EVALUATION OF 9-METHYLAMINO-METHYLANTHRACENE AS A CHEMICAL LABEL FOR TOTAL REACTIVE ISOCYANATE GROUP - A COMPARISON OF MONO-ISOCYANATE AND DIISOCYANATE MONOMERS
Rj. Rando et al., EVALUATION OF 9-METHYLAMINO-METHYLANTHRACENE AS A CHEMICAL LABEL FOR TOTAL REACTIVE ISOCYANATE GROUP - A COMPARISON OF MONO-ISOCYANATE AND DIISOCYANATE MONOMERS, Journal of liquid chromatography, 16(18), 1993, pp. 3977-3996
9-Methylamino-methylanthracene (MAMA) is a secondary amine compound co
mmonly used for derivatization and quantitation of specific commercial
isocyanate compounds by HPLC with detection by fluorescence and ultra
-violet light absorbance. The determination of airborne total reactive
isocyanate group (TRIG) compounds arising from partially polymerized
polyurethanes and thermal decomposition products of fully cured polyur
ethanes is of interest in industrial hygiene. The potential applicatio
n of MAMA to the measurement of TRIG has been evaluated using a series
of 11 model isocyanate compounds, including aliphatic and aromatic, m
ono-, and di-isocyanates. After synthesis, purification, and character
ization, the 11 isocyanate-MAMA urea derivatives were analyzed by reve
rsed phase HPLC using three detection/quantitation modes: fluorescence
with excitation at 245 nm and emission at 414 nm, and UV absorbance a
t 245 and 370 nm. ANOVA of the observed response factors showed statis
tically significant differences among the isocyanates for each of the
detection modes. The most variable was fluorescence with an overall co
efficient of variation of 55%, whereas absorbance at 245 nm and at 370
nm showed coefficients of variation of only 14% and 8.6%, respectivel
y. The ratios of response factors for absorbance at 245 nm and at 370
nm were relatively constant across isocyanates, with a mean of 10.46 a
nd standard deviation of 0.87 (8.3%). Certain structure/response relat
ionships were observed, particularly the enhancement of UV absorbance
by aromatic isocyanate derivatives and a general decrease in fluoresce
nce by derivatives containing unhindered aromatic rings conjugated to
the urea group. These results suggest that the ratio of UV absorbance
at 245 nm to that at 370 nm may be used for reliable identification of
unknown MAMA-derivatized TRIG and that quantitation of MAMA-derivatiz
ed TRIG may be achieved with satisfactory accuracy using absorbance de
tection at 370 nm.