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2-(4-Fluorophenyl)-2-Propanol

    • Product Name 2-(4-Fluorophenyl)-2-Propanol
    • Alias Alphaprodine
    • Einecs 226-367-8
    • 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
    VTB
    Specifications

    HS Code

    402111

    Iupac Name 2-(4-Fluorophenyl)propan-2-ol
    Molecular Formula C9H11FO
    Molar Mass 154.18 g/mol
    Cas Number 402-44-8
    Appearance White to off-white solid
    Melting Point 54-58 °C
    Boiling Point 220-222 °C
    Density 1.09 g/cm³
    Solubility In Water Slightly soluble
    Smiles CC(C)(O)C1=CC=C(C=C1)F

    As an accredited 2-(4-Fluorophenyl)-2-Propanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-(4-Fluorophenyl)-2-Propanol, 25g." Sealed cap, hazard warnings, and chemical supplier details printed clearly.
    Shipping **Shipping Description:** 2-(4-Fluorophenyl)-2-Propanol should be shipped in tightly sealed containers, away from incompatible substances, and stored in a cool, dry environment. Ensure packaging prevents leaks and complies with local, national, and international transport regulations. Appropriate safety labeling and documentation must accompany the package to indicate chemical hazards during transit.
    Storage 2-(4-Fluorophenyl)-2-Propanol should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Store at room temperature and keep away from sources of ignition. Ensure proper labeling and follow all safety regulations and institutional guidelines for chemical storage.
    Application of 2-(4-Fluorophenyl)-2-Propanol

    Applications of 2-(4-Fluorophenyl)-2-Propanol in Industrial Manufacturing

    2-(4-Fluorophenyl)-2-Propanol serves as a key intermediate in several industrial sectors, including pharmaceuticals, agrochemicals, polymers, and specialty coatings. As a manufacturer, we maintain strict process control and batch consistency to support complex downstream integration and regulatory compliance. Below, we detail core application scenarios from a production perspective, with process, compliance, and end product specifics.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical companies use this material as a building block for synthesizing beta-adrenergic receptor antagonists, particularly in the manufacturing of propranolol analogs. The compound delivers the fluorinated phenyl group necessary for optimizing bioactivity, and downstream processes employ Grignard reactions or Friedel-Crafts acylation, followed by chiral resolution when targeting enantiomeric APIs. Manufacturers rely on this intermediate due to its demonstrated performance under controlled GMP conditions and proven downstream compatibility in batch reactor and continuous flow processes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF standards for input materials in drug synthesis
    • European Pharmacopoeia (Ph. Eur.) monographs for active ingredient intermediates
    • FDA cGMP 21 CFR Part 210/211

    Typical usage ratio

    • Utilized at 0.95–1.05 molar equivalents with respect to the downstream core structure, with fine adjustment based on targeted yield and process scale

    Downstream process integration

    • Introduced in early-stage condensation or alkylation steps during multi-step API synthesis; process sequence includes purification and chiral separation if required

    Final product types

    • Chiral and racemic beta-blocker APIs
    • Propranolol-related drug substances
    • Intermediates for cardiovascular therapies
    • Bulk pharmaceutical chemicals

    2. Agrochemical Active Intermediate Production

    Agrochemical manufacturers select this compound in the production of systemic fungicides and select herbicides, especially for the construction of fluoroaromatic rings. The material enters selective hydrogenation or etherification reactions, producing responsive intermediates for protective crop agents. Downstream process chemists control the parameter range tightly to manage reactivity and purity, supporting batch and continuous reactor systems with multi-metric in-process QC for global market supply.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 for chemical registration
    • ISO 9001:2015 Quality Management System
    • OECD guidelines for testing of chemicals

    Typical usage ratio

    • Applied at 10–30% w/w within the core reaction blend, adjusted based on method of fluorine introduction and yield targets

    Downstream process integration

    • Added at the initial step of active ingredient assembly, preceding halide exchange or acylation in agrochemical synthesis pipelines

    Final product types

    • Systemic triazole fungicides
    • Selective herbicide intermediates
    • Crop protection additive precursors
    • Pesticide formulation components

    3. Polymer Modifier Additive Manufacturing

    Producers in the specialty polymer sector use 2-(4-Fluorophenyl)-2-Propanol as a chain-modifying agent for fluorinated copolymers and high-performance plastics. The secondary alcohol group and fluoroaromatic moiety impart chemical resistance and glass transition temperature adjustment capabilities to final polymers. Manufacturing approaches like melt polycondensation or solution-phase free-radical processes feature controlled feed of this additive, with integration in reactor feedstock to support functional polymer property tuning for electronics and engineering applications.

    Industry compliance standards

    • ISO 14001 Environmental Management relating to chemical processing
    • ASTM D638 for testing of polymer mechanical properties
    • RoHS Directive (2011/65/EU) where applicable to end-use
    • EU REACH chemical registration requirements for polymer additives

    Typical usage ratio

    • Employed within 0.2–2.0% by total monomer weight, with dosage based on the molecular weight target and desired fluorine content

    Downstream process integration

    • Fed as a co-monomer or terminal chain-modifier during melt or solution polymerization, with blending and in-situ monitoring of conversion

    Final product types

    • Fluorinated polystyrene copolymers
    • Engineering thermoplastics for electronics
    • Chemically resistant membrane materials
    • Specialty films and adhesives

    4. Specialty Coating Intermediate Sourcing

    Coating manufacturers use this raw material to synthesize high-performance fluorinated resins for protective, anti-graffiti, or chemical-resistant surfaces. The compound introduces desired hydrophobicity and solvent resistance through dehydration, esterification, or crosslinking. Plant protocols include staged feeding to reactor vessels with in-process FTIR and GC monitoring, enabling tailored resin formulation for automotive, marine, and industrial coatings with stringent batch reproducibility demands.

    Industry compliance standards

    • ISO 12944 for corrosion protection coatings
    • ASTM D4060 for abrasion resistance testing in coatings
    • Directive 2004/42/EC on VOC content in paints and varnishes
    • GMP guidelines for material traceability in coating raw materials

    Typical usage ratio

    • Ranged from 1–5% in resin matrix formulations, with dosing based on targeted hydrophobicity and UV stability

    Downstream process integration

    • Integrated during pre-polymer mixing or as a functionalizing crosslinker post-emulsion polymerization in resin production lines

    Final product types

    • Anti-graffiti architectural coatings
    • Marine and automotive surface coatings
    • Chemical-resistant tank and pipeline linings
    • Protective floor finishes
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    Certification & Compliance
    More Introduction

    2-(4-Fluorophenyl)-2-Propanol: Experienced Manufacturer’s Perspective

    Introduction to 2-(4-Fluorophenyl)-2-Propanol

    As a chemical manufacturer with years in the field, we focus on delivering products that not only meet requirements but also provide real, measurable value for downstream users. 2-(4-Fluorophenyl)-2-Propanol holds a unique position in organic synthesis and specialty intermediates. This compound serves as a vital building block for pharmaceutical development and advanced material science, with a molecular structure that lends itself to reliable downstream transformations.

    Our manufacturing history gives us insight into both the technical and practical aspects of 2-(4-Fluorophenyl)-2-Propanol. Based on rich operational data and hands-on experience, we understand the challenges and the reliability users expect from their raw chemical materials. Every lot we produce reflects strict attention to control parameters, analytical verification, and consistent technical support.

    Chemical Model and Specifications

    The fundamental identity of 2-(4-Fluorophenyl)-2-Propanol stems from its symmetrical arrangement and the presence of the 4-fluoro substituent on the phenyl ring. The chemical formula is C9H11FO, accompanied by a molecular weight of about 154.18. Our routinely offered grade records assay values upwards of 99%, with moisture and volatile content tightly monitored through Karl Fischer titration and gas chromatography.

    We own and operate reactors built for heteroaromatic coupling and controlled aliphatic modifications. The synthesis of 2-(4-Fluorophenyl)-2-Propanol starts with the careful handling of its fluorinated precursors, followed by stepwise purification stages like reduced-pressure distillation, phase separation, and recrystallization. Each batch undergoes HPLC and NMR verification against international standards, not because regulations prescribe it, but because we have seen first-hand how downstream disruptions often trace back to overlooked minor impurities.

    Most users receive our standard crystalline powder, white to off-white in appearance, packed under nitrogen to arrest hydrolysis and oxidative change. Typical lot certificates include a robust panel of physical and chemical attributes—melting range, residue on ignition, chloride content, and elemental analysis—all stamped with signatures from our in-house quality control experts.

    Usage Patterns and Practical Applications

    Input from end-users, process chemists, and formulators have shaped the way we tailor our product. 2-(4-Fluorophenyl)-2-Propanol features in several industrial settings, but its strongest adoption comes from pharmaceutical research where it is a core intermediate for the synthesis of chiral auxiliaries, antidepressants, and antipsychotic molecules. Its secondary alcohol group offers a versatile position for further functionalization such as oxidation, esterification, and ether formation. Experience tells us that this flexibility saves downstream process steps, reduces waste, and opens up alternative synthesis routes that are otherwise blocked by more rigidly substituted analogues.

    In agrochemical pipelines, companies incorporate it into advanced pesticide and herbicide frameworks. The fluorine atom, introduced at the para-position, brings unique electronegativity and metabolic stability. While there are many phenylpropanol derivatives on the market, the 4-fluoro version stands apart for its dual benefits: improved biological activity and marked resistance to oxidative degradation. Recognizing the significance of these traits came from iterations in scale-up and pilot studies, with process teams repeatedly returning to this material for late-stage modifications.

    Outside the life sciences, we see our product in specialty polymers and liquid crystal manufacture, particularly in those applications where the combination of aromatic stability and polar substituents delivers new material properties. Custom application data shows improvements in optical and dielectric properties—factors manufacturers cannot secure by generic phenylpropanols.

    Application engineers call for not just a reagent, but a material they can trust to behave as expected batch after batch. Our internal tests emphasize not only purity, but batch-to-batch consistency measured using chromatographic fingerprints and reproducible melting behavior. The solvent compatibility, crystal morphology, and thermogravimetric stability we track with every batch directly respond to feedback from real-world use.

    Differences Compared to Other Phenylpropanol Compounds

    With several decades of product development under our belt, we see clear performance distinctions among aromatic alcohols. Many customers approach us initially considering more basic phenylpropanol isomers—either the unfluorinated version or those with different substitution patterns. Our technical team has consistently recorded several practical advantages offered by 2-(4-Fluorophenyl)-2-Propanol.

    Adding a fluorine atom at the 4-position changes both electronic and steric effects. The result is a notable boost in both chemical and metabolic stability. Standard non-fluorinated propanols typically show higher rates of oxidation in both synthetic and biological settings, raising concerns about product shelf life, downstream purity, and final product reproducibility. In high-throughput discovery campaigns, this instability leads to more frequent batch failures—and based on client input, switching to the fluoro-derivative consistently obviates these issues.

    Another major distinction lies in reactivity. The 4-fluoro group modulates electron density in the aromatic system, which can either activate or deactivate the ring toward further functionalizations. Real process data from multiple scale-ups demonstrate smoother reaction kinetics and higher isolated yields in stepwise modifications, particularly for halogen exchange, nucleophilic aromatic substitutions, and aldol-type condensations. By contrast, positional isomers without the 4-fluorine show erratic behavior: sometimes, they resist required transformations, other times, they undergo side-reactions that bloat costs or introduce unpredictable downstream profiles.

    We have also seen a difference in practical work-up and purification. Non-fluorinated analogues, for example, often come with higher volatility and lower phase separation efficiency. Every time production teams run a comparative re-crystallization or solvent extraction, the product recovery rates with 2-(4-Fluorophenyl)-2-Propanol consistently outperform the alternatives. Ease of filtration, color stability, and tendency to form stable crystals all reinforce this material’s superior processability.

    When considering toxicity and handling, our users find that 2-(4-Fluorophenyl)-2-Propanol offers an advantage. Many halogenated compounds present notable concerns in handling, storage, and transport. Yet, with our process controls and analytical screens, each lot demonstrates low residual solvent carryover, no detectable heavy metals, and high resistance to photolytic breakdown. This matters operationally: cleaner operations and less downtime for cleaning or changeover enables teams to focus on value-adding process steps, not unplanned shutdowns.

    Real-World Manufacturing Insights

    Running a chemical plant brings practical challenges that theory seldom predicts. The synthesis of 2-(4-Fluorophenyl)-2-Propanol calls for careful control over reaction temperature, dosing rates, and byproduct management. Through experience, we adopted an approach emphasizing closed handling and real-time monitoring, using online analytics to flag process drifts before they create quality issues. One critical insight: at the exotherm-prone alkylation stage, reaction selectivity depends strongly not only on feed purity, but also on agitation speeds and micro-oxygen intrusion. Years of troubleshooting taught us that even minor oxygen ingress oxidizes the intermediate, forcing costly rework or scrapping material.

    We continuously review our protocols, not only relying on published literature but also embracing custom engineering upgrades, such as inert-gas blanketing and redundant filtration to catch submicron solids. As a manufacturer, real feedback from the floor—such as operator notes and quality alerts—drives our ongoing investment in validation and analytics. For example, the installation of in-line NMR and advanced chromatography systems has reduced the time from synthesis to batch clearance, enabling us to deliver fresher material and tighter production cycles.

    The downstream utility of our product depends not just on chemical form, but its physical properties and batch consistency. We work with both large-volume buyers and small-lot specialty users, taking pride in our flexible production arrangements. Over the years, shifting customer demands have steered us toward both dedicated production campaigns and standard campaign-mode manufacturing. Our process control methodologies were adapted in partnership with scientists and engineers who depend on batch reproducibility—no matter the order size.

    Sustainability, Reliability, and Regulatory Experience

    Modern chemical manufacturing faces rising scrutiny over environmental impact, worker safety, and regulatory compliance. We made it a point to invest in closed reactor systems, vapor recovery, and scrupulous residue management. The production of 2-(4-Fluorophenyl)-2-Propanol doesn’t just happen behind closed doors. Each stage of solvent use, energy input, and waste output is tracked and optimized. For example, by switching to high-efficiency distillation columns and reusing process solvents in a closed-loop, we cut both solvent costs and net emissions. Fielding audit teams and regulatory inspectors gave us practical know-how for tracking critical traces—be it residual monomers or micro-level contaminants.

    Markets now demand longer shelf-lives, traceable documentation, and real-time transparency. Each batch produced comes backed by multi-tiered analytical records and up-to-date regulatory status reports. We respond to queries from customers and regulators alike, providing not just standard documentation—lot certification, analysis reports, but also custom validation for those working under specialized or geo-specific guidelines.

    Our own experience with international supply chains highlighted the need for robust packaging and logistic controls. In earlier years, temperature excursions during transit led to isolated product yellowing or crystallization changes. We responded by investing in moisture and oxygen-barrier packaging, along with temperature loggers that ensure product arrives in original condition. This is not simply a matter of compliance; it pays real dividends in reduced returns and better end-user reliability.

    Solutions to Process and Supply Chain Challenges

    Manufacturers face constant pressure for shorter lead times and greater predictability. We regularized our forecasting and batch scheduling, keeping buffer stock and alternate raw material sources on hand during periods of supply disruption. COVID-era shortages drove home the lesson: relationships with upstream fluorochemicals suppliers and logistics partners determine downstream reliability. By qualifying and auditing alternate sources for key precursors, we maintained unbroken supply while others ran into shortages or price spikes.

    On the customer side, we found that communication and transparency build loyalty. Whenever possible, technical advice comes from process veterans and chemists who know the hands-on difficulties of running multi-step syntheses. We offer in-lab troubleshooting and support during scale-up trials, based not on marketing literature but on accumulated feedback, failed runs, and successful recovery stories.

    Risk management in chemical manufacturing is rarely discussed openly, yet it shapes every run, shipment, and delivery. By embracing a mindset of preemption—routine analytical checks, proactive change management, and direct operator feedback into process revisions—we sidestep issues before they introduce cost or quality risk. Familiarity with global regulations, export controls, and customs documentation eliminates most headaches at points of cross-border transfer.

    Looking Ahead: Continuous Improvement and Customer Focus

    No two production runs are ever identical. Minor shifts in utility performance, feedstock grade, or even weather can influence batch performance. Our plant teams and chemists use real production data to identify new opportunities for improvement, whether by optimizing energy consumption, trialing greener solvents, or exploring safer and more robust process routes. Day-to-day, our priorities focus on consistent output, traceable documentation, and approachable technical support.

    Over the course of many successful (and occasionally difficult) production campaigns, we learned that trust rests on three things: material reliability, communication, and ownership of both problems and solutions. 2-(4-Fluorophenyl)-2-Propanol is no longer an obscure niche compound; it is a respected and central intermediate in many innovative technologies and life science pipelines across the globe.

    Our experience in the manufacturing trenches has shaped every investment, every process improvement, and every customer interaction concerning this product. By blending technical rigor with a practical, customer-centered approach, we continue to deliver not only high-quality material but also a long-term partnership for every customer relying on our expertise.