Warning: hardcore chemistry!
I asked the question a while back as to whether FOs have sap values, because of an experiment I did in which some of the KOH appeared to be reacted by the oil.
Now, I think that the answer we get from FO suppliers - that FO "doesn't saponify" and therefore has no sap value, while technically correct, may be misleading. It's not saponifying, to be sure . . . but something IS happening otherwise trace would not accelerate, ricing would never occur, etc.
I think it would be more correct to ask of the supplier "what is the
equivalent to a sap value caused by this FO?"
The reason why I am thinking along these lines is that when I used to teach organic chemistry (not at any high level I hasten to add) I learned that aldehydes and ketones were often present in aromatics. Now, as illustrated in the link below,
www.chem.missouri.edu/chem2050/Dibenzylacetone.doca mixture of aldehydes and ketones will indeed react with NaOH to form aldols. (molecules composed of alcohols and aldehydes)
Sorry if this really bores you. I'm a bit of a maniac for tracking things down, probably because I am an aspie!
And anyway I might be on the wrong track.