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5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole

    • Product Name 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole
    • Alias TFPT
    • Einecs 695-178-8
    • 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

    197712

    Chemical Name 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole
    Cas Number 18039-42-4
    Molecular Formula C8H5F3N4
    Molecular Weight 214.15
    Appearance White to off-white solid
    Melting Point 139-142°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, in a dry place
    Smiles FC(F)(F)c1ccc(cc1)c2nnn[nH]2
    Inchikey CYYNUYOXWKEKAD-UHFFFAOYSA-N
    Synonyms 4-(Trifluoromethyl)phenyl-1H-tetrazole

    As an accredited 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 10g amber glass bottle with a secure screw cap, labeled with chemical name, hazard symbols, lot number, and storage conditions.
    Shipping 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is transported as a hazardous material, following all regulatory guidelines for chemical safety. Ensure proper labeling and use secondary containment to prevent leakage during transit. Store in a cool, dry environment upon arrival.
    Storage Store 5-[4-(Trifluoromethyl)phenyl]-1H-tetrazole in a tightly sealed container under cool, dry conditions, away from direct sunlight and sources of ignition. Keep it in a well-ventilated area, segregated from incompatible substances such as oxidizing agents and strong acids. Use gloves and eye protection when handling. Ensure proper chemical labeling and restrict access to trained personnel.
    Application of 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole

    Applications of 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole in Industrial Manufacturing

    As a direct chemical raw material manufacturer with global clients, we deliver 5-[4-(Trifluoromethyl)Phenyl]-1H-Tetrazole to key downstream industries where its structural features and reactivity are indispensable for advanced synthesis, safety system innovation, and pharmaceutical intermediate production. Below, we outline specialized industrial applications, each detailing regulatory adherence, formulation practices, integration into downstream protocols, and resulting finished goods manufactured by our clients worldwide.

    1. Synthesis of Energetic Materials for Airbag Gas Generators

    Automotive safety component suppliers integrate this tetrazole derivative into energetic formulations for airbag inflators due to its favorable gas-yield efficiency, thermal stability, and low-toxic byproducts. Its precise function as a nitrogen donor enables manufacturers to control inflation dynamics and side-product minimization, while supporting cost-effective, scalable production runs.

    Industry compliance standards

    • ISO 26262 Functional Safety Standard
    • United Nations ECE R94/R95 Automotive Safety Regulations
    • National Highway Traffic Safety Administration (NHTSA) Specifications
    • Automotive Industry Quality Management (IATF 16949)

    Typical usage ratio

    • Usage rates typically range from 1.5% to 5% by weight in the azide-free generant blend, adjustable based on required gas output, inflator volume, and desired burn profile.

    Downstream process integration

    • Blending into generant formulations in high-shear mixers prior to pelletization
    • Tableting and incorporation into airbag inflator assemblies under dust-controlled conditions
    • Thermal and pressure-testing performed before final device manufacturing

    Final product types

    • Driver and passenger airbag modules
    • Side curtain airbag inflators
    • Seatbelt pretensioner gas generators
    • State-of-the-art azide-free automotive inflator systems

    2. High-Performance Pharmaceutical Intermediate for Novel API Synthesis

    Leading pharmaceutical manufacturers select this material as a critical heterocyclic building block in the synthesis of select investigational and approved active pharmaceutical ingredients, particularly those requiring trifluoromethylated aromatic motifs for metabolic stability and bioavailability improvement. Its usage is closely defined by strict process and quality demands owing to target API purity and regulatory regimes.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) per 21 CFR Parts 210/211
    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP–NF and European Pharmacopoeia monographs for intermediates
    • REACH Registration for substances used in pharmaceutical synthesis

    Typical usage ratio

    • Applied at 0.8–2.2 molar equivalents relative to coupling partner, specifically controlled by route of synthesis and target yield optimization; precise charge determined by pilot batch titration and validated process transfer.

    Downstream process integration

    • Used directly in heterocycle-forming condensation, click chemistry, and nucleophilic substitution for intermediate construction
    • Integration into semi-continuous reactor processes for multi-step API synthesis
    • Purification by preparative chromatography and inline HPLC verification

    Final product types

    • Investigational cancer therapeutics with trifluoromethyl functionality
    • CNS-active compounds under clinical development
    • Marketed antiviral drug intermediates
    • Small-molecule pharmaceutical building blocks supplied for CDMO operations

    3. Click Chemistry Reagent for Advanced Polymer and Material Synthesis

    Specialty polymer and performance material manufacturers rely on this tetrazole for azide–alkyne cycloaddition (“click”) reactions targeting functionalized polymers, coatings, and diagnostics. Its unique electronic and steric profile allows for clean, high-yielding triazole ring formation with minimal side reactions, supporting production of advanced materials with tunable surface or bulk properties.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • EU REACH Regulation (EC) No. 1907/2006 for monomer and additive handling
    • ANSI/ASTM polymer labeling and safety standards
    • OECD Guidelines for Testing of Chemicals (if product exported as polymer additive)

    Typical usage ratio

    • Loading typically at 0.5–4 wt% in prepolymer or surface modification mixtures; specific ratio selected by desired functional group density and post-polymerization analysis.

    Downstream process integration

    • Precursor activation prior to click addition in solution-phase synthesis or bulk melt blending
    • Inline flow chemistry setups for continuous modification of polymer chains
    • Post-reaction purification using solvent extraction or membrane filtration

    Final product types

    • Biosensor surface coatings
    • Functionalized polymer resins for photonics
    • Diagnostic microarray substrates
    • High-performance adhesives for electronics

    4. Custom Ligand Synthesis for Metal-Catalyzed Cross-Coupling Reactions

    Catalyst technology companies and specialty reagent developers apply this compound for ligand framework construction in homogeneous catalysis, notably for forming stable, electron-rich tetrazole–metal complexes to enhance catalytic turnover, selectivity, and handling in industrial-scale cross-coupling processes spanning fine chemicals and agrochemical intermediates.

    Industry compliance standards

    • Responsible Care Global Charter for catalyst manufacturing
    • ISO 14001 Environmental Management Systems for chemical processing
    • SHE (Safety, Health, Environment) guidelines for metal handling
    • Custom catalyst quality control (internal and customer-defined QC protocols)

    Typical usage ratio

    • Ligand charge typically in 0.02–0.2 equivalents per metal center, adjusted by substrate/catalyst ratio and turnover frequency requirements for each specific process.

    Downstream process integration

    • Employed in ligand-exchange stages during palladium, copper, or nickel catalyst synthesis
    • Purification through crystallization or chromatography prior to catalyst complexation
    • Incorporation into batch or continuous-flow catalytic processes for cross-coupling reactions

    Final product types

    • Fine chemical intermediates for agrochemical synthesis
    • Electron-rich metal catalysts for pharmaceutical synthesis
    • Custom cross-coupling catalyst kits for chemical R&D
    • Advanced catalyst formulations for industrial process scale-up

    5. Light-Sensitive Material Component in Laser Igniter and Safety Devices

    Manufacturers of industrial and aerospace pyrotechnic devices incorporate this tetrazole derivative for its rapid photothermal decomposition and high energy density, supporting precision ignition in equipment such as electronic initiators or laser igniters. Stringent regulatory and QMS oversight guide its selection and qualification in sensitive applications.

    Industry compliance standards

    • ATEX EU Directives (2014/34/EU) for explosive atmospheres
    • CEN/TS 13763-27 for pyrotechnic and initiator device testing
    • EN ISO 9001:2015 for aerospace device manufacturing
    • NFPA 1124 for manufacture, storage, and handling of pyrotechnics

    Typical usage ratio

    • Blend proportions range from 3% to 8% by weight in composite initiator charge, determined by ignition voltage, heat flux, and laser wavelength compatibility.

    Downstream process integration

    • Weighing and high-shear blending with oxidizers and binders in inert-atmosphere chambers
    • Compression molding or filling into micro-initiator housings under strict environmental monitoring
    • Performance validated through laser ignition and ignition delay time measurements

    Final product types

    • Laser-based initiator pellets
    • Safety fuse heads for aerospace
    • Electronic detonator assemblies for mining and tunneling
    • Photo-initiators for microactuator launch devices
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