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4-Bromo-3-Methylphenylacetic Acid

    • Product Name 4-Bromo-3-Methylphenylacetic Acid
    • Alias 4-Bromo-3-methylbenzeneacetic acid
    • Einecs 694-876-0
    • 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

    109786

    Productname 4-Bromo-3-Methylphenylacetic Acid
    Casnumber 90275-01-9
    Molecularformula C9H9BrO2
    Molecularweight 229.07
    Appearance White to off-white solid
    Meltingpoint 110-113°C
    Boilingpoint No data available
    Density No data available
    Purity Typically >98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=C(C=CC(=C1)Br)CC(=O)O
    Inchi InChI=1S/C9H9BrO2/c1-6-7(5-9(11)12)3-2-4-8(6)10/h2-4H,5H2,1H3,(H,11,12)
    Synonyms 2-(4-Bromo-3-methylphenyl)acetic acid
    Storageconditions Store at 2-8°C
    Hazardclass Irritant

    As an accredited 4-Bromo-3-Methylphenylacetic 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 4-Bromo-3-Methylphenylacetic Acid

    Applications of 4-Bromo-3-Methylphenylacetic Acid in Industrial Manufacturing

    4-Bromo-3-methylphenylacetic acid is an advanced intermediate widely adopted by pharmaceutical and fine chemical plants. Its structure enables specific transformations, making it crucial for synthesis routes across regulated sectors. Below, we detail practical, industry-specific downstream applications directly supported by our process and compliance expertise.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Manufacturers use this intermediate during the multistep synthesis of specialty APIs, especially within certain antihypertensive and central nervous system drug groups. The unique brominated aromatic structure enables selective coupling, crucial for consistency in API batch production. Our product consistently passes trace impurity analysis during scale-up and meets process checks such as residual solvent and halide monitoring. Close control over raw material quality supports seamless tech transfer and audit preparedness for global customers.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7) for regulated intermediates
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) monograph requirements
    • Chinese Pharmacopoeia (ChP) recommendations for process impurities

    Typical usage ratio

    • Use in 1:1 to 1:2 molar ratio with downstream coupling reagents
    • Ratio adjusts based on API final yield targets and side product minimization

    Downstream process integration

    • Charged at mid-stage of synthesis, after pre-functionalization or halide exchange step
    • Feeds into condensation or amidation reactions
    • In-process controls verify identity and residual halide content before further transformation

    Final product types

    • Small molecule antihypertensive drugs
    • Central nervous system pharmaceutical agents
    • Advanced pharmaceutical intermediates for further custom synthesis

    2. Agrochemical Intermediate for Herbicide Manufacturing

    Many herbicide compound producers integrate this brominated aromatic acid as a key intermediate during active ingredient development. Its use enables introduction of specific substituents that increase selectivity for target weeds, optimizing field efficacy and lowering phytotoxic side effects. Our technical supply supports residue analysis and trace element control throughout pilot to commercial scaling.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance systems
    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO pesticide specification limits for content and impurities
    • REACH Annex VII-VIII registration compliance for intermediate usage

    Typical usage ratio

    • Typically introduced at 0.8–1.2 equivalents per synthetic batch
    • Ratio depends on desired substitution pattern and downstream reactivity

    Downstream process integration

    • Added post-nitration for selective coupling or halogen exchange
    • Blended with alkylation reagents in monitored batch reactors
    • Impurity checks at each step for EC and FAO compliance

    Final product types

    • Selective post-emergence herbicides
    • Precursor intermediates for fungicides
    • Active compounds for crop protection formulations

    3. Advanced Dye Intermediate for Specialty Colorants

    The fine chemical sector leverages the acid as a coupling building block to produce high-performance azo and anthraquinone dyes. These processes demand high purity and consistent halogenation to achieve repeatable final dye quality. Our controlled crystallization and packaging prevent unwanted contamination in colorant production environments, as verified by batch consistency reports.

    Industry compliance standards

    • ISO 14001:2015 for environmental management
    • Zero Discharge of Hazardous Chemicals (ZDHC) requirements for textile processing
    • REACH SVHC regulations on aromatic amine content
    • OEKO-TEX® Standard 100 testing for residual contaminants

    Typical usage ratio

    • 0.5–1.3 molar equivalents relative to chromogenic partner
    • Adjusted based on desired dye chroma and end-use substrate

    Downstream process integration

    • Introduced during coupling step post-diazotization in continuous or batch reactors
    • Purity measured via HPLC before high-temperature dye formation
    • Residue testing for halogen and isomer content in every batch

    Final product types

    • High-brightness azo textile dyes
    • Specialty colorants for leather finishing
    • Anthraquinone derivatives for automotive coatings

    4. Research and Development: Custom Synthesis Platforms

    Chemical and pharmaceutical R&D teams use the acid as a starting point for synthesis libraries and candidate molecule design. Its reactivity profile supports rapid analog generation through halogen exchange or functional group modification, critical for SAR studies and initial screening. We provide detailed batch records, impurity profiles, and analytical data to support project filing and patent application documentation.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for regulated laboratory workflows
    • OECD Principles of Good Laboratory Practice
    • REACH Article 26 notification for R&D uses
    • Corporate quality protocols for traceability and record retention

    Typical usage ratio

    • Flexible, typically 0.5–2.0 molar equivalents per synthesis run
    • Optimized per target molecule structure and desired analog throughput

    Downstream process integration

    • Used either as initial building block or transformation target in multi-parallel reactions
    • Integrated into automated synthesis platforms
    • QC verified using GC-MS and LC-MS at each screening stage

    Final product types

    • Analogs for preclinical pharmacology
    • Patent-submittable scaffold molecules
    • Lead compounds for medicinal chemistry projects

    5. Fine Chemical Synthesis of Specialty Fragrance Intermediates

    The aromatic character of this compound allows fragrance chemical manufacturers to use it in the preparation of high-value musk or woody note intermediates. The bromine enables direct substitution, facilitating the introduction of functional groups critical to olfactory thresholds. Batch reproducibility and impurity profiles proved effective for major fragrance operations, meeting export batch clearance by major inspection authorities.

    Industry compliance standards

    • IFRA Standards for fragrance ingredient purity
    • ISO 22716:2007 (Cosmetic GMP) for fragrance chemical production
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • REACH registration for specific intermediate status

    Typical usage ratio

    • 1.0–1.2 equivalents per target intermediate batch
    • Adjusted for ring substitution reactivity and target note intensity

    Downstream process integration

    • Reacted with acylation agents following pre-purification
    • Subjected to specific hydrogenation or Grignard steps for note adjustment
    • Analytical release using GC/FID and NMR before downstream blending

    Final product types

    • Musk-type fragrance intermediates
    • Woody-note compounds for perfumery
    • Blending agents for high-end fine fragrances
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    Certification & Compliance
    More Introduction

    4-Bromo-3-Methylphenylacetic Acid: Real Value in Research and Industry

    An Experienced Look at a Trusted Chemical Workhorse

    Getting reliable performance out of specialty chemicals sometimes boils down to the small details. Take 4-Bromo-3-Methylphenylacetic Acid as an example. I remember walking into a university lab, seeing drums labeled with the chemical formula C9H9BrO2, and realizing how much time and resources ride on its consistency and proven character. With a purity above 98% and a deliberate focus on trace impurities, this compound has earned a place in the toolkit of pharmaceutical development and material synthesis. It’s more than just one more product among aromatic acids.

    Chemists often ask about physical properties before anything else. Here, you get a pale crystalline powder with a molecular weight of 229.08 g/mol and a melting point within 118-122°C, tight enough to trust for repeated workups and syntheses. It doesn’t cake under standard storage. Once, during a medicinal chemistry project, we relied on this predictability to avoid setbacks in high-throughput synthesis, where having to rerun a reaction means wasted days.

    Why This Compound? Practical Experience Speaks

    Talk to anyone who’s spent late nights scaling reactions from milligrams to hundreds of grams. Having 4-Bromo-3-Methylphenylacetic Acid with solid batch-to-batch consistency just makes a difference. Some aromatic acids tend to clump or pull in moisture, throwing off stoichiometry. This one stays manageable from scoop to flask. I’ve seen how that single difference at the bench translates directly to yield and project timelines. When a team leans on this chemical, they know what to expect, which brings real peace of mind.

    There’s also the functional group advantage. Drop a bromine atom onto the ring at the 4-position and you open up rich possibilities through cross-coupling. Tack a methyl group onto the 3-position and you get tweaks in the electron density of the aromatic system, translating to distinctive reactivity. I’ve found that Suzuki and Heck reactions run cleaner compared to other halogenated phenylacetic acids. That gives synthetic chemists an edge when building out complex molecules, whether it’s an intermediate for an active pharmaceutical ingredient or a novel material.

    When companies talk about their R&D pipelines, most of the attention flies to the shiniest, most exotic compounds. Lost in the noise, you’ll often spot foundational reagents like this one quietly keeping entire workflows on track. Even highly automated labs benefit once they realize this acid’s predictable performance cuts down trial-and-error, especially with scale-up batches.

    Where It Shows Up: Real-World Impact

    One of the most personally satisfying projects I've witnessed involved using 4-Bromo-3-Methylphenylacetic Acid as a precursor in the stepwise synthesis of a kinase inhibitor. The compound’s reactivity allowed the team to introduce specific groups to the molecule’s aromatic ring without extra purification steps. Replacing lower-purity alternatives that forced us through multiple chromatographies, this upgrade quite literally saved weeks off the drug discovery process.

    The utility isn’t just limited to pharmaceuticals. In material chemistry, it acts as a key intermediate in making organic dyes and optoelectronic polymers. During scale-ups for electronics prototypes, quick, clean coupling reactions allowed downstream steps to stay on schedule. Consistent physical properties meant no extra calibrations, allowing synthesis to transition from 10-gram trials to kilogram runs without adjusting protocols. That flexibility and dependability set it apart from other, less-refined analogues.

    While other phenylacetic acids may crowd the marketplace, offering generic performance, not every variant brings this same balance of reactivity and stability. Sometimes, buyers settle for the least expensive substitute, imagining they’re saving money, but the hidden costs creep into low yields, more impurities, and headaches with reproducibility. Based on my own repeated side-by-side trials, choosing the right compound quickly becomes a question of whether the immediate savings outweigh days lost from unexpected side reactions or sluggish reactivity.

    The Place of Purity in Specialty Synthesis

    Skeptics sometimes say, “A carboxylic acid is a carboxylic acid.” Anyone who’s spent enough time running NMRs or walking the line between product and by-product knows that isn’t the case. Here’s what separates 4-Bromo-3-Methylphenylacetic Acid: consistently sharp spectra, minimal byproducts, and no mystery peaks littering up the end-stage analysis. For a junior researcher, having that certainty means trusting your starting material isn’t the culprit if something odd shows up downstream. For an experienced chemist, it translates into more time spent solving problems that matter, not just cleaning up someone else’s mistake.

    Being able to trace every batch with spectral analysis offers another layer of guarantee. Solid manufacturers put their batch records front and center—so you never have to cross your fingers, wondering if the purity claim was generous. My years spent ordering from catalogues taught me to look beyond the datasheet and call support directly, digging for real answers about trace contaminants. With this compound, the pattern was clear: published purity claims matched reality in every delivery I checked.

    Those details matter in industrial environments, where a slip in quality can cascade into lost production time, wasted raw materials, or even delayed regulatory filings. I’ve seen cases where an off-spec batch forced a full plant shutdown for revalidation. By comparison, working with a well-characterized material like 4-Bromo-3-Methylphenylacetic Acid keeps projects on the rails, sparing entire teams from unplanned overtime and cost overruns.

    From Bench to Market: Defining Differences that Matter

    There’s a world of difference between mass-market intermediates and targeted research compounds. You’ll find the market flooded with alternative phenylacetic acids, brominated or otherwise, sometimes produced for bulk fragrance or flavor industries. In those cases, impurities take a back seat to price, and analytical data tends to be less robust. By contrast, suppliers focused on the research sector provide full Certificates of Analysis with every batch, often including HPLC, NMR, and GC-MS data. From my own ordering and testing, these elevated standards in 4-Bromo-3-Methylphenylacetic Acid narrow down the risk when the stakes rise.

    One overlooked strength here is the lower level of common byproducts like 3-bromo-4-methylphenylacetic acid or residual brominated solvents. Several times, I ran side-by-side comparisons for early-stage projects, watching how these contaminants threw off LC-MS readings or forced researchers into extra cleanup stages. Every avoided side reaction means a cleaner workflow and more convincing data, especially when regulatory filings or IP protection depend on cleaner synthetic routes.

    In custom synthesis work, being able to count on each step, starting with this compound, can mean the difference between a two-week sprint and a month of dead ends. Every process chemist knows there are enough curveballs already; starting from a dependable, well-documented source lessens risk. This reliability doesn’t just improve comfort in the lab—it often shapes whether a project even reaches pilot scale.

    Safe Handling, Practical Storage

    Everyone in the lab understands that the best results come with the right habits. 4-Bromo-3-Methylphenylacetic Acid comes packaged to resist moisture uptake and light degradation, making it easier to keep stable over time. In my labs, we store it in amber bottles, away from acid-sensitive reagents, with no elaborate precautions necessary beyond standard chemical storage. It holds up well under ambient conditions, so users don’t get nasty surprises after just a day or two out of refrigeration.

    The crystal form pours easily, so measuring out precise amounts stays straightforward for routine batch work. This can seem like a small convenience, but anyone who’s worked with sticky or granular reagents knows the difference. Wasting several minutes scraping a caked bottle or trying to reconstitute a partially hydrolyzed intermediate can get old fast in a tight workflow.

    Good suppliers print manufacturing and expiry dates, along with handling tips, directly on the label—or in digital batch records. This traceability helps everyone, from undergraduate researchers to industry process leads, keep tabs on chemical quality. There’s comfort in knowing exactly where a batch fits in its lifecycle, reducing the odds of expired or off-spec material slipping into an important reaction.

    Comparing Alternatives: Real Results, Not Just Paper

    I’ve sat at roundtables where colleagues debated switching to a lower-cost analogue, convinced the savings would stack up. After a few rounds of parallel syntheses, the intangible costs bled into every column—lower yields, murky TLC streaks, unexpected odor profiles, or quantifiable hits to purity. Across a whole R&D budget, those hidden setbacks dwarf the original price tag. With 4-Bromo-3-Methylphenylacetic Acid from a reputable source, I watched our workflow streamline—no reruns, no head-scratching over new mystery peaks, and no impromptu troubleshooting at midnight.

    Anyone familiar with green chemistry initiatives knows that cleaner reactions, which need fewer purifications and generate less waste, are better for the environment and bottom line. Using a purer starting material like this compound cuts down on volumes of solvents used during post-reaction workups. I kept records comparing side products after coupling reactions using different grades of the same compound. Every time, the better pedigree gave cleaner mass balances, translating directly into less waste to neutralize or dispose of.

    Some buyers still get seduced by low sticker prices, but every mistake in a development pipeline costs more than just the price of a bottle. Replace questionable material with well-characterized 4-Bromo-3-Methylphenylacetic Acid, and even skeptical engineers start to trust the numbers again. Clean processes make regulatory filings smoother and reduce the burden on quality control, letting teams focus on R&D rather than redoing routine batches gone wrong.

    Contribution to Safer, Smarter Workflows

    Safety teams appreciate a chemical with clear characterization and well-documented hazards. 4-Bromo-3-Methylphenylacetic Acid doesn’t bring exceptional toxicity risks beyond other aromatic acids. Full SDS documentation supports everyday lab protocols. Labs I’ve worked in often standardize on this compound for initial trials in new reaction schemes, since reliable, well-known performance trims the learning curve and limits the number of unknowns in hazard assessments.

    Its compatibility with standard glassware and disposables, along with routine ventilation, means no special equipment list. This becomes important in lean startup labs or education settings where resources stay tight. Clear, practical labeling and batch history anchor safety reviews, making it easier for all experience levels to stay prepared.

    Students and new chemists benefit from predictable results as much as industry veterans. Every unexpected side product is a teaching moment, but too many unpredictabilities can frustrate learning or derail a senior project’s timeline. Providing a foundation of trust in the starting materials, as this compound does, builds better chemists—people who can focus on mechanisms, optimization, or invention rather than playing detective with questionable reagents.

    Potential Pitfalls and Honest Discussion

    Of course, no product works miracles. Over the years, there have been rare batches affected by environmental shipping mishaps. Courier delays or poor storage before delivery can lead to slight discoloration or excess moisture. Still, experienced suppliers get ahead of these issues with tight QC and responsive customer support. Anyone buying at volume should call ahead, confirm shipping conditions, and open shipments right away—something I always recommend regardless of the compound.

    On occasion, synthetic chemists experimenting with new coupling catalysts notice subtle differences in reaction rates or selectivity compared to other bromo- or methyl-substituted acids. This is less a fault of the compound itself and more a function of nuanced reactivity, as the electron-donating methyl and withdrawing bromo groups tug and pull on the aromatic system. Most experienced synthetic teams know to run small pilots to tune protocols. Anyone expecting identical performance between this compound and, say, 4-bromo-phenylacetic acid, will have to adjust stoichiometry or reaction conditions.

    No standard exists without knowledgeable handling. Carelessness can always result in cross-contamination, hydrolysis, or unintended exposure. Prompt use of gloves, goggles, and appropriate lab attire remains a must, no matter how reliable the chemical in question.

    Moving Forward: Smarter Choices for Labs and Industry

    More institutions and companies now emphasize full traceability from raw materials to end products. As regulatory and environmental reporting becomes more stringent, transparent supply chains matter more than ever. The dependable history of 4-Bromo-3-Methylphenylacetic Acid—its clear audit trail, robust documentation, and long stretches of consistent performance—keeps projects inspection-ready and simplifies collaborative work across partnerships or contract research arrangements.

    Feedback from seasoned process chemists and R&D leaders strengthens the case for purposeful sourcing. Many teams are willing to pay a premium for a product with fewer out-of-spec surprises, not just out of convenience, but because it anchors project schedules and reduces headaches. This is especially true for small to mid-sized operations, where one failed batch can wipe out weeks of progress.

    Looking to the horizon, the future calls for even tighter specifications and better sustainability records in specialty chemicals. Suppliers with a solid track record for 4-Bromo-3-Methylphenylacetic Acid continue to invest in greener production practices, recycling solvents, optimizing reaction conditions, and packaging in recyclable materials. Having spent years charting both performance and environmental impact, I’ve watched the best results come from vendors that focus not just on sales but on honest answers and transparent reporting.

    In sum, 4-Bromo-3-Methylphenylacetic Acid has quietly become an anchor in research, innovation, and industrial workflows. Scientists and engineers looking for more than the lowest price find value in provable quality, batch history, and supplier accountability. Choosing this compound signals a commitment to trustworthy, reliable results—whether on the academic bench or the industrial scale-up floor.