|
HS Code |
611541 |
| Product Name | 4-Chloro-3-Fluorobenzoic Acid |
| Cas Number | 403-41-8 |
| Molecular Formula | C7H4ClFO2 |
| Molecular Weight | 174.56 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 174-176 °C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents (ethanol, methanol, DMSO) |
| Density | 1.53 g/cm³ |
| Smiles | C1=CC(=C(C=C1C(=O)O)Cl)F |
| Inchi | InChI=1S/C7H4ClFO2/c8-6-2-1-4(7(10)11)3-5(6)9/h1-3H,(H,10,11) |
| Storage Temperature | Store at room temperature (2-8°C) |
As an accredited 4-Chloro-3-Fluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle with a tight screw cap, labeled "4-Chloro-3-Fluorobenzoic Acid, 25g," including hazard symbols and chemical details. |
| Shipping | 4-Chloro-3-Fluorobenzoic Acid is shipped in tightly sealed containers to prevent moisture entry and contamination. The package is clearly labeled with hazard information, handled as a non-combustible, stable solid. It is shipped in accordance with local regulations, typically via ground or air freight, and must be stored in a cool, dry place. |
| Storage | 4-Chloro-3-Fluorobenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect it from moisture and direct sunlight. Store at room temperature and ensure that the container is properly labeled. Follow all relevant safety, health, and environmental regulations when handling and storing this chemical. |
Applications of 4-Chloro-3-Fluorobenzoic Acid in Industrial ManufacturingWe supply 4-Chloro-3-Fluorobenzoic Acid for specialized industrial applications. Our material supports core production in high-value chemical sectors, offering reliable input for precise chemical synthesis across advanced downstream manufacturing verticals. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical facilities incorporate 4-Chloro-3-Fluorobenzoic Acid as a key intermediate in the production of systemic APIs, specifically targeting heterocyclic and substituted benzoic core-based compounds. The acid group and halogen moieties enable site-selective coupling, halogen exchange, and condensation in custom route design, particularly for oncology therapeutics, CNS drugs, and anti-inflammatory agents. Production chemists adjust stoichiometry to achieve yield targets in multistep syntheses. All operations maintain cGMP compliance at every phase, with extensive in-process and final batch analytical verification. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis for Herbicide and Fungicide Active IngredientsMajor agrochemical producers integrate this compound for the synthesis of halogenated aromatic rings used in selective herbicides and fungicides, particularly for products targeting broadleaf weeds and resistant fungal strains. The fluorinated and chlorinated benzoic acid backbone facilitates downstream esterification, amidation, and heterocycle formation, yielding high stability end products. Batch sizing and application vary based on regulatory pre-harvest interval (PHI) and crop-specific residue tolerances, with documentation for agricultural and environmental compliance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Building Block for Liquid Crystal Monomer SynthesisManufacturers of liquid crystal monomers employ 4-Chloro-3-Fluorobenzoic Acid as an essential raw material for producing mesogenic compounds used in high-definition display technologies. The strategically positioned halogen atoms impart thermal stability and defined electronic properties necessary for high-performance optoelectronics. Stringent purity standards apply, as the consistency of the acid influences downstream alignment layers and switching parameters. Integration follows upstream purification and activation for high-yield esterification or amidation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Precursor in High-Performance Polymer ManufacturingProducers of specialty polymers and copolymers utilize this benzoic acid derivative to introduce tailored halogen functionality into polymer chains, enhancing chemical resistance, flame retardancy, and mechanical stability. Applications include advanced coatings, industrial adhesives, and specialty films. The acid serves as a comonomer or chain end modifier, depending on the specific synthetic route. Precise dosage and reaction sequencing ensure target molecular weight distribution and polymer architecture. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Intermediate for Fine Chemical and Specialty Chemical SynthesisManufacturers in the fine chemicals sector use our material to introduce dual halogen and carboxyl functionality into custom molecules, serving as a scaffolding for the synthesis of specialty aromatics, advanced organic building blocks, and performance additives. The compound functions as a substrate for decarboxylation, halogen exchange, or directed ortho-metalation, enabling multi-step synthesis of tailored molecules demanded in electronics, advanced coatings, and analytical standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-Chloro-3-Fluorobenzoic 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 sales7@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
We manufacture 4-chloro-3-fluorobenzoic acid from raw materials handled within our own facilities, so every batch reflects hands-on experience gathered over years of production. This specialty compound, with the chemical formula C7H4ClFO2 and CAS number 1645-83-6, stands out as a crucial building block for pharmaceutical synthesis, crop protection research, and advanced material applications. Our team has worked closely with formulators and process engineers across several sectors, seeking out where this molecule truly makes a difference.
The distinct combination of a chlorine atom at the four position and a fluorine atom at the three position on the benzene ring gives this benzoic acid derivative unique reactivity. We observe that its electron distribution enables highly selective downstream functionalization, making it popular among chemists aiming for efficient construction of more complex products. The acid group also provides a stable anchor point for further derivatization, opening multiple synthetic routes in both laboratory and manufacturing environments.
Throughout our manufacturing, we monitor batch purity using HPLC and NMR, reaching a minimum purity of 99%. Purity control is not just a number – it determines whether your reactions deliver the same outcome consistently. Impurities in these kinds of acids often act as poisons in later synthesis steps, so direct control over the upstream inputs pays off in the reliability and yield of customer reactions downstream. Moisture, color, and trace contaminants all affect the ease with which you can isolate or purify your final products.
4-chloro-3-fluorobenzoic acid sets itself apart from isomeric or related fluoro/chloro-substituted benzoic acids by the unique reactivity of its specific substitution pattern. Colleagues in medicinal chemistry repeatedly report improved regioselectivity and enhanced yields in cross-coupling or amide-formation reactions, compared to more common analogs like 2-chloro-4-fluorobenzoic acid or plain 4-fluorobenzoic acid. The electron-withdrawing effect of both halogens, arranged ortho and meta to the acid group, creates a scaffold for constructing more complex heterocycles or for introducing new substituents with precision.
One key difference we offer versus stock-bottle distributors lies in process transparency. Because we run the whole synthesis under our roof—from halogenation to final acidification and purification—control over every step allows us to adjust to unique customer specifications. Customers frequently approach us to tweak aspects like particle size, crystalline form, or grade requirements. Staying close to the actual chemistry, rather than pushing paperwork, means we target these adjustments quickly.
Years of running halogenations in a purpose-built reactor train has taught us vigilance. Both selective fluorination and chlorination bring challenges for yield and impurity control. Rather than rely on bulk halogenated benzoic acids (which can suffer batch-to-batch variability), we draw on our own optimization work: altering reaction times, solvent ratios, and quench conditions to hit the purity and flow properties the market expects. Finished product comes as a white or off-white crystalline powder, free-flowing, with bulk density measured with each lot. This lets downstream handlers calibrate their dosing and handling—tiny details that translate to lower waste and easier processing.
In pharmaceuticals, intermediates like 4-chloro-3-fluorobenzoic acid serve as starting points for nonsteroidal anti-inflammatory drug candidates, some kinase inhibitors, and APIs under investigation for treatment of viral infections. Crop protection researchers find value in this building block, especially where both halogens provide metabolic stability in field trials. Our own engagement with these sectors lets us understand which lot attributes matter most—low impurity burden, controlled moisture, and persistent free-flowing consistency (even in humid climates).
In manufacturing settings, every minute spent cleaning blocked hoppers or troubleshooting poor solubility can mean hours lost. We learned that too fine a particle size means dusting and handling loss, while too coarse causes handling and mixing issues. Working with customers, we dial in a controlled particle size range to minimize such headaches. Our adjustment of drying conditions and grinding protocols comes straight from long stints in our own process areas—not a one-size-fits-all specification, but a partnership approach.
The carboxylic acid group on 4-chloro-3-fluorobenzoic acid offers options for converting into amides, esters, or for participating in coupling with a variety of heterocycles and APIs. Medicinal chemists use this intermediate to rapidly test new analogs, often relying on its unique substitution to produce bioactive molecules with fine-tuned properties. Specialized polymers and liquid crystals also take advantage of substituted aromatic acids for enhanced temperature stability or unique dielectric profiles, bringing the reach of this compound well beyond pharmaceuticals.
Controlling halogenated intermediates raises safety and environmental stakes. From raw material sourcing through to shipment, we comply with local and international regulations, including REACH and applicable TSCA reporting requirements, to ensure stakeholders stay informed about what’s entering their process stream. Our waste management and effluent treatment have been shaped by years of dealing with halogen byproducts. In addition to internal audits and staff training, we continuously review ventilation, containment, and PPE requirements, adjusting procedures to maintain high standards.
We blend process chemistry with practical packaging. All shipments are vacuum-sealed and nitrogen-purged where moisture matters. Packaging materials resist halogen-induced brittleness and provide a barrier against ingress of contaminants. Years ago, using off-the-shelf containers led to trace moisture issues during ocean shipping—resulting in clumping in the final product. Redesigning the packaging and including humidity indicators during transport saved downstream users from surprise headaches, especially in tropical or high-humidity locations.
During project discussions, researchers often ask about differences compared to similar compounds. The structural difference between 4-chloro-3-fluorobenzoic acid and others like 2-chloro-4-fluorobenzoic acid or 3,5-dichlorobenzoic acid goes beyond the raw position of substituents. Our bench-scale R&D group reports that this compound enables higher selectivity in Suzuki couplings or amidation reactions, largely because the combined electron-drawing effects fine-tune reactivity both at the ring and carboxyl positions.
While simpler benzoic acid derivatives, such as 4-fluorobenzoic acid or 4-chlorobenzoic acid, can be easier to source, results in advanced applications can be unpredictable. Unreacted or over-reacted impurities have a way of deactivating catalysts or introducing byproducts with similar chromatographic retention times to desired targets. Seeing these issues in our own downstream pilot lines taught us the necessity of clean, high-purity starting material. Even a 0.2% impurity by HPLC sometimes pushed product yields down by over 10%, especially in sensitive transformations.
Our product draws demand not because of broad use in commodity chemistry, but from tasks where subtle differences in substitution mean the difference between good and great experimental outcomes. The chlorofluoro pattern provides an optimal balance for those needing reliable reactivity without sacrificing compound longevity under process heating or storage. Our in-house experience with long-term storage conditions means each drum can be relied upon, even after months in a customer warehouse.
Over time, close relationships with research labs and process chemists have deepened our understanding of practical needs. For those developing proprietary routes to APIs or agrochemical actives, access to reliable, clean, and specification-compliant intermediates makes the difference in bringing new molecules to commercial scale. Years ago, a partner’s scale-up for an investigational oncology drug candidate stalled when contaminants from a substitute supplier knocked the subsequent ring closure off target. After switching to our controlled-purity input, yields stabilized, and their pilot lot finally cleared QA.
The lesson remains: consistency at this intermediate stage shapes both speed and success of final-stage development. Across the product lifecycle—from early discovery, through development, and into commercial runs—minimizing input variability translates to fewer surprises and shorter troubleshooting cycles. Feedback from scale-up chemists shows they value batch records and traceability over generic paperwork alone; our lot documentation traces every input through production and final QC release, supporting robust documentation needs during regulatory filings.
Customizations have grown more common. Higher-purity single lots, streamlined particle sizing, and limited ultra-low metal specifications often arrive as customer requests. Because we control every processing variable ourselves, these are rarely obstacles: we adjust our dry-down or purification steps in direct response to technical needs, not marketing language. This feedback loop shapes both technical specs and our long-term process improvements.
Supply chain disruptions in recent years have reiterated how crucial it is to work directly with producers who stay invested in technical control and documentation. Our ongoing investments in analytical equipment and user training keep us ahead of the curve, not just for internal assurance, but for customer audits and regulatory submission support. We do not outsource production; every drum originates on our own lines, and technical staff stand ready for clarifications when project teams require traceability or deeper analytical details.
Our technical managers have walked customers through solubility studies, reactivity trials, and even on-site recalibration of their handling systems. Application engineers working with us lean on our direct experience with how crystal habit or moisture load influences process yields and storage behavior—not only in controlled-lab settings, but in pilot and production-scale realities. Our feedback loop with end-users shapes our future adjustments and emphasizes our dedication to reproducible outcomes batch after batch.
With continued interest in halogenated benzoic acid derivatives, we anticipate growing demand from both pharmaceutical and specialty chemical spaces. New methods in synthetic chemistry continually redefine what intermediates bring the most value. Our focus remains on robust purity, reliable supply, and actionable technical support, since these factors directly drive project timelines and quality. Every year, regulatory environments grow more complex, and audit expectations climb. Our open-book approach allows partners to track chain of custody and compliance details rapidly.
From a broader perspective, sustainability remains high on our agenda. The manufacture and handling of halogenated aromatic compounds demand careful control of emissions, waste, and resource consumption. Our operations incorporate solvent recycling, waste minimization, and ongoing upgrades to both containment technology and worker safety measures. By choosing to keep all steps within our organization, we offer direct accountability not just on product specs, but on environmental stewardship as well.
Real-world experience reminds us that success in specialty chemicals comes from unwavering attention to the details—from impurity profiling and logistics to technical dialogue and after-sales support. For 4-chloro-3-fluorobenzoic acid, the quality of the intermediate often acts as an early warning system for any broader development issues. To our team, every lot tells a story of chemistry, collaboration, and continuous process evolution.