Jose Ramos-Díaz, Sonja Suvanto, Elina Forsten, Laila Seppa
Content of 3-methyl-1-butanol
seems to correlate with the overall fla-
vor intensity. Based on Figure 5, the
overall flavor intensity can be related
to the concentration of compounds
such 2-butanone-3-hydroxide, hexanal
and hexanol-1. The concentration of 2-
bu-tanone-3-hydroxide was higher in
the NH samples, stored for 14 days; 2-
bu-tanone-3-hydroxido also had a high
correlation with the total intensity of
aromas. The second largest concentra-
tion of 2-butanone-3-hydroxide cor-
responds to NH samples, stored for 7
days, and the third largest concentra-
tion of this compound corresponds to
H samples, stored for 7 days (slightly
higher than H samples stored for 14
days). The concentration of 1-hexanol
was the greatest in NH samples, stored
for 7 days; these samples are character-
ized by a strong aroma of fresh peas. In
H samples, the concentration of 1-hex-
anol was low compared to NH
samples. Given the intensity of
grassiness and the high concentrations
of 1-hexanol, it is reasonable to think
that this com-pound is somehow
related to perceived grassiness.
Based on Figure 5, the intensity of
grassy aroma correlated with various
compounds such as 2-heptanone, oc-
tane, 2-octanone, 3-methyl butanal, 2-
nonanol, and 2-methyl butanal, but
only the concentration of 3-methyl-
butanal has been observed in H sam-
ples, stored for 7 days. The aroma of
fresh pea was strongly associated with
2-pentylfuran, but this compound was
found in low concentrations in every
sample. Interestingly, the results of sen-
sory evaluation showed that the aro-ma
of fresh peas was one of the most
intense. This suggests that there is no
direct correlation between the aroma of
fresh peas and the 2-pentylfuran, or that
the compound causes a strong
aroma even at low concentrations.
Fresh samples presented aromas of
low intensity and, generally, very low
concentration of volatile compounds.
2-methylfuran had the highest concen-
tration in fresh samples, but was also
detected in samples stored for 7 days.
At 14-day storage, 2-butanone
and 2,3-butane were detected in NH
samples while acetic and butyr-ic
acid were detected in H samples.
DISCUSSION
The panellists were able to differentiate
between the following aromatic descrip-
tors: Fresh peas, yeast-like, musty, bitter
and grassy. More reliable results would
have been obtained with a greater num-
ber of panellists and longer training.
Despite this, panellists’ performance
was acceptable. The effect of the inter-
action between replication and storage
time on musty aroma was significant (p
= .03), which may indicate some dis-
crepancy among panellists (Kälviäinen,
Roininen, & Appelbye, 2005). Panellists
may not have understood attributes same
way, or the samples were not suf-
ficiently distinguishable. It is believed
that the interaction with replicate and the
large standard deviations may have
resulted from insufficient training.
As mentioned in the introduction, the
characteristic aroma of the beans and the
generation of volatile com-pounds have
been a topic of some study (Vara-Ubol
et al., 2004; Bott & Cham-bers, 2006).
The head-space analyses of H and NH
samples, stored for up to 14 days,
allowed the identification of vari-ous
oxidation products such as hexanal, 1-
hexanol, 2-heptanone, 2-pentylfu-ran, 1-
octen- 3-ol, and hexanoic acid. From
these, the concentration of 1-hex-anol
was high in most samples. In addi-tion
to 1-hexanol, the concentration of
20 | Cátedra Villarreal | V. 4 | No. 1 | enero -junio | 2016 |