Salicylamide

• Formula: C₇H₇NO₂
• Molecular weight: 137.1360
• IUPAC Standard InChI: InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10) Copy

  
• IUPAC Standard InChIKey: SKZKKFZAGNVIMN-UHFFFAOYSA-N Copy
• CAS Registry Number: 65-45-2
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Benzamide, 2-hydroxy-; o-Hydroxybenzamide; Acket; Afko-Sal; Algamon; Algiamida; Allevin; Amid-Sal; Amidosal; Anamid; Benesal; Cetamide; Cymidon; Dolomide; Dropsprin; Liquiprin; Morsarinas; Novecyl; Oramid; OHB; Panithal; Raspberin; Salamid; Salamide; Saliamid; Saliamin; Salicim; Salicylic Acid amide; Salipur; Salizell; Salrin; Salymid; Serramida; Urtosal; 2-Carbamoylphenol; 2-Hydroxybenzamide; Andasol; Benzamide, o-hydroxy-; Eggosalil; Flarpirina; Amid kyseliny salicylove; Cidal; H.P. 34; Salicilamide; Salicylamid; Samid; 2-Carboxamidophenol; NSC 3115; SR 4326
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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Phase change data

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

Enthalpy of fusion

References

Go To: Top, Phase change data, Notes

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

Grady, Hays, et al., 1973
Grady, L.T.; Hays, S.E.; King, R.H.; Klein, H.R.; Mader, W.J.; Wyatt, D.K.; Zimmere, R.O., Drug purity profiles, J. Pharm. Sci., 1973, 62, 459. [all data]

Bernardes and Minas da Piedade, 2008
Bernardes, Carlos E.S.; Minas da Piedade, Manuel E., Energetics of the O-H Bond and of Intramolecular Hydrogen Bonding in HOC ₆ H ₄ C(O)Y (Y = H, CH ₃ , CH ₂ CH«58875»CH ₂ , C«58876»CH, CH ₂ F, NH ₂ , NHCH ₃ , NO ₂ , OH, OCH ₃ , OCN, CN, F, Cl, SH, and SCH ₃ ) Compounds, J. Phys. Chem. A, 2008, 112, 40, 10029-10039, https://doi.org/10.1021/jp804455u . [all data]

Ribeiro da Silva and Araújo, 2007
Ribeiro da Silva, Maria D.M.C.; Araújo, Nuno R.M., Thermochemical studies on salicylaldehyde and salicylamide, The Journal of Chemical Thermodynamics, 2007, 39, 10, 1372-1376, https://doi.org/10.1016/j.jct.2007.03.006 . [all data]

Nordström and Rasmuson, 2006
Nordström, Fredrik L.; Rasmuson, Åke C., Solubility and Melting Properties of Salicylamide, J. Chem. Eng. Data, 2006, 51, 5, 1775-1777, https://doi.org/10.1021/je060178m . [all data]

Notes

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• Symbols used in this document:
  

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

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