Actually it is not the question if one hormone is stable to heat, as you mean : safe for autoclaving. If you have a special hormone in mind, just trythe medium with the hormone autoclaved with the medium and and next to it the medium autoclaved and later adding the hormone at 50C. Do some tubes, add tissue and compare the response! Maybe even it is not so bad that the autoclaving cleaves the hormone, maybe the pieces of the hormones are effective too .
Gibberellins are rapidly degraded by elevated temperatures,
and the biological activity of a freshly prepared solution of GAj was
reduced by more than 90% as a result of autoclaving . The auxins NAA, IAA,
and 2,4-D are thermostabie. AlthoughIAA is unaffected by autoclaving under normal conditions, it is subjectto decomposition by other factors found under in vitro conditions.
For better results you can add the millipore filtered (whatman filter paper) PGR solution (Use autoclaved millipore water for preparing stock solutions of PGR'S) after autoclaving the media and then add according to the proportionate concentration required. (because these PGR's may lose activity after autoclaving Picloram, NAA, IAA, IBA)
Mostly we add after boiling the media and before poring in test tubes. yes autoclave effects its performance, but if we add it after autoclave, contamination control is more big issue.
Adding PGRs after autoclaving is better for good results. BA, NAA, IBA 2,4 D can be added before autoclave with no big deal in efficiency. However, Zeatin, TDZ , IAA can perform better if added after autoclave.