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2-Chloro-6-Fluorobenzyl Alcohol

    • Product Name 2-Chloro-6-Fluorobenzyl Alcohol
    • Alias 2-Chloro-6-fluorobenzyl alcohol
    • Einecs 630-947-5
    • 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

    234915

    Cas Number 700-28-3
    Molecular Formula C7H6ClFO
    Molecular Weight 160.57
    Appearance Colorless to pale yellow liquid
    Boiling Point 235-237°C
    Purity Typically ≥98%
    Density 1.336 g/cm³
    Refractive Index 1.554
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles OCc1c(Cl)cccc1F
    Synonyms 2-Chloro-6-Fluorobenzyl Alcohol; Benzyl Alcohol, 2-chloro-6-fluoro-
    Storage Conditions Store at 2-8°C, tightly closed container
    Flash Point 108°C
    Ec Number 615-698-2

    As an accredited 2-Chloro-6-Fluorobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100g of 2-Chloro-6-Fluorobenzyl Alcohol, labeled with hazard symbols, tightly sealed for safety.
    Shipping 2-Chloro-6-Fluorobenzyl Alcohol is shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. Packaging complies with international regulations for hazardous materials. Proper labeling and documentation accompany each shipment to ensure safe transport. Handling instructions and emergency measures are provided to minimize risks during transit. Suitable for air, sea, and ground shipping.
    Storage **2-Chloro-6-Fluorobenzyl Alcohol** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, strong oxidizers, acids, and bases. Store at room temperature and protect from moisture and direct sunlight. Properly label the container and restrict access to trained personnel only. Use appropriate secondary containment if necessary.
    Application of 2-Chloro-6-Fluorobenzyl Alcohol

    Applications of 2-Chloro-6-Fluorobenzyl Alcohol in Industrial Manufacturing

    2-Chloro-6-Fluorobenzyl Alcohol functions as an essential chemical intermediate in several specialized industrial production chains. The following sections detail its practical downstream integration in multiple real manufacturing environments, referencing relevant compliance, formulation, processing, and final-product factors observed by our customers and manufacturing partners.

    1. Synthesis of Pharmaceutical Intermediates

    Pharmaceutical ingredient manufacturers use 2-Chloro-6-Fluorobenzyl Alcohol during multi-step API synthesis, particularly for selective fluorinated benzyl derivatives. The alcohol group enables introduction into nucleophilic substitution reactions, supporting side chain extension in targeted molecules. The correct input ratio and purity are critical for downstream yield and regulatory compliance, especially in commercial scale GMP operations focused on APIs such as aryl benzylamines and select central nervous system agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for APIs
    • US FDA 21 CFR Part 211 (for final drug manufacturing)
    • EU EudraLex Vol. 4 GMP
    • USP and Ph. Eur monograph references for related intermediates

    Typical usage ratio

    • 10–35 mol% relative to final molecule; adjusted based on yield targets and impurity control in specific API synthesis routes

    Downstream process integration

    • Charged during Grignard-type and Suzuki coupling stages
    • Introduced to protected benzylation reactions for aromatic substitution controls
    • Used in the purification and crystallization step for intermediate isolation

    Final product types

    • Central nervous system drug APIs (e.g., substituted phenethylamines)
    • Oncology API intermediates
    • Commercial active pharmaceutical intermediates with fluoro- and chloro-benzyl frameworks

    2. Agrochemical Intermediate Production

    Agrochemical formulators employ 2-Chloro-6-Fluorobenzyl Alcohol as a building block in herbicide and insecticide intermediate syntheses, where aromatic halogenation and benzylation reactions are required. The compound supports creation of molecules with tailored field stability and selective uptake properties, vital to meet regulatory residue and environmental impact benchmarks established in key markets. Close control of input ratio avoids generation of toxic byproducts during scale-up.

    Industry compliance standards

    • FAO/WHO Guidelines for Quality Control of Pesticides
    • EU Regulation (EC) No 1107/2009 (Plant Protection Product)
    • US EPA 40 CFR Part 158 (Data requirements for pesticides)
    • REACH registration for industrial intermediates

    Typical usage ratio

    • 8–20 wt% in benzylation and halogenation steps; modified for desired active group incorporation and reaction completeness

    Downstream process integration

    • Reacted in batch reactors for stepwise halogen substitution
    • Fed at controlled rates during continuous stirred tank processing
    • Isolated after key conversion for immediate downstream coupling or further derivatization

    Final product types

    • Herbicide intermediate precursors featuring fluorinated side chains
    • Pyridine and phenyl-based insecticide intermediates
    • Active raw materials for branded agrochemical actives

    3. Fine Chemical Custom Synthesis

    Specialty fine chemical manufacturers utilize 2-Chloro-6-Fluorobenzyl Alcohol for constructing complex, high-value molecules where precise halogen and benzyl group positioning is required. The molecule integrates early in multi-step syntheses via selective activation, including etherification, esterification, and halogen exchange. Manufacturers prioritize consistency in purity and reactivity to streamline batch repeatability and minimize rework or purification overhead, especially in CDMO supply arrangements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Responsible Care® chemical safety management
    • REACH registration for supplied intermediates
    • Client-validated in-house QC protocols and traceability

    Typical usage ratio

    • 5–18 mol% as starting material or intermediate, based on complexity of target molecule structure

    Downstream process integration

    • Fed as initial substrate for chain-extension synthesis
    • Converted via oxidation or protection-deprotection schemes for later cyclization or substitution
    • Controlled addition to avoid excessive side product formation during scale-up

    Final product types

    • Custom aromatic ether and ester compounds
    • Functionalized halogenated building blocks for advanced materials
    • Contract-manufactured research chemicals

    4. Electronic Chemical Intermediates

    Producers in the electronic and specialty materials sectors incorporate 2-Chloro-6-Fluorobenzyl Alcohol in syntheses that generate functionalized aromatics for high-performance resins and photoresists. The molecule’s chloro and fluoro substitutions enable direct modification of electronic band structure and chemical resistance properties in end materials. Input ratios and impurity levels require careful management to meet downstream semiconductor manufacturing qualification standards, given the high sensitivity to trace contaminants and batch-to-batch reproducibility demands.

    Industry compliance standards

    • IPC-4101 (Base Materials for Rigid and Multilayer Printed Boards)
    • JEDEC JESD625A (Requirements for Handling Electrostatic-Discharge-Sensitive Devices)
    • ISO 14001 (Environmental Management in chemical processing for electronics)
    • OEM-specific PPAP for electronic chemical supply

    Typical usage ratio

    • 3–12 wt% in synthesis route; optimized for desired functional group density and minimal residual metals/halides

    Downstream process integration

    • Reacted in step-growth polymerization for pre-polymers
    • Added in controlled sequence to safeguard electronic grade purity
    • Subjected to vacuum distillation and filtration to meet photolithography-grade specs

    Final product types

    • Advanced polymer resins for printed circuit boards
    • Photoinitiators and photoresist precursors
    • Specialty monomers for optoelectronic materials and coatings
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    Certification & Compliance
    More Introduction

    2-Chloro-6-Fluorobenzyl Alcohol: Hands-On Experience from the Manufacturer’s Perspective

    Understanding 2-Chloro-6-Fluorobenzyl Alcohol in a Busy Lab

    In real manufacturing floors and pilot plants, every raw material and intermediate finds its purpose through actual results. We’ve worked with 2-Chloro-6-Fluorobenzyl Alcohol for years, in environments ranging from steady multi-ton batches to custom syntheses where every parameter counts. This compound, distinguished by its specific substitution pattern on the benzyl alcohol core, brings a set of clear physical and chemical advantages that real process chemists notice — not just on spec sheets, but while running reactions where consistency and specificity are key.

    Our standard product comes as a colorless to pale yellow liquid, with a purity exceeding 98% on GC. That narrow window of contamination means most pilot lines won’t need much extra purification, which can save cost and time — every reaction starts with confidence in the input material. On the ground level, this purity results in better yield control in downstream synthesis, especially for those building more elaborate molecules for pharma, crop protection, or material science projects.

    Why “2-Chloro-6-Fluoro” Stands Out

    In a world full of benzyl alcohol derivatives, small structural tweaks lead to big changes in chemical behavior. Adding a chlorine at the 2-position and a fluorine at the 6-position doesn’t just alter the molecular weight. Chemically, it changes the electron density of the aromatic ring, which gives our version very different reactivity in coupling reactions, oxidations, and nucleophilic substitutions. This isn’t academic theory — our chemists see less undesired ortho substitution during downstream halogenations and alkylations. The electron-withdrawing effects help reduce some side-products, and that’s been proven batch after batch in real workups and purifications.

    Fluorinated aromatics always command special attention because they behave differently from non-fluorinated cousins. Years of screening different benzyl alcohols for the agrochemical sector showed this: the 2-chloro-6-fluoro substitution increases the persistence and thermal stability of target molecules such as active intermediates or building blocks for more complex herbicides and insecticides. Our partners in contract manufacturing often bring feedback about easier process optimization because this intermediate does not devolve into sticky resinous by-products like less-substituted analogs sometimes do under elevated process temperatures.

    From Lab Synthesis to Tonne-Scale Runs

    At kilo-plant scale, achieving consistent purity and color in 2-Chloro-6-Fluorobenzyl Alcohol takes more than a simple distillation. Our process routes rely on clean starting halobenzenes, staged addition protocols, and temperature control to minimize off-colored materials and unwanted regioisomers. For regular bulk orders, we handle everything from resin-bound purification systems all the way up to glass-lined reactors. This gives us hands-on experience with the practical details that aren’t always visible in published procedures.

    We’ve seen many requests from clients swapping other benzyl alcohols for 2-Chloro-6-Fluoro. They often think it’s a straight substitution, but the molecule’s altered electron profile shifts downstream reactivity and final product stability. For example, in some pharmaceutical routes, the presence of both halogens improves metabolic resistance, a property that’s supported by animal-model data and cited in regulatory dossiers from end users familiar with our material.

    Performance in production isn’t a guess. We have monitored GC and HPLC data on multiple lots across multi-month periods, documenting that batches maintain their composition with little drift. This helps with regulatory process validation and cuts requalification headaches out of the schedule. Years of real shipment logistics also tell us that our product maintains its color and spec in standard packaging — we typically see no yellowing or breakdown unless shipments are exposed to extreme conditions far beyond standard storage.

    Regulatory and Environmental Considerations

    Every manufacturer producing chlorinated and fluorinated intermediates faces strict compliance expectations. Our processes align with the most recent trends in environmental management. We made specific choices to keep quenching and workup protocols as mild as possible, limiting generation of spent acid and halide waste streams. With on-site scrubbers and neutralization, we catch most by-product halides before they escape. Suppliers and clients have brought up increasingly tough demands for lifecycle transparency, and our documentation reflects actual batch traceability — not just a theoretical “green” claim, but a paper trail from starting raw materials through every production lot.

    REACH and local environmental agencies rightly pay extra attention to haloaromatics. We prepare full dossiers covering raw material origins, worker exposure controls, and waste handling procedures. For many clients this level of transparency speeds qualification or handles agency questions before they become roadblocks. Many of our regular customers in the EU and East Asia have commented that dealing with a full producer and not a third-party consolidator gives them a faster, more reliable regulatory audit pathway.

    Applications: From Ideas to Implementation

    The most frequent uses our customers report involve this alcohol as a building block for custom syntheses in pharmaceuticals, specifically where further substitution or derivatization on the benzyl alcohol core is required. Because the two halogens make the aromatic ring less reactive in certain positions, chemists can guide later functionalization with greater precision. This translates into higher selectivity and fewer purification headaches with downstream intermediates.

    Crop protection projects rely heavily on this material for preparing ether and ester derivatives. In these settings, process scale-ups show that the dual halogen pattern allows for robust coupling chemistry and results in intermediates that survive the harsh oxidative and metabolic environments encountered in real field application. Several feedback cycles with agricultural partners drove changes in our purification scheme, minimizing trace contaminants any sensitive bioassays might pick up.

    We have worked side-by-side with researchers from specialty materials companies looking for heat-stable, halogen-rich monomers. When compared directly against simple benzyl alcohols or even mono-halogenated versions, the dual halogen scheme of 2-Chloro-6-Fluorobenzyl Alcohol improves the flame-retardant qualities and environmental persistence of final polymers. Repeat runs and accelerated weathering tests from customers point to increased longevity, and we designed mild stabilization agents into our packaging to further prevent degradation before use.

    Handling and Storage Insights from the Factory Floor

    Years of hands-on storage and sampling provide more lessons than any database will ever show. The material isn’t overly volatile, so there’s little loss to evaporation, but we still use tight-seal containers to prevent slow air-oxidation. In modern warehouse conditions, with controlled temperature, we see no appreciable change in color or purity for well over a year. Opened drums or sample bottles hold up well across routine lab schedules, provided users avoid direct sun and keep caps on tight.

    Safety isn’t abstract when you work with these chemicals every day. Our in-house occupational health monitoring, reflecting years of accepted exposure limits for related compounds, has never recorded a reading close to action limits. Training for handling focuses mostly on hygiene and splash protection, since low volatility means inhalation risk is low compared to more mobile solvents or reagents.

    Comparisons: Other Benzyl Alcohols and Structural Impacts

    Colleagues often ask why not use simpler benzyl alcohols or less highly-substituted analogs. From our side, two key differences stand out. First, the 2-chloro-6-fluoro variant simply reacts less in positions prone to over-alkylation or unwanted oxidations. This lets end-users make more selective molecules, cutting down on side-pathways that eat up time and solvent in purification.

    Second, its combination of halogens boosts environmental, metabolic, and chemical resistance in products made from it. Direct experience shows the downstream value: more stable drugs, harder-wearing coatings, and crop protection agents that break down only when and where needed. Regular benzyl alcohols tend to give more unpredictable by-products if run under high temperature or with aggressive agents — something we see less often with this halogenated alcohol, as long as standard production controls are in place.

    Mono-halogenated benzyl alcohols (like 2-chlorobenzyl alcohol or 6-fluorobenzyl alcohol) each have their uses, but our feedback from the field shows that the combination brings more reliable selectivity and improvement in yield for the relevant reactions. For producers looking for “one-pot” synthesis steps, the dual halogen pattern consistently survives longer synthetic sequences, particularly where later functionalization relies on the ring’s resistance to unwanted substitution.

    Weighing the Downstream Value

    For every customer, the main question remains: why pay a premium for a dual-halogenated benzyl alcohol? After watching dozens of project launches, process optimizations, and actual kilogram-to-tonne scale-ups, the answer comes down to consistency and reduction of downstream losses. Lost time purifying off-pathway by-products costs more in labor and solvents than the slightly higher initial input material cost. When you cut out even a single extra chromatography run, or save a week on repeated purity checks, you notice the value in day-to-day manufacturing.

    Several large-scale pharmaceutical and agrochemical companies have documented yield and purity improvements with this alcohol as a key intermediate. Process engineers who test head-to-head reactions with simpler alcohols often cite fewer distillation fractions, clearer endpoint signals in analytical runs, and lower batch-to-batch variance. That’s partly down to the molecular structure — but also to years of fine-tuning route controls, solvent removal, and in-situ stabilization steps that only come from lived experience running real batches.

    Continuous Improvement, Backed by Experience

    New challenges always arrive. We regularly review the newest academic research and field reports, adjusting routes to minimize environmental load, quicken throughput, or satisfy new downstream conversion demands. Lately, pressure to lower residual solvent levels has led us to upgrade solvent-stripping techniques — resulting in lower trace organics for several client pharmaceutical submissions. Our R&D teams run pilot assays simulating real customer conditions. This rapid feedback loop lets us catch lot-to-lot deviations before they ever reach the customer, and learn which process tweaks actually matter.

    In one recent case, developers in specialty chemicals raised flags about trace metal content. After root cause analysis, we improved filtration and tweaked workup pH — and after follow-up testing, saw contamination levels drop by over 80%. We talk regularly with process chemists, so our manufacturing, purification, and packing logistics stay tuned not just to the theory, but to the realities on customers’ production lines.

    The Final Word from the Manufacturer’s Viewpoint

    From inside the plant, 2-Chloro-6-Fluorobenzyl Alcohol is more than a spec or a commodity. Hands in gloves, eye on the product during every transfer, care with the final purification — these steps translate directly to reliability when our material goes into someone else’s multi-million-dollar process. Everything from how shipments are labeled to how incoming feedback shapes our next production run comes from lived experience, not just what’s written in the reference literature.

    For developers who have struggled with inconsistent results, unwanted by-products, or difficulties in scaling up, the choice of a precisely made, carefully monitored intermediate like 2-Chloro-6-Fluorobenzyl Alcohol can make the difference between a failed run and a validated, repeatable process. Every batch we send out reflects the sum total of our technical know-how, real-world quality controls, and those small adjustments that only come from making the material ourselves. This isn’t just inventory — it’s the outcome of repeated cycles of direct problem solving and commitment to what works in real synthesis.

    As the industry evolves, the importance of proven intermediates made by direct producers only grows. Through each batch, each feedback loop, and each technical hurdle, we keep learning, refining, and building a knowledge base others can rely on. That’s how reliable chemistry happens — and why 2-Chloro-6-Fluorobenzyl Alcohol continues to earn its place in advanced synthesis pipelines worldwide.