Theophylline

• Formula: C₇H₈N₄O₂
• Molecular weight: 180.1640
• IUPAC Standard InChI: InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9) Copy

  
• IUPAC Standard InChIKey: ZFXYFBGIUFBOJW-UHFFFAOYSA-N Copy
• CAS Registry Number: 58-55-9
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-; Elixophyllin; Elixophylline; Lanophyllin; Liquophylline; Optiphyllin; Parkophyllin; Pseudotheophylline; Solosin; Teofyllamin; Theocin; Theofol; Theograd; Theophyllin; 1,3-Dimethylxanthine; Acet-theocin; Aerolate III; Diphyllin; Doraphyllin; Elixex; GS 2591A; Maphylline; Medaphyllin; Nuelin; NSC 2066; Purine-2,6(1H,3H)-dione, 1,3-dimethyl-; Respbid; Synophylate-L.A. Cenules; Tefamin; Teolair; Theacitin; Theo-11; Theocontin; Theolair; Theophyl-225; Theophylline, anhydrous; Theovent; X 115; Xanthine, 1,3-dimethyl-; Xantivent; 3,7-Dihydro-1,3-dimethyl-1H-purine-2,6-dione; Elixicon; Euphylline; Slo-phyllin; Teofilina; Theal tabl.; Theo-Dur; Theolix; Theophyline; Theona P; Theodel; Unifyl; Uniphyl; Uniphyllin; Xanthium; Unicontin CR; Quibron T/SR; 1H-Purine-2,6-dione, 3,9-dihydro-1,3-dimethyl-; Physpa; PulmiDur; Accurbron; Aerobin; Diffumal; Duraphyl; Telbans; Teocen 200; Teonova; Theopek; Slo-Bid; component of Bronkotabs (Salt/Mix); component of Dicurin Procaine (Salt/Mix); component of Hecadrol (Salt/Mix); component of Primatene (Salt/Mix); component of Quibron (Salt/Mix); component of Quibron Plus (Salt/Mix); component of Tedral (Salt/Mix); component of Theo-Organidin (Salt/Mix); component of Mudrane GG elixir (Salt/Mix); component of Primatene tablets (Salt/Mix); component of Quibron-T/SR (Salt/Mix); component of Slo-phyllin GG (Salt/Mix); component of Theo-organdin (Salt/Mix); component of Theolair plus (Salt/Mix); 1,3-Dimethylxanthine (theophylline)
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • References
  • Notes
• Other data available:
  • UV/Visible spectrum
  • Gas Chromatography
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Phase change data

Go To: Top, IR Spectrum, Mass spectrum (electron ionization), References, Notes

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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of sublimation

Enthalpy of fusion

IR Spectrum

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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 by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Gas Phase Spectrum

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Additional Data

Mass spectrum (electron ionization)

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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 by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

References

Go To: Top, Phase change data, IR Spectrum, Mass spectrum (electron ionization), Notes

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

Bruns, Reichelt, et al., 1984
Bruns, S.; Reichelt, J.; Cammenga, H.K., Thermochemical investigation of theophylline, theophylline hydrate and their aqueous solutions, Thermochim. Acta, 1984, 72, 31. [all data]

Fokkens, van Amelsfoort, et al., 1983
Fokkens, J.G.; van Amelsfoort, J.G.M.; de Blaey, C.J.; de Kruif, C.G.; Wilting, J., A thermodynamic study of the solubility of theophylline and its hydrate, International Journal of Pharmaceutics, 1983, 14, 1, 79-93, https://doi.org/10.1016/0378-5173(83)90116-3 . [all data]

Emmenegger and Piccand, 1999
Emmenegger, F.; Piccand, M., Organometallics, 1999, 57, 1, 235-240, https://doi.org/10.1023/A:1010100531350 . [all data]

Good and Rodriguez-Hornedo, 2009
Good, David J.; Rodriguez-Hornedo, Nair, Solubility Advantage of Pharmaceutical Cocrystals, Crystal Growth & Design, 2009, 9, 5, 2252-2264, https://doi.org/10.1021/cg801039j . [all data]

Gondová, Králik, et al., 1989
Gondová, T.; Králik, P.; Gonda, J., Determination of some thermodynamic characteristics of melting of 8-alkyltheophyllines by the DSC method, Thermochimica Acta, 1989, 156, 1, 147-155, https://doi.org/10.1016/0040-6031(89)87180-1 . [all data]

SUZUKI, SHIMOMURA, et al., 1989
SUZUKI, Etsuko; SHIMOMURA, Kikuko; SEKIGUCHI, Keiji, Thermochemical study of theophylline and its hydrate., Chem. Pharm. Bull., 1989, 37, 2, 493-497, https://doi.org/10.1248/cpb.37.493 . [all data]

Notes

Go To: Top, Phase change data, IR Spectrum, Mass spectrum (electron ionization), References

• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion
  ΔsubH	Enthalpy of sublimation
  ΔsubH°	Enthalpy of sublimation at standard conditions

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