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3-Carboxypropanesulfonamide

    • Product Name 3-Carboxypropanesulfonamide
    • Alias ACES
    • Einecs 241-721-9
    • 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

    270939

    Productname 3-Carboxypropanesulfonamide
    Casnumber 2719-48-0
    Molecularformula C4H7NO4S
    Molecularweight 165.17 g/mol
    Appearance White to off-white solid
    Meltingpoint 188-192°C
    Solubility Soluble in water
    Purity Typically ≥98%
    Boilingpoint Decomposes before boiling
    Functionalgroups Carboxylic acid, sulfonamide
    Synonyms β-Carboxyethanesulfonamide
    Chemicalstructure HSO2NHCH2CH2COOH
    Storageconditions Store at 2-8°C, keep container tightly closed
    Pka Carboxylic acid: ~4.7 (estimated), sulfonamide: ~10 (estimated)

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

    Packing & Storage
    Packing A 25g amber glass bottle labeled "3-Carboxypropanesulfonamide," featuring hazard symbols, batch number, and tightly sealed with a screw cap.
    Shipping 3-Carboxypropanesulfonamide is shipped in tightly sealed containers to prevent moisture ingress and contamination. It is labeled according to chemical safety regulations, with all relevant hazard and handling information. Typically transported via ground or air freight as a non-hazardous chemical, it should be stored in a cool, dry location upon arrival.
    Storage 3-Carboxypropanesulfonamide should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers. Properly label the container and avoid exposure to extreme temperatures. Personal protective equipment should be used when handling to prevent skin or eye contact.
    Application of 3-Carboxypropanesulfonamide

    Applications of 3-Carboxypropanesulfonamide in Industrial Manufacturing

    3-Carboxypropanesulfonamide is a highly specialized chemical intermediate that has found purposeful integration in several advanced industrial fields. Recognized for its unique functional group structure, this material supports key transformations within selected manufacturing value chains. Below, we detail principal downstream sectors that deploy this raw material at industrial scale, alongside process-focused guidance and regulatory information.

    1. Advanced Pharmaceutical Synthesis: Sulfonamide Drug Intermediate

    Within pharmaceutical API production, 3-Carboxypropanesulfonamide acts as a sulfonamide building block during the creation of targeted antimicrobial and diuretic agents. Process chemists utilize it in amidation and condensation steps to construct core molecular structures, ensuring strict batch consistency and traceability. The use and purity specification adhere tightly to drug master file requirements and validations for final API registration in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP / EP / JP monographs where applicable
    • 21 CFR Part 210 and 211 (US FDA)
    • EDQM Certification of Suitability (CEP)

    Typical usage ratio

    • 0.7% to 2.5% w/w in core reaction intermediates, adjusted based on target yield and molecular weight of the desired final API

    Downstream process integration

    • Introduced during the amide coupling or sulfonation stage in multi-step organic synthesis, following solvent charging and in-process QC verification

    Final product types

    • Sulfonamide antibiotics (e.g., sulfamethoxazole derivatives)
    • Thiazide-related diuretics
    • Specialty custom APIs for clinical research supplies

    2. Industrial Water Treatment: Chelating Compound Precursor

    In the water treatment chemicals industry, manufacturers employ 3-Carboxypropanesulfonamide as a precursor for producing proprietary chelating agents. These agents target scale, heavy metal capture, and membrane antiscalant formulations. Producers control addition rates to comply with residual regulatory thresholds and application-specific performance, particularly in regions mandating effluent composition limits.

    Industry compliance standards

    • NSF/ANSI Standard 60: Drinking Water Treatment Chemicals
    • EN 15040: Chemicals Used for Treatment of Water Intended for Human Consumption
    • REACH Registration (EC 1907/2006, Europe)
    • EPA Clean Water Act Section 307

    Typical usage ratio

    • 0.2% to 1.0% w/w in chelating agent synthesis reactions, optimized for sequestration efficiency and compatibility with blending polymers

    Downstream process integration

    • Dosed into aqueous phase during the chelating ligand formation stage, generally after initial polymer backbone assembly but before pH neutralization and filtration

    Final product types

    • Reverse osmosis antiscalant additives
    • Industrial water softening agents
    • Metal ion sequestrant blends for circuit board manufacture

    3. Electroplating and Metal Surface Treatment: Functional Additive for Bath Stabilization

    For complex metal finishing and electroplating operations, 3-Carboxypropanesulfonamide serves as a critical bath additive, contributing to enhanced layer uniformity and reduction of dendritic growth during electrodeposition. Technical teams maintain precise dosing according to substrate type and current density criteria, ensuring process compliance for high-quality surface metallization on sensitive parts used in electronics or automotive subassemblies.

    Industry compliance standards

    • ISO 6158:2018 (Metallic and Other Inorganic Coatings—Electroplated Coatings of Zinc with Additives)
    • ASTM B700: Standard Specification for Electrodeposited Coatings
    • RoHS Directive 2011/65/EU for end use in electronics
    • IEC 62321 Serial for hazardous substance screening

    Typical usage ratio

    • 10 ppm to 75 ppm, calculated based on bath volume and substrate area; periodic adjustment with inline process monitoring

    Downstream process integration

    • Directly injected into plating bath after initial metal salt and brightener introduction; incorporated before parts loading and continuously monitored for ion stability

    Final product types

    • Printed circuit board functional coatings
    • Precision automotive fastener plating
    • Decorative and corrosion-resistant metal parts

    4. Specialty Polymers: Sulfonated Copolymer Monomer Feedstock

    In advanced polymer synthesis facilities, 3-Carboxypropanesulfonamide is adopted as a comonomer or functionalizing agent in sulfonated polymer chains. Polymer engineers calculate loading based on desired ion-exchange capacity or hydrophilicity, regulating process inputs to meet the physical property targets required by downstream OEMs for membranes or specialty films.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for plastics manufacture
    • FDA 21 CFR 177.1520 for food contact polymers (when applicable)
    • REACH SVHC (Substance of Very High Concern) restrictions
    • ASTM D883 for plastics terminology and characterizations

    Typical usage ratio

    • 1.5% to 4.0% by weight of total monomer feed, selected according to balance of sulfonation degree and polymer molecular weight targets

    Downstream process integration

    • Fed to the reactor vessel post-initiation during bulk or emulsion copolymerization; inline viscosity and conversion monitoring control addition

    Final product types

    • High-performance ion exchange membranes
    • Sulfonated polyamide or polyester process films
    • Specialist hydrophilic coatings for filtration and battery separators

    5. Laboratory Fine Chemicals: Reference Standard Material Production

    Manufacturers of analytical standards and high-purity laboratory reagents utilize tightly specified 3-Carboxypropanesulfonamide batches for preparing calibration compounds and control samples. Purity and contamination traceability prove critical for this segment, and addition levels depend on reference concentration requirements for method validation and regulatory lot release.

    Industry compliance standards

    • ISO 17034:2016 (Reference Material Producers)
    • IUPAC purity designation guidelines
    • ISO/IEC 17025 for analytical laboratory testing
    • USP Reagent Standards

    Typical usage ratio

    • 0.05% to 0.2% in batch reference solutions; calculated by intended reference material concentration and protocol guidance of regional pharmacopeias

    Downstream process integration

    • Weighing under controlled atmosphere and addition to solvent phase or carrier matrix during primary reference material preparation, followed by QC validation and certification

    Final product types

    • Certified analytical reference materials (CRM)
    • Internal standards for chromatographic and spectroscopic analysis
    • Pharmacopoeial secondary standards
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    Certification & Compliance
    More Introduction

    3-Carboxypropanesulfonamide: A Trusted Intermediate from the Producer’s Bench

    Behind the Molecule: Building Reliability in Chemical Synthesis

    At our facility, we handle a lot of complex chemistry. Over the years, one molecule that keeps coming up in R&D and scale-up meetings is 3-Carboxypropanesulfonamide. This isn’t new for us; we’ve manufactured it on campaigns big and small, across several years of market fluctuations and laboratory trends. Chemistry teams ask about its purity, consistency and handling, and since we’re the source, our focus stays fixed on batch reliability and open data. Our plant engineers know firsthand that most bottlenecks show up not at the design table, but in day-to-day plant operation — temperature controls, material compatibility, waste management — and our experience with this sulfonamide means we can spot the trouble areas early.

    Defining the Compound: Lifting the Hood on 3-Carboxypropanesulfonamide

    This compound, classified chemically as a sulfonamide bearing a carboxylic acid on a propyl chain, has found solid ground as a versatile intermediate. Labs turn to it for its dual-functionality: both the sulfonamide and carboxyl groups lend themselves to a range of coupling and derivatization reactions. We get calls from pharmaceutical researchers who use it to build out heterocyclic scaffolds, crop protection teams interested in its routes to functionalized sulfonamides, and specialty material innovators seeking novel polar monomers.

    Sulfonamide intermediates are crowded with options. But in our process, 3-Carboxypropanesulfonamide delivers a strong combination of selective reactivity and physical stability. Unlike analogues with longer or branched chains, this molecule keeps reactivity balanced without introducing unwanted side-products or overly aggressive conditions. Over the years, we’ve seen both seasoned chemists and young research associates choose it to circumvent tougher processes attached to bulkier sulfonamides or less stable carboxylic partners.

    Specifications Forged in Production: Purity, Appearance, and Handling

    Our plant never takes shortcuts with raw material quality or purification for this compound. We isolate 3-Carboxypropanesulfonamide as a white crystalline solid, paying attention to minimize colored impurities that complicate downstream synthesis. Orders from long-term partners usually demand assay purities exceeding 98%. There’s a reason for this: minor sulfonic or carboxy degradation fragments might not show up in spot tests but can wreak havoc in multistep pharmaceutical synthesis or polymer grafting.

    The melting point remains consistent from batch to batch, a detail synthetic chemists pick up quickly when chasing robust reaction controls. Our internal specifications include visual appearance checks, moisture content characterization (since even trace water can skew coupling yields), and thorough HPLC/GC profiles. Packing is never an afterthought. We use chemical- and moisture-resistant liners because we’ve seen firsthand that the tiniest leak during extended transit leads to avoidable hydrolysis and color formation. Stability trials guide our shelf life estimates, and we share these data openly with collaborators.

    Practical Uses Unearthed Over Decades

    Customers keep sharing new routes every year, but the bread and butter for 3-Carboxypropanesulfonamide centers on pharmaceutical and fine chemical synthesis. For a while, it was seen mostly as a sulfonamide-building pre-cursor, serving as a reliable nucleophile or coupling partner in amide bond formation. Pharma process chemists appreciate its straightforward behavior in alkylation and acylation reactions. As we watched the agrochemical market pick up pace, teams began using it for tailored incorporation into small-molecule herbicides and fungicides, exploiting both its aqueous solubility and unique pKa balance.

    More recently, we’ve supplied larger polymer makers, who leverage the carboxy and sulfonamide functions as polar handles in specialty copolymers, increasing hydrophilicity or inducing targeted cross-linking in medical materials and membrane technology. We’ve also seen growing interest from teams working on dye intermediates and complexing agents, pointing to its ability to anchor stable linkers.

    Distinguishing Features: How This Compound Measures Up

    Chemists often need to choose among a range of propanesulfonamides, so direct comparisons come up in almost every discussion. We know the limits of close analogues: longer-chain sulfonamides get waxy and sticky, turning simple handling into a headache. The shorter ones sometimes fall short in building more robust scaffolds, leaving teams with unreactive intermediates or hard-to-purify byproducts.

    Unlike the well-known 1,3-propanesulfonic acid, the amide in this molecule gives stable physical handling and improved shelf life, without the unpleasant hygroscopic drift we’ve tracked in pure-acid stocks. We keep hearing from labs struggling with side reactions when they use more basic amine analogues; switching to our grade of 3-Carboxypropanesulfonamide means fewer purification cycles and less fiddling with pH or solvent loads.

    Solid-phase or solution-phase, it resists degradation by light and air, so long as basic moisture limits are respected. For teams developing active pharmaceutical ingredients, these seemingly minor differences become crucial — fewer side products, predictable yields, and no late-stage surprises. The hands-on work on the plant floor — watching how quickly the product powders fill out drums, how they transfer with simple scoops, how the surfaces don’t cake or clump — all these qualities matter more over time than the figures on a spec sheet.

    Supporting Quality at Scale: Insights from Real Production

    Our operation scaled 3-Carboxypropanesulfonamide from bench to pilot long ago, and every expansion taught us new lessons. Initially, controlling the exotherm during amidation was the trickiest part; it took rounds of experimentation to find just the right cooling intervals. Our crew shifted from glass-lined to steel reactors after finding the sulfonamide held up better than expected, with stainless finishing cutting downtime for cleaning cycles. Every improvement stemmed from hands-on problem solving, feedback from our process operators, and in-plant dialogue.

    Moving from pilot to multi-ton lots, filtration and drying became the pinch points. Early on, small filter aids seemed fine, but particle size distributions on scale shifted fastest in humid weather. We learned the hard way that even a few grams out of spec leads to bottlenecks down the line, especially in pharma workshops running continuous processes. Regular in-process QC checks, with every batch tracked in plant logs, built confidence among our R&D partners and allowed us to keep production windows tight. Every step of the operation — charging reactants, agitation, temperature ramp, and downstream work-up — has been adapted and tuned through experience. It’s this in-house expertise that guides steady product quality, year after year.

    Handling, Storage, and Safety—A Producer’s Perspective

    Material safety comes from years of vigilance, not a one-time checklist. We store our finished 3-Carboxypropanesulfonamide in clean, dry bulk bins, using only new packaging for each load. Every loaded pallet moves under controlled humidity, with documentation accompanying each dispatch. If weather swings threaten stability, our on-site QA tracks temperature profiles and dispatch routes, logging every delay proactively.

    We’ve trained every member of the floor team on best handling practices: wearing gloves, avoiding dust clouds in decanting, checking drum seals before moving product to bulk storage. We don’t leave compliance to chance; our shop keeps standard operating procedures posted in each work area, and periodic refresher training stays in place. These routines are built on previous troubleshooting — moisture ingress on rainy days, stray powders near open drains, even the energy costs tied to longer drying cycles. Every piece of it feeds into better, safer material for laboratories and production shops downstream.

    On the safety front, 3-Carboxypropanesulfonamide delivers fewer surprises than more volatile sulfonamides or compounds with unstable leaving groups. It doesn’t fume, it doesn’t creep up containment hoods, and we don’t see aggressive corrosivity. We encourage safe handling with goggles and ventilation, but most personnel find that by staying disciplined, the risks stay manageable. Our on-site emergency drills include slow-release simulations, to cover even the rarest mishaps.

    Application Stories: What Real-World Experience Teaches

    We talk with customers from five-person startups through to global multinationals. Everyone has their favorite story of how a batch worked better than expected — or a time when a minor impurity threw off days of work. One research team working on N-alkylated derivatives for enzyme inhibitors reported that switching to our high-purity sulfonamide reduced purification steps so substantially that their project timeline accelerated by nearly a week. They’d been roadblocked on yield trim across dozens of pilot reactions.

    In material science, one group exploring hydrophilic membrane prototypes came across a persistent clogging problem with a branched analogue. Our 3-Carboxypropanesulfonamide showed improved solubility and dispersed better with their standard polymer backbones. Their pilot runs yielded cleaner films by every metric — transparency, tensile strength, and ease of handling.

    In the regulatory sphere, major pharmaceutical accounts have pushed us to strengthen our impurity tracking and process documentation. Feedback from their own audits led to additional stability trials and expanded chromatographic testing, ensuring our outputs conform to their stringent standards. This information loop has made us better producers. We fail less often on repeat orders and can back up claims with a deep archive of analytical records.

    Real-world anecdotes keep us grounded. Some users need economy, running simple coupling reactions and extracting only the required functionality; others need every impurity counted and tracked. We keep hearing that stability, repeatability, and ease of scaling are more important than the latest molecular trend. Practical laboratory wins drive persistent demand for reliable intermediates, and we've built our operation around that.

    Addressing Challenges: Supporting Chemists Beyond the Drum

    Raw material prices move. Regulatory lists change. These things strain even the best-run synthesis programs. Over time, we've realized that direct communication and open sharing of data matter more to users than hollow guarantees. When our solvent suppliers make unannounced tweaks in their own formulations, downstream color changes or filterability issues might show up in our customers’ runs. We proactively share updated analytical certificates and batch notes so that any drift in specs is tracked early.

    For groups scaling up for the first time, we're happy to share what we've learned about reaction compatibility, solvent performance, or quenching methods — not just the glossy highlights, but the practical pitfalls. Anyone can copy a batch procedure from a paper, but only producers with boots on the ground can warn about thermal runaways or the little quirks of scale-dependent process changes.

    For international buyers, regulatory alignment can become a hurdle. We keep material compatibility and local customs data up-to-date, and we collaborate with technical teams on import paperwork or safe use documentation. Years ago, we built feedback loops with quality teams at both ports of entry and user facilities to eliminate shipment delays or surprise compliance requests. We stay responsive for any questions that pop up once material starts moving.

    Continuous Improvement: Listening to Experience, Not Just Equipment

    Our product teams never treat process improvements as a one-and-done fix. Instead, every batch run in scale builds a record. When downstream partners report residual solvent beyond tolerance, or caking in hot climates, it feeds into next season’s procedures. A few years back, a rise in temperature at a customer’s remote receiving site led to minor discoloration — something we only solved by re-engineering our packaging protocols, including desiccant upgrades and double-bagging on every shipment to certain markets.

    We track user feedback carefully. Practical lessons from failed pilot reactions and on-site assessments are brought directly into production improvement meetings. These can range from fine-tuning particle size for automated feeders, to adjusting drying cycles for high-humidity months. Our analytics department keeps detailed logs not just for internal compliance, but so that any customer can request the history behind their specific lot and learn exactly what’s changed.

    Sometimes changes come from outside. Environmental regulations evolve, pushing us to further curtail waste and optimize process yields. Waste stream management and solvent recovery became a focus after new local ordinances required tracking even trace emissions. These improvements keep downstream users shielded from compliance risks. Open knowledge of audit trails, re-test procedures, and waste segregation now forms part of regular communication with our partners.

    Navigating Tomorrow: Why Methodical Production Remains Central

    The specialty chemical market keeps shifting, with new players and new applications showing up at our door each year. But the bedrock principles we stick to every week — measured process control, documentation, and honest dialogue — remain the difference between a fleeting commodity producer and a long-view supplier partners trust. 3-Carboxypropanesulfonamide, for us, represents not just another molecular tool, but a showcase for what proper chemical manufacturing delivers. Reliable supply, measurable properties, and support born from real experience.

    We trust this molecule because we know every step it’s taken — every improvement, every hiccup — just like other trusted intermediates we've produced through the years. So whether your work sits in drug discovery, crop science, or materials development, our focus stays on providing a consistent, well-characterized supply, backed by decades of hands-on manufacturing experience.