All additives
E950·sweetener

Acesulfame K

Limit

Overview

Acesulfame potassium (acesulfame K, E950) is a synthetic, calorie-free sweetener approximately 200 times sweeter than sucrose, first developed by Hoechst chemist Karl Clauss in 1967. Its chemical structure — a six-membered oxathiazinone ring with a potassium sulphonate group — is completely stable under pasteurisation, baking, and the acidic conditions of carbonated beverages, making it one of the most heat- and acid-stable high-intensity sweeteners available. It is frequently blended with aspartame (E951) or sucralose (E955) to improve flavour profile, as acesulfame K alone has a bitter-metallic aftertaste at higher concentrations that synergistic blending mitigates. Applications include soft drinks, desserts, confectionery, chewing gum, and tabletop sweeteners.

JECFA established an ADI of 15 mg/kg body weight per day for acesulfame K (evaluated 2006), and the European Food Safety Authority confirmed the same 15 mg/kg ADI in its 2000 opinion. This agreement between JECFA and EFSA is notable given their occasional divergence on other additives. The ADI was derived from long-term carcinogenicity and reproductive toxicity studies in rats and mice, with the critical study showing a NOAEL of 2,000 mg/kg/day and an uncertainty factor of 100 applied. Estimated dietary exposure from food additive use is generally well below the ADI except in very high-consuming individuals drinking multiple servings of acesulfame K-sweetened diet beverages daily.

Acesulfame K is authorised under EU Regulation (EC) No 1333/2008 and US FDA 21 CFR §172.800 with specific maximum permitted levels in designated food categories. Unlike aspartame, it is stable under all food processing conditions and carries no phenylketonuria (PKU) warning requirement. Emerging research has examined potential effects on glucose metabolism and gut microbiota from high doses in animal models, but human clinical evidence at achievable dietary exposures does not support adverse metabolic effects. Several beverage manufacturers have moved away from acesulfame K in consumer-facing reformulations for clean-label reasons, despite its robust safety record and regulatory clearance in over 100 countries.

Generated from verified JECFA, EFSA, and regulatory data. All numerical values are sourced from the WHO/FAO JECFA Combined Compendium and EFSA OpenFoodTox 3.0.

Safety Assessment

BodyAcceptable Daily Intake (ADI)Year
JECFA0–15 mg/kg body weight/day · JECFA 19901990
EFSA15 mg/kg body weight/day

ADI = the amount of a substance a person can consume every day over a lifetime without appreciable health risk. Expressed as mg per kg body weight per day. Source: WHO/FAO JECFA Combined Compendium; EFSA OpenFoodTox 3.0.

Regulatory Status

JurisdictionStatusNotes
AEApproved (GCC/GSO standards)
CNApproved per GB 2760
European UnionApproved; EFSA ADI 9 mg/kg/day (under re-evaluation)
GBFSA approved with usage limits
INFSSAI approved with category limits
JapanApproved with usage limits
South KoreaApproved (MFDS)
THApproved with usage limits
United StatesGRAS; FDA ADI 15 mg/kg/day
VNApproved with usage limits

Chemical Identity

IUPAC name
potassium 6-methyl-2,2-dioxo-1-oxa-2lambda6-thia-3-azanidacyclohex-5-en-4-one
CAS number
55589-62-3
PubChem CID
11074431

Primary Sources

Products on Looksee containing Acesulfame K

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