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Pentamethyl Dinitrobenzene

    • Product Name Pentamethyl Dinitrobenzene
    • Alias Sym-Trinitrobenzene
    • Einecs 254-762-8
    • 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
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    Specifications

    HS Code

    883903

    Chemical Name Pentamethyl Dinitrobenzene
    Molecular Formula C11H16N2O4
    Molecular Weight 240.26 g/mol
    Appearance Yellow to orange crystalline solid
    Melting Point Approximately 120-130°C
    Boiling Point Decomposes before boiling
    Solubility In Water Poorly soluble
    Density Approx. 1.18 g/cm3
    Cas Number 618-78-2
    Functional Groups Methyl, Nitro
    Odor Characteristic aromatic odor
    Stability Stable under recommended storage conditions
    Hazards May be harmful if swallowed or inhaled
    Storage Conditions Store in a cool, dry, well-ventilated area

    As an accredited Pentamethyl Dinitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of Pentamethyl Dinitrobenzene supplied in a sealed amber glass bottle with hazard labeling and tamper-evident cap for safety.
    Shipping Pentamethyl Dinitrobenzene should be shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard information. Transport under ambient temperature, away from heat, ignition sources, and incompatible substances. Follow all local, national, and international regulations for hazardous materials. Ensure carriers are trained for chemical emergencies, and provide accompanying Material Safety Data Sheets (MSDS).
    Storage Pentamethyl dinitrobenzene should be stored in a tightly sealed container, away from direct sunlight and sources of heat or ignition. Keep it in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizers and acids. Clearly label the container, and ensure it is placed in a designated chemical storage cabinet for organics or nitro compounds.
    Application of Pentamethyl Dinitrobenzene

    Applications of Pentamethyl Dinitrobenzene in Industrial Manufacturing

    Pentamethyl Dinitrobenzene serves specialized roles in several highly controlled industrial sectors. As an original manufacturer, we support downstream users with precise material characteristics and production knowledge. Below, we detail its established B2B applications by distinct industry process, with specific notes on compliance, formulation, integration, and final product output.

    1. Energetic Materials Synthesis for Propellant Formulations

    Manufacturers in the defense and aerospace sector utilize pentamethyl dinitrobenzene as a targeted intermediate in the fine synthesis of energetic materials, specifically for melt-cast and composite propellants. Its specific nitration profile and methyl substitution pattern aid in controlling the detonation velocity and thermal stability during batch synthesis. Integration occurs at an early stage of propellant matrix preparation, where precise solvent and temperature conditions ensure complete integration and minimize risk of hot spots in the finished energetic mixtures. Final propellants using this intermediate undergo rigorous crystallization, granulation, and solvent removal processes before QA release.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods – Manual of Tests and Criteria
    • EU Regulation (EC) No 1907/2006 (REACH) for chemical safety assessment
    • US CFR Title 49 – Hazardous Materials Regulations
    • STANAG 4170 (NATO standard for explosives)

    Typical usage ratio

    • 5%–20% by weight in propellant matrix; ratios depend on performance requirements and environmental conditions
    • Adjusted by thermal and rheological testing results during pilot formulation

    Downstream process integration

    • Charged into high-shear blending equipment post-initial binder melt
    • Added before phlegmatizer to control energetic properties
    • Integrated at solvent mixing phase in slurry process for composite propellants
    • Subjected to controlled cooling and granulation for uniform particle size

    Final product types

    • Solid rocket propellants
    • Insensitive munitions compositions
    • Pyrotechnic delay charges
    • Military and civilian rocket motor grains

    2. Custom Synthesis of Aromatic Intermediates for High-Performance Dyes

    Chemical companies in the specialty dye sector employ pentamethyl dinitrobenzene as a crucial benzenoid scaffold for direct nitration and downstream amination reactions. This approach enables the creation of advanced azo and nitro dyes with tailored chromatic and fastness properties, preferred for technical textiles and nonfood packaging. Material intake is closely monitored for moisture and residual acidity, as these directly impact yield and dye purity. Process steps span from nitro reduction to diazotization and coupling, under inert atmosphere and at strictly controlled temperatures.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile chemical safety)
    • REACH Annex XVII – Restrictions on certain azo colorants
    • ZDHC Chemicals Management System
    • ISO 105-B02:2014 (color fastness to light—textiles)

    Typical usage ratio

    • 10%–35% by molar proportion in dye intermediate blends
    • Ratio varies for chromophore intensity and shade-matching in custom blends

    Downstream process integration

    • Nitration occurs in multi-stage reactors under continuous monitoring
    • Reductive amination is performed as second-stage modification
    • Diazotization and azo coupling are carried out in jacketed glass-lined vessels
    • Crude dye is isolated, washed, and dried before refining and blending

    Final product types

    • Disperse dyes for polyester fibers
    • High-performance pigment precursors
    • Nitro azo dyes for industrial imaging toners
    • Color masterbatches for plastics applications

    3. Antioxidant Synthesis for Synthetic Lubricant Additives

    Formulators in the lubricant industry incorporate pentamethyl dinitrobenzene as an aromatic base for manufacturing custom phenolic and aminic antioxidants. Through controlled hydrogenation and alkylation reactions, the resulting antioxidants exhibit excellent resistance to thermal and oxidative degradation, essential for long-life lubricants in turbines and compressors. The raw material is introduced at the initial synthesis phase, followed by multi-stage purification to yield high-purity stabilizers compatible with ester- and PAO-based oils. Finished additives undergo routine batch testing for effectiveness and compatibility before large-scale blending into commercial lubricant packages.

    Industry compliance standards

    • ASTM D3241 (thermal stability of turbine oils)
    • API Base Oil Interchange Guidelines
    • European EELQMS (Lubricant Quality System)
    • ISO 9001:2015 certification for process management

    Typical usage ratio

    • 0.5%–3% by weight of finished antioxidant concentrate
    • Adjusted based on OEM-specific oxidation requirements and baseline oil reactivity

    Downstream process integration

    • Base chemical charged into alkylation reactor with controlled temperature and pressure
    • Hydrogenation catalysis performed under inert atmosphere
    • Purified concentrate blended into finished lubricant formulations in centralized bulk mixers
    • Product undergoes stability testing before distribution

    Final product types

    • Industrial turbine and compressor lubricants
    • Automotive synthetic engine oils
    • Hydraulic oil additive packages
    • Industrial grease formulations

    4. Building-Block Intermediate for Agrochemical Synthesis

    Leading agrochemical manufacturers use pentamethyl dinitrobenzene as a specialized building-block for the synthesis of selective herbicide and insecticide actives, leveraging its methylated and nitrated aromatic structure. The compound enters multi-step transformations including nucleophilic substitution and directed ortho-metalation, enabling precise placement of additional functional groups crucial for bioactivity. Stringent quality assurance starts with incoming raw analysis for trace by-products and chiral purity, as downstream requirements for crop protection agents demand controlled impurity profiles and regulatory traceability.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025:2017 laboratory standards for analytical testing
    • EPA FIFRA (US Federal Insecticide, Fungicide, and Rodenticide Act)
    • EU Regulation (EC) No 1107/2009 for placing plant protection products on the market

    Typical usage ratio

    • 15%–28% by molar ratio as a starting material in active ingredient synthesis
    • Adjusted for yield, crop selectivity, and environmental fate results

    Downstream process integration

    • Introduced during initial condensation or substitution steps of active ingredient synthesis
    • Reacted with specific reagents to form final bioactive intermediates
    • Material purification and crystallization for analytical certification
    • Further formulated with adjuvants and carriers by downstream formulators

    Final product types

    • Selective broadleaf herbicides
    • Systemic insecticide actives
    • Pre-emergent seed treatment compounds
    • Specialty crop protection solutions

    5. Research Intermediate for Advanced Performance Polymers

    Polymer manufacturers and R&D institutes employ pentamethyl dinitrobenzene as a multifunctional intermediate to create high-thermal-stability polyarylenes and specialty copolymers for electronic applications. The molecule’s electron-rich aromatic core and multiple methyl groups result in unique chain flexibility and dielectric properties, favored for insulating films and high-temperature components. Process integration typically involves nucleophilic aromatic substitution polymerizations in polar aprotic media, combined with custom monomer feeds and specific molecular weight targets. Consistent monitoring of residual nitro content and molecular distribution secures downstream process control and application-specific film properties.

    Industry compliance standards

    • IEC 60216 (Electrical insulating materials – thermal endurance properties)
    • RoHS 2011/65/EU Directive (hazardous substances in electronics)
    • ISO 6721 (Determination of dynamic mechanical properties of polymers)
    • UL 94 (Polymer flammability rating)

    Typical usage ratio

    • 2%–18% by mol as co-monomer or chain modifier, tailored to thermal or physical property targets
    • Adjusted during process scale-up via pilot trials and QC analysis

    Downstream process integration

    • Charged during the prepolymerization step with other aromatic dihalides or nucleophiles
    • Polymerization carried out under controlled nitrogen atmosphere at raised temperature
    • In-process control monitors for complete conversion and molecular weight distribution
    • Finished polymer is granulated or cast into films for further processing

    Final product types

    • High-temperature electrical insulation films
    • Semiconductor encapsulant resins
    • Printed circuit board substrates
    • Structural composites for electronic housings
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