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Methyl 4'-Bromomethylbiphenyl-2-Carboxylate

    • Product Name Methyl 4'-Bromomethylbiphenyl-2-Carboxylate
    • Alias Methyl 4'-bromomethyl-[1,1'-biphenyl]-2-carboxylate
    • Einecs 841-813-4
    • 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

    831135

    Productname Methyl 4'-Bromomethylbiphenyl-2-Carboxylate
    Molecularformula C16H13BrO2
    Molecularweight 317.18 g/mol
    Casnumber 60762-18-9
    Appearance White to off-white solid
    Purity Typically ≥98%
    Meltingpoint 75-80°C
    Solubility Soluble in organic solvents like DMSO, chloroform
    Smiles COC(=O)C1=CC=CC=C1C2=CC=C(CBr)C=C2
    Inchi InChI=1S/C16H13BrO2/c1-19-16(18)15-9-4-5-13(11-15)12-6-8-14(10-17)7-2-3-12/h2-11H,1H3
    Storagetemperature 2-8°C (refrigerated)

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

    Packing & Storage
    Packing The chemical is packaged in a 25-gram amber glass bottle with a tamper-evident cap and clear hazard labeling for safety.
    Shipping Methyl 4'-Bromomethylbiphenyl-2-Carboxylate is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with regulatory standards for hazardous chemicals. Adequate labeling and documentation are provided for safe handling and transport. Shipping is typically via specialized carriers, with temperature and handling precautions taken to ensure product integrity.
    Storage Methyl 4'-Bromomethylbiphenyl-2-Carboxylate should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Use appropriate safety containers and ensure clear labeling. Store at recommended temperatures, typically between 2–8°C, and avoid humidity and direct sunlight.
    Application of Methyl 4'-Bromomethylbiphenyl-2-Carboxylate

    Applications of Methyl 4'-Bromomethylbiphenyl-2-Carboxylate in Industrial Manufacturing

    As the original manufacturer, we supply Methyl 4'-Bromomethylbiphenyl-2-Carboxylate to numerous industrial clients engaging in advanced synthesis. This specialty intermediate finds distinct use in several precision-driven downstream sectors, serving as a key building block for high-value specialty compounds. The following application scenarios represent our core customer segments, based on established market experience and direct supply chain participation.

    1. Pharmaceutical API Intermediate Synthesis

    Major pharmaceutical manufacturers source this material as a core intermediate in the multistep synthesis route for several small-molecule APIs benefiting from the biphenyl scaffold, especially in new-generation antihypertensives and CNS-active agents. QC teams emphasize the precise introduction of the bromomethyl group for controlled downstream functionalization and linking. Plant engineers integrate the compound during early-stage route development and scale-up optimization, ensuring dimensional consistency and reliable reactivity at each batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP 35–NF 30 Monograph (relevant sections on intermediate quality)
    • EU GMP Part II Basic Requirements for APIs
    • FDA 21 CFR Part 211 (finished pharmaceuticals quality considerations)

    Typical usage ratio

    • Ranges from 0.08 to 0.16 mol per mol of intended target molecule; subject to step yield and protection strategy in route design

    Downstream process integration

    • Loaded into the second or third step of multistage synthesis via controlled addition to N-alkylation or Suzuki coupling vessels
    • Deployed under anhydrous conditions, usually at 65–85°C to maximize selectivity towards desired active structure

    Final product types

    • Cardiovascular medications (antihypertensive tablets, injectable CNS drugs)
    • Novel small-molecule investigational drugs submitted for US FDA IND
    • Patent-protected branded pharmaceutical substances

    2. Specialty Liquid Crystal Monomer Precursor

    Leading electronic material producers leverage this compound for constructing custom monomers blending biphenyl units. Downstream, the bromomethyl side chain offers a selective anchor point for later mesogen attachment, ensuring consistent molecular orientation in advanced display manufacturing. Production teams deploy it at the start of key liquid crystal monomer syntheses where purity and unique substitution patterns boost final optical performance and thermal behavior, directly influencing device stability and image clarity.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • IEC 62899-201 standards for Printed Electronics Materials
    • ISO 9001:2015 (general QC and traceability for advanced chemical inputs)
    • Joint Industry Guide (JIG 101 Ed. 4) on Materials Composition

    Typical usage ratio

    • Incorporated at 4–8% by weight in initial feed for mesogen precursor synthesis lines; adjustable depending on desired viscosity and birefringence specification

    Downstream process integration

    • Added to the base reactor charge at the start of Grignard coupling or Friedel–Crafts alkylation operations
    • Batch QC samples withdrawn post-coupling for HPLC evaluation before downstream conversion to functionalized LC monomers

    Final product types

    • Liquid crystal display (LCD) alignment layers
    • OLED panel custom monomers
    • High-durability organic electronic films for optical and sensor applications

    3. Advanced Agrochemical Active Ingredient Synthesis

    Agrochemical formulators utilize this material as a critical intermediate while manufacturing select crop protection actives, especially biphenyl-based fungicides and pre-emergent herbicide actives. The bromomethyl group allows for selective downstream derivatization by nucleophilic substitution, promoting high conversion rates and product consistency. Production chemists integrate the material after initial cyclization steps, choosing conditions matched to the sensitivity of crop-targeted molecules, optimizing batch-to-batch effectiveness in field trials and regulatory submissions.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) Guidelines
    • EPA 40 CFR Part 180 (Tolerances and exemptions for pesticide chemicals in food)
    • ISO 17025 Certified Laboratory Analysis
    • REACH Annex XVII Safety Registration (EU active ingredient registration)

    Typical usage ratio

    • Applied at 5–12% of the total batch mass during intermediate formation; varies by targeted crop protection activity spectrum

    Downstream process integration

    • Fed into the key alkylation step after initial ring formation and dehalogenation
    • Reaction parameters controlled for minimal side reactions impacting environmental fate characteristics

    Final product types

    • Biphenyl-based systemic fungicides (suspension concentrates and wettable powders)
    • Pre-emergence herbicide formulations for major row crops
    • Active technical ingredient for post-patent pesticide synthesis

    4. Performance Polymer and High-Temperature Resin Synthesis

    Polymer producers employ this material to introduce functional biphenyl structures and bromomethyl crosslinking sites into high-performance specialty resins. Its controlled incorporation supports downstream synthesis of heat-resistant polyarylate and polyimide matrices, providing both rigid backbone and selective reactivity. The compound directly impacts resin curing profile and final material attributes such as dimensional stability, dielectric strength, and continuous use temperature per customer application testing.

    Industry compliance standards

    • UL 94 Standard for Flammability of Plastic Materials
    • ASTM D5948-18 — Compounds for Molding Polymeric Materials
    • ISO 1043-1:2011 Identification of Plastics — Polymers and Additives
    • RoHS Substance Restrictions for Electronics Polymers

    Typical usage ratio

    • Added at 1.5–4% of resin mass during prepolymer stage; loading depends on target glass transition temperature and crosslink density

    Downstream process integration

    • Introduced to the resin synthesis reactor during primary chain extension or as a branching agent prior to final polycondensation
    • QC validated at prepolymer and final curing stages

    Final product types

    • High-temperature printed circuit board substrates (polyarylate/PI matrix)
    • Automotive electronic enclosure resin compounds
    • Specialty molded components for aerospace and industrial electric modules
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