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4,4,4-Trifluorobutan-2-One

    • Product Name 4,4,4-Trifluorobutan-2-One
    • Alias Perfluoroethyl methyl ketone
    • Einecs 213-668-1
    • 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

    934729

    Iupac Name 4,4,4-Trifluorobutan-2-one
    Molecular Formula C4H5F3O
    Molar Mass 126.08 g/mol
    Cas Number 461-20-3
    Appearance Colorless liquid
    Boiling Point 89-91 °C
    Melting Point -82 °C
    Density 1.252 g/cm³
    Refractive Index 1.349
    Flash Point 16 °C
    Solubility In Water Miscible
    Smiles CC(=O)CC(F)(F)F
    Pubchem Cid 10674

    As an accredited 4,4,4-Trifluorobutan-2-One 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 4,4,4-Trifluorobutan-2-One, tightly sealed with a screw cap and labeled with hazard symbols.
    Shipping 4,4,4-Trifluorobutan-2-One should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport according to local, national, and international regulations for hazardous chemicals. Keep away from heat and direct sunlight. Proper labeling and documentation, including Safety Data Sheet (SDS), are required to ensure safe handling and compliance during shipment.
    Storage 4,4,4-Trifluorobutan-2-one should be stored in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep the container tightly closed and protected from moisture and incompatible substances such as strong oxidizers or acids. Store in a chemical-resistant, labeled container. Use appropriate secondary containment and follow all relevant chemical safety regulations.
    Application of 4,4,4-Trifluorobutan-2-One

    Applications of 4,4,4-Trifluorobutan-2-One in Industrial Manufacturing

    4,4,4-Trifluorobutan-2-One functions as a specialized fluorinated intermediate in several advanced chemical manufacturing processes. As an experienced producer, we supply this material to well-documented downstream sectors, and we support customers with technical data for compliance and optimized integration into their production lines. Below are the principal industrial application scenarios and their technical requirements.

    1. Pharmaceutical Synthesis—Active Pharmaceutical Ingredient (API) Intermediate

    Many pharmaceutical manufacturers use 4,4,4-Trifluorobutan-2-One as a building block in the synthesis of new fluorinated APIs. It participates in nucleophilic substitution and coupling reactions to introduce a trifluoromethyl group for enhanced metabolic stability in target molecules such as antiviral and oncological candidates. The material requires precise handling under GMP guidelines, and quality documentation must accompany every lot.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 211 US cGMP Regulations
    • European Pharmacopoeia Monograph 5.10 (Impurities)
    • REACH Registration for pharmaceutical intermediates

    Typical usage ratio

    • Between 0.6 and 2.5 molar equivalents per reaction step, depending on targeted substitution patterns and overall process yield

    Downstream process integration

    • Introduction during early or middle-stage chemical transformations via a controlled batch or continuous flow addition
    • Monitored by in-process HPLC to minimize side products
    • Often coupled with catalytic hydrogenation or alkylation steps
    • Isolated by distillation or crystallization after reaction completion

    Final product types

    • Intermediate salts for antiviral compounds
    • Fluorinated amine intermediates for kinase inhibitors
    • Reference standards for metabolite profiling
    • Final API forms supplied to formulation sites

    2. Agrochemical Synthesis—Herbicide and Fungicide Intermediate

    Crop protection manufacturers rely on 4,4,4-Trifluorobutan-2-One as a key intermediate in the assembly of advanced herbicide and fungicide molecules. The trifluoromethyl group boosts the bioactivity and environment persistence of actives. The compound serves as a precursor in multistep synthesis for the preparation of active ingredient cores.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • ISO 9001:2015 Quality Management System
    • Globally Harmonized System (GHS) for classification and labeling

    Typical usage ratio

    • 0.7–1.8 mole per mole of co-reactant, adjusted per specific molecule requirements and yield targets

    Downstream process integration

    • Introduced in the initial condensation or acylation step in a multistage batch synthesis
    • Process requires controlled addition under inert atmosphere due to volatility
    • Intermediate purification by short-path distillation or column chromatography
    • Followed by derivatization to introduce heterocyclic motifs

    Final product types

    • Trifluorinated phenyl herbicides
    • Fungicidal pyrimidines
    • Pre-mix technical concentrates
    • Granular and liquid agrochemical formulations

    3. Electronic Chemicals—Photolithography Solvent and Fluorinated Developer Component

    Semiconductor fabrication specialists incorporate 4,4,4-Trifluorobutan-2-One as a high-purity solvent and functional additive in photolithography and etching solutions. Its unique volatility profile and compatibility with modern advanced patterning processes enable fine feature definition on silicon wafers, particularly in ArF immersion and EUV photoresist formulations.

    Industry compliance standards

    • SEMI C1: Specifications for Chemicals
    • IATF 16949 for quality in electronic component supply
    • RoHS Directive (2011/65/EU)
    • Transparency per SEMI E49 for trace metal impurities

    Typical usage ratio

    • In the range of 8–20% w/w in developer or rinse blends, depending on the targeted lithography process and wafer material

    Downstream process integration

    • Added during preparation of photoresist developer solutions for 90–14 nm processes
    • Filtered through sub-micron IP-rated cartridges to remove particulates
    • Controlled delivery to spin-coating and developer tracks in a cleanroom (ISO Class 5 or better)
    • Recovered and recycled using vacuum distillation units

    Final product types

    • Photoresist developers
    • Wafer rinse liquids
    • Advanced ArF immersion solutions
    • EUV-compatible photochemical blends

    4. Fine Chemical Manufacturing—Synthesis of Specialty Fluorinated Building Blocks

    Producers of specialty chemicals and advanced materials utilize 4,4,4-Trifluorobutan-2-One to construct mono- and polyfunctional fluorinated building blocks. Its electrophilic properties facilitate controlled substitutions, enabling access to valuable intermediates for polymer and crystal engineering. These applications demand high purity and batch-to-batch consistencies to satisfy final product performance criteria.

    Industry compliance standards

    • ISO 9001:2015 for batch production and traceability
    • REACH Compliance for specialty chemical registration
    • Responsible Care® Global Charter for safe chemical handling
    • GHS/CLP labeling per European and North American standards

    Typical usage ratio

    • 1.0–2.2 molar equivalents per reaction, customized for the structure and yield of the targeted fluorinated block

    Downstream process integration

    • Added to controlled reaction vessels operating under anhydrous conditions
    • Supports one-pot, multi-component assembly for fluorinated alcohols or ketones
    • Reaction monitored by GC/MS to confirm unreacted ketone removal
    • Purification via acid-base extraction or fractional distillation

    Final product types

    • Trifluoromethylated ether derivatives
    • Fluorinated aldehyde and carboxylate intermediates
    • Building blocks for specialty polymers
    • Fine chemicals for analytical reference standards

    5. Polymer Industry—Modification Agent for Fluorinated Acrylic Resins

    Advanced resin manufacturers employ 4,4,4-Trifluorobutan-2-One to introduce fluorinated motifs into acrylic copolymers, enhancing their chemical resistance and hydrophobicity. Consistent quality and controlled trace metal content remain critical in this segment, especially for high-performance coatings and electronics encapsulants.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in polymers
    • ASTM D256 for resin impact resistance tests
    • EN 13523-20 for coating durability
    • REACH compliance for monomer import and use

    Typical usage ratio

    • 0.5–3.5% by weight of the monomer feed, determined by targeted surface energy and end-use durability

    Downstream process integration

    • Dosed into the main monomer feed prior to radical polymerization initiation
    • Mixed under nitrogen to prevent premature oxidation
    • Integrated fully by post-polymerization reflux or stripping of unreacted monomer
    • Batch tested for non-volatile residue

    Final product types

    • Fluorinated acrylic resins for marine coatings
    • High-durability architectural paints
    • Electronics encapsulation compounds
    • Automotive topcoat resins

    6. Organic Synthesis R&D—Building Block in Advanced Fluorination Studies

    Research and development labs engaged in organic synthesis use 4,4,4-Trifluorobutan-2-One as a versatile module for late-stage fluorination experiments. Its presence in combinatorial libraries and patentable molecular frameworks supports innovation in medical, agrochemical, and materials chemistry.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for chemical testing
    • REACH Annex XVII for restricted uses in R&D volume
    • Local university or institutional EH&S chemical guidelines
    • Precautionary labeling per GHS Classification

    Typical usage ratio

    • 0.2–1.0 equivalents per reaction based on experiment design, screening focus, and scale of synthesis

    Downstream process integration

    • Introduced as a discrete reagent in a parallel synthesis array
    • Often used in automated liquid handling and microwell reactors
    • Work-up procedures adapted to scale-down and fast purification
    • Product characterization supported by LC-MS and NMR

    Final product types

    • Combinatorial fluorinated analogs
    • Lead compounds for pharmaceutical screening
    • Novel fluorinated scaffolds for patent applications
    • Building blocks for further chemical elaboration
    Free Quote

    Competitive 4,4,4-Trifluorobutan-2-One prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4,4,4-Trifluorobutan-2-One: Precision Chemical for Advanced Synthesis

    Expertise from the Manufacturer’s Floor

    Years of experience in producing specialty fluorinated chemicals have sharpened our understanding of what matters most during synthesis. 4,4,4-Trifluorobutan-2-One offers a unique balance between reactivity and selectivity, influenced directly by the presence of the trifluoromethyl group. Our team has focused on purity and consistent quality, knowing that each batch affects downstream processes for customers who need reliability above anything else.

    Model and Specifications

    Each batch is manufactured in-house under a robust quality system. We produce 4,4,4-Trifluorobutan-2-One to achieve a purity surpassing 99%. The product appears as a colorless liquid, free from suspended matter and visible contamination. Controlled moisture content and minimal residue on evaporation characterize each lot, based on regular analytical testing following both internal controls and industry best practices.

    The substance presents with a defined boiling range and low levels of non-volatile impurities. NMR and GC-MS documentation accompanies each shipment. Over the years, input from process chemists has guided us to adjust and optimize parameters, ensuring the product integrates smoothly with established and next-generation synthetic routines.

    Role in Advanced Organic Synthesis

    Many research labs and production sites depend on the clean reactivity of 4,4,4-Trifluorobutan-2-One, especially when seeking to introduce the trifluoromethyl functionality into larger molecules. The compound’s keto group, combined with the electron-withdrawing effect of the CF3 group, tunes its reactivity profile for a variety of synthetic steps, from nucleophilic additions to enolate chemistry. Our team stands in conversation with leading chemists, using feedback from application trials and published literature to adapt our approach and deliver a material that fits both industrial workflow and academic investigation.

    Most demand comes from pharmaceutical and agrochemical sectors. These industries rely on tightly controlled reactivity in multi-step processes, often under patent timelines or tight project schedules. Over time, our customers have stressed the value of traceability, reproducible results and the confidence that comes from knowing every batch meets the same tough standards. We build final shipment lots from drums tracked by ISO procedures, but hands-on testing and experience on the line still drive our confidence that each bottle matches the last.

    Comparative Differences with Analogous Ketones

    Our team has compared 4,4,4-Trifluorobutan-2-One against both standard butanone and other trifluoromethylated ketones in practical reaction setups. The triple-fluorine substitution produces behavioral differences not captured by general tables. In cross-aldol reactions, for example, trifluoromethylation suppresses self-condensation and enables straightforward product isolation in cases where methyl ethyl ketone would complicate workup. Experienced chemists remark on the improved chemical shifts during NMR analysis, aiding faster structural elucidation and product verification across complex pathways.

    Finding a reliable source with real process control over trace by-product levels has helped several partners break through scale-up barriers. The subtle reactivity and volatility shifts distinguished by the CF3 group often help avoid side-product formation found in less substituted ketones or insufficiently pure competitive offerings. This has proven especially true in the design of fluorinated building blocks for modern material science and high-performance polymer synthesis.

    Building Trust through Real-World Solutions

    Chemical manufacturing remains a hands-on discipline. From the tank farm valves to the reactor vessel, every phase involves human systems as much as molecular structures. Through steady customer conversations, we’ve learned that providing extra analytical detail often uncovers sources of process drift that standard specifications miss. In supporting a fluorination partner scaling from bench to pilot plant, we identified how upshifts in water content—two decimal points above standard—led to product crystallization failures. This led us to invest in on-line Karl Fischer titration and reinforce solvent separation during final purification, resulting in shipment lots with tighter spec margins than before.

    Software models can predict a lot, but feedback from process bottlenecks, off-smell complaints, or unusual chromatograms shapes every batch. This on-the-ground reality takes time. The trust we’ve built with long-term partners mirrors the way many professionals choose their sources: attention to detail, willingness to find root causes, and the courage to re-run lots that do not meet the highest standards. We ship after reviewing every batch record, aware that repercussions show up in our clients’ yields, not just in our own documentation.

    Broadening Research Horizons

    4,4,4-Trifluorobutan-2-One has enabled progress in bioconjugation, fluorinated surfactant development, and next-gen electronic materials. Its chemical behavior, shaped by our focus on purity and consistent handling, underpins results from research partners making discoveries in areas we couldn’t anticipate at the outset. Several leading university and industrial groups have mapped novel reactivities onto the core structure, using our material as the starting point for unique chemical patents and publications.

    As the industry pushes into new methodologies—photoredox, late-stage fluorination, metal-mediated cross-coupling reactions—our product lines adjust to meet this movement. Researchers relying on 4,4,4-Trifluorobutan-2-One often need reliable access to both hundred-gram and kilogram quantities with the same chemical fingerprint. We set up production streams with flexible batch sizes and tightly monitored lot tracking, using input from university partners and pilot plant teams to ensure both scale and purity remain on target.

    Supporting Safety and Compliance

    Handling perfluorinated chemicals imposes unique safety and environmental responsibilities. Our experience with regulatory frameworks—borne out of countless audits, inspections, and years of shipping under global compliance regulations—guides both production and post-sale support. We train each handling team member in fluorinated solvent behavior, accident response, and proper containment so that every liter ships out according to best practice guidelines.

    Documentation for transportation, exposure management and environmental fate reflect our on-site experience, not just regulatory language. Each staff member has seen how small changes in process or packaging affect safe delivery downstream. Partnering with global companies has shown us the value of upfront clarity and shared safety data. Down-the-line staff—whether in warehouse, transport, or lab—work best with clear instructions that reflect practical plant experience.

    Reducing Contamination and Unwanted By-Products

    Years of troubleshooting have highlighted the impact even trace contaminants can have on high-sensitivity syntheses. In working with customers synthesizing pharmaceutical intermediates, we’ve tracked minor impurity peaks back to subtle upstream factors—small solvent carryovers, minor temperature swings, or run-time filtration delays. Our process team countered these by automating critical inspection points and reviewing each batch with a battery of analytical tools before approval.

    We learned that impurity thresholds must reflect customer application, not one-size-fits-all company policies. Our technical support team, with decades inside chemical manufacturing, works directly with users to profile their target specifications, testing for outliers particular to each end-use case. This effort results in practical shipment formats—bottles, drums, or custom totes—filled under conditions matched to the customer’s process flow.

    Serving Emerging Technology Fields

    Our product’s robust performance in medicinal chemistry extends into other high-tech sectors. Electronics manufacturers use the compound in thin-film deposition and specialty material synthesis. It finds pathways into battery technologies, energy storage, and microelectronic fabrication, thanks to its stability and highly defined structural attributes. We listen to project feedback and use this to anticipate next-generation requirements, adjusting product handling protocols and packaging to fit each specialized flow.

    The emergence of greener chemistry practices has shaped our own plant procedures. Recovery and safe neutralization of fluorinated process streams prevents environmental release and recycles value. We’ve engineered loop systems for internal recovery and staff training programs emphasizing safe material management, aligning our manufacturing with the highest standards for responsible production.

    Listening and Adapting to Customer Challenges

    Every partnership with a customer brings new questions, fresh challenges, and opportunities to improve. We’ve adapted product documentation, packaging designs, even shipping schedules based on customer feedback. Several industrial partners in high-output pharma production once faced delays due to product sensitivity in bulk storage. After fielding their concerns, our technical team re-engineered storage recommendations and tightened bottle cap specifications, resulting in reduced spoilage and improved usability at their end.

    We keep an open line with groups needing process validation, supporting their work with technical packs drawn from actual production data, not boilerplate. The spirit in our factory combines procedural diligence and personal pride. Whether it’s a single analyst confirming a GC trace or an engineer overseeing reactor pressure curves, each person knows their work contributes to the reliability users experience in every bottle and drum of 4,4,4-Trifluorobutan-2-One.

    Continuous Improvement and Future Directions

    Tomorrow’s chemistry will set tougher challenges. We expect customers to demand higher purity, lower trace impurities, and broader application data. As usage of 4,4,4-Trifluorobutan-2-One increases across pharmaceuticals, specialty polymers, and high-value intermediates, our path forward builds on what we’ve learned: detailed tracking, operator training, and system redundancy. Our investment in analytical equipment, automation and staff expertise reflects the stakes involved. Each batch delivered demonstrates not just compliance, but the real-life performance users build into their discoveries and products.

    Our commitment to quality has a personal dimension for every person on the team. We see daily how the details—minute chromatography differences, subtle reactivity features, timely communication—shape the work of partners near and far. The product stands as a reflection of decades of practice, problem-solving, and drive to support the next generation of molecular innovation.