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Furanone, 5-ethyl-3-hydroxy-4-methyl

DIMETHYL-3-HYDROXY -2(5H)-FURANON 3-HYDROXY-4-METHYL-5-ETHYL 2(5H)-FURANON FURFURYL-MERCAPTANE 2-METHYL FURAN-3-THI0L... [Pg.394]

H)-Furanone, dihydro-5-(3-ethyl-4-methyl-1-pentenyl)-3-hydroxy-5-methyl- 4249 ... [Pg.154]

Hydroxy-2-methyl-4-pyrone 5-Ethyl-2(5H)-furanone a-TerpinoIene Octanal ... [Pg.119]

Ethyl-4-methyl-l-pentenyI)-4,5-dihydro-3-hydroxy-5-methyl-2(3 furanone, 9Ci... [Pg.168]

Ethyl-3-methyl-2,4,6-nonatriene, E-30154 5-(3-Ethyl-4-methyl-1 -pentenyl )-4,5-dihydro-3-hydroxy-5-methyl-2(3//)furanone, E-30155... [Pg.455]

A rapid and efficient one-pot synthesis of substituted 2(5H)-furanones has been reported starting from 3-hydroxy-3-methyl-2-butanone 88 and ethyl... [Pg.230]

Ethyl-4-hydroxy-5-methyl-3(2//)-furanone [27538-10-9] and 5-Ethyl-4-hydroxy-2-methyl-3(2//)-furanone [27538-09-6]... [Pg.147]

Trade Names. Sugar lactone (Treatt), Fenugreek lactone (Vioryl). 5-Ethyl-3-hydroxy-4-methyl-2(5)-furanone [698-10-2], abhexone... [Pg.154]

Twenty-nine odour-active compounds were detected by using aroma extract dilution analysis (AEDA) [60]. The results of AEDA together with GC-MS analysis showed ethyl 2-methylbutanoate (described as fruity flavour), followed by methyl 2-methylbutanoate and 3-methylbutanoate (fruity, apple-like), 4-hydroxy-2,5-dimethyl-3(2H)-furanone (sweet, pineapple-like, caramel-like), d-decalactone (sweet, coconut-like), l-( ,Z)-3,5-undecatriene (fresh, pineapple-like), and a unknown compound (fruity, pineapple-like) as the most odour-active compounds. [Pg.197]

The influence of the sensitivity of the assessors on AEDA has been studied [11], with the result that the differences in the FD factors determined by a group of six panellists amount to not more than two dilution steps (e.g. 64 and 256), implying that the key odorants in a given extract will undoubtedly be detected. However, to avoid falsification of the result by anosmia, AEDA of a sample should be independently performed by at least two assessors. As detailed in [6], odour threshold values of odorants can be determined by AEDA using a sensory internal standard, e.g. ( )-2-decenal. However, as shown in Table 16.6 these odour threshold values may vary by several orders of magnitude [8] owing to different properties of the stationary phases. Consequently, such effects will also influence the results of dilution experiments. Indeed, different FD factors were determined for 2-methyl-3-furanthiol on the stationary phases SE-54 and FFAP 2 and 2 , respectively. In contrast, 5-ethyl-3-hydroxy-4-methyl-2(5H)-furanone showed higher FD factors on FFAP than on SE-54 2 and 2, respectively. Consequently, FD factors should be determined on suitable GC capillaries [8]. However, the best method to overcome the limitations of GC-O and the dilution experiment is a sensory study of aroma models (Sect. 16.6.3). [Pg.373]

Ethyl-3-hydroxy-4-methyl-2(5H)-furanone [2H3]ethyl Blank et al., 1993... [Pg.1019]

Blank, I., Schieberle, P., and Grosch, W. 1993. Quantification of the flavour compounds 3-hy-droxy-4,5-dimethyl-2(5H)-furanone and 5-ethyl-3-hydroxy-4-methyl-2(5H)-furanone by stable isotope dilution assay. In Progress in Flavour and Precursor Studies (P. Schreier and P. Winterhalter, eds.). Allured Publishing, Wheaton, 111. [Pg.1022]

Blank, I., Fay, L.B., Lakner, F.J., and Schlosser, M. 1997. Determination of 4-hydroxy-2,5-di-methyl-3(2/f)-furanone and 2(or 5)-ethyl-4-hy-droxy-5(or 2)-methyl-3(2/f)-furanone in pentose sugar-based Maillard model systems by isotope dilution assays. J. Agric. Food Chem. 45 2642-2648. [Pg.1022]

Ethyl 3-Hydroxy 4-Methyl 2(5H)-Furanone View Flavor Chemical... [Pg.706]

Dimethoxy Phenol 3,4-Dimethyl 1,2-Cyclopen tandione 5-Ethyl 3-Hydroxy 4-Methyl 2(5H)-Furanone 3-Ethyl Pyridine Furfuryl Mercaptan Geranyl Isovalerate 2,3 -Heptandione (Z)-3-Hexenyl Butyrate (Z)-3-Hexenyl Formate Hexyl Butyrate Hexyl Hexanoate Isoamyl Isobutyrate Isobutyl Formate Isobutyl Hexanoate Linalool Oxide... [Pg.1028]

Ethyl-4-hydroxy-2-methyl-3(2H)-furanone Ethyl trans-cinnamate... [Pg.41]

The volatiles of fresh pineapple (Ananas comosus [L] Merr.) crown, pulp and intact fmit were studied by capillary gas chromatography and capillary gas chromatography-mass spectrometry. The fnjit was sampled using dynamic headspace sampling and vacuum steam distillation-extraction. Analyses showed that the crown contains Cg aldehydes and alcohols while the pulp and intact fruit are characterized by a diverse assortment of esters, h rocarbons, alcohols and carbonyl compounds. Odor unit values, calculated from odor threshold and concentration data, indicate that the following compounds are important contributors to fresh pineapple aroma 2,5-dimethyl-4-hydroxy-3(2H)-furanone, methyl 2-methybutanoate, ethyl 2-methylbutanoate, ethyl acetate, ethyl hexanoate, ethyl butanoate, ethyl 2-methylpropanoate, methyl hexanoate and methyl butanoate. [Pg.223]

Figure 5.2.10. Cellulose pyrolysate obtained at 59CP C by Py-GC/MS. The separation was done on a Carbowax type column. 1 CO2, 2 acetaldehyde, 3 acetone, 4 2-butanone, 5 2,3-butandione, 6 toluene, 7 water, 8 cyclopentanone, 9 methylfuran, 10 3-hydroxy-2-butanone, 11 hydroxypropanone, 12 cyclopent-1-en-2-one, 13 2-methylcyclopentenone, 14 acetic acid, 15 acetic acid anhydride, 16 furancarboxaldehyde, 17 methylcyclopentenone, 18 dimethylcyclopentenone, 19 5-methylfurancarboxaldehyde, 20 2,3-dihydro-2-furanone, 21 furan-2-methanol, 22 3-methylfuran-2-one, 23 2(5H)-furanone, 24 hydroxycyclopentenone, 25 3,5-dimethylcyclopentan-1,2-dione, 26 2-hydroxy-3-methyl-2-cyclopenten-1-one, 27 2-hydroxy-3-ethyl-2-cyclopenten-1-one, 28 2,3-dimethyl-2-cyclopenten-1-one, 29 phenol, 30 dimethylphenol, 31 3 thyl-2,4(3H,5H)-furandione, 32 3-butenoic acid, 33 1,4 3,6-dianhydro-a-D-glucopyranose, 34 5-(hydroxymethyl)-furfural. Figure 5.2.10. Cellulose pyrolysate obtained at 59CP C by Py-GC/MS. The separation was done on a Carbowax type column. 1 CO2, 2 acetaldehyde, 3 acetone, 4 2-butanone, 5 2,3-butandione, 6 toluene, 7 water, 8 cyclopentanone, 9 methylfuran, 10 3-hydroxy-2-butanone, 11 hydroxypropanone, 12 cyclopent-1-en-2-one, 13 2-methylcyclopentenone, 14 acetic acid, 15 acetic acid anhydride, 16 furancarboxaldehyde, 17 methylcyclopentenone, 18 dimethylcyclopentenone, 19 5-methylfurancarboxaldehyde, 20 2,3-dihydro-2-furanone, 21 furan-2-methanol, 22 3-methylfuran-2-one, 23 2(5H)-furanone, 24 hydroxycyclopentenone, 25 3,5-dimethylcyclopentan-1,2-dione, 26 2-hydroxy-3-methyl-2-cyclopenten-1-one, 27 2-hydroxy-3-ethyl-2-cyclopenten-1-one, 28 2,3-dimethyl-2-cyclopenten-1-one, 29 phenol, 30 dimethylphenol, 31 3 thyl-2,4(3H,5H)-furandione, 32 3-butenoic acid, 33 1,4 3,6-dianhydro-a-D-glucopyranose, 34 5-(hydroxymethyl)-furfural.
Figure 5.2.11. Cellulose pyrolysate obtained at 59(P C and separated on a methyl silicone with 5% phenyl silicone type column. 1 acetic anhydride, 2 pentanal, 3 2-hydroxybutanedialdehyde, 4 1,4-dioxadiene, 5 tetrahydro-2-furanmethanol, 6 2-(hydroxymethyl)-furan, 7 3-methyl-2-hexanone, 8 2-methoxy-2,3-dihydrofuran, 9 2(5H)-furanone, 10 1-acetyloxypropan-2-one, 11 hydroxycyclopentenone, 12 5-methylfurfural, 13 2,3-dihydro-5-methylfuran-2-one, 14 1-cyclopentylethanone, 15 2-hydroxy-3-methyl-2-cyclopenten-1-one, 16 3,5-dimethylcyclopentan-1,2-dione, 17 unknown, 18 3-ethyl-2,4(3H,5H)-furandione, 19 6-methyl-1,4-dioxaspiro[2,4]heptan-5-one, 20 1-hydroxy-3,6-dioxabicyclo[3.2.1]octan-2-one, 21 1,4 3,6-dianhydro-a-D-glucopyranose, 22 5-(hydroxymethyl)-furfural, 23 4-cyclopenten-1,2,3-triol, 24 5-ethyl-3-hydroxy-4-methyl-tetrahydrofuran-2-one, 25 levoglucosan, 26 1,6-anhydro-p-D-glucofuranose. Figure 5.2.11. Cellulose pyrolysate obtained at 59(P C and separated on a methyl silicone with 5% phenyl silicone type column. 1 acetic anhydride, 2 pentanal, 3 2-hydroxybutanedialdehyde, 4 1,4-dioxadiene, 5 tetrahydro-2-furanmethanol, 6 2-(hydroxymethyl)-furan, 7 3-methyl-2-hexanone, 8 2-methoxy-2,3-dihydrofuran, 9 2(5H)-furanone, 10 1-acetyloxypropan-2-one, 11 hydroxycyclopentenone, 12 5-methylfurfural, 13 2,3-dihydro-5-methylfuran-2-one, 14 1-cyclopentylethanone, 15 2-hydroxy-3-methyl-2-cyclopenten-1-one, 16 3,5-dimethylcyclopentan-1,2-dione, 17 unknown, 18 3-ethyl-2,4(3H,5H)-furandione, 19 6-methyl-1,4-dioxaspiro[2,4]heptan-5-one, 20 1-hydroxy-3,6-dioxabicyclo[3.2.1]octan-2-one, 21 1,4 3,6-dianhydro-a-D-glucopyranose, 22 5-(hydroxymethyl)-furfural, 23 4-cyclopenten-1,2,3-triol, 24 5-ethyl-3-hydroxy-4-methyl-tetrahydrofuran-2-one, 25 levoglucosan, 26 1,6-anhydro-p-D-glucofuranose.
Maltol, ethyl maltol, 4-hydroxy-2,5-dimethyl- 3(2H)-furanone, 4-hydroxy-5-methyl-3(2H)- furanone Enhance odour impressions, e.g. fruity, creamy maltol and ethyl maltol improve the mouthfeel of low fat foods... [Pg.352]

DIMETHYL-3-HYDROXY 3(2H)>FURANON 5-METHYL-2-ETHYL-4-HYDROXY 3(2H)-FURANON 2,5-D METHYL-4-METHOXY 3(2HFFURANON 3-METHYL CYCLOPENT -2-EN-2-OL-1-ON... [Pg.394]


See other pages where Furanone, 5-ethyl-3-hydroxy-4-methyl is mentioned: [Pg.198]    [Pg.198]    [Pg.234]    [Pg.245]    [Pg.129]    [Pg.607]    [Pg.236]    [Pg.37]    [Pg.270]    [Pg.270]    [Pg.270]    [Pg.374]    [Pg.416]    [Pg.556]    [Pg.84]    [Pg.198]    [Pg.580]    [Pg.716]   
See also in sourсe #XX -- [ Pg.154 ]

See also in sourсe #XX -- [ Pg.165 ]




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1-Ethyl-2-methyl-5-hydroxy

3 -Furanon

3- Ethyl-5-hydroxy

4-Hydroxy-5-methyl-3 -furanone

5-Ethyl-4-hydroxy-2-methyl-3 -furanon

5-Ethyl-4-hydroxy-2-methyl-3 -furanon

Furanone 5-methyl

Hydroxy ethylation

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