Acetone cyanohydrin

Acetone cyanohydrin
Names
IUPAC name
2-Hydroxy-2-methylpropanenitrile[1]
Other names
Cyanohydrin-2-propanone[2]

α-Hydroxyisobutyronitrile[2]
2-Hydroxy-2-methyl-propionitrile[2]

2-Methylactonitrile[2]
Identifiers
75-86-5 YesY
3DMet B00479
605391
ChEBI CHEBI:15348 YesY
ChemSpider 6166 YesY
DrugBank DB02203 YesY
EC Number 200-909-4
Jmol interactive 3D Image
KEGG C02659 YesY
MeSH acetone+cyanohydrin
PubChem 6406
RTECS number OD9275000
UN number 1541
Properties
C4H7NO
Molar mass 85.11 g·mol−1
Appearance Colourless liquid
Density 932 mg mL−1
Melting point −21.2 °C; −6.3 °F; 251.9 K
Boiling point 95 °C (203 °F; 368 K)
Vapor pressure 2 kPa (at 20 °C)
1.399
Thermochemistry
−121.7–−120.1 kJ mol−1
−2.4514–−2.4498 MJ mol−1
Hazards
Safety data sheet fishersci.com
GHS pictograms
GHS signal word DANGER
H300, H310, H330, H410
P260, P273, P280, P284, P301+310
T+ N
R-phrases R26/27/28, R50
S-phrases (S1/2), S27, S45
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 4: Very short exposure could cause death or major residual injury. E.g., VX gas Reactivity code 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g., phosphorus Special hazards (white): no codeNFPA 704 four-colored diamond
1
4
2
Flash point 75 °C (167 °F; 348 K)
Explosive limits 2.25–11%
Lethal dose or concentration (LD, LC):
  • 15.8 mg kg−1 (dermal, rabbit)
  • 18.65 mg kg−1 (oral, rat)
US health exposure limits (NIOSH):
none[2]
C 1 ppm (4 mg/m3) [15-minute][2]
N.D.[2]
Related compounds
Related alkanenitriles
Related compounds
 DBNPA
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Acetone cyanohydrin (ACH) is an organic compound used in the production of methyl methacrylate, the monomer of the transparent plastic polymethyl methacrylate (PMMA), also known as acrylic. It is extremely toxic.

Preparation

The compound is generated as part of the acetone cyanohydrin route to methyl methacrylate. It is treated with sulfuric acid to give the sulfate ester of the methacrylamide, methanolysis of which gives ammonium bisulfate and MMA.[3] In the laboratory, this compound may be prepared by reacting sodium cyanide with acetone, followed by acidification:[4]

A simplified procedure involves the action of sodium or potassium cyanide on the sodium bisulfite adduct of acetone prepared in situ. This gives a less pure product that is suitable for most syntheses.[5]

Natural occurrence

Cassava tubers contain linamarin, a glucoside of acetohydrin, and the enzyme linamarinase for hydrolysing the glucoside. Crushing the tubers releases these compounds and produces acetone cyanohydrin.

Safety

Acetone cyanohydrin is classified as an extremely hazardous substance in the US Emergency Planning and Community Right-to-Know Act. The principal hazards of acetone cyanohydrin arise from its ready decomposition on contact with water, which releases highly toxic hydrogen cyanide.

References

  1. ↑ "acetone cyanohydrin - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification. Retrieved 8 June 2012.
  2. 1 2 3 4 5 6 7 "NIOSH Pocket Guide to Chemical Hazards #0005". National Institute for Occupational Safety and Health (NIOSH).
  3. ↑ Bauer, Jr., William (2002), "Methacrylic Acid and Derivatives", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a16_441, ISBN 3-527-30673-0.
  4. ↑ Cox, R. F. B.; Stormont, R. T. "Acetone Cyanohydrin". Org. Synth.; Coll. Vol. 2, p. 7
  5. ↑ Wagner, E. C.; Baizer, Manuel. "5,5-Dimethylhydantoin". Org. Synth.; Coll. Vol. 3, p. 323

External links

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