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2-Bromo-4-Methoxy-Benzoic Acid

    • Product Name 2-Bromo-4-Methoxy-Benzoic Acid
    • Alias 2-Bromo-p-anisic acid
    • Einecs 620-048-3
    • 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
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    Specifications

    HS Code

    336541

    Chemical Name 2-Bromo-4-Methoxy-Benzoic Acid
    Molecular Formula C8H7BrO3
    Molecular Weight 231.05 g/mol
    Cas Number 85068-36-6
    Appearance White to off-white solid
    Melting Point 172-175°C
    Solubility In Water Slightly soluble
    Smiles COC1=CC(=C(C=C1)Br)C(=O)O
    Iupac Name 2-Bromo-4-methoxybenzoic acid
    Storage Conditions Store at room temperature, in a dry place, away from light

    As an accredited 2-Bromo-4-Methoxy-Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-4-Methoxy-Benzoic Acid

    Applications of 2-Bromo-4-Methoxy-Benzoic Acid in Industrial Manufacturing

    2-Bromo-4-methoxy-benzoic acid serves as a vital intermediate in multiple specialized industrial manufacturing sectors. Below, we present key application fields based on established downstream processing, with practical details for real business use.

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

    Pharmaceutical manufacturers use this raw material in the multi-step chemical synthesis of specific APIs, particularly for anti-inflammatory and anti-cancer drugs. The product acts as a critical building block in the preparation of advanced heterocyclic intermediates required for targeted therapies. Reactors introduce this compound in the early synthetic stages, where its stability and selectivity influence yield and impurity profiles. Process development teams optimize reaction ratios based on route-specific conversion efficiency, considering scaling and purification parameters to comply with regulatory filings.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF Monographs (where applicable for intermediates)
    • EU EudraLex Vol. 4 Part II (GMP for Intermediates)
    • FDA DMF (Drug Master File) referencing

    Typical usage ratio

    • Applied at 0.95 – 1.15 molar equivalents relative to primary amine or coupling partner; adjusted for route selectivity and impurity control.

    Downstream process integration

    • Charged as a starting material during initial condensation or coupling stages in continuous or batch reactors.
    • Undergoes bromide displacement, esterification, or amidation transformations during intermediate steps.
    • Removal of excess by crystallization or liquid-liquid extraction before pre-final purification.

    Final product types

    • Nonsteroidal anti-inflammatory drug intermediates
    • Advanced precursor in anti-tumor agents
    • Substituted benzoic acid-based pharmaceutical APIs
    • Chemical building blocks for patented small molecules

    2. Custom Synthesis of Agrochemical Intermediates

    Crop protection and agricultural chemical manufacturers require this material for the synthesis of herbicide and pesticide intermediates, especially where brominated aromatic precursors are essential. Process engineers design routes that use this compound’s high reactivity for selective protection or substitution steps. Its role ensures high product fidelity during downstream transformations under strictly monitored batch or continuous production, and adjustments in process parameters reflect seasonal and regional regulatory demand.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Material
    • ISO 9001:2015 Quality Management Systems
    • National agrochemical registration guidelines (EPA, REACH registration, China ICAMA)
    • GLP (Good Laboratory Practice guidelines for R&D)

    Typical usage ratio

    • 0.8 – 1.2 equivalents per downstream coupling partner; adapted per impurity profile and catalyst presence.

    Downstream process integration

    • Fed as an initial core aromatic in heterocycle synthesis or protective group addition.
    • Direct bromide substitution or methoxy-directed cross-coupling in closed-system reactors.
    • Residuals managed via aqueous workup based on environmental emission limits.

    Final product types

    • Herbicide intermediates for rice or wheat protection agents
    • Pesticide active intermediate compounds
    • Growth-regulator synthesis precursors
    • Auxiliary agents in select biopesticide manufacturing

    3. Polymer Additive and Specialty Monomer Manufacturing

    High-performance polymer and specialty resin producers turn to this material for use as a fine chemical monomer precursor, particularly in specialty polyesters and advanced materials where both bromine and methoxy functionalities contribute to flame retardancy and tailored electronic properties. Its precise integration ensures consistent molecular weight distribution, with reactivity monitored to control branching and end-group effects important for final end-use requirements in plastics and films.

    Industry compliance standards

    • ISO 14001 Environmental Management System
    • RoHS Directive (2011/65/EU) for electronic and flame retardant components
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ASTM D4066 for plastic resin composition

    Typical usage ratio

    • 1–5% wt/wt as a co-monomer or additive in resin polymerization batches; varies with desired retardancy and resin properties.

    Downstream process integration

    • Introduced as a fine chemical intermediate before melt polymerization or copolymerization steps.
    • Pre-treated via deprotection or functional group activation prior to main chain growth.
    • Excess monitored and recycled or destroyed to avoid property inconsistencies.

    Final product types

    • Flame-retardant polyester pellets
    • High-heat resistance plastic films
    • Engineered resin components for electronics
    • Functional copolymer additives

    4. Fine Chemical Synthesis for Dye and Pigment Manufacturing

    Producers in the dyes and specialty pigment industry use this compound in designer aromatic coupling routes for azo and anthraquinone dye chemistry. The bromine and methoxy groups serve as activation or protection platforms, enabling tailored lightfastness and shade properties. Quality control ensures that raw material purity and stoichiometry directly influence color consistency and batch yield, particularly for demanding textile and plastics applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 safety for textile chemicals
    • ISO 9001 Certification for pigment and dye manufacturing
    • REACH compliance for dye substances in the EU
    • ZDHC MRSL for restricted substances in coloration agents

    Typical usage ratio

    • Used at 0.7 – 1.0 equivalents relative to primary dye intermediate; optimized for depth and purity of color in finished lots.

    Downstream process integration

    • Combined with aromatic amines or acids during diazotization/coupling steps in batch reactors.
    • Functional group transformations conducted under controlled temperature and pH to direct chromophore structure.
    • Byproduct separation managed in line with effluent control standards for colorant manufacturing.

    Final product types

    • Azo dye intermediates for textile printing
    • Anthraquinone pigments for engineering plastics
    • High-purity organic photoinitiators
    • Specialty colorants for automotive coatings
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    More Introduction

    2-Bromo-4-Methoxy-Benzoic Acid: More Than Just a Chemical Name

    Unlocking the Story Behind 2-Bromo-4-Methoxy-Benzoic Acid

    Anyone working in research or fine chemicals gets familiar with names like 2-Bromo-4-Methoxy-Benzoic Acid pretty early on. It rolls off the tongue in a way that says, “I belong in a complex lab,” but in reality, this compound does not just hide behind its name. For researchers, chemists, and process engineers, it brings value at every stage, from method development to industrial scale reactions. Years spent in various academic and industry labs have shown me that the journey from small vial to kilogram supply often shapes decisions as much as raw specs.

    Let’s start with what makes 2-Bromo-4-Methoxy-Benzoic Acid different. This compound is an aromatic carboxylic acid, set apart by its dual functional groups: a bromo attached to the second carbon of the benzene ring, and a methoxy on the fourth. Each group sets the stage for a unique chemistry performance. The bromo atom turns the compound into a natural fit for cross-coupling reactions, taking part in Suzuki, Heck, or Sonogashira type transformations that build more complex structures. The methoxy group has an electron-donating effect, slightly changing the property of the molecule and tuning reaction outcomes. That opens up doors in medicinal chemistry where such tweaks often spell the difference between lead optimization and an unworkable path.

    Getting Down to the Details: Model, Specs, and Where It Fits

    In most labs, we look for crystal-clear purity. For 2-Bromo-4-Methoxy-Benzoic Acid, the modern standard is over 98% purity, with a molecular formula of C8H7BrO3 and a molecular weight of roughly 231.05 g/mol. You can spot it as a white to off-white powder, and it tends to melt between 172–176°C, which puts it in a comfortable range for handling without thermal worries. Analytical verification usually relies on NMR, IR, and HPLC. Anyone with a solid benchtop spectrometer can confirm its identity by checking the distinctive aromatic peaks and the carboxyl stretch. I remember one batch years ago that failed quality control because its bromination step was off, and we found out fast how crucial analytical rigor is for this kind of intermediate.

    Labs often order 2-Bromo-4-Methoxy-Benzoic Acid at the gram scale for method scouting, but pilot plant teams think in kilograms for downstream building block integration. What’s striking is the way supply and finishing purity become just as important as yield or cost. Academic researchers care about trace metals, industrial chemists focus on streamlined purification protocols, and both scan for unwanted isomers. I’ve seen projects derail because a trace contaminant slipped through, ruining an expensive follow-up step. That awareness usually leads to more care in sourcing and documentation, even if it means a longer procurement process.

    Why Bromo and Methoxy Make a Difference

    Not every benzoic acid brings the same punch to an organic transformation. The bromo group on the ortho position is not just decorative; it allows for nucleophilic aromatic substitution or cross-coupling chemistry. Medicinal chemists know this feature well because it allows them to tack on fragments and test new analogs without reworking an entire synthesis plan. Take the rush to synthesize kinase inhibitors or calcineurin pathway probes. Adding the right bromo-benzoic acid shortens synthetic steps, which in projects with tight deadlines or expensive reagents, spells a break-even between publishing a paper and missing a conference entirely.

    For the methoxy group, its electron-donating nature helps steer reactivity. Synthesis teams working on more complex molecules find these attributes make for cleaner reactions, leading to less tar formation and fewer side products. I’ve watched teams debate between a methoxy and a methyl group for hours, knowing how even small changes alter not just yield but downstream purification requirements.

    Where It Shines: Applications Across Fields

    In pharma, the discussion around benzoic acids often leads straight to their role in forming core scaffolds. 2-Bromo-4-Methoxy-Benzoic Acid helped a colleague as the linchpin in a Suzuki coupling, connecting aryl boronic acids to create lead compounds in anti-inflammatory research. Outside of medicinal chemistry, material scientists look for ways to add functionality to polymers, and 2-Bromo-4-Methoxy-Benzoic Acid finds a place here too. Its halide and methoxy group bring reactivity needed for grafting onto backbone polymers, improving conductivity or light absorption in emerging materials.

    Qualitative stories make the message stick. During my stint in an early biotech startup, we tried half a dozen benzoic acid derivatives before landing on 2-Bromo-4-Methoxy-Benzoic Acid. The difference came down to predictable reactivity. Competing compounds without both the right halogen and oxygen substituents required extra steps – protecting groups, longer reaction times, repeated purification – all burning through our modest funding fast.

    Differences from Similar Compounds: Why the Details Matter

    Compound substitution sounds simple. Swap out a methoxy for an ethoxy or move the bromo around the ring, and the downstream effects ripple across synthesis and biological testing. Take 4-bromo-2-methoxy-benzoic acid as an example—the rearranged positions mean a very different electronic environment, changing the reactivity profile in Pd-catalyzed coupling reactions. In another case, a plain 2-bromo-benzoic acid might show less solubility and less selectivity, affecting both batch yield and consistency. The stories add up in the lab: solvents that once worked need rethinking, yields slip, and impurities spike.

    I’ve watched teams regret cutting corners here. A team aiming to scale production switched to a cheaper mono-substituted benzoic acid, only to run into persistent solubility issues in the final API (active pharmaceutical ingredient) step. The cost savings evaporated in redoing failed batches, and after three months of headaches, they circled back to the more expensive, better-spec’d 2-Bromo-4-Methoxy-Benzoic Acid. These practical lessons remind us that choosing intermediates isn’t just about what “should” work; it’s about what removes variables and increases reliability.

    The Importance of Reliable Characterization and Sourcing

    For those new to chemical sourcing, the buying process can seem straightforward: check the catalogue, select the right purity, hit order. Seasoned researchers watch for red flags—ambiguous batch history, gaps in spectral data, inconsistent melting points. It only takes one off-spec order to understand what’s at stake. Once, in a CRO lab, we received a batch with yellowing and irregular melting behavior. Further analysis found oxidative damage, likely from improper storage during shipping. The consequences ranged from a week of extra labor to delayed project milestones and strained customer relationships.

    Trusted suppliers often work closely with clients, providing detailed certificates of analysis with NMR, LC-MS, and HPLC traces. For regulated markets like pharmaceuticals, the extra steps in auditing suppliers and confirming proper documentation bring peace of mind. A thorough lab manager keeps backup suppliers but rarely compromises on documentation. Traceability, batch-to-batch consistency, and the ability to pinpoint the root cause in case of anomalies matter more with each uptick in production scale.

    Responsibility in Handling and Safety

    Anyone using 2-Bromo-4-Methoxy-Benzoic Acid has a duty to respect its safety profile. The bromo group can bring moderate risks, requiring proper gloves and, often, work in fume hoods. Overexposure can risk irritation or worse—something any experienced hand learns early, either by training or through those minor mishaps that burn a lesson into memory. Labs keep their safety data sheets nearby and ensure spill kits are on hand when handling larger volumes.

    Disposal considers both halogen content and carboxylic acid degradation products. Environmental safety means working with accredited waste services and logging each transfer—a routine I saw fastidiously followed in regulated labs but sometimes overlooked in busier, underfunded university settings. Attention here helps institutions avoid fines, protects workers, and staves off hazardous exposure.

    Where Problems Show Up: Scale-Up and Synthesis Pitfalls

    Lab synthesis of gram-scale 2-Bromo-4-Methoxy-Benzoic Acid often runs smoothly, using time-tested bromination and methoxylation steps on appropriate aromatic platforms. In scale-up settings, new issues crop up: batch uniformity, reaction exotherms, and purification at larger volumes challenge even skilled teams. My experience tells me that solvent selection at kilogram scale changes everything; what worked for a 100 mg prep might turn into a bottleneck or trigger unanticipated crystal fouling in a reactor. Companies often allocate resources for robust process development, adding calorimetry or real-time analytics to spot trouble before full-scale production.

    Problems vary by context. In some labs, air-sensitive raw materials complicate logistics and storage. In others, a surprise drop in yield points to undetected trace impurities lurking from upstream intermediates. I remember chasing down a persistent side product that only became apparent in pilot batches—a lesson in how crucial analytical depth is beyond basic purity checks.

    The Impact on Research and Product Development

    2-Bromo-4-Methoxy-Benzoic Acid quietly powers breakthroughs across chemistry, from crafting next-generation pharmaceuticals to fine-tuning new organic materials. By serving as a reliable link between early discovery and finished products, its consistency saves time and sharpens focus. On the research bench, time saved by not reworking failed reactions adds up; weeks regained can mean faster publications or a crucial funding renewal.

    For product development teams, predictability reduces risk. Pharmaceutical research has no patience for one-off anomalies or unpredictable batch results. The molecular toolkit grows strategically, where each new building block like 2-Bromo-4-Methoxy-Benzoic Acid extends the reach of medicinal chemists or material scientists. For those building light-absorbing polymers, adding a methoxy- and bromo-functionalized benzoic acid brings both modularity and flexibility, thanks to the compound’s ease of derivatization.

    Quality, Documentation, and the Path to Regulatory Approval

    For products destined for the clinic, regulatory expectations shape every step. Documentation covers origin, purity, impurity profile, and trace element analysis. Investment in reliable analytical methods pays off: agencies require full method validation, not just a quick HPLC run. Suppliers supporting this market often offer full traceability, impurity reference standards, and multi-step verification.

    I’ve sat through more meetings than I can count where a regulatory reviewer requested spectral overlays to verify that building blocks like 2-Bromo-4-Methoxy-Benzoic Acid met specification in every batch. The time spent upfront to secure high-integrity documentation saves headaches years later, especially for projects advancing towards IND filings or medical device submissions. A mistake at this stage could set a project back months or even cancel it outright—a risk few can afford.

    Navigating the Marketplace: Price, Availability, and Authenticity

    With the global demand for specialized reagents rising, price swings and supply chain vulnerabilities challenge even the best-laid plans. COVID-19 taught the industry tough lessons about just-in-time procurement and the importance of supply chain diversity. 2-Bromo-4-Methoxy-Benzoic Acid, while not the rarest chemical, has seen spikes when raw material shortages or transport bottlenecks hit. Researchers often budget for backup suppliers instead of chasing the cheapest price.

    Authenticity checks matter more than ever. The rise of grey-market chemicals poses real risks, especially where regulatory compliance and product liability come into play. Experienced lab managers ask for batch-level analytical verification and track supplier track records over time, trusting established relationships over unknown sources, no matter the savings.

    Environmental and Sustainability Factors

    Modern laboratories and companies recognize their impact on the environment. The synthesis of 2-Bromo-4-Methoxy-Benzoic Acid generates byproducts and wastes that need responsible handling. As industry seeks greener pathways, research teams look for less toxic solvents, lower-waste reactions, and better ways to reclaim or recycle spent chemicals. My own experience at a contract manufacturing organization showed that process optimization not only saves money but also reduces the environmental footprint—a strong selling point for eco-conscious clients.

    Some teams experiment with alternative catalysts or renewable feedstocks in place of petrochemical sources. While these experiments often add costs or complexity, the reputational gain—and the gradual tightening of environmental regulations—pushes the effort forward. For companies in competitive markets, a greener or more sustainable process can serve as a market differentiator.

    Challenges in Global Transport and Regulations

    Shipping chemicals across borders introduces complications that only multiply with scale. 2-Bromo-4-Methoxy-Benzoic Acid requires careful documentation to move easily through customs, especially as global regulators watch for dual-use materials. Regulations shift often, putting additional pressure on suppliers to maintain clear, complete paperwork. Delays caused by missing or unclear material safety data sheets mean project slowdowns or even cancelled shipments.

    Reliable transport partners and customs brokers offer peace of mind—saving days or weeks of back-and-forth by preemptively covering regulatory bases. For time-sensitive pharmaceutical projects, these logistics matter as much as the underlying science.

    Paths Forward: Improving Access and Reliability

    Better access to quality 2-Bromo-4-Methoxy-Benzoic Acid starts with transparent relationships between suppliers and researchers. Comprehensive, real-world data on performance and impurities brings trust. For buyers, clear technical communication and direct questions about specifications often reveal more than a generic product sheet can. In my experience, open feedback loops turn into tighter quality cycles—a win for both customers and producers.

    Discovery-stage chemists look for affordable milligram samples, but process teams want five-nines reliability on multi-kilogram orders. The challenge is matching responsive service at every stage, staying flexible without sacrificing standards. Online marketplaces help, but seasoned researchers know the value of picking up the phone to resolve ambiguities before a project hits a wall.

    Conclusion Is Not Furnished, Only Continuous Growth

    Looking at 2-Bromo-4-Methoxy-Benzoic Acid, the heart of the matter rests not just in its chemical structure but in the network of people, systems, and methods that bring it from a catalog entry to a pivotal role in research and production. The careful interplay of technical detail, real-world experience, and high standards shapes every decision, lesson, and breakthrough. The path from the first spark of an idea to proved synthesis to a finished product is where value grows, challenge by challenge, batch by batch, all the way from bench to factory floor.