BUTYRONITRILE Property

Melting point:

−112 °C(lit.)

Boiling point:

115-117 °C(lit.)

Density 

0.794 g/mL at 25 °C(lit.)

vapor density 

2.4 (vs air)

vapor pressure 

23 mm Hg ( 25 °C)

refractive index 

n20/D 1.384(lit.)

Flash point:

62 °F

storage temp. 

Flammables area

solubility 

slightly soluble in water; soluble in alcohol, ether and dimethylformamide

form 

Liquid

color 

Clear

explosive limit

1.6% (v/v)

Water Solubility 

Miscible with benzene, alcohol, ether and dimethylformamide. Slightly soluble in water.

Merck 

14,1597

BRN 

1361452

Exposure limits

TLV-TWA 22.5 mg/m³ (8 ppm) (NIOSH).

Dielectric constant

20.7（21℃）

Stability:

Stable. Combustible. Substances to be avoided include strong acids, strong bases, strong oxidizing agents and strong reducing agents.

LogP

0.401 at 30℃

CAS DataBase Reference

109-74-0(CAS DataBase Reference)

EPA Substance Registry System

Butanenitrile (109-74-0)

Safety

Hazard Codes 

T,F

Risk Statements 

10-23/24/25-11

Safety Statements 

45-63-36/37-16

RIDADR 

UN 2411 3/PG 2

OEB

A

OEL

TWA: 8 ppm (22 mg/m3)

WGK Germany 

1

RTECS 

ET8750000

Autoignition Temperature

910 °F

Hazard Note 

Toxic

TSCA 

Yes

HazardClass 

3

PackingGroup 

II

HS Code 

29269095

Hazardous Substances Data

109-74-0(Hazardous Substances Data)

Toxicity

LD50 orally in rats: 0.14 g/kg (Smyth)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H225Highly Flammable liquid and vapour

H330Fatal if inhaled

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

BUTYRONITRILE Chemical Properties,Usage,Production

Chemical Properties

colourless liquid

Chemical Properties

n-Butyronitrile has a sharp suffocating odor. Forms cyanide in the body. Butyronitrile [109-74-0], propyl cyanide, butanenitrile, CH3(CH2)2CN, is a colorless liquid slightly miscible with water, miscible with ethanol and diethyl ether. The physical properties are listed in Table 1. Butyronitrile is usually obtained by the catalytic gase-phase reaction of butanol or butyraldehyde with ammonia. Its major use is the manufacture of the poultry drug amprolium.

Uses

Basic material in industrial, chemical, and pharmaceutical intermediates and products; poul- try medicines.

Uses

Butyronitrile serves as an intermediate in the chemical and pharmaceutical industries. It is also involved in the preparation of n-butylamine, butanamide and butyric acid. It acts as a precursor to the poultry drug amprolium. Further, it reacts with phosphorochloridic acid diethyl ester to prepare (1-cyano-propyl)-phosphonic acid diethyl ester. It is also employed to study the effect of stereochemical factors on intervalence charge transfer. In addition to this, it is used in electrolyte composition in dye-sensitized solar cells.

Uses

Butyronitrile is used as a chemical intermediate.

Definition

ChEBI: A nitrile that is hydrogen cyanide in which the hydrogen has been replaced by a propyl group.

Production Methods

n-Butyronitrile is prepared from 1-butanol by controlled cyanation with NH₃ at 300°C in the presence of Ni-Al₂0₃ or zinc phosphide catalysts.

General Description

A clear colorless liquid. Flash point 76°F. Less dense than water. Vapors heavier than air. Produces toxic oxides of nitrogen during combustion. Used in the manufacture of other chemicals.

Air & Water Reactions

Highly flammable. Slightly soluble in water.

Reactivity Profile

BUTYRONITRILE can react vigorously with oxidizing reagents, when heated to decomposition, BUTYRONITRILE emits highly toxic fumes of cyanides and oxides of nitrogen [Sax, 9th ed., 1996, p. 609]. Nitriles may polymerize in the presence of metals and some metal compounds. They are incompatible with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give carboxylic acids (or salts of carboxylic acids). These reactions generate heat. Peroxides convert nitriles to amides. Nitriles can react vigorously with reducing agents. Acetonitrile and propionitrile are soluble in water, but nitriles higher than propionitrile have low aqueous solubility. They are also insoluble in aqueous acids.

Hazard

Flammable, dangerous fire risk.

Health Hazard

n-Butyronitrile is considered a highly hazardous material and full precautions should be used to prevent skin contact or inhalation of the vapor. Inhaled n-butyronitrile is about 2.4 times as toxic as acetonitrile. In order to protect workers, the recommended TWA limit is obtained by dividing that for acetonitrile by the factor 2.4. NIOSH has therefore recommended that employee exposure should not exceed 8 ppm (v/v) (22 mg/m³) compound as a TLV-TWA.

Health Hazard

Butyronitrile showed moderate to high toxicity on test animals. It is an acute toxicant by all routes: inhalation, ingestion, and absorption through skin. The target organs are the liver, kidney, central nervous system, lungs, and sense organs, as well as the peripheral nerve. Its toxicity is on the same order as that of propionitrile; its inhalation toxicity is slightly lower than that of propionitrile, and its oral toxicity is slightly greater than that of propionitrile.
Inhalation can cause nausea, respiratory distress, and damage to liver. Willhite (1981) reported a LC50 value of 249 ppm in mice from 1 hour exposure to its vapor. It produced ataxia, dyspnea, and corneal damage in test animals when given intraperitoneally. The toxic symptoms from subcutaneous applications are tremor, dyspnea, respiratory depression, and spastic paralysis. It is toxic only at low levels by skin absorption.
LD50 value, oral (mice): 27.7 mg/kg
There is no report on its teratogenicity. The reproductive effect of this compound is expected to be similar to that of propionitrile.

Health Hazard

Dizziness, rapid respirations, headache, drowsiness, drop in blood pressure and pulse, delayed symptoms. May cause cyanosis (blue-grey coloring of skin and lips due to lack of oxygen)

Fire Hazard

Special Hazards of Combustion Products: Toxic cyanide fumes

Flammability and Explosibility

Highly flammable

Industrial uses

n-Butyronitrile is used as an industrial solvent, an intermediate in the chemical industry and in poultry medicines.

Safety Profile

A poison by ingestion, skin contact, intraperitoneal, and subcutaneous routes. Moderately toxic by inhalation. Experimental reproductive data. A skin irritant. Dangerous fire hazard when exposed to heat, flame, or oxidizers. To fight fire, use alcohol foam. When heated to decomposition it emits toxic fumes of NOx and CN-.

Purification Methods

Treat it with conc HCl until the smell of the isonitrile had gone, then dry with K2CO3 and fractionally distil [Turner J Chem Soc 1681 1956]. Alternatively it is twice heated at 75o and stirred for several hours with a mixture of 7.7g Na2CO3 and 11.5g KMnO4 per L of butyronitrile. The mixture is cooled, then distilled. The middle fraction is dried over activated alumina. [Schoeller & Wiemann J Am Chem Soc 108 22 1986, Beilstein 2 IV 806.]

Waste Disposal

Burning in a chemical incinerator equipped with an afterburner and scrubber is the most effective way to destroy the compound. Oxidation with ethanolic–KOH can convert butyronitrile to nonhazardous cyanate.