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Isobutyronitrile

Product Name
Isobutyronitrile
CAS No.
78-82-0
Chemical Name
Isobutyronitrile
Synonyms
iso-C3H7CN;2-Cyanopropane;Isobutyronitril;Isopropylcyanid;Isopropylkyanid;Isobutanenitrile;Isopropylnitrile;ISOBUTYRONITRILE;Isobutylronitrile;isiobutyronitrile
CBNumber
CB9854381
Molecular Formula
C4H7N
Formula Weight
69.11
MOL File
78-82-0.mol
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Isobutyronitrile Property

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
Stability:
Stable. Flammable. May form explosive mixtures with air. Incompatible with strong oxidizing agents.
CAS DataBase Reference
78-82-0(CAS DataBase Reference)
NIST Chemistry Reference
Propanenitrile, 2-methyl-(78-82-0)
EPA Substance Registry System
Isobutyronitrile (78-82-0)
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Safety

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
Hazardous Substances Data
78-82-0(Hazardous Substances Data)
Toxicity
LD50 (mg/kg): 25 i.p. in mice; 200 orally in rats (Zeller); LD50 orally in male mice: 0.3652 mmol/kg (Tanii)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Hazard statements

H225Highly Flammable liquid and vapour

H301Toxic if swalloed

H311Toxic in contact with skin

H330Fatal if inhaled

Precautionary statements

P320Specific treatment is urgent (see … on this label).

P330Rinse mouth.

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

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P405Store locked up.

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N-Bromosuccinimide Price

TCI Chemical
Product number
I0112
Product name
Isobutyronitrile
Purity
>98.0%(GC)
Packaging
500mL
Price
$29
Updated
2021/12/16
TCI Chemical
Product number
I0112
Product name
Isobutyronitrile
Purity
>98.0%(GC)
Packaging
25mL
Price
$15
Updated
2021/12/16
Alfa Aesar
Product number
L14470
Product name
Isobutyronitrile
Purity
99%
Packaging
250ml
Price
$30.5
Updated
2021/12/16
Alfa Aesar
Product number
L14470
Product name
Isobutyronitrile
Purity
99%
Packaging
1000ml
Price
$68.6
Updated
2021/12/16
TRC
Product number
I868310
Product name
Isopropylnitrile
Packaging
10g
Price
$55
Updated
2021/12/16
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Isobutyronitrile Chemical Properties,Usage,Production

Chemical Properties

colourless liquid

Uses

Solvent.

Uses

Isobutyronitrile can be derived from isobutyraldehyde and is used in organic synthesis and as a gasoline additive.

Uses

Used in the synthesis of gasoline additives, as a catalyst in the production of polyethylene.

Production Methods

Isobutyronitrile is prepared from isobutyraldehyde by cyanation with ammonia.

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. 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 .
Isobutyronitrile was implicated in several cases of industrial poisoning. Thiess and Hey reported that a worker became unconscious following isobutyronitrile exposure. His immediate symptomatology included convulsive movements of upper limbs, soft and thready pulse, dilated pupils, shallow and gasping breathing and secretion of viscous mucus. After hospital admission, an exacerbation of the condition occurred with tonic-clonic movements of the upper extremities. The patient was cyanotic, the pulse faint and thready. The patient was treated intravenously with noradrenaline (1 mg) followed by amyl nitrite, sodium nitrite, and sodium thiosulphate. The man's cyanotic condition diminished and his pulse strengthened, although his gasping breath and upper limb convulsions continued. He was given intravenous injections of lobeline and phenobarbital. Rapid improvement occurred and the patient recovered gradually, leaving the hospital symptom-free at 14 d after admission. Two milder inhalation exposures of isobutyronitrile were reported by Zeller et al in which an unknown concentration of vapor produced headache, dizziness, and vomiting at 10-60 min after exposure. The intensity of symptoms varied with the concentration and duration of exposure.

Health Hazard

Poisonous; 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.

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.

Industrial uses

Isobutyronitrile is used in organic synthesis, as a catalyst in the polymerization of ethylene and in the petroleum industry as a gasoline additive.

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.]

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Isobutyronitrile Suppliers

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