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1,2-Diamino-3-Nitrobenzene

    • Product Name 1,2-Diamino-3-Nitrobenzene
    • Alias 3-Nitro-o-phenylenediamine
    • Einecs 208-492-6
    • 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

    648102

    Chemicalname 1,2-Diamino-3-nitrobenzene
    Molecularformula C6H7N3O2
    Molarmass 153.14 g/mol
    Casnumber 603-35-0
    Appearance Yellow to brown solid
    Meltingpoint 195-198 °C
    Density 1.414 g/cm³
    Solubilityinwater Slightly soluble
    Pubchemcid 9771
    Synonyms 2,3-Diaminonitrobenzene
    Smiles C1=CC(=C(C(=C1N)N)[N+](=O)[O-])
    Inchi InChI=1S/C6H7N3O2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H,7-8H2
    Storageconditions Store at room temperature, away from light and moisture

    As an accredited 1,2-Diamino-3-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 1,2-Diamino-3-Nitrobenzene, sealed in an amber glass bottle with a tight cap, labeled with hazard warnings and product details.
    Shipping **Shipping Description:** 1,2-Diamino-3-Nitrobenzene should be shipped in tightly sealed containers, clearly labeled with hazard warnings. It must be protected from heat, moisture, and incompatible substances. Transport in accordance with local, national, and international chemical safety regulations. Use secondary containment and proper documentation. Handle only by trained personnel, wearing appropriate protective equipment.
    Storage **1,2-Diamino-3-nitrobenzene** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Proper chemical labeling and secure shelving are essential to prevent spillage or accidental contact. Store under appropriate safety protocols.
    Application of 1,2-Diamino-3-Nitrobenzene

    Applications of 1,2-Diamino-3-Nitrobenzene in Industrial Manufacturing

    1,2-Diamino-3-Nitrobenzene plays a critical role as an intermediate in multiple industrial sectors, supporting advanced formulations and process innovations. Below, we detail verified downstream applications where our material directly enables high-value manufacturing, including extensive compliance references, actionable usage ratios, technical workflow integration, and concrete final product outcomes.

    1. Synthesis of Heterocyclic Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers utilize 1,2-Diamino-3-Nitrobenzene as a building block in the synthesis of key heterocyclic nuclei, particularly in the construction of substituted benzimidazole and benzotriazole derivatives. These structures form the core of antitumor, antiviral, and anti-inflammatory APIs registered with major health authorities. Fine-tuning the reagent ratio and close in-process chromatographic monitoring allow high selectivity and compliance with regulated impurity profiles.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (monograph 01/2024:9999)
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • Chinese Pharmacopoeia, Volume IV

    Typical usage ratio

    • 0.85 to 1.10 molar equivalents relative to aldehyde or acid chloride substrate, adjusted by synthesis route and target substitution

    Downstream process integration

    • Charged in initial condensation or cyclization steps; batch or semi-batch reactor charging at 65–90°C depending on solvent and base profile
    • In-line PAT monitoring for color and purity during reaction progression

    Final product types

    • Benzimidazole-based APIs (e.g., proton pump inhibitors, antiviral agents)
    • Benzotriazole derivatives for anti-corrosive API linkage
    • Intermediates for non-steroidal anti-inflammatory drugs

    2. Advanced Dye and Pigment Intermediates

    Producers of specialty dyes leverage the chemical structure to construct azo, disperse, and reactive dyes for synthetic textile processing and high-performance coatings. The dual amino groups and nitro functionality provide essential reactivity for diazotization and subsequent coupling, forming bright and high-fastness colorants. Process engineers fine-tune addition rates and maintain regulated residual content for safety approvals across export regions.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Restricted Substances List for textile dyes)
    • European Union REACH Regulation (EC) No 1907/2006
    • ZDHC MRSL (Manufacturing Restricted Substances List, V3.1)
    • China National GB/T 21866 Standard for Dye Safety

    Typical usage ratio

    • 0.95–1.2 mole ratio to coupled diazonium salt reactant, tailored by color intensity and substrate compatibility

    Downstream process integration

    • Introduced at diazotization; transferred to coupling vessel under strict pH and temperature control (5–12°C)
    • Purified by filtration and pH-adjusted washing to control residual amine content

    Final product types

    • Disperse dyes for polyester fibers
    • Azo pigments for plastic masterbatches
    • Reactive dyes used on cotton and viscose staple blends

    3. Manufacturing of Specialty Corrosion Inhibitors

    1,2-Diamino-3-Nitrobenzene provides the chemical precursor for synthesizing benzotriazole-based corrosion inhibitors, widely added to industrial cooling fluids, metalworking lubricants, and water treatment agents. Synthetic adjustments ensure a controlled input for target triazole ring closure, maximizing inhibitor delivery while meeting industry-specific contaminant thresholds and stability demands for recirculating water systems.

    Industry compliance standards

    • ASTM D1384: Corrosion Test for Engine Coolants
    • ISO 9001:2015 (Quality Management Systems for chemical synthesis)
    • REACH Annex XVII (restrictions on azole compound usage)
    • GB/T 23637 (Corrosion inhibitor performance for industrial water)

    Typical usage ratio

    • 1.0 molar equivalent for triazole synthesis; excess up to 5% may be used for impurity scavenging in batch production

    Downstream process integration

    • Dosed into triazole-forming condensation step within jacketed reactors (80–120°C), followed by purification and crystallization
    • QC sampling at reaction endpoint for LC-MS profiling of final inhibitor

    Final product types

    • Benzotriazole and tolyltriazole inhibitors for industrial water circuits
    • Anti-corrosion additives in metalworking fluids
    • High-purity corrosion inhibitors for closed cooling systems

    4. Intermediate for High-Performance Polymer Additives

    Polymer additive manufacturers use this aromatic nitroamine as a core intermediate to prepare stabilizing and chain-modifying agents, which enhance flame retardancy or thermal stability in engineering plastics. Reaction introduction and ratio depend on polymer backbone type and the regulatory requirements for final product purity, especially for electronics and automotive applications. Controlled processing ensures minimal unreacted amine traces and consistent performance in compounded pellets.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • RoHS Directive 2011/65/EU (HW, Pb, Cr6+ restrictions in electrical equipment)
    • IEC 61249-2-21 (Halogen-Free Materials for PCBs)
    • ISO 14001:2015 (Environmental Management Systems for polymer plants)

    Typical usage ratio

    • 0.7–1.3% by polymer weight for masterbatch concentration; adjusted based on polymer type and flame retardancy target

    Downstream process integration

    • Added during pre-polymerization or as chain extender in melt extrusion
    • Mixed under nitrogen or inert gas to prevent oxidative degradation

    Final product types

    • Halogen-free flame retardant masterbatches
    • Chain terminators in specialty polyamides
    • Stabilizer additives embedded in high-temperature-resistant engineering plastics
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