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3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde

    • Product Name 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde
    • Alias 3-Bromo-4-hydroxy-5-ethoxybenzaldehyde
    • Einecs 629-351-8
    • 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

    826374

    Chemical Name 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde
    Molecular Formula C9H9BrO3
    Molecular Weight 245.07 g/mol
    Cas Number 16532-79-7
    Appearance Off-white to light yellow solid
    Solubility Soluble in organic solvents
    Purity Typically ≥ 98%
    Iupac Name 3-Bromo-5-ethoxy-4-hydroxybenzaldehyde
    Smiles CCOC1=CC(=C(C=C1Br)O)C=O
    Storage Conditions Store at room temperature, in a dry and dark place

    As an accredited 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde is securely sealed in an amber glass bottle with a tamper-evident cap.
    Shipping 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It’s packed according to hazardous material regulations, with clear labeling and appropriate cushioning. Ensure transport complies with chemical safety standards, using temperature control if required, and provide documentation including Material Safety Data Sheets (MSDS).
    Storage 3-Bromo-5-ethoxy-4-hydroxybenzaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Store at room temperature and handle under conditions that minimize exposure to air and humidity to ensure chemical stability.
    Application of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde

    Applications of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde in Industrial Manufacturing

    As a specialized producer of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde, we serve key downstream sectors where this fine chemical plays a critical role in advanced synthesis. Below, we detail its real-world applications in industrial lines where the material integrates into demanding processes, referencing the compliance and processing requirements of each sector.

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

    Our material is widely adopted by pharmaceutical manufacturers as a core intermediate in the multi-step synthesis of selective kinase inhibitors and other aromatic drug scaffolds. It enters as an essential building block in heterocyclic condensation reactions, supporting the construction of complex molecules used in targeted therapies. Its purity and specific reactivity directly affect final product yield and batch-to-batch reproducibility in API synthesis.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF (United States Pharmacopeia / National Formulary) for impurity profiling
    • EU GMP Guidelines (EudraLex, Volume 4, Part II)
    • China Pharmacopoeia (ChP) requirements for chemical intermediates

    Typical usage ratio

    • Batch formulations typically use a molar ratio of 1.0–1.2 equivalents per target scaffold. Exact dosage adjusts based on route of synthesis and yield optimization parameters.

    Downstream process integration

    • Introduced at the aromatic ring functionalization stage via amide or imine coupling.
    • Participates in Suzuki, Heck, or Sonogashira cross-coupling sequences in synthesis trains.
    • QC checked for residual bromide and aldehyde content before further derivatization.

    Final product types

    • Oral kinase inhibitor tablets
    • Injectable formulations (oncology drugs)
    • Research-grade small molecule compounds

    2. Agrochemical Synthesis for Fungicide and Herbicide Active Ingredients

    Major crop protection manufacturers utilize our product as a core aromatic intermediate in the synthesis of substituted benzaldehyde frameworks key to next-generation fungicide and herbicide actives. Its defined reactivity supports reproducible synthesis of aryl-ether derivatives, enhancing molecular stability and biological activity against resistant strains.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Quality Control
    • REACH Regulation (EC) No 1907/2006 registration as industrial chemical
    • China “GB” National Standards: GB 24689 for pesticide preparations
    • ISO 9001:2015 traceability in supply chain

    Typical usage ratio

    • Formulation processes use 0.8–1.5 equivalents, titrated based on the agrochemical backbone and side-chain selectivity during condensation and reduction steps.

    Downstream process integration

    • Enter synthesis at the protected phenol aromatic ring introduction stage.
    • Undergoes m-ethoxy functionalization prior to cyclization or halogen exchange.
    • Batch-wise residual solvent removal followed by integration into bulk technical concentrate lines.

    Final product types

    • Systemic triazole fungicides (formulated liquids and powders)
    • Selective post-emergence herbicide actives (formulated granules)
    • Pre-mix technical grade intermediates supplied to pesticide formulators

    3. Fine Chemical Intermediate for Liquid Crystal Material Production

    Our compound is specified by advanced materials manufacturers developing high-purity liquid crystal monomers for thin-film transistor (TFT) and display applications. Its functionalized aromatic aldehyde structure lends tailored alignment and polarity properties, supporting the precise molecular architecture required in LCD mixtures for high-contrast and fast-switching displays.

    Industry compliance standards

    • IEC 61249-2-41 standards for display materials
    • RoHS Directive (2011/65/EU) regarding hazardous substance restrictions
    • ISO 9001:2015 certification for batch traceability
    • Internal QC analytics (HPLC, GC, NMR) to maintain trace-level impurity compliance

    Typical usage ratio

    • Typically introduced at 0.5–2.0% by mass within LC precursor synthesis, adjusted according to desired polarity index and viscosity targets for downstream blending.

    Downstream process integration

    • Condensed with mesogen precursors in high-vacuum distillation reactors.
    • Intermediates protected and deprotected during high-pressure etherification steps.
    • Final crystallinity and purity controlled before LC monomer polymerization.

    Final product types

    • Liquid crystal mixtures for TFT-LCD devices
    • High birefringence specialty LC formulations
    • Film alignment agents used in e-paper and display manufacturing

    4. Synthesis Block for Fragrance Intermediate Manufacturing

    In fragrance ingredient manufacturing, our product serves as a controlled aromatic intermediate used to generate aldehydic, phenolic, and ether notes in high-end perfumery bases. The selective reactivity of its ortho-hydroxy/ethoxy substitution pattern allows chemists to construct novel tones and expand fragrance libraries for both fine fragrance and home care applications.

    Industry compliance standards

    • IFRA (International Fragrance Association) standards for aromatic aldehyde derivatives
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 9235 standards for aroma chemical raw materials
    • Ingredient disclosure per California Proposition 65

    Typical usage ratio

    • Typically applied at 0.2–0.7 equivalents per final aldehyde tonality note in the synthetic scheme, with precise ratio determined by desired olfactive intensity and regulatory maximum levels per finished product type.

    Downstream process integration

    • Used in multi-step synthesis of aldehydic bridge compounds for high-value base notes.
    • Advanced via Grignard or Wittig couplings before formation of final aromatic frameworks.
    • Batch post-treatment includes solvent exchange and isomeric purity control prior to blending into perfume concentrates.

    Final product types

    • Fine fragrance concentrates for luxury eau de parfum
    • Detergent and personal care fragrance bases
    • Air care and home fragrance liquid refills
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    Certification & Compliance
    More Introduction

    3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde: Reliable Foundations for Advanced Synthesis

    Understanding the Value of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde

    Producing 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde has always called for a deep appreciation of both chemistry and the persistent demands of the growing pharmaceutical and specialty chemical industries. The journey from raw materials to the final refined aldehyde means more than simply reacting chemicals together; it means respecting every stage—reaction, purification, and final quality assessment—because every gram matters to the scientific community relying on precise molecular tools.

    This compound, structurally known as 5-Ethoxy-4-hydroxy-3-bromobenzaldehyde, forms a foundation for several advanced molecules. Demand has steadily risen from research chemists, custom synthesis units, and specialty drug developers who need aromatic aldehydes with unique substitution patterns for targeted synthetic programs. Over years of hands-on manufacturing, certain lessons ring true: purity, traceability, and reaction predictability separate well-produced chemicals from unreliable intermediates.

    Production Insights Only a Manufacturer Can Offer

    Our line has seen the full range of aromatic aldehyde production, and each batch of this brominated, ethoxylated benzaldehyde brings its own challenges and rewards. The bromine atom at the three-position enables pathways to further functionalization, either for halogen-lithium exchange reactions, cross-coupling, or selective activation during subsequent steps. Retaining both the ethoxy substituent and the hydroxy group on the aromatic ring makes the molecule appealing for library synthesis or for building blocks in pharmacologically active frameworks.

    Consistency sets our material apart. We control and monitor hydroxy protection-deprotection steps and bromination conditions closely, avoiding trace contaminants that complicate later transformations. A single uncontrolled variable—temperature excursion, incomplete phase separation, even minute solvent impurities—might introduce unpredictable by-products that undermine months of research. By refining our protocols year after year, we deliver an aldehyde with minimal impurities, supporting both scale-ups and sensitive development projects.

    Specifications That Enable Progress

    Every result in synthetic chemistry starts with the properties of the starting materials themselves. Our 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde leaves our facility with a minimum purity of 98%, confirmed by well-maintained HPLC and NMR. The careful isolation of this compound ensures a fine crystalline form, low in residual solvents and protected from moisture, which keeps reactivity and storage stability on target. We avoid casual shortcuts—each batch undergoes strict moisture and residual solvent checks, as slight hydration or solvent residue may directly affect the reactivity in downstream pathways.

    From our earliest small-scale runs to full commercial batches, the specifications we hold to go beyond a checklist. For instance, color clarity verifies the absence of trace oxidation, while melt point spreads and spectral checks ensure clean aromatic substitution. Our long partnership with packaging suppliers limits any possibility of leaching or unintended contamination. We warehouse each lot in humidity-controlled environments after triple-verifying labeling and traceability.

    What Sets Our Material Apart in Research and Production

    Synthetic projects set to begin with this compound often aim to construct benzofuran, benzopyran, or other oxygen- and halogen-rich frameworks. Directing groups and electron density tuning, thanks to both the hydroxy and ethoxy components, aid regioselectivity or ortho/para directing effects—subtle features appreciated by chemists seeking to avoid side reactions. Unlike lower-grade aldehydes that arrive with boarder melt ranges, visible particulate, or batch-to-batch variability, our product consistently meets the demands of sensitive downstream chemistry.

    The refinements made locally, at the source of manufacture, impact performance directly. Several chemists across the industry have commented on the color quality that results from fresh, careful crystallization. We see these features as not only indicators of our technical skill but confirmations that material will behave as expected, batch after batch.

    Reproducibility is what every development team counts on. Even minor residual acidity, or peroxide contamination, derails catalyst-driven reactions built on our aldehyde. When you know your starting material will not introduce such risks, you can design your synthetic approach for maximum efficiency rather than troubleshooting unwanted surprises. That's the real-world difference made by a dedicated manufacturer.

    Applications and Insights From Ongoing Work

    Over the years, the bulk of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde customers have come from pharmaceutical and agrochemical discovery units. Their project goals frequently target heterocycle synthesis, intermediate building for proprietary molecules, or method development where access to unique aromatic frameworks unlocks new biological activity. Some groups focus on coupling this aldehyde with active methylene or amine partners, using the product in classical Knoevenagel, Mannich, or Pictet-Spengler strategies. The ethoxy and hydroxy features open doors to both hydrogen bonding and electronic modulation, making this benzaldehyde versatile for structure-activity exploration.

    In our own work, we've noticed that handling remains straightforward when precautions are respected—tightly sealed glass containers prevent hydrolysis, and temperature control during storage avoids decomposition. Strong nucleophiles react as expected at the aldehyde carbonyl, while the hydroxy group can take part in intermolecular chemistry or be protected as needed. Our technical support often fields questions about aldehyde selectivity, and having experience running these reactions at production-scale allows genuine guidance, not just textbook answers.

    Differences That Matter: Real-World Comparisons With Other Aldehydes

    Researchers sometimes debate the value between this specific halogenated, hydroxy-ethoxy benzaldehyde and more common options. Plain benzaldehydes, those lacking the bromine or with only methoxy substitutions, do not allow for targeted cross-coupling or selective derivatization. For libraries where diversity and late-stage functionalization matter, the bromo group offers a unique handle. The ethoxy substituent distinguishes reactivity from simpler methoxy analogs—its electronic and steric effects methodically shift reaction pathways. Hydroxy groups, concurrently, enable direct interaction or site-specific protection.

    Another aldehyde, such as 3-bromo-4-hydroxybenzaldehyde, does not bring the ethoxy group to bear. Results in model reactions confirm different reactivity and solubility that affect workups or downstream analytics. The specialty role of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde is not theoretical; we've watched teams run parallel syntheses and observe improved yields or better selective outcomes using our material, particularly in Suzuki, Heck, or Ullmann couplings. Tracing performance directly to molecular structure, instead of batch inconsistency, saves weeks of troubleshooting.

    Less refined material often cuts costs upfront but leads to project backtracking, instrument fouling, or ambiguous assay results. We understand first-hand how those headaches slow down both R&D and production schedules, with each missed target or extra purification translating directly into missed deadlines and ballooning expenses. It's in these details where experienced manufacturing pays off for everyone further down the development line.

    Supporting Chemists Through Technical Experience

    As much as chemistry textbooks discuss theory, laboratory and plant realities reward careful observation. Each campaign teaches new lessons, and we approach every run of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde looking for microscopic signs of change—color shifts, viscosity changes, spectral nuances. Small changes regularly arise from raw material variations or subtle seasonal shifts in ambient humidity, so we build in multiple points of control, logging every deviation to understand long-term trends.

    We see chemists in academic, pharmaceutical, and fine chemical sectors relying on in-house production data to inform their choices. By sharing technical support —reaction notes, optimal storage conditions, observations on incompatible partners—we directly address challenges faced in live projects. Three-way troubleshooting calls with analysts, customer process teams, and our own operators lead to more straightforward scale-ups and cleaner results.

    Aldehyde intermediates sometimes require custom specification: alternative particle sizes, solvent removal, or packaging changes for air or moisture sensitive applications. Over time, we've tailored solutions, tracking every adjustment in batch records and confirming any changes do not affect long-term stability or performance. Most buyers care deeply about these adjustments only after the fact, once unexpected challenges appear during larger scale-ups or analytical validations.

    Environmental and Regulatory Considerations

    Modern laboratory and industrial users increasingly demand transparency around environmental impacts and regulatory status. By manufacturing in-house, we keep a close watch over effluents, side-reactions, and waste processes. The bromination step carries its own hazards, so containment and scrubbing protocols keep exposure risks in check. Each batch runs with recorded compliance to local permit requirements, monitored by dedicated safety staff present during all hazardous operations. Updates in national and international regulatory frameworks mean consistent review and documentation.

    Efforts to recover and reuse solvents have increased steadily, with our technical team driving new recycling systems. End-users often value the assurance that their intermediates come from facilities committed to pollution reduction and low-waste processes. Documentation trails frequently accompany shipments for this compound, enabling customers to complete their own safety and environmental audits with confidence.

    Innovation Rooted in Practical Experience

    The best progress occurs where technical skill meets on-the-ground experience. Each new project poses unique demands. We've worked with clients who modify the 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde with custom substituents or request tailored purities for their targets. These partnerships challenge us to improve not just reaction yields but operational reliability—batch reproducibility, robust storage, and detailed analytics.

    In one notable application, a specialty pharmaceutical R&D group required kilogram-scale runs with exacting trace metal content due to a sensitive downstream coupling. Stepping up from benchtop synthesis to full reactor production, we navigated changes in agitation, temperature control, and isolation that might have introduced micro-impurities. By reviewing our records and running side-by-side analysis at scale-up, we met the specification without sacrificing output. Instead of generic responses, real-world data, and years of line-side work, proved decisive.

    Innovations extend to improved packaging—using vacuum-sealed, amber-lined vessels, we limit light-initiated decomposition. More than a technical upgrade, these packaging tweaks help researchers avoid time-consuming re-purification. Responding to these needs as they arise fast-tracks experimentation, safeguarding investment in both time and resources.

    Real-World Challenges and Forward-Looking Solutions

    The hands-on experience of making and supporting 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde runs deeper than generic technical advice. One recurring challenge involves moisture pick-up in humid climates, where even minor aldehyde hydration impacts downstream transformations. To counter this, we double-seal containers and use desiccant packing for every export shipment—keen awareness learned over years of batch failures and customer troubleshooting calls.

    Cross-contamination, often overlooked, is managed through dedicated reactor trains and cleaning protocols. Not every chemical supplier invests in such infrastructure, but our operations prove these steps essential for offering truly high-purity intermediates. What might look like extra time and expense in the short-term repeatedly pays off, with long-term partners reporting fewer failed experiments and better analytical results.

    Our industry also faces regulatory shifts surrounding hazardous reagents, changing permitted concentrations, and stricter waste disposal standards. Instead of waiting for changing rules to mandate action, we proactively adapt processes, phase out legacy reagents, and share regulatory updates transparently with our customers. Every update and documentation checkpoint means more clarity for downstream quality control audits.

    The Manufacturer’s Perspective on Quality and Reliability

    From firsthand experience, laboratory and pilot plant teams benefit most from predictable material that arrives as described—consistent appearance, consistent purity, and complete documentation. What may look like small advantages in one batch become decisive factors across large numbers of syntheses. Years spent producing 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde in high volume have shown us how every detail—right down to how material is filtered, dried, and packed—translates into less risk for chemists and process engineers alike.

    Reliability never results from a one-time effort. It takes continuous review, re-testing, and open collaboration with the scientific community. The value of listening to researchers who use the chemical daily cannot be overstated. Their practical warnings, checklist tweaks, and proposed optimizations return to us as invaluable feedback, helping us iterate and upgrade our operating procedures. That’s why every batch reflects the combined wisdom of both our plant staff and our customers.

    With every shipment of 3-Bromo-5-Ethoxy-4-Hydroxybenzaldehyde, we remind ourselves of our commitment—not simply to meet a number on a specification sheet but to underpin the progress of research with true confidence in starting materials. Trust comes from experience—ours and our customers’—shared through every single batch we prepare.