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4-Cyanobenzyl Bromide

    • Product Name 4-Cyanobenzyl Bromide
    • Alias 4-Bromomethylbenzonitrile
    • Einecs 221-665-2
    • 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

    836238

    Chemical Name 4-Cyanobenzyl Bromide
    Cas Number 17201-35-3
    Molecular Formula C8H6BrN
    Molecular Weight 196.04 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 68-72°C
    Boiling Point 328.9°C at 760 mmHg
    Density 1.41 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and dichloromethane
    Refractive Index 1.600
    Purity Typically ≥98%
    Synonyms p-Cyanobenzyl bromide; 1-(Bromomethyl)-4-cyanobenzene
    Smiles N#CC1=CC=C(C=C1)CBr
    Inchi InChI=1S/C8H6BrN/c9-6-7-1-3-8(10)4-2-7/h1-4H,6H2

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

    Packing & Storage
    Packing The 25g bottle of 4-Cyanobenzyl Bromide is packaged in a brown glass container with a secure, tamper-evident cap and hazard labeling.
    Shipping 4-Cyanobenzyl Bromide is classified as a hazardous material and should be shipped in tightly sealed, chemical-resistant containers. It must be packed and labeled according to international and local regulations for toxic and corrosive substances. Shipping should be via certified carriers, with appropriate documentation, hazard labels, and safety data sheets included.
    Storage 4-Cyanobenzyl bromide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong bases and oxidizing agents. Protect from moisture and direct sunlight. Use appropriate chemical-resistant storage cabinets, and ensure proper labeling. Handle under a fume hood, wearing suitable protective clothing and gloves.
    Application of 4-Cyanobenzyl Bromide

    Applications of 4-Cyanobenzyl Bromide in Industrial Manufacturing

    4-Cyanobenzyl Bromide serves as a crucial intermediate in numerous fine chemical manufacturing pathways. Our facility provides this material for well-established downstream industries that demand consistent quality and stringent compliance, as outlined in the following industrial application scenarios.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ 4-cyanobenzyl bromide as a key alkylating agent when building nitrile-containing pharmacophores essential for active pharmaceutical ingredients, including atypical antipsychotics and beta-blockers. Its controlled reactivity supports substitution reactions, ensuring the integration of the cyanobenzyl moiety onto diverse heterocyclic and aromatic ring systems used in drug development.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia (Ph. Eur.) monograph guidance for intermediates
    • U.S. FDA 21 CFR Part 211 (for API process steps)
    • REACH Regulation (EC) No 1907/2006—Registration, Evaluation and Authorization of Chemicals

    Typical usage ratio

    • 0.75–1.25 molar equivalents relative to the target nucleophile, with ratio adjustments based on coupling efficiency and process scale to minimize side-product formation.

    Downstream process integration

    • Incorporated at the nucleophilic substitution (alkylation) stage during multi-step API synthesis, following pre-conditioning of target amines or heterocycles under controlled temperature and solvent conditions.

    Final product types

    • Pharmaceutical raw materials: precursor blocks for antipsychotic agents, cardiovascular drugs, CNS-active molecules
    • Custom fine chemical intermediates for CDMO and CRO sectors

    2. Agrochemical Intermediate Manufacturing

    In crop protection and pesticide synthesis, formulators use this compound to introduce cyanobenzyl functionality into target molecules, fostering the creation of efficient herbicides and fungicides. Its selective bromination characteristics allow process chemists to achieve high conversion rates with limited by-product accumulation, directly translating to cost-efficient agrochemical production cycles.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for the Registration of Pesticide Intermediates
    • ISO 9001:2015 Certified Quality Management Systems
    • Chinese Ministry of Agriculture standards for agrochemical intermediates (GB/T 1604, GB/T 1250)
    • REACH Pre-registration (for import and use within the EU)

    Typical usage ratio

    • 0.9–1.1 molar equivalents, with adjustment according to the molecular complexity of the end agrochemical product and presence of catalyst systems.

    Downstream process integration

    • Participates in early-stage intermediate synthesis or late-stage functionalization step in the production of phenylcyanobenzyl-based herbicides or fungicides, frequently under controlled temperature batch reactors.

    Final product types

    • Herbicide active ingredients with cyanobenzyl substitutions
    • Fungicide intermediates for grain, vegetable, and fruit crop protection
    • Pesticidal precursors for new-generation plant treatment agents

    3. Liquid Crystal Monomer Production

    Display material manufacturers incorporate the cyanobenzyl group by executing reliable coupling reactions for the synthesis of high-purity monomers used in advanced liquid crystal (LC) mixtures. Accurate introduction of the nitrile and benzyl functionalities ensures precise control over mesogenic core properties, which is vital for the optical and electrochemical behavior of thin-film displays.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for specialty chemical production
    • IEC 61747 standards for liquid crystal devices
    • REACH and TSCA registration
    • Internal industrial LC purity and trace analysis protocols

    Typical usage ratio

    • 1.0–1.05 molar equivalents, controlled to minimize oligomer formation, with further adjustments based on solvent and process route.

    Downstream process integration

    • Enters the synthetic scheme at the etherification or esterification coupling stage, mainly in the synthesis of biphenyl nitrile LC monomers where the bromine acts as a leaving group under palladium-catalyzed or nucleophilic aromatic substitution conditions.

    Final product types

    • Liquid crystal monomer cores for LCD and OLED displays
    • Functionalized oligomers used in high-contrast display screens and specialty touch technologies

    4. Dyes and Functional Pigment Intermediate

    In dye manufacturing, chemists rely on the stability and reactivity of the cyanobenzyl group to synthesize key chromophore intermediates, particularly within the textile and specialty pigment sectors. This building block supports the assembly of high-intensity, photostable dye molecules used in fiber coloration and precision printing applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textile applications
    • EN 71-3:2019 (Safety of toys—Migration of certain elements, relevant for pigment use)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) stewardship requirements
    • ISO 14001:2015 for environmentally conscious production

    Typical usage ratio

    • 0.8–1.15 molar equivalents per chromophoric amine or hydroxyl, tailored based on dye structure and targeted shade intensity.

    Downstream process integration

    • Employed at the condensation or amination step to construct core chromogenic scaffolds, preceding final sulfonation or metal-complex formation in the pigment synthesis workflow.

    Final product types

    • Textile dyes with enhanced lightfastness
    • Functional pigments for plastics, inks, and specialty coatings
    • Intermediates for high-performance organic colorants

    5. Specialty Polymer Intermediate Manufacture

    In high-value polymer production, such as for engineering plastics or advanced resins, process engineers use the compound to introduce polar aromatic structures that impart controlled rigidity and crosslinking capacity. Its role in nucleophilic aromatic substitution reactions supports scalable synthesis of monomeric units essential for polymer backbone customization.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (Polymer manufacturing)
    • RoHS Directive 2011/65/EU for electronic polymer use
    • ASTM D256 for polymer impact resistance (relevant for downstream product QC)
    • REACH compliance for monomer import/export

    Typical usage ratio

    • 0.95–1.05 molar equivalents, closely monitored to maintain molecular weight distribution and batch repeatability; adjusted for degree of polymerization required.

    Downstream process integration

    • Introduced at the step-growth or chain-growth initiation phase to synthesize specialty monomers or pre-polymers with pendant nitrile groups, subsequently copolymerized to target material properties.

    Final product types

    • High-performance engineering plastics with improved chemical resistance
    • Advanced thermosetting resins for aerospace and electronics
    • Specialty copolymers for optical materials and adhesives
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