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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 | 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. |
Applications of 4-Cyanobenzyl Bromide in Industrial Manufacturing4-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 SynthesisPharmaceutical 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
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2. Agrochemical Intermediate ManufacturingIn 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
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3. Liquid Crystal Monomer ProductionDisplay 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
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4. Dyes and Functional Pigment IntermediateIn 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
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5. Specialty Polymer Intermediate ManufactureIn 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
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