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2-Hydroxychalcone

    • Product Name 2-Hydroxychalcone
    • Alias 2’-Hydroxychalcone
    • Einecs 216-245-3
    • 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

    517772

    Cas Number 1668-44-4
    Iupac Name 1-(2-Hydroxyphenyl)-2-phenylethan-1-one
    Molecular Formula C15H12O2
    Molecular Weight 224.26 g/mol
    Appearance Yellow solid
    Melting Point 66-69°C
    Solubility Slightly soluble in water, soluble in ethanol and organic solvents
    Density 1.17 g/cm³ (approximate)
    Smiles C1=CC=C(C=C1)C=CC(=O)C2=CC=CC=C2O
    Pubchem Cid 75826
    Flash Point >110°C

    As an accredited 2-Hydroxychalcone 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, tightly sealed, labeled "2-Hydroxychalcone," includes hazard warnings, lot number, and company branding.
    Shipping 2-Hydroxychalcone is shipped in tightly sealed containers, protected from light, moisture, and air. Packaging complies with chemical safety standards, ensuring safe handling during transit. Standard shipping methods are used unless otherwise specified by regulations. Proper labeling and documentation accompany the shipment for identification, storage, and hazard communication purposes.
    Storage 2-Hydroxychalcone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from light and sources of ignition. It should be kept at room temperature, protected from moisture, and isolated from incompatible substances such as strong oxidizers. Appropriate labeling and adherence to safety protocols are recommended to ensure safe handling and storage.
    Application of 2-Hydroxychalcone

    Applications of 2-Hydroxychalcone in Industrial Manufacturing

    As the original manufacturer of 2-Hydroxychalcone, we support partners across multiple downstream industries with consistent, quality-controlled supply. Below are focused, real-world scenarios where our material is integrated into industrial-scale end-product manufacturing, each with unique requirements for formulation, process, regulatory standards, and targeted outputs.

    1. Pharmaceutical Intermediates for API Synthesis

    In the pharmaceutical sector, 2-Hydroxychalcone serves as a core intermediate during active pharmaceutical ingredient (API) production, especially for synthesis of flavonoid-based drug structures with anti-inflammatory, antimicrobial, or anticancer properties. Production facilities implement robust controls and documentation per good manufacturing practice, as minor impurity profile variations can affect downstream purity and compliance. Typically, operators introduce this compound at the condensation step, reacting it with specific acids or amines, closely monitored by in-line HPLC for batch consistency. Final APIs produced using this intermediate target prescription drugs and over-the-counter products regulated by stringent pharmacopoeial standards.

    Industry compliance standards

    • USP, EP, JP pharmacopoeias (where applicable to APIs)
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EudraLex Volume 4 GMP guidelines

    Typical usage ratio

    • Used at 0.7–1.5 mol equivalents relative to target core structure; exact mole count adjusted based on desired API yield and purity requirements

    Downstream process integration

    • Introduced during aldehyde-ketone condensation (Claisen-Schmidt reaction) for subsequent cyclization, purification by crystallization, and multi-step functionalization into the final API framework

    Final product types

    • Flavonoid-based pharmaceuticals (tablets, injectables, topical creams)
    • Semi-synthetic antimicrobial and anti-inflammatory drugs
    • API intermediates exported for contract drug manufacturing

    2. UV-Absorbing Agents in Cosmetic Formulation

    Manufacturers in the personal care and cosmetic industry utilize 2-Hydroxychalcone as a UV-absorbing moiety in formulations targeting photoprotective performance, particularly in premium sunscreen and anti-aging lines. Its chromophore properties provide efficient absorption within the UV-A/B spectrum without significant discoloration or odor in final emulsions. Technicians introduce the compound to the oil or aqueous phase at controlled temperatures, maintaining compliance with cosmetic ingredient listings and permissible concentrations by market. The process integrates functionality with sensory appeal, balancing regulatory adherence and consumer demand for safe sun care products.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • US FDA Title 21 CFR Part 700–740 (where regulated as a cosmetic ingredient)
    • China GB 7916 Hygienic Standard for Cosmetics
    • INCI registration and labeling

    Typical usage ratio

    • Usually 0.05–0.5% w/w in final emulsified sunscreen matrix; upper limit determined by regional photostability tests and patch test results

    Downstream process integration

    • Added during emulsion pre-mix or homogenization step; disperses with surfactants or stabilizers before final fragrance adjustment

    Final product types

    • Broad-spectrum sunscreen lotions and sprays
    • UV-protective day creams and anti-aging serums
    • Foundation makeup with SPF labeling

    3. Pigment Precursor in Specialty Dye Manufacturing

    In the specialty dye industry, technical formulators rely on 2-Hydroxychalcone as a key precursor for producing anthocyanin analogs and advanced organic pigments. The compound’s reactive sites enable tailored color tuning via subsequent oxidation, reduction, or glycosylation, supporting custom shades in industrial ink and textile dye production. Precise weighing and batch additions prevent tonal variation and pigment instability, with each lot undergoing spectrophotometric assessment for hue accuracy. Compliance with downstream textile and ink regulatory requirements drives process validation routines throughout the manufacturing chain.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textiles
    • REACH Annex XVII (restrictions on certain hazardous substances)
    • ISO 8780-6:2018 (Pigments and extenders for paints and varnishes)
    • DIN EN 71-3 (Toy safety—migration of certain elements, for relevant applications)

    Typical usage ratio

    • 1.5–7% w/w as a pigment precursor in bulk dye synthesis; adjusted for targeted chromaticity and pigment concentration in each formula

    Downstream process integration

    • Fed into reaction vessels post-alkali fusion or enzymatic catalysis step, followed by purification through membrane filtration and spray drying for pigment finishing

    Final product types

    • Textile dyes used in fabric printing and dyeing lines
    • Colorant pastes for plastics and industrial coatings
    • Inkjet and offset printing inks for paper and packaging

    4. Antioxidant Component in Functional Food Additives

    The food ingredient manufacturing sector applies 2-Hydroxychalcone as a minor antioxidant compound within certain functional food additive blends. Its polyphenol backbone acts to delay lipid oxidation in stabilized beverage and confectionery systems, mainly as part of antioxidant premixes. Food technologists incorporate it in micronized powder batches or encapsulated beadlets, with all formulations subject to food safety regulations and dietary supplement labeling requirements. Trained personnel manage blending under hygienic conditions, using in-process sampling to confirm absence of contaminant carryover in line with global food safety standards.

    Industry compliance standards

    • GB 2760-2023 (China Food Additives Standard)
    • FAO/WHO Codex Alimentarius—General Standard for Food Additives
    • FSSC 22000 (Food Safety System Certification)
    • HACCP process verification

    Typical usage ratio

    • Micro-addition at 5–40 ppm in total batch; exact ppm set by product type, regional maximum residue levels, and oxidative stability targets

    Downstream process integration

    • Weighed into antioxidant preblend at dry mix or liquid feed stage; followed by direct addition to beverage concentrates or final confectionery pre-extrusion batching

    Final product types

    • Functional beverages and teas
    • Nutrition bars and fortified candies
    • Stabilized bakery pastes and fillings

    5. Corrosion Inhibitor Intermediate for Industrial Coatings

    2-Hydroxychalcone finds practical application as a synthetic intermediate in the production of corrosion inhibitors incorporated into industrial coatings and anti-rust metal primers. Chemical engineers select this compound for its chelation potential and enhanced bonding with ferrous and non-ferrous metal substrates, delivering sustained protection under aggressive atmospheric and marine conditions. Standard operating procedures dictate its addition at the pre-polymerization or monomer modification stage, where it reacts with alkyd or phenolic resins before colloid-mill dispersion and quality control for viscosity and adhesion metrics. Regulatory and end-use testing reinforce reliability for critical asset protection projects.

    Industry compliance standards

    • ISO 12944 (Paints and varnishes—Corrosion protection of steel structures by protective paint systems)
    • ASTM D3359 (Adhesion by Tape Test)
    • RoHS Directive 2011/65/EU for hazardous substance limits
    • REACH Regulation (EC) No. 1907/2006 (for chemicals in coatings)

    Typical usage ratio

    • Integrated at 0.2–1.2% w/w within corrosion inhibitor component prior to coating blend-up; variation based on exposure class and substrate reactivity

    Downstream process integration

    • Charged into reactor at monomer modification step; followed by full dispersion into paint matrix and post-add curing/stabilization

    Final product types

    • Industrial anti-corrosion primers for structural steel
    • Protective marine coatings for shipbuilding
    • Heavy-duty machinery paints and restoration products
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    Certification & Compliance
    More Introduction

    2-Hydroxychalcone: Reliable Foundation for Synthesis and Research

    Authenticity Starts in the Lab

    Working with 2-Hydroxychalcone from the production end means hands-on experience with every step, right from raw material handling to batch cGMP practices. This compound, known to the bench chemist simply as a hydroxy-substituted chalcone, offers a bright yellow powder that rarely surprises—its stability and well-documented melting range provide predictability project after project. Every lot we release draws from refined filtration, careful crystallization, and archive-standard quality controls. There’s a craftsmanship to working with 2-Hydroxychalcone. Staff monitor batches like clockwork, checking for the faintest impurity, so customers avoid unexpected noise in their results.

    Over two decades in the field has taught us to respect the nuance of aromatic intermediates. The phenolic OH on the 2-position seems like a minor tweak, but seasoned organic chemists appreciate how much of a difference it creates—improving solubility for researchers, modifying reactivity in downstream transformations, and providing a launchpad for tailored ligand chemistry or the next cycle in a biological screen. If someone asks for specs, they usually care about purity, water content, absence of starting materials, and sometimes trace metals. Achieving clean 2-Hydroxychalcone usually means column-free workup, constant drying under vacuum, and no shortcuts.

    Specifications that Serve Real Projects, Not Stock Lists

    The metrics customers regularly ask about include GC or HPLC area normalization, NMR-integrity, and sometimes LC-MS screening for tough applications. Achieving >98% by HPLC or NMR requires a stubborn approach to washing, recrystallizing, and monitoring the process right up to packaging. Moisture can lead to clumping and affects measured mass, so we keep all final material sealed under dry nitrogen until it leaves for delivery. Our analysts, some with years on the same product line, keep running the thin layer chromatography plates and spectroscopic scans to spot tiny variances batch to batch. This isn’t about ticking boxes—it’s about making sure customers hit their endpoints without needing extra troubleshooting.

    Discussing specifications means talking real-world impact for phosphorescence studies, starting materials in organic synthesis, or as an in-house intermediate for pharma lead optimization. 2-Hydroxychalcone, thanks to its hydroxyl group on the aromatic ring, can behave as both a nucleophile and a hydrogen bond donor, opening the door to more selective synthesis routes, cyclization studies, or functional group transformations under mild conditions. What’s ground truth for us as manufacturers: customers value analytical reports that match results, batch-to-batch consistency, and straightforward packaging that doesn’t degrade the compound en route.

    Application: From Bench to Scale-Up

    Chemists order 2-Hydroxychalcone for broad purposes—offering both a flexible Michael acceptor and a useful starting point for synthesizing flavonoids, heterocycles, and functionalized building blocks for agrochemicals or medicinal chemistry programs. In our experience, medicinal chemists often reach for 2-Hydroxychalcone as a tool in structure–activity relationship studies or to create analog libraries for enzyme inhibition assays. The phenolic group boosts interaction potential and may bring low-level antioxidative properties, making it relevant in biochemical research probing enzyme or receptor activity.

    Small-scale researchers gravitate toward this compound for predictable crystallization, allowing for easy purification via common solvents—ethyl acetate, methanol, or dichloromethane, to name three that feature in daily production. The chalcone scaffold itself, with its double bond and conjugated system, provides a solid foundation for UV-Visible spectral studies, a must in photochemistry and analytical labs. Working with downstream partners, we’ve seen 2-Hydroxychalcone serve as a starting point in Suzuki couplings, Claisen–Schmidt condensations, and even multi-step syntheses where yields matter at every stage.

    What Makes 2-Hydroxychalcone Unique in Our Toolbox

    Compared with basic or unsubstituted chalcones, the presence of a 2-hydroxyl group changes the rules of engagement. Reactivity ramps up in cases involving electrophilic aromatic substitution, cyclizations, and functional modifications, all due to the directional effects and electron-donating nature of the attached OH. Bench chemists we’ve supported prefer our 2-Hydroxychalcone because fewer side products build up during post-condensation steps, meaning columns run faster and downstream analysis takes less time. Stability in storage, both from chemical and moisture perspectives, stands out compared to other substituted chalcones or more reactive hydroxyketones. End users working with scale-up for heterocycle projects know that this compound doesn’t degrade easily, even over several months.

    Our technical team often fields questions comparing this product with similar derivatives—say, 4-Hydroxychalcone or methoxy-substituted analogues. The 2-position hydroxyl generally delivers more pronounced effects on conjugation along the chalcone backbone, influencing not only color and solubility but also downstream functionalization strategies. For customers exploring enone chemistry or photoreactive compounds, the twist created by the ortho-hydroxyl facilitates unique cyclization possibilities that the para or meta analogues struggle to deliver. Beyond theory, those practical distinctions shape real decisions: vendors for research-scale syntheses don’t want guesswork when choosing between chalcone derivatives.

    Quality Rooted in Knowledge, Not Just Certificates

    Any lab with a chromatography system and basic spectral tools can identify a decent batch of 2-Hydroxychalcone, but consistently delivering ultra-high purity calls for deep process know-how. Our facility invests in full-batch NMR checks, FTIR overlays for incoming and outgoing lots, and periodic external lab verifications. We store detailed batch histories and can offer retrospective data reviews for major customers working on regulated development projects. These steps often exceed industry minimums because researchers designing animal studies, pharmaceutical screens, or crystal growth studies can’t afford to risk surprise contaminants.

    Product quality stems from more than suitable cleanroom tech or compliant equipment. A good batch of 2-Hydroxychalcone starts with trained personnel who understand why phenolic oxidation matters or why temperature gradients during crystallization can cause subtle color changes—a sign of product breakdown or overreaction. Every product line relies on tight collaboration between synthetic scale-up teams and analytical chemists, translating to a product scientists can trust with key experiments. Experience, both on the bench and manufacturing floor, has refined how quickly we adapt protocols to block emerging impurities or pin down process drift before it affects quality.

    Story of a Batch: Lessons from Root Cause Analysis

    A few years back, we logged a sequence of batches with slightly higher UV impurities—enough to trouble several pharmaceutical partners. Instead of simply rerunning those lots for purity, shop-floor and QC teams reviewed the entire production stream. They found solvent recovery tanks had developed trace metal leaching, reacting subtly with chalcone’s phenolic group and shifting its UV absorbance. By replacing liners and refocusing on single-use vessels, we brought impurity levels down below customer cut-off points. That experience reemphasized the need for detailed traceability in aromatic compound manufacturing, proving how minor process adjustments can keep output reliable and project timelines intact.

    Stories like these offer more than “quality improvement” platitudes. At the synthesis scale, even a minor change—temperature, solvent, cleaning regimen—can push products like 2-Hydroxychalcone out of spec. Continuous improvement has to go hand-in-hand with deep chemistry knowledge, not just compliance checklists. This attitude keeps customer confidence high, especially when our product serves as a building block in FDA or EMA-driven research pipelines.

    Ensuring Safe Handling and Longevity

    Every milligram of 2-Hydroxychalcone leaves the plant sealed, labeled for moisture and light-sensitivity. Storage in cool, dry conditions preserves its yellow color and keeps peroxide formation at bay. Early in our process development, leaving even partially open containers led to off-odors and color changes, which later showed up as out-of-trend HPLC peaks. Preventing cross-contamination and ensuring robust packaging isn’t just about shelf aesthetics—it protects research output and guarantees accurate weight measurements for microgram-sensitive dosing in pharma studies.

    Transport partners know to avoid high humidity and heat spikes during transit. We track each shipment, not because customers expect it, but because repeat deliveries have to be as reliable as the first. Our teams remain available for post-delivery support, fielding questions about solubility, handling, or clean-up. If a unique customer process calls for smaller or custom aliquots, we adapt our filling lines to maintain integrity down to the gram.

    How 2-Hydroxychalcone Drives Discovery

    Research teams appreciate how flexible the 2-hydroxyl group makes downstream synthesis. Across dozens of customer projects, we’ve seen it play a role as a Michael acceptor in enamine chemistry, serve as a precursor for natural product analogues, and hold up to cycloaddition or reduction without generating unpredictable byproducts. Whether exploring enzyme inhibition, new light-reactive materials, or bioactive scaffolds, labs trust the predictability: batch after batch, crystallization, purity, and spectral properties stay consistent.

    The material supports work in analytical chemistry. UV-Vis and fluorescence measurements on pure 2-Hydroxychalcone provide clean reference spectra for method development. Graduate students and senior scientists alike benefit from its well-known reactivity, allowing clear validation of synthetic steps without losing time troubleshooting unexpected peaks or complex mixtures. For those driving projects toward preclinical testing, knowing the starting material behaves the same between lots means fewer failed runs and more focused troubleshooting.

    Applications Beyond the Lab

    Beyond the bench, agricultural companies engage with 2-Hydroxychalcone research to build new fungicide and herbicide leads. The phenolic group lends itself to derivatization into more complex bioactive molecules with promising systemic movement and environmental breakdown. With pharma and biopharma, product quality and absence of trace contaminants outweigh cost—reproducible lead analogs for early pipeline evaluation matter more than a cheap, flexible substrate.

    Formulators in specialty pigment projects choose this specific chalcone for color intensity, solubility, and batch stability—especially when other derivatives pose oxidation or handling headaches. Our R&D group shares methodologies and practical advice with major partners: methods to avoid metal contamination, best recrystallization solvents, and effective storage to stop unwanted dimer formation. They draw not only on internal batch data, but decades of feedback from scientific partners who call out where handling or analytical support is needed, closing process gaps nationwide and even globally.

    Differences from Other Chalcones and Derivatives

    Over the years, comparisons with other chalcone products reveal the real practical advantages of 2-Hydroxychalcone. The ortho-phenolic group provides increased resonance stabilization without provoking autocondensation or unmanageable side reactions. In large-scale manufacturing, this means a higher first-pass yield and fewer purification cycles than with other hydroxy- or methoxy-chalcones. For researchers, this translates to less time spent on cleanup and more time exploring actual chemistry.

    Discussions with downstream processors highlight how 2-Hydroxychalcone generally outperforms para- or meta-hydroxy analogues for high-efficiency coupling reactions, photoinitiator synthesis, or as a benchmark in spectroscopic calibration. Its characteristic yellow hue and spectral fingerprint set it apart from both basic chalcones and heavier halogen-substituted analogs, letting method developers confirm product identity quickly and with high confidence. Product feedback over the years consistently shows that the ortho substitution encourages easier crystallization and better solution stability, reducing time spent troubleshooting solubility limits or gradual degradation.

    Supporting Research and Industry with Direct Know-How

    Customers benefit from more than material. Our production chemists host discussion calls with university teams, industrial analytical labs, and pharma process chemists who raise concerns about method development, yield drops, or unexpected side products. This type of support isn’t optional. Decades of scale-up experience and direct collaboration with researchers gives our teams the experience to troubleshoot, tailor, and refine technical protocols, not just ship generic product or standard certificates.

    Guidance extends to process improvements for clients scaling their own syntheses. Over time, our facility has shared optimized crystallization protocols, safe solvent recommendations, and analytical references that allow customers to hit target purities and achieve reliable batch replication. Feedback loops with clients influence our internal process tweaks and inspire further R&D, ensuring product upgrades mirror the evolving needs of scientific research and industrial customers.

    Climate, Sustainability, and Responsibility

    Responsible chemical manufacturing isn’t a buzzword here. Every lot of 2-Hydroxychalcone passes sustainability checks—tracking waste reduction, selecting greener solvents when possible, and engineering safer waste disposal pathways. Knowledge gained from in-house research now informs solvent recycling and emission reduction strategies, while supply chain audits help ensure environmentally and socially sound procurement for all raw materials.

    Modern research teams care about green chemistry. We’ve worked to minimize the footprint of 2-Hydroxychalcone production by revising the condensation stage to run at lower temperatures, cutting energy demand and reducing byproduct load. Waste solvents follow engineered collection and recycling programs; analysis teams develop and share less toxic workup options so bench chemists can avoid hazardous reagents from start to finish.

    Looking Ahead: Evolution Through Experience

    Expectations for aromatic intermediates, especially those with bioactive interest, keep rising. Longstanding partnerships with industry and academic groups help us anticipate needs before they become headaches. Our team aims to support both high-end pharma and practical bench researchers by maintaining clear communication, technical transparency, and ongoing investment in both process control and product improvement.

    2-Hydroxychalcone continues to anchor chemical discovery projects across disciplines not because of high profile marketing, but through reliable chemistry, grounded know-how, and a willingness to help troubleshoot when conditions in the field shift. From the plant floor to the shipping dock to the R&D office, every stage brings valuable experience. Those lessons shape the next batch, influence the upgrades we engineer into our processes, and reinforce the trust customers place in our materials.

    Summary: Substance Over Promise

    Anyone manufacturing 2-Hydroxychalcone at scale knows its quirks, advantages, and the hurdles that never show up on data sheets. Getting it right means more than batch numbers or purity percentages—it means understanding what research depends on, how specs relate to lab performance, and why detailed support can unlock better results for every project. Reliable science demands reliable starting points, and our commitment remains the same: bring experience to bear, listen to the people who rely on these compounds, and keep pushing for ever better outcomes in both chemistry and service.