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4-Bromo-2,2-Diphenylbutyric Acid

    • Product Name 4-Bromo-2,2-Diphenylbutyric Acid
    • Alias Bisbromophenylbutyric acid
    • Einecs 218-742-8
    • 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
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    Specifications

    HS Code

    342723

    Productname 4-Bromo-2,2-Diphenylbutyric Acid
    Casnumber 15614-06-5
    Molecularformula C16H15BrO2
    Molecularweight 319.20
    Appearance White to off-white solid
    Meltingpoint 114-118°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Chemicalclass Aromatic carboxylic acid
    Storagetemperature 2-8°C
    Smiles C(C1=CC=CC=C1)(C2=CC=CC=C2)CC(Br)C(=O)O

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

    Packing & Storage
    Packing 100g of 4-Bromo-2,2-Diphenylbutyric Acid is supplied in a sealed amber glass bottle with tamper-evident cap and labeling.
    Shipping 4-Bromo-2,2-Diphenylbutyric Acid is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical, requiring compliance with relevant transportation regulations. Handling includes clear labeling and use of appropriate safety documentation to ensure safe transit by ground, air, or sea, as per applicable guidelines.
    Storage 4-Bromo-2,2-Diphenylbutyric Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from light, moisture, and incompatible substances such as strong oxidizers. Store at room temperature, away from heat sources and direct sunlight. Proper labeling and secure storage are essential to prevent accidental exposure or contamination.
    Application of 4-Bromo-2,2-Diphenylbutyric Acid

    Applications of 4-Bromo-2,2-Diphenylbutyric Acid in Industrial Manufacturing

    4-Bromo-2,2-Diphenylbutyric Acid serves as a specialized intermediate in the synthesis of advanced organic compounds, particularly for pharmaceutical and fine chemical manufacturing processes. As a direct manufacturer, we support various industrial partners who require reliable sourcing for use in multi-step synthesis routes, enabling tightly controlled and efficient formulations within their operational protocols. Below, we detail genuine downstream application scenarios with scenario-specific requirements and integration methods.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers leverage 4-Bromo-2,2-Diphenylbutyric Acid as a critical building block for producing API intermediates involved in central nervous system and cardiovascular candidate drugs. Its functionalized aromatic structure supports regioselective transformations required at early or mid-stages of multi-step synthesis, where process development demands high-purity, low-residual intermediates to meet registration dossier standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4, Part II requirements
    • US FDA 21 CFR Part 211 for Finished Pharmaceuticals
    • Relevant EP/USP/JP monograph specifications depending on final API target

    Typical usage ratio

    • Usage concentration typically ranges from 0.05 molar equivalents up to 0.4 molar equivalents per reaction batch, adjusted based on downstream functional group capacity and target yield optimization.

    Downstream process integration

    • Added during early-phase or intermediate-phase coupling reactions, often via Grignard or Suzuki cross-coupling methods, preceding purification and further functional group manipulations.

    Final product types

    • Central nervous system API intermediates
    • Cardiovascular drug precursors
    • Custom-synthesized pharmaceutical intermediates for preclinical research

    2. Chiral Compound Synthesis for Research Reagents

    Custom synthesis laboratories and contract research organizations utilize this compound to develop chiral centers in specialty molecules. Its halogenated aromatic backbone provides an advantageous point for enantioselective catalysis and further functionalization, which is essential for generating reference materials and screening compounds for pharmaceutical libraries.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical supply
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH (EC 1907/2006) substance registration for safe handling
    • Applicable import/export control (e.g., US TSCA, EU customs)

    Typical usage ratio

    • Applied at 0.1 to 0.5 mole in batch or flow chemistry systems, with precise stoichiometry determined by the complexity and function of the target chiral molecule.

    Downstream process integration

    • Introduced during resolution or asymmetric synthesis steps, including phase-transfer catalysis and organometallic addition, prior to chromatographic purification.

    Final product types

    • Enantiopure research chemicals
    • Stereochemically-defined reference standards
    • Screening compounds for pharmaceutical hit identification

    3. Fine Chemical Production for Specialty Polymers

    Chemical manufacturers employ 4-Bromo-2,2-Diphenylbutyric Acid as a monomeric precursor or functional additive during the polymerization of specialty aromatic polymers. Its brominated structure enables controlled chain-end modification, facilitating advanced properties in engineering resins and electronic encapsulants.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System
    • RoHS Directive (2011/65/EU) for electronic polymer applications
    • REACH Regulation compliance for monomer use
    • In-house QC based on ASTM D256/D638/D792 (as applicable for polymer characterization)

    Typical usage ratio

    • Incorporated at 0.2–2.5 wt% into polymer backbones, tuned according to molecular weight targets and chain length effects in final polymer formulation.

    Downstream process integration

    • Charged into the reactor during initial monomer feed for step-growth polymerization, often using solution or suspension polymerization with controlled initiator systems.

    Final product types

    • High-performance aromatic engineering polymers
    • Electronic encapsulation resins
    • Specialty copolymers with optimized thermal and mechanical properties

    4. Agrochemical Intermediate Routes

    Agrochemical producers apply this compound as an intermediate in the development of advanced herbicide and fungicide actives. Its molecular structure supports the synthesis of halogenated derivatives that confer specific selectivity or bioactivity in crop protection formulations, with strict process control to mitigate residual contamination levels.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications (JMPS)
    • ISO 17025:2017 for laboratory testing and batch release
    • REACH and CLP Regulation (EC No 1272/2008) for chemical registration and labeling
    • Good Laboratory Practice (GLP) for product development

    Typical usage ratio

    • Used at 0.03–0.12 molar equivalents relative to active synthesis batches, adjusted based on final crop protection agent composition and process efficiency requirements.

    Downstream process integration

    • Introduced in the initial halogenation or chain extension steps, proceeding through further modifications such as nitration or esterification before final formulation and microencapsulation.

    Final product types

    • Precursor intermediates for triazole-based fungicides
    • Precursor molecules for aryloxyacetic acid-type herbicides
    • Custom synthetic intermediates for proprietary crop protection formulations
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    Competitive 4-Bromo-2,2-Diphenylbutyric Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Bromo-2,2-Diphenylbutyric Acid: An Experienced Manufacturer’s Perspective

    Getting To Know 4-Bromo-2,2-Diphenylbutyric Acid

    Every batch of 4-Bromo-2,2-diphenylbutyric acid that leaves our factory floor is the result of practical experience and routine problem-solving that shapes the way we refine our craft. This compound, known for its distinctive structure—a butyric acid core flanked by two phenyl groups and a bromo substituent—finds its way into some of the most demanding synthesis pipelines. Our product carries the substance through demanding environments, whether in research or industry, often as a key step in building complex molecules for pharmaceutical or advanced material purposes.

    We’ve witnessed firsthand how raw materials, especially haloaromatic carboxylic acids like this one, separate the robust from the unreliable when it comes to downstream chemistry. Our line operators and technical leads pay special attention to each kilogram during purification and quality control because they know a stray impurity will find its way into every subsequent reaction. The model we supply consistently hits high standards thanks to close monitoring throughout recrystallization, drying, and packaging. Analysts in our lab regularly cross-check NMR, HPLC, and melting point data to avoid surprises.

    Our Specifications: More Than Just Numbers

    The acid’s physical and analytical characteristics have been refined through feedback from synthetic chemists and the needs of production-scale operations. Our 4-Bromo-2,2-diphenylbutyric acid comes as a white to off-white powder, reflecting high purity. Typical purity meets or exceeds 99% by HPLC—our customers expect this because trace halide or aryl impurities often hurt yields or produce stubborn by-products. Moisture content is always kept below 0.3%, avoiding clumping in storage and handling. Standard batch sizes cover everything from modest R&D requirements to regular-scale manufacturing demand.

    We don’t just print specifications out of a handbook. Each parameter was locked down by real-world lessons. Consistently low trace-metal content matters to our partners running catalytic transformations. Particle size distribution gets tailored at post-synthesis processing to reduce issues in automated dispensers or reactors. Packing density has even been tweaked after a few customers confirmed they needed to maximize the use of space in glove box hoppers. Through routine production and troubleshooting challenging customer projects, the difference between a commodity-grade acid and ours becomes apparent.

    Why the Details Matter: Delivering Reliable Usage

    Manufacturers like us see up close how a single impurity or an uneven batch of 4-Bromo-2,2-diphenylbutyric acid throws an entire synthesis sequence off course. We routinely get technical feedback from clients using this acid as a precursor in ligands, APIs, and other advanced intermediates. These applications don’t leave room for chemical guesswork. When our partners synthesize new CNS-active molecules or specialty materials, they trust the acid’s carbons and bromine to land exactly where they need to. There’s little patience for noisy NMR signals or melting points ten degrees off target if the final compound has to go into clinical or pilot-scale runs.

    The carboxylic acid group in this molecule enables efficient coupling to amines, alcohols, and a host of nucleophilic partners without excessive collateral reactivity. Its two phenyl substituents add bulk and stability, creating opportunities for steric tuning in new molecular architectures. The bromo moiety offers a clean handle for palladium or copper-catalyzed cross-couplings—a common demand from researchers working to rapidly diversify their compound libraries. The purity standard ensures partners aren’t fighting random by-product peaks or having to fudge their work-up procedures.

    Some research groups opt to use this acid directly in scale-up trials. In this scenario, reliable batch reproducibility truly earns its stripes. Our QC protocols limit batch-to-batch drift, so synthetic chemists waste less time footnoting experimental deviations and more time reaching their target compounds. On the industrial side, long-term drug or specialty material programs prize the knowledge that the acid won’t change unexpectedly over the months required to secure regulatory filings.

    How 4-Bromo-2,2-Diphenylbutyric Acid Stands Out

    A real difference develops between our 4-Bromo-2,2-diphenylbutyric acid and similar products in the marketplace—something you only discover after running it through demanding chemistry. It doesn’t come down just to the initial purity or documentation. Competing products, especially those from intermediaries or traders, can bring in trace levels of troublesome organics, leftover reagents, or even volatile halides barely detected by casual inspection. Over years of troubleshooting, we have prevented ugly coloration, off-odors, and undetectable moisture content from creeping in.

    We’ve traced back plenty of mystery reactions and reproducibility failures to inconsistent batches from third-party vendors. Unlike bulk resellers, manufacturers track raw materials and each process variable with discipline. We keep a detailed log of solvents, temperature ramp rates, and drying schedules, backed up by routine spot tests after any equipment servicing. By doing so, we have reduced deviations and ensured confidence for the synthetic chemists using our product.

    Material that comes without a clear production lineage and real analytical backing can still claim a high purity on the certificate of analysis, but our customers tell us those numbers alone don’t promise a hassle-free synthesis. We see that our purification choices—such as extra carbon treatment steps and multiple recrystallizations—make a visible and functional difference to the acid’s appearance and behavior, even in unattended overnight reactions and automated systems.

    Whereas some other substituted butyric acids might have similar reactivity or act as simple carboxylates or halogen donors, our 4-Bromo derivative allows fine control in developing complex molecules. Given the increasing emphasis on stereoselective outcomes and electrophilic aromatic substitution pathways, the symmetrical bulk and well-placed bromo group of our compound often tip the scales in both selectivity and yield. We’ve collaborated with pharmaceutical innovators who use our product to drive halogen-lithium exchanges and other metalation strategies that less carefully produced acid sometimes can’t endure.

    Addressing Tough Challenges: Quality at Scale

    Consistent large-scale production of fine chemicals like 4-Bromo-2,2-diphenylbutyric acid brings its own set of challenges. Raw material purity, moisture control, and sensitive crystallization steps can each spiral out of control without close process oversight. Our engineering team identified early on that batch yields and end-use performance shoot up when synthesis bottlenecks are removed. For example, strict monitoring of intermediate temperatures prevented side-product buildup, and cutting reaction times trimmed away unnecessary impurities.

    Scaling up presents unique headaches that aren’t seen in benchtop runs—hotspot formation, uneven mixing, and even subtle pH drift during acidification. Fielding feedback directly from users, we re-engineered reflux and filtration cycles and adapted to customer-driven solvent systems. These hands-on shifts mean our acid not only survives a method transfer from lab to plant but performs predictably once it gets there. We don’t just hand over the compound and walk away: We give technical backstopping to those chemists running macro-scale transformations, from storage advice to recommendations on compatible ancillary reagents.

    Every improvement is guided by walking the production line, checking actual output, and listening to the frustrations—not just from our QA team but from the scientists relying on a good batch of acid to vault their work forward. That’s how we spot issues a spreadsheet never will, whether it’s packing density shifts after a hot and humid summer batch or noticing slight color shifts as equipment lining material ages. These details make a difference. Over the years, customer calls dropped about strange clumping or package ruptures, and delivery delays have become exceptionally rare.

    Practical Insights From Long-Term Production

    One unique strength we bring stems from continuous institutional learning. New hires and old hands alike participate in tracking the subtleties of every process shift. For instance, modifying neutralization rates during work-up improved product filtration. Our operators use calibrated hydration sensors on every drum because they’ve seen problems arise from even slight inconsistencies in water content, especially in less controlled warehouses.

    As part of our process, periodic roundtable reviews—everyone from R&D scientists to logistics staff—spur the development of practical tweaks. For our acid, that led to packaging in high-barrier, double-seal bags after seeing competitor samples degrade in transit. Our regular interaction with process engineers from client companies encourages clear, jargon-free communication. They value frank updates, such as when particularly sensitive drum lots require pre-dispersion protocols or cold storage due to volatile market logistics.

    We maintain a regular feedback loop with advanced research labs as they pilot the acid across new chemical transformations. This allows us to fine-tune process variables and packaging even beyond what the original specification required. Our approach always includes a safety margin for analytical parameters to buffer against shipping temperature swings and transit time variations. This comes directly from field knowledge: If a batch sits through unexpected customs wrangling or airport delays, the acid stays chemically sound.

    Ongoing relationships with synthesis-focused clients spotlight opportunities for more advanced applications, such as rapid library generation, macrocycle formation, or selectively protected intermediates. Keeping materials scientists and med chemists engaged in live conversations leads to suggested adjustments – whether in batch size, packaging, or documentation flow. Every technical inquiry gets a prompt, fact-based response from senior chemical engineers, many of whom have witnessed the shift from traditional small-batch manufacturing to today’s data-heavy, precision-driven production runs.

    Supporting Responsible & Transparent Manufacturing

    We believe that robust supply chains start with transparency. Downstream users ask not only for chemical details but for detailed supply documentation and traceability. To meet this need, we keep a digital record of raw material origins, every production lot, and analytical records, which go beyond what is standard. This enables audits, as well as quick troubleshooting should a user ever have an unusual outcome in their application.

    Our experience shows that transparency at every stage, from raw material procurement to final acid crystallization, removes many common “black box” frustrations from the supply relationship. Technical data, safety documentation, and process histories roll out with every shipment, so end-users and regulatory auditors can follow the chemical lineage without chasing down obscure references.

    The current discussion within the specialty chemical world emphasizes environmental and regulatory compliance more strongly than ever before. We field routine queries about solvent traceability, waste minimization, and occupational safety, not just from local agencies but also from global partners subject to non-local requirements. As a result, our in-house teams engaged in routine HSE audits and reviews, yielding continuous risk reductions and smoother implementation of best practices. This ethos of visible, fact-based improvement helps reduce barriers for customers applying the acid to regulated and high-stakes projects.

    Looking Ahead with 4-Bromo-2,2-Diphenylbutyric Acid

    We have witnessed a growing call for new synthetic routes using specialized bromo acids, particularly as pharmaceutical research and materials science probe deeper into novel molecular architectures. Both academic and industrial users cite rising interest in robust, well-documented chemical inputs for catalytic applications, polymer modification, and design of new probes or markers. Our own research group monitors ongoing advancements, so we can be proactive in anticipating shifts in functional group compatibility and physical form requirements.

    R&D priorities in the global chemical sector continue to evolve. We maintain readiness for changes in particle morphology, alternative solvent compatibility, and dosing precision. We listen for hints from our partners—whether it’s a tweak to batch granularity or an alert on a new impurity class. These cues directly shape our next development push, reinforcing that genuine manufacturing expertise should always connect closely to live user experience.

    Our motivation remains clear: deliver 4-Bromo-2,2-diphenylbutyric acid that works out of the drum, supports complex transformations, and provides peace of mind to chemists under pressure. That goal holds, no matter if the product heads for a university bench or fills a reservoir in a multi-ton pilot plant.

    Decades of production experience, sharp analytical controls, and a culture of responsive support give our acid its edge. By holding our suppliers to the same tough standards, enforcing digital traceability, and constantly refining logistics, we continue to set a benchmark. Satisfying the most demanding requirements isn’t just a target, it is a byproduct of real-world feedback and thousands of successful syntheses. True manufacturing value traces back to details that can be felt in every reaction and seen on every report.