Aspartame is an artificial sweetener, roughly 200 times sweeter than sucrose, widely used in food and beverages as a sugar substitute. Chemically, it is the methyl ester of aspartic acid/phenylalanine dipeptide and is marketed under brand names like NutraSweet and Equal. Discovered in 1965, it gained approval from the FDA in 1974, although this was briefly revoked before being re-approved in 1981.
In 1965, James M. Schlatter, a chemist, accidentally discovered aspartame's sweet taste while working for G.D. Searle & Company.
In 1965, aspartame was discovered as an artificial sweetener, being 200 times sweeter than sucrose.
In 1974, aspartame was initially approved by the US Food and Drug Administration (FDA).
In 1975, an FDA task force team reviewed 25 studies submitted by the manufacturer, including 11 on aspartame and reported "serious deficiencies in Searle's operations and practices".
In 1979, the Center for Food Safety and Applied Nutrition (CFSAN) concluded that many problems with the aspartame studies were minor and did not affect the conclusions and the studies could be used to assess aspartame's safety.
In 1980, the FDA convened a Public Board of Inquiry (PBOI) and it concluded aspartame does not cause brain damage, but it recommended against approving aspartame at that time, citing unanswered questions about cancer in laboratory rats.
In 1981, aspartame was re-approved by the FDA after its initial approval was briefly revoked.
In 1983, the FDA approved aspartame for use in carbonated beverages.
In 1985, Monsanto bought G.D. Searle, and the aspartame business became a separate Monsanto subsidiary, NutraSweet.
In 1987, European use patents on aspartame expired.
In 1992, the US patent on aspartame expired.
In 1993, the FDA approved aspartame for use in other beverages, baked goods, and confections.
In 1994, aspartame received EU-wide approval.
In 1996, the FDA removed all restrictions from aspartame, allowing it to be used in all foods.
In March 2000, Monsanto sold NutraSweet to J.W. Childs Associates Equity Partners II L.P.
In 2000, Ajinomoto acquired its aspartame business from Monsanto for $67 million.
In 2002, the Scientific Committee on Food (SCF) reviewed subsequent safety studies and reaffirmed the approval of aspartame.
In 2004, aspartame traded at about $30 per kilogram and sucralose traded at around $300 per kilogram.
In 2004, the market for aspartame, in which Ajinomoto had a 40% share, was 14,000 metric tons a year.
In 2006, The European Food Safety Authority (EFSA) reported that the previously established Acceptable daily intake (ADI) was appropriate, after reviewing yet another set of studies.
In 2006, the Holland Sweetener Company left the sweetener industry due to oversupply and price erosion.
In 2007, Asda was the first British supermarket chain to remove all artificial flavourings and colours in its store brand foods.
In 2008, Ajinomoto sued Asda for a malicious falsehood action concerning its aspartame product when the substance was listed as excluded from the chain's product line.
In July 2009, a British court ruled in favor of Asda in the lawsuit with Ajinomoto.
In November 2009, Ajinomoto announced a new brand name for its aspartame sweetener — AminoSweet.
In June 2010, an appeals court reversed the decision, allowing Ajinomoto to pursue a case against Asda to protect aspartame's reputation.
In 2011, the lawsuit was settled with Asda choosing to remove references to aspartame from its packaging.
In December 2013, the EFSA released a report stating that after examining the evidence, it ruled out the "potential risk of aspartame causing damage to genes and inducing cancer" and deemed the amount found in diet sodas safe to consume.
As of 2017, reviews of clinical trials showed that using aspartame reduces calorie intake and body weight in adults and children.
In 2019, a policy statement by the American Academy of Pediatrics concluded that there were no safety concerns about aspartame in fetal or childhood development or as a factor in attention deficit hyperactivity disorder.
In 2021, the FDA reviewed the scientific information included in IARC's review and identified significant shortcomings in the studies on which IARC relied, disagreeing with IARC's conclusion that these studies support classifying aspartame as a possible carcinogen to humans.
As of May 2023, the FDA stated that it regards aspartame as a safe food ingredient when consumed within the acceptable daily intake level of 50 mg per kg of body weight per day.
In July 2023, scientists for the International Agency for Research on Cancer (IARC) concluded that there was "limited evidence" for aspartame causing cancer in humans, classifying the sweetener as Group 2B (possibly carcinogenic).
As of 2023, regulatory agencies, including the FDA and EFSA, and the US National Cancer Institute, have concluded that consuming aspartame is safe within acceptable daily intake levels and does not cause cancer.
In 2023, the $67 million acquisition from 2000 was equivalent to $113 million.
In 2023, the World Health Organization recommended against the use of common non-sugar sweeteners (NSS), including aspartame, to control body weight or lower the risk of non-communicable diseases.
The World Health Organization WHO is a specialized agency of...
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