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3-Bromo-1,1,1-Trifluoropropane

    • Product Name 3-Bromo-1,1,1-Trifluoropropane
    • Alias 1-Bromo-3,3,3-trifluoropropane
    • Einecs 205-858-6
    • 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

    568141

    Productname 3-Bromo-1,1,1-Trifluoropropane
    Casnumber 460-41-7
    Molecularformula C3H4BrF3
    Molecularweight 178.96
    Appearance Colorless liquid
    Boilingpoint 76-78°C
    Density 1.581 g/mL at 25°C
    Refractiveindex 1.358
    Meltingpoint -63°C
    Solubility Insoluble in water
    Purity Typically >=98%
    Synonyms 1,1,1-Trifluoro-3-bromopropane
    Smiles C(CBr)C(F)(F)F
    Inchikey OAGXHTOMHYVWEU-UHFFFAOYSA-N

    As an accredited 3-Bromo-1,1,1-Trifluoropropane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Bromo-1,1,1-Trifluoropropane is supplied in a 100 mL amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 3-Bromo-1,1,1-Trifluoropropane is shipped as a hazardous material, typically in sealed, UN-approved containers to prevent leaks or exposure. The chemical is transported under regulated conditions, following all relevant safety, labeling, and documentation standards as required for flammable, toxic, or halogenated organic compounds. Proper handling and storage guidelines must be observed.
    Storage 3-Bromo-1,1,1-Trifluoropropane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep separate from strong oxidizing agents. Store at room temperature, but avoid excessive moisture. Use secondary containment to prevent leaks or spills, and ensure appropriate labeling in accordance with safety regulations.
    Application of 3-Bromo-1,1,1-Trifluoropropane

    Applications of 3-Bromo-1,1,1-Trifluoropropane in Industrial Manufacturing

    3-Bromo-1,1,1-Trifluoropropane acts as a key building block in several specialized chemical industries. As the original manufacturer, we maintain traceable quality control throughout each process step to meet high downstream demands. The following sections present actual industrial application segments with verified regulatory and process specifics.

    1. Synthesis of Fluorinated Agrochemical Intermediates

    Several manufacturers in the agrochemical field use this compound to introduce trifluoromethyl groups in syntheses for advanced technical active molecules. Its reactivity allows controlled substitution in multi-step organic synthesis for generating herbicide and insecticide intermediates. Integration typically occurs during the halogen-exchange stage or in nucleophilic substitution reactions under controlled parameters and inert atmospheres to minimize byproduct formation. Process engineers manage reagent ratios and temperature profiles to ensure regulatory compliance for environment and worker safety.

    Industry compliance standards

    • European Union REACH Regulation (EC) No 1907/2006
    • US EPA TSCA compliance
    • ISO 9001:2015 for process quality management
    • ILO chemical exposure guidelines for plant operations

    Typical usage ratio

    • 0.8 – 1.2 molar equivalents relative to target substrate
    • Adjusted based on substitution efficiency and impurity profile
    • Lab-scale to pilot: 100g – 10kg batches, scaling up to metric tons for commercial production

    Downstream process integration

    • Inserted after initial functional group introduction and before final heterocycle closure
    • Used in glass-lined or stainless reactors equipped for halogen handling
    • Residues are neutralized according to waste management protocols
    • Monitored via LC-MS for unreacted bromide removal

    Final product types

    • Herbicide intermediates for sulfonylureas
    • Insecticide precursors containing trifluoropropyl moieties
    • Pre-cursors for selective fungicide actives
    • Intermediate active building blocks traded under custom synthesis contracts

    2. Pharmaceutical Intermediate Synthesis (API Route Development)

    Custom synthesis of pharmaceutical intermediates often uses this compound to construct trifluoromethyl-containing side chains for select APIs in cardiovascular, CNS, and antiviral therapy candidates. The compound typically reacts under anhydrous conditions to minimize side-reactions, and batch records comply with GMP process documentation. Reaction scale, purity, and traceability remain critical from gram-scale pilot runs to full industrial campaigns. Cold chain management applies where product stability requires.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU Guidelines EudraLex Volume 4
    • USP–NF monograph input ingredient requirements

    Typical usage ratio

    • 1.0 – 1.3 molar equivalents depending on desired conversion
    • Use rate optimized in route scouting phase
    • Pilot to industrial: 50g for route development, up to 500kg per synthesis batch

    Downstream process integration

    • Added in derivatization steps for side chain introduction
    • Charged under nitrogen protection with dry solvents
    • Synthesis monitored for residual bromide by ion chromatography
    • Product purified via recrystallization or preparative HPLC

    Final product types

    • Chiral drug intermediates with trifluoropropyl side arms
    • Final-stage intermediates for CNS and antiviral APIs
    • Protected amino acid analogues for peptide-based drugs
    • Building blocks for advanced medicinal chemistry libraries

    3. Key Intermediate in Fire Suppressant Gas Manufacture

    Producers employ this material as a critical precursor in synthesizing next-generation halogenated fire extinguishing agents, especially for clean agent gas blends. The process involves stepwise halogen-exchange and fluorination, meeting stringent purity requirements to limit residual brominated by-products. Reactors feature specialist materials for corrosion resistance. Gas handling SOPs reference hazardous substances management under respective regional guidelines, and continuous in-line GC testing manages blending accuracy.

    Industry compliance standards

    • NFPA 2001: Standard on Clean Agent Fire Extinguishing Systems
    • ISO 14520 Clean Agent Fire Extinguishing Systems
    • EU Regulation No 517/2014 on fluorinated greenhouse gases
    • US EPA SNAP (Significant New Alternatives Policy) List

    Typical usage ratio

    • 0.9 – 1.05 molar equivalents to perfluorination agent
    • Exact blend ratio depends on agent specification (usually 5–15% by mass in pre-reactor mix)
    • Monitored per batch via on-line mass balance systems

    Downstream process integration

    • Introduced in closed-system fluorination reactions
    • Processed in high-pressure reactors to yield desired agent
    • All steps documented for environmental and health audit trails
    • Impurity residues destroyed or recovered per safety protocols

    Final product types

    • Clean fire suppression gases (e.g., HCFC, HFC blends)
    • System fill agents for server room protection
    • Pressurized cylinder contents for industrial fire safety
    • Raw blend stock for further halogenation or formulation

    4. Sourcing Agent in Advanced Polymer Modification

    Producers of specialty fluorinated polymers and copolymers rely on this chemical as a sourcing agent for introducing short-chain trifluoropropyl units during free-radical or ionic polymerization. Its precise introduction influences polymer flexibility, chemical inertness, and dielectric properties. The addition occurs under regulated conditions, using specific initiators and temperature programs. Residual monomer control and solvent recovery form part of standard QC, as does the analysis of final polymer composition by NMR and FTIR techniques.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical sites
    • RoHS 3 (Directive 2015/863/EU) for electronics-related polymers
    • ASTM D3839 Standard Practice for Quality Polymer Sourcing
    • REACH Annex XVII SVHC restrictions where applicable

    Typical usage ratio

    • 2–10% by weight in monomer feed, tailored for performance target
    • Adjustment guided by melt index or dielectric property requirements
    • Pilot study ratios determined prior to full-scale implementation

    Downstream process integration

    • Mixed with base monomers at feedstock charging stage
    • Polymerization under controlled temperature and pressure
    • Off-gas and residual monomer captured via abatement units
    • Resulting copolymers pelletized or compounded for sale

    Final product types

    • Fluorinated elastomers for chemical-resistant gaskets
    • Insulating materials for advanced cable sheathing
    • Fluoropolymer films for electronic packaging
    • High-durability coating materials for industrial application

    5. Precursor for Specialty Fluorinated Solvents

    Chemical formulators utilize this substance as a starting material in the creation of specific fluorinated solvents tailored for electronics cleaning, dry etching, and precision degreasing. The downstream process includes sequential substitution and hydrodehalogenation, refining the product through distillation to meet high-purity specifications. Site operators rigorously track batch records for each solvent lot and maintain documentation for exposure and emissions control.

    Industry compliance standards

    • US EPA 40 CFR Part 63 (NESHAP) for solvent emission
    • OSHA 29 CFR 1910 for workplace chemical handling
    • SEMATECH industry guidance for electronics processing chemicals
    • ISO 16100:2010 for solvent performance testing

    Typical usage ratio

    • 0.95 – 1.2 equivalents charged relative to transformation target
    • Solvent yield varies by final boiling point cut and purity requirements (typically 8–20% recovered mass yield per batch)

    Downstream process integration

    • Charged to halogenation system during first reactant blend
    • Crude product purified by multi-stage fractional distillation
    • Final solvent passed through activated carbon to meet residue specs
    • Quality assurance by GC and solvent-specific conductivity tests

    Final product types

    • High-purity fluorinated solvents for semiconductor manufacturing
    • Precision degreasing agents for metallic components
    • Nonflammable cleaning solutions for optical equipment
    • Photoresist-removal chemicals for microelectronics
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