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Isobutyronitrile

CAS No.
78-82-0
Chemical Name:
Isobutyronitrile
Synonyms
2-METHYLPROPIONITRILE;2-METHYLPROPANENITRILE;isiobutyronitrile;ISOPROPYL CYANIDE;Azobis (2-methylpropionitrile);iso-C3H7CN;2-Cyanopropane;Isobutyronitril;Isopropylcyanid;Isopropylkyanid
CBNumber:
CB9854381
Molecular Formula:
C4H7N
Molecular Weight:
69.11
MDL Number:
MFCD00001873
MOL File:
78-82-0.mol
Last updated:2023-11-28 16:31:44

Isobutyronitrile Properties

Melting point -72 °C (lit.)
Boiling point 107-108 °C (lit.)
Density 0.770 g/mL at 20 °C (lit.)
vapor density 2.38 (vs air)
vapor pressure 100 mm Hg ( 54.4 °C)
refractive index n20/D 1.372(lit.)
Flash point 39 °F
storage temp. Flammables area
solubility slightly soluble in water and acetone, very soluble in alcohol and ether
form Liquid
color Clear colorless to light yellow
Water Solubility 35 g/L (20 ºC)
Merck 14,5156
BRN 1340512
Dielectric constant 23.9(Ambient)
Stability Stable. Flammable. May form explosive mixtures with air. Incompatible with strong oxidizing agents.
CAS DataBase Reference 78-82-0(CAS DataBase Reference)
FDA UNII 699AWF2WV2
NIST Chemistry Reference Propanenitrile, 2-methyl-(78-82-0)
EPA Substance Registry System Isobutyronitrile (78-82-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS06
Signal word  Danger
Hazard statements  H225-H300+H310+H330
Precautionary statements  P210-P233-P240-P280-P303+P361+P353-P304+P340+P310
Hazard Codes  F,T
Risk Statements  11-23/24/25-36/37/38
Safety Statements  9-16-24/25-26-36/37/39-45-23
RIDADR  UN 2284 3/PG 2
WGK Germany  2
RTECS  TZ4900000
Hazard Note  Highly Flammable/Toxic
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29269095
Toxicity LD50 (mg/kg): 25 i.p. in mice; 200 orally in rats (Zeller); LD50 orally in male mice: 0.3652 mmol/kg (Tanii)
NFPA 704
3
3 0

Isobutyronitrile Chemical Properties,Uses,Production

Chemical Properties

Colorless liquid with a foul odor. Insoluble in water, easily soluble in ethanol and ether.

Uses

Isobutyronitrile can be derived from isobutyraldehyde. It is used in organic synthesis, as a catalyst in the polymerization of ethylene and in the petroleum industry as a gasoline additive. Isobutyronitrile is also used to synthesize the intermediate 2-isopropyl-4-methyl-6-hydroxypyrimidine of the organophosphorus insecticide diazinon.

Production Methods

Isobutyronitrile is prepared from isobutyraldehyde by cyanation with ammonia.

Definition

ChEBI: Isobutyronitrile is an aliphatic nitrile that is acetonitrile in which two of the hydrogens have been replaced by methyl groups. It has a role as a polar aprotic solvent. It is an aliphatic nitrile and a volatile organic compound.

Production Methods

Isobutyronitrile is usually obtained by the catalytic gas-phase reaction of isobutyraldehyde or isobutanol with ammonia. Its major use is the synthesis of the insecticide diazinon.

General Description

A clear colorless liquid. Flash point 47°F. Less dense than water. Vapors heavier than air. Toxic oxides of nitrogen produced during combustion.

Air & Water Reactions

Highly flammable. Slightly soluble in water.

Reactivity Profile

Isobutyronitrile is incompatible with the following: Oxidizers, reducing agents, strong acids & bases .

Hazard

Toxic by ingestion, inhalation, and skin absorption.

Health Hazard

Isobutyronitrile is considered highly hazardous and full precautions should be taken to prevent skin contact or inhalation of vapor. Inhaled isobutyronitrile is about 2.4 times as toxic as acetonitrile in rats. may be fatal if inhaled, swallowed, or absorbed through skin. Contact may cause burns to skin and eyes. (Non-Specific -- Nitriles) Primarily, they are skin and eye irritants. Large doses cause collapse and stop breathing. 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 p.p.m. (22 mg/m3) for either compound as a TLV-TWA.

Fire Hazard

Vapor may explode if ignited in an enclosed area. Toxic oxides of nitrogen are produced during combustion. Isobutyronitrile is a flammable/combustible material and may be ignited by heat, sparks, or flames. Vapors may travel to a source of ignition and flash back. Container may explode in heat of fire. Vapor explosion and poison hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Hazardous polymerization may not occur.

Metabolism

Thiocyanate was present in the urine of rats dosed orally with isobutyronitrile.

Purification Methods

Shake the nitrile with conc HCl (to remove isonitriles), then with water and aqueous NaHCO3. After a preliminary drying with silica gel or Linde type 4A molecular sieves, it is shaken or stirred with CaH2 until hydrogen evolution ceases, then decanted and distilled from P2O5 (not more than 5g/L, to minimize gel formation) or Drierite (b 101-103o/760mm). Finally it is refluxed with, and slowly distilled from CaH2 (5g/L), taking precautions to exclude moisture. [Beilstein 2 H 294, 2 I 129, 2 II 263, 2 III 655, 2 IV 853.]

Isobutylronitrile #niso-Butyronitrile ISOBUTYRONITRILE, 99.6% 1-Cyano-1-methylethane 2-Cyanopropane 2-methyl-propanenitril 2-methyl-propanoicacinitrile alpha-Methylpropanenitrile Dimethylacetonitrile Isobutanenitrile Isobuttersαurenitril isobutyricacidnitrile Isobutyronitril iso-C3H7CN Propane-2-carbonitrile 2-Methylpropanrnitrile 2-Methylpropanenitrile, 2-Methylpropionitrile, Isopropyl cyanide 2-Methylpropannitrile alpha-Methylpropionitrile Isobutyronitrile,99% ISOBUTYRONITRILE FOR SYNTHESIS Isopropylcyanid Isopropylkyanid Isopropylnitrile Propanenitrile,2-methyl- Propenenitrile,2-methyl- α-Methylpropanenitrile α-Methylpropionitrile ISOPROPYL CYNAIDE ISOBUTYRONITRILE Azobis (2-methylpropionitrile) 2-METHYLPROPANENITRILE 2-METHYLPROPIONITRILE isiobutyronitrile ISOPROPYL CYANIDE Voriconazole Impurity 30 Prasugrel Impurity 32 78-82-0 CH3CHCH3CN CH32CHCN 78820 Organic Building Blocks Nitrogen Compounds Cyanides/Nitriles Building Blocks C1 to C5 Organics