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1-(4-Bromophenyl)-2-Hydroxyethan-1-One

    • Product Name 1-(4-Bromophenyl)-2-Hydroxyethan-1-One
    • Alias 4-Bromomandelic acid
    • Einecs 259-401-6
    • 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

    871879

    Chemical Name 1-(4-Bromophenyl)-2-hydroxyethan-1-one
    Molecular Formula C8H7BrO2
    Molecular Weight 215.05 g/mol
    Cas Number 2652-63-7
    Appearance White to off-white crystalline powder
    Melting Point 112-116 °C
    Boiling Point Unknown
    Purity Typically ≥98%
    Solubility Soluble in organic solvents like ethanol and DMSO
    Density Unknown
    Smiles C1=CC(=CC=C1C(=O)CO)Br
    Inchi InChI=1S/C8H7BrO2/c9-7-3-1-6(2-4-7)8(11)5-10/h1-4,10H,5H2
    Refractive Index Unknown

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

    Packing & Storage
    Packing The 25g of 1-(4-Bromophenyl)-2-Hydroxyethan-1-One is securely sealed in a clear amber glass bottle with detailed labeling.
    Shipping The chemical **1-(4-Bromophenyl)-2-hydroxyethan-1-one** is shipped in secure, sealed packaging to prevent contamination and moisture exposure. It is transported according to relevant chemical safety guidelines, typically under ambient conditions unless otherwise specified. Proper labeling and documentation ensure compliance with international and local shipping regulations for laboratory chemicals.
    Storage Store 1-(4-Bromophenyl)-2-Hydroxyethan-1-One in a tightly sealed container, away from direct sunlight, heat, and moisture, ideally in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as oxidizing agents. Ensure proper labeling and adhere to all relevant safety guidelines when handling and storing the compound to prevent accidental exposure or contamination.
    Application of 1-(4-Bromophenyl)-2-Hydroxyethan-1-One

    Applications of 1-(4-Bromophenyl)-2-Hydroxyethan-1-One in Industrial Manufacturing

    As a primary manufacturer, we provide 1-(4-Bromophenyl)-2-Hydroxyethan-1-One for downstream industries where its unique chemical structure plays a critical role in synthesis, process efficiency, and finished-product quality. The following use cases highlight the compound’s specialized role across real-world industrial applications, detailing compliance, formulation ratios, plant integration points, and examples of end products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    This compound acts as a key building block in the synthesis of advanced pharmaceutical intermediates, particularly for the preparation of substituted phenylethanol derivatives. QC teams value its reliable performance in multi-step synthetic pathways, especially in halogenated intermediates required for cardiovascular and central nervous system drug candidates. Process chemists precisely control addition rates to balance reactivity and minimize side-products.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs for related APIs
    • European Pharmacopoeia (Ph. Eur.) requirements for raw material traceability
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Reactant input: 1.1–1.3 molar equivalents relative to target API intermediate, adjusted according to yield optimization data and batch scale

    Downstream process integration

    • Charged to the main reaction kettle after solvent charging and inert gas blanketing; undergoes nucleophilic or condensation reactions under controlled temperature profiles
    • Purified by recrystallization prior to downstream derivatization steps on pilot and commercial scale

    Final product types

    • Halogenated phenylethanol pharmaceutical intermediates
    • Active pharmaceutical ingredients (APIs) for CNS, anti-inflammatory, and cardiovascular therapies
    • Clinical research chemicals for preclinical testing

    2. Fine Chemical Synthesis for Agrochemical Precursors

    Fine chemical manufacturers select this compound as an integral intermediate in producing substituted aromatic building blocks for crop protection agents, especially for triazole and azole fungicides. The compound’s selective bromination pattern enhances site-specific reactivity, supporting downstream alkylation or ring-closure processes pivotal to engineered pesticide formulations designed for residual field stability.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • EU REACH Registration, Evaluation, Authorisation and Restriction of Chemicals Regulations
    • FAO/WHO Specifications for Agrochemical Technical Materials
    • OECD GLP Guidelines for downstream toxicological testing

    Typical usage ratio

    • Direct intermediate: 0.8–1.2 molar equivalents relative to target agrochemical backbone, set according to cycle efficiency and impurity control parameters

    Downstream process integration

    • Added to nitration or acylation reaction vessels following catalyst charging; monitored via HPLC for complete conversion before workup
    • Acts as an input in column isolation procedures leading to solid or liquid technical-grade intermediates for further formulation

    Final product types

    • Triazole fungicide intermediate chemicals
    • Selective herbicide precursors
    • Eco-toxicological research compounds for regulatory submission

    3. Organic Synthesis for Aromatic Fragrance Ingredients

    Specialty fragrance and aroma compound producers utilize this raw material to construct complex aromatic ketones for high-value perfumery and cosmetics. Its defined reactivity enables controlled acylation and hydroxy group transformations, supporting the manufacture of brominated aromatic blends that anchor long-lasting odor profiles in consumer fragrances and personal care formulations.

    Industry compliance standards

    • IFRA Code of Practice for safe use in fragrances
    • ISO 9001:2015 for process controls in flavor and fragrance manufacturing
    • EU Cosmetic Regulation (EC) No 1223/2009 for raw material assessment
    • REACH Annex XVII for restricted substances in consumer goods

    Typical usage ratio

    • Synthesis input: 0.5–2.5% wt/wt of total fragrance batch input, level selected based on olfactory strength calibration and reaction kinetics

    Downstream process integration

    • Introduced during Friedel–Crafts acylation steps in batch reactors; reaction parameters adjusted for purity and aroma retention
    • Refined via distillation or flash chromatography before final blending with natural extracts and essential oils

    Final product types

    • Aromatic ketone fragrance ingredients
    • End-use perfumes and personal care scent bases
    • Cosmetic additive aroma stabilizers

    4. Synthesis Intermediate for Laboratory Chemical Reagents

    Chemical reagent manufacturers incorporate this compound as a reference standard and reactive intermediate during the synthesis or calibration of analytical standards in research laboratories worldwide. Its well-defined functional groups allow method validation in developing custom reagents for high-precision chemical, biological, and analytical workflows, where both halogen and hydroxy substitutions are essential for method specificity.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Competence
    • ACS Reagent Chemicals Specifications
    • GLP (Good Laboratory Practice) for batch traceability
    • ISO Guide 34 Reference Material Production for certified standards

    Typical usage ratio

    • Formulation: 0.05–0.5% wt/wt in analytical solution or 5–10 mg per reference standard, optimized for instrument calibration and shelf-life

    Downstream process integration

    • Dissolved or weighed directly into standard solution preparations; precise weighing ensured by automated microbalance systems under controlled environments
    • Undergoes secondary synthesis for producing high-purity analytical standards with stringent impurity profiling using NMR and MS

    Final product types

    • Certified reference chemical standards
    • Analytical reagent kits for LC/MS, GC/MS detection
    • Calibration materials for pharmaceutical and environmental quality labs
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    Certification & Compliance
    More Introduction

    1-(4-Bromophenyl)-2-Hydroxyethan-1-One: Essential Intermediate Designed for Real-World Chemical Synthesis

    A Closer Look at Our Main Product

    1-(4-Bromophenyl)-2-hydroxyethan-1-one stands out as more than a specialty chemical. For years, we have tailored its production through batch consistency, strict raw material selection, and time-tested operational controls. Chemical manufacturers, research institutions, and pharmaceutical developers rely on intermediates that go beyond the catalog entry—products that match process requirements day after day. Our direct production gives us fine-grain control of purity, color, and stability, so each lot supports precise outcomes in targeted end use.

    Knowing the Structure and Nature of the Compound

    Chemically, this compound—sometimes called 4'-bromo-α-hydroxyacetophenone—carries both a brominated aromatic ring and a hydroxy ketone moiety. This combination drives its value in synthesis. The bromine group, positioned on the para portion of the phenyl ring, enables straightforward substitution, coupling, and cross-coupling reactions. The hydroxy functionality unlocks further reactivity, facilitating reductions, esterifications, and protective chemistry. Many colleagues in the pharmaceutical industry focus on these two groups to build scaffolds for bioactive molecules, including anti-inflammatories and central nervous system candidates. Over time, this dual functionalization has made it indispensable in both discovery and scale-up projects.

    Our Manufacturing Experience and Specifications

    As direct producers, we refine every aspect of 1-(4-Bromophenyl)-2-hydroxyethan-1-one. We manage bromination, condensation, and crystallization steps, examining reaction profiles to prevent side reactions and ensure lot uniformity. Each batch meets a minimum purity of 98% by HPLC, with melting points between 118°C and 123°C, confirmed through repeated runs. Water content typically registers below 0.5%, as checked by Karl Fischer titration. These benchmarks reflect both sound chemistry and routine feedback from downstream users who require high assay levels for process predictability.

    Over the years, we have improved particle morphology and color consistency. Rather than accept a yellowish or off-white product, we’ve zeroed in on minimizing chromophoric byproducts, especially over multi-ton runs. The result is a white crystalline powder, free-flowing and straightforward to weigh, dissolve, or handle in automated lines and small-lot glassware alike. Though some alternate preparations outside our factory might yield a technical grade, we focus on robust, predictable lots meant for regulated environments and advanced synthesis.

    Everyday Uses in Synthesis and Research

    Many partners look to 1-(4-bromophenyl)-2-hydroxyethan-1-one as a versatile building block. In our experience, it performs reliably in the synthesis of substituted benzofuran and benzopyran derivatives. Chemists value its ability to undergo etherification, alkylation, and Grignard additions. We've seen extensive adoption in medicinal chemistry projects, with its ability to serve as a stepping stone to complex heterocyclic cores.

    One research group working on antitumor compounds relies on our product’s purity and controlled impurity profile during the synthesis of thienopyridine and quinolinone fragments. Shifting to electronic materials, another client routinely couples this intermediate under palladium catalysis to build arylated analogs for organic semiconductors. In custom synthesis, the hydroxy and keto motifs have encouraged the exploration of diverse protective strategies during iterative coupling and deprotection steps, a feedback line we remain tuned into while adjusting our crystallization process.

    Why Control in Production Matters

    A manufacturer’s shop floor is not the same as a sales desk or trading company. We carry out reactions in equipment selected over years of trial and knowledge—not just laboratory glass but scalable reactors, material handling tools, and built-in safety checks for bromine and strong base handling. Each operator works within documented procedures. Tighter in-process controls and validated cleaning regimes keep our product from picking up unintended moisture or contamination. We systematically sample each lot, perform in-house gas chromatography and mass spec analysis, and only release barrels once they match the stability and purity ranges we’ve become known for.

    Many years ago, a customer flagged the presence of a persistent isomer byproduct seen only in high-throughput UPLC screening. Rather than ship a replacement blindly, we stopped batch release, dug into the relevant production stage, and revised our workup and recrystallization methods. Today, lots that leave our facility can be traced back to these moments of proactive adjustment. Working under a compliance framework, our team ensures that documentation supports every batch, from raw material origin to final certificate of analysis, because consistency and traceability stem from direct hands-on production.

    Differences From Non-Directly Produced and Technical Grades

    A common question from buyers is why they should insist on material straight from the source. In our experience, technical grade materials from trading houses often fail in process-sensitive steps—specifically, when minor variability in impurity profile or residual moisture causes chain stops in downstream reactions. Our quality standards eliminate these unknowns. Each kilogram of our 1-(4-bromophenyl)-2-hydroxyethan-1-one supports process validation for both pharmaceutical and fine chemical routes. Analytical comparisons have shown that off-white, aged technical lots build up trace degradation products over long storage and poorly controlled shipping, which can call for additional purification and delay project timelines.

    We keep the product fresh, shipping directly after quality control approval. Process lines are washed, dried, and subject to air and dust monitoring, minimizing introduction of foreign material. The analytical fingerprint—specifically, the HPLC retention time, UV absorbance peak, and NMR signatures—lines up consistently across sequential lots. This repeatability enables research and manufacturing groups to scale up reactions without devoting time to pre-inspection or repeated pilot reactions to recheck the behavior of the starting material.

    How We Respond to Changing Requirements

    Manufacturing comes with surprises. Regulatory shifts, new process control standards, and stricter raw material provenance checks push us to make continuous improvements. By sourcing bromine only from audited and traceable suppliers, we limit upstream variability. Routine spectroscopic identity checks (1H, 13C NMR and FT-IR) ensure that each batch matches the intended structure, right down to the last peak. If a customer requests a specific particle size or solubility range, we work openly with their project chemists—running test milled lots, solubility trials, or drying studies until the final product integrates smoothly into their route.

    For shipping, we use containers lined with inert film, documented pre-shipment for cleanliness and compliance. Regular storage checks keep stocks within temperature and humidity limits, preventing cake formation or hydrolysis. We do not repackage or mix lots, maintaining a one-to-one link from production run to delivered material. This traceability has supported customers’ regulatory filings and helped us address rare deviation claims with transparency and real data.

    Supporting Green Chemistry and Safe Operations

    The chemical industry faces growing pressure to cut environmental risks and enhance worker safety. Years ago, our team began developing closed bromination systems that minimize releases and secondary waste. Spent bromides are collected and sent to certified recovery facilities. By adopting aqueous workups and recirculating process water, we reduced effluent chemical load. Regular air monitoring and operator safety training—hands-on, not just procedural—ensure a safer production environment.

    We didn’t stop at the plant floor. Our R&D group supports clients exploring biocatalytic and lower-emission synthetic options. In several pilot projects, we have supplied analytical samples to customers using solid-state and solvent-free reactions, and have heard positive feedback on reactivity and product quality. By staying open to these approaches, we help our partners experiment with new, greener methods, making sure that the material serves emerging needs without trade-offs on quality.

    Why Choice of Intermediate Quality Changes Outcomes

    Some may view intermediates as interchangeable, but after years supplying both small and large labs, we see the difference crop up at every stage. The predictable reactivity and controlled impurity background of our product often translate to higher yields and smoother downstream purifications. Researchers avoid time-consuming troubleshooting, minimizing column loads and material loss. In process scale-up, the careful control over batch moisture and trace metal content heads off batch failures—an issue we’ve seen when clients trialed lower-grade alternatives from non-direct sources and encountered catalytic poisoning in Suzuki or Buchwald-Hartwig couplings.

    It isn’t just research flows that benefit. Commercial manufacturing partners trust our supply chain transparency, with real-time COA release, direct shipment from factory floor to end site, and accessible technical support. These factors matter most once the pressure of a go-live date ramps up, regulatory inspections start, and every deviation is scrutinized. Teams depend on a supplier with skin in the game—the kind of commitment that comes from being the original manufacturer, willing to work closely to resolve batch-specific questions.

    Feedback Loop: Listening and Adapting

    No two clients run the same process, and over the years, the feedback we gather has shaped how we work. Synthetic chemists, process developers, and even storage managers share challenges and preferences on solubility, filtration, or seasonal shipment temperatures. Whenever a new isolation problem or crystallization challenge surfaces, we dig into it, often modifying our drying cycles or tweaking particle size distribution to address real bottlenecks.

    Handling feedback is a two-way street. Our dedicated technical staff interact not only with purchasing contacts but with end-user chemists. Late one summer, a customer working over 30°C logged more rapid clumping of material, threatening batch homogeneity. We started packing that season’s production with enhanced desiccants, rolled out oversight on shipment transport, and followed up post-delivery to make sure the issue had closed. Many of today’s process controls trace their roots to stories like this—real-world challenges, solved through direct conversation rather than generic responses.

    Pushing the Envelope—New Applications and Process Improvement

    While the bread and butter lies in pharmaceutical and fine chemical intermediates, we continue to see new uses for 1-(4-bromophenyl)-2-hydroxyethan-1-one. Custom electronics groups develop fluorescent compounds from our material, leveraging the electron-rich hydroxy function to tweak emission spectra. Academic groups head up photochemical and polymerization projects, demanding a stable and high-purity intermediate to assure clean transformation and robust material properties. In every case, the journey from bench to factory is smoothed when the starting material delivers batch after batch, rising to technical challenges as the applications shift and grow.

    Demonstrating Real Commitment and Expertise

    Operating as a direct manufacturer isn’t just a selling point—it defines our mentality. We see our work as a stewardship of process, product, and partnership. Every kilogram of 1-(4-bromophenyl)-2-hydroxyethan-1-one leaving our doors has the mark of hands-on expertise, a track record of adaptation, and a shared understanding of what downstream users need. That shared understanding comes from conversation and from years behind the reactor, where hiccups and successes inform the next shift and the next improvement.

    We invite inquiry and collaboration, drawing on a team with real process experience—not reading from stock sheets but responding to fresh technical requirements. Each engagement becomes a chance to refine both our compound and our approach, ensuring that the next batch produced fits the ever-shifting landscape of chemical synthesis. In this way, our intermediate forms more than a part of a reaction—it shapes real outcomes for researchers and manufacturers working to make the next breakthrough or raise the standard for their own products.

    Conclusion: Why Origin and Production Matter

    Choosing 1-(4-bromophenyl)-2-hydroxyethan-1-one directly from a dedicated producer speaks to more than specification compliance. It reflects a preference for reliability, deep technical support, and an open feedback channel. As the industry moves toward more stringent regulatory, analytical, and sustainability demands, we stand ready to meet those needs—continuing to provide compounds shaped not only by chemistry but by lived manufacturing experience.