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HS Code |
288562 |
| Chemical Name | 2',4'-Dihydroxy-3'-Methylacetophenone |
| Molecular Formula | C9H10O3 |
| Molecular Weight | 166.18 g/mol |
| Cas Number | 4433-79-8 |
| Appearance | White to off-white solid |
| Melting Point | 115-117 °C |
| Boiling Point | No data available |
| Solubility | Soluble in organic solvents like ethanol and methanol |
| Synonyms | 4-Acetyl-2-hydroxy-3-methylphenol |
| Smiles | CC(=O)C1=CC(=C(C=C1)O)C |
| Inchi | InChI=1S/C9H10O3/c1-6-5-7(2)8(10)3-4-9(6)12-11/h3-5,10H,1-2H3 |
| Pka | No data available |
| Storage Conditions | Store in a cool, dry place and keep container tightly closed |
| Purity | Typically ≥98% (depending on supplier) |
As an accredited 2',4'-Dihydroxy-3'-Methylacetophenone 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, securely sealed, with a white screw cap and detailed chemical labeling for 2',4'-Dihydroxy-3'-Methylacetophenone. |
| Shipping | 2',4'-Dihydroxy-3'-Methylacetophenone is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a potentially hazardous chemical, requiring proper labeling and adherence to local, national, and international transportation regulations. Ensure compatibility with shipping materials and include a safety data sheet (SDS) with the consignment. |
| Storage | **2',4'-Dihydroxy-3'-Methylacetophenone** should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it separate from incompatible substances such as strong oxidizing agents. Store at room temperature, avoiding excessive heat. Properly label the container and follow institutional guidelines for safe chemical storage and handling. |
Applications of 2',4'-Dihydroxy-3'-Methylacetophenone in Industrial ManufacturingOur direct manufacturing expertise with 2',4'-Dihydroxy-3'-Methylacetophenone enables industry clients to efficiently integrate this specialty intermediate into advanced downstream processes. Below, we detail major market applications where this raw material delivers measurable performance in targeted formulations. 1. Pharmaceutical Intermediate for Antipyretic and Analgesic APIsPharmaceutical manufacturers incorporate this compound as a key phenolic intermediate during the synthesis of antipyretic and analgesic actives, especially within paracetamol analogues. Its dual hydroxyl functionalization enables effective acetylation or etherification steps, supporting production of established pain-relief formulations where stringent traceability and impurity control are required. The input ratio and integration point are precisely adjusted based on the desired pharmacological activity and yield targets. Industry compliance standards
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2. Synthesis of UV-Absorbing Agents in Cosmetic FormulationsLeading cosmetic ingredient suppliers rely on this molecule for the synthesis of benzophenone derivatives widely used as UV filters in sunscreen and daily-wear skincare products. Its ortho- and para-hydroxyl groups improve photoprotective capacity when modified via selective methylation or condensation reactions. The precise input quantity is determined by target SPF value and compatibility with other photostable ingredients in compliance-driven batches. Industry compliance standards
Typical usage ratio
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3. Dye Intermediate for High-Fastness Disperse Dye ProductionTextile dye producers use this raw material as a specific coupling component in the manufacturing of disperse dyes designed for polyester and acetate fiber coloration. Its methylated acetophenone structure enables formation of color-stable azo and anthraquinone chromophores via diazotization or condensation reactions. Usage ratios depend on chromatographic hue requirements and fiber affinity, ensuring regulatory limits on free aromatic amines are met during batch validation. Industry compliance standards
Typical usage ratio
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4. Intermediate for Plastic Stabilizer AdditivesManufacturers of plastic additives select this compound in the synthesis pathway of phenolic antioxidants and stabilizers formulated for polyolefin and engineering plastic resin modification. The meta-methyl and dihydroxy configuration serve as a building block for high-performance non-discoloring stabilizer molecules produced by alkylation or sulfuration routes. The input level and stage are driven by stabilization curve requirements and finished resin application, under strict residual monomer controls. Industry compliance standards
Typical usage ratio
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5. Fine Chemical Synthesis for Agrochmical IntermediatesManufacturers of crop protection chemicals utilize this intermediate in specific derivative synthesis routes to generate phenolic scaffolds required for herbicide and plant growth regulator formation. Its unique substitution pattern allows for regioselective reactions in constructing target molecules with high biological selectivity. The material input is closely controlled according to seasonal demand for downstream actives and must align with traceability schemes for regulatory registration. Industry compliance standards
Typical usage ratio
Downstream process integration
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Producing 2',4'-Dihydroxy-3'-Methylacetophenone stems from years of hands-on work and observation on the manufacturing line. Over time, a close familiarity with this compound has developed—not because it’s another line item on a catalog, but because of how consistently it delivers reliability and flexibility across many applications. Manufactured in our facilities, the care we take shows through each batch.
2',4'-Dihydroxy-3'-Methylacetophenone belongs to the family of hydroxy acetophenones, sporting a methyl group at the 3' position and hydroxyl groups at the 2' and 4' positions of the aromatic ring. As the dry, pale yellow powder emerges from the reactor, the distinctive patterns in solubility and reactivity come into play. The molecule’s specific substitution pattern shapes its behavior in chemical processes—this isn’t just a faint structural anomaly, but a driving factor in reactivity.
In the laboratory, this compound demonstrates more selective reactivity than other acetophenones, owing particularly to the positions of its functional groups. Subtle changes in substitution have a way of turning yield predictions inside out or changing purification requirements. With experience, it becomes clear which structural nuances translate to total synthesis outcomes and which produce more unwanted side products.
From the raw material stage through to final handling, every production step is chosen based on its impact on the composition and purity. Typical batches produce a material with purity exceeding 98%, achieved through a sequence of recrystallization and vacuum drying, in addition to routine screening for trace impurities. Moisture content remains low. Particle sizing is controlled through sieving, avoiding agglomeration and ensuring good dispersibility. Aroma and color, though not primary quality indicators, give early clues if something has deviated during synthesis.
Years of running reactors—watching for those moments when temperature curves threaten to slip off track or when a minor raw material variability leads to a messier product—teach that rigorous process controls make the difference. It’s these hard-earned lessons that transform a standard quality checkpoint into an opportunity for improvement in every new campaign.
Every manufacturer who handles hydroxy acetophenones sooner or later learns something that textbooks gloss over: these compounds play more than one role in formulation chemistry. In-house trials and feedback from downstream chemical engineers confirm the wide applicability of 2',4'-Dihydroxy-3'-Methylacetophenone, from acting as a building block in pharmaceutical syntheses to its selective use in organic pigment development.
In pharmaceutical research, it serves as a starting material for synthesizing more complex molecules. Its arrangement of hydroxyl and methyl groups lends itself well to further modifications—each group can be harnessed without too much risk of cross-reactivity with other parts of the molecule. The relatively straightforward reactivity enables more efficient protection and deprotection steps, which speeds up reaction sequences and reduces the need for excess reagents. Simpler purification downstream means less waste. Laboratory teams have reported fewer chromatographic runs after incorporating this intermediate, cutting down on time and solvent use.
For pigment manufacturing, the compound's stability and color development potential stand out. Consistent pigment output relies on reproducible starting materials; small deviations in melting range or moisture can throw off entire batches. That’s why a close relationship with production is important—making corrections before anyone downstream needs to spot an off-spec input.
Not all acetophenones share the same pattern of action. Compared with plain hydroxyacetophenone or 4'-hydroxy derivatives, the dual hydroxyl and single methyl combination in this compound pushes reaction pathways towards higher regioselectivity and better yields in esterification or alkylation. The 3'-methyl group, in particular, offers protection from unwanted side reactions during multi-step syntheses, acting much like a traffic barrier in an urban grid—directing traffic, not just slowing it down.
The shape and charge distribution of the molecule enable tighter control in downstream chemistry. Take its performance under Friedel-Crafts acylation conditions: the exact placement of functional groups reduces side-product formation, resulting in cleaner isolations. Discussions with research chemists from multiple fields confirm the same advantage: easier clean-up, meaning fewer purification headaches, especially on scale-up.
The dual-hydroxyl structure also creates a stronger hydrogen bonding network than in mono-hydroxy acetophenones. This affects how the compound dissolves and recrystallizes—not just an academic issue, but one with substantial impact in actual manufacturing. Solubility profiles in different solvents open or close doors to downstream steps, and the right balance is essential, especially when engineering crystallization protocols for further derivatives.
Scaling up organic synthesis brings unexpected hurdles, from heat transfer limitations to impurity build-up. The experience gained from repeated production cycles of 2',4'-Dihydroxy-3'-Methylacetophenone allows for pinpointing where scalable solutions pay off. By carefully tuning reagent ratios and stirring speeds, batch outcomes now match lab-scale precision far more often than they did in early campaigns.
Final product consistency benefits not only our inventory but also the work of researchers and plant engineers using it downstream. As feedback from long-term partners shows, switching to our material often means fewer surprises in their analytical results, whether preparing a new library of pharmaceutical candidates or blending pigments for specialty coatings.
The chemical sector has seen more than enough supply chain disruptions in the past decade. Experience with domestic and international logistics means learned the importance of robust packaging, streamlined documentation, and quick adaptation to transport challenges. Custom packaging options—tailored after real customer requests—help address variables such as humidity, temperature, and transit duration.
Handling questions about shelf life and storage, insight from actual experience makes a difference. Stored at room temperature and away from moisture, 2',4'-Dihydroxy-3'-Methylacetophenone maintains stability at least two years post-manufacture, proven by ongoing stability tests. Problems like caking or color change usually reveal themselves only when packaging or warehouse conditions slip; these issues get addressed by routine audits and rapid response if a customer ever flags something amiss.
Quality does not rest only on certificate paperwork. It grows out of run-by-run adjustments, listening to real user feedback, and honest evaluation of process strengths and weaknesses. Regular testing—using HPLC, GC, and melting point determination—quantifies what experience already suggests. Any variation outside the norm triggers not just paperwork, but full root-cause investigation and, when necessary, batch reprocessing.
Analytical teams sometimes spot signals in the data before they become obvious in the finished product. These early warnings help prevent subpar material from ever leaving the site. Every month, insights from these checks get discussed not only with lab staff, but also across production and maintenance. This keeps improvement running as an ongoing process, not just an annual formality.
Manufacturing organic intermediates brings unavoidable environmental and safety concerns. By staying close to the process, issues like waste management, solvent recovery, and employee health become part of the daily discussion. Routine air monitoring and effluent treatment keep emissions well inside current regulatory limits. Solvent use and recycling practices have been refined with each campaign to drive down hazardous waste volumes.
Worker safety receives the same level of attention as product purity. Routine operator training, thorough emergency drills, and a transparent reporting culture have reduced workplace incidents over the past five years. Many improvements stem from direct shop-floor feedback—small changes in layout or workflow often produce a larger positive shift than sweeping top-down mandates.
Many advances in formulation chemistry or pharmaceutical R&D depend on reliable, well-characterized building blocks like 2',4'-Dihydroxy-3'-Methylacetophenone. Supporting the innovation of research partners involves more than filling a purchase order; it means working alongside development teams to answer complex questions about reactivity, compatibility, and impurity profiles, based on lived experience.
Over the years, the manufacturing team has tackled unusual requests—alternative particle sizes, minimal residual solvents, compatibility with bespoke reaction systems. These special runs allow the core production team to stretch its skills and draw on decades of process familiarity, resulting in new protocols that often become standard for future projects.
Feedback from external researchers frequently points to the value of transparent dialogue with manufacturing—not just exchanging spec sheets, but open technical discussions about product behavior. Some customers share analytical data from their own work, leading in turn to further process improvements or batch customization, which benefits both parties.
Practice sometimes outpaces published literature. Issues have cropped up in crystallization sequences or solvent mixture selection that standard guides never mention, but repeated production cycles make certain practical workarounds obvious. A minor tweak in solvent ratio or temperature ramp speed sometimes boosts yield or purity more reliably than theoretical predictions—this is know-how that grows only from years in the plant, discussing with shift technicians and lab analysts.
Continuous process verification, using regular analytical sampling and data review, keeps product outcomes aligned with customer needs. Each change, even incremental ones, starts with trial-scale runs and close monitoring for unintended effects. Once a proven modification exists, it gets institutionalized not with bureaucracy, but with training and updated process charts for every operator on shift.
The facility produces several hydroxy and methylated acetophenone variants, each serving a different segment. Cross-comparisons in physical property and reaction performance drive the more nuanced positioning of 2',4'-Dihydroxy-3'-Methylacetophenone relative to its chemical cousins. For customers accustomed to other acetophenones, the nuanced differences—whether in melting range, reaction pH, or post-run crystallization—drive decision-making in formulation and scale-up.
By directly fielding application-specific questions, it has become clear that this compound does not merely substitute for mono-hydroxy or plain methyl acetophenones in every case. The unique combination of groups addresses gaps not covered by others, particularly where selectivity and reaction speed matter most. Internal data, corroborated by customer case studies, support these distinctions in actual end-use settings.
Years spent moving from bench to pilot plant to full-scale production have stamped practical wisdom on every aspect of handling 2',4'-Dihydroxy-3'-Methylacetophenone. Rather than relying on generic product claims, continual improvement relies on daily experience, learning from close calls, yield surprises, and real customer dialogues.
Future developments—whether in greener synthesis, finer impurity control, or expanded customization—draw momentum from this grounded approach. Each success or setback loops back as another data point, driving further enhancements in how the product is made, packaged, and delivered. The most useful insights rarely come from protocol manuals alone; they grow from working shoulder-to-shoulder with production staff, handling real challenges as they arise.
There is no substitute for the kind of hands-on expertise that grows from years on the production floor. Whether for researchers seeking a stable building block, or manufacturers needing a reliable input, 2',4'-Dihydroxy-3'-Methylacetophenone benefits from this continual blend of process learning and honest, open collaboration. Each kilogram represents not just a chemical, but the trust built from unbroken supply, repeatable quality, and straightforward problem solving.