2-FLUOROBENZONITRILE

PRODUCT IDENTIFICATION
CAS NO. 394-47-8

2-FLUOROBENZONITRILE
EINECS NO. 206-897-7
FORMULA C7H4FN
MOL WT. 121.11
H.S. CODE 2926.90
TOXICITY  
SYNONYMS o-Cyanofluorobenzene; o-Fluorobenzonitrile;
o-Fluorophenyl cyanide; 2-Fluorobenzoic acid nitrile; o-Fluorophenyl cyanide; 1-Fluoro-2-cyanobenzene; 24-Fluorobenzonitrilo (Spanish);
SMILES 
 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES
PHYSICAL STATE clear liquid
MELTING POINT

 
BOILING POINT 90 C (20hPa)
SPECIFIC GRAVITY

1.11 - 1.12
SOLUBILITY IN WATER Insoluble (soluble in alcohol and ether)
AUTOIGNITION

 
pH  
VAPOR DENSITY  
NFPA RATINGS Health: 2; Flammability: 2; Reactivity: 0

REFRACTIVE INDEX

 1.5089
FLASH POINT 67 C
STABILITY Stable under ordinary conditions

APPLICATIONS
Nitrile is an organic compounds containing cyano group (-C》N, containing trivalent nitrogen) which is attached to one carbon atom with the general formula RC》N. Their names are corresponding to carboxylic acids by changing '-ic acid' to the suffix, '-onitrile' which denotes only the 》N atom (triply bound) excluding the carbon atom attached to it, or  the suffix, '-carbonitrile' where the carbon atom in the -CN is included, whichever preserves a single letter O. Examples are acetonitrile from acetic acid and benzonitrile from benzoic acid. The prefix,  'cyano-' is used as an alternative naming system to indicate the presence of a nitrile group in a molecule for the compounds of salts and organic derivatives of hydrogen cyanide (HC》N). Isocyanides are salts and hydrocarbyl derivatives from the isomer, HN+》C-. Sodium cyanide, NaCN; potassium cyanide, KCN; calcium cyanide, Ca(CN)2; and hydrocyanic (or prussic) acid, HCN are examples. Chemically, the simple inorganic cyanides resemble chlorides in many ways. Organic nitriles act as solvents and are reacted further for various application including;

  · Extraction solvent for fatty acids, oils and unsaturated hydrocarbons
  · Solvent for spinning and casting and extractive distillation based on its     selective miscibility with organic compounds.
  · Removing agent of colouring matters and aromatic alcohols
  · Non-aqueous solvent for titrations and for inorganic salts
  · Recrystallization of steroids
  · Parent compound for organic synthesis
  · Solvent or chemical intermediate in biochemistry ( pesticide sequencing and     DNA synthesis)
  · High-pressure liquid chromatographic analysis
  · Catalyst and component of transition-metal complex catalysts
  · Stabilizer for chlorinated solvents
  · Chemical intermediate and solvent for perfumes and pharmaceuticals

Benzonitrile, derived mainly from benzoic acid reaction with lead thiocyanate by heating, is a clear liquid; boils at 191 C; It reacts violently with strong acids to produce toxic hydrogen cyanide. It decomposes on heating producing very toxic fumes, hydrogen cyanide, nitrous oxides.  Benzonitrile is used as a solvent and chemical intermediate for the synthesis of pharmaceuticals, dyestuffs and rubber chemicals through the reactions of alkylation, condensation, esterification, hydrolysis, halogenation or nitration. Benzonitrile and its derivatives are used in the manufacture of lacquers, polymers and anhydrous metallic salts as well as intermediates for pharmaceuticals, agrochemicals, and other organic chemicals.
SALES SPECIFICATION

APPEARANCE

 clear to white semi solid
PURITY (GLC)

98.0% min
TRANSPORTATION
PACKING 200kgs in drum
HAZARD CLASS 6.1 (Packing Group: III)
UN NO. 3276
OTHER INFORMATION
Hazard Symbols: XN, Risk Phrases: 20/21/22-36/37/38, Safety Phrases: 26-36/37/39