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2-Bromo-5-Hydroxybenzaldehyde

    • Product Name 2-Bromo-5-Hydroxybenzaldehyde
    • Alias 2-Bromo-5-formylphenol
    • Einecs 259-984-6
    • 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

    488583

    Chemical Name 2-Bromo-5-Hydroxybenzaldehyde
    Molecular Formula C7H5BrO2
    Molecular Weight 201.02 g/mol
    Cas Number 703-94-8
    Appearance Light yellow to beige solid
    Melting Point 114-118°C
    Boiling Point No data available (decomposes)
    Density 1.8 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Synonyms 2-Bromo-5-formylphenol
    Smiles C1=C(C=C(C(=C1)Br)O)C=O
    Inchi InChI=1S/C7H5BrO2/c8-6-2-1-5(4-9)3-7(6)10/h1-4,10H

    As an accredited 2-Bromo-5-Hydroxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Bromo-5-Hydroxybenzaldehyde, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 2-Bromo-5-Hydroxybenzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous material, requiring appropriate labels and safety documentation. The substance is transported in compliance with relevant chemical and hazardous goods regulations to ensure safe delivery and environmental protection.
    Storage 2-Bromo-5-Hydroxybenzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from direct sunlight and moisture. Store at room temperature and avoid excessive heat. Use appropriate secondary containment and clearly label the container to prevent accidental misuse or contamination.
    Application of 2-Bromo-5-Hydroxybenzaldehyde

    Applications of 2-Bromo-5-Hydroxybenzaldehyde in Industrial Manufacturing

    2-Bromo-5-hydroxybenzaldehyde is a specialty aromatic intermediate produced for demanding industrial sectors. This compound features a halogenated and phenolic functional structure, supporting reliable performance in advanced synthesis environments. As a trusted manufacturer, we integrate tight process controls and analytical backup, ensuring quality suitable for pharmaceuticals, fine chemicals, specialty polymers, and related applications.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (API) Synthesis

    Pharmaceutical producers employ this material as a building block in the multi-step production of certain pharmaceutical actives, especially within the categories of anti-infectives and investigational new drugs. The compound’s ortho-bromo and para-hydroxy functionalization has enabled selective formylation and halogenated substitutions, increasing yield in heterocycle construction. We supply customers who incorporate this aldehyde into their regulated API manufacturing, where tight impurity control, reactivity, and traceability drive batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia (Ph. Eur.) monographs for impurities limits and purity
    • 21 CFR Part 210/211 (FDA cGMP requirements)
    • Custom impurity profiling and documentation for DMF submissions

    Typical usage ratio

    • Employed at 0.2–0.7 molar equivalents relative to primary amines or hydrazines during core API scaffold formation
    • Adjusted in coupling or condensation steps based on reaction efficiency and regulatory impurity thresholds

    Downstream process integration

    • Reacts during early to mid-stage synthesis after initial aromatic substitution
    • Used as a key reactant for introducing the bromo-functionalized aromatic ring into API scaffolds under controlled conditions
    • Subject to QC at both incoming material and post-coupling steps for confirmation of conversion and residuals

    Final product types

    • Intermediates and APIs for antibacterials, antifungals, and selective receptor modulators
    • Pilot and commercial scale finished drug substances containing heterocyclic cores

    2. Intermediate for Agrochemical Synthesis

    Producers of modern crop protection chemicals use this material in the preparation of brominated phenolic intermediates critical for formulated fungicides and insecticides. The compound promotes regioselective synthesis of benzoxazole, benzimidazole, and benzothiazole rings, offering high conversion for active ingredient backbones. This application demands assured contaminant profiling and consistency, especially for export-compliant active ingredient manufacturing.

    Industry compliance standards

    • ISO 9001:2015 quality management systems for chemical intermediates
    • REACH EU Regulation (EC) No 1907/2006 compliance for downstream handling and transport
    • Technical specification agreements for impurity content with global agrochemical companies

    Typical usage ratio

    • Used at 10–23% by weight of total reactants in benzothiazole or benzimidazole synthesis
    • Optimized according to target product and yield considerations, with adaptation to proprietary flow or batch protocols

    Downstream process integration

    • Acts as a starting material in condensation and cyclization reactions under catalytic or basic conditions
    • Integrated following solvent extraction and purification of parent phenolic derivatives
    • Monitored for carryover during isolation steps preceding formulation

    Final product types

    • Benzoxazole-based fungicides and protective seed treatments
    • Benzimidazole derivatives for systemic pesticide active ingredients
    • Bulk intermediates for custom crop protection AI synthesis

    3. Dye and Pigment Industry Intermediate (Functional Azo Dyes)

    Manufacturers of high-performance functional dyes integrate this compound to achieve precise electron-donating and -withdrawing effects in advanced azo systems. Its halogen and phenol functionalities allow superior colorfastness, lightfastness, and molecular rigidity in specialty textile and leather auxiliaries. Producers require assured color value, consistent aldehyde group reactivity, and low background fluorescence.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textile auxiliaries
    • EN 71-3 (Safety of Toys) – migration limits for aromatic amines
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) Conformity

    Typical usage ratio

    • Used at 1–8% by mass of azo coupling components in dye synthesis
    • Adjusted as required for deeper chroma or for precise metamerism in technical textiles and pigments

    Downstream process integration

    • Chemical introduction occurs during the diazotization/coupling stage with aromatic amines
    • Serves as a color-modifying substituent through controlled formyl and halogen substitution
    • Batch color value confirmation and impurity screening conducted prior to granulation or formulation

    Final product types

    • Specialty azo and anthraquinone dyes for high-fastness applications
    • Technical dyes for textiles, leathers, and plastics with demanding color migration control requirements
    • Pigment intermediates for high-performance coatings

    4. Synthesis of Specialty Polymers and Resins

    Producers of engineered polymeric materials use this aromatic aldehyde to introduce bromo and hydroxy functional groups that enhance crosslinking and adhesion in tailored resins. These modifications benefit molecular engineering of photoresists, specialty coatings, and heat-resistant plastics, and require tight content control and documented residue management. Resin manufacturers select this intermediate for molecular insertion in process-controlled environments.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems for chemical and polymer sectors
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94 (Tests for Flammability of Plastic Materials)

    Typical usage ratio

    • 0.5–3.5% by weight in formulation batches for cross-linked phenolic or epoxy systems
    • Adjusted based on polymer target properties, crosslink density, and performance testing

    Downstream process integration

    • Added during resin monomer modification phase or as a chain stopper in condensation polymerization
    • Mixed under controlled temperature and catalyst dosage to prevent unwanted side reactions
    • Integrated with in-process controls to monitor unreacted aldehyde for downstream quality acceptance

    Final product types

    • High-performance photoresists for microelectronics
    • Fire-retardant and adhesive resins for automotive and appliance applications
    • Specialty cross-linked polymers for advanced coatings and electronics encapsulation

    5. Biochemical Research and Diagnostic Reagents Synthesis

    Producers of fine biochemical reagents and diagnostic intermediates utilize this compound as a selective derivatization agent for target enzyme assays, clinical diagnostic kit components, and research markers. The aldehyde-hydroxy-bromo structure offers fluorescence quenching and specific reaction points, facilitating analytically pure marker synthesis for laboratory and industrial use. This application demands the tightest quality and trace residue profiling.

    Industry compliance standards

    • ISO 13485:2016 Quality Management Systems for medical devices and diagnostics
    • Good Laboratory Practice (GLP) guidelines (OECD)
    • USP/NF analytical reagent standards, especially regarding purity and trace contaminants

    Typical usage ratio

    • Utilized at 0.05–0.4 mmol per mmol of target substrate in conjugation reactions or functionalization steps
    • Adjusted depending on targeted signal intensity, background requirements, and protocol scale

    Downstream process integration

    • Introduced during marker conjugation or substrate labeling, often in aqueous-organic phases
    • Monitored with LC/MS and HPLC to assure purity and reactivity for diagnostic use
    • QC analytics performed post-conjugation before release into reagent filling sections

    Final product types

    • Diagnostic enzyme assay reagents for laboratory and clinical use
    • Chemically tagged substrates for imaging and biochemical pathway studies
    • Analytical standards and quality control materials for in vitro diagnostic kits
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Hydroxybenzaldehyde: Manufacturer's Insight into a Precision Intermediate

    Understanding the Foundation of 2-Bromo-5-Hydroxybenzaldehyde

    In chemical manufacturing, precision and consistency drive both product quality and business reliability. 2-Bromo-5-Hydroxybenzaldehyde, known by its CAS number 27125-03-7, stands as a key intermediate for diverse synthetic processes. Experience on the plant floor shows that handling brominated aromatic compounds requires not just textbook knowledge but hands-on skill to keep every batch up to specifications. Our team knows that each step in its preparation – from bromination through careful isolation and purification – creates direct consequences in application downstream.

    Working with this compound, we have found that subtle changes in moisture, batch timing, or temperature profiles during synthesis make a visible difference to product color and purity. The crystalline powder should run between off-white and faint beige, indicative of careful process control and gas flow optimization. Melt point range offers early clues – batch after batch, we rely on consistent melting between 128–132 °C as a sign that contaminants have been kept in check and no unreacted precursors remain.

    Experienced Observations on Specifications

    Our standard production protocol pursues a purity of no less than 98% by high-performance liquid chromatography – a threshold reflective of real-world demands from both pharma and fine chemical partners. Impurities such as residual bromide ions, chlorinated analogs, or partially oxidized byproducts can disrupt later reactions, particularly those involving amide coupling or Suzuki cross-coupling. We learned quickly that even low-level contaminants, below the eye’s detection, tie directly into yields and efficacy on the user’s side.

    For those with stricter needs, including API synthesis, additional recrystallization passes or column chromatography might be implemented, though rarely required with our continuous improvement in process control. Water content, monitored by Karl Fischer titration, stays strictly under 0.5% in our usual lots, aiding in long-term stabilities and solution-phase applications.

    Packaging practice has evolved in response to the compound’s sensitivity to moisture and light. Over years, we have transitioned from basic glass to inert, nitrogen-flushed amber bottles. Production teams understand that oxidation, though slow, can cause not just color changes but deeper loss in chemical reactivity. This knowledge, gained during off-site client support, emphasized the importance of practical solutions like insulation, smaller pack sizes, and UV-opaque containers.

    Applications Speak Louder Than Theory

    A lot of talk about chemical intermediates can sound academic, but the proof lies in what partners make with the product. 2-Bromo-5-Hydroxybenzaldehyde has found its place as a primary starting block for pharmaceuticals and dyes. In laboratories and industrial reactors alike, it enters Suzuki and Heck reactions, flowing effortlessly into biphenyl scaffolds or heterocyclic architectures. The aldehyde group combined with bromine at the ortho position gives a reactive handle; it welcomes nucleophilic attacks, Grignard additions, and condensation reactions head on.

    Some partners in pharma use this material as a precursor for advanced serotonin modulators or antihypertensives, with purity and trace moisture levels affecting downstream bioactivity. In polymer chemistry, we’ve watched it build out complex phenolic resins where any residual acidic impurities can radically change curing rates. On the life sciences end, small batches often end up incorporated into assay development tools. Every case highlights how small variances ripple through entire product pipelines – which is why process reproducibility is always top-of-mind when feedback comes in from the field.

    Electronics manufacturers have flagged up the need for colorimetric consistency and lowest possible halide contamination, requesting extra batch certificates tailored to their own device standards. Their devices can fail from just minor traces of unanticipated contaminants, an issue we now test for preventively.

    Industry Feedback Shapes Production Choices

    Direct conversations with R&D teams across different applications taught us to focus on batch-to-batch reproducibility rather than just chasing ultra-high purities for marketing. Consistency beats chasing decimals after the purity percentage, and discrepancies often show up not as failed analyses, but as unexplained side products in downstream chemistry. We have invested in inline sensors and digital batch logs so that customers can both trace and trust the process from raw material intake to end product.

    A common challenge for manufacturers who order end-to-end: Some struggle with the balance between cost and specification. We learned that tightening specification parameters – for instance, lower allowed halide levels – increases production cost by requiring more elaborate purification, but that payoff appears downstream as shorter reaction times and lower rejection rates in finished pharmaceuticals.

    Authentic feedback from end-users impacts how we calibrate everything from drying temperatures to packaging sizes. For certain medicinal chemists, a kilogram packed under dry argon in a custom bottle makes all the difference during route scouting and scale-up. Others building colorants for the textile or ink industries demand stability over months and stricter color tolerance, leading to the adoption of specialty stabilizers during storage.

    What Distinguishes 2-Bromo-5-Hydroxybenzaldehyde from Similar Aromatic Reagents?

    Stepping back from technical bullet points, real-world experience shows us that 2-Bromo-5-Hydroxybenzaldehyde’s utility comes from its structure. Plenty of brominated benzaldehydes populate catalogs, but the position of the hydroxy and bromo groups impacts the chemistry that follows. Take 4-bromo-2-hydroxybenzaldehyde as a side-by-side comparison: the substitution pattern means nucleophilic or electrophilic aromatic substitution proceeds at different positions, changing which frameworks become possible in later steps.

    Our customers share that for Suzuki couplings or Stille reactions, 2-bromo substitution avoids unwanted side-chain reactivity seen in para-analogs and offers more stability during storage and shipping. This specificity leads to higher yield and less byproduct. The ortho relationship in our product unlocks different biological activities when building pharmaceutical candidates, thanks to changes in steric and electronic character upon subsequent functionalization.

    Over the years, we noticed that while standard benzaldehydes exhibit similar reactivity in condensation chemistry, they can introduce complications due to undesired cross-coupling or product instability. By delivering a product with strictly controlled isomer content and directed bromination, we enable our partners to skip unnecessary purification downstream. These nuanced structural effects matter, especially in stepwise synthesis on both lab and pilot scales, and represent subtleties only found through repeated practice and customer feedback.

    Manufacturing Challenges: Learning and Adapting

    Anyone producing aromatic intermediates at scale appreciates that small changes slip past if quality checks aren’t robust or continuous. Early in our experience, simple glassware choices or changes in bromine addition rates gave inconsistent yields. Over multiple campaigns, experimentation and failure led us to automate certain stages and standardize agitation rates and reaction times. Human intuition, particularly among veteran technicians, guided improvements that ultimately shaped today’s product lines.

    Handling the product’s sensitivity to thermal degradation shifted our philosophy around equipment setup and cleaning protocols. In the past, a single misstep in rinsing led batch to fail purity specs by introduction of trace basic or acidic residues. Such details rarely show up in text or datasheets, but in reality they mark the difference between a pass and a fail at QA.

    We respond to environmental demands by optimizing solvent recovery and treating process effluent. Regulatory requirements are getting stricter every year. Team efforts to minimize emissions, recover solvents, and reprocess wash waters have paid off in a more sustainable operation, which matters increasingly to downstream buyers evaluating supply chain environmental responsibility.

    Partnerships, Not Transactions

    Most of our best process improvements stem from conversations with experienced users. One customer, from an agricultural lab focused on developing new herbicide structures, challenged us on color consistency and shelf-life stability, pressing for product improvements which led to extended testing and adjusted packaging – a move that not only kept the customer but enhanced our practices across the product portfolio.

    Another case involved a global pharmaceutical company scaling up rapid syntheses where small amounts of unreacted bromine sabotaged their catalytic cycles. Our answer involved installing inline detection and refining purification steps, delivering measurable results in their own process performance. Genuine feedback from such users steers both R&D and daily production. On our end, talking to specialists who react the product in tough, multi-step syntheses keeps us honest and grounded about how real-life variability impacts outcomes.

    These stories underline why we prioritize real operational feedback over anonymous market research. It’s not about shipping chemicals without care; it’s about delivering a product that supports efficient, reliable synthesis, batch after batch.

    Facing Ongoing Supply Chain and Regulatory Pressures

    We have seen consistent supply chain stress, especially with imported bromine and specialty solvents. Advance planning and local sourcing, wherever possible, have helped buffer many of the price spikes and delays that ripple through the industry. We track all suppliers with annual audits and documented trail of origin so our customers can stay compliant with traceability requirements.

    Labeling regulations and safety documentation have trended toward greater transparency. In practice, that means more rigorous analysis and extra documentation hours for every lot. No shortcut exists here: we assign dedicated personnel to manage quality records, and all our batches go through full HPLC, NMR, and elemental analysis before release. This layer of consistency, while adding cost, returns value to customers who are increasingly called upon by regulators to prove origin and composition for all intermediates.

    What the Future Brings

    Looking ahead, demand for high-fidelity intermediates like 2-Bromo-5-Hydroxybenzaldehyde continues to grow as pharmaceutical innovation and specialty materials evolve. A few trends already shape the field: stricter specifications from end-users, more rigorous environmental footprints, and a nearly universal expectation of traceability from raw materials to delivered product.

    Automatic process control and digital batch management are here to stay. By giving customers clear visibility into production histories and deviations, we help them meet their own regulatory needs and reduce chances of miscommunication or error. Robotics have taken a firm hold in both small and medium-scale batchwork, providing unprecedented reproducibility and verifiable cleanliness for each lot.

    Process chemistry never stands still. Raw materials can fluctuate in purity or availability, and year-to-year climatic variability can even influence reaction yields in large-scale plants. Staying close to the chemistry, not just the theory, and keeping lines of dialogue open with research users and plant engineers has provided our best insurance against unexpected challenge.

    Practical Takeaways from the Manufacturer’s Floor

    Repeated hands-on production cycles underscore a few truths worth sharing. Specifications only matter when they consistently support customer goals, especially in complicated synthetic routes where one intermediate can become the difference between a breakthrough and a blind alley. Handling and storage protocols perform best when tailored to the realities of logistics and actual use, not hypothetical worst-case scenarios.

    Faced with increasing consumer expectations around sustainability, we have upgraded solvent recovery systems and instituted internal recycling – both of which have improved the actual cost of goods sold as well as our responsible standing in the market. The push for environmentally-responsible supply chains, though challenging, proves compatible with the efficiency demands of quality chemical production.

    Transparent, efficient operations result from investing in both human expertise and technological upgrades. Senior process chemists working hand-in-hand with automated reactors, diligent packaging teams using state-of-the-art moisture protection, and quality control staff empowered with modern analytical tools – all contribute directly to customer satisfaction and product reliability.

    Summary Reflections

    For those procuring 2-Bromo-5-Hydroxybenzaldehyde, choosing a direct manufacturer yields dividends in responsibility, traceability, and real dialogue. We have learned through years of hands-on experience, collaborative problem-solving, and feedback-driven improvements that consistent, high-quality intermediates enable smarter, more reliable discoveries downstream. Each bottle reflects purposeful choices, from raw material scrutiny to the final, tightly sealed cap – aiming not for the lowest price, but for the level of reliability that catalyzes effective innovation.

    Our biggest advances come not from chasing abstract ideals, but from listening carefully to end users, responding with real process upgrades, and sharing technical knowledge earned from the manufacturing front lines. In this way, the story of 2-Bromo-5-Hydroxybenzaldehyde continues as a genuine partnership between those who make it and those who put it to work in the advancement of science, technology, and medicine.