Isobutyric acid

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Isobutyric acid[1][2]
Skeletal formula of isobutyric acid
Ball-and-stick model of the isobutyric acid molecule
Names
Preferred IUPAC name
2-Methylpropanoic acid[3]
Other names
Isobutyric acid (no longer recommended)[3]
2-Methylpropionic acid
Isobutanoic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.001.087
KEGG
UNII
Properties
C4H8O2
Molar mass 88.11 g/mol
Density 0.9697 g/cm3 (0 °C)
Melting point −47 °C (−53 °F; 226 K)
Boiling point 155 °C (311 °F; 428 K)
Acidity (pKa) 4.86[4]
-56.06x10−6 cm3/mol
Hazards
NFPA 704
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g., diesel fuelHealth code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentineReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
2
1
0
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

Isobutyric acid, also known as 2-methylpropanoic acid, is a carboxylic acid with structural formula (CH3)2CHCO2H. It is a colorless liquid with a somewhat unpleasant odor. It is soluble in water and organic solvents. Isobutyric acid is an isomer of n-butyric acid. Deprotonation or esterification of isobutyric acid gives derivatives called isobutyrates. Isobutyric acid is found in the free state in carobs (Ceratonia siliqua), in vanilla, and in the root of Arnica dulcis, and as an ethyl ester in croton oil.[5]

Production[edit]

Isobutyric acid is prepared by the oxidation of isobutyraldehyde, which is a byproduct of the hydroformylation of propylene.[6]

It can also be prepared by the high pressure hydrocarboxylation (Koch reaction) from propylene:[6]

CH3CH=CH2 + CO + H2O → (CH3)2CHCO2H

Niche methods[edit]

Many routes are known including the hydrolysis of isobutyronitrile with alkalis and the oxidation of isobutanol with potassium dichromate in the presence of sulfuric acid,[7] In the presence of proton donors, the action of sodium amalgam on methacrylic acid also gives isobutyric acid.[5]

Isobutyric acid can also be manufactured commercially using engineered bacteria using a sugar feedstock.[8]

Reactions[edit]

When heated with a chromic acid solution it is oxidized to acetone. Alkaline potassium permanganate oxidizes it[5] to α-hydroxyisobutyric acid, (CH3)2C(OH)-CO2H.

Isobutyric acid is a retained trivial name under the IUPAC rules.[9]

References[edit]

  1. ^ Merck Index, 11th Edition, 5039
  2. ^ "{title}". Archived from the original on 2015-02-17. Retrieved 2015-03-13. 
  3. ^ a b Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 748. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. 
  4. ^ Bjerrum, J.; et al. (1958). Stability Constants. London: Chemical Society. 
  5. ^ a b c Wikisource Chisholm, Hugh, ed. (1911). "Butyric Acid". Encyclopædia Britannica. 4 (11th ed.). Cambridge University Press. p. 892. 
  6. ^ a b Riemenschneider, Wilhelm; Bolt, Hermann (2000). "Esters, Organic". Ullmann's Encyclopedia of Industrial Chemistry: 10. doi:10.1002/14356007.a09_565. Retrieved 17 December 2013. 
  7. ^ I. Pierre and E. Puchot (1873). "New Studies on Valerianic Acid and its Preparation on a Large Scale". Ann. Chim. Phys. 28: 366. 
  8. ^ "Biological pathways to produce methacrylate". Archived from the original on 2012-05-02. Retrieved 2011-10-07. 
  9. ^ Panico R, Powell WH, Richer JC, eds. (1993). "Recommendation R-9.1". A Guide to IUPAC Nomenclature of Organic Compounds. IUPAC/Blackwell Science. ISBN 0-632-03488-2.