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6-Chloro-2-Fluoro-3-Methylbenzoic Acid

    • Product Name 6-Chloro-2-Fluoro-3-Methylbenzoic Acid
    • Alias 6-Chloro-2-fluoro-m-toluic acid
    • Einecs 662-056-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    789431

    Productname 6-Chloro-2-Fluoro-3-Methylbenzoic Acid
    Molecularformula C8H6ClFO2
    Molecularweight 188.59 g/mol
    Casnumber 935272-21-6
    Appearance White to off-white solid
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO, methanol
    Purity Typically ≥ 98%
    Smiles Cc1cccc(C(=O)O)c1ClF
    Inchi InChI=1S/C8H6ClFO2/c1-5-2-3-6(8(11)12)7(9)4-10-5/h2-4H,1H3,(H,11,12)
    Storagetemperature Store at 2-8°C

    As an accredited 6-Chloro-2-Fluoro-3-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "6-Chloro-2-Fluoro-3-Methylbenzoic Acid, 25g, for research use only," with tamper-evident seal.
    Shipping 6-Chloro-2-Fluoro-3-Methylbenzoic Acid is shipped in a tightly sealed container, with clear labeling and documentation. The package is cushioned to prevent breakage and handled as a chemical substance, complying with relevant regulations for safe transport. Avoid exposure to extreme temperatures, moisture, and direct sunlight during shipping.
    Storage 6-Chloro-2-Fluoro-3-Methylbenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Keep away from incompatible materials such as strong oxidizers and bases. Ensure the storage area is clearly labeled, and that access is restricted to trained personnel, following standard chemical safety protocols.
    Application of 6-Chloro-2-Fluoro-3-Methylbenzoic Acid

    Applications of 6-Chloro-2-Fluoro-3-Methylbenzoic Acid in Industrial Manufacturing

    6-Chloro-2-Fluoro-3-Methylbenzoic Acid serves as a key intermediate in several high-value industry chains. Our production quality, batch consistency, and traceability support manufacturers in active pharmaceutical ingredient synthesis, agrochemical intermediate formation, specialty dye engineering, and advanced polymer development.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    This compound functions as a core building block during the multi-step synthesis of third-generation fluoroquinolone antibiotics and other halogenated benzoic acid derivatives used in prescription drug manufacturing. Its halogenated aromatic structure enables coupling reactions in the downstream multistep process, contributing chlorine and fluorine sites vital for intended pharmacological activity and metabolic profile manipulation. In regulated settings, our on-site QC and impurity tracking ensures downstream partners meet stringent pharma guidelines for product safety and regulatory compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs)
    • China NMPA guidelines for pharmaceutical raw materials
    • US Pharmacopeia (for intermediates traceability, not direct APIs)

    Typical usage ratio

    • 5–18% by mass in key stages, adjusted based on specific pharmaceutical target and coupling partner reactivity
    • Stoichiometric or slight excess for coupling reactions to ensure complete conversion and minimize downstream purification

    Downstream process integration

    • Introduced at the initial acylation or halogen-exchange step during pharmaceutical intermediate synthesis
    • Used during Pd-catalyzed cross-coupling or amidation with elaborated side chains following Grignard or Suzuki processes
    • Input at step two or three in fluoroquinolone backbone construction

    Final product types

    • Oral and injectable fluoroquinolone APIs (e.g., besifloxacin, finafloxacin, nemonoxacin)
    • Other halogenated benzoic acid derivatives for generic APIs
    • Intermediates for anti-infective or anti-inflammatory drugs

    2. Agrochemical Synthesis Building Block

    Our 6-Chloro-2-Fluoro-3-Methylbenzoic Acid plays a fundamental role as a carbon framework precursor in the agrochemical pipeline for active ingredients targeting pest and weed management. In high-volume herbicide and fungicide manufacture, formulators leverage its reactive halogen groups to introduce further substituents under controlled conditions, supporting yield stability and compound specificity in the final formulation. Melting point control, isomeric purity, and minimal metal residuals are tightly monitored for downstream scale-up batches.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • ISO 9001:2015 for process documentation
    • China GB 2763 for residue control in agrochemicals
    • REACH registration for use in European plant protection products

    Typical usage ratio

    • 14–22% by weight in the initial synthetic stage of target agrochemicals
    • Batch-specific ratios set by required ring substitution pattern for active structures

    Downstream process integration

    • Fed into initial condensation or chlorination sequence during synthesis of agrochemical actives
    • Employed in halogen rearrangement steps before formulation blending
    • Processed in solution-phase or solid-phase synthesis reactors

    Final product types

    • Selective herbicide technical concentrates
    • Fungicidal active ingredients for foliar spray
    • Pre- and post-emergence weed control formulations

    3. Specialty Dye and Pigment Manufacturing

    6-Chloro-2-Fluoro-3-Methylbenzoic Acid is utilized for constructing highly specific halogenated and fluorinated dye intermediates in colorant production. Dye manufacturers require stable ring frameworks for color-fastness and light resistance in technical textile coatings and high-surface-area plastics. Manufacturers tune molecular substitutions via controlled reaction with diazo or azo coupling partners, resulting in improved dye structural integrity and intense color yield for automotive, industrial, and electronic applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for textile safety and environmental requirements)
    • ISO 9001:2015 for specialty dye batch control
    • RoHS Directive (for electronic device pigment use)
    • REACH Annex XVII (restrictions on aromatic amines and halogenated substances)

    Typical usage ratio

    • 8–16% by molar ratio depending on multi-ring colorant structure
    • Adjusted for desired aromatic ring density and hue characteristics

    Downstream process integration

    • Charged at diazotization or coupling reaction phase for azo dye precursor synthesis
    • Used during directed nitration prior to pigment cyclization
    • Input at ring-substitution stage for high-performance pigment manufacture

    Final product types

    • High-stability textile dyes for performance fabrics
    • Aromatic pigment intermediates for plastics and films
    • Special colorants for electronic ink and automotive coatings

    4. Fluorinated Polymer and Advanced Material Components

    The raw material acts as a specialty monomer precursor in high-durability fluorinated and chlorinated polymer systems. Industrial polymer engineers incorporate this benzoic acid into sidechain-modified polyesters and polyamides requiring improved chemical resistance, thermal stability, and wettability for technical coatings, electronics encapsulation, and membrane materials. Our material quality ensures molecular weight control, lot-to-lot reproducibility, and assures low ionic contaminant content for high-purity applications.

    Industry compliance standards

    • ISO 14001 for environmental management in polymer operations
    • ASTM D638, D790 for mechanical property validation
    • RoHS Directive (for high-performance technical application safety)
    • UL 94 flammability classification for end-use polymers

    Typical usage ratio

    • 3–9% by mass as co-monomer or end-capping agent in specialty resin production
    • Modification level determined by polymer performance target (e.g., higher for chemical resistance, lower for flexibility)

    Downstream process integration

    • Added during polycondensation as structural modifier or end-group capping agent
    • Incorporated at copolymer synthesis stage with other halogenated units
    • Used in feedstock blending for membrane or encapsulant extrusions

    Final product types

    • Fluorinated polyester and polyamide technical films
    • Durable coatings for electronics and automotive surfaces
    • Membrane materials for filtration and separation processes
    Free Quote

    Competitive 6-Chloro-2-Fluoro-3-Methylbenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 6-Chloro-2-Fluoro-3-Methylbenzoic Acid

    Practical Insights Straight from the Production Floor

    We have spent years working with aromatic halogenated acids, and much of our expertise comes from making sure every batch meets the requirements voiced by professionals in fine chemicals, agrochemicals, and pharmaceutical research. 6-Chloro-2-Fluoro-3-Methylbenzoic Acid, known by its CAS number 158062-76-1, stands out in our line-up. The structure features a chlorinated position at the 6th carbon, with fluoro and methyl substituents at the 2nd and 3rd carbons. This gives it an advantage in many synthesis sequences, especially where handling select substitution matters just as much as the acid’s performance in subsequent steps.

    During years of production, our teams quickly discovered that the dual halide arrangement in this molecule supports unique reactivity—it is favored in building blocks for specialty intermediates. The pronounced electron-withdrawing influence from the chlorine and fluorine atoms impacts how this acid behaves in electrophilic aromatic substitution, which draws attention for those working with complex halogenated pharmaceuticals. When comparing this compound to similar benzoic acids, the difference in reactivity becomes clear. The methyl group on the 3-position offers a distinct twist—fine-tuning physical properties like melting point, solubility, and downstream compatibility.

    Technical requirements are not just numbers on paper for us. Product consistency depends on tight batch control and the habit of checking incoming and outgoing purity, color, and moisture data. Through regular feedback from partners in applied research, we maintain purity levels not lower than 98%, with typical results running above 99%. Our HPLC and GC methods get checked against trusted primary standards. Lumps, caking, and contamination are issues we don’t ignore; our production teams handle these complications with strict attention to storage conditions and immediate reprocessing when needed. End users see the benefit—material behaves predictably whether run on pilot scale or in full production.

    Comparing Chemical Performance and Application Reach

    Aromatic carboxylic acids may seem interchangeable at first glance, but we noticed over time that professionals spot subtle differences during actual use. Substitution patterns strongly affect yield and selectivity in coupling reactions or halogen-metal swaps. Either in esterification or amidation, this molecule’s activity profile is impressive. The electron density shaped by the halides and methyl group moves certain transformation points, so each reaction step draws a different kind of outcome than a simple benzoic acid or an ortho/meta-substituted version.

    Those producing crop protection agents often prefer 6-Chloro-2-Fluoro-3-Methylbenzoic Acid due to cleaner conversion rates, with less troublesome by-products from over-halogenation or side-chain elimination. Chemical engineers in pharmaceutical plants have told us for years that this material can survive harsher process conditions. The reason—its halide confidence, delivering robust resistance to hydrolytic and oxidative agents that tend to degrade other carboxylic acids. When pressure mounts in downstream filtrations or crystallizations, our fine crystalline product allows low-dust handling, reducing material loss in humid or open-air production environments.

    We built our batch protocols based on real trial-and-error. Each alteration to crystallization or solvent removal shows up right away in the quality of the acid. Early on, residual solvents like chlorobenzene or acetonitrile raised alarms; our crew switched to optimized systems, using rotary evaporation and vacuum tray dryers to drive solvent content below 0.2%. Customers in regulated markets prioritized this, since solvent carryover interfered with trace analysis further down the production line. Consistency matters, not just for documentation, but in the real cost of plant downtime or explosive waste reactions.

    Quality from Source to Shipment

    Selection of chlorinated aromatic starting materials is something we managed very carefully. Even the smallest difference in feedstock purity or supplier contamination triggers deviations in our acid’s analytical profile. Operators pre-filter every batch, involving multi-stage liquid-liquid washing and fine filtration before drying. Silica gel columns and activated carbon columns find heavy use in our QA department, stripping away colored impurities and stabilizing the finished acid’s visual appearance. Most of our batches leave the plant as a free-flowing white or faintly off-white solid, avoiding the discoloration found with less controlled operations.

    Solid handling may seem mundane, but it matters. Our staff discovered that too much agitation or temperature cycling ruined crystal quality; that in turn caused stickiness or powdering when packed. Tightly-sealed polyethylene liners and stored containers inside climate-stable rooms proved invaluable, especially during hot and humid months. The difference becomes obvious when side-by-side with competingly-sourced material. Bulk purchasers and lab-scale chemists both commented on this, finding less caking and easier dissolution.

    Shipping complications can undermine the hardest work if not planned for. Moisture ingress and vessel transfer are points where less-stable carboxylic acids degrade. We warehouse this product in dehumidified spaces and move through dedicated, short-distance couriers for domestic clients, and we contract only bulked chemical logistics partners for exports. Traceability on every drum or bag connects back to our production log and in-house QC release, so auditing and recall—with full paperwork—moves ahead without delay. This process keeps research partners and quality teams confident at every stage.

    Use Cases in Synthesis and Industry

    Planned usage extends from research benches up through continuous-flow reactors in industrial synthesis. Most teams using 6-Chloro-2-Fluoro-3-Methylbenzoic Acid seek out specific performance: constructing substituted benzene rings that eventually turn into selective herbicides, insecticides, or active pharmaceutical ingredients. The chemical backbone from this acid serves as a springboard in Suzuki-Miyaura and Buchwald-Hartwig couplings, since the halides at C-6 and C-2 allow for creative pathways in introducing various heterocycles or alkyl chains.

    Our technical partners have reported that, compared with 3-methylbenzoic acid or common 2,6-dichlorobenzoic acid, this material grants more versatility. The different steric and electronic layout reduces unwanted side reactions—especially hydrodehalogenation or ortho-substitution typical of less-orchestrated precursors. Plants producing veterinary drugs using this route observed smoother purifications; university researchers isolating related compounds offered similar feedback about higher yields from the same input material.

    Demand from the crop protection sector keeps growing. Application chemists have pointed out how the acid’s resistance to photodegradation translates into greater shelf life for formulated intermediates. Downstream, this simplifies storage and inventory management. On our side, we address requests to scale up quickly, and we do this with emphasis on process repeatability. Small pilot runs get sampled at multiple checkpoints, and our operators ensure that transition to 500-kg or 1-ton lots delivers the same particle size, flow, and chemical purity as the lab samples.

    Year-round customers have included companies designing new fungicides. Oral bioavailability and metabolic routes for experimental APIs rely on this backbone, since its halide mix alters rates of liver and gut breakdown in preclinical models. Analytical chemists working at the evaluation stage consistently mention less interference in readouts, a result of cleaner starting-acid profile. That same predictability makes scale-up formulations less risky when changing solvents or processing speeds in pilot and commercial plants.

    How We Handle Safety and Regulatory Concerns

    Safe handling and regulatory awareness dictate both production and distribution. The halogen profile of this acid means operators wear extra PPE, including chemical goggles and gloves rated for acid and solvent resistance during all handling. On-site, all reactions take place in closed reactors vented through active carbon scrubbers, minimizing emissions and protecting our crew from inhalation risks. Our safety staff lead regular drills and chemical storage walkthroughs, verifying labeling and quarantine zones for all hazardous materials.

    For every lot, our team prepares full material traceability documentation, including chain-of-custody logs, impurity chromatograms, and environmental monitoring records from the plant. These are essential for customers importing our product, as regulatory authorities across North America, Europe, and parts of Asia request detailed, authenticated records for all chemical imports. Our certifications cover routine regional requirements, and we stay ahead of updates in compliance rules as they develop.

    Waste generated from process steps is tightly regulated. Solvent streams are collected separately and sent through on-site recovery distillation, with only trace residues going to certified waste handlers. This reduces both environmental impact and disposal costs. Solid and liquid acid residues are neutralized using controlled sodium carbonate processing, ceasing all hazardous evolution before shipment off-site. These steps reflect our commitment to responsible manufacturing and reassure downstream users wary of contamination risks tied to less-vigilant operations.

    Our team takes feedback from both auditors and end users to heart. If a customer flags a packaging concern, or doubts about analytical matching in a particular batch, we can trace the root cause within the day. Staff reviews supplement our audits, and deviations—whether operator error or equipment malfunction—trigger root-cause analysis and corrective strategy adjustments. Such responsiveness wins trust not just with buyers but with lab personnel who value genuine problem-solving over bureaucratic half-measures.

    Continuous Improvement—What Sets Our Production Apart

    Improvements come from collaboration. Our chemists routinely visit plants using our acid, talking directly to staff about integration points and bottlenecks. Field reports guide upgrades in filtration, powder handling, and active monitoring for solvent compatibility. Only actual use feedback—melt flow, filtration time, batch-to-batch reproducibility—cuts through statistics and tells us what changes to pursue. Plant upgrades in air handling or crystal separation often come straight from the suggestions of those further down the supply chain.

    We test every new process in house before rollout, inviting feedback from established partners. If a new solvent proves superior, or if an anti-caking agent alters reactivity, we trial it in real-world conditions before making a switch. Trace test records link sample changes to production logs. This prevents surprises later—there is no guessing about why a crystallization failed or why a shipment arrived less pure than expected.

    Not many manufacturers can say they track in-process yields as closely, from the moment raw materials land at our gate to shipment of the finished acid. Sensors and automated readouts watch for deviations in pH, color, and temperature. If a batch sits longer than intended or deviates in any measurable way, our QA teams intervene, running side-by-side lots to determine the best corrective action. Early intervention beats late correction, and years of work have proven that proactive troubleshooting avoids waste, costly recalls, and lost relationships.

    Operators and supervisors receive routine cross-training across roles—lab, plant, warehouse, and logistics all exchange team members during busy production phases. This develops a deeper understanding at every level and cuts down error rates. When something goes wrong, people fix it fast because they have experienced the problem themselves. Customers notice this, especially during scale-ups and fast turnarounds on development projects.

    Looking Forward—Building Value Together

    Built into every batch of our 6-Chloro-2-Fluoro-3-Methylbenzoic Acid is a hard-won appreciation for the realities of fine chemical production. Close attention to every link—from selecting pure feedstocks, through solvent elimination, to vigilant packaging and logistics—keeps the product reliable. Process changes never occur in a vacuum. They come out of real industry needs, employee ingenuity, and customer feedback. These shared efforts drive incremental gains and sometimes spark breakthrough improvements in how aromatic acids are produced and delivered.

    The market for specialty halogenated acids will keep pushing for more precise compliance, greater purity, and faster delivery. Our investments point in these directions because ongoing conversations with end users in pharmaceuticals, crop protection, and applied R&D continue to shape our decisions. Every time we adjust a parameter or overhaul a filtration line, we do so grounded by conversations, not just spreadsheets. This pattern makes every drum we ship a little bit sharper, safer, and ready for demanding applications.

    Reliability grows out of practice. Our people, equipment, and partner relationships keep maturing, grounded by stubborn attention to detail and natural skepticism of shortcuts. Every complaint gets investigated, and every improvement gets documented. We owe dedicated customers chemical lots that perform without surprises, and we keep pushing until that promise holds, batch after batch.

    From benchtop experiments to turnkey industrial production, 6-Chloro-2-Fluoro-3-Methylbenzoic Acid supplies the leverage, purity, and proven consistency demanded by the toughest users. Our manufacturing team stands behind every order, ready for direct feedback, technical discussion, and the kind of hands-on support that drives innovation in modern chemistry.