1997
DOI: 10.1016/s0008-6215(97)00234-6
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Thermal decomposition of ascorbic acid

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Cited by 83 publications
(56 citation statements)
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“…Its identification as a thermal degradation product of thiamin has been described previously (Hartman, Carlin, Scheide, & Ho, 1984). A possible pathway for the formation of 2-methyltetrahydrothiophen-3-one involves aldol condensation between acetaldehyde, derived from cysteine or ASA, and pyruvaldehyde, formed from ASA (Vernin et al, 1998). The aldol condensation product reacts with hydrogen sulphide to produce 2-methyltetrahydrothiophen-3-one.…”
Section: Thiophenonesmentioning
confidence: 87%
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“…Its identification as a thermal degradation product of thiamin has been described previously (Hartman, Carlin, Scheide, & Ho, 1984). A possible pathway for the formation of 2-methyltetrahydrothiophen-3-one involves aldol condensation between acetaldehyde, derived from cysteine or ASA, and pyruvaldehyde, formed from ASA (Vernin et al, 1998). The aldol condensation product reacts with hydrogen sulphide to produce 2-methyltetrahydrothiophen-3-one.…”
Section: Thiophenonesmentioning
confidence: 87%
“…They are the major volatile products in the reaction of glucose with cysteine (Zhang & Ho, 1991). These alicyclic S-compounds can be formed from the condensation of aldehydes, H 2 S, and mercaptoacetaldehyde (Chen & Ho, 2002), all of which are thermal breakdown products of cysteine and ASA (Mottram & Whitfield, 1995;Vernin, Chakib, Rogacheva, Obretenov, & Párkányi, 1998). It has been suggested that 3,5-dimethyl-1,2,4-trithiolane can be formed by the reaction of two molecules of acetaldehyde with hydrogen sulphide (Takken, van der Linde, de Valois, van Dort, & Boelens, 1976).…”
Section: Alicyclic S-compoundsmentioning
confidence: 99%
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“…Although ascorbic acid is known to produce acetaldehyde and glycolaldehyde when heated at 180 o C (Vernin et al, 1998) and thus, in theory, can produce furan through aldol condensation, however, due to the ease of oxidation and hydrolysis of ascorbic acid in food (Liao and Seib, 1987) and subsequent formation of 2,3-diketogulonic acid (DKG), Perez and Yaylayan (2004), based upon carbohydrate degradation mechanism, proposed the formation of similar four carbon precursors such as an aldotetrose and 2-deoxy-aldotetrose that could be converted into furan (Fig. 6).…”
Section: Figmentioning
confidence: 99%
“…All the presented mechanism of ascorbic acid degradation are quite complex, there are about 200 different products reported in the literature so far. Upon literature review degradation of ascorbic acid was investigated by different methods: HPLC and spectrophotometry (Jingyan et al 2013), GC-MS (Vernin et al 1998) TG (Lerdkanchanaporn et al 1996). Information about degradation products containing vitamin C are very interesting and useful in terms of safety and effi cacy of food and medical products .…”
Section: Introductionmentioning
confidence: 99%