A. Buldt et U. Karst, N-methyl-4-hydrazino-7-nitrobenzofurazan as a new reagent for air monitoring of aldehydes and ketones, ANALYT CHEM, 71(9), 1999, pp. 1893-1898
The synthesis of N-methyl-4-hydrazino-7-nitrobenzofurazan (MNBDH) and its a
pplication as a new reagent for the determination of aldehydes and ketones
are described. MNBDH reacts with carbonyl compounds in acidic media to the
corresponding MNBD-hydrazones. In contrast to the established reagent 2,4-d
initrophenylhydrazine (DNPH), MNBDH is oxidized by both ozone and nitrogen
dioxide quantitatively to only one product, N-methyl-4-amino-7-nitrobenzofu
razan (MNBDA), This can easily be separated from the hydrazones of lower al
dehydes by means of HPLC. Due to larger molar absorptivities and absorption
maxima at wavelengths over 470 nm, selectivity is higher and limits of det
ection are lower for the new reagent compared to DNPH. MNBDH reacts slightl
y faster than DNPH with carbonyl compounds and significantly faster than ot
her N-alkylated hydrazine reagents.