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4-Bromophenylpropanol

    • Product Name 4-Bromophenylpropanol
    • Alias 4-(4-Bromophenyl)-1-propanol
    • Einecs 252-036-8
    • 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

    900192

    Chemicalname 4-Bromophenylpropanol
    Casnumber 1527-30-4
    Molecularformula C9H11BrO
    Molecularweight 215.09
    Appearance White to off-white solid
    Meltingpoint 53-56°C
    Boilingpoint 145-147°C at 7 mmHg
    Density 1.43 g/cm³
    Solubility Soluble in organic solvents, low solubility in water
    Purity Typically >98%

    As an accredited 4-Bromophenylpropanol 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-Bromophenylpropanol

    Applications of 4-Bromophenylpropanol in Industrial Manufacturing

    As a core manufacturer specializing in fine chemical intermediates, we supply 4-Bromophenylpropanol for precise applications across advanced industrial sectors. The following sections outline real deployment scenarios in downstream manufacturing, each defined by actual regulatory requirements, formulation guidance, production workflow, and real-world end product classes.

    1. Pharmaceutical Intermediate Synthesis for Beta-Blockers

    4-Bromophenylpropanol serves as a critical building block in pharmaceutical synthesis, particularly for selective beta-blocker APIs. Its high purity and defined reactivity enable precise coupling in the side-chain construction required by patented active moieties. During API manufacture, chemists incorporate this raw material into the controlled regioselective functionalization step, which determines both the safety and clinical performance profile of downstream agents. Markets sourcing this intermediate demand rigorous compliance from input qualification to batch traceability, as outlined by global agency frameworks.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF and Ph. Eur. documentation for API production inputs
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice)
    • EDQM CEP requirements for registered intermediates

    Typical usage ratio

    • 5–8% w/w relative to the targeted API batch yield; process chemists adjust this concentration based on target molecule and side-chain substitution pattern requirements.

    Downstream process integration

    • Introduced during the side-chain assembly phase as a coupling precursor for propanol-substituted aromatic rings, frequently in a halide-exchange or reduction-alkylation stage, under GMP-controlled conditions.

    Final product types

    • Finished beta-blocker tablets (e.g., bisoprolol, metoprolol derivatives)
    • Bulk API for finished dosage forms
    • Pharmaceutical export-grade intermediates

    2. Fine Agrochemical Intermediate for Selective Herbicide Synthesis

    In the agrochemical sector, this material supports the preparation of specialized phenylpropanoid-based herbicides. Agrochemical formulators use it in multi-step synthesis lines, tailoring aromatic ring substitution to create actives with targeted crop selectivity and environmental compliance. Downstream users require traceable input batches, with precisely measured charges that align with permitted residue and emission guidelines as directed by crop-protection authorities.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Quality Management Systems for input qualification
    • REACH registration for European ingredient supply

    Typical usage ratio

    • 3–6% w/w per active batch, tuned according to the required substitution efficiency and the specifications of the final agricultural formulation.

    Downstream process integration

    • Fed into the functionalization step of aromatic intermediates, forming part of the phenylpropanoid skeleton assembly. It is subjected to substitution or coupling reactions in controlled reactors under monitored temperature and inert atmosphere.

    Final product types

    • Selective herbicide actives with propanol substituents
    • Emulsifiable concentrates for field application
    • Technical-grade active ingredient for global agrochemical brands

    3. Fragrance Ingredient Precursor in Fine Aromatics Synthesis

    The fragrance and aroma chemical industry utilizes 4-Bromophenylpropanol as a precursor in the synthesis of high-value aromatic alcohols and aldehydes, especially for niche perfumery bases. This compound participates in chain extension and aromatic modification reactions, allowing for precise odor profile adjustment in finished bases. Feedstock tracking, allergen control, and compliance with market-specific olfactory purity requirements drive demand for analytically characterized input batches.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Updates
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9001:2015 for ingredient traceability and quality management
    • REACH compliance for fragrance intermediates in Europe

    Typical usage ratio

    • 1–4% w/w, depending on the volatility and final concentration of desired aromatic alcohols or aldehydes in the finished base.

    Downstream process integration

    • Enters the olfactive molecule assembly during aromatic core modification steps, typically via Grignard or reduction pathways to yield fragrance building blocks for subsequent esterification or acetalization.

    Final product types

    • Blended perfume bases for fine fragrance houses
    • Specialty aroma chemicals (aromatic alcohols, aldehydes)
    • Cosmetic and toiletry ingredient concentrates

    4. Intermediate for Imaging Chemical Synthesis (Color Developer Precursors)

    Photographic and imaging industries require carefully functionalized aromatic compounds as key precursors in developer and color-forming agent production. In these workflows, 4-Bromophenylpropanol is charged in the developer synthesis process for constructing high-purity, propanol-functionalized aromatic units, impacting both processing time and end product tonal quality. Strict analytical and impurity controls are imposed by end-users for compatibility with global imaging chemistry requirements.

    Industry compliance standards

    • ISO 18902:2020 (Imaging materials — Processed imaging materials — Photographic films and papers — Storage practices)
    • RoHS Directive 2011/65/EU for heavy metals in photo-related chemicals
    • REACH substance registration for the European market
    • Company SOPs for chemical batch traceability and purity

    Typical usage ratio

    • 2–5% w/w, adjusted based on the molar mass and structure of the color developer synthesis route chosen by the downstream manufacturer.

    Downstream process integration

    • Fed into the nucleophilic aromatic substitution or coupling steps that build key color developer fragments, with close QC oversight for residual heavy metals and organic impurities.

    Final product types

    • Color developer concentrates for photo processing
    • Ready-to-use and replenisher developer kits
    • Precursor chemicals for color photographic paper and film emulsions

    5. Advanced Polymer Additive Intermediate (Functionalized Monomers for Specialty Polymers)

    High-performance polymer manufacturers use this compound as an intermediate for synthesizing functional monomers incorporated into tailored resins and specialty copolymers. By leveraging specific brominated aromatic reactivity, polymer chemists produce modified propanol-derived units that impart desired polarity, flexibility, or reactivity to engineered polymers. Strict adherence to customer specifications and international standards regarding extractables, downstream handling, and compositional disclosure is essential in these applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH regulations (Europe), TSCA (USA) for input registration
    • RoHS Directive compliance for extrudable resins in electronic or automotive settings
    • Customer-imposed technical specification limits for residual bromide and alcohol groups

    Typical usage ratio

    • 0.5–3% w/w as a functional monomer, varying by the degree of modification desired and the performance target of the specialty resin or copolymer.

    Downstream process integration

    • Dosed into the polymerization or pre-polymer synthesis stage, where it acts as a functionalized segment to introduce targeted chemical groups within the resin matrix, followed by purification and extrusion or molding as required for the end-use sector.

    Final product types

    • Specialty copolymers for electronics encapsulation
    • Engineered resins for automotive coatings
    • Functionalized thermoset and thermoplastic components
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    More Introduction

    Introducing 4-Bromophenylpropanol: A Real-World Perspective on a Versatile Chemical

    Anyone working in fine chemical synthesis likely knows the hurdles that come with finding reliable, high-purity intermediates for advanced research. Not all starting materials behave the same way, and in my years working with aromatic alcohols, some compounds always seemed to create bottlenecks, either due to impurities, reactivity quirks, or trouble during scale-up. 4-Bromophenylpropanol stands out from the crowd, both for its dependable performance in synthetic routes and its unique niche in a crowded field of substituted phenylpropanols. Sharing some firsthand experience with this compound might help clear the fog for scientists looking for an edge in their procedures.

    Why 4-Bromophenylpropanol Draws Attention in the Lab

    The world of phenylpropanols is wide, but 4-Bromophenylpropanol carves out a specialty for itself thanks to a defining feature: Its para-bromo substituent brings a new layer of reactivity while keeping the core integrity of the phenylpropanol structure. Some folks underestimate how much the bromine atom changes the chemistry here. The molecule becomes more than just a subtle variant; it’s a building block for targeted modification because bromine, unlike many other groups, enables efficient coupling reactions. Anyone looking to connect aromatic rings using Suzuki or Heck reactions, for example, finds the presence of a bromine at the para-position opens doors that plain phenylpropanol slams shut.

    Plenty of researchers spend months wrestling with stubborn side reactions in their search for pharmaceutical building blocks, fragrances, or advanced materials. 4-Bromophenylpropanol tends to ease that frustration. Its purity remains consistent thanks to mature extraction and purification methods. In my own experience, the difference between using a low-grade starting material and a well-prepared 4-Bromophenylpropanol is night and day. Unwanted by-products go down, the need for laborious post-reaction cleanups shrinks, and success rates climb. The compound’s crystalline nature, moderate melting point, and predictable solubility create a more straightforward purification process, a detail every chemist who has juggled columns and rotavaps will appreciate.

    Usage Patterns: Insight from Bench to Pilot Plant

    4-Bromophenylpropanol finds most of its demand in fields where selective substitution rules the day. Pharmaceutical chemists, especially those focused on small-molecule drugs, understand its utility in designing new candidates with precise structural tweaks. Brominated aromatics serve as key inputs in cross-coupling, giving rise to ethers, amines, or other complex fragments with minimal trouble. In fragrance chemistry, this compound’s structural backbone remains stable under typical formulation conditions, granting fine-tuned control over volatility and sensory profile.

    I’ve observed that with the right setup, the benzylic alcohol group of 4-Bromophenylpropanol sits ready to undergo further modification—oxidation, protection, or even conversion to other functional groups—without risking unwanted shifts on the aromatic ring. This separation of reactivity lets chemists manipulate one domain without sabotaging another. Such flexibility is rare. Many researchers end up looking at their glassware late at night, hoping an unpredictable side reaction hasn’t ruined their yield. Compared to unhalogenated phenylpropanols, or derivatives with more reactive nitro or amino substituents, the bromo group offers controlled branching points but has fewer compatibility issues with diverse reagents or catalysts.

    Specifications and What Sets This Compound Apart

    Most suppliers provide 4-Bromophenylpropanol in fine crystalline powder, usually with purity levels above 98%. Moisture content typically stays low due to stable packaging, but anyone pulling this bottle off the shelf should keep an eye on hygroscopic tendencies, common for benzylic alcohols. Analytical reports based on HPLC or NMR consistently reflect tight quality control in trusted sources. From my observations, physical handling remains straightforward—there’s little clumping, dustiness is minimal, and the odor is faint, lacking the sharpness you sometimes notice in lower-quality aromatic alcohols.

    What really separates this compound from others is not just its bromine substituent, but the way it sits on the molecule. Para-bromination pushes the electronic environment into a sweet spot: Reactivity is dialed in without destabilizing the aromatic system, so over-reactions and polymerization remain rare. Compounds with ortho- or meta-bromo groups often don’t play as nicely in complex coupling reactions or fall apart during prolonged exposure to heat. The para-bromine, in contrast, keeps the molecule both accessible and manageable, which opens up more consistent reaction planning.

    Comparing 4-Bromophenylpropanol to Other Aromatic Alcohols

    Chemists shopping for intermediates often face a wall of choices. Phenylpropanol, 4-chlorophenylpropanol, 3-bromophenylpropanol, and dozens of others crowd the shelves. It’s tempting to imagine any will do if the rest of the route lines up, but that rarely works out. I’ve tried knocking together the same series of reactions with 4-chlorophenylpropanol; the results didn’t match in yield, and some downstream coupling partners simply fizzled. Chlorine, for instance, can make products trickier to purify, and it may limit the scope of available cross-coupling partners.

    Other researchers have spent entire quarters running parallel trials with the meta-brominated version, only to find their target fragments carried persistent impurities—byproducts that resisted every trick in the book. Comparing results, 4-Bromophenylpropanol won hands down for clarity in workup and flexibility with Pd- or Ni-catalyzed systems. Reactivity can be tuned up or down; you want a fast coupling, just dial up temperature and catalyst, but things rarely veer out of control. I’ve rarely seen para-bromo compounds fall prey to wild side reactions unless handled with gross negligence.

    There’s something to be said for predictability in research, especially when budgets and timelines run tight. Some buyers aim to save money and settle for phenylpropanol itself, convinced that installing a halogen can come as a later step. What those strategies miss: Skipping direct purchase of 4-Bromophenylpropanol adds extra steps, extra hazards, and more waste streams. It’s rarely practical to subject bulk lots of alcohols to bromination just to shave a few dollars off procurement. Starting with the right intermediate cuts weeks, not just days, off development projects.

    Impact on Industry and Research

    Modern pharmaceutical development depends on reliable intermediates, and new compounds entering clinical study have only gotten more complex. Every small gain in efficiency can cascade throughout the process. 4-Bromophenylpropanol appears in more patent filings every year, and companies relying on robust, modular synthesis value these kinds of functionalized aromatics. Patented kinase inhibitors, for instance, list this compound as a key precursor. The same applies in agrochemical R&D, where regulatory approval processes demand high-purity, traceable intermediates.

    The academic scene benefits as well: Graduate students working on SAR (structure-activity relationship) studies lean heavily on compounds like 4-Bromophenylpropanol to build out analog libraries. Students asked to source alternatives often report more failed syntheses and higher costs. In teaching labs, I’ve seen instructors offer this compound during cross-coupling modules because it’s forgiving for beginners. Mistakes, naturally, happen, but this compound doesn’t punish minor protocol errors with hazardous or noxious byproducts, which cannot be said for some other bromoaromatics.

    Challenges and Solutions in Sourcing 4-Bromophenylpropanol

    Even a well-loved reagent faces sourcing challenges. Counterfeit or mischaracterized material has popped up in less-reputable supply chains, so real experience counts when vetting suppliers. Chromatographic profiles and NMR signatures don’t lie, and colleagues swapping stories about inconsistent batches stress the need for up-to-date analytical verifications. Some university labs, especially those in lower-resourced regions, occasionally gamble on off-brand intermediates. Most times, trouble follows: Impurities show up in spectra, actual yields slide downward, and project times balloon. Having dealt once with a tainted batch—filled with hints of dibromo impurities and oxidized byproducts—I learned to demand full traceability and reference spectra up front.

    Frustrations aside, one practical solution remains: Invest in sourcing from suppliers with solid track records, independent third-party test results, and transparent batch histories. A single reliable provider cuts risk, saves repeat ordering, and eliminates time wasted on troubleshooting unexpected analytical results. During a high-throughput library build at my old lab, one minor supplier shipped batches containing unexpected isomers. Productivity took a hit, but once switched back to a verified source, everything fell back into line.

    Sustainability and Green Chemistry Considerations

    A compound’s utility should go hand in hand with its environmental impact. In many organizations, procurement now must answer to sustainability audits. Traditional bromination reactions leave behind hazardous waste, but direct acquisition of 4-Bromophenylpropanol—both as a time-saver and as a cost-cutter—lets chemists bypass at least one high-impact synthetic step. Some advanced producers now employ continuous-flow techniques or use greener solvents to reduce the environmental burden in production. This pushes the product toward better compliance with green chemistry standards without sacrificing quality or accessibility.

    In the lab, benign solvent choices like ethyl acetate or even greener options align with recent recommendations to limit exposure to halogenated waste. Anyone who has managed barrels of spent brominating agents or cleaned up a fume hood can appreciate the improvement. Conversations about waste handling, especially with leaner lab staff, feel less stressful when 4-Bromophenylpropanol comes straight from the bottle, ready for use.

    Looking Ahead: Emerging Applications and Trends

    The landscape for this type of aromatic intermediate keeps shifting. Advances in polymer chemistry have created a need for reliable monomers and crosslinking agents, and 4-Bromophenylpropanol’s dual functional groups catch the eye of materials scientists. Electrochemistry and photoactive research spaces, hungry for new, scalable building blocks, also see rising orders for bromoaromatics. A few notable start-ups developing next-generation OLEDs list 4-Bromophenylpropanol derivatives as precursors because the bromine drives site-selective incorporation into complex backbones.

    Younger synthetic chemists, sometimes unfamiliar with the subtleties of fine-tuned substitution, benefit from industry commentary highlighting comparative studies and real-world outcomes. More conference talks now report side-by-side yield comparisons and failed attempts with other substituted phenylpropanols. This open sharing has broadened the knowledge base, giving the new generation a faster path up the learning curve. Those seasoned in the craft nod in recognition: a well-chosen starting material can make or break a month’s work.

    Quality, Compliance, and Research Integrity

    Any commentary on advanced chemical intermediates comes back to the issue of verification and transparency. As regulatory expectations rise, researchers must keep robust paper trails for every compound that enters the lab. Pharmaceutical and fine chemical companies demand explicit purity metrics, contaminant traces, and batch documentation. Such requirements help keep data credible and reproducible. In my case, regular audits went more smoothly each time our team relied on suppliers with digital batch histories and quick access to analytical data.

    There’s also a growing expectation for ethical sourcing and responsible chemicals management. For 4-Bromophenylpropanol, its broad use brings industry pressure to avoid supply chains linked to environmental harm or substandard manufacturing. Most reputable suppliers now seek third-party audits, and as more customers ask about supply origins, transparency keeps improving. Reproducibility suffers when chemistry shortcuts lead to incompletely characterized intermediates. Open communication between buyers and sellers, rooted in technical expertise, keeps standards high and reduces batch-to-batch surprises.

    4-Bromophenylpropanol: Where It Matters Most

    Having worked on a handful of patent filings and development projects, I’ve seen firsthand how the selection of a single intermediate shapes not just costs and timelines but team morale. The lab operates better when smaller frustrations disappear, when clean spectra arrive on the first try, and when workups don’t turn into a week of grinding chromatography. Experienced hands in research and development pick 4-Bromophenylpropanol because it provides real, lasting advantages: flexible reactivity, reliable supply, and environmental responsibility.

    For anyone stepping into new synthetic territory—from undergraduate classes to advanced industrial labs—taking the time to choose an intermediate with a proven track record delivers results. I’ve sat through project meetings where post-mortems focus on avoidable delays caused by unreliable starting materials. Major discoveries sometimes hinge on the routine steps, the parts of synthesis that just need to work. In the hierarchy of fine chemicals, 4-Bromophenylpropanol doesn’t just serve as a stepping stone; it quietly supports breakthroughs across diverse research domains.

    Research is always a balancing act. One eye stays fixed on budgets, another on deadlines, a third—every experienced chemist grows a third—on the unexpected. Getting the starting materials right reduces risk at every step down the line. In my experience, 4-Bromophenylpropanol does more than just sit on shelves. It earning trust, delivering value, and making tough chemistry look easy.