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1 be present in Kosher and Halal foods such as saffron.
2 ethod for safranal quantity determination in saffron.
3 t and quantify safflower as an adulterant in saffron.
4 accurate tools were proposed to authenticate saffron.
5 enes during the development of the stigma in saffron.
6 vorably used to discriminate between Spanish saffron.
7 for the first time in the quality control of saffron.
8 in Spain of unknown origin, labeled Spanish saffron.
9 dress the quality and authenticity issues of saffron.
10 hich was used to prepare mixtures with fresh saffron.
11 e determination of aroma-active compounds of saffron.
12 sible compound matches for peaks observed in saffron.
13 tal of 28 aroma compounds were identified in saffron.
14 hieve a representative aromatic extract from saffron.
15 and prediction of authentic and adulterated saffron.
17 iency of established methodologies to detect saffron adulteration with plant adulterants, the method
19 applied for improved analytical accuracy of saffron analysis, by using retention indices in the two-
21 ars to be restricted to the stigma tissue in saffron and other Crocus species and was correlated with
22 ne vision technology for characterization of saffron and shows how it can be employed in practical us
23 inary study for the detection of adulterated saffron and the identification of the adulterant used by
24 cleave zeaxanthin, the presumed precursor of saffron apocarotenoids, both in Escherichia coli and in
25 nt analysis applied to the UV-vis spectra of saffron aqueous extracts revealed a clear differentiatio
26 enoid-derived compound is characterised by a saffron aroma and is here reported in grape for the firs
31 ntification of each Sudan dye in adulterated saffron can be utilised for quantitative (1)H NMR (qHNMR
32 thms can be made available for prediction of saffron characteristics such as color as well as for pro
34 remost parameters that define the quality of saffron (crocetin esters, picrocrocin and safranal); the
36 Aroma and aroma-active compounds of Iranian saffron (Crocus sativus L.) were analyzed by gas chromat
38 1 is a new glucosyltransferase isolated from saffron (Crocus sativus) that localizes to the cytoplasm
39 sis (PCA) revealed clear differences between saffron cultivated and packaged in Spain, protected desi
48 The GC data for several samples of powdered saffron from different origins were compared to specific
50 ived materials utilised as bulking agents in saffron, i.e., Crocus sativus stamens, safflower, turmer
53 arkers as a result of a metabolomic study of saffron (kaempferol 3-O-glucoside, kaempferol 3-O-sophor
54 presence of two major flavonoid compounds in saffron: kaempferol-3-O-beta-D-glucopyranosyl-(1-2)-beta
56 , protected designation of origin (PDO), and saffron packaged in Spain of unknown origin, labeled Spa
57 ions on the secondary metabolite contents of saffron produced in the area of Cascia, in central Italy
68 severe validation conditions (30% and 50% of saffron samples in the evaluation set), correct predicti
73 r to compare spectra in pseudo-absorbance of Saffron samples with different geographical origins thro
74 Crocus sativus stigmas are the source of the saffron spice and accumulate the apocarotenoids crocetin
76 amounts of floral bio-residues are wasted in saffron spice production, which need to be stabilized be
81 eq datasets of three developmental stages of saffron stigma allowed the determination of alternative
82 R technique to the quality control of traded saffron that suffers various types of fraud or mislabell
84 preprocessing strategy for image analysis of saffron thin layer chromatographic (TLC) patterns was in
85 was developed to assess the authenticity of saffron through the analysis of a group of kaempferol de
89 that can be applied to several posts of the saffron trade chain to specifically detect adulteration
92 We attempted geographical classification of saffron using UV-visible spectroscopy, conventionally ad
97 n the range of 0.1-20% (w/w) of safflower in saffron, which was successfully validated and applied to
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