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624-79-3

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624-79-3 Usage

Description

Ethyl isocyanide, also known as ethyl isonitrile, is an organic compound with the chemical formula C3H5N. It is a colorless, volatile liquid with a characteristic pungent odor. Ethyl isocyanide is a simple alkyl isonitrile and is used in various applications due to its unique chemical properties.

Uses

Used in Toxicology:
Ethyl isocyanide is used as a reagent in toxicology for the characterization of cytochrome P450 isozymes. It plays a crucial role in understanding the behavior and function of these enzymes, which are essential for the metabolism of various drugs and toxins in the body.
Used in Enzyme Research:
Ethyl isocyanide is used as a probe molecule in enzyme research, particularly for studying the properties of cytochrome P450 enzymes. When ethyl isocyanide interacts with the reduced form of cytochrome P450, it forms a characteristic optical difference spectrum with two peaks in the Soret region (type III). The pH equilibrium point, which is the pH at which the two peaks are of equal height, varies between different isozymes, providing valuable information about their structure and function.

Preparation

CAUTION: The reaction and distillation should be conducted behind a safety shield. Precautions for handling toxic cyanides should be observed.To a three-necked flask equipped with a condenser and ground glass stirrer (or Hershberg stirrer) is added 116 gm (0.75 mole) of ethyl iodide and 100 gm (0.75 mole) of silver cyanide. The mixture is refluxed for 2 hr, the stirrer blade raised, the mixture cooled, filtered (see Note a), the solid washed with ether, dried, and 260 gm of a 50% solution of potassium cyanide (2.0 moles) added. The reaction mixture is distilled to afford a mixture of isonitrile and water (see Note b). The crude isonitrile 49.5- 52.3 gm (90-95%) is separated after being salted out of the water. The isonitrile is washed twice with 24-ml portions of ice-cold saturated sodium chloride solution, dried over magnesium sulfate, and fractionally distilled, to afford 25.9-30.3 gm (47-55%), b.p. 77-79°C (760 mm Hg).

Check Digit Verification of cas no

The CAS Registry Mumber 624-79-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 624-79:
(5*6)+(4*2)+(3*4)+(2*7)+(1*9)=73
73 % 10 = 3
So 624-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N/c1-3-4-2/h3H2,1H3

624-79-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name isocyanoethane

1.2 Other means of identification

Product number -
Other names ethyl isocyanide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:624-79-3 SDS

624-79-3Relevant articles and documents

Bolton et al.

, p. 1 (1969)

The Question of Tautomerism of Alkylnitrile and Isonitrile Cations

Chess, Edward K.,Lapp, R. L.,Gross, Michael L.

, p. 475 - 480 (2007/10/02)

The isomeric pairs+. and +. and +. and +. have been established as stable, noninterconverting structures.The conclusion derives from studies of collision induced decomposition spectra.The same conclusion pertains for the ions +. and +., and for +., +. and HNCCHCHCNH>+..The energy barrier of a -hydrogen shift, a possible isomerization mechanism, is determined to be at least 163kJ mol-1 for the +. and +. pair, and the barrier may be as high as 318kJ*mol-1.The C3H5N and C4H4N2 radical cations decompose before they can be activated with 318 kJ mol-1 of internal energy.

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