Empirical data obtained through scientific experimentation that supports the formation of α-Hydroxydialkylnitrosamines during the solvolysis of α-(Acyloxy)dialkylnitrosamines at pH-1.
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Acetic acid, dichloro-, (methylnitrosoamino)phenylmethyl ester
(3aR,6R,7S,7aS)-2,2-Dimethyl-6-(p-tolylamino-methyl)-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6,7-diol
1H-Indene, 2,3-diphenyl-1-(phenylmethyl)-
allyl 3,4-di-O-benzyl-2-O-p-methoxybenzyl-α-L-rhamnopyranoside
3-(methylthio)but-3-enyl tosylate
{3-[4-(2-Benzyloxycarbonylamino-acetylamino)-butylamino]-propyl}-carbamic acid tert-butyl ester
ETHYL TRIMETHYLACETOPYRUVATE
benzaldehyde N,N-dimethyl-N-(p-bromobenzyl)hydrazonium bromide
1-(3-(trifluoromethyl)benzyl)-4-phenyl-1H-1,2,3-triazole
