|
HS Code |
480812 |
| Productname | 3-Chloro-4-Fluorothiophenol |
| Molecularformula | C6H4ClFS |
| Molecularweight | 162.61 g/mol |
| Casnumber | 852140-51-9 |
| Appearance | Light yellow to brown liquid |
| Boilingpoint | 219-221°C |
| Density | 1.43 g/cm³ |
| Purity | Typically ≥97% |
| Synonyms | 3-Chloro-4-fluorobenzenethiol |
| Chemicalclass | Aromatic thiol |
| Smiles | C1=CC(=C(C=C1S)F)Cl |
| Inchikey | ILJLZHYZMMUOCB-UHFFFAOYSA-N |
| Storagetemperature | 2-8°C |
| Solubility | Soluble in organic solvents |
As an accredited 3-Chloro-4-Fluorothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, screw cap sealed, white hazard label showing chemical name, CAS number, hazard symbols, and handling precautions. |
| Shipping | **Shipping Description:** 3-Chloro-4-Fluorothiophenol is shipped in tightly sealed containers under cool, dry conditions. It should be clearly labeled as a corrosive and toxic substance, with appropriate hazard warnings. Transport complies with local regulations for handling hazardous materials, ensuring protection from moisture, heat, and incompatible chemicals during transit. |
| Storage | **3-Chloro-4-Fluorothiophenol** should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, well-ventilated area away from heat, moisture, and incompatible substances such as strong oxidizing agents. Store in a dedicated flammable cabinet and protect from direct sunlight. Properly label all storage containers. |
Applications of 3-Chloro-4-Fluorothiophenol in Industrial ManufacturingOur expertise in the synthesis and production of 3-Chloro-4-Fluorothiophenol enables consistent integration across multiple advanced industrial applications. Below, we detail key downstream uses, each supported by practical data on compliance, dosage, processes, and finished goods in the international marketplace. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)3-Chloro-4-Fluorothiophenol is widely used in pharmaceutical manufacturing as a critical building block for certain APIs, notably for molecules in anti-inflammatory and anti-infective drug classes that require halogenated aromatic thiophenol intermediates. The material undergoes nucleophilic substitution and C-S bond formation at the early stage of synthetic pathways, allowing precise placement of chloro and fluoro substituents critical for later pharmacophore assembly. Secure material handling, validated process documentation, and batch traceability are mandatory for GMP batch synthesis and subsequent scale-up stages. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient SynthesisIn agrochemical manufacturing, 3-Chloro-4-Fluorothiophenol functions as a key intermediate for the synthesis of crop protection agents such as fungicides and insecticides that rely on halogenated thiophenol motifs for biological activity. The product’s molecular structure enables the introduction of selective substitution patterns essential for specificity in pesticide formulations. Downstream, it participates in thioetherification and subsequent heterocycle ring-closure, which is critical for the formation of active agrochemical compounds subjected to regulatory scrutiny and environmental risk assessment. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemicals for Semiconductor and Display MaterialsIn the electronics industry, 3-Chloro-4-Fluorothiophenol serves as a functionalized thiol intermediate for manufacturing custom organic semiconductors, particularly in the construction of thiol-functionalized compounds used in OLED display assemblies and high-performance circuit substrates. The molecular moiety offers excellent electron-withdrawing characteristics, making it suitable for fine-tuning electrical properties and anchoring layers in multi-material thin films through controlled thiolation steps. Strict purity and metal content control are required for use in cleanroom and microelectronics production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer Modification3-Chloro-4-Fluorothiophenol is integral as a modifier in specialty polymer synthesis, where its thiophenol group participates in chain-end functionalization or backbone modification during step-growth polymerization. The dual halogen substitutions enable precise alteration of thermal and chemical resistance in engineering plastics, with the compound most frequently entering polythioether and copolymer synthesis streams at the monomer or pre-polymer stage. Application requires audit trails and certified process control, especially for plastics used in regulated industries. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Chloro-4-Fluorothiophenol 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!
In the world of chemical synthesis, even minor variations in a single molecule can lead to significant shifts in performance and outcome. Over many years working on the production side, we have seen first-hand how demand for finely-tuned thiophenols has grown in pharmaceutical research, fine chemicals, and electronic materials. Out of this landscape, 3-Chloro-4-Fluorothiophenol—known across development teams by its CAS number 101814-81-3—has found a regular place on order lists thanks to its unique mix of reactivity, selectivity, and compatibility.
We step beyond simply preparing a chemical for market; our work starts in the pilot plant, where every production parameter finds careful optimization for purity and reproducibility. With 3-Chloro-4-Fluorothiophenol, having control over each stage is essential. It isn’t just another building block—it represents a turning point for R&D teams pushing for cleaner reactions and fewer by-products. From our own reaction vessels to the finished product, oversight doesn’t leave our hands.
We synthesize this compound in small-to-medium batch runs, not by outsourcing but with in-house crews well versed in halogenated aromatic chemistry. Every batch undergoes GC, HPLC, and NMR analysis, reflecting standards real clients request for their projects. What we find is that maintaining above 98% assay purity eliminates the headaches downstream—less workup, fewer surprises in scale-up, and reliable behavior during coupling or cross-linking reactions.
The physical profile comes out as a pale yellow to off-white crystalline solid, melting in a manageable range that makes isolation straightforward. Moisture and air stability mean storage doesn’t turn into a shelf-life gamble. Our practical experience tells us that slight impurities or lower conformational purity can skew subsequent synthetic steps, particularly when pursuing active pharmaceutical ingredients or advanced intermediates. We tune drying conditions and packaging to block atmospherics from interfering, not simply to tick a QC checklist but because returns or failed syntheses cost everyone more time than most realize.
Buyers often see a long list of suppliers of 3-Chloro-4-Fluorothiophenol, but the difference lands in the details. As direct manufacturers, we know every stage from initial halogenation to controlled thiolation. Our process minimizes the introduction of disulfides, which frequently crop up as contaminants during storage or shipping. These by-products—often difficult to separate without re-crystallization or laborious column work—cause problems in Suzuki coupling, reductive amination, or polymer preparation.
Many commercial options on the market originate from multiple subcontracted sources, which can introduce minute but detectable shifts batch-to-batch. Chemists in scale-up development quickly see these variations when a routine step suddenly returns an unexpected TLC spot or NMR impurity. Supplying from a single controlled system means analytical fingerprints remain stable, not drifting with every invoice number. That consistency benefits projects where reproducibility is not just a nice-to-have but keeps expensive medicinal chemistry programs on track.
Physical handling also plays a role. Our team witnesses how powder flow, granule size, and tap density directly affect dosing accuracy in automated feed systems. A lumpy, poorly milled product chokes a reactor feed and draws out even simple weighing tasks. We use filtration and drying protocols fine-tuned for this molecule to avoid clumping and tough-to-break-up masses. Feedback from bench and pilot customers pushed us to refine these steps, since their throughput relies on small improvements at our end.
3-Chloro-4-Fluorothiophenol serves as a core fragment for the preparation of more complex molecules with reactivity difficult to match through other scaffolds. Medicinal chemists often build upon its backbone to generate compounds intended for testing as kinase inhibitors, anti-inflammatory candidates, or precursor motifs for agricultural chemistry.
Its native chloro and fluoro functions lend both electron-withdrawing character and versatile reactivity, opening up cross-coupling and nucleophilic substitution reactions. We have worked closely with partners tailoring lead candidates, where using our material shortened purification cycles and improved yields compared with lower-purity lots. Some clients choose it for preparing fluorinated aryl thioethers and sulfonyl derivatives that enter electronic materials or specialty coatings. The reliability of a fresh, authentic batch lets them develop process improvements with confidence it won’t falter at pilot or full-scale.
Our technical teams assist with integration into existing flows. Whether it’s solubility adjustment, compatibility with metal catalysts, or stability in complex multistep processes, direct knowledge of what happens from our drum to your flask gives our partners a point of contact grounded in practical experience.
Chemists often ask why not just use plain 4-fluorothiophenol or other simple aryl thiols. The difference lies in electronic and steric impacts; the ortho-chloro substituent modulates reactivity, either shielding or activating adjacent positions depending on reaction conditions. In C–S bond-forming reactions, this can dictate selectivity or suppress side-product formation. In aromatic substitutions, the pattern resists overactivation and narrows product profiles, saving work during isolation.
Our experience shows that analogs lacking chlorine at the 3-position can behave unpredictably with some palladium-catalyzed strategies, leading to more tar, side-chain fragmentation, or protracted purification. Over time, researchers tell us these differences become magnified when moving from milligram to hundred-gram scale. When teams switch to less specialized thiophenols, overall throughput suffers. The extra few percent impurity, moisture, or trace metal content often introduce more than just a purity penalty—they set off chain reactions of lost work, extra solvent use, and even failed regulatory audits.
For industries working with sensitive active ingredients or high-purity electronics, such distinctions are not just academic. Customer feedback routinely underlines the costs of roadblocks linked to inconsistent input materials—added downtime, drawn-out investigations, and even regulatory concerns. We see the reality of these issues and continue to invest in process refinement, batch tracking, and staff training to raise the bar.
Quality in specialty chemicals is a moving target. Regulators, end-users, and manufacturers all shoulder responsibility for environment, safety, and community health. Every batch of 3-Chloro-4-Fluorothiophenol produced in our plants carries traceable batch records, raw material origin details, and full supplier declarations for all additives used in synthesis.
We have moved away from obscure supply chains and mystery intermediates, opting for vertical integration wherever possible. Our in-house analytical teams provide audit records and monitoring updates. We believe transparency goes hand-in-hand with chemical stewardship. Many of our downstream partners work under Good Manufacturing Practice (GMP) or similar systems, so we echo those standards upstream, restricting the use of certain process agents and documenting every handoff.
Waste minimization and safe handling of hazardous reagents remain a constant focus. Using directly controlled halogen sources cuts the risks of off-specification by-products. Comprehensive training for everyone in synthesis and finishing areas ensures safety, right down to how empty containers get cleaned and managed. By producing specialized chemicals with a responsible eye on both output and environmental impact, we add value beyond the drum or bag.
Real insight does not arise from spreadsheets or spec sheets alone. It comes from seeing what works and what falters day to day. Over the years, we have collected practical lessons that influence every aspect of our workflow: how certain solvents accelerate chlorination, which filtration setups end up clogging, and even what kind of packaging holds up best under cyclical humidity during shipping.
Switching from glass-lined to high-grade stainless vessels, we stopped occasional leaching issues that could taint trace analysis work or bio-research applications. After a handful of problematic customer returns linked to poorly sealed containers, our logistics crew transitioned fully to moisture-tight, tamper-evident drums—taking advice straight from the users who saw the last mile of risk.
We do not see improvements as one-off fixes, but as iterative gains. Each year, we review analytics data, listen to partner site reports, and walk through plant tours with fresh eyes. That continuous circle of feedback, adjustment, and action means we close the gap between lab concept and commercial run. Our customers—from hands-on R&D teams to production supervisors—stay engaged through every batch, not just the first test order.
Too often, chemical users discover too late that their supplier lacks real process data. Delays mount, contracts go unfulfilled, and scavenger hunts for technical support eat into project timelines. We take a different approach, opening our doors to dialogue and troubleshooting before an order goes out the door.
Our in-house synthesis experts consult regularly with process engineers at customer sites. Whether the issue is forming a tight thiophenol-metal catalyst complex, avoiding hydrolysis during storage, or troubleshooting plugged pipelines, our staff base answers on what works, not just what theory says. By keeping every aspect under direct control from start to finish, we can adapt formulations, suggest alternative solvents, or supply documentation needed for regulatory submissions—without endless redirection.
We also recognize that commercial projects face tight schedules and cost pressures. Unplanned downtime from inconsistent intermediates can cascade rapidly into expensive overruns. With hands-on oversight, we shore up reliability and eliminate the surprises that disrupt process validation, pilot runs, or clinical manufacture. In one case, a major pharmaceutical client traced sporadic chromatographic ghost peaks back to residue from externally prepared thiophenols. Together, we redesigned their sampling and introduced in-line QC at both ends until the process ran clean.
By investing in end-to-end operations, we do more than supply material; we carry through on hands-on support that stands up to the real world, not just idealized trials.
The landscape for specialized aromatic intermediates continues to evolve. We remain committed to advancing our manufacturing capability for 3-Chloro-4-Fluorothiophenol by monitoring advances in green chemistry, automation, and emission reduction. Customers increasingly ask not just for material on time, but with ever-clearer provenance, predictable handling, and fewer environmental burdens.
We invest in catalyst recycling schemes to cut down on precious metal waste. Regular reviews of waste management protocols and implementation of solvent swaps keep our process in line with tougher regulatory and client-driven targets. Technical staff run trials with new purification columns, more efficient condensers, and real-time monitoring to raise both quality and sustainability standards.
By working directly with those at the forefront of pharmaceutical and high-tech manufacturing, we draw fresh inspiration and stay ahead of shifting demands. Where clients see a gap—in shelf-life, compatibility, or documentation—we roll those findings into process upgrades. For example, a shift to cleaner, lower-odor packaging met emerging health and safety standards on customer sites. The lessons stick, shaping our future batches for wider application and easier integration.
Our approach with 3-Chloro-4-Fluorothiophenol is shaped by direct involvement in every step and a shared understanding that reliable chemical supply underpins innovation. Whether your application pushes toward novel bioactives, performance materials, or next-generation research, our firsthand experience as manufacturers aligns our product with your success. Reliable chemistry seldom results from wishful thinking or luck. It grows from constant attention to process, dialogue with users, and a willingness to invest where it matters.
Through these practices, we have built trust not just in the product itself, but in our commitment to those who depend on it. Direct market access, controlled supply chains, and hands-on support allow us to deliver 3-Chloro-4-Fluorothiophenol that offers more than just specification—it becomes a tool for progress in the hands of skilled scientists and engineers.