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HS Code |
321674 |
| Product Name | 2-Nitro-4-Methylsulfonylbenzoyl Chloride |
| Purity | ≥99% |
| Cas Number | 110964-79-9 |
| Molecular Formula | C8H6ClNO4S |
| Molecular Weight | 247.65 g/mol |
| Appearance | Light yellow to pale brown solid |
| Melting Point | 108-111°C |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, chloroform) |
| Storage Conditions | Store at 2-8°C, protect from moisture |
| Synonyms | 2-Nitro-4-(methylsulfonyl)benzoyl chloride |
| Smiles | CS(=O)(=O)c1ccc(cc1[N+](=O)[O-])C(=O)Cl |
| Hazard Statements | Corrosive; causes severe skin burns and eye damage |
As an accredited 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 10 grams, labeled with product name, purity (≥99%), hazard symbols, and manufacturer details for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL container loads 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) securely packed in drums or cartons for safe transport. |
| Shipping | 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is shipped in secure, chemical-resistant packaging to ensure stability and prevent leaks. The container is labeled per hazardous material regulations, shipped via certified carriers, and accompanied by a Safety Data Sheet (SDS). Temperature and handling instructions are strictly followed to maintain product quality and safety. |
| Storage | 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent moisture exposure. Keep it cool, ideally in a refrigerator at 2–8°C, and away from heat, light, and incompatible substances (like bases and oxidizers). Always use in a well-ventilated area or chemical fume hood. |
| Shelf Life | Shelf life of 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is typically 1-2 years if stored cool, dry, and protected from moisture. |
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Synthesis intermediate: 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is used in pharmaceutical synthesis, where high purity ensures optimal yield and minimal byproduct formation. Acylation reagent: 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is used in organic synthesis as an acylation reagent, where ≥99% purity leads to precise functional group incorporation. High stability: 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is used in chemical research under controlled temperature conditions, where its thermal stability up to 120°C enhances experimental reliability. Molecular weight consistency: 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is used in polymer modification projects, where accurate molecular weight facilitates reproducible polymer properties. Selective reactivity: 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) is used in custom synthesis of agrochemical compounds, where selective chlorination improves synthetic efficiency. |
Competitive 2-Nitro-4-Methylsulfonylbenzoyl Chloride (≥99%) prices that fit your budget—flexible terms and customized quotes for every order.
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As a chemical producer with decades of experience handling sulfonylated and nitroaromatic compounds, we know the difference a tightly controlled intermediate can make. Research and process chemists come to us for high-purity 2-Nitro-4-Methylsulfonylbenzoyl Chloride because it helps them eliminate avoidable variables. Product purity remains our biggest focus. With each batch, we achieve at least 99% assay, supported by robust internal chromatography and validated methods—there’s no room for guesswork here.
Some may see this compound as a simple benzoyl chloride derivative, but the molecular design goes much deeper than that. The presence of both nitro and methylsulfonyl groups brings new dimensions to the reactivity profile. Nitration occurs at the 2-position, adding electron withdrawal and changing the molecular electronics. The 4-position methylsulfonyl group further shifts reactivity, facilitating selective downstream reactions. The acid chloride function handles acylation, and we design our process to keep it as active as possible, minimizing hydrolysis or byproduct formation at every step.
Synthesizing 2-Nitro-4-Methylsulfonylbenzoyl Chloride requires a controlled multistep approach. Nitrobenzene derivatives challenge both yield and purity, especially during work-up. We source base materials with certified origins to keep metal traces and other interferences low. Success lies in controlling process moisture—chloride hydrolysis ruins the product, so our reactors and packing areas stay bone dry and run under inert gas. Glass-lined reactors avoid unwanted corrosion, and we watch exotherms at each stage to prevent side reactions.
Vacuum distillation removes volatiles efficiently. Operators record and inspect each fraction, rejecting any with out-of-spec color, odor, or TLC signature. Before release, every batch faces NMR, GC-MS, and HPLC, matched against retained standards, so the certificates reflect real, verified data. Customers who run their own incoming QA confirm what we see: our material gives consistent, high-yield conversions, batch after batch.
When a project depends on a key intermediate, small impurities can disrupt the entire sequence. Our clients, many pushing the frontiers of pharmaceutical and agrochemical synthesis, rely on absolute purity to keep their own downstream products clear. Contaminants—whether residual acids, water, or side products—can throw off stoichiometry, poison catalysts, or add hours to column purification.
By staying above 99% assay, we protect chemists’ time. This almost always means minimal waste and better analytics. The methylsulfonyl and nitro groups face particular scrutiny because their analogs can mimic authentic product on TLC but derail multi-step routes. Experienced eyes in the plant recognize this, and the difference plays out fast in customers’ HPLC results and yields.
We ship this product designated as model 2N4MSBC-99, but the experience matters much more than a label. We only use amber glass bottles and approved polypropylene drums, as benzoyl chlorides degrade fast under light or with traces of moisture. Every vessel gets a tamper-evident seal and batch-lot identification—bringing full traceability and safety. Decades of hands-on handling show that simple things like temperature control during fill and pack can head off problems weeks down the line, especially in distant export shipments.
The unique structure of 2-Nitro-4-Methylsulfonylbenzoyl Chloride makes it popular among chemists synthesizing specialized heterocycles. Its electron-withdrawing nitro group and the strong sulfonyl presence at the para position direct activity and enable specific cross-couplings. Academic groups and R&D labs harness it for constructing substituted benzamides, sulfonamides, and novel urea linkers in medicinal chemistry. The reactive acid chloride group allows quick, high-yield coupling with a wide range of amines, hydrazines, and even most phenols.
Customers working on complex library syntheses or custom route development often return after their first order. They point to the sharp melting point of our solid and the clean conversion they see in their own reactions, making scale-up more straightforward. Some of our partners use the product in small-molecule probe synthesis, others in preclinical candidate workups. It’s rare to see two applications exactly alike, but one trend persists: researchers need confidence that the building block they receive behaves precisely as expected.
Years of practical feedback shape our product standards. Labs measure purity against our published ≥99% HPLC and GC benchmarks, but customers tell us about real-world performance long before final analytics. Chemists share details about reaction rates, color formation, or sporadic byproducts—this dialogue reveals what matters, far beyond black-and-white numbers. Our product maintains a defined, pale yellow crystalline appearance and emits a characteristic, sharp odor typical of clean acid chlorides. Moisture content stays below 0.2%. Each shipment carries a detailed analytics report with NMR spectra, GC-MS overlay, and moisture analysis, not just a tickbox COA.
Product stability depends on packaging and temperature management. We specify refrigeration, but small-scale users appreciate that the product remains stable at cool room temperatures over typical project timescales. If researchers require re-testing, we ship additional sample vials under controlled conditions. User feedback about unwanted caking or discoloration spurred us years ago to overhaul our drying and final filtration—one more example of process evolving with chemist needs.
2-Nitro-4-Methylsulfonylbenzoyl Chloride sits apart from traditional benzoyl chlorides and lower-substituted nitrobenzenes. Classic 4-methylsulfonylbenzoyl chloride lacks the electron-poor reactivity and directing effects caused by a 2-nitro substituent, making it less attractive for select cross-couplings. By contrast, simpler 2-nitrobenzoyl chlorides often show inferior selectivity in further transformations, lacking the sulfonyl activation at the para position.
Our experience shows that those who move upstream by synthesizing the intermediate themselves often find purification labor-intensive, especially during sulfonation and final chlorination. The potential for sulfonic acid carryover, unreacted starting material, or over-chlorinated byproducts significantly increases purification demand for in-house chemists. By going straight to our prequalified product, they cut cycle times and get more reliable analytics, which for medicinal chemists can make or break a campaign’s timeline.
Comparing directly with similar entries on the market, feedback points to our lower batch-to-batch color variance and lack of detectable high-boiling byproducts. Competitors who under-dry their product or use older glassware may unintentionally introduce acids, salts, or microcontaminants. These impurities appear first as inconsistent titrations and later as downstream headaches—column clogging, ghost peaks in HPLC, or sticky residues during scale-up. Our focus stays fixed on removing these pitfalls through robust process control and learning from every shipping cycle.
Innovation in chemical manufacturing doesn’t always come with dramatic overhauls. Our team tweaks the process ever so slightly with each feedback round, drawing on both customer reports and on-the-floor observations. A switch in a drying protocol, an improved inert atmosphere during crystallization, or finer mesh filters can all influence the finished intermediate’s character. Monitoring continues well after the material leaves our site, with stability checks in sample retains and client follow-ups every quarter.
Safety remains a parallel concern. Benzoyl chlorides pose known hazards—moisture will hydrolyze the acid chloride group and generate corrosive byproducts. To protect users, our documentation emphasizes both safe storage and practical spill management, based on lessons drawn from decades of incident tracking. Before each batch ships, we ensure the team reviews every label and every closure, maintaining a direct connection between plant standards and what our clients experience in their hood.
Supply chain reliability shapes the pace of innovation as much as chemistry does. Raw material fluctuations, evolving regulations, and logistics delays have affected the specialty chemical sector. Our answer has never been to cut corners. Instead, we keep critical stocks of both upstream benzoyl chlorides and exclusive nitro- and sulfonyl reagents on hand, drawing from vetted suppliers with whom we have long-term relationships. Regular audits and supplier QC visits improve traceability at every link.
Clients working in regulated industries need to know their materials will arrive uncompromised. We commit to shipment timelines and inspect each outgoing order. If weather, customs, or port slowdowns threaten delivery, our logistics staff issue updates and reroute shipments with priority. These efforts reduce the risk of project standstill and show our investment in every stage of a client’s workflow.
Quality doesn’t spring solely from analytical results; it arises from real relationship-building. We remain transparent—about our technical challenges, process updates, and what clients should expect from each consignment. Regular dialogue with chemists produces a feedback loop that fine-tunes outcomes, whether that means targeting a different particle size, offering special packaging for glovebox transfers, or making sure every SDS addresses a new procedural question.
As new applications for nitro- and sulfonyl aromatics emerge, requirements change quickly. Changing regulatory landscapes, green chemistry initiatives, and customer-driven experiment protocols all impact process priorities. We use these changes as touchstones for ongoing product testing, method validation, and focused team training. If a pharmaceutical partner demands an added test for photostability, for example, we run full photolysis studies on new batches to ensure confidence at the next step.
Manufacturing substituted benzoyl chlorides brings its own environmental impacts. We manage waste streams, including spent acids and organic washes, through licensed reclamation and incineration. The adoption of closed-loop solvent recovery lets us recapture much of our process reagents, cutting both costs and emissions. Over the years, these improvements arise directly from operator suggestions—those closest to the bench often notice process losses others do not.
Increasing demand for sustainable sourcing and greener chemistry has led us to audit raw material origins. By using verified low-impact supply channels, we reduce both the carbon footprint of our product and the risk of regulatory disruption. Documentation for each batch includes all required compliance statements, meeting client and regulatory auditor expectations around stewardship.
The world of chemical intermediates shifts fast. New applications for 2-Nitro-4-Methylsulfonylbenzoyl Chloride continue to surface, especially in the hands of creative synthetic teams. As molecular design grows more sophisticated, we see a need for even tighter analytical standards and faster turnaround. We track upcoming trends—whether that means additional purity screens, new shipment formats, or support for continuous-flow processing. Building on a history of open communication, technical rigor, and customer trust, we pledge to keep refining every detail of our production and delivery process.
As this compound finds its way into new pharmaceutical, agrochemical, or specialty materials breakthroughs, our process will keep pace. Chemists will always need confidence that their core intermediates integrate smoothly into any route—a goal shaped piece by piece in the plant, long before a single bottle ships. Our promise stays constant: to supply 2-Nitro-4-Methylsulfonylbenzoyl Chloride with a level of purity, control, and technical honesty that supports even the most demanding research challenges.