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4'-Hydroxychalcone

    • Product Name 4'-Hydroxychalcone
    • Einecs 212-109-4
    • 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

    899459

    Chemical Name 4'-Hydroxychalcone
    Molecular Formula C15H12O2
    Molecular Weight 224.25 g/mol
    Cas Number 42013-20-7
    Appearance Yellow crystalline powder
    Melting Point 110-112°C
    Solubility Slightly soluble in water, soluble in ethanol and DMSO
    Iupac Name 1-(4-hydroxyphenyl)-3-phenylprop-2-en-1-one
    Smiles C1=CC=C(C=C1)C=CC(=O)C2=CC=C(C=C2)O

    As an accredited 4'-Hydroxychalcone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 4'-Hydroxychalcone; features a white screw cap and a detailed product label with safety instructions.
    Shipping 4'-Hydroxychalcone is shipped in accordance with standard laboratory chemical regulations. The product is securely packaged in sealed containers to prevent contamination and degradation. Shipping is typically at ambient temperature, unless otherwise specified, and is accompanied by relevant safety documentation (SDS/MSDS) to ensure safe handling and compliance with local and international transport guidelines.
    Storage 4'-Hydroxychalcone should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry place. Store at room temperature or as specified by the chemical supplier, away from incompatible materials such as strong oxidizers. Ensure good ventilation in the storage area, and label the container clearly to avoid accidental misuse or exposure.
    Application of 4'-Hydroxychalcone

    Applications of 4'-Hydroxychalcone in Industrial Manufacturing

    4'-Hydroxychalcone provides essential functional benefits as a fine chemical intermediate and additive in select downstream industries. Our manufacturing expertise ensures consistent supply to customers integrating this compound into regulated industrial processes. Explore dedicated application scenarios where this material delivers measurable value:

    1. Active Pharmaceutical Ingredient (API) Synthesis for Anticancer Drug Intermediates

    Pharmaceutical manufacturers utilize 4'-Hydroxychalcone as a key synthetic building block in the processing of certain chalcone-based APIs with cytotoxic and antiproliferative functions. The material enters the synthetic route during the early-stage formation of heterocyclic frameworks, contributing its hydroxy functional group for subsequent transformation steps such as cyclization or selective functionalization. Sourcing material that adheres strictly to pharmacopeia impurity limits and residual solvent regulations is central to API quality and regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) specifications for intermediates
    • European Pharmacopoeia (Ph. Eur.) monograph guidelines
    • FDA 21 CFR Part 211 (if for US markets)

    Typical usage ratio

    • 0.5% – 3% w/w in multi-step reaction sequences (actual charge varies by reaction yield and scale; adjusted according to stoichiometric requirements and side reaction minimization)

    Downstream process integration

    • Direct addition during aldol condensation or Claisen-Schmidt reaction stage of small-molecule API synthesis;
    • Employed in batch or continuous synthesis reactors under temperature-controlled and inert conditions;
    • Material shows stability for in-situ handling with subsequent transformations (hydrogenation, oxidation, cyclization re-routing based on the molecule design)

    Final product types

    • Antineoplastic API intermediates for oral and injectable dosage forms
    • Heterocyclic pharmaceutical compounds for further derivatization
    • Reference standards for oncology research and clinical development

    2. Cosmetic Ingredient for Skin Brightening Formulations

    Within the cosmetics sector, formulators incorporate 4'-Hydroxychalcone in brightening serums, creams, and facial lotions owing to its function as a polyphenolic antioxidant and melanin synthesis modulator at controlled concentrations. The ingredient must comply with international cosmetic ingredient inventories and demonstrate stability through formulation, processing, and shelf life. Manufacturers achieve consistency through validated blending and emulsification protocols, integrating the compound post-emulsification or during cool-down phases to avoid degradation.

    Industry compliance standards

    • Cosmetic Ingredient Review (CIR) safety assessments
    • EU Cosmetics Regulation (EC) No. 1223/2009
    • China IECIC (Inventory of Existing Cosmetic Ingredients in China)
    • ASEAN Cosmetic Directive compliance (if supplied to SE Asia)

    Typical usage ratio

    • 0.05% – 0.5% w/w depending on product type such as serums (higher) or rinse-off cleansers (lower); precise level determined by toxicological data, formula stability tests, and end-use regional limits

    Downstream process integration

    • Dispersed in the oil or aqueous phase prior to homogenization
    • Incorporated post-emulsification in heat-sensitive formulations
    • Subjected to microbiological and antioxidant activity QC after batch blending

    Final product types

    • Skin brightening day creams and night creams
    • Facial serums targeting pigmentation spots
    • Anti-aging emulsions and lotions

    3. Food Additive for Functional Beverage Color Stabilization

    Functional beverage producers add 4'-Hydroxychalcone as a natural polyphenolic additive to stabilize color profiles in clear drinks and teas, as well as to support shelf-life extension by suppressing oxidative browning. Regulations require careful documentation of additive identity, batch traceability, and maximum ingestible limits. Processing depends on beverage category and thermal treatment parameters, typically post-extraction or in late-stage blending tanks with protection from light and oxygen exposure to preserve compound activity.

    Industry compliance standards

    • US FDA 21 CFR Part 172 – Food Additives Permitted for Direct Addition to Food
    • EU Regulation (EC) No. 1333/2008 on food additives
    • JECFA (Joint FAO/WHO Expert Committee on Food Additives) assessments
    • China GB 2760 – National Food Safety Standard for Food Additives Use

    Typical usage ratio

    • 5 – 30 ppm (mg/kg) for ready-to-drink teas and plant-based juices; final dosage based on product color, total polyphenol content, and target sensory characteristics validated during pilot trials

    Downstream process integration

    • Added to blending tank immediately before pasteurization or cold filling
    • Subjected to fine filtration to ensure clarity
    • Homogeneous mixing under inert atmosphere when necessary to minimize oxidation

    Final product types

    • Ready-to-drink herbal teas and infusions
    • Functional juices and health beverages
    • Liquid dietary supplements positioned for antioxidant claims

    4. Organic Synthesis Intermediate for Flavonoid Pigment Manufacturing

    Companies manufacturing specialty pigments for textile, printing, and food colorant industries employ 4'-Hydroxychalcone in targeted condensation and catalytic processes to generate specific flavonoid pigment structures, such as aurones and other yellow chromophores. Production operations must maintain strict controls on reaction purity and byproduct formation to deliver pigments with consistent color strength and regulatory status for their intended uses. Plant operators monitor incoming raw material batches for defined impurity and moisture specifications to support downstream yield and pigment tonality.

    Industry compliance standards

    • REACH (EC 1907/2006) registration and safety documentation for pigment intermediates
    • OEKO-TEX® Standard 100 compliance (for textile pigments)
    • FDA 21 CFR §73.260 Color Additive Exempt from Certification (applicable to food-contact pigments)
    • ISO 9001 Quality Management System for production documentation and traceability

    Typical usage ratio

    • 2% – 10% molar basis in flavonoid/aurone pigment synthesis batches, dependent on target pigment intensity and molecular yield after final condensation steps

    Downstream process integration

    • Introduced as a starting material in base-catalyzed Claisen-Schmidt condensations
    • Subjected to further cyclization and oxidation for pigment core development
    • Incorporated with co-reactants at controlled pH and temperature for chromophore formation

    Final product types

    • Aurone-based yellow pigments for food or textile applications
    • Natural colorants for inkjet and offset printing
    • Specialty organic pigments for coatings and plastics

    5. Research Chemical for Structure-Activity Relationship (SAR) Studies in Medicinal Chemistry Labs

    Academic and biotechnology institutions frequently require 4'-Hydroxychalcone as a reference compound or starting material for medicinal chemistry projects focused on structure-activity relationship mapping. These research activities demand materials with high analytical purity, traceable batch documentation, and clear certificate of analysis data. Application protocols usually involve small-scale reactions and advanced characterization as researchers investigate modifications to parent chalcone frameworks for biological screening.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for analytical and preclinical studies
    • ISO/IEC 17025 (Testing and calibration laboratories)
    • Material transfer compliance according to university or institutional guidelines
    • MSDS and hazard communication per GHS (Globally Harmonized System)

    Typical usage ratio

    • 5 – 100 mg per parallel experiment (scaling dependent on target yield for screening or crystallographic assessments; kept minimal to focus on analytical outputs and reaction repeatability)

    Downstream process integration

    • Direct weighing into reaction vials for library synthesis
    • Integration with automated parallel synthesis platforms
    • Purification by preparative HPLC following reaction completion

    Final product types

    • Small-molecule libraries for inhibitory and cytotoxicity assays
    • Structural analogs for target validation in medicinal research
    • Reference samples for publication or patent filing
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    Competitive 4'-Hydroxychalcone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4'-Hydroxychalcone: More Than a Chemical Name

    What Sets 4'-Hydroxychalcone Apart

    On the production floor, 4'-Hydroxychalcone stands out for its consistency and clarity. Every chemist with a jar of this pale yellow powder knows that its structure—an aromatic ketone with a hydroxy group on the para position—offers a distinct pathway compared to unsubstituted chalcones or their methoxy cousins. After years working with flavonoid chemistry, it’s easy to spot the subtle differences this hydroxy group brings. Reactions run smoother, solubility changes in organic solvents become noticeable, and downstream modifications hit higher yields.

    We manufacture our batches with high-purity benchmarks. Our 4'-Hydroxychalcone hits a minimum assay of 98% by HPLC, a level we track from raw material screening up through every filter and distillation. Crystallization and drying steps aren’t rushed, so purity feels visible in the final material. Water content matters, especially to researchers and formulators who intend to push this intermediate into fine chemical or pharmaceutical spaces. Our team targets moisture below 1.5%, keeping stability numbers predictable. The powder feels free-flowing with mild floral notes on the nose—a small detail, but one regulars in the lab quickly notice.

    People on the outside like to talk about chalcones as a group. On the inside, there’s an appreciation for what a para-hydroxy does to the molecule. Compared with raw chalcone, the hydroxy variant resists oxidation a little more, but it still reacts eagerly in hydroxylation or methylation chemistry. Modifiers and polymer scientists prize this extra grip, watching as it becomes a seed for flavones, isoflavonoids, or custom ligands. That isn’t sales jargon. In mass spectrometry, the difference jumps off the report. In practical cross-couplings, it shapes the outcome.

    Production Runs Built on Real-World Details

    This product didn’t emerge overnight. Early efforts presented us with sticky residues and off-color material, forcing process tweaks through trial and repeated runs. We shifted solvents, experimented with temperature profiles, and learned to charge reactants at just the right moment. Today, operators know well that letting the system drift five degrees makes filtering a headache and leaves trace by-products. Through all of this, documentation gets updated, and small equipment changes ripple into easier cleaning cycles. This is why our plant’s batch records carry footnotes from the actual hands who solved the problems.

    We’ve met customers who had thrown up their hands after getting inconsistent material from third-party operators or batches with residual aldehydes. It’s not hard to spot freshly made hydroxychalcone from an old one because color changes from bright yellow to a brownish tone—the result of uncontrolled moisture or light exposure during storage. Our warehouse crew seals every drum under nitrogen, and regular stability checks kick out any suspect lot before it makes it onto a truck.

    Pharmaceutical, agrochemical, and cosmetic interests all lean on 4'-Hydroxychalcone, but each group needs something different. One formulator might need sharp melting point data (ours lands reliably around 83–85°C) to set process windows on their end. A biologist might request a contaminant profile or ensure that the product goes through one extra round of recrystallization. For every inbound request, our technical team looks over the actual production history and, if necessary, takes out samples from current lots. We run extra purity checks as requested—it comes from understanding that no universal spec sheet can fit every real project.

    Why Purity and Traceability Matter

    The end users we serve rarely operate in a vacuum. Their results depend on sample consistency, and they come back to the same manufacturer for a reason: predictability. A lot that checks out at 97.8% may as well be a different material when you’re scaling pilot processes or planning regulatory filings. Difference between 96% and 98% purity is not academic—it shifts crystallization points, alters reactivity, and leaves extra work for downstream analytics. A procedural shortcut on our end ends up as a failed batch or a flagged result downstream. Every lot we produce ties back to a batch record with precise timestamps, operator initials, and digital signatures that can be traced sample by sample. It’s routine for us to run side-by-side chromatograms for every lot and keep reference spectra archived for years.

    Mistakes in this line of work have a way of surfacing eventually. We don’t just validate by instrumental readings but back it with observations: dryness, flow, color stability in air, and test reactions with established side chains. Proof of purity isn’t a randomly assigned number but something measured over hundreds of kilograms and years of reactivity testing on our end.

    Handling and Safety Without The Hype

    Talk of “handling precautions” almost always misses the small details that make a plant run safe and clean. Echoing every safety data sheet isn’t enough; our team found through direct work that hydroxychalcones dust easily, so we upgraded local extraction and implemented non-slip mats at weighing stations. Not all chemicals in the plant need as much respect for eye protection, but this powder will sting if workers are careless. The team switched from standard cotton lab coats to reinforced sleeves for this very reason. Monthly training drills, unglamorous as they are, keep the newer hires from becoming overconfident.

    We ship with data sheets and clear hazard labeling, making sure receivers don’t risk storage in high humidity. True, 4'-Hydroxychalcone isn’t as volatile as the parent chalcone nor as tricky as nitro-aromatics, but regular audits have shown that a few seasonal errors—storing near open warehouse doors or skipping desiccant checks—can cost thousands in rework. The product does not tolerate plastic bag storage for long; drums with foil linings keep the surface from yellowing. Every small logistic lesson came from issues encountered and solved, not proclamations in a spec book.

    Research and Applications Move the Product Forward

    People sometimes ask what actually happens with all this hydroxychalcone leaving our facility. In truth, the variety rivals anything in specialty chemical manufacturing. Several academic groups order by the gram for their screening work, characterizing antioxidant or anti-inflammatory effects. More established pharmaceutical clients go the synthetic route, building up scaffolds for trial candidates. Raw material consistency soaks up a lot of concern on their end.

    In the field, agricultural work points to 4'-Hydroxychalcone as a precursor in pathway studies of plant metabolites—projects that often circle back for more, especially as gene editing and metabolic engineering gain traction. Cosmetics R&D labs check for new photoprotective actives, and they need detailed impurity breakdowns, not just a COA printout.

    Inside our own technical development center, we run predictive reactions to support application requests. Some clients submit their own procedures for pilot trials, wanting to confirm yields and intermediates align with claims. We know the difficulties of scaling up from test tubes to 100-liter reactors, and more than one formulation specialist has thanked us for keeping the standard deviations to a minimum batch-to-batch. A scientist counting on a kilo batch expects the analytical profile to match the original 50-gram lot; our facility delivers that match because of the groundwork laid by operators and QC staff.

    We also work alongside innovators developing building blocks for polymers or resins. The para-hydroxy functionality plays a role in promoting crosslinking, giving new material properties that standard chalcones can’t provide. The creative potential appears even stronger in light-driven curing studies and specialty pigment syntheses—projects that show how every subtle shift in raw material reflects downstream.

    Supply Challenges and Solutions

    Supply chain scrutiny defines modern chemical manufacturing. Even a short disruption ripples across customers counting on delivery schedules. A few years back, raw acetophenone and p-hydroxybenzaldehyde feeds took a price leap and availability tightened. Many producers passed along costs or failed to fill standing orders, leaving R&D teams scrambling at the last minute.

    Our solution focused on securing multiple vetted supply lines and investing in local source development for critical starting reagents. We built our safety stock buffers high enough to weather quarter-long interruptions—always a delicate balance with costs and warehouse space. Throughout, our purchasing team pushed for supplier transparency, reviewing audits in-person, and not just over email. Each input comes with its own set of certificate checks and laboratory confirmations by our own analysts. That upfront work filters out the contamination risks and keeps us from price shocks. Internal teams coordinate daily on inventory and logistics, supported by direct feedback from production managers. These steps sound routine, but without them, product integrity slips fast, as dozens of customer stories have shown.

    Customer communication tops most lists in this field, but consistency in follow-through is what keeps operations healthy. If any order faces a supply-side hiccup, our support staff loops in with project managers to share documentation, offer alternatives, or work on delayed staging. We do not shy away from difficult news, and our reputation reflects this.

    Comparisons to Similar Products

    A question crops up with nearly every new customer: why not substitute 4'-Methoxychalcone, 3',4'-Dihydroxychalcone, or just plain chalcone itself? Real-world experience shows that even tiny shifts in substitution change the game. Take 4'-Methoxychalcone—the methoxy group adds higher lipophilicity and lowers hydrogen bonding potential, which becomes crucial in biological screening or resin synthesis. Comparisons in antioxidant studies regularly show that the extra hydroxy in 4'-Hydroxychalcone boosts radical quenching, verified repeatedly in lab-scale tests.

    We watched some users invest in bulk chalcone to save a line item, only to discover through stability trials and LC-MS results that their conversion rates dropped and impurity levels spiked. 3',4'-Dihydroxychalcone, though a promising variant for antioxidant libraries, introduces synthetic complications—double hydroxyls demand more controlled storage and involve higher oxidation risk during handling.

    Every substitution must pass the reactor, the analysis, and practical formulation hurdles. Process chemists know the value of sticking with the molecule designed for the reaction, especially when scale rises. Our plant has fine-tuned equipment settings so that every lot remains true, avoiding excess solvents or process drift that alternative molecules bring along. While academic literature offers substitution studies, nothing beats the record of full-run industrial experiences.

    Feedback-Driven Improvements

    Over years of making and shipping this product, customer requests have pushed us to tweak more than just the synthesis. Feedback loops sparked light-block packaging, extra analytical options (NMR, MS, UV), more documentation control, and even sample retention for long-term support. Some end-users approached us with novel application profiles, such as its use in studying metabolic pathways, enzymatic inhibitor libraries, or function as a precursor in multi-step synthetic routes. These conversations sharpen our offering.

    Not every request can be met, especially with hazardous or highly specialized modifications. Yet, our process allows for custom packing, select analytical runs, and, when possible, consulting to enable specific project timelines. These efforts grow from direct relationships with long-term partners—not one-off sales. Preserving that trust lands at the core of why our product draws new and repeat customers.

    R&D doesn’t happen in isolation. Our in-house development team routinely checks new literature, updating protocols if a safer, cleaner, or higher-yielding process comes to light. Sometimes a minor solvent change or an updated purification resin can cut impurities down by half. These improvements flow back into our mainline production, keeping the product competitive and reliable.

    Long-Term Perspective

    4'-Hydroxychalcone has become a mainstay for advanced chemical synthesis, and progress in the field keeps demand steady. Universities, startups, and multinationals all rely on a chain of dependable supply from a manufacturer who stakes reputation on quality, traceability, and technical support. Years of experience at the reactor and in the QC lab come together in this one intermediate. This isn’t a box-ticking exercise, but an evolving partnership with the scientific community.

    That’s why each drum carries weight beyond its gross mass—it’s the result of careful process development, repeated analytical checks, decades of scale-up experience, and willingness to adapt. As methods and regulations tighten in every sector, reliability in raw materials turns from a preference to a requirement. Our goal keeps pace: deliver 4'-Hydroxychalcone as a trusted building block, shaped by feedback and guided by daily experience on the shop floor.

    We look forward to further advances—be they in tandem catalysis, photochemistry, or biological applications—confident that the product our people craft will anchor the next wave of discoveries.