Butanal, 3-methyl-

• Formula: C₅H₁₀O
• Molecular weight: 86.1323
• IUPAC Standard InChI: InChI=1S/C5H10O/c1-5(2)3-4-6/h4-5H,3H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: YGHRJJRRZDOVPD-UHFFFAOYSA-N Copy
• CAS Registry Number: 590-86-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Other names: Isovaleraldehyde; β-Methylbutanal; Isopentanal; Isovaleral; Isovaleric aldehyde; Isovalerylaldehyde; 3-Methylbutan-1-al; 3-Methylbutanal; 3-Methylbutyraldehyde; iso-C4H9CHO; Butyraldehyde, 3-methyl-; Isoamylaldehyde; Isopentaldehyde; 1-Butanal, 3-methyl-; 2-Methylbutanal-4; 3-Methyl-1-butanal; NSC 404119
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal boiling point

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Markovnik, Sachek, et al., 1979
Markovnik, V.S.; Sachek, A.I.; Peshchenko, A.D.; Shvaro, O.V.; Andreevskii, D.N.; Olizarevich, N.M., Termodin. Org. Soedin., 1979, 107. [all data]

Lecat, 1949
Lecat, M., Tables Azeotropiques, Vol. 1, 10th ed., Brussels, Belgium, 1949. [all data]

Lecat, 1947
Lecat, M., Orthobaric Azeotropes of Sulfides, Bull. Cl. Sci., Acad. R. Belg., 1947, 33, 160-82. [all data]

Friend and Hargreaves, 1944
Friend, J.N.; Hargreaves, W.D., LXXI. viscosities and rheochors of aldehydes, nitriles and of secondary and tertiary amines., Philos. Mag., 1944, 35, 619. [all data]

Komarewsky and Smith, 1944
Komarewsky, V.I.; Smith, L.G., The Action of Chromia Cat. on Aliphatic Iso-Alcohols and Iso-Aldehydes, J. Am. Chem. Soc., 1944, 66, 1116-7. [all data]

Bohnsack, 1943
Bohnsack, H., Chem. Ber., 1943, 76, 564. [all data]

Platt, Rusoff, et al., 1943
Platt, J.R.; Rusoff, I.I.; Klevens, H.B., J. Chem. Phys., 1943, 11, 535. [all data]

Coomber and Partington, 1938
Coomber, D.I.; Partington, J.R., Studies in dielectric polarisation part xxiii the dipole moments of some aliphatic and aromatic aldehydes and of anthrone, J. Chem. Soc., 1938, 1938, 1444. [all data]

Kohlraush and Koppl, 1934
Kohlraush, K.W.F.; Koppl, F., Z. Phys. Chem., Abt. B, 1934, 24, 370. [all data]

Pringsheim and Leibowitz, 1923
Pringsheim; Leibowitz, Chem. Ber., 1923, 56, 2034. [all data]

Harries, 1916
Harries, C.D., Ozone and Its Action on Organic Compound, 1916. [all data]

Sabatier and Mailhe, 1914
Sabatier, P.; Mailhe, A., C. R. Hebd. Seances Acad. Sci., 1914, 158, 985. [all data]

Sabatier and Mailhe, 1909
Sabatier, P.; Mailhe, A., New Applications of the General Method of Hydrogenation with Various Metals, Ann. Chim. Phys., 1909, 16, 70. [all data]

Semmler, 1909
Semmler, F.W., Chem. Ber., 1909, 42, 2014. [all data]

Sabatier and Senderens, 1903
Sabatier, P.; Senderens, J.B., C. R. Hebd. Seances Acad. Sci., 1903, 137, 302. [all data]

Nef, 1901
Nef, J.V., Justus Liebigs Ann. Chem., 1901, 318, 137. [all data]

Schroder, 1871
Schroder, A., Chem. Ber., 1871, 4, 400. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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