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5-(4-Nitro-Phenyl)-2H-Tetrazole

    • Product Name 5-(4-Nitro-Phenyl)-2H-Tetrazole
    • Alias NPT
    • Einecs 261-093-0
    • 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

    748083

    Chemical Name 5-(4-Nitro-Phenyl)-2H-Tetrazole
    Cas Number 10114-59-3
    Molecular Formula C7H5N5O2
    Molecular Weight 191.15 g/mol
    Appearance Yellow to orange solid
    Melting Point 222-224 °C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%

    As an accredited 5-(4-Nitro-Phenyl)-2H-Tetrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 5-(4-Nitro-Phenyl)-2H-Tetrazole (10g) is a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping Shipping of 5-(4-Nitro-Phenyl)-2H-Tetrazole requires secure, approved packaging in accordance with local and international hazardous materials regulations. Due to its energetic and potentially explosive nature, it must be handled by trained personnel and shipped with clear labeling, documentation, and may require temperature control and restricted transportation methods.
    Storage 5-(4-Nitro-Phenyl)-2H-Tetrazole should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep the container tightly closed and protected from direct sunlight. Store separately from incompatible materials such as strong acids, bases, and reducing agents. Handle with caution, as this compound may be sensitive or potentially explosive under certain conditions.
    Application of 5-(4-Nitro-Phenyl)-2H-Tetrazole

    Applications of 5-(4-Nitro-Phenyl)-2H-Tetrazole in Industrial Manufacturing

    5-(4-Nitro-Phenyl)-2H-Tetrazole has become a key intermediate and energetic compound used across several specialized industrial sectors. Our manufacturing experience and repeat supply to regulated manufacturers support applications in pyrotechnics, initiator chemicals, pharmaceutical synthesis, and energetic device assembly. Below we provide a detailed overview for each authenticated downstream field, guiding technical decision makers through compliance, formulation, process inclusion, and end products.

    1. Initiating Compounds for Primary Explosives Manufacturing

    This compound is widely incorporated into lead-free primary explosive design due to its favorable energetic profile and thermal stability. R&D and production teams in explosive manufacturing use 5-(4-Nitro-Phenyl)-2H-Tetrazole during the compounding of non-azide primary charges for initiator assemblies, developing safer and environmentally responsible detonating devices. Our product enables technical flexibility for direct substitution or co-formulation with other energetic synergists.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods – Manual of Tests and Criteria (UN Orange Book)
    • REACH Regulation (EC) No 1907/2006
    • US Bureau of Alcohol, Tobacco, Firearms, and Explosives (ATF) Regulation 27 CFR Part 555
    • EU Explosives Precursors Regulation (EU) 2019/1148

    Typical usage ratio

    • 10 – 25% in composite lead-free priming mixes, fine-tuned for ignition sensitivity and stability based on end device sensitivity class and environmental storage requirements.

    Downstream process integration

    • The compound is wet-mixed with oxidizers, metallic fuel components, and stabilizers during final charge slurry preparation. Operators typically add it after pH adjustment to guarantee homogeneous incorporation and prevent premature decomposition. The wet mix then undergoes granulation, drying, and subsequent pressing or casting into detonator assemblies.

    Final product types

    • Electric detonators (e.g., automotive airbag initiators, blasting caps)
    • Pyrotechnic initiators for military and civilian applications
    • Lead-free percussion primers
    • Energy transfer fuses for industrial safe igniters

    2. Gas Generator and Airbag System Formulation

    Automotive and aerospace suppliers rely on 5-(4-Nitro-Phenyl)-2H-Tetrazole as a source of non-toxic, high-gas-output propellant charges in pyrotechnic gas generators. Gas generator module manufacturers formulate this raw material with metallic reducers and gas-yielding oxidizers to achieve controlled burn profiles and inflation rates for occupant restraint systems. Rigorous incoming QC and traceability to batch source are standard for program audits.

    Industry compliance standards

    • ISO 19014-1:2018 (Safety of pyrotechnic articles - General requirements for airbags and pre-tensioner systems)
    • IATF 16949:2016 Automotive Quality Management System
    • FMVSS No. 208 (US Federal Motor Vehicle Safety Standards – Occupant Crash Protection)
    • JSS 0259-09 (India Defense Standards for energetic materials)

    Typical usage ratio

    • 18 – 28 wt% within total gas generant charge, with the specific formulation balanced according to required chamber pressure and desired gas evolution profile for the device application.

    Downstream process integration

    • Batch-reacted directly into primary gas generant doughs following metered addition of oxidizer (e.g., potassium nitrate) powders. The blended mix undergoes controlled extrusion, pelletization, and precise drying before module assembly. Automated weighing and traceback records ensure compliance to PPAP and full lot recall capabilities.

    Final product types

    • Automotive airbag inflators
    • Seat belt pre-tensioner gas generators
    • Micro gas generator modules for industrial safety equipment
    • Emergency evacuation slide inflators

    3. Synthesis Intermediate for High Performance Energetic Materials

    Chemical synthesis plants use 5-(4-Nitro-Phenyl)-2H-Tetrazole as a core building block during multi-step synthesis of tetrazole-based energetic compounds. These downstream molecules see use in performance explosive compositions and research into next-generation insensitive munitions for defense. Manufacturers require strict source documentation and impurity control to guarantee batch-to-batch molecular consistency for subsequent synthetic reactions.

    Industry compliance standards

    • International Traffic in Arms Regulations (ITAR, 22 CFR 120-130)
    • EU Regulation (EC) No 428/2009 (Dual-Use Items)
    • ISO 9001:2015 Quality Management for chemical intermediates
    • GMP (as applied to non-pharmaceutical, high-purity energetic intermediates)

    Typical usage ratio

    • Stoichiometric equivalents based on desired molecular ratio in cycloaddition or ring-substitution reactions; typically 1.0–2.5 molar equivalents per target energetic molecule synthesized.

    Downstream process integration

    • The compound is dissolved or suspended in anhydrous solvent systems and reacts with nitrating, alkylating, or ring-contracting reagents. All operations take place in explosion-proof synthesis blocks, with QC checkpoints after both reaction and purification before transfer to subsequent synthetic steps such as chlorination or additional azole ring fusion.

    Final product types

    • Nitramino-tetrazole explosives (e.g., used in military booster charges)
    • Insensitive munitions formulation precursors
    • Specialized detonator charge precursors for oil & gas perforation
    • Energetic binders for composite solid propellants

    4. Research Chemical for Laboratory Pyrotechnics and Safety Detonators

    Universities, government research institutes, and product development centers utilize 5-(4-Nitro-Phenyl)-2H-Tetrazole when developing new energetic formulations with controlled ignition and decomposition characteristics. The material supports experimental work on reduced-toxicity, high-yield gas output, and temperature-adapted ignitor systems. Strict laboratory safety review and regulatory reporting are required for all research orders shipped from our plant.

    Industry compliance standards

    • OSHA Laboratory Safety Standards (29 CFR 1910.1450, US)
    • International Air Transport Association (IATA) Dangerous Goods Regulations for shipping
    • Institutional review and permitting for handling energetic materials
    • ISO/IEC 17025:2017 (General requirements for testing and calibration laboratories)

    Typical usage ratio

    • 0.1 – 2 g per bench-scale experiment; up to 50 g for pilot-scale safety detonator work. Dosing is adapted to experimental requirements with documented scale adjustments and chemical compatibility review.

    Downstream process integration

    • Material enters at the formulation stage, combined with candidate oxidizers or binders in small-scale mixers or micro-reactors. After composition, samples are pressed or cast into test articles and subjected to instrumented sensitivity and decomposition studies.

    Final product types

    • Lab-developed test detonators and initiator compositions
    • Proof-of-concept airbag and propellant charge samples
    • Pyrotechnic demonstration samples for ignition property analysis
    • Experimental gas generating charges for automotive and aerospace R&D
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