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Acesulfame potassium

Calorie-free sugar substitute


Summary

Calorie-free sugar substitute

| NFPA-H = 1 | NFPA-F = 1 | NFPA-R = 0 Acesulfame potassium (, or ), also known as **acesulfame K ** or Ace K, is a synthetic calorie-free sugar substitute (artificial sweetener) often marketed under the trade names Sunett and Sweet One. In the European Union, it is known under the E number (additive code) E950. It was discovered accidentally in 1967 by German chemist Karl Clauss at Hoechst AG (now Nutrinova). Acesulfame potassium is the potassium salt of 6-methyl-1,2,3-oxathiazine-4(3H)-one 2,2-dioxide. It is a white crystalline powder with molecular formula and a molecular weight of 201.24 g/mol.

Properties

Acesulfame K is 200 times sweeter than sucrose (common sugar), as sweet as aspartame, about two-thirds as sweet as saccharin, and one-third as sweet as sucralose. Like saccharin, it has a slightly bitter aftertaste, especially at high concentrations. Kraft Foods patented the use of sodium ferulate to mask acesulfame's aftertaste. Acesulfame K is often blended with other sweeteners (usually sucralose or aspartame). These blends are reputed to give a more sucrose-like taste whereby each sweetener masks the other's aftertaste, or exhibits a synergistic effect by which the blend is sweeter than its components. Acesulfame potassium has a smaller particle size than sucrose, allowing for its mixtures with other sweeteners to be more uniform.

Unlike aspartame, acesulfame K is stable under heat, even under moderately acidic or basic conditions, allowing it to be used as a food additive in baking, or in products that require a long shelf life. Although acesulfame potassium has a stable shelf life, it can eventually degrade to acetoacetamide, which is toxic in high doses. In carbonated drinks, it is almost always used in conjunction with another sweetener, such as aspartame or sucralose. It is also used as a sweetener in protein shakes and pharmaceutical products, especially chewable and liquid medications, where it can make the active ingredients more palatable. The acceptable daily intake of acesulfame potassium is listed as 15 mg/kg/day.

Acesulfame potassium is widely used in the human diet and excreted by the kidneys. It thus has been used by researchers as a marker to estimate to what degree swimming pools are contaminated by urine.

Other names for acesulfame K are potassium acesulfamate, potassium salt of 6-methyl-1,2,3-oxothiazin-4(3H)-one-2,3-dioxide, and potassium 6-methyl-1,2,3-oxathiazine-4(3H)-one-3-ate-2,2-dioxide.

Effect on body weight

Acesulfame potassium provides a sweet taste with no caloric value. There is no high-quality evidence that using acesulfame potassium as a sweetener affects body weight or body mass index (BMI).

Discovery

Acesulfame potassium was developed after the accidental discovery of a similar compound (5,6-dimethyl-1,2,3-oxathiazin-4(3H)-one 2,2-dioxide) in 1967 by Karl Clauss and Harald Jensen at Hoechst AG. After accidentally dipping his fingers into the chemicals with which he was working, Clauss licked them to pick up a piece of paper. Clauss is the inventor listed on a United States patent issued in 1975 to the assignee Hoechst Aktiengesellschaft for one process of manufacturing acesulfame potassium. Subsequent research showed a number of compounds with the same basic ring structure had different levels of sweetness. 6-methyl-1,2,3-oxathiazine-4(3H)-one 2,2-dioxide had particularly favourable taste characteristics and was relatively easy to synthesize, so it was singled out for further research, and received its generic name (acesulfame-K) from the World Health Organization in 1978. Acesulfame potassium first received approval for table top use in the United States in 1988.

Safety

The United States Food and Drug Administration (FDA) approved its general use as a safe food additive in 1988, and maintains that safety assessment, as of 2025.

In a 2000 scientific review, the European Food Safety Authority determined that acesulfame K is safe in typical consumption amounts, and does not increase the risk of diseases.

Other sources

References

References

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  3. (2012-03-14). "Current EU approved additives and their E Numbers". Food Standards Agency.
  4. (1973). "Oxathiazinone Dioxides - A New Group of Sweetening Agents". Angewandte Chemie International Edition.
  5. (1998). "Commercial, Synthetic Nonnutritive Sweeteners". Angewandte Chemie International Edition.
  6. [https://web.archive.org/web/20170430070157/http://patft.uspto.gov/netacgi/nph-Parser?patentnumber=5336513 United States Patent 5,336,513] (expired in 2006)
  7. (November 2006). "Customizing Sweetness Profiles". Food Product Design.
  8. Mullarney, M.; Hancock, B.; Carlson, G.; Ladipo, D.; Langdon, B. "The powder flow and compact mechanical properties of sucrose and three high-intensity sweeteners used in chewable tablets". ''Int. J. Pharm''. 2003, 257, 227–236.
  9. Findikli, Z.; Zeynep, F.; Sifa, T. Determination of the effects of some artificial sweeteners on human peripheral lymphocytes using the comet assay. ''Journal of toxicology and environmental health sciences 2014'', 6, 147–153.
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  11. Whitehouse, C.; Boullata, J.; McCauley, L. "The potential toxicity of artificial sweeteners". ''AAOHN J.'' 2008, 56, 251–259, quiz 260.
  12. Erika Engelhaupt. (March 1, 2017). "Just How Much Pee Is In That Pool?". NPR.
  13. (September 2014). "Low-calorie sweeteners and body weight and composition: a meta-analysis of randomized controlled trials and prospective cohort studies". The American Journal of Clinical Nutrition.
  14. (July 2017). "Nonnutritive sweeteners and cardiometabolic health: a systematic review and meta-analysis of randomized controlled trials and prospective cohort studies". CMAJ.
  15. (September 2015). "Does low-energy sweetener consumption affect energy intake and body weight? A systematic review, including meta-analyses, of the evidence from human and animal studies". International Journal of Obesity.
  16. O'Brien-Nabors, L.. (2001). "Alternative Sweeteners". Marcel Dekker.
  17. (1991). "Biotechnology and Food Ingredients". Van Nostrand Reinhold.
  18. Newton, D. E.. (2007). "Food Chemistry (New Chemistry)". Infobase Publishing.
  19. "Process for the manufacture of 6-methyl-3,4-dihydro-1,2,3-oxathiazine-4-one-2,2-dioxide".
  20. (2006). "Low-Calorie Sweeteners and Other Sugar Substitutes: A Review of the Safety Issues". [[Comprehensive Reviews in Food Science and Food Safety]].
  21. (27 February 2025). "Aspartame and Other Sweeteners in Food". US Food and Drug Administration.
  22. Scientific Committee on Food. (2000). "Opinion - Re-evaluation of acesulfame K with reference to the previous SCF opinion of 1991". EU Commission.
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