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1,3-Benzenedisulfonyl Chloride

    • Product Name 1,3-Benzenedisulfonyl Chloride
    • Alias m-Benzenedisulfonyl chloride
    • Einecs 214-290-3
    • 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
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    Specifications

    HS Code

    513782

    Chemicalname 1,3-Benzenedisulfonyl Chloride
    Casnumber 98-68-0
    Molecularformula C6H4Cl2O4S2
    Molecularweight 275.13 g/mol
    Appearance White to off-white solid
    Meltingpoint 96-98 °C
    Boilingpoint Decomposes
    Density 1.8 g/cm3 (approximate)
    Solubility Reacts with water; soluble in organic solvents like chloroform
    Synonyms isophthalic disulfonyl chloride, 1,3-benzenedisulfonic dichloride
    Smiles C1=CC(=CC=C1S(=O)(=O)Cl)S(=O)(=O)Cl

    As an accredited 1,3-Benzenedisulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, high-density polyethylene (HDPE) bottle containing 100 grams of 1,3-Benzenedisulfonyl Chloride, labeled with hazard symbols and product details.
    Shipping **Shipping Description for 1,3-Benzenedisulfonyl Chloride:** This chemical should be shipped in tightly sealed containers, away from moisture and incompatible materials. Clearly label the package as corrosive. Comply with relevant regulations (e.g., DOT, IATA, IMDG). Ensure appropriate hazard labels are visible. Handle with care to avoid leaks or spills during transport.
    Storage 1,3-Benzenedisulfonyl chloride should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizers. Keep the container tightly closed and properly labeled. Avoid exposure to heat and direct sunlight. Use corrosion-resistant shelving and secondary containment to prevent leaks or spills, and store under inert atmosphere if possible.
    Application of 1,3-Benzenedisulfonyl Chloride

    Applications of 1,3-Benzenedisulfonyl Chloride in Industrial Manufacturing

    1,3-Benzenedisulfonyl Chloride acts as a core sulfonating and chlorinating agent, essential in the synthesis of specialty chemicals across multiple sectors. As a direct manufacturer, we serve high-value downstream fields demanding reliable lot traceability, process documentation, and regulatory compliance. The following segments reflect real industrial demand and established usage.

    1. Pharmaceutical Intermediate Synthesis

    Pharma manufacturers incorporate this compound to introduce sulfonyl chloride moieties during the multi-step synthesis of advanced drug intermediates, especially sulfonamide antibiotics and antidiabetic APIs. Its high reactivity enables functional group integration under mild conditions, providing higher selectivity and yield. Chemical engineers calibrate the reagent’s loading per target product profile, considering reaction efficiency, downstream purification, and regulatory impurity limits. We supply material with complete audit trails and solution-phase compatibility certificates to support continuous and batch operations.

    Industry compliance standards

    • Good Manufacturing Practice (EU GMP Part II, ICH Q7)
    • USP-NF and Ph. Eur. raw material standards
    • 21 CFR Part 211 (cGMP - APIs and intermediates)
    • ICH Q3A/B (impurity limits)

    Typical usage ratio

    • Employed at 0.9–1.2 molar equivalents relative to target amine/functionalized substrates
    • Dynamic adjustment based on batch size, stoichiometry, and reaction purity, verified by LC-MS

    Downstream process integration

    • Charged after substrate dissolution and solvent pre-conditioning
    • Reacts at controlled temperature (5–35°C) with amine/amide compounds
    • Integration with inline pH and impurity monitoring

    Final product types

    • Sulfonamide antibiotic intermediates
    • Antidiabetic precursor molecules (e.g., sulfonylureas)
    • Specialty drug linkers
    • CRO/CDMO small-molecule libraries

    2. Sulfonated Polymer Manufacturing

    Producers of high-performance membranes and ion-exchange resins use this reagent for controlled sulfonation of aromatic polymers such as polyether ether ketone (PEEK) or polystyrene. During sulfonation, its chloride groups activate the polymer backbone, introducing sulfonic acid functionality that imparts ion conductivity and chemical resistance. This step requires precise dosing and temperature management to regulate sulfonation degree, avoid gelation, and validate final polymer MW distribution.

    Industry compliance standards

    • ISO 9001:2015 (Quality management systems)
    • EN 13641 (Ion-exchange resin requirements)
    • REACH Registration (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • FDA CFR 177.2440 (Polystyrene and copolymer use in food contact)

    Typical usage ratio

    • 5–25% by wt. versus polymer substrate, depending on target sulfonation level
    • Ratio set via pilot trial, monitored by titration and FTIR

    Downstream process integration

    • Dosed into polymer slurry in organic solvent under inert atmosphere
    • Gas scrubbing and post-sulfonation quench step mandatory
    • Product purification by washing and neutralization prior to extrusion or granulation

    Final product types

    • Proton exchange membranes for fuel cells
    • High-capacity ion-exchange resins (water treatment, bioprocessing)
    • Engineering plastics with enhanced flame retardance
    • Specialty polymer masterbatches

    3. Agrochemical Active Ingredient Production

    Agrochemical synthesis routes employ this intermediate for the manufacture of key sulfonylurea herbicides and fungicides. The reagent introduces sulfonyl groups onto aromatic cores, tailoring the bioactivity and field persistence of crop protection compounds. Operators carefully adjust feed rates and temperature control to prevent byproduct formation and ensure compliance with residue legislation. Full batch-COA supply and chain-of-custody documentation remain critical for global registrations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD guidelines on pesticide manufacturing
    • ISO 17025 (Analytical QC for active content validation)
    • Regulation (EC) No 1107/2009 (EU agrochemical approval)

    Typical usage ratio

    • 0.8–1.5 molar equivalents relative to aniline or amino precursor
    • Proportions optimized to minimize downstream purification cost and product reactivity loss

    Downstream process integration

    • Fed-batch or continuous reaction with aromatic base substrates
    • Integration with dichlorination or nitro-reduction process units
    • Final product crystallization and drying under regulated containment

    Final product types

    • Sulfonylurea herbicides (e.g., metsulfuron-methyl)
    • Broad-spectrum agricultural fungicides
    • Formulated crop protection solutions
    • Intermediate supply to global agro majors

    4. Specialty Dyes and Optical Brighteners

    Dye manufacturers integrate the material in sulfonation reactions to increase water solubility, color brightness, and fastness of azo and phthalein dyes. The chloride substituents activate aromatic intermediates, enabling high selectivity in diazo coupling and sulfonic acid function introduction. Operations demand tight QC to meet shade consistency, purity classes, and ecotoxicity levels for downstream textile and paper applications. Purity and residual analysis data must accompany each bulk shipment.

    Industry compliance standards

    • OEKO-TEX 100 Annex 4 (Eco-toxicological acceptance)
    • EN 71-3 (Toy safety: colorant migration limits)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • ISO 13007 (Dye purity for industrial applications)

    Typical usage ratio

    • Between 1–3 molar equivalents relative to substrate for primary sulfonation
    • Optimized to achieve specified dye shade/depth and solubility in line with client technical sheets

    Downstream process integration

    • Dosed post-nitration/pre-condensation in dye molecule synthesis
    • Sulfonation staged prior to coupling agent addition
    • Followed by neutralization, solvent recovery, and fine filtration

    Final product types

    • Direct dyes for textile finishing
    • Acid dyes for leather and paper coloration
    • Optical brighteners for detergent and pulp bleaching
    • Azo-based technical dyes

    5. Fluorinated Sulfonate Synthesis for Advanced Performance Materials

    Manufacturers use this reagent to produce fluorinated organosulfonates required in high-performance lubricants, surfactants, and selective membranes. The dual sulfonyl chloride groups react with fluorinated alcohols or amines, resulting in compounds with exceptional thermal stability and surface activity. Quality labs verify product integrity with NMR and titration prior to downstream fluorination or blending operations. All shipments are covered with detailed COA and batch traceability.

    Industry compliance standards

    • ISO 9001:2015 (Quality assurance in specialty chemicals)
    • GHS/CLP regulations on hazardous material transport
    • Internal QC: HPLC and ^19F-NMR data files per lot
    • Responsible Care® chemical management

    Typical usage ratio

    • 1.0–1.4 molar equivalents depending on reactivity of the fluorinated reactant
    • Adjusted to meet target sulfonation degree, validated by gravimetry and spectral analysis

    Downstream process integration

    • Reacted with perfluoroalkyl alcohols under basic or solvent-free conditions
    • Process includes phase separation, neutralization, and stripping of byproduct hydrochloric acid
    • Critical purge and dry-keep before product moving to formulation lines

    Final product types

    • Fluorinated sulfonate surfactants (oil & gas, electronics)
    • Membrane materials for fuel cells and water electrolysis
    • Performance lubricants with high thermal/chemical tolerance
    • Surface active agents for technical fluids
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    Certification & Compliance
    More Introduction

    1,3-Benzenedisulfonyl Chloride: Practical Experience from the Production Floor

    A Closer Look at 1,3-Benzenedisulfonyl Chloride

    1,3-Benzenedisulfonyl chloride (also known as m-benzenedisulfonyl chloride or m-phenylenedisulfonyl chloride) occupies a unique space among aromatic sulfonyl chlorides. Our teams have worked with this compound under a range of conditions for years, adjusting processes to ensure that each batch meets high purity standards demanded by specialty synthesis and advanced polymer industries. With a repeated molecular arrangement—sulfonyl chloride groups located at the 1 and 3 positions on the benzene ring—this compound demonstrates a balance between reactivity and selectivity that other sulfonyl chlorides sometimes lack.

    Understanding the Model and Purity

    Consistent quality represents a major part of our production philosophy. Each drum of 1,3-benzenedisulfonyl chloride rolling off our line contains carefully controlled material. Typical product comes as off-white to pale yellow crystalline solid. From practical experience, the real determinant of usefulness lies in purity. The majority of downstream syntheses—whether for polymers, pharmaceuticals, or custom organic intermediates—benefit from our product’s minimum purity specification, which we hold at >98%. We focus on keeping moisture and hydrolyzable impurities as low as technically feasible since even minor contamination can cause issues during sulfonation or crosslinking steps.

    Working with the Chemistry: Applications Seen in Practice

    Few compounds in our catalog bridge so many projects as 1,3-benzenedisulfonyl chloride. We’ve shipped this product for work on specialty polyimides—those high-performance plastics found in aerospace and microelectronics. The difunctional structure makes it suitable for linking diamines, where the reaction between sulfonyl chlorides and amines forms sturdy sulfonamide bonds. Research labs often request it for advanced pharmaceutical syntheses, especially when selective functionalization at the aromatic ring is required.

    Researchers and process engineers often arrive at 1,3-benzenedisulfonyl chloride after comparing it with its positional isomer, 1,2-benzenedisulfonyl chloride. That small change—moving from ortho to meta positions—directly affects polymer network formation, crosslink geometry, and solubility of the resulting product. In practice, we see that the meta arrangement in our compound gives greater flexibility in polymer backbone design and leads to resins with distinct heat and chemical resistance. Many downstream projects benefit from these nuances, particularly laser-stable imaging coats or solvent-resistant membranes.

    Handling and Operational Considerations

    Experience has taught us to respect the hydrolysis sensitivity of sulfonyl chlorides. Any exposure to ambient moisture triggers decomposition and produces hydrogen chloride gas—a familiar but unwelcome guest in the production area. Our process minimizes moisture ingress from the moment crude is separated, relying on sealed equipment and prompt packaging to keep the active component intact. Even at the customer’s bench, safe handling calls for a drybox or nitrogen environment. Such operational discipline protects both the end product and the operator’s health.

    From a logistics perspective, we’ve learned to avoid extended transport in humid climates. During peak summer, our logistics team leverages insulated containers wherever possible. Experience counts, and careful packaging under nitrogen or with desiccants makes all the difference.

    Process Reliability and Real-World Expectations

    On our shop floor, equipment design responds to the realities of aromatic sulfonyl chloride chemistry. All wetted parts use passivated steel or corrosion-resistant alloys. Batch integrity depends on temperature control: heat or excess time will promote sulfonic acid byproducts. Over many years, we’ve dialed in our crystallization and filtration steps. Reliable supply, in our view, rests on more than just shipping correct paperwork. The reactors, centrifuges, and drying lines see constant checks—no one benefits from a formula that works in theory but disappoints in practice.

    Customers share feedback from pilot to industrial scale. Some have noticed minor yellowing in finished polyimides if byproduct content increases, especially during runs using less pure sulfonyl chloride. We consistently address this by pushing our manufacturing standards for lower free acid content. Our practical knowledge and process controls, not just lab analysis, keep lot-to-lot variations minimal.

    Comparison with Other Sulfonyl Chlorides

    1,3-Benzenedisulfonyl chloride carves its niche beside single-site or ortho/para isomers. While p-toluenesulfonyl chloride and benzenesulfonyl chloride deliver classic monosulfonyl chemistry for protecting groups in organics or routine coupling, our difunctional aromatic system introduces options for building complexity. In certain crosslinked networks or advanced membrane research, that matters. Customers in polymer R&D have shared that our meta-disulfonyl chloride helps produce tighter pore size control in sulfonated membranes, compared to more flexible aliphatic disulfonyl analogs.

    We’ve seen chemists test 1,3-benzenedisulfonyl chloride against alternatives—looking for higher thermal stability, improved hydrophilicity, or better controlled crosslink density. Each adjustment in structure ripples through the end-use performance. Our team assists with technical questions so users can tailor their processes accordingly. Sometimes a single methyl group swap or isomer change tips a project from success to failure. Those details drive our attention to consistent production quality and open communication with research teams worldwide.

    Supply Assurance with Regulatory Confidence

    Producers bear the responsibility of safety as much as chemistry. Over time, we’ve aligned our operations with evolving local and global environmental guidelines. While not subject to the same high profile as a pharmaceutical intermediate, aromatic sulfonyl chlorides still face regulatory scrutiny. We meet these requirements through continual audits and well-documented safety data, acting long before a regulatory body mandates documentation.

    Our teams maintain up-to-date analytical records and traceability for each batch. Sampling, sealed documentation, and logistics coordination reduce interruptions for customers. More than once, users have called us for support with compliance documentation when border authorities request unusual details on byproducts or synthetic origins. We help them get paperwork right, drawing on firsthand experience in audits and customs reviews. That confidence and transparency benefit everyone in the value chain, starting from our gate all the way to the research lab or plant floor.

    Challenges and Learning Through Experience

    Complex molecules demand more than a recipe and a list of raw materials. During process scaleup, we faced more than one challenge controlling chlorination and sulfonation selectivity—undesired isomers or polysubstituted byproducts cropped up in early batches. Overcoming these hurdles needed steady troubleshooting, hands-on purification, and hours at the process controls. This practical insight now shapes our internal training and drives gradual improvements to reactor design and analytical protocols.

    Handling solid aromatic sulfonyl chlorides at commercial scale can become troublesome due to caking or agglomeration under humid conditions. Through trial and error, we transitioned from simple drum lining to the use of specialized inner liners and moisture-scavenging inserts. Our experience: a little preventive action up front saves customers significant downstream pain. Technical support doesn’t end at shipment; customers sometimes reach back to discuss process adaptations for application-specific needs, such as optimizing reaction times during polyamide synthesis or troubleshooting unexpected side products in pharmaceutical manufacturing.

    Listening and Supporting Researchers

    Because our history as a manufacturer predates trends in membrane science and modern specialty polymers, we’ve watched application landscapes shift over time. Ten years ago, most orders targeted established reactive intermediates for dyes or pigments; today, more requests focus on advanced resin systems, lithium battery separators, and fuel cell membranes. We’ve collaborated with university researchers on exploratory projects, sharing stability data or supplying custom particle size cuts for experiments. Shared learning benefits both sides—our customers gain from our process practicalities, and we gain from the innovations they bring to application fields.

    New users often seek advice on dissolving and incorporating the compound into their systems. From our own lab trials, we know that dry acetonitrile or chlorinated solvents work best; water must remain excluded at every step. Those small details, often learned the hard way by a junior chemist at midnight, make a noticeable impact on outcome. Embedded technical notes and support documents draw from real setbacks and solutions tested in full-scale production—not just theory or datasheets.

    Our Role: Reliable Partnership, Not Just Supply

    Engagement doesn’t stop with a shipment notice. Our technical representatives regularly gather project feedback from labs and factories who use 1,3-benzenedisulfonyl chloride in new synthesis or production environments. Sometimes users are working under evolving process constraints or dealing with downstream regulatory reviews. Our track record shows that keeping access open to practical troubleshooting, process suggestions, or even slight customizations in packaging avoids costly delays and ensures product is genuinely fit for the purpose.

    Customers have asked for modifications ranging from scaled-down test lots to pre-weighed, low-moisture small packs for handling in glove boxes. Our flexible approach has grown out of responding directly to these needs, rather than offering rigid, “take it or leave it” supply. Such adaptability requires deep knowledge of the product, ongoing process monitoring, and honest two-way communication—a standard we keep because the reality of real-world projects rarely matches idealized catalog conditions.

    Fostering Safe Use and Sustainable Practice

    Safety underpins our daily operations. Our production team trains on sulfonyl chloride handling as a matter of routine, using experience with spills, emergency responses, and proper storage techniques to cement best practice. Each incident report or near-miss becomes tomorrow’s training example. Efforts extend beyond our walls; we partner with shipment handlers and key customers, passing along learnings and recommendations for safe storage or mitigation in case of accidental release.

    In today’s evolving market, sustainability matters too. Aromatic sulfonyl chlorides touch many chemical lifecycles, some with environmental implications. Where production generates recoverable byproducts, our facility reclaims and recycles as much as possible, documenting the process for customer transparency. Our approach aims not only for regulatory compliance but for continuous reduction of inefficiency and impact in day-to-day operations.

    Looking Ahead: What Stays Consistent

    The role of 1,3-benzenedisulfonyl chloride continues to evolve in new processes and markets. Whether the focus is the highest performance polyimide fibers or targeted pharmaceutical intermediates, technical details keep shifting. Still, one thing holds true: hands-on manufacturing expertise, close customer contact, and a willingness to improve beat the standard “off the shelf” supply model. Through decades of trial, dialogue, and adjustment, our team has turned this sulfonyl chloride from a specialty curiosity into a go-to solution for complex synthesis and material science projects worldwide.

    As expectations rise, we continue to build on our core practice: marrying process discipline with transparency, steady improvement, and precise technical support. The result shows in every batch—real chemistry, made reliable through experienced hands and careful listening.