\\ Species Tag: & 34004 & Name:& H2O2 \\ Version: & 4 & & Hydrogen peroxide, \\ Date: & Sept. 1995 & & H$_2$O$_2$, \\ Contributor:& J. C. Pearson & & first 5 torsional states \\ & & & \\ Lines Listed: & 38357 & Q(300.0)=& 9785.505 \\ Freq. (GHz) $<$ & 9999 & Q(225.0)=& 5760.578 \\ Max. J: & 60 & Q(150.0)=& 2814.265 \\ LOGSTR0= & -10.0 & Q(75.00)=& 895.518 \\ LOGSTR1= & -10.0 & Q(37.50)=& 288.930 \\ Isotope Corr.: & 0.0 & Q(18.75)=& 88.856 \\ Egy. (cm$^{-1}$) $>$& 0.0 & Q(9.375)=& 26.680 \\ $\mu_a$ = & & A=& 301878. \\ $\mu_b$ = & & B=& 26211.9 \\ $\mu_c$ = & 1.5724 & C=& 25099.14 \headend The spectral lines and method of calculation are from D. T. Petkie, T. M. Goyette, J. J. Holton, F. C. De Lucia and P. Helminger, 1995, J. Mol. Spect. {\bf 171}, 145-159. This paper included the previous lines of P. Helminger, W. C. Bowman and F. C. De Lucia, 1981, J. Mol. Spect. {\bf 85}, 120. E. A. Cohen and H. M. Pickett, 1981, J. Mol. Spect. {\bf 87}, 582. Also used in the analysis were energy levels from C. Cammy-Peyret, J.-M. Flaud, J. W. C. Johns and M. Noel, 1992, J. Mol. Spect. {\bf 155}, 84-104. Dipoles are from A. Perrin, J.-M. Flaud, C. Camy-Peyret, R. Schermaul, M. Winnewisser, \mbox{J.-Y.} Mandin, V. Danna, M. Badaoui, and J. Koput, Line Intensities in the Far-Infrared Spectrum of H$_2$O$_2$, in preparation. The dipole moment is c-type in all cases. The value given is for the ground state transitions only. The vibrational quantum number designation is as follows: \begin{center}\begin{tabular}{cccc} v(catalog) & n & $\tau_{even}$ & $\tau_{odd}$ \\ 0 & 0 & 1 & 2 \\ 1 & 1 & 1 & 2 \\ 2 & 2 & 1 & 2 \\ 3 & 0 & 4 & 3 \\ 4 & 1 & 4 & 3 \\ \end{tabular}\end{center} $\tau_{even}$ is the value of $\tau$ when K$_a$ is even, and $\tau_{odd}$ is the value of $\tau$ when K$_a$ is odd. The analysis must be separated into $\tau$ = odd and $\tau$ = even parts due to torsional staggering.