|
HS Code |
435475 |
| Iupac Name | 1-(2-methyl-4-sulfonic acid-6-chlorophenyl)-3-methyl-5-pyrazolone |
| Molecular Formula | C11H11ClN2O4S |
| Molecular Weight | 302.74 g/mol |
| Appearance | Light yellow to yellow crystalline powder |
| Solubility In Water | Soluble |
| Melting Point | Approximately 200-210°C (decomposes) |
| Cas Number | 5281-04-9 |
| Chemical Class | Pyrazolone derivative |
| Functional Groups | Sulfonic acid, methyl, chloro, pyrazolone |
| Boiling Point | Decomposes before boiling |
| Ph Of 1 Aqueous Solution | Approximately 3-4 |
| Storage Conditions | Store in a cool, dry, and well-ventilated place |
As an accredited 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 500g high-density polyethylene bottle, clearly labeled with product name, purity, and hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 16-18 metric tons of 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone packed in 25kg bags. |
| Shipping | **Shipping Description:** 1-(2'-Methyl-4'-sulfonic acid-6'-chloro)phenyl-3-methyl-5-pyrazolone should be shipped in tightly sealed containers, protected from moisture and light. The package must be clearly labeled, handled with care, and comply with local and international regulations for chemicals. Use appropriate cushioning and temperature control if necessary during transit. |
| Storage | **Storage Description:** Store 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and sources of ignition. Use appropriate chemical storage cabinets and label clearly. Handle with personal protective equipment to avoid contact with skin and eyes. |
| Shelf Life | Shelf life: Store in a cool, dry place; stable for at least 2 years when kept in tightly sealed containers, away from light. |
Competitive 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone prices that fit your budget—flexible terms and customized quotes for every order.
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From the earliest days in our production halls, 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone has been one of the core intermediates in our line-up. Teams here know it by its shorthand, often referring to its structure more than its complex name, but conversations in both R&D and manufacturing regularly come back to its versatility and strength. Its rich methylation, sulfonic group, and chlorination pattern turn it into a go-to building block for a range of azo dyes—especially those known for stable colorfast properties on textiles, leathers, and paper.
On the factory floor, this compound comes off the line as a pale to golden yellow solid, highly soluble in water. Filtration and refining steps demand close attention. Anyone trying to push it rapidly risks carryover impurities, which any cobwebbed batch reactor operator here will tell you, directly impacts crude dye yields and downstream shades. In the earliest years, batches would sometimes show variation due to imprecise sulfonation or incomplete methylation of the phenyl ring, so control over these core steps remains a constant point of pride on the shop floor. Over time, investment in flow reactors and monitoring tech has tightened reproducibility—a fact newer chemical operators appreciate but often take for granted compared to those of us who recall the hand-stirred reaction days.
Application chemists, whether working in dye plants or customer laboratories, regularly report that the main challenge in using dye intermediates lies in controlling unwanted shade shifts and impurity-based dulling of color. The direct consequence of a minor change in the sulfonic acid substitution level becomes painfully clear on long machine runs in textile mills. One odd spot of an off-tint roll can translate into dozens of meters of wasted fabric. This pain echoes back all the way to us at the production end.
Our quality labs regularly analyze each batch's sulfonic acid content and chlorination. The most critical threshold centers on limiting bis-chlorinated or partially methylated byproducts, as even a trace creates problems by shifting bath behavior in coloring steps. Any batch with UV or HPLC outliers is held back, and process control data always gets shared with R&D. This kind of hand-in-glove feedback with application users shapes our process tweaks. It reduces downtime for both our lines and those of customers. You're far less likely to see shade drift or uneven exhaustion in dyeing when the chemistry starts from a tightly-controlled pyrazolone of this particular isomer.
What stands out for this compound is its functional group arrangement. Not every phenyl-pyrazolone intermediate boasts a methyl group at position 2', a sulfonic acid at 4', and a chlorine at 6'. The electron-withdrawing chlorine stabilizes the molecule, reducing unwanted side reactions during azo-coupling. Meanwhile, the sulfonic acid increases water solubility, supporting even distribution through dye baths, and methylation helps maintain color brilliance by reducing oxidative degradation once applied.
Compare this profile to older-generation intermediates, such as the non-chlorinated or unsubstituted pyrazolones. While those had lower production costs, their limitations became evident in fastness testing and after extended light/atmospheric exposures. Textile laboratories and color development teams confirm that dyes based on this specific compound maintain bolder hues after extended weathering or laundering, which remains a key selling point for many brands downstream of our plant product.
In day-to-day manufacturing, our teams mainly supply 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone for use as a coupling component in the synthesis of azo dyes. Its core function revolves around reacting with diazonium salts, often derived from nitroaniline or other aromatic amines, to create complex mono- and di-azo compounds with high bath exhaustion and deep shade development.
In many dye houses, this intermediate has a clear following. Colorists cherish its ability to yield reddish and yellowish azo dyes that stand up to aggressive finishing treatments and resist washing, chlorination, and light exposure. Case studies from printworks and tannery color shops show consistent batches maintain key standardized colors on a wide variety of fibers, from cellulose to polyamide blends. This level of flexibility comes from the way the molecule holds together and interacts within dye chemistry, not just from theoretical qualities on a datasheet.
Our batches typically range in active compound from 98.0-99.2%, with trace byproducts kept well below 0.5%. Moisture content in packaged drums sits under 1%, which avoids issues of clumping or unexpected reactions in blending tanks at customer sites. Operators tasked with weighing out feedstock for the diazotization and coupling processes report that the flow properties and solid granule form help keep cleanup quick—less dust, reduced risk of spillage, and smoother transfer to primary reactors.
Repetition in processing isn’t just about hitting the spec sheet—anyone who’s faced a process upset knows how even the smallest impurity shift plays out over hours in production. That’s why upstream control of methylation and final product isolation, with regular filter and solvent system checks, has remained a major focus as batch volumes have scaled up.
Manufacturers producing alternative pyrazolone intermediates, especially those based on simpler methyl or sulfonic substitutions, see savings in basic raw material costs. Yet the trade-off is evident wherever longevity and day-to-day reproducibility enter the conversation. For any dye house or textile finishing operation aiming for tight color standards and resistance profiles, this intermediate stands apart in real-world use.
Our in-plant trails and external user reports highlight three big shifts versus older, cheaper alternatives. First, the robust electron structure means final dyes need lower stabilizer additions, cutting down on unwanted buildup in tanks and application lines. Second, pigment synthesis using this compound often delivers higher yields, since couplings proceed with less side chain fragmentation or hydrolysis. Third, storage stability in finished dye stock remains higher, which translates into less waste—crucial for customers producing in variable climate zones or with extended shipping routes.
Our daily work with textile partners shows a steady shift toward higher-strength, more resilient dyes, many still based on this compound’s molecular backbone. Circular economy demands and changing regulations limit options for some heavy metal-based colorants—pushing azo dye development back toward organosulfonic intermediates with improved safety and lower toxicity profiles. In this setting, precise control over each functional group becomes not just a technical curiosity, but a requirement set by downstream certification labs and brand compliance teams.
Process engineers from some of our longest-standing dye house customers still visit every year or two, bringing swatches and test prints from their new lines. Their decision to stick with this intermediate comes down to reliability across shift changes and temperature swings in the dye pit—a problem that flares up all too often with less tailored intermediates or off-spec batches from lower-tier producers. This isn’t just theory; it’s a lived problem, especially in regions where water quality varies or environmental controls are more stringent. Delivering on these expectations sits squarely with our manufacturing design and execution teams.
Over the years, both regulators and large-brand purchasers have tightened monitoring of all dye intermediates for safety and traceability. Sulfonic acid intermediates with controlled chlorination and defined substitution patterns find much wider acceptance in these audits, due to their lower persistence and proven degradation in end-use scenarios.
As countries increasingly demand cleaner water discharge and limit certain aromatic amines, the lure of cheaper, less specific alternatives diminishes. In audits and certification reviews, documentation showing trace impurity control and validation of molecular structure gives our downstream customers added confidence. Production records and regular third-party testing form the backbone of our compliance efforts. The absence of heavy metals and persistent, non-degradable substitution groups in our product gives a clear edge during REACH, ZDHC, and similar sustainability checks.
Improvements over the last decade—such as inline analysis for reaction endpoint validation, closed-filtration drying, and adoption of more precise methylating agents—come straight from the feedback loop with users and inspection authorities. People often underestimate the complexity of keeping such an intermediate stable across thousands of kilograms per month, particularly in monsoon or dry seasons where humidity, reagent purity, or power disruption threaten tight control. These tweaks in process control and worker training have freed up operators to focus on high-volume output without sacrificing batch-to-batch equality.
Operators and shift supervisors point out that washdowns and clean-in-place techniques, adopted in the last few years, have cut cross-contamination between runs close to zero. Less time spent on cleaning means more productive hours in the reactor bay. All these changes feed back into cost savings for buyers—fewer product complaints, less downtime, no unscheduled rework. In the big picture, this means greater headroom to invest in both environmental controls and new product variants.
From experience, advances in dye performance start with reliable intermediates. Product development teams often rely on the consistent performance of 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone when scaling up from lab samples to pilot plant and then to full industrial production. The margin for error shrinks drastically as run sizes grow; even a small drop in intermediate quality shows up magnified in final applications. Printing houses pushing for new color effects or textile finishers aiming for multi-treatment resistance often work with our technical consultants to tweak azo dye synthesis, using our intermediate as the base.
Direct feedback from pilot projects has spurred small but meaningful adjustments in our production streams—such as optimizing solvent ratios or adjusting feed rates in response to seasonal or raw material variability. Some of the most innovative shade creations in the market today, especially those in high-visibility sportswear, outdoor gear, or specialty home goods, start from this consistent building block. Growing interest in sustainable, high-durability dyes offers our teams regular technical challenge and inspiration.
While the technical and performance arguments favor this compound, practical issues still show up. Transporting and storing a solid dye intermediate means facing climate differences, unpredictable customs delays, and potential drum handling errors at various steps. Years of watching customers handle incoming batches taught us to focus on stable packaging, moisture barriers, and clear labeling to circumvent degradation risk. Frequent engagement with logistics partners keeps breakage and contamination problems to a minimum.
Within the plant, recurring process headaches—such as reducing the formation of bis-chlorinated side-products—required tighter control over reagent addition sequence and using more precise batch times. A critical eye on filtration efficiency, along with routine maintenance of gaskets, valves, and dryer units, prevents costly slipups. Regular checks of off-gas content and residue solvent recovery further tighten the environmental belt, so discharge limits into air and water remain inside regulatory targets without crisis-management firefighting.
A growing number of finished goods manufacturers signal the need for sustainability across the full dye value chain, not just at the stage of final coloration. For suppliers of dye intermediates, this shift demands not only transparency in production—such as detailed batch analytics—but also ongoing reduction of process waste, lower energy use per kilogram, and improved end-of-life fate for the product. Our plant management teams meet these evolving expectations by conducting regular process efficiency audits and working to reduce the carbon and water footprint per batch.
Diversification of supply chains, pressure to reduce transportation emissions, and the growing use of renewable feedstocks press us to revisit established methods. For example, our R&D section continues pilot trials of alternative sulfonating agents and greener methylation pathways, aiming to cut both reagent costs and the environmental load. Success in these areas could open the door to next-generation dye intermediates with even lower hazardous material profiles.
Producing specialty chemical intermediates—especially one as widely relied upon as 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone—means more than just checking boxes for bulk sales. It means making the daily effort to resolve on-the-ground issues before they affect quality, reliability, or downstream performance. Our technical teams and process workers stand behind every drum and every batch with a clear understanding that color integrity, material resilience, and consistent shade delivery rest on disciplined production and open technical dialogue.
The combination of specialty structure, high purity, and proven daily performance ensures this compound’s continued use in a demanding industry. Those who have worked through its manufacturing, quality control, logistics, and final application know well that reliable chemistry comes less from luck or theory, and more from hands-on experience, collaboration with users, and targeted improvement day after day. This approach shapes each run of our 1-(2'-methyl-4'-sulfonic acid-6'-chloro) phenyl-3-methyl-5-pyrazolone, and it reflects in the trust of every customer relying on our intermediate for their critical color work.