I was looking and I cant seem to find much information on increasing stability of harm(al)ine during the manske style salting process.
On my last big batch I got to one point where nice clean orangish yellow crystals reverted to dirty orange on the next manske cycle. Whatever red-orange-brown decomposition product contaminates the harmalas can clearly form during a manske.
Has an effort been done to determine what pH, contaminant metal salts, temperatures, etc. harm purity?
I'm guessing previously boiled water is preferable to reduce oxygen. Is demineralized water good enough or does distilled make a consistent difference? A touch of vinegar? That sort of thing.
I'm running a 31 gram crystallization of already half pure harm(al)ine now in which I first dissolved 0.31 grams of ascorbic acid in previously boiled water and I can at least say it did not decolorize the dissolved harmalas, it looked like 450 ml of coffee.
I dont want my crystals dirty orange-brown!