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4-Bromo-2-Nitrobenzaldehyde

    • Product Name 4-Bromo-2-Nitrobenzaldehyde
    • Alias 4-Bromo-2-nitrobenzalaldehyde
    • Einecs 410-340-5
    • 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

    584008

    Chemicalname 4-Bromo-2-nitrobenzaldehyde
    Molecularformula C7H4BrNO3
    Molecularweight 230.02 g/mol
    Casnumber 50890-83-0
    Appearance Light yellow to orange solid
    Meltingpoint 120-124°C
    Solubility Slightly soluble in organic solvents, insoluble in water
    Density 1.80 g/cm³ (approximate)
    Purity Typically ≥98%
    Smiles C1=CC(=C(C=C1Br)[N+](=O)[O-])C=O
    Inchi InChI=1S/C7H4BrNO3/c8-5-1-2-7(6(3-5)9(11)12)4-10/h1-4H
    Synonyms 4-Bromo-2-nitrobenzaldehyde; p-Bromo-o-nitrobenzaldehyde
    Storage Store at room temperature, keep container tightly closed

    As an accredited 4-Bromo-2-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Bromo-2-Nitrobenzaldehyde, securely sealed with labeling for chemical identification and hazard information.
    Shipping 4-Bromo-2-Nitrobenzaldehyde is shipped in tightly sealed containers to prevent exposure to air and moisture. It is packaged according to chemical safety regulations, with clear hazard labeling. The shipment follows all relevant transportation guidelines for hazardous materials, ensuring safe handling and storage during transit to the designated destination.
    Storage 4-Bromo-2-nitrobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances like strong oxidizers and reducing agents. Keep the chemical away from sources of ignition and moisture. Properly label the container, and ensure appropriate protection from physical damage. Store according to standard laboratory safety protocols.
    Application of 4-Bromo-2-Nitrobenzaldehyde

    Applications of 4-Bromo-2-Nitrobenzaldehyde in Industrial Manufacturing

    Our company supplies 4-Bromo-2-Nitrobenzaldehyde for use in specialized downstream sectors, supported by years of formulation and process integration experience. The following application fields represent the material's established role across global industries. Each section details regulatory standards, inclusion ratios, processing stages, and the relevant manufactured goods.

    1. Pharmaceutical Intermediate for API Synthesis

    4-Bromo-2-Nitrobenzaldehyde functions as a crucial intermediate in the manufacture of specific active pharmaceutical ingredients (APIs) that require a brominated nitrobenzaldehyde core. Its reactivity allows targeted modifications during multi-step synthesis routes, which are commonly applied in the development of anti-infective or anticancer compounds. Commercial API production demands rigorous quality control and batch traceability throughout processing, with this intermediate typically undergoing further condensation or reduction reactions to construct the desired molecular scaffolds.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) requirements for starting materials
    • United States Pharmacopeia (USP) reference for intermediates
    • FDA CFR Title 21 for traceability and impurity profiling

    Typical usage ratio

    • Applied at 0.8–1.2 molar equivalents relative to target substrate, with adjustment based on molecular weight and target API yield

    Downstream process integration

    • Introduced during the initial or mid-stage condensation step in the synthesis of heterocyclic precursors or direct functionalization of aromatic rings
    • Pre-purification may involve recrystallization, followed by reaction in inert atmospheres with controlled temperature profiles

    Final product types

    • Intermediates leading to third- and fourth-generation cephalosporin antibiotics
    • Precursor molecules for selective kinase inhibitors for oncology applications
    • Specialty anti-tubercular agent intermediates

    2. Building Block in Agrochemical Synthesis

    Formulators in the agrochemical sector use this material primarily for the synthesis of specialty crop protection agents, where nitro and bromo-substituted aromatics form part of fungicide or herbicide active molecules. Its unique electronic properties provide required reactivity in subsequent substitution or reduction steps, enabling development of agents with targeted biological profiles for regulated crop markets.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • FAO/WHO Specifications for Plant Protection Products
    • REACH (Regulation EC No 1907/2006) substance registration for European use
    • Chinese ICAMA registration protocols for active ingredient intermediates

    Typical usage ratio

    • Standard 1.0–1.5 molar equivalents relative to downstream synthesis targets; ratios may be increased for higher-yield batch processes or tailored molecular designs

    Downstream process integration

    • Employed during the core aromatic modification, typically in nitration, reduction or Suzuki-type couplings to build up the active backbone
    • Material undergoes chlorination, methylation, or cyclization depending on the final agrochemical structure required

    Final product types

    • Triazole-based fungicide intermediates
    • Pyrimidine or imidazole herbicide intermediates
    • Precursors for insecticide actives targeting resistant pest populations

    3. Fine Chemical Intermediate for Dye Synthesis

    Chemical dye manufacturers incorporate 4-Bromo-2-Nitrobenzaldehyde into synthetic routes for specialty colorants where high-purity aromatic aldehydes contribute to chromophoric structures. These intermediates participate in controlled condensations, acylations, and azo-coupling steps to generate advanced dyes that meet regulatory and colorfastness specifications for industrial and textile applications. Consistent aldehyde content is monitored batchwise to support reproducible dye qualities and compliance with export quality standards.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for restricted substances in dyestuffs
    • ZDHC Manufacturing Restricted Substances List for textile input chemicals
    • Global Organic Textile Standard (GOTS) requirements for dye intermediates
    • China Textile Certification (GB/T 23344-2009, AATCC 61 for color fastness)

    Typical usage ratio

    • Applied at 0.5–1.3 weight percent of total batch, with variations determined by the specific dye structure being targeted and batch scale

    Downstream process integration

    • Introduced during the formation of azo or anthraquinone dye intermediates; may be subjected to condensation with amines or phenols in solvent systems
    • Careful pH monitoring and temperature control to prevent byproduct formation and ensure maximum incorporation into the chromophore skeleton

    Final product types

    • Reactive and direct dyes for cotton and wool substrates
    • Acid dyes for nylon or silk applications
    • Specialty pigments for printing inks used in industrial and packaging sectors

    4. Synthesis of Liquid Crystal Compounds

    Within the electronics and optical materials field, our material serves as a starting point for precision organic syntheses used in liquid crystal display (LCD) compounds. Its rigid, highly substituted aromatic structure imparts essential mesogenic properties, and downstream chemists employ this intermediate in the stepwise construction of complex liquid crystal molecules. Such formulations require meticulous attention to material purity and functional group arrangement to meet demanding performance thresholds in display panel manufacturing.

    Industry compliance standards

    • ISO 9001:2015 for quality management in electronic materials
    • RoHS (Restriction of Hazardous Substances Directive, EU 2011/65/EU)
    • IEC 61249-2-41 for base material compounds in PCB and display applications
    • Japan’s JIS C 5101-1 for electronic material specifications

    Typical usage ratio

    • Formulators add at 2–12 mol% in liquid crystal precursor mixtures, fine-tuning this range based on molecular alignment demands for finished display systems

    Downstream process integration

    • Reacted in selective alkylation or etherification steps to form mesophase-stabilizing aromatic cores
    • Undergoes final purification by column chromatography or distillation prior to formulation into liquid crystal blends

    Final product types

    • Molecules for twisted nematic (TN) and in-plane switching (IPS) LCD formulations
    • Advanced LC host materials for electronic paper and OLED display matrices
    • Optical alignment media for precision display orientation layers

    5. Advanced Polymer Additive Production

    Polymer producers utilize this raw material as a functional additive precursor, where its electron-withdrawing substituents enable tailored monomer synthesis for specialty polymer backbones. These are often developed for high-performance plastics requiring enhanced chemical resistance or dielectric properties for demanding engineering and electronic applications. Process control includes strict monitoring of the intermediate conversion rate to minimize residual monomer content and ensure compliance with downstream regulatory and mechanical property requirements.

    Industry compliance standards

    • REACH Annex XVII for polymer building blocks
    • ASTM D256 and D648 for plastic product specification
    • UL 94 flammability standard for electrical polymer applications
    • China GB/T 9341 for flexural properties of plastics

    Typical usage ratio

    • Intermediate concentrations ranging from 0.3–2.0 weight percent of total monomer feed, depending on desired functional group density and polymerization method

    Downstream process integration

    • Undergoes nucleophilic aromatic substitution or co-polymerization in the initial monomer synthesis step of technical-grade plastics production
    • Incorporated through melt-processing or solution polymerization with later-stage granule blending for unique performance attributes

    Final product types

    • High-temperature polyimides and polyamides for structural applications
    • Functionalized epoxy resins for electronics encapsulation
    • Specialty foams for chemical and microelectronic filtration media
    Free Quote

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