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Methyl 3,5-Dibromobenzoate

    • Product Name Methyl 3,5-Dibromobenzoate
    • Alias methyl_3_5_dibromobenzoate
    • Einecs 841-867-6
    • 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
    VTB
    Specifications

    HS Code

    475077

    Cas Number 67430-92-0
    Molecular Formula C8H6Br2O2
    Molecular Weight 293.94 g/mol
    Appearance White to off-white solid
    Melting Point 82-85°C
    Boiling Point 334.7°C at 760 mmHg
    Density 1.924 g/cm3
    Purity ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles COC(=O)C1=CC(Br)=CC(Br)=C1
    Inchi InChI=1S/C8H6Br2O2/c1-12-8(11)6-2-5(9)3-7(10)4-6/h2-4H,1H3
    Synonyms Methyl m-dibromobenzoate, 3,5-Dibromobenzoic acid methyl ester
    Refractive Index 1.634 (est)
    Ec Number 614-076-7

    As an accredited Methyl 3,5-Dibromobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White powder packed in a 25g amber glass bottle, tightly sealed, with a printed label indicating “Methyl 3,5-Dibromobenzoate."
    Shipping Methyl 3,5-Dibromobenzoate is shipped in tightly sealed, labeled containers to prevent leakage and contamination. It is transported according to local and international regulations for hazardous chemicals. The package is protected from moisture, heat, and direct sunlight, and handled by trained personnel using appropriate personal protective equipment (PPE).
    Storage Store Methyl 3,5-Dibromobenzoate in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Clearly label the container and keep it in a chemical storage cabinet, following all local regulations and safety guidelines for hazardous organic chemicals.
    Application of Methyl 3,5-Dibromobenzoate

    Applications of Methyl 3,5-Dibromobenzoate in Industrial Manufacturing

    Methyl 3,5-Dibromobenzoate plays a crucial role as a specialty intermediate across various fine chemical sectors. As a direct manufacturer, we supply this compound to established global plants engaging in advanced synthesis, where its controlled reactivity, purity, and specific halogenated structure support performance and compliance needs throughout stringent production environments.

    1. Pharmaceutical Active Ingredient Synthesis

    This compound acts as a brominated aromatic intermediate in multi-stage production of APIs, especially for selective serotonin reuptake inhibitors (SSRIs) and certain analgesics. Process chemists prefer it for introducing high-purity halogen groups during molecule assembly, with tightly controlled reaction sequences to avoid side reactions. Its predictable reactivity delivers consistent yields and helps maintain narrow impurity profiles. Downstream, manufacturers integrate this intermediate into controlled building block libraries under cGMP to support regulated product development.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU GMP Directives (2017/1572/EU)
    • Chinese Pharmacopoeia (when supplying China-based pharmaceutical plants)

    Typical usage ratio

    • 0.2–1.2 molar equivalents per target API synthesis batch, adjusted for target yield and process efficiency

    Downstream process integration

    • Used in early-stage halogenation or esterification steps
    • Often reacts with organolithium or Grignard reagents in stepwise functionalization
    • Enters automated batch reactors during multi-step syntheses
    • Subjected to in-process QC as part of standard pharma intermediate workup

    Final product types

    • Antidepressant APIs
    • CNS-acting intermediates
    • Analgesic APIs
    • Intermediates for peptide-based drugs

    2. Agrochemical Active Compound Manufacturing

    The compound serves as a fundamental halogenated intermediate for selected herbicide and fungicide molecules, particularly in the synthesis of benzoyl-substituted actives. Its dual bromine substitution supports targeted functional group introductions for improved biological performance. Agrochemical formulators rely on this intermediate for batch-to-batch reproducibility, adhering to pesticide regulatory frameworks governing precursor control and traceability throughout downstream steps.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009
    • US EPA 40 CFR Part 170—Pesticide Worker Protection Standard
    • ISO 9001:2015 for agrochemical manufacturing

    Typical usage ratio

    • 5–18% w/w relative to total batch weight, according to target active ingredient and multi-step process scale

    Downstream process integration

    • Introduced in initial halogenation or acylation stages
    • Converted through cross-coupling or further substitution in automated glass-lined reactors
    • Subjected to wet-chemistry analysis and LC-MS impurity screening before next synthesis stage
    • Handled under documentation for controlled raw material traceability

    Final product types

    • Herbicide actives (substituted benzoyl family)
    • Fungicide actives
    • Formulated crop protection products
    • Precursor chemicals for biocidal ingredient synthesis

    3. Development of Advanced Performance Polymers

    Materials scientists employ this compound in the synthesis of high-value specialty polymers requiring brominated aromatic monomer input. Notably, it features in the creation of flame-retardant polyesters and high glass transition polymers used for electronics and automotive coatings. Manufacturers precisely meter its dosage based on end-use mechanical and fire safety targets, ensuring both efficient polymerization and compliance with global consumer and electronics safety standards.

    Industry compliance standards

    • UL 94: Standard for Safety of Flammability of Plastic Materials
    • REACH Regulation (EC) No 1907/2006
    • RoHS Directive (2011/65/EU) for electronic applications
    • ISO 14001: Environmental Management in chemical synthesis

    Typical usage ratio

    • 2–12% molar fraction of total monomers, tailored by polymer chain design and fire safety requirements

    Downstream process integration

    • Dosed as co-monomer during melt or solution polymerization
    • Introduced prior to catalyst initiation under nitrogen blanketing
    • Undergoes in-line quality control to confirm bromine incorporation
    • Early precursor for copolymerizable resins and masterbatch granules

    Final product types

    • Flame-retardant polyesters
    • High-Tg engineering polymers
    • Electronic encapsulation resins
    • Protective coatings for automotive and appliance industries

    4. Custom Fine Chemical and Dye Synthesis

    Specialty dye manufacturers and fine chemical producers use this intermediate in precision synthesis of halogenated aromatic compounds with unique colorimetric or electronic properties. Its selectivity helps control final chromophore structures in dyes and permits targeted modifications in pigments for plastics and textiles. Operators choose this intermediate for scale-up under batch or semi-batch conditions, considering solvent compatibility and required substitution efficiency.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemical safety
    • EN 71-3: Safety of Toys—Migration of Certain Elements (for dyes used in toys)
    • ISO 9001:2015 Quality Management
    • REACH Annex XVII substance restrictions

    Typical usage ratio

    • 0.7–5% w/w in global dye synthesis processes, with variation based on chromophore and desired shade

    Downstream process integration

    • Added during primary aromatic functionalization or halogen exchange step
    • Often dissolved in high-boiling solvents to maximize yield and selectivity
    • Allows controlled substitution for precise color adjustment in synthetic dyes
    • Integrated within closed reactor setups for hazardous material handling

    Final product types

    • Specialty azo and anthraquinone dyes
    • Halogenated pigments for plastics
    • Color additives for synthetic fibers
    • Intermediates for specialty fine chemical libraries

    5. Electronic Chemical Intermediate Production

    Electronics chemical producers incorporate this compound as a halogenated building block for manufacturing modified aromatic esters and specialty monomers, especially those used in the fabrication of printed circuit boards and photoresists. The dual bromine configuration enhances patternability, dielectric stability, and substrate adhesion in the final chemical systems. Manufacturers monitor halogen content precisely and implement multi-stage purification to ensure downstream reliability in high-purity applications.

    Industry compliance standards

    • IPC-4101: Specification for Base Materials for Printed Boards
    • RoHS Restriction (2011/65/EU), specifically for controlled brominated compound levels
    • JEDEC JESD709C for electronic materials reliability
    • ISO/TS 16949 for automotive electronics quality management

    Typical usage ratio

    • 3–9% moles per total monomer or intermediate matrix, based on device specifications

    Downstream process integration

    • Enters primary reaction for halogenated monomer synthesis
    • Used under dry, inert atmosphere to prevent side reactions
    • Integrated with automated analytical verification (elemental, halogen balance)
    • Supplied as high-purity input for monomer customization in electronics

    Final product types

    • Modified polyimide film precursors
    • PCB dielectric layer monomers
    • Photoresist components
    • Electronic adhesive raw materials
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