purification columns, pushing finished 2-fluorobenzoyl chloride to a minimum GC assay above 99% on a lot basis, and holding hydrolyzable chloride levels stable. Every drum we fill comes off a line designed around these reactions, not adapted to them.
Laboratory-sourced batches may register a sharp, colorless appearance, but it’s in multi-ton production that subtle challenges arise—water ingress from storage, variable ambient humidity, or residual solvent from purification. We keep moisture content below 0.3% and stick to environmentally stable packaging, not just for transportation safety, but because even slight hydrolysis during storage can sabotage downstream acylation steps. Customers working with pharmaceutical or fine chemical targets frequently provide feedback on how reduced trace moisture cuts down purification steps and improves finished yields. We produce 2-fluorobenzoyl chloride in liquid form, targeting a density consistent with 1.32–1.34 g/ml at ambient temperatures, which supports automated dosing on complex assembly lines.
Processors find this intermediate most valuable when producing fluorinated benzamides, esters, or fine agrochemical compounds. The ortho-fluoro positioning influences reactivity across a range of subsequent derivatizations—not simply as a novelty, but because electron-withdrawing substitutions tweak both lability during coupling reactions and the stability of final active ingredients. Over the years, we have adjusted batch parameters based on close technical dialogues with customers developing APIs such as fluoroquinolone antibiotics or tailored photovoltaic materials, where a small impurity can create regulatory headaches or unexpected photostability problems.
End users often ask us about switching between 2-fluorobenzoyl and its isomers, like 4-fluorobenzoyl chloride, or stepping back to non-fluorinated benzoyl chloride. These are not interchangeable. The 2-fluoro group brings a steric twist and electron-density effect that changes both reactivity and by-product formation during amide coupling and Friedel–Crafts installation. We’ve helped process engineers troubleshoot unexpected tar formation when attempting a direct swap with para-fluoro analogs. The ortho effect manifests not only in lab data, but in the speed and clarity of final product crystallization—an aspect that carries real consequence for waste management and solvent recycling.
Running hundreds of tonnes through our system each year, we routinely validate batch reactivity using high-throughput microreactors—never just spot-check HPLC. Routine analysis traces batch-to-batch consistency for color (APHA less than 20), acidity, and trace metal content, providing a profile that synthetic chemists can trust. These figures go beyond generic claims: one pharmaceutical customer noted a reduction in by-product load during amide formation, tying directly to our process purity improvements implemented in 2021. These types of improvements, hard-won through iterative batch engineering, enable formulation chemists to streamline downstream workups.
Maintaining the integrity of 2-fluorobenzoyl chloride calls for care, since it reacts with moisture and produces sharp, irritating fumes. Factory experience has led us to shift from bulk barrels to lined jerry cans for smaller customers, protecting against product degradation in humid seasons. In our own facility, we deploy closed-transfer systems and rapid venting lines to prevent pressure buildup—not just out of regulatory obligation, but because residual pressure and unplanned venting can contaminate both the finished material and the work environment. All these adaptations grew directly out of real incidents, not just regulatory recommendations.
Many specialty companies still hand-charge these intermediates under fume hoods, but our own in-house fine chemical department runs jacketed, automated vessels that meter in 2-fluorobenzoyl chloride under controlled temperature with nitrogen blanketing. Monitoring everything from pressure spikes to thermal exotherms, we get clear data on how small shifts in reagent grade and dosing speed affect coupling efficiency, especially during synthesis of fluorinated benzanilides. Several customers in the dye and pigment industry have integrated our material straight into automated batch synthesis, thanks in part to its consistent flow characteristics and reliable reaction profile.
Lab-scale methods frequently hide limitations, especially related to solvent miscibility and heat release. We have scaled up 2-fluorobenzoyl chloride production using a proprietary multi-stage chlorination system, which responds tightly to real-time temperature feedback. This approach reduces risk of secondary halogenation, an issue that arises in older glass-lined reactors when scaling up from gram to multi-ton batches. We also judge every new batch of raw material against in-process titration results, not just supplier certificates, based on a lesson learned years ago after a run of out-of-specification product led to a significant recall for a downstream API manufacturer.
Having walked the production floor through two decades of shifting regulations—including updates in ICH impurity guidelines—we continue refining our protocols to keep phosphate, heavy metal, and other residuals to levels far below regulatory maxima. This matters to our partners, especially during FDA and EMA audits, where certificate data alone cannot substitute for a verifiable, reproducible manufacturing history. The difference between good and great batches often shows up in HPLC baseline flatness, not just peak value, and this is where continuous process control pays off.
Repeated exposure to chlorinated aromatics demands strict procedures. Our operators suit up with appropriate canister masks and triple-gloved handling protocols—a routine developed after visible corrosion to valve seats highlighted air moisture ingress several years back. Regular air-quality monitoring and emergency stopper stations line our workspaces for this reason. These may seem like small details, but anyone who’s cleaned up a spill in humid weather can appreciate what’s at stake both for worker safety and for the final compound’s purity.
Every batch we release tracks back to root-cause analysis when a deviation arises, whether it’s brought up by in-house teams or long-standing clients. A few years back, an uptick in carbonyl impurity pinpointed to a heat exchanger inefficiency pushed us to invest in titanium-lined cooling coils. This update resulted in better control over the exothermic chlorination phase and, ultimately, a step increase in product stability. Simple fixes such as vacuum-purged drying cycles have likewise trimmed residual moisture, bringing measurable improvements for synthesizing downstream products like fluorinated pharmaceutical intermediates.
Consistent communication with customers running pilot or full-scale operations shapes our approach. One partner in the agrochemical field shared that the reduction in trace acid contaminants allowed direct transfer into esterification, skipping a pre-neutralization wash. In the solar material sector, producers commented on the lessened off-gassing and how it shortened their post-reaction cycling time. Feedback like this steers us toward process changes; over the years, it has nudged our quality group to implement online FTIR for quicker, tighter QC.
Worldwide demand patterns for fluorinated aromatic intermediates shift in response to regulatory changes and new material science innovations. As US and European markets set stricter impurity control thresholds for pharma precursors, our team uses this knowledge to plan upgrades—a shift from batch documentation to real-time data logging, or investments in refrigerated storage that extends shelf life and prevents in-transit degradation. Each adjustment flows not from boardroom theory, but directly from shifts we witness on the shop floor and in our clients’ requests.
Chemically, subtle differences add up to significant process impacts. The ortho-fluorine atom lowers electron density near the acyl chloride, accelerating certain acyl substitution reactions while boosting selectivity in those needing both electron-withdrawing and steric effects. Our teams worked with research labs facing low yields from generic benzoyl chloride and observed marked improvements (in both yield and crystallization speed) using this compound, with fewer insoluble by-products formed. These improvements carry straight through to commercial-scale synthesis, where batch consistency makes or breaks project deadlines.
Each batch we produce reflects knowledge gained in demanding settings—where operational stability and performance trump catalog specs. We engage with end-users from synthetic organic chemists to scale-up engineers, incorporating their feedback into every run. Control over feedstock quality, combined with process integrity and an unwavering commitment to safe, reproducible outcomes, sets our 2-fluorobenzoyl chloride apart in a crowded field. We bring product to market that lives up to real-world needs, not just theoretical claims—a philosophy that’s earned us trust among both established and cutting-edge process innovators.