Benzyl Cyanide

Other Trading Names:

  • Phenylacetonitrile
  • α-Tolunitrile
  • Benzeneacetonitrile
  • Benzonitrile
  • α-Phenylacetonitrile

CAS Number: 140-29-4

HS Code: 29269095

Types of Packaging:

  • 1 Kg/ Aluminum Foil Bag
  • 1 Kg/ Aluminum Tin
  • 25 Kg/ Aluminum Drum
Inquiry right-arrow $100.00
Availability: In stock
SKU
Benzyl Cyanide

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Molecular Formula

C8H7N

Appearance

Clear liquid

Purity

99%

Moisture

0.5%

Melting Point

-11°C

Boiling Point

230-235°C

Density

1.02 g/mL

Refractive Index

1.527-1.529

Chemical Description

  • Benzyl cyanide, also known as phenylacetonitrile or benzeneacetonitrile, is a clear liquid with a distinct almond-like odor.
  • It is primarily used as an intermediate in the synthesis of various compounds, including pharmaceuticals, fragrances, and pesticides.
  • Benzyl cyanide is a versatile chemical, often employed as a precursor in the production of benzyl derivatives, such as benzyl alcohol and benzylamine.
  • The chemical structure of benzyl cyanide consists of a benzene ring attached to a cyanide group, providing reactivity for diverse chemical reactions.
  • Due to its high purity and stability, benzyl cyanide is favored in industrial processes requiring precise control over reaction conditions.
  • In pharmaceutical applications, benzyl cyanide serves as a key building block for the synthesis of pharmaceutical intermediates, contributing to the development of various drugs.
  • Its use in fragrance manufacturing adds a distinctive almond-like aroma to perfumes and personal care products.
  • Benzyl cyanide is also utilized in the synthesis of agrochemicals, aiding in the formulation of effective pesticides and herbicides.
  • With stringent quality control measures in place, our Benzyl Cyanide meets the highest industry standards, ensuring reliability and consistency in diverse applications.
  • Benzyl cyanide possesses unique chemical properties that make it valuable in organic synthesis.
  • Its cyano group (–CN) renders it reactive towards nucleophilic substitution and addition reactions, allowing for the introduction of various functional groups.
  • The benzene ring provides aromaticity, which can influence the reactivity and stability of benzyl cyanide derivatives.
  • In addition to its role as a precursor, benzyl cyanide itself exhibits some interesting biological activities, including insecticidal and antimicrobial properties.
  • Despite its toxicity in high concentrations, benzyl cyanide is handled safely in controlled industrial environments, following strict safety protocols.
  • Its relatively low volatility and moderate solubility in water make it suitable for a range of industrial processes, facilitating efficient separation and purification methods.
  • Benzyl cyanide's versatility extends to its compatibility with a wide range of solvents and reaction conditions, offering flexibility in synthetic routes and process optimization.
  • The distinct almond-like odor of benzyl cyanide, reminiscent of bitter almonds, is attributed to its chemical structure and is utilized in the flavor and fragrance industry to enhance product profiles.
  • With its importance spanning multiple sectors, benzyl cyanide remains a key molecule in organic chemistry, contributing to advancements in drug discovery, material science, and agrochemical development.
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Benzyl Cyanide