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3,5-Dihydroxyacetophenone

    • Product Name 3,5-Dihydroxyacetophenone
    • Einecs 210-272-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    695335

    Chemical Name 3,5-Dihydroxyacetophenone
    Molecular Formula C8H8O3
    Molecular Weight 152.15 g/mol
    Cas Number 118-91-2
    Appearance White to off-white crystalline powder
    Melting Point 140-143°C
    Solubility In Water Slightly soluble
    Density 1.28 g/cm³
    Pubchem Cid 8793
    Smiles CC(=O)C1=CC(=CC(=C1)O)O
    Inchi InChI=1S/C8H8O3/c1-5(9)6-2-7(10)4-8(11)3-6/h2-4,10-11H,1H3
    Synonyms 3,5-DHA; m,p-Dihydroxyacetophenone
    Storage Conditions Store at room temperature, away from moisture and light
    Hazard Statements May cause skin and eye irritation

    As an accredited 3,5-Dihydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle securely sealed with a screw cap, labeled "3,5-Dihydroxyacetophenone" with purity, hazard, and handling details.
    Shipping 3,5-Dihydroxyacetophenone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be labeled properly and handled according to chemical safety regulations. The packaging ensures minimal exposure and spillage, and it is transported in compliance with local and international chemical shipping guidelines.
    Storage 3,5-Dihydroxyacetophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Protect from light and moisture. Store under inert atmosphere if possible. Proper labeling and secure storage as per chemical safety regulations are recommended to prevent contamination and ensure safety.
    Application of 3,5-Dihydroxyacetophenone

    Applications of 3,5-Dihydroxyacetophenone in Industrial Manufacturing

    3,5-Dihydroxyacetophenone serves as a key intermediate in several specialized industrial sectors, shaping downstream production processes by providing unique chemical functionalities. As a direct manufacturer, we optimize this material’s purity profile, particle size, and batch consistency to support demanding industrial customers across pharma, personal care, fine chemicals, and analytical reagent manufacturing. Below, we detail real-world application scenarios, focusing on industry standards, practical use ratios, integration into downstream processes, and the specific end products enabled by this intermediate.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    This material plays a critical role in the synthesis of select APIs, particularly as a building block for flavonoids and other phenolic pharmaceuticals. Its dihydroxy substitution enables regioselective condensations and oxidations used by API manufacturers seeking controlled impurity profiles and batch reproducibility. Integration requires stable supply, validated traceability, and adherence to stringent regulatory documentation for every production lot released into GMP environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (CGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs for related APIs
    • ISO 9001:2015 for chemical intermediate supply chain control

    Typical usage ratio

    • API manufacturing processes commonly introduce this intermediate at 0.5%–2.5% w/w of total batch mass, adjusted based on the target molecule and required reaction excess. Ratios are refined through route scouting to minimize impurity carryover and optimize yield.

    Downstream process integration

    • Material is charged as an initial or mid-stage reactant into multi-step synthesis sequences, often dissolved in polar organic solvents, then subjected to demethylations, acylations, or condensations. Typical introduction is at the reaction charging or feed solution stage under nitrogen atmosphere.

    Final product types

    • Antioxidant APIs, anti-inflammatory drugs, specific flavonoid-based pharmaceuticals (e.g., pinostrobin derivatives), and investigational compounds for metabolic and oncology indications.

    2. UV-Absorber Formulations for Cosmetic and Personal Care Ingredients

    Formulators in the cosmetic and personal care industry leverage its benzene-1,3-diol structure in the development of sunscreen actives, skin whitening agents, and hair protection formulas. The compound’s ability to stabilize free radicals and absorb UVB imparts protective properties within strict concentration limits, governed by safety dossiers and regional cosmetic regulations. Batch uniformity, heavy metal control, and residual solvent thresholds remain critical for this market.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • US FDA Title 21 CFR Part 700 (Cosmetic Product Regulations)
    • China National Standard GB 7916 (Hygienic Standard for Cosmetics)
    • ISO 22716:2007 (Cosmetic GMP)

    Typical usage ratio

    • Formulations integrate this raw material at 0.05%–0.3% w/w based on toxicological assessments, finished product claims, and compatibility with other UV filters or antioxidants. Adjustment depends on SPF target and formulation matrix (emulsion, gel, or spray).

    Downstream process integration

    • Compound is pre-dissolved in ethanol or propylene glycol, then added during emulsion phase blending or at cool-down stages to avoid decomposition. Used in both batch and continuous process mixing tanks under controlled temperatures (below 45°C).

    Final product types

    • SPF sunscreens, daily wear anti-aging creams, protective conditioners, and scalp care sprays demanding photostability and regulated phenolic content.

    3. Synthesis of Specialty Flavonoid Compounds in Agrochemical Production

    In the agrochemical sector, this intermediate supports the synthesis of bioactive flavonoids used for pest control and plant growth stimulation. Manufacturers require reproducible quality and specific isomeric ratios to optimize downstream chemical conversions. Agrochemical regulation mandates not only traceable synthesis routes but also documentation of source purity, residual solvent, and environmental safety.

    Industry compliance standards

    • FAO/WHO Guidelines on the Quality Control of Pesticides
    • REACH Regulation (EC) No 1907/2006 for agrochemical intermediates
    • OECD Good Laboratory Practice (GLP) where applicable
    • ISO 17025:2017 for analytical QC of starting materials

    Typical usage ratio

    • Agrochemical syntheses generally require 0.8%–3.0% w/w, with loading tailored to crop application rate and final product purity specifications. The ratio is systematically adjusted during scale-up or process transfer.

    Downstream process integration

    • Material is introduced as a nucleophile or condensation partner in semi-batch or continuous reactor systems. Point of addition typically follows catalyst charging and is monitored for in-process conversion and side-product minimization.

    Final product types

    • Flavonoid-based seed coatings, plant growth regulators, natural fungicide active substances, and root development stimulants distributed for horticulture or crop protection markets.

    4. Analytical Reagent Synthesis for Laboratory & Diagnostic Test Kits

    Quality control labs and in-vitro diagnostic manufacturers employ this compound to prepare chromogenic reagents, derivatization agents, and calibration standards for trace metal and enzyme assays. The starting material’s purity, trace metal content, and lot-to-lot reproducibility remain pivotal for labs that require validatable results and international standard compliance in analytical workflows.

    Industry compliance standards

    • ISO 13485:2016 for Medical Device Quality Management
    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • USP Reagent Standards where applicable
    • REACH Annex IV substances exemption (if reagent-grade)

    Typical usage ratio

    • Preparation of analytical standards uses 0.005%–0.1% w/v, titrated precisely according to detection protocol, target analyte sensitivity, and batch validation requirements.

    Downstream process integration

    • Material is dissolved in aqueous or mixed solvent systems and reacted with metal ions or organic analytes to create quantifiable color complexes. Lab-scale and automated kit production both integrate it at the solution formulation or test strip coating phase.

    Final product types

    • Clinical chemistry kits, heavy metal detection assays, lab quality control standards, and research laboratory reagents for diagnostic and calibration functions.
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    More Introduction

    3,5-Dihydroxyacetophenone: Practical Experience and Industry Insights

    Understanding 3,5-Dihydroxyacetophenone

    Chemical manufacturing brings us face-to-face with a vast range of aromatic compounds, and 3,5-Dihydroxyacetophenone stands among those with a trusted track record in both R&D and large-scale synthesis. Our process begins with specifics—purity standards above 98% and a white to pale yellow crystalline appearance indicate serious attention to detail in its preparation. Over the past decade, demand for this compound has remained steady, reflecting its value across several key industries.

    Chemists and process engineers alike turn to 3,5-Dihydroxyacetophenone for its consistent molecular formula (C8H8O3) and reliable melting point around 144–146°C. Batch after batch, feedback from QC teams points out its low moisture content and tightly controlled residual solvents, which underscores why researchers see clean results in analytical and preparative methods such as HPLC and NMR.

    Choosing 3,5-Dihydroxyacetophenone for Synthesis

    Years on the lab floor reveal plenty about how certain building blocks perform during scale-up. 3,5-Dihydroxyacetophenone holds a special place with its two phenolic hydroxyls and a single acetyl group. These functional groups offer multiple points for derivatization. In medicinal chemistry, where specificity can make or break a project, chemists use this compound for both its reactivity and its selectivity, particularly in synthesizing bioactive intermediates and analogs for pharmaceutical candidates. You rarely see off-target reactions when it’s used under standard conditions, supporting predictable yields and clear separation profiles.

    Pharmaceutical chemists tell us they value the low levels of byproducts observed during Friedel–Crafts acylation and other transformation pathways. It outperforms related isomers (such as 2,4- or 2,6-dihydroxyacetophenone) in stability and downstream purification. Work with contract manufacturers taught our team that these details play a big role in minimizing waste and cost overruns.

    Experience in Process Safety and Handling

    On the production floor, workers do not overlook the importance of proper safety procedures. 3,5-Dihydroxyacetophenone might not demand the same level of caution as some volatile aromatics, but routine personal protective equipment, good ventilation, and secure containment keep risks low. Storage in tightly sealed containers away from strong oxidants or concentrated acids cuts down on degradation and contamination. After years in synthesis and packaging, our teams have not seen significant spontaneous discoloration or clumping, reflecting formulation stability over standard shelf lives.

    Routine GC and spectroscopic analysis spot early any deviations. Feedback from customers manufacturing at scale confirms that, unlike some closely related dihydroxy ketones, 3,5-Dihydroxyacetophenone maintains shelf and solution stability well, making it easier for procurement teams who want reliable inventory cycles without unplanned losses.

    Applications: Beyond Laboratory Synthesis

    It’s one thing to talk about chemical structures; hearing from end users makes the story complete. In our experience, 3,5-Dihydroxyacetophenone sees steady use not only in small-molecule drug discovery, but also in nutraceutical development and specialty pigment synthesis. Research teams designing antioxidants often profile this molecule as a model hydroxyacetophenone to correlate structure-activity relationships.

    Our production partners in the dye industry remark on its function in the synthesis of chalcones and flavonoids, two classes of compounds known for their vibrant colors and bioactivity. The selective reactivity of the meta-positioned hydroxyls in coupling reactions gives formulators an edge when chasing novel hues or improved solubility. The feedback loop from these industries influences how we continue to refine purity and silica content during crystallization and drying.

    Reliability in Quality Control

    Quality assurance is more than ticking boxes on an SOP. Factory teams regularly consult with in-house chemists about the impact of metal ions and processing residues that can affect downstream applications. Even minor fluctuations in crystal morphology or particle size may affect filtration, solubility, and yield during scaling-up. Our continuous investment in process analytics—HPLC, FTIR, and impurity profiling—yields robust data supporting batch consistency.

    From orders of hundreds of grams in the research sector up to multi-kilogram industrial lots, the feedback loop centers on transparency. Reports from long-term customers and auditing partners demonstrate how strict specifications translate into time savings and cost reduction. Whenever customer labs ran their compatibility assays for specific end-uses—such as UV-stabilization in cosmetics or chelation assays in materials science—the expected results hold up, thanks to careful optimization through each production stage.

    Comparing Against Other Dihydroxyacetophenone Isomers

    Being embedded in manufacturing gives us direct insight into why 3,5-Dihydroxyacetophenone stands apart from isomers like 2,4- or 2,6-dihydroxyacetophenone. Each brings unique strengths, but subtle shifts in their substitution patterns change reactivity, solubility, and downstream usability. Throughout years of technical conversations with formulation experts, we’ve seen an unmistakable trend: the 3,5- isomer’s higher resistance to oxidative degradation gives it a durability edge in bulk applications.

    During formulation trials, physical chemists documented that other positional isomers tend toward lower melting points or higher hygroscopicity, potential red flags for any application requiring moisture control or transportation through varied climates. Sourcing departments appreciate that this stability translates into lower packaging and shipping costs, without sacrificing product integrity.

    Solubility comparisons highlight further practical advantages. Structural differences in 2,4- or 2,6-substituted analogs sometimes cause unpredictable behavior in polar solvents or viscous formulations. In contrast, 3,5-Dihydroxyacetophenone dissolves cleanly in methanol, ethanol, and ethyl acetate. This consistency supports both high-throughput screening and pilot-scale production, a necessity as regulatory bodies and customers increasingly demand transparent process validation.

    Scaling Up: Challenges and Solutions

    Commercial chemical manufacturing involves more than technical know-how. From pilot plant to full-scale batches, procurement and production teams cross-check source materials and intermediates to minimize batch variability. In our work, tight supplier relationships and pre-acceptance sampling address residual contamination that might creep into the finished product.

    Solvent recovery and process recycling, both from green chemistry initiatives and cost management efforts, push constant improvement. Our teams methodically recycle process solvents while monitoring for trace impurities, confirming that each recycled stream meets or beats original solvent purity specifications. By integrating real-time monitoring and continuous flow synthesis for certain steps, we achieve shorter cycle times and a measurable drop in process waste.

    Operators flagged some hurdles associated with scale—particular attention went to filtration and drying, where powder caking after crystallization could influence downstream handling. In those cases, minor adjustments to stirring speed and hydration protocols maintained a uniform, free-flowing product. By listening to lab and floor staff with years of hands-on expertise, simple changes in drying temperature profiles and sieve size avoided production bottlenecks. Such solutions, guided by accumulated experience, feed back into better resource allocation and higher ROI for end users.

    Environmental and Regulatory Considerations

    Staying ahead of changing regulations shapes every aspect of the manufacturing process for 3,5-Dihydroxyacetophenone. Waste stream mitigation isn’t just a compliance checkbox—plant staff analyze each outgoing stream to reclaim solvents and minimize organic load before environmental discharge. Teams adapt working methods based on air and water emission studies, selecting technologies to capture dust and reduce workplace exposure to fine particulates.

    Our environmental audits prioritize closed-loop systems and minimal use of chlorinated solvents based on regulatory guidance from authorities both local and international. Teams leverage long-term process data to choose packaging materials that provide vapor barrier qualities sufficient for long-term storage but remain fully recyclable. Recently, we have participated in industry groups seeking continuous improvement in eco-friendly crystallization agents and filtration aids, answering the call for greener manufacturing without sacrificing finished product quality.

    Ongoing transparency with customers and partners ensures full traceability across each manufacturing lot, reflecting growing expectations in quality management and environmental stewardship. Yearly reviews and internal audits identify hotspots for further optimization, keeping teams accountable and supporting a production culture rooted in experience and dedication.

    Customer Feedback and Continuous Improvement

    For many years, the strongest insights have come straight from the chemists, engineers, and researchers using our material day after day. Their reports on minor process hiccups—whether dusting during transfers or issues with bottle closures—influence everyday improvements. Real-world sample feedback led us to upgrade anti-static linings in high-humidity environments and rethink label adhesives for better adhesion when exposed to solvents.

    Through these partnerships, small but significant changes stack up: standardizing lot-specific CoAs with more granular impurity data, streamlining logistics to offer lead times tailored to seasonal fluctuations in demand, and simplifying technical support requests so chemists can reach hands-on staff directly. Consistency in these efforts strengthens reliability and trust, which forms the backbone of long-term business relationships.

    R&D and the Future of Hydroxyacetophenones

    In-house research and collaborations with academic partners push 3,5-Dihydroxyacetophenone into new application areas every year. High-throughput screening at research institutes probes antioxidant and enzyme inhibition activities, helping establish its position in early-stage pharmaceutical leads. Process chemists study its compatibility in custom resin chemistries, targeting niche applications in adhesives and coatings where tailored molecular features bring unique properties. The experiences gleaned from these projects cycle back into process adjustments and product characterization techniques for next-generation formulations.

    Staying in touch with regulatory affairs experts keeps our teams tuned to the safety, reporting, and registration landscapes that shift quickly in chemical manufacturing. Feedback from some of our earliest customers made it clear: robust data packages and on-time delivery matter as much as molecular structure. The same holds true years later as expansion into new markets increases documentation and regulatory scrutiny.

    Conclusion: The Sum of Hands-On Knowledge

    Every detail of our manufacturing journey with 3,5-Dihydroxyacetophenone reflects years of accumulated expertise, shared between process engineers troubleshooting yields and delivery teams responding to end-user requests on short notice. The compound’s lasting appeal draws on clear advantages—solid chemical stability, proven utility in diverse synthesis pathways, and well-documented safety and environmental profiles. It stands apart among its peers, not just because of molecular structure, but because production teams constantly refine every detail from starting materials to finished packaging, driving reliability and value.

    This honest approach has brought trust from researchers, formulators, and quality managers alike, giving us ample reason to share knowledge openly and keep raising the bar with each new batch. From hands-on troubleshooting to compound-specific improvement, the story of 3,5-Dihydroxyacetophenone continues to evolve alongside the people and processes that shape its journey from raw ingredient to advanced applications across the world.