2010
DOI: 10.1021/je9008427
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Solubility of Sucralose in Different Solvents from (283.15 to 333.15) K

Abstract: The solubility of sucralose in water, methanol, ethanol, and isopropyl alcohol from (283.15 to 333.15) K was measured by an isothermal method. The results show that the solubility of sucralose in the four solvents increases with the increasing temperature. The experimental solubility data were correlated by the modified Apelblat equation, and the calculated values were in good agreement with the experimental data.

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Cited by 14 publications
(7 citation statements)
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References 9 publications
(13 reference statements)
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“…These particular solvents are often used to extract lipid components from mixtures ( Ramesh et al, 1979 ; Goldsmith et al, 1988 ; Mao-Qiang et al, 1996 ; Cabrini et al, 1992 ; Crabbe et al, 2001 ; Lin et al, 2004 ). The fact that sucralose is readily soluble in alcohols was corroborated by others ( Bennett et al, 1992 ; Anderson et al, 2006 ; Li et al, 2010 ).…”
Section: Potential Toxicity From Habitual Sucralose Ingestionsupporting
confidence: 60%
See 2 more Smart Citations
“…These particular solvents are often used to extract lipid components from mixtures ( Ramesh et al, 1979 ; Goldsmith et al, 1988 ; Mao-Qiang et al, 1996 ; Cabrini et al, 1992 ; Crabbe et al, 2001 ; Lin et al, 2004 ). The fact that sucralose is readily soluble in alcohols was corroborated by others ( Bennett et al, 1992 ; Anderson et al, 2006 ; Li et al, 2010 ).…”
Section: Potential Toxicity From Habitual Sucralose Ingestionsupporting
confidence: 60%
“…The decrease in the concentration of a xenobiotic compound as it passes through the GIT and liver is termed the “first-pass effect” ( Riegelman and Rowland, 1973 ; Iwamoto and Klaassen, 1977 ; Shimomura et al, 2002 ; Watkins, 1997 ; Paine and Thummel, 2003 ; Paine, 2009 ). The intestinal component of the first-pass effect is especially significant in the disposition of sucralose because the majority of this OC sweetener is reportedly unabsorbed from the small intestine after ingestion ( Grice and Goldmith, 2000 ) even though it is an amphiphilic compound with appreciable lipid solubility ( Hough and Khan, 1978 ; 1989 ; Anderson et al, 2006 ; Li et al, 2010 ). Further, higher doses of orally administered sucralose in humans are associated with lower urinary excretion that suggests sucralose absorption is reduced at increased concentrations ( Roberts et al, 2000 ).…”
Section: Effects Of Sucralose On Presystemic Detoxification Mechanismmentioning
confidence: 99%
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“…Because the analyses were performed on a set of sample extracts archived for 36–48 months at −80 °C, there are concerns with sample integrity during long-term storage. Sucralose has been shown to be a relatively inert and stable molecule, and is known to be very soluble in the storage solvent, methanol . There were several duplicate samples collected throughout the study for source, finished drinking and distribution water.…”
Section: Resultsmentioning
confidence: 99%
“…For example, it is used to help improve adherence to medication by masking the bitter taste of drugs and is used in personal hygiene products such as toothpaste and mouthwashes (Gupta et al, 2012;Budanur et al, 2016). The range of products utilising sucralose is larger than most other artifical sweeteners mainly due to its physico-chemical properties (see Section 6.4), in particular its solubility in both water and alcohol (Bennett et al, 1992;Anderson et al, 2006;Li et al, 2010) which enables its use in both fat-and water-based food and beverage applications including alcoholic drinks. This is in contrast to other common artificial sweeteners such as aspartame, saccharin, and acesulfame-K that are only slightly soluble in alcohol (O'Neal, 2006) and so have more limited product applications.…”
Section: Introductionmentioning
confidence: 99%