Triphenylmethyl hydroperoxide

Triphenylmethyl hydroperoxide
Names
Other names
Trityl hydroperoxide
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 609-978-9
  • InChI=1S/C19H16O2/c20-21-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,20H
    Key: ILNQBWPWHQSSNX-UHFFFAOYSA-N
  • C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)OO
Properties
C19H16O2
Molar mass 276.335 g·mol−1
Density 1.27 g/ mL
Melting point 87.5–88.5 °C (189.5–191.3 °F; 360.6–361.6 K)
Hazards
GHS labelling:[1]
Danger
H271, H315, H319, H335
P210, P220, P261, P264, P264+P265, P271, P280, P283, P302+P352, P304+P340, P305+P351+P338, P306+P360, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P371+P380+P375, P403+P233, P405, P420, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Triphenylmethyl hydroperoxide is the organic compound with the formula (C6H5)3COOH. It is the hydroperoxide (OOH-containing) derivative of triphenylmethane. A colorless solid, it is an unusual example of a thermally robust hydroperoxide.[1]

Triphenylmethyl hydroperoxide is prepared from by treating triphenylmethanol with hydrogen peroxide in the presence of acid:[1]

(C6H5)3COH + H2O2 → (C6H5)3COOH + H2O

References

  1. ^ a b Rossiter, Bryant E.; Frederick, Michael O. (2013). "Triphenylmethyl Hydroperoxide". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rt363m.pub2. ISBN 978-0-471-93623-7.