Acetonitrile

Not to be confused with Acetyl cyanide.

Acetonitrile

Skeletal formula of acetonitrile Skeletal formula of acetonitrile with all explicit hydrogens added
Ball and stick model of acetonitrile Spacefill model of acetonitrile
Names
Preferred IUPAC name Acetonitrile [1]
Systematic IUPAC name Ethanenitrile [1]
Other names Cyanomethane [2] Ethyl nitrile [2] Methanecarbonitrile [2] Methyl cyanide [2] MeCN ACN
Identifiers
CAS Number	75-05-8  Y
3D model (JSmol)	Interactive image
Beilstein Reference	741857
ChEBI	CHEBI:38472  Y
ChEMBL	ChEMBL45211  Y
ChemSpider	6102  Y
ECHA InfoCard	100.000.760
EC Number	200-835-2
Gmelin Reference	895
MeSH	acetonitrile
PubChem CID	6342
RTECS number	AL7700000
UNII	Z072SB282N  Y
UN number	1648
CompTox Dashboard (EPA)	DTXSID7020009
InChI InChI=1S/C2H3N/c1-2-3/h1H3 Y Key: WEVYAHXRMPXWCK-UHFFFAOYSA-N Y
SMILES CC#N
Properties
Chemical formula	C2H3N
Molar mass	41.053 g·mol−1
Appearance	Colorless liquid
Odor	Faint, distinct, fruity
Density	0.786 g/cm3 at 25°C
Melting point	−46 to −44 °C; −51 to −47 °F; 227 to 229 K
Boiling point	81.3 to 82.1 °C; 178.2 to 179.7 °F; 354.4 to 355.2 K
Solubility in water	Miscible
log P	−0.334
Vapor pressure	9.71 kPa (at 20.0 °C)
Henry's law constant  (kH)	530 μmol/(Pa·kg)
Acidity (pKa)	25
UV-vis (λmax)	195 nm
Absorbance	≤0.10
Magnetic susceptibility (χ)	−28.0×10−6 cm3/mol
Refractive index (nD)	1.344
Thermochemistry
Heat capacity (C)	91.69 J/(K·mol)
Std molar entropy (S⦵298)	149.62 J/(K·mol)
Std enthalpy of formation (ΔfH⦵298)	40.16–40.96 kJ/mol
Std enthalpy of combustion (ΔcH⦵298)	−1256.03 – −1256.63 kJ/mol
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H302, H312, H319, H332
Precautionary statements	P210, P280, P305+P351+P338
NFPA 704 (fire diamond)	2 3 0
Flash point	2.0 °C (35.6 °F; 275.1 K)
Autoignition temperature	523.0 °C (973.4 °F; 796.1 K)
Explosive limits	4.4–16.0%
Lethal dose or concentration (LD, LC):
LD50 (median dose)	2 g/kg (dermal, rabbit) 2.46 g/kg (oral, rat)
LC50 (median concentration)	5655 ppm (guinea pig, 4 hr) 2828 ppm (rabbit, 4 hr) 53,000 ppm (rat, 30 min) 7500 ppm (rat, 8 hr) 2693 ppm (mouse, 1 hr) [3]
LCLo (lowest published)	16,000 ppm (dog, 4 hr) [3]
NIOSH (US health exposure limits):
PEL (Permissible)	TWA 40 ppm (70 mg/m3) [4]
REL (Recommended)	TWA 20 ppm (34 mg/m3) [4]
IDLH (Immediate danger)	500 ppm [4]
Related compounds
Related alkanenitriles	Hydrogen cyanide Thiocyanic acid Cyanogen iodide Cyanogen bromide Cyanogen chloride Cyanogen fluoride Aminoacetonitrile Glycolonitrile Cyanogen Propionitrile Aminopropionitrile Malononitrile Pivalonitrile Acetone cyanohydrin
Related compounds	DBNPA
Supplementary data page
Acetonitrile (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y  verify  (what is  YN ?) Infobox references

Acetonitrile, often abbreviated MeCN (methyl cyanide), is the chemical compound with the formula CH₃CN and structure H₃C−C≡N. This colourless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not classed as organic). It is produced mainly as a byproduct of acrylonitrile manufacture. It is used as a polar aprotic solvent in organic synthesis and in the purification of butadiene. ^[5] The N≡C−C skeleton is linear with a short C≡N distance of 1.16  Å. ^[6]

Acetonitrile was first prepared in 1847 by the French chemist Jean-Baptiste Dumas. ^[7]

Applications

Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower. Heat is then employed in the separating tower to separate the butadiene.

In the laboratory, it is used as a medium-polarity solvent that is miscible with water and a range of organic solvents, but not saturated hydrocarbons. It has a convenient liquid range and a high dielectric constant of 38.8. With a dipole moment of 3.92  D, ^[8] acetonitrile dissolves a wide range of ionic and nonpolar compounds and is useful as a mobile phase in HPLC and LC–MS.

It is widely used in battery applications because of its relatively high dielectric constant and ability to dissolve electrolytes. For similar reasons it is a popular solvent in cyclic voltammetry.

Its ultraviolet transparency UV cutoff, low viscosity and low chemical reactivity make it a popular choice for high-performance liquid chromatography (HPLC).

Acetonitrile plays a significant role as the dominant solvent used in oligonucleotide synthesis from nucleoside phosphoramidites.

Industrially, it is used as a solvent for the manufacture of pharmaceuticals and photographic film. ^[9]

Organic synthesis

Acetonitrile is a common two-carbon building block in organic synthesis ^[10] of many useful chemicals, including acetamidine hydrochloride, thiamine, and α-napthaleneacetic acid. ^[11] Its reaction with cyanogen chloride affords malononitrile. ^[5]

As an electron pair donor

Acetonitrile has a free electron pair at the nitrogen atom, which can form many transition metal nitrile complexes. Being weakly basic, it is an easily displaceable ligand. For example, bis(acetonitrile)palladium dichloride is prepared by heating a suspension of palladium chloride in acetonitrile: ^[12]

${\displaystyle {\ce {PdCl2 + 2 CH3CN -> PdCl2(CH3CN)2}}}$

A related complex is tetrakis(acetonitrile)copper(I) hexafluorophosphate [Cu(CH₃CN)₄]⁺. The CH₃CN groups in these complexes are rapidly displaced by many other ligands.

It also forms Lewis adducts with group 13 Lewis acids like boron trifluoride. ^[13] In superacids, it is possible to protonate acetonitrile. ^[14]

Production

Acetonitrile is a byproduct from the manufacture of acrylonitrile. Most is combusted to support the intended process but an estimated several thousand tons are retained for the above-mentioned applications. ^[15] Production trends for acetonitrile thus generally follow those of acrylonitrile. Acetonitrile can also be produced by many other methods, but these are of no commercial importance as of 2002. Illustrative routes are by dehydration of acetamide or by hydrogenation of mixtures of carbon monoxide and ammonia. ^[16] In 1992 ^[update] , 14,700 tonnes (32,400,000 lb) of acetonitrile were produced in the US.

Catalytic ammoxidation of ethylene was also researched. ^[17]

Acetonitrile shortage in 2008–2009

Starting in October 2008, the worldwide supply of acetonitrile was low because Chinese production was shut down for the Olympics. Furthermore, a U.S. factory was damaged in Texas during Hurricane Ike. ^[18] Due to the global economic slowdown, the production of acrylonitrile used in acrylic fibers and acrylonitrile butadiene styrene (ABS) resins decreased. Acetonitrile is a byproduct in the production of acrylonitrile and its production also decreased, further compounding the acetonitrile shortage. ^[19] The global shortage of acetonitrile continued through early 2009.^{[ needs update ]}

Safety

Toxicity

Acetonitrile has only modest toxicity in small doses. ^{[11] [20]} It can be metabolised to produce hydrogen cyanide, which is the source of the observed toxic effects. ^{[9] [21] [22]} Generally the onset of toxic effects is delayed, due to the time required for the body to metabolize acetonitrile to cyanide (generally about 2–12 hours). ^[11]

Cases of acetonitrile poisoning in humans (or, to be more specific, of cyanide poisoning after exposure to acetonitrile) are rare but not unknown, by inhalation, ingestion and (possibly) by skin absorption. ^[21] The symptoms, which do not usually appear for several hours after the exposure, include breathing difficulties, slow pulse rate, nausea, and vomiting. Convulsions and coma can occur in serious cases, followed by death from respiratory failure. The treatment is as for cyanide poisoning, with oxygen, sodium nitrite, and sodium thiosulfate among the most commonly used emergency treatments. ^[21]

It has been used in formulations for nail polish remover, despite its toxicity. At least two cases have been reported of accidental poisoning of young children by acetonitrile-based nail polish remover, one of which was fatal. ^[23] Acetone and ethyl acetate are often preferred as safer for domestic use, and acetonitrile has been banned in cosmetic products in the European Economic Area since March 2000. ^[24]

Metabolism and excretion

Compound	Cyanide, concentration in brain (μg/kg)	Oral LD50 (mg/kg)
Potassium cyanide	700 ± 200	10
Propionitrile	510 ± 80	40
Butyronitrile	400 ± 100	50
Malononitrile	600 ± 200	60
Acrylonitrile	400 ± 100	90
Acetonitrile	28 ± 5	2460
Table salt (NaCl)	—	3000
Ionic cyanide concentrations measured in the brains of Sprague-Dawley rats one hour after oral administration of an LD50 of various nitriles. [25]

In common with other nitriles, acetonitrile can be metabolised in microsomes, especially in the liver, to produce hydrogen cyanide, as was first shown by Pozzani et al. in 1959. ^[26] The first step in this pathway is the oxidation of acetonitrile to glycolonitrile by an NADPH-dependent cytochrome P450 monooxygenase. The glycolonitrile then undergoes a spontaneous decomposition to give hydrogen cyanide and formaldehyde. ^{[20] [21]} Formaldehyde, a toxin and a carcinogen on its own, is further oxidized to formic acid, which is another source of toxicity.

The metabolism of acetonitrile is much slower than that of other nitriles, which accounts for its relatively low toxicity. Hence, one hour after administration of a potentially lethal dose, the concentration of cyanide in the rat brain was 1⁄20 that for a propionitrile dose 60 times lower (see table). ^[25]

The relatively slow metabolism of acetonitrile to hydrogen cyanide allows more of the cyanide produced to be detoxified within the body to thiocyanate (the rhodanese pathway). It also allows more of the acetonitrile to be excreted unchanged before it is metabolised. The main pathways of excretion are by exhalation and in the urine. ^{[20] [21] [22]}

See also

• Trichloroacetonitrile – a derivative of acetonitrile used to protect alcohol groups, and also used as a reagent in the Overman rearrangement

References

1. Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 902. doi:10.1039/9781849733069-FP001. ISBN   978-0-85404-182-4.
2. "Material Safety Data Sheet: Acetonitrile" (PDF). TedPella.com.
3. "Acetonitrile". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
4. NIOSH Pocket Guide to Chemical Hazards. "#0006". National Institute for Occupational Safety and Health (NIOSH).
5. "Archived copy" (PDF). Ashford's Dictionary of Industrial Chemicals, Third edition. p. 76. Archived from the original (PDF) on 2011-05-16. Retrieved 2011-03-31.
6. Karakida, Ken'ichi; Fukuyama, Tsutomu; Kuchitsu, Kozo (1974). "Molecular Structures of Hydrogen Cyanide and Acetonitrile as Studied by Gas Electron Diffraction". Bulletin of the Chemical Society of Japan. 47 (2): 299–304. doi: 10.1246/bcsj.47.299 .
7. Dumas, J.-B. (1847). "Action de l'acide phosphorique anhydre sur les sels ammoniacaux" [Action of anhydrous phosphoric acid on ammonium salts]. Comptes rendus. 25: 383–384.
8. Steiner, P. A.; Gordy, W. (1966). "Journal of Molecular Spectroscopy". 21: 291.
9. Spanish Ministry of Health (2002), Acetonitrile. Summary Risk Assessment Report (PDF), Ispra (VA), Italy: European Chemicals Bureau, Special Publication I.01.65, archived from the original (PDF) on 2008-12-17
10. DiBiase, S. A.; Beadle, J. R.; Gokel, G. W. "Synthesis of α,β-Unsaturated Nitriles from Acetonitrile: Cyclohexylideneacetonitrile and Cinnamonitrile". Organic Syntheses .; Collective Volume, vol. 7, p. 108
11. Philip Wexler, ed. (2005), Encyclopedia of Toxicology, vol. 1 (2nd ed.), Elsevier, pp. 28–30, ISBN   0-12-745354-7
12. Jürgen-Hinrich., Fuhrhop (2003). Organic synthesis : concepts and methods. Li, Guangtao, Dr. (3rd, completely rev. and enl. ed.). Weinheim: Wiley-VCH. p. 26. ISBN   9783527302727. OCLC   51068223.
13. B. Swanson, D. F. Shriver, J. A. Ibers, "Nature of the donor-acceptor bond in acetonitrile-boron trihalides. The structures of the boron trifluoride and boron trichloride complexes of acetonitrile", Inorg. Chem., 2969., volume 8, pp. 2182-2189, {{doi:10.1021/ic50080a032}}
14. Haiges, Ralf; Baxter, Amanda F.; Goetz, Nadine R.; Axhausen, Joachim A.; Soltner, Theresa; Kornath, Andreas; Christe, Kalr O. (2016). "Protonation of nitriles: isolation and characterization of alkyl- and arylnitrilium ions". Dalton Transactions. 45 (20): 8494–8499. doi:10.1039/C6DT01301E. PMID   27116374.
15. Pollak, Peter; Romeder, Gérard; Hagedorn, Ferdinand; Gelbke, Heinz-Peter. "Nitriles". Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_363.
16. US 4179462,Olive, G.&Olive, S.,"Process for preparing acetonitrile",published 1979-12-18, assigned to Monsanto Company  
17. Rhimi, B.; Mhamdi, M.; Ghorbel, A.; Narayana Kalevaru, V.; Martin, A.; Perez-Cadenas, M.; Guerrero-Ruiz, A. (15 May 2016). "Ammoxidation of ethylene to acetonitrile over vanadium and molybdenum supported zeolite catalysts prepared by solid-state ion exchange". Journal of Molecular Catalysis A: Chemical. 416: 127–139. doi:10.1016/j.molcata.2016.02.028.
18. Lowe, Derek (2009). "The Great Acetonitrile Shortage". Science Translational Medicine.
19. A. Tullo (2008). "A Solvent Dries Up". Chemical & Engineering News. 86 (47): 27. doi:10.1021/cen-v086n047.p027.
20. Institut national de recherche et de sécurité (INRS) (2004), Fiche toxicologique no. 104 : Acétonitrile (PDF), Paris: INRS, ISBN   2-7389-1278-8, archived from the original (PDF) on 2011-07-28, retrieved 2008-08-19
21. International Programme on Chemical Safety (1993), Environmental Health Criteria 154. Acetonitrile, Geneva: World Health Organization
22. Greenberg, Mark (1999), Toxicological Review of Acetonitrile (PDF), Washington, DC: U.S. Environmental Protection Agency
23. Caravati, E. M.; Litovitz, T. (1988). "Pediatric cyanide intoxication and death from an acetonitrile-containing cosmetic". J. Am. Med. Assoc. 260 (23): 3470–73. doi:10.1001/jama.260.23.3470. PMID   3062198.
24. "Twenty-Fifth Commission Directive 2000/11/EC of 10 March 2000 adapting to technical progress Annex II to Council Directive 76/768/EEC on the approximation of laws of the Member States relating to cosmetic products". Official Journal of the European Communities . L65: 22–25. 2000-03-14.
25. Ahmed, A. E.; Farooqui, M. Y. H. (1982), "Comparative toxicities of aliphatic nitriles", Toxicol. Lett., 12 (2–3): 157–64, doi:10.1016/0378-4274(82)90179-5, PMID   6287676
26. Pozzani, U. C.; Carpenter, C. P.; Palm, P. E.; Weil, C. S.; Nair, J. H. (1959), "An investigation of the mammalian toxicity of acetonitrile", J. Occup. Med., 1 (12): 634–642, doi:10.1097/00043764-195912000-00003, PMID   14434606

External links

• WebBook page for C₂H₃N
• International Chemical Safety Card 0088
• National Pollutant Inventory - Acetonitrile fact sheet
• NIOSH Pocket Guide to Chemical Hazards
• Chemical Summary for Acetonitrile (CAS No. 75-05-8), Office of Pollution Prevention and Toxics, U.S. Environmental Protection Agency
• Simulation of acetonitrile
• How Did Organic Matter Reach Earth? Cosmic Detectives Trace Origin of Complex Organic Molecules, on: SciTechDaily. September 10, 2020. Source: Tokyo University of Science: Acetonitrile found in molecular cloud Sgr B2(M) at the center of our galaxy.