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1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One

    • Product Name 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One
    • Einecs 413-790-8
    • 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
    VTB
    Specifications

    HS Code

    447147

    Iupac Name 1-(3-acetyl-2,4,6-trihydroxyphenyl)ethan-1-one
    Molecular Formula C10H10O5
    Molar Mass 210.18 g/mol
    Appearance solid (exact color may vary)
    Solubility In Water Slightly soluble
    Cas Number 4547-24-4
    Smiles CC(=O)C1=C(C(=C(C(=C1O)O)O)C(=O)C)O
    Pubchem Cid 22297524
    Functional Groups Phenol, ketone, acetyl
    Stability Stable under recommended storage conditions
    Storage Conditions Cool, dry place, protected from light

    As an accredited 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 10g, sealed with a screw cap; chemical name, molecular formula, CAS number, and safety labeling on the exterior.
    Shipping **Shipping Description:** 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)ethan-1-one is shipped in tightly sealed containers, protected from moisture and light. It is handled as a chemical substance, requiring proper labeling and documentation according to regulatory guidelines. Ensure compliance with local and international shipping regulations for safe transport and storage.
    Storage Store 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)ethan-1-one in a tightly-sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers or bases. Label the container clearly, avoid prolonged exposure to air, and ensure access is restricted to trained personnel. Use appropriate personal protective equipment when handling.
    Application of 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One

    Applications of 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One in Industrial Manufacturing

    1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One finds its utility in several established specialized manufacturing sectors, each with distinct application protocols, process requirements, and regulatory demands. As the original producer, we focus on supplying material that meets stringent criteria for quality, traceability, and batch consistency demanded by large-volume downstream industries. Below we highlight specific industrial segments where our product directly contributes to value-added transformations.

    1. Pharmaceutical Intermediate for API Synthesis

    Major pharmaceutical synthetic routes utilize this compound as a key intermediate during the construction of polyphenolic and benzaldehyde-based APIs. Its unique phenolic structure allows for precise functionalization required in advanced medicinal chemistry. Pharmaceutical manufacturers integrate this intermediate into regulated GMP lines, maintaining strict traceability and impurity profiles throughout synthesis to comply with registration dossiers for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monographs (for intermediate and API quality)
    • European Pharmacopoeia 10.0 and supplements
    • China Pharmacopoeia ChP, applicable cycle

    Typical usage ratio

    • Batch-level conversion: 0.5%–6% w/w relative to the main reaction substrate, titrated based on reaction scale and API architecture requirements.

    Downstream process integration

    • Used at the pharmaceutical intermediate stage in multi-step synthesis after initial methylation or protection group addition; isolated by crystallization and passed to coupling or condensation step to form target active cores.

    Final product types

    • Custom and generic small molecule APIs for oncology, anti-inflammatory, or cardiovascular treatment
    • Advanced pharmaceutical intermediates for CDMO-scale drug substance production

    2. Polymer Additive in High-Performance Resins

    Polymer resin manufacturers rely on this raw material for its controlled reactivity within phenolic, epoxy, and polyurethane resin recipes to impart targeted thermal resistance and molecular crosslinking. It enters resin pre-polymerization phases, reacting under monitored temperature and pH to enhance stability and anti-aging properties in engineering plastics and coatings. Large-scale resin operators require consistent analytical profiles and supply.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 Registration for polymer applications
    • ASTM D3536 Standard for Polyphenolic Additives
    • ISO 9001:2015 Quality Management for chemical raw material supply
    • UL Yellow Card Compliance for electrical & flame resistance additives

    Typical usage ratio

    • 0.1%–1.5% by resin mass; the adjustment aligns with resin backbone reactivity and desired crosslink density, determined through pilot compounding trials.

    Downstream process integration

    • Added during pre-polymer or monomer mixing, introduced before catalyst stages in batch or continuous mixer systems, followed by polymerization and post-curing.

    Final product types

    • Phenolic composites for automotive friction materials
    • High-durability electrical insulation panels
    • Heat-resistant coatings for industrial equipment

    3. Analytical Reagent in Laboratory Diagnostics and Quality Control

    Producers of analytical kits and reference materials deploy this compound as a colorimetric reagent owing to its specific chromophoric properties and ability to chelate transition metals for photometric analysis. Manufacturers emphasize batch homogeneity and impurity management, meeting documentation requirements for traceability under laboratory standards in regulated regions.

    Industry compliance standards

    • ISO 17034 Reference Material Producer Accreditation
    • ISO/IEC 17025 Laboratory Competence Standard
    • FDA 21 CFR Part 211 for reagent production used in diagnostic settings
    • European Union In Vitro Diagnostic Regulation (IVDR) 2017/746

    Typical usage ratio

    • Stock solution preparations: 0.01%–0.5% by solution volume; optimized for sensitivity and background absorbance in enzymatic and biochemical assays.

    Downstream process integration

    • Dissolved in stabilized aqueous or solvent-based solutions; filtered and aliquoted into diagnostic test kits or laboratory standards for photometric and spot tests.

    Final product types

    • Certified colorimetric assay kits
    • Trace element diagnostics and calibration standards
    • Laboratory quality control reagents for industrial QC labs

    4. Fine Chemical Precursor for Dyes and Pigments

    Industrial dye and pigment producers process this compound to synthesize specialty colorants for inks, textiles, and coatings. Its tri-hydroxy substitution enables development of metal-complex and lake pigments via controlled condensation and chelation, contributing to colorfastness and stability in application. Our production batches maintain defined purity and trace metal content to match color specification protocols.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for pigment and dye manufacturing
    • OEKO-TEX® Standard 100 for consumer textiles
    • EU Regulation (EC) No 1223/2009 for colorants in cosmetics, where applicable
    • EN 71-3:2019 Safety of toys — migration of certain elements (for pigments used in toys and children’s articles)

    Typical usage ratio

    • 0.5%–4% as a chromophoric component in dye synthesis; proportion varies depending on desired hue and pigment fixation pathway.

    Downstream process integration

    • Entered during dye condensation or pigment chelation; reacted with coupling agents and metal salts, followed by purification, milling, and formulation into dispersions.

    Final product types

    • Textile reactive dyes and complex lake pigments
    • Offset and inkjet printing color concentrates
    • Colorants for solvent-based and waterborne coatings

    5. Antioxidant Component for Cosmetic Formulations

    Cosmetic product manufacturers incorporate this ingredient as a functional antioxidant in advanced skincare and haircare formulations, leveraging its polyphenolic structure to inhibit oxidative degradation of emulsions and active botanicals. cGMP-compliant cosmetic operators require declaration of purity, residual solvent control, and validated analytical support for raw material lots intended for use in formulations destined for regulated markets.

    Industry compliance standards

    • ISO 22716:2007 (Cosmetic GMP guidelines)
    • EU Cosmetic Regulation (EC) No 1223/2009
    • US FDA 21 CFR 700 Subpart B—Ingredient restrictions and labeling
    • Japan Ministry of Health, Labour and Welfare—List of Permitted Cosmetic Ingredients

    Typical usage ratio

    • 0.05%–0.5% w/w in emulsion bases or aqueous phases, adjusted to meet stability testing endpoints and compatibility with other antioxidants.

    Downstream process integration

    • Integrated during pre-emulsification or after main hydrophilic phase preparation, dissolved under controlled temperature before homogenization and finished product filling.

    Final product types

    • Face creams for oxidative stress reduction
    • Leave-in conditioners with anti-aging claims
    • Serum bases marketed for environmental skin protection
    Free Quote

    Competitive 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Introducing 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)Ethan-1-One: A Direct View from Our Factory

    A Chemical Born from Practical Demands

    Producing 1-(3-Acetyl-2,4,6-Trihydroxyphenyl)ethan-1-one feels like ground-level chemistry work. Over the years on our shop floor, we’ve seen requests for this compound rise, mostly from clients who don’t have space or time to run acetylation reactions in their own labs. We know the precise logic behind that request. The compound delivers a unique combination of structure and reactivity that fits niche research and manufacturing goals, with each batch reflecting a bridge between fundamental chemistry knowledge and a line operator’s experience.

    We don’t need to look far for the reason behind its value. Three hydroxy groups and an acetyl group on the same aromatic ring build in functionality that’s not easy to access through simpler intermediates. Consistent output means more than “purity on a spec sheet.” In our facility, that equates to how the batch stirs, how it filters, and how repeat users respond. The crystal habit, moisture retention, and color impact downstream processes in ways few non-chemists notice.

    Specifications Rooted in Production Reality

    Speaking from the factory floor, we work with a product that carries a real weight in solid form. 1-(3-Acetyl-2,4,6-trihydroxyphenyl)ethan-1-one is usually a fine crystalline powder, with coloring that may run from off-white to pale beige when impurities are under control and drying parameters stay tight. Typical melting range, checked batch after batch, hovers in the ballpark we build our process around, reflecting not just the chemistry but the air handling, filtration, and solvent drying we maintain with more vigilance than any spreadsheet could log.

    Specs get detailed attention. Purity by HPLC or NMR, typically not less than 98%, drives both confidence and predictability. Water content, checked by Karl Fischer titration, matters greatly, especially to formulators concerned about product shelf life or stability under ambient warehouse conditions. Residual solvent matters too—so we run rigorous vacuum drying under controlled heat. Particle size distribution, often overlooked, impacts those who need to weigh and blend on-site. These metrics aren’t abstractions; they match direct requests from partners who tell us where an odd clump or sticky sample has interfered with their own batch consistency.

    Bulk density, while rarely prioritized on a spec sheet, still comes into play for scale-up operations, especially for anyone preparing suspensions or slurries. We don’t skip over this because we’ve fielded the odd call from a customer whose mixing tanks don’t handle certain chemicals easily—often because a manufacturer skipped the small details.

    There is no single, definitive “grade,” though research and industrial buyers both expect lots to reference the same analytical standards. Stability under room temperature is reliable, but we like to stress airtight containers and away-from-light storage, not out of theory, but from years of seeing samples degrade when shelving or repackaging slips.

    The Real Application Frontlines

    Why would a team specify this compound? In laboratory synthesis and pilot-scale research, 1-(3-Acetyl-2,4,6-trihydroxyphenyl)ethan-1-one brings a set of reactive handles, especially those three hydroxyls, that few chemicals can match. We’ve seen this product picked by developers working on heterocyclic construction, seeking to anchor polyhydroxy substitutions into target molecules. The acetyl group offers a ready point for further extension, especially for those pushing deeper into methods that build complexity through condensation reactions or mild oxidations.

    More than one customer, in both pharmaceutical and dye chemistry, has related how hard it is to build the scaffold from less functionalized precursors. Upstream, a few have tried alternatives sourced from commercial resellers but found contaminants hard to remove or yields inconsistent. Our control over every step—starting from raw hydroxylated aromatics, control over acetylating agents, and exclusion of side products—lets us give a clean and dependable base for exploratory work in these fields.

    Research chemists have fed back on uses in the elaboration of natural products, and enzymatic transformations where position-selective reactivity is critical. We’ve seen skilled organic teams turn to our batches because they want all three hydroxy groups unprotected and available for further manipulation or direct assay.

    On the non-pharma side, the dye and pigment sector brings its own list of requirements. Their focus sometimes falls less on absolute purity and more on batch-to-batch processability and amenability to upscale production. There, input on solubility characteristics in different carriers makes its way back to us. By tuning our drying cycle, we can land the right product feel, something we continue to improve with each feedback cycle.

    What Sets This Product Apart in Practice

    Direct control is the short answer. As actual chemical manufacturers, we know where routine producers stumble. Some suppliers work with intermediates, buying from a series of handoffs and risking variable trace impurity content. That can mean formaldehyde residues from poor-quality acetylating steps, or unexpected coloration indicating decomposition at a packaging stage. Because we own the entire chain, down to solvents and filtration aids, we can guarantee not just compliance to stated specs but actual batch-to-batch predictability.

    Lab techs who work with actual powder from us notice cohesion and tendency to cake or flow, which we manage by choosing the right balance of milling step versus crystal form. Plant operators want samples that push cleanly through feeders—something we found only after running hundreds of kilograms through our own processing lines, not based on theoretical properties alone.

    Differences from other suppliers also show up in logistics and packaging. Many producers or resellers view storage and shipping as an afterthought, meaning users sometimes receive material with moisture gain, or inconsistent particle size due to poor secondary packaging. We pack under dry nitrogen when seasonal humidity demands it and use tamper-evident, re-sealable primary containers. Feedback from bulk consumers highlighted the risk of small packaging bottle failures, which led us to switch to heavier-gauge containers for multi-kilo shipments.

    On another front, sustainability matters. In our experience, buyers rarely want greenwashing – they prefer evidence that process solvent is recycled or that resource efficiency is not just a buzzword. For our own production runs, solvent recovery loops for the acetylation stage allow us to recover much of the acetic anhydride and lower the waste burden.

    We also cut out the “mystery batch” issue that sometimes arises from trading platforms. Our batches trace directly from in-house records—no repackaging blind spots or uncertainty over raw material lots. If a client has questions about analytical data for a certain lot, we connect them straight to the records (and the staff) that handled their material, not a generic call-center contact.

    In the Manufacturer’s Hands: Solving Customer Problems

    Solving technical and logistical issues comes from understanding the hands-on difficulties chemical users face. We’ve received samples back from customers, accompanied by clear notes on unexpected residual solvents or stuck filtration during their own processing. Instead of deflecting, production staff have run root cause analyses and sent out a better-optimized batch at our own cost. Every error, fix, and success gets fed back into updated process controls—and that kind of refinement doesn’t come from third-party sellers or out-of-house logistics chains.

    One real-world case involved a research facility running into bottlenecks trying to derivatize an intermediate. The problem appeared as batch variation in melting point and reactivity. Their original sample came from a trading firm with ambiguous paperwork. After testing our product, they witnessed more consistent downstream results, zeroing in on purity and particle size as the keys. The difference for them showed up in saved hours during purification and less ambiguity in analytical readouts. Their team pivoted to us for subsequent lots, eliminating maintenance headaches mid-campaign.

    Sometimes a minor adjustment on our side—slowing down a drying phase or using a finer sieve during final packaging—solves a months-long customer issue. We don’t just respond to purchase orders with a boxed commodity; we listen, compare batch records to field results, and make micro-adjustments at the request of real scientists and engineers actually using these chemicals.

    Processing teams rely on materials that blend, dissolve, or react as predicted. That sounds simple, but as anyone running a kilo-scale synthesis knows, minor variations cause hours or days of troubleshooting. By producing 1-(3-Acetyl-2,4,6-trihydroxyphenyl)ethan-1-one in-house, controlling the incoming materials, and letting our staff sign off every batch, we shield partners from the runaround that comes with brokerage intermediaries or piecemeal logistics.

    Quality and Consistency: More Than Just Test Data

    Customers depend on reliability, not just a single spec pass. Every order reflects a web of process controls from raw material sampling, through in-line reaction monitoring, to tight outbound testing that covers not only core chemical identity, but also more subtle markers: UV-Vis scans for chromophores, LC data for trace byproducts, and hands-on inspection for color, flow, and “feel.” We train our operators to notice and report subtle differences, feeding those observations back into production planning.

    In our facility, equipment maintenance, solvent cleanliness, and clear line assignments for different product grades cut the risk of cross-contamination. From experience, overlapping production lines can lead to small carryover amounts, which become problematic for downstream analytical applications. That’s why we keep lines distinct, schedule rigorous cleanout runs, and change filters and seals on documented cycles.

    Documented processes and process history matter for regulatory work, registration, and audits. For many downstream buyers working toward regulated markets, traceable batch documentation cannot wait until problems show up. We supply analytical records within days of request, and we’re honest when a lot doesn’t meet the end-user’s threshold, either sending a replacement or adjusting processes in real time.

    Supporting Research and Industrial Growth through Direct Partnership

    Each kilogram we send out represents not just a chemical but an ongoing conversation with the teams who use it. As our partners push into new chemistry, analytical techniques, or process changes, they give feedback we use to adjust our manufacturing, from solvent selection to packaging design. Whether someone builds a dye intermediate or probes a pharmaceutical target, our crews work behind the scenes, absorbing every technical detail and fielding every batch-specific request.

    Scale-up users see benefits beyond paper specifications. They get precise documentation, minimized exceptions, and the confidence that comes from talking straight to the people who manufactured their product. If packaging needs to change, or analytical needs evolve, we make the shift at source. In bigger runs, we can afford to fine-tune operations for custom particle size, solubility range, or blending properties, based on real feedback and clear references to user experiences.

    Smaller buyers, including academic research groups, aren’t left behind. We treat modest-scale orders with the same diligence—overpacking sensitive compounds, sending representatives to demonstrate sample handling, and troubleshooting batch issues on a call or site visit instead of bouncing emails between logistics partners and unknown intermediaries.

    Navigating Market Shifts and Supply Chain Challenges

    In recent years, market volatility, supply chain constraints, and regulatory shifts have added layers of pressure to all chemical manufacturing. What keeps us afloat isn't just a focus on compliance, but long-standing supplier relationships and flexibility in raw material sourcing. By building redundancy into our raw input streams, and holding higher-than-average inventory of uncommon intermediates, we weather sudden disruptions—something end-buyers are increasingly keen to ask about before committing to scale-up purchases.

    Regulatory expectations continue rising, especially for those shipping into North America, Europe, and East Asia. We keep up through site audits, up-to-date documentation, and nimble adaptation to any announced rules. As a direct manufacturer, we can respond rapidly to rule changes, adjust lot labeling, or adopt a new handling protocol within our teams. That agility beats the lag that comes when product needs to run through a chain of brokers before changes filter through to the production level.

    From our perspective, being present at every step—sourcing, production, packaging, shipment—means we get early warnings of potential delays or inconsistencies and have levers for direct intervention. We keep contingency plans in place, coordinate with licensed carriers familiar with specialty chemical requirements, and brief our own people on the unique shipping hazards for each compound.

    The Manufacturer’s View: A Commitment to Practicable Solutions

    Every time a batch leaves our dock, we see it as part of a story—one that includes chemistry, practicalities, and partnership. As direct producers of 1-(3-Acetyl-2,4,6-trihydroxyphenyl)ethan-1-one, we understand the stakes involved with each shipment. With hands in every vessel, and eyes on every analytic readout, we aim to supply not just a reagent, but a measurable difference in the workflow of every end user who relies on our dedication to reliability, communication, and ongoing refinement.