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HS Code |
592358 |
| Chemical Name | 3-Nitrobenzenesulfonyl Chloride |
| Cas Number | 636-95-3 |
| Molecular Formula | C6H4ClNO4S |
| Molecular Weight | 221.62 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 72-76°C |
| Solubility | Reacts with water, soluble in organic solvents |
| Density | 1.65 g/cm³ |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | O=[N+]([O-])C1=CC=CC(Cl)(S(=O)(=O))=C1 |
| Synonyms | m-Nitrobenzenesulfonyl chloride |
As an accredited 3-Nitrobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Nitrobenzenesulfonyl Chloride is supplied in a tightly sealed amber glass bottle with hazard labeling and tamper-evident cap. |
| Shipping | 3-Nitrobenzenesulfonyl chloride should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It must comply with regulations for hazardous materials, typically classified as corrosive and an irritant. Proper labeling, secondary containment, and documentation are required to ensure safe transport and handling during shipping. |
| Storage | 3-Nitrobenzenesulfonyl chloride should be stored in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizing agents. Keep the container tightly closed and protected from direct sunlight. Store under an inert atmosphere if possible to minimize moisture exposure, as it hydrolyzes readily, releasing irritating and toxic gases. |
Applications of 3-Nitrobenzenesulfonyl Chloride in Industrial ManufacturingAs a direct manufacturer with deep technical expertise in aromatic sulfonyl chlorides, we supply 3-Nitrobenzenesulfonyl Chloride to global B2B partners for precise, critical synthesis steps in their production lines. This material plays an irreplaceable role in select pharmaceuticals, dyes, pesticide intermediates, and specialty chemical transformations. Below, we detail key industrial applications supported by our supply, with information based on actual downstream adoption and regulatory requirements. 1. Pharmaceutical Sulfonamide Intermediate SynthesisOriginating as a preferred sulfonylating reagent, this compound is widely adopted by manufacturers specializing in the development of sulfonamide-based antibiotics and selective enzyme inhibitors. Its electrophilic sulfonyl chloride group enables highly efficient coupling with amines under controlled reaction settings, providing reliable throughput for regulated drug production pipelines. Pharmaceutical producers rely on its consistent reactivity and purity when scaling, especially in multi-step synthesis for active pharmaceutical ingredients (API). Industry compliance standards
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2. Azo Dye Intermediate ManufacturingDye producers utilize this material when constructing sulfonyl-bearing aromatic amines as precursors for vivid, water-soluble azo dyes. It serves as a key sulfonating agent during diazotization and coupling steps, ensuring dye molecules maintain strong bathochromic shifts and optimal fastness profiles. Its nitro substituent preserves chromatic intensity while supporting high-yield conversion rates in continuous reactor setups. Industry compliance standards
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3. Agrochemical Sulfonamide Precursor ProductionAgrochemical formulators select this material primarily for the preparation of advanced sulfonamide herbicide or fungicide intermediates. It reacts with appropriate amine carriers, granting high selectivity and conversion rate in large-volume plant scales. Its low impurity load and reliable supply chain help agrochemical contractors maintain process efficiency and purity approval standards for finished plant protection agents. Industry compliance standards
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4. Specialty Chemical Building Block for SulfonylationChemical processors apply this compound during selective sulfonylation steps when constructing advanced intermediates for electronics, polymer additives, or fluorination reagents. It manifests high utility in producing functionally substituted benzenesulfonyl derivatives, enabling downstream transformations like cross-coupling and nucleophilic substitution. Plant chemists value its stage-specific reactivity, allowing for tunable functional group introduction without over-sulfonation or product instability. Industry compliance standards
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5. Analytical Chemistry Derivatization ReagentsProducers of advanced analytical reactivity kits leverage this compound as a derivatization agent to selectively tag and quantify amines, peptides, and amino acids in both pharmaceutical QC and research settings. Its unique reactivity profile and the resulting tagged derivatives offer improved chromatographic characteristics, detection sensitivity, and identification accuracy in HPLC and LC-MS protocols. Controlled batch consistency enables certified reference material producers to meet both research and industry demands for high-purity standards. Industry compliance standards
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In the chemical plant, every reaction step takes place under a watchful eye. Among the chemicals that make routines at our site specific and valuable, 3-nitrobenzenesulfonyl chloride (CAS 636-73-7), often referred to as NBSCl for brevity among technical staff, stands out. All employees here know the yellowish crystalline compound, not as another inventory number, but as a crucial building block for a wide set of synthesis processes. Our batches run from kilograms for R&D labs to full tonnage for larger pharmaceutical campaigns.
We never treat the quality of this compound as an afterthought. Years of hands-on process tuning have shown the levels of purity directly affect success rates in downstream applications. A conversion step using a sample with 98% purity doesn’t compare at all with a carefully refined 99.5%, especially in the hands of a medicinal chemist trying to avoid side reactions or purification headaches.
Inside our plant, we control the multi-step synthesis, guaranteeing the powerful sulfonyl chloride group attaches precisely in the 3-nitro position. Our production lines don’t just pass raw benzenesulfonyl chloride and nitric acid through; we have invested in multiple-stage purification that strips away impurities — unreacted precursor, isomeric by-products, and especially moisture, which tends to degrade the resulting acid chloride in storage.
Our standard shipment leaves the warehouse crystal-dry, pale yellow, and rigorously several times filtered. Moisture content drops consistently below 0.2%, and most customers come to us asking for at least 99% assay by HPLC. Some projects, including specialized electronics and pharma work, push for higher purity, which we have developed on-demand without scaling headaches.
Particle size comes up sometimes in customer discussions. Typical material from our lines averages in the 200-400 micron range, which reduces clumping in automated feeders and fits most batch reactors. Researchers with solid phase synthesis requests sometimes ask for a different cut. We schedule those on dedicated equipment, not as an afterthought or side job, so cross-contamination stays absent from our records.
We have found that packing matters just as much as purity for this compound. Our line workers double-bag under nitrogen, directly inside the cleanroom, with the inner packaging designed to minimize light exposure and atmospheric ingress. That simple discipline cuts down on hydrolysis and keeps the product consistent even after transcontinental shipment.
In large-scale workshops, customers bring up questions about why this particular sulfonyl chloride — out of a whole catalog full of them — matters. From our perspective, nothing highlights this better than its dual reactivity and precise substitution.
3-Nitrobenzenesulfonyl chloride reacts with amines, alcohols, and other nucleophiles, forming sulfonamide or sulfonate linkages. That feature isn’t unique; what distinguishes it is the electron-withdrawing nitro group positioned at the meta point. Over years of supplying to peptide chemistry labs, we’ve seen how this configuration slows hydrolysis and self-coupling, compared to other isomers or unsubstituted benzenesulfonyl chloride.
R&D chemists have pointed out that the 3-nitro substitution restrains electron density enough to offer selective deprotection in stepwise organic syntheses. For example, after coupling with an amino acid, clever use of reductive or basic cleavage removes only the desired protecting group, leaving others untouched. Our partners in dye manufacture utilize the meta nitro group’s altered UV absorbance, letting them tailor their chromophores for high-stability pigment systems.
Every week brings new questions about alternatives — why not the 4-nitrobenzenesulfonyl chloride, or the unsubstituted analog? Real experience has shown us three-nitro’s position gives unique reactivity. The para isomer, for example, brings increased activation and higher hydrolysis rates, which sometimes triggers byproduct formation or handling risks. In our factory, we notice the para form turns brown rapidly with just a whiff of damp air, while our three-nitro lines store and ship with color and purity stable for many months.
Researchers developing diagnostics repeatedly confirm the value of lower background signals from three-nitro-linked labels, compared to less substituted analogs. Through their feedback, and our own regular use tests (we blend small batches in the onsite test lab for QC itself), we confirm claims with data, not desk research.
One overlooked detail in the chemical manufacturing world is how aging plants or third parties sometimes pinch costs in their process. We take pride that our three-nitrobenzenesulfonyl chloride lines never mix recycled solvents from unrelated runs. Each campaign gets fresh reactants, and we dedicate all glassware, powder transfer equipment, and filter systems, reducing batch-to-batch variability. That attention avoids traces of heavy metals or unwanted aromatic residues, troublesome in sensitive pharmaceutical or electronic applications.
Our QC department spends real hours running both in-house titration and chromatographic fingerprinting, not just the minimum HPLC scan a spec sheet demands. Over the years, these extra checkpoints have reduced customer complaints about misbatches and avoided costly reshipments.
We keep linesafe logs and production records for every lot. That culture matters more than any marketing claim. When a batch triggers a question or special observation, scientists doing the work check back through original run conditions and can often pinpoint the step where variation began.
Our operators note even the subtle odors and color shifts during preparation, which is a real advantage over fully automated, hands-off feeds. Three-nitrobenzenesulfonyl chloride emits an acrid, but not overpowering fume, and that sensory input often flags process issues before they turn into paperwork.
Downstream users employ this compound extensively for intermediate steps in pharmaceuticals, specialty chemicals, and diagnostics. In industry discussions, drug designers emphasize the need for efficient, orthogonal protecting group chemistry. Our product finds its role in several patented peptide and oligonucleotide programs because the nitro group’s electron-withdrawing power modulates both reaction rate and selectivity.
Diagnostic device developers need stable, robust labeling agents. With three-nitrobenzenesulfonyl chloride, our site’s QC data shows lot-to-lot signal reproducibility, in contrast to more reactive alternatives, where shelf instability or cross-reactivity leads to higher calibration failures.
From hands-on pilot projects years ago, we have seen manufacturers turn away from benzene sulfonyl chlorides lacking the nitro group once they run small-molecule coupling reactions on real-world scales. Losses from premature hydrolysis, problems with extraction, and trouble in downstream purification all surface during scale-up. Through real process experience, we learned the value that three-nitro substitution adds.
In our R&D unit, chemists have experimented with the compound’s behavior in polymer modification and fine-tuned its integration into functionalized resins for ion-exchange and chromatography. The meta-nitro pattern brings stability in storage, slow baseline drift, and resistance to fouling in long-term use.
Anyone working with acid chlorides spends plenty of time discussing safety, but it goes beyond following broad rules. Even within our own warehouse, three-nitrobenzenesulfonyl chloride’s reactivity, dusting behavior, and hydrolysis make for unique handling compared to its chemical cousins. Suiting up in goggles, thick gloves, and proper masks isn’t just a formality; fine powder can cause fast irritation, and any exposure to open humid air sets off fuming.
Long experience shows that bins must seal tightly and air purges on transfer lines need continual monitoring to keep moisture out. While pure product rarely triggers fires, secondary reactions with trace water get hot fast. Our facility uses dedicated local scrubbers and immediate neutralization stations, rather than relying only on plant-wide safeguards.
We take a hands-on approach to waste handling. Reaction residues treated with ammonium solutions or simple base neutralize quickly, and we regularly monitor for any traces of organosulfonic acid leaking into the effluent stream. The controlled procedure has prevented regulatory issues and costly environmental audits over the years.
With chemical investments in staff training and minor on-site modifications, we have kept incident records clear of inhalation problems for more than a decade now, even while handling tonnages that would overwhelm sites that try to cut corners. Our safety program runs on continual retraining, direct feedback from operators, and monthly review rather than sporadic after-the-fact fixes.
Logistics for an air- and moisture-sensitive intermediate like three-nitrobenzenesulfonyl chloride introduces unique hoops. Over the years, we stopped relying on generic packaging suppliers and developed relationships with a select group that can pre-purge and seal lined drums before arriving at our dock. Any exposure during transit affects product stability, especially for the high-end pharmaceutical formulations.
Real incidents have shown us what happens when poorly bagged samples sit on tarmacs or in customs, soaking up damp air. Several batches lost their purity and required costly disposal. Based on those hard lessons, every box leaving our warehouse includes datalogger strips to monitor temperature and relative humidity. This transparent feedback loop allowed us to retrain logistics partners and cut out weak links that don’t respect the specialized nature of the material.
Smaller lots for research or prototyping move in smaller vials, again sealed in nitrogen-filled foil to avoid accidental exposure in universities or startup labs, which often lack sophisticated storage. By offering flexibility in shipment sizes, we prevent accidental waste and lower entrance barriers for R&D teams.
As a manufacturer, far removed from the trading desk, we keep regulatory paperwork embedded in all production and testing stages. Trace-level control matters when supplying to clients designing molecules destined for regulatory review. Our records for three-nitrobenzenesulfonyl chloride include real-time QC results, certificate archives, and clear digital audit trails.
Over the years, we have worked with auditors from pharmaceutical and agricultural chemical companies to line out clear impurity profiles that meet global Pharmacopeia and REACH requirements. We routinely share data with clients who require full batch histories, which boosts confidence when a regulatory body comes knocking.
Genuine producers know the difference between real manufacturing and bulk reselling. We get questions from buyers who have struggled with uneven supply and inconsistent quality after working with traders or unknown offshore sources. Our commitment to in-house synthesis — every precursor, every handling step — sets us apart, and we keep this transparent.
In direct feedback calls with regular clients, we often hear that quick shipping means little if the delivered material fails in the real workflow. There is no point in selling a “high-purity” label if the batch can’t stand up to rigorous intermediate use. Live process know-how, not paper claims, is what lets us troubleshoot quickly when a client runs into a process block.
Peer-to-peer advice within our technical sales and support team keeps information flowing both ways. We never promise an application fit that we haven’t run in our own small-scale plant tests. Manufacturing discipline means beating deadlines through reliable infrastructure instead of outsourcing to the cheapest outside party.
Chemists rarely work in isolation, and our experience has reinforced the value of real dialogue. We routinely participate in collaborations ranging from process trouble-shooting for scale-up to tailored customization for research groups refining next-generation reaction schemes. This collaboration starts with technical transparency, not salesmanship.
We take pride in providing open-access information from the plant floor — sometimes inviting clients to witness production steps, analyze our in-house QC results, and see firsthand the controls we have in place. Updates based on feedback from these exchanges have led to meaningful innovations in drying, packaging, and documentation, and they continue to drive our improvements.
University and industry partners have shaped our product development, especially in requests for lower-dust formats for high-throughput screening and ultra-dry batches for sensitive electronics fabrication. Rolling out these changes comes from direct feedback, with every tweak and new configuration tested in our own applications lab before scaling commercially.
In the world of specialty chemicals, three-nitrobenzenesulfonyl chloride will continue to find ever-more technical demand. We have invested in ongoing process improvements to ensure consistency, safety, and customization at scale. As newer synthetic methods and greener practices evolve, our aim stays fixed on minimizing environmental impact without sacrificing the product purity or reliability that our long-term clients depend on.
Continuous feedback drives our evolution — both from in-house R&D and from regular technical discussions with end-users. By honestly reporting both strengths and limits, and by sticking to hard-earned manufacturing discipline, we aim to remain the preferred supplier to both industry and academic innovators. Our door is open for serious technical inquiry, direct application feedback, and collaborative development of new use cases for this essential intermediate.