Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone

    • Product Name 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone
    • Alias 3-(Trifluoromethyl)phenyl 2-chloroethyl sulfone
    • Einecs 629-707-2
    • 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

    896112

    Product Name 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone
    Cas Number N/A
    Molecular Formula C9H8ClF3O2S
    Molecular Weight 276.68 g/mol
    Appearance White to off-white solid
    Melting Point N/A
    Boiling Point N/A
    Solubility Slightly soluble in water, soluble in organic solvents
    Density N/A
    Purity Typically >98%
    Refractive Index N/A
    Storage Conditions Store in a cool, dry place, tightly closed
    Smiles C1=CC(=CC(=C1)S(=O)(=O)CCCl)C(F)(F)F
    Inchi InChI=1S/C9H8ClF3O2S/c10-6-7-16(14,15)8-3-1-2-7(4-8)9(11,12)13/h1-4H,5-6H2

    As an accredited 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled "2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone, 25 grams," hazard pictograms, and lot number.
    Shipping **Shipping Description:** 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone is shipped in tightly sealed, chemical-resistant containers suitable for hazardous organic compounds. The packaging complies with ADR/IATA regulations for flammable and toxic substances. Material safety data sheets (MSDS) are included. Ensure transport in a cool, dry environment, away from incompatible substances, with appropriate hazard labeling.
    Storage 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone should be stored in a tightly sealed container within a cool, dry, and well-ventilated area, away from moisture, heat sources, and direct sunlight. Keep it separate from incompatible substances such as strong bases and oxidizing agents. Proper chemical labeling and secure storage in accordance with local regulations are essential to prevent accidental exposure or reactions.
    Application of 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone

    Applications of 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone in Industrial Manufacturing

    2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone has established itself as a key intermediate in several highly specialized chemical manufacturing processes. As a direct producer, we support innovation in downstream sectors by delivering consistently high-purity sulfone that fits stringent performance and compliance needs. Below, we outline the primary industrial application areas where this compound directly impacts synthesis workflows and finished product characteristics.

    1. Pharmaceutical Intermediate for Antineoplastic and Antiviral Agents

    Major pharmaceutical manufacturers rely on this sulfone as a building block for certain classes of oncology and antiviral active pharmaceutical ingredients (APIs), primarily due to its unique trifluoromethylated aromatic structure. It enters the route of synthesis at the stage of arylsulfonylalkylation, enabling precise molecular modifications demanded by modern chemotherapeutic and antiviral molecule design. Production workflows incorporate it during the late-stage intermediate synthesis, so quality and bioburden control remain closely monitored. Final APIs commonly deploy the trifluoromethyl-phenyl sulfone motif as part of their pharmacophore, warranting high traceability and batch reproducibility from our supplied material.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 Current GMP for Finished Pharmaceuticals
    • EU Guidelines for GMP (EudraLex, Volume 4)
    • Japanese Pharmacopoeia (where regionally applicable)

    Typical usage ratio

    • 5–12% molar ratio in step-growth synthesis stages; actual loading depends on the target API structure and balance of competing nucleophile/electrophile reactions in the process route

    Downstream process integration

    • Used during the arylsulfonylation and alkylation steps; typically charged to the reactor during the key chain-extension or nucleophilic aromatic substitution sequence, with process controls set for temperature-sensitive operations to prevent unwanted side reactions

    Final product types

    • Antineoplastic APIs for targeted cancer therapies
    • Antiviral APIs for respiratory and systemic infection treatments
    • Chiral intermediates for advanced pharmaceutical research

    2. Advanced Agrochemical Intermediates

    This sulfone is crucial for the synthesis of agrochemical actives involving trifluoromethyl-aryl scaffolds, such as certain new-generation sulfonylurea herbicides and insecticidal agents. The electron-withdrawing sulfone and trifluoromethyl groups impart the necessary reactivity for selective alkylation and modification steps in multi-stage agrochemical molecule assembly. As part of the setup for large-scale synthesis, producers utilize this intermediate under strictly controlled addition, usually during the core scaffold formation stage, which confers the desired metabolic stability and bioactivity profile unique to modern agrochemicals.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 – Quality Management Systems for Crop Protection Products
    • Regulation (EC) No 1107/2009 – EU Plant Protection Products Regulation
    • US EPA Guidelines for Pesticide Active Ingredients

    Typical usage ratio

    • 7–15% by mass relative to total aromatic intermediates; this loading depends on the complexity of the downstream substituent modification and final active strength required by the agrochemical formulation

    Downstream process integration

    • Added during the initial aromatic sulfonylation or subsequent alkylation phase, typically under inert atmosphere and monitored for by-product minimization in pilot and production batch reactors

    Final product types

    • Sulfonylurea herbicides
    • Systemic insecticidal actives
    • Growth regulator intermediates for seed and crop coating solutions

    3. Specialty Polymer Additives for High-Performance Materials

    Within the high-performance polymer sector, formulators incorporate this compound as a functional group donor in the production of heat- and chemical-resistant polymers, notably in the synthesis of custom sulfone-based engineering resins. Its integration into the polymer backbone—often through co-polymerization with other aromatic monomers—imparts high glass transition temperatures and outstanding oxidative stability. Real-world production entails a carefully balanced feed using this sulfone intermediate during solvent- or melt-phase condensation reactions, supporting strict batch reproducibility needed for advanced manufacturing segments, including electronics and aerospace composites.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in Polymer Manufacturing
    • UL 94 Flammability Standards (for electrical and electronic end uses)
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EU)
    • RoHS Directive 2011/65/EU (where applicable for electronics housing components)

    Typical usage ratio

    • 3–9% by weight of total monomer content; often adjusted to tune polymer mechanical and chemical resistance, or as dictated by the chain extender loading in the engineered formulation

    Downstream process integration

    • Fed into the polymerization reactor at the co-monomer stage, either by pre-dissolving in carrier solvents for solution polymerization or direct melt-phase addition for step-growth processes; reaction usually performed under reduced pressure or inert gas to control molecular architecture

    Final product types

    • Sulfone-based engineering plastics
    • High-temperature thermoplastic composites
    • Specialty films for electronics and automotive connectors

    4. Organic Synthesis Intermediate for Custom Fine Chemicals

    Contract and custom synthesis plants utilize this chemical as an indispensable linchpin for assembling a variety of fine chemical intermediates. Its reactivity promotes regioselective alkylation and cross-coupling reactions vital for specialty molecule building, particularly where the electron-withdrawing and steric properties of the trifluoromethyl and sulfone groups influence product selectivity. Such synthesis routes often employ it during the late intermediate or penultimate step, after other functional group modifications, in order to guarantee the intended downstream reactivity and physical characteristics of specialty fine chemicals.

    Industry compliance standards

    • ISO 9001:2015 for custom chemical manufacture
    • Responsible Care® Management System (chemical industry best practices)
    • OECD Guidelines for the Testing of Chemicals (relevant for process development and environmental acceptance)

    Typical usage ratio

    • Variable, usually between 2–10% by mole in the step where its substituent function is directly incorporated; the ratio depends on the target fine chemical and downstream conversion efficiency

    Downstream process integration

    • Introduced during advanced alkylation or cross-coupling reaction stages, typically after protection/deprotection sequences, as its reactive sites enable precise downstream modifications without excessive side product formation

    Final product types

    • Specialty intermediates for photographic chemicals
    • Custom fluorinated aromatics for electronics or analytical reagents
    • Building blocks for organic dyes and pigments
    Free Quote

    Competitive 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    About 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone: From Concept to Industrial Application

    Understanding 2-Chloroethyl-(3-(Trifluoromethyl)Phenyl)Sulfone

    2-Chloroethyl-(3-(trifluoromethyl)phenyl)sulfone stands as one of the distinct sulfone intermediates we manufacture in our facility. Most of our team, from process engineers to technical quality supervisors, have worked hands-on with this compound—often just called “3-TFMPCE sulfone” around the plant. In the chemical industry, intermediates like this one rarely get the spotlight, yet decades of hard-won experience have taught us that consistency in both performance and high purity can make or break entire production chains.

    A 2-chloroethyl group and a 3-(trifluoromethyl)phenyl group both attached to sulfur form a rigid, stable molecule. On paper, that sounds straightforward; in practice, subtle differences in the process—reaction temperatures, solvent choice, filtration rate—have noticeable effects on the final properties. It's the kind of insight you develop only after running hundreds of batches and tackling real-world challenges, not just reading technical monographs.

    Meeting the Quality Demands of Downstream Chemistries

    Our core motivation is straightforward: provide a starting material that works, batch after batch, in the demanding conditions of large-scale synthesis. Pharmaceutical and crop protection manufacturers rely on specificity, traceability, and reliable reactivity. This compound’s dual halogenation and electron-withdrawing trifluoromethyl group make it uniquely reactive in nucleophilic substitution and further elaboration. A typical usage sees it acting as a synthon for various benzenesulfonyl derivatives, arylthioethers, or asyl intermediates. Fine-tuning stoichiometry during downstream reactions means even trace impurities or physical inconsistencies can cause costly downtime—these facts became obvious after a single lot caused issues in a pilot run years ago.

    Specifications that Matter in Day-to-Day Manufacturing

    In chemical manufacturing, claims about purity and analytics must always line up with the facts. Each batch undergoes HPLC, NMR, and GC-MS checks right here on-site, with spectral records reviewed by veteran chemists. Published “certificate of analysis” sheets are only as useful as the trust behind them, and nothing replaces the habit of walking the line and checking crystal morphology by eye. We maintain melting points precisely, typical ranges around 60–62 °C, but we pay closer attention to color and particulate characteristics. Experience taught us: subtle yellowing hints at low-level sulfoxide byproducts, which tie directly to trace oxygen ingress during the chlorination stage.

    Process Insights: Avoiding Routine Pitfalls

    Preparing this sulfone at scale brought early headaches. Some competitors struggle with reproducibility because the trifluoromethyl group can complicate purification—it loves to stick to glassware and can cause losses. Years ago, our R&D team overhauled filtration methods after yield reports showed creeping product retention. By adopting new filtration media and controlling pH at workup, we’ve essentially eliminated visible product clumping—saving much grief come packaging time.

    Solvent management also sets real-world manufacturers apart. The presence of the 3-(trifluoromethyl)phenyl group makes trace organic residues challenging to wash away. We invested in closed-loop solvent recovery partly out of regulatory necessity, but mostly because successive chromatography showed that trace aromatics, if left unchecked, could skew downstream reactivity.

    Benefits for End Users: What Years in Manufacturing Reveal

    Chemists in downstream plants benefit from a physically stable, free-flowing sulfone, rarely clumping and effortlessly weighed. Those benefits follow from strict control of granulation and humidity. In a damp season, supervisors in our facility adjust drying cycles. No amount of technical data replaces actual batches tested on your own equipment to verify that pouring, blending, and dosing unfold as planned.

    The compound’s chemical profile—chloroethyl group paired with the electron-withdrawing trifluoromethyl-phenyl—makes selective reactivity more accessible in C–S, C–N, and C–O bond formation. We’ve had multiple partners in medicinal chemistry point out how certain impurity profiles (minor deschloro or over-chlorinated forms) hampered their catalyst selections and stability tests; that’s led us to rework selectivity at the sulfonylation stage each year.

    Differences From Other Products: A Manufacturer’s Perspective

    Within the sulfone class, comparable products exist—simple phenyl sulfones, methyl sulfones, or even other halogenated derivatives. Yet the combination of chloroethyl and the trifluoromethyl-phenyl group offers an inflection point for selectivity and solubility. These two substituents not only alter reactivity in cross-coupling conditions but also affect partitioning in multi-phase extraction. Years of practical chemistry have demonstrated that, for specific alkylation or nucleophilic aromatic substitution projects, this sulfone outperforms its methyl or plain phenyl counterparts.

    Physical handling reveals further distinctions. Our 3-TFMPCE sulfone retains crystalline, non-dusty characteristics even at larger scales, which is rarely the case for methyl or ethyl sulfones that tend to compact or “cake” when stored. Years of observing customer feedback prompted enhanced packaging—from triple-layered polyethylene for intermediate storage to bulk containers with gas-purged liners—to inhibit both static build-up and accidental moisture exposure.

    Some suppliers deliver cheaper analogues with broader impurity ranges, but repeated trials leave their batches prone to unpredictable color shifts and decomposition under light or heat. In our experience, close oversight at the re-chlorination and sulfonylation steps consistently outperforms attempts at cheaper processing.

    Real-World Challenges: Addressing Scale-up and Environmental Safety

    Scaling bench chemistry to ton-scale sulfone production meant confronting process safety and waste minimization at every step. The handling of chlorinated precursors and volatile solvents created perennial demands for new exhaust scrubbing and updated PPE protocols. Our project engineering leads remember numerous trial runs held back not by yield but by thermal hot spots or minor byproduct formation that changed off-gas profiles. We accept these iterative improvements, recognizing that most innovation comes from thoroughly understanding every failure mode, not just as a regulatory obligation but as a culture of safety and reliability.

    Supply Chain Transparency and Batch Traceability

    As regulations grow tighter, customers rarely want only the chemical—they seek assurance about origin, transport, and compliance. We document every step, from raw trifluoromethylbenzene and ethylene glycol dichloride, through multi-stage chlorination and sulfonation, to final drying. Internal audits, third-party monitors, and digital batch tracking allow customers to reference in-depth batch histories. Events in recent years, especially global logistics disruptions, reminded us that “just-in-time” delivery only succeeds when manufacturers maintain buffer stocks, flexible scheduling, and direct transport oversight.

    We keep technical files not just for compliance but so that plant staff and partners can consult with full knowledge of synthetic origin, impurity spectra, and intermediate handling. Some partners have shifted procurement away from non-transparent sources after encountering unreproducible test results; our customers routinely cite batch consistency as a deciding factor for long-term contracts.

    Application-Centric Focus: The Role in Advanced Synthesis

    In complex organic synthesis, this sulfone often acts as a coupling partner where the electron-deficient aromatic ring governs regioselectivity. Customers in agrochemical synthesis and specialty materials count on repeat performances—successful sulfonyl group transfer, robust yields, and little need for repeated purification cycles. Modern pharmaceutical approach values not just the theoretical accessibility of a functional group but the consistency in how that functionality carries across dozens of high-throughput screening reactions.

    Feedback, Evolution, and Continuous Improvement in Manufacturing

    Plant data, customer feedback, and collaborative test projects form a cycle that keeps our product improving. Over the years, client-side chemists have identified new synthetic routes where minor changes in crystal habit or hygroscopicity affected downstream mixing or solubilization. Acting on this input has led us to modify drying temperatures, recrystallization solvents, and even introduced new analytical checkpoints.

    We consider every unexpected result a clue for improvement. Product managers meet regularly with process operators to review deviations—having a chemist at the drum-filling station and inside the QC lab shortens troubleshooting time dramatically. We learned early that manufacturing is less a linear process and more a living, iterative exchange of lab work, plant experience, and customer reality.

    Responsible Production and Environmental Commitment

    Every round of sulfonation generates not only product but also acidic byproducts and spent solvents. Over years, we’ve upgraded scrubbing and recycling systems, minimizing both local and downstream environmental impact. We test wastewater for trace sulfonyl residues and have learned that pre-neutralization and staged clarification reduce emissions well below statutory limits. In the broader community, our credibility depends not just on what we deliver in drums, but also on the standards we uphold in waste management and emissions tracking.

    Recommendations and Future Directions

    Market needs and regulatory climates continue to evolve, and so does the profile of intermediates like 2-chloroethyl-(3-(trifluoromethyl)phenyl)sulfone. Precision in terms of purity and documentation remains non-negotiable. Some clients now request micro-scale lots for preclinical projects, while others ask for ton-scale annual reserves. Flexibility isn’t just about switching output volumes but about adapting QC benchmarks, lead times, and documentation to match new expectations.

    Some current partnerships are experimenting with catalytic transformation strategies where even minor changes in the sulfone structure affect result reproducibility. We see our role as more than just providing a molecule. We create a foundation for our partners to test, iterate, and scale their innovations.

    Concluding Thoughts: What Sets This Product Apart

    2-Chloroethyl-(3-(trifluoromethyl)phenyl)sulfone—built through rigorous process control, daily plant experience, and a tradition of open feedback—demonstrates the core of industrial chemistry done right. It supports teams seeking reliability, safety, and clear answers to commercial and technical challenges. Through each batch, we reinforce the value of experienced hands and open communication between plant and customer.

    While the molecular formula remains the same, it’s the knowledge, precautions, and responsive attitude behind each drum that define its real-world performance. That cumulative experience underpins the trust customers place in this essential sulfone, batch after batch, year after year.