Monobenzone

• Formula: C₁₃H₁₂O₂
• Molecular weight: 200.2332
• IUPAC Standard InChI: InChI=1S/C13H12O2/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9,14H,10H2 Copy

  
• IUPAC Standard InChIKey: VYQNWZOUAUKGHI-UHFFFAOYSA-N Copy
• CAS Registry Number: 103-16-2
• 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: Phenol, 4-(phenylmethoxy)-; Phenol, p-(benzyloxy)-; p-(Benzyloxy)phenol; p-Hydroxyphenyl benzyl ether; Agerite alba; Alba-Dome; Benoquin; Benzoquin; Benzyl p-hydroxyphenyl ether; Carmifal; Depigman; Dermochinona; Hydroquinone benzyl ether; Hydroquinone monobenzyl ether; Leucodinine; Monobenzon; Monobenzyl ether hydroquinone; Monobenzyl hydroquinone; Pigmex; Superlite; 4-(Benzyloxy)phenol; para-(Benzyloxy)phenol; Benzyl hydroquinone; Hydrochinon monobenzylether; 4-(Phenylmethoxy)phenol; Monobenzyl ether of hydroquinone; Agerite; NSC 2132; Superlite (antioxidant)
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
• Options:
  • Switch to SI units

Gas phase ion energetics data

Go To: Top, 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:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

Ionization energy determinations

Appearance energy determinations

References

Go To: Top, Gas phase ion energetics data, Notes

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

Weschke, Timpe, et al., 1979
Weschke, W.; Timpe, H.-J.; Just, G., Untersuchungen an EDA-Komplexen von Benzylarylethern, J. Prakt. Chem., 1979, 321, 605. [all data]

Ward, Cooks, et al., 1969
Ward, R.S.; Cooks, R.d.; Williams, D.H., Substituent effects in mass spectrometry. Mass spectra of substituted phenyl benzyl ethers, J. Am. Chem. Soc., 1969, 91, 2727. [all data]

Notes

Go To: Top, Gas phase ion energetics data, References

• Symbols used in this document:
  

  AE	Appearance energy

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.