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Imre Blank

Researcher at Nestlé

Publications -  117
Citations -  6110

Imre Blank is an academic researcher from Nestlé. The author has contributed to research in topics: Maillard reaction & Amadori rearrangement. The author has an hindex of 36, co-authored 110 publications receiving 5470 citations. Previous affiliations of Imre Blank include University of Stuttgart.

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Acrylamide from Maillard reaction products

TL;DR: It is shown that acrylamide can be released by the thermal treatment of certain amino acids (asparagine, for example), particularly in combination with reducing sugars, and of early Maillard reaction products (N-glycosides).
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A Review of Acrylamide: An Industry Perspective on Research, Analysis, Formation, and Control

TL;DR: This review addresses the analytical and mechanistic aspects of the acrylamide issue and summarizes the progress made to date by the European food industries in these key areas and presents experimental results generated under laboratory model conditions, as well as under actual food processing conditions.
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In-depth mechanistic study on the formation of acrylamide and other vinylogous compounds by the maillard reaction.

TL;DR: Evidence is shown that certain glycoconjugates play a major role in acrylamide formation and it is suggested that this thermal pathway may be common to other amino acids, resulting under certain conditions in their respective vinylogous reaction products.
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Potent odorants of the roasted powder and brew of Arabica coffee

TL;DR: Aroma extract dilution analysis (AEDA) revealed 13 compounds as important contributors to the aroma of roasted coffee (powder): 2-methyl-3-furanthiol (I), 2-furfurylthiol (II), methional (III), 3-mercapto-3 -methylbutylformate (IV), 3isopropyl-2-methoxypyrazine (V), 2ethyl-3,5-dimethylpyrazine(VI), 2,3-diethyl-5-methylpyrazINE
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Formation of furan and methylfuran by maillard-type reactions in model systems and food.

TL;DR: The formation of furan and 2-methylfuran was studied in model systems based on sugars and selected amino acids and indicated two major formation pathways for both furans: from the intact sugar skeleton and by recombination of reactive C(2) and/or C(3) fragments.