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HS Code |
372620 |
| Product Name | 4-Chloro-3-Nitrophenyl Methyl Sulfone |
| Cas Number | 52514-34-6 |
| Molecular Formula | C7H6ClNO4S |
| Molecular Weight | 235.64 g/mol |
| Appearance | Light yellow to yellow powder |
| Melting Point | 112-116 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents such as DMSO |
| Purity | >98% (typical) |
| Smiles | CS(=O)(=O)C1=CC(=C(C=C1)Cl)[N+](=O)[O-] |
| Inchikey | JPXYJKRKFWXSNU-UHFFFAOYSA-N |
| Synonyms | Methyl 4-chloro-3-nitrophenyl sulfone |
| Storage Temperature | Store at 2-8°C, protected from light and moisture |
As an accredited 4-Chloro-3-Nitrophenyl Methyl Sulfone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Chloro-3-Nitrophenyl Methyl Sulfone, sealed with a screw cap and hazard labeling. |
| Shipping | 4-Chloro-3-nitrophenyl methyl sulfone is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be kept in a cool, dry place and handled with care. Shipping complies with all relevant hazardous material regulations, including appropriate labeling, documentation, and protective packaging to ensure safe transport. |
| Storage | 4-Chloro-3-Nitrophenyl Methyl Sulfone should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, moisture, and incompatible substances such as strong oxidizing agents. Avoid exposure to direct sunlight. Proper labeling and containment are essential to prevent leaks or contamination. Store at room temperature and follow all relevant safety protocols. |
Applications of 4-Chloro-3-Nitrophenyl Methyl Sulfone in Industrial Manufacturing4-Chloro-3-Nitrophenyl Methyl Sulfone serves as a specialty intermediate across selected technical fields. Our production consistently meets industrial requirements, supporting defined synthesis routes in high-value downstream segments. Each application below addresses specific use cases, compliance, dosage guidance, processing methods, and typical finished goods. 1. Agrochemical Intermediate SynthesisMajor agrochemical producers employ this compound as a custom intermediate in the preparation of advanced herbicides and fungicides. The electron-withdrawing nitro and sulfone groups enable precise substitution reactions, supporting synthesis pathways for selective pesticides. Our material's consistency and purity remain critical for subsequent coupling and condensation steps, ensuring target yield and activity in crop protection product development. Industry compliance standards
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2. Pharmaceutical Intermediate for Active Ingredient PreparationPharma manufacturers utilize this sulfone derivative as a building block in syntheses of targeted APIs, particularly where specific aromatic substitution enhances pharmacological profiles. Its reliable reactivity profile, consistent particle size, and high-purity specification support strict downstream GMP protocols, allowing for reproducible batch synthesis and traceable process validation during multi-step API manufacturing routes. Industry compliance standards
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3. Dye and Pigment SynthesisDye manufacturers adopt this sulfone as a functionalized aromatic feedstock to introduce reactive anchor points for chromophore assembly. The compound’s chloro-nitro groups facilitate introduction of color-giving azo or anthraquinone bridges. Companies specify tight quality controls to ensure batch-to-batch uniformity in shades and stability in textile and industrial applications. Industry compliance standards
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4. Electronic Chemicals for Specialty Polymer ManufactureProducers of high-performance engineering polymers use this chemical to introduce stability and electronic rigidity in advanced monomer formulations, especially in the electronics sector. The compound enhances polymer backbones for improved thermal resistance and dielectric performance. Downstream manufacturers benefit from consistent impurity profiles to meet stringent device reliability requirements in microelectronic and optoelectronic assembly. Industry compliance standards
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5. Custom Synthesis for Fine Chemical ProductionContract manufacturers and specialty chemical producers source this molecule to unlock precise aromatic sulfone chemistry in multi-step fine chemical routes. Its defined reactivity aids in generating rare sulfone, nitro, or chloro containing fragments, supporting creation of advanced functional chemicals required in flavor, fragrance, or specialty additive sectors. The batch lot and full-traceability records we supply meet high expectations for contract QC traceability. Industry compliance standards
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Experience in the chemical industry offers a front-row view of how demand for fine organic building blocks has evolved. Among the myriad of specialty compounds, 4-Chloro-3-Nitrophenyl Methyl Sulfone stands out in our catalog, valued for its stability and selectivity across several synthetic contexts. Our workshops run it through demanding quality metrics, ensuring consistent crystalline properties. Every batch meets purity expectations essential for research and production in advanced pharmaceuticals, agrochemical discovery, and dyestuff developments.
In our laboratory, 4-Chloro-3-Nitrophenyl Methyl Sulfone draws chemical architects for its reliable electron-withdrawing sulfone and nitro groups. These groups influence reactivity, making the compound a powerful moiety for stepwise elaboration in both academic and commercial projects. Most requests come from teams working to build heterocycles for first-in-class biologically active molecules. Chemists recognize that this intermediate brings more than mere structural novelty; it offers a defined reactivity profile, reducing off-target reactions and helping streamline purification.
In process development, the compound’s predictable melting point and solubility behavior help reduce troubleshooting. Its absence of labile functionalities means we rarely encounter batch-to-batch variability that plagues other nitroaromatics. Approved for use in multiple regulated environments, its reliable profile has encouraged further bridge-building into API synthesis campaigns.
We keep a steady eye on reproducibility. 4-Chloro-3-Nitrophenyl Methyl Sulfone is not just a lot number in our inventory; it represents a carefully built model of quality control. Each batch undergoes identity confirmation through NMR, LC-MS, and IR checks. Low-level impurities typically fall below thresholds for advanced synthesis, a direct result of rigorous process optimization. Chemists in our QC team understand the significance of these standards, especially as downstream transformations often depend on such starting materials for high-yielding, clean reactions.
Anecdotes from customers highlight the convenience of our consistently high-purity material. Some of these teams mention shortened project timelines and reduced purification workloads, outcomes only possible with fewer side-products and negligibly low trace contaminants. Our experience confirms that taking short-cuts on purification or flexibility in processes quickly triggers inconsistencies, so we champion routine and controlled parameters above all.
Hands-on production teaches that specifications can’t rest on paper guarantees. Commercial, kilo-scale orders demand the same faithful adherence to spec as 10-gram research packs. Our user base—whether contract research or in-house development crews—counts on solids without clumping, discoloration, or excessive dust that could compromise measurements or cause unsafe exposure. Hygroscopicity tests inform the storage guidance we pass on; the compound’s well-packed crystalline form helps minimize environmental moisture uptake, and direct handling experience tells us the additional nitrogen group imparts more physical stability than most sulfone benchmarks.
Our trained staff carefully avoid static buildup during weighing—a small detail, but one with a real impact when transferred to high-throughput experimentation platforms. As a result, the compound supports automated dosing lines, which feature wider in pharma pilot plants. This real-world compatibility doesn’t get captured in spec sheets. Years of product handling, drying techniques, and packaging adjustments permit precise repetition every cycle.
Clarifying the merits of 4-Chloro-3-Nitrophenyl Methyl Sulfone sometimes obliges a quick chemistry lesson. Nitroaromatics share a family resemblance, but nuances set this specific intermediate apart. Incorporating a chloro substituent at the para position directs downstream reactivity, boosting selectivity for specific Suzuki or nucleophilic aromatic substitutions. Synthetic schemes that pivot on such reactivity often see fewer byproducts and increased yields compared to analogues like 4-nitrophenyl methyl sulfone, which misses the electron-shuffling chlorine atom.
Other sulfone intermediates, though structurally similar, can lack the simultaneous electron-rich and electron-deficient environment created by the joint nitro and chloro pairing. This feature expands the chemical window, letting medicinal chemists cross into transformations usually off-limits for conventional aryl sulfones. Comparing with 3-nitrophenyl methyl sulfone or even multi-substituted analogues, our in-house trials and customer feedback confirm this combination uniquely enables certain regioselective syntheses. Over years of campaigns, our observation tracks with these reports: when selectivity matters, most teams circle back to this compound after running pilot reactions on others.
Optimization efforts in chemical manufacturing gain a boost when supplied intermediates behave as expected. Experienced teams rely on reactions that don’t drift from standard conditions—whether scaling up a Grignard pathway, aromatic substitution, or esterification. The properties of 4-Chloro-3-Nitrophenyl Methyl Sulfone, including its resistance to reduction and steady solubility in common polar solvents, help steer synthetic sequences toward robust, high-yield results. As a manufacturer, we invest in early-stage work-up protocols alongside our clients to cut the learning curve on new processes.
The compound’s compatibility with established protecting group strategies lets researchers and process chemists innovate without roadblocks. We have consulted with external teams experimenting with sulfone deprotection or targeted photolytic releases; each time, the crystalline stability and clean reactions support repeatable outcomes. Testimonies from groups moving toward scale-up have frequently credited our quality with simplifying their transfer from milligram screens to pilot or manufacturing scale.
Modern chemical production cannot overlook the environmental and safety aspects surrounding specialty intermediates. We invest in responsible sourcing of starting reagents. Our sulfur dioxide and aromatic feedstock come from established, certified supply streams, with full traceability to minimize risk. Waste streams from the synthesis of 4-Chloro-3-Nitrophenyl Methyl Sulfone are routed through approved treatments to ensure regulatory harmony and workplace safety.
We continuously audit both energy consumption and solvent cycles for greener alternatives. Where text-book syntheses may rely on chlorinated solvents or aggressive oxidizers, we routinely review and adapt our processes to drop environmental burden where feasible, without sacrificing product performance. These investments in sustainability present both a responsibility and a business requirement, as more formulators and end-users request both supply chain transparency and concrete actions to reduce chemical waste.
As a direct manufacturer, we take feedback from our warehouse and shipping teams as seriously as from our lab staff. The durability of the compound’s packaging, resilience to accidental impact, and the clarity of labeling help keep overall process safety uncompromised. Industry requirements demand more than compliance; our stake in responsible handling sets a model many downstream partners now expect us to help enforce up the value chain.
From our vantage point, a significant part of product satisfaction does not end with synthesis. Controlled drying conditions and packaging lines ensure batches remain free from excess particulate and moisture. In response to research and pilot plant customers, our workflow has evolved from standard drums to smaller, single-use liners and moisture-barrier bags. This helps teams handling only a few hundred grams avoid product caking or losses, while also supporting easy access for large-scale refills in process development settings.
Custom order requests have become frequent. We accommodate needs ranging from high-load, multi-kilo deliveries for industrial pilot runs to small vials for boutique research. Each shift, our staff double-check weights and inspect seals, adopting the practice that an overlooked tear or improper cap will multiply issues down the line. As a manufacturer, solving these small but persistent problems eliminates backlogs and upholds the level of trust we have with repeat partners.
Internal logistics staff coordinate with couriers and bulk freight providers, ensuring regulated documentation and rapid traceability from the moment a request enters our system to dispatch. Many of our clients report fewer interruptions related to transit damage compared to past experiences with less robust packages. Labeling ties into batch-level records, supporting full backward tracing if any questions about specifications or compliance standards ever arise.
Working on this compound, extensive collaborative cycles with regulatory teams have clarified many functional requirements. 4-Chloro-3-Nitrophenyl Methyl Sulfone is not a controlled substance, which enables smoother transit across most commercial and research borders. Still, we maintain documentation on heavy metals, residual solvents, and genotoxins in line with ICH and Reach guidelines where assay results verify compliant levels.
We coordinate frequently with clients in contract manufacturing and academic centers working on pre-clinical targets. Project leads count on our prompt documentation: certificates of analysis, material safety records, and—crucially—detailed transparency about any process changes. Our approach builds confidence, not by over-promising, but by maintaining the discipline to back technical claims with documentation rooted in verified results.
Technical support draws from practical experience with the material, not just a reference to standard guidelines. Research labs reach out seeking reaction optimization, not only because we know the core synthesis, but because we’ve seen pitfalls in failed attempts. We regularly troubleshoot setbacks during nucleophilic substitutions or coupling protocols, sharing what our team has already overcome in upstream and scale-out adjustments. Over years, this approach shortens feedback cycles and prevents repeated errors, particularly for less common scale-up issues where literature falls short.
Chemists want real engagement, not scripted scripts. Sharing practical solutions, backed by internal experiments and scaled trials, proves more valuable than long lists of theoretical protocol steps. Teams working with demanding regulatory or technical timelines benefit from these exchanges, where manufacturing experience closes the gap between raw material supply and successful product development.
Innovation cycles grow sharper as pharmaceutical and fine chemical companies pivot toward faster project launches. 4-Chloro-3-Nitrophenyl Methyl Sulfone serves as a versatile and reliable intermediate with the adaptability to meet new challenges. Industry analysts project growing interest in substituted aryl sulfones for next-generation drug candidates. In response, our R&D and production engineers engage in regular process reviews, preparing for increased scale demands and new technical collaborations.
As new synthetic targets emerge, our staff partners with external method developers to validate 4-Chloro-3-Nitrophenyl Methyl Sulfone’s place in cutting-edge synthetic flows, anticipating shifts in selective functional group transformations and late-stage elaboration. Research feedback suggests increasing exploration of this intermediate in photoredox and palladium-catalyzed methodologies. Our continued investment in scale-flexible manufacturing lines ensures rapid responses as these advanced protocols progress from discovery to pre-clinical supply.
Field knowledge tells us that reliability, transparency, and technical familiarity with our product outperform generic or commodified inventories. We work to ensure that each shipment delivers on these expectations, positioning 4-Chloro-3-Nitrophenyl Methyl Sulfone as a trusted solution for project teams demanding more than off-the-shelf performance. By continually refining our approach—through ongoing dialogue with chemists, active data gathering, and visible commitment to environmental and operational standards—we support genuine progress for our partners across research and industry.
Manufacturing specialty chemicals means living with the results of every synthesis and shipment, not just pushing paperwork or moving boxes. Our years in this business, handling and delivering 4-Chloro-3-Nitrophenyl Methyl Sulfone, have built up more than just operational know-how. The connections formed with scientists and engineers inform every production tweak and support call. Experience proves that every detail matters, from equipment calibration and fine-tuned purification, all the way to customer advice on reaction troubleshooting and scale-up support.
As new applications for this intermediate continue to emerge, our proactive approach—rooted in practical experience and ongoing improvement—anchors its reputation as a preferred choice across demanding arenas. Our approach delivers more than a chemical sample: it delivers a partner committed to reliability and technical integrity where every batch, and every reaction, can move forward without hesitation.