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2-Fluorodiphenylmethane

    • Product Name 2-Fluorodiphenylmethane
    • Alias Benzyl fluoride
    • Einecs 216-038-4
    • 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

    187091

    Compound Name 2-Fluorodiphenylmethane
    Molecular Formula C13H11F
    Molecular Weight 186.23 g/mol
    Cas Number 1012-25-1
    Iupac Name 2-fluorophenyl(phenyl)methane
    Appearance Colorless to pale yellow liquid
    Boiling Point 288-290°C
    Density 1.104 g/cm3
    Refractive Index n20/D 1.581
    Smiles C1=CC=C(C(=C1)F)C(C2=CC=CC=C2)
    Pubchem Cid 144671
    Solubility Insoluble in water, soluble in organic solvents
    Flash Point 119°C
    Storage Conditions Store in a cool, dry, well-ventilated area

    As an accredited 2-Fluorodiphenylmethane 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 100 grams of 2-Fluorodiphenylmethane, sealed with a screw cap and labeled with hazard and handling information.
    Shipping 2-Fluorodiphenylmethane is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It must be handled according to standard chemical shipping regulations, including appropriate labeling and documentation. Transport should ensure stable temperatures and prevent physical damage or leakage, in compliance with local, national, and international chemical transport guidelines.
    Storage 2-Fluorodiphenylmethane should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from light and moisture. Use appropriate chemical storage cabinets if available. Handle with suitable personal protective equipment to avoid contact and inhalation.
    Application of 2-Fluorodiphenylmethane

    Applications of 2-Fluorodiphenylmethane in Industrial Manufacturing

    As a direct manufacturer of 2-Fluorodiphenylmethane, we supply this specialty intermediate to several high-value industrial sectors. The following application segments reflect real downstream use cases, each with distinct regulatory, formulation, processing, and finished goods characteristics.

    1. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical producers use 2-Fluorodiphenylmethane in the synthesis of fluorinated benzyl derivatives, essential for generating several classes of active pharmaceutical ingredients (APIs), especially within anti-inflammatory and CNS drug research pipelines. It is introduced at key multistep reaction stages, where the fluorine atom provides metabolic stability and target selectivity. Integration into GMP manufacturing lines involves controlled handling, validated cleaning protocols, and precise in-process measurements to ensure compliance with pharmacopoeial purity standards for downstream APIs such as fluoroarene-containing tablets or injectables.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP)
    • EU EMA Guidelines for Starting Materials
    • USP-NF General Chapters
    • FDA 21 CFR 211

    Typical usage ratio

    • 5-15% molar equivalent relative to target API precursor, adjusted based on target fluorination and product yield optimization.

    Downstream process integration

    • Loaded during the alkylation or Friedel–Crafts condensation step followed by monitoring of impurity profiles and specific fluorine incorporation.

    Final product types

    • Fluorinated Active Pharmaceutical Ingredients (e.g., CNS modulators, anti-inflammatory drugs)
    • Research-grade intermediates for clinical candidate development

    2. Liquid Crystal Monomer Synthesis for Display Technology

    Manufacturers of advanced display panels utilize 2-Fluorodiphenylmethane as a core building block for producing liquid crystal monomers with tailored electro-optical properties. These monomers improve contrast, response times, and reliability in LCD screens for mobile devices and automotive clusters. Processing lines require stringent contamination control, detailed batch recording, and adherence to RoHS directives regarding fluorinated intermediates used in electronics.

    Industry compliance standards

    • IEC 62474 (Material Declaration for Electronic Industry)
    • RoHS Directive (2011/65/EU) on hazardous substances
    • ISO 9001:2015 Quality Management System for Electronics Manufacturing
    • JIS C61000 (Japanese Industry Standards for display components)

    Typical usage ratio

    • 3-7% by weight in custom monomer formulations, balancing between molecular rigidity and dielectric anisotropy, tailored to the optical requirements of each screen brand.

    Downstream process integration

    • Used in early-stage organic synthesis for monomer functionalization, followed by purification and copolymer blending for mass production of liquid crystal mixtures.

    Final product types

    • Liquid Crystal Display (LCD) monomers and blends
    • Advanced screen components for smartphones and automotive displays

    3. Agrochemical Building Block for Herbicide Development

    Producers in the crop protection sector deploy 2-Fluorodiphenylmethane as a precursor to synthesize substituted aryl herbicides. It imparts selectivity and persistence to actives targeting resistant weed species. Downstream processes require exacting control of residual solvents and unreacted intermediates to meet national agrochemical safety and export standards. Each batch must pass multi-residue analysis as per regulatory protocols before market clearance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Test Guidelines for Chemical Safety
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • EPA 40 CFR Part 180 (US Pesticide Residue Limits)

    Typical usage ratio

    • 10-25% by weight in coupled reactions, depending on downstream active concentration targets and regulatory residue allowances.

    Downstream process integration

    • Introduced during heteroaryl coupling followed by downstream halogenation or alkylation steps, culminating in the formulation of technical-grade herbicide actives.

    Final product types

    • Selective herbicide active concentrates
    • Post-emergence weed control formulations

    4. Specialty Polymer Synthesis for Engineering Plastics

    In the engineering plastics industry, 2-Fluorodiphenylmethane acts as a functional comonomer to modify properties of high-performance thermoplastics such as polyaryletherketones (PAEKs). Its inclusion enhances thermal stability and chemical resistance, critical for automotive and aerospace components. Polymerization lines require continuous monitoring of the monomer feed ratio and polymer Mw distribution, also strictly maintaining REACH safety documentation for polyfluorinated intermediates used in final polymer lots.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (EU chemicals safety)
    • ISO 17855-1 (ISO Standard for Polyaryletherketone Plastics)
    • UL 94 (Flammability of Plastic Materials)
    • TSCA Inventory listing (US chemicals management)

    Typical usage ratio

    • 2-8% molar in the monomer mix, with adjustments based on required end-use temperature resistance and flow characteristics.

    Downstream process integration

    • Charged during initial step-growth polymerization, co-reacted with bisphenol and diarylketone species, followed by extrusion and granulation for shipment to molding shops.

    Final product types

    • High-temperature engineering polymers
    • Precision injection-molded auto parts
    • Fluorinated aerospace thermoplastics

    5. Organic Electronic Materials for OLED Synthesis

    Manufacturers in the advanced materials sector apply 2-Fluorodiphenylmethane in the development of novel organic semiconductors, specifically hole-transport and electron-blocking layers in OLED device stacks. The fluorine moiety enhances carrier mobility and device longevity. Every process stage must trace the incoming raw material, keeping within purity thresholds and following high-purity electronic grade internal specifications and IPC standards to ensure consistent device performance.

    Industry compliance standards

    • IPC-6012 (Qualification and Performance Specification for Rigid Printed Boards)
    • ISO 14644 (Cleanrooms and Associated Controlled Environments)
    • IEC 62341 (Standards for OLED panels)
    • JIS K1557 (Japanese Standard for Organic Semiconductors)

    Typical usage ratio

    • 1-5% by mol in target compound synthesis, based on the targeted layer thickness and charge transport requirements in the OLED stack design.

    Downstream process integration

    • Incorporated via Buchwald–Hartwig or Suzuki–Miyaura cross-coupling in the early synthetic phase, purified under high-vacuum before spin-coating on device substrates.

    Final product types

    • OLED display stack materials
    • Organic electronic components for flexible screens
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    Certification & Compliance
    More Introduction

    Introducing 2-Fluorodiphenylmethane: A Perspective from Our Manufacturing Floor

    Working with 2-Fluorodiphenylmethane Every Day

    People in the chemical business know how often the small differences between raw materials can decide the outcome of a project. Over the years, our team has specialized in refining and scaling up aromatic compounds, and 2-Fluorodiphenylmethane has become a regular topic. While some chemicals pass through the plant only once in a while, this molecule turns up again and again, thanks to its utility wherever selective fluorination adds value — especially in the world of fine chemicals, agrochemicals, and custom synthesis.

    Out here, where synthesis and purification meet real-world pressure, the practical differences between similar-sounding compounds become more than just catalog entries. We do not treat 2-Fluorodiphenylmethane as a mere commodity but as a key intermediate that helps unlock complex molecular structures.

    Product Overview: Specifications That Matter

    Every batch of 2-Fluorodiphenylmethane (CAS No. 345-88-6) leaves our site after passing rigorous analysis by GC-MS and NMR, ensuring high chemical identity and minimal impurities. Standard purity levels usually exceed 98%, since lower purities often fail to satisfy the needs of end users in pharmaceutical research and electronic material development. Colorless, oily liquid at room temperature, it comes with a faint aromatic odor that signals its sharp, clean structure.

    During production, we keep detailed records on physical properties: boiling points, density, and fluorine content. These aren’t mere stats for a datasheet. They influence how operators set up distillation, how QC teams choose analytical standards, and how our logistics crew handle packaging. Storing this material in amber glass or high-density polyethylene helps minimize any potential degradation during transit and across extended storage periods.

    Usage in the Real World: Where 2-Fluorodiphenylmethane Fits In

    Chemists look for precise results. A single misplaced atom in a synthetic route can send a project off-course. 2-Fluorodiphenylmethane’s structure — a benzylic methylene linking two aromatic rings, with the fluorine snug on one of them — has made it especially valuable as a starting material for several fluorinated building blocks. In pharmaceutical labs, teams try to introduce fluorine atoms at specific positions because these atoms can dramatically change drug metabolism and bioavailability. Our product’s consistency and low contaminant profile help chemists avoid surprises in yields and downstream reactions.

    Agrochemical innovation also relies on the ability to modify aromatic compounds quickly. Those seeking to synthesize new crop protection molecules have come to recognize that using high-purity 2-Fluorodiphenylmethane can cut unnecessary side reactions and reduce waste in multi-step synthesis. Our clients frequently provide feedback that minimization of unknown impurities saves both purification costs and time, especially as regulatory scrutiny grows for end-use formulations.

    We’ve also seen electronic and functional material researchers request this material. In these fields, the presence of halogens and fine-tuned electronic properties can make or break a batch of OLED materials, specialty polymers, or advanced surface treatments. By sticking closely to tight batch-to-batch QC specs, we help these clients avoid troublesome rework or device failures down the line.

    Experience at Scale: Manufacturing Learnings and Best Practices

    Consistency is everything. The key to reproducible syntheses lies in controlling each variable from raw material selection through reaction step, right to purification and logistics. Our operation runs continuous small-scale pilots alongside industrial-scale reactors to monitor process drift. The most persistent challenges involve controlling by-products in fluorination steps and ensuring thermal stability when scaling batch size.

    Operator know-how comes into play often. Adjusting reaction temperatures by even a few degrees can set purity margins back. Because 2-Fluorodiphenylmethane tends to resist hydrolysis, we catch fewer problems with moisture sensitivity than with some related compounds, but airborne particulate and trace acids still demand vigilant monitoring. Residual catalyst metals, if left untended, carry over into the final product and compromise performance for our most demanding clients. We continue pushing internal discussions between R&D and Quality to sharpen our detection methods: more sensitive HPLC, targeted trace-element analysis, and better chromatographic separations.

    Every change on the plant floor, from distillation columns to solvent composition, ripples through the process. We’ve added extra filtration points and built custom glassware assemblies to reduce contamination. Packing final product in drums, bottles, or ampules follows strict protocols — less for regulatory boxes to tick, more to safeguard hard-won batch quality.

    Real Differences: Comparing 2-Fluorodiphenylmethane to Close Relatives

    People sometimes ask what sets 2-Fluorodiphenylmethane apart from its non-fluorinated or isomeric cousins. The answer’s easy to overlook unless you work closely with synthesis routes. Compared with ordinary diphenylmethane, fluorination at the ortho-position changes not only the electron distribution across the rings but also influences reactivity toward electrophiles and nucleophiles. Downstream reactions such as Friedel–Crafts alkylations, oxidative couplings, or selective hydrogenations often hinge on nuances like these.

    For chemists aiming at specific fluorophenyl architectures, 2-Fluorodiphenylmethane forms key linkages that regular diphenylmethane can’t replicate efficiently. Some selectivity shifts appear subtle on paper but translate into significant improvements when making multi-gram or multi-kilogram quantities. This molecule shows less tendency to byproduct formation than its 3- or 4-fluoro analogs during common functionalization steps. These facts emerge clearly after years at the bench and in the plant, not through catalog copy.

    Storage stability also varies with small structural changes. 2-Fluorodiphenylmethane’s chemical robustness means fewer headaches in warehousing, especially when bulk materials need to ship cross-border over weeks. Analogues with more delicate substituents risk polymerization or color changes — not so here.

    We have serviced projects where researchers first spec’d a substitute, thinking all diphenylmethane derivatives behave the same, only to encounter solubility puzzles or downstream selectivity losses. Once they switched to our material, yields picked up and trouble tickets fell away. These are the cases that stick with you, project after project, as a manufacturer.

    Supporting Modern R&D: Why Reliable 2-Fluorodiphenylmethane Makes a Difference

    Industry conversations these days focus on speeding up discovery cycles and moving from bench to pilot scale faster. Opaque chemical suppliers or thin traceability records slow everything down. We field direct requests from research leaders who share that even a week of analytical back-and-forth can derail an R&D timeline. Each batch we release can be traced, with records of precursors, reaction dates, protocols, and analysis logs. Many of our long-term clients cite this transparency as the reason for choosing not just a product, but a reliable manufacturing partner.

    Beyond consistency, custom packaging and safety documentation play a role. Hazards in handling aromatic fluorinated compounds aren’t theoretical. Our own EHS teams live with these risks and have developed specific protocols for spills, waste streams, and personnel training. This practical experience shows up in the thorough documentation that travels with each shipment, not only to meet regulatory needs but also to help chemists in the field avoid preventable incidents.

    Supply chain resilience has become a louder topic. Disruptions hit harder for specialty products that have few producers with true technical depth. We’ve invested in raw material sourcing partnerships and backup routes because a single weather event shouldn’t put all downstream projects at risk. Planners count on steady, predictable batch readiness — and we ship as scheduled even during market stress periods.

    Insights from Custom Projects: Collaboration Improves Real-World Results

    Over the past few years, our shop has handled dozens of custom synthesis projects centered on 2-Fluorodiphenylmethane’s core structure. These collaborations illustrate why off-the-shelf product specs rarely tell the whole story. In one recent engagement, a client needed extremely tight impurity profiles for a pharmaceutical intermediate. Their original approach, using commercially available lots, returned inconsistent NMR signals and purification headaches that stalled preclinical work. After onsite visits and joint troubleshooting, we adjusted fluorination agents and upgraded purification trains, ultimately producing lots that cleared their synthetic bottleneck.
    Another case came from the materials science world. A client struggled with polymerization challenges in specialty coatings, ultimately solved by moving from a blended raw material to a higher-purity, freshly packed 2-Fluorodiphenylmethane batch. The chain reaction downtime and cost savings were documented — and repeated during later scale-up.

    Feedback like this drives us to keep refining our process and to keep communication lines open. Troubleshooting real-world applications, not just shipping product, gives us as much insight as process simulation software or ISO compliance hits on paper. Close, candid dialogue with users forms the backbone of better manufacturing — and it means each batch that leaves the gate carries lessons learned right up to the moment of delivery.

    Looking Ahead: Growing Demand and Responsible Manufacturing

    Growth in demand for 2-Fluorodiphenylmethane signals broader changes in specialty chemical markets. Research teams want cleaner, better-characterized molecules to serve as platforms for more complex chemistry. Pharma and agrochemical sectors shape their projects around reliable intermediates, increasingly seeking molecules with higher traceability and compliance assurances. Expectations for environmental responsibility and process efficiency headline more RFPs and review meetings now than in years past.

    In our own plant, shifts like solvent minimization, heat recovery, and automated sampling aren’t buzzwords — they’re the outcome of internal workshops to cut emissions and streamline steps. Manufacturing teams see waste treatment and emissions as daily priorities, not quarterly review topics. By building real know-how on batch recovery and safe effluent handling, we give clients material that meets not only chemical specs, but also growing environmental expectations.

    We have also expanded digital batch tracking, adopting software platforms that log each critical event for cross-team review. Traceability becomes more valuable as regulations tighten globally. End users benefit when they can access detailed certificates and audit trails without delays.

    Commitment to Ongoing Improvement: Beyond the Product Sheet

    Reflecting on years as a direct manufacturer, one theme recurs: only ongoing dialogue and technical honesty build trust. No matter how tightly a process runs, the best lessons come from problems solved hand-in-hand with customers. Whether through analytical troubleshooting, process optimization, or regulatory navigation, we stay involved past the point of basic delivery.

    Most of our best advances track directly to user feedback — requests for smaller or specialized lots, pre-scaleup consultation, or introductions of new analysis protocols to match unique R&D workflows. Our operators perform better in the field, not by memorizing procedures, but by understanding the reasons behind every step. By combining manufacturing muscle with respect for lab-level precision, we deliver batches that enable novel research, faster launches, and real-world reliability.

    Every drum, bottle, or ampule of 2-Fluorodiphenylmethane that leaves our site represents hundreds of small decisions, countless hours of discussion, and a persistent drive to do better. This slow, steady work — owning the process from raw materials to final QC — provides the foundation clients count on when pushing the frontiers of chemical science.