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Erythritol (, ) is an , the naturally occurring four-carbon (or ). It is the reduced form of either D- or L- and one of the two reduced forms of . It is used as a and . It is synthesized from corn using and . Its formula is , or HO(CH2)(CHOH)2(CH2)OH.

Erythritol is 60–70% as sweet as . However, erythritol is almost completely

(2026). 9789350905302, Jaypee Brothers Medical Publishers (P) Ltd.
and does not affect blood sugar or cause . Japanese companies pioneered the commercial development of erythritol as a sweetener in the 1990s.


Etymology
The name "erythritol" derives from the Greek word for the color red ( erythros or ). That is the case even though erythritol is almost always found in the form of white crystals or powder, and chemical reactions do not turn it red. The name "erythritol" is adapted from a closely related compound, , which turns red upon oxidation.
(2026). 9783110611069, de Gruyter. .


History
Erythritol was discovered in 1848 by the Scottish chemist The discovery of erythritol, which Stenhouse called "erythroglucin", was announced in and first isolated in 1852.

Starting from 1945, American chemists applied newly-developed techniques of to and , finding in 1950 that erythritol was present in molasses fermented by yeast.

It was first approved and marketed as a sweetener in Japan in 1990, and in the US in 1997.

(2001). 9780824704377, CRC Press. .
In February 1997, Holding Co., Mitsubishi Chemical Co., and Nikken Chemicals Co. submitted a formal generally recognized as safe (GRAS) affirmation petition with the US FDA., 6 March 1997. However, in April 1997 the FDA replaced the GRAS affirmation petition process with the current GRAS notification process, a notice was first filed by Cerestar in April 2001, and the FDA responded with "no questions" in September 2001.


Occurrence
Erythritol occurs naturally in some fruits (watermelons, pears, and grapes in minimal amounts), and in - foods.


Uses
Since 1990, erythritol has had a history of safe use as a sweetener and flavor-enhancer in food and beverage products and is approved for use by government regulatory agencies in more than 60 countries., Quote: "In 2003, the European Union (EU) Scientific Committee on Food (SCF) concluded that erythritol is safe for use in foods. ... the SCF opinion stated that the threshold may be exceeded, especially by young consumers, ... the ANS Panel concluded that the acute bolus consumption of erythritol via non-alcoholic beverages at a maximum level of 1.6 % would not raise concerns for laxation."

Beverage categories for its use are coffee and tea, liquid dietary supplements, juice blends, , and flavored water product variations, with foods including , biscuits and cookies, tabletop sweeteners, and sugar-free chewing gum. The mild sweetness of erythritol allows for a volume-for-volume replacement of sugar, whereas sweeter sugar substitutes need fillers that result in a noticeably different texture in baked products.


Absorption and excretion
Erythritol is absorbed rapidly into the blood, with peak amounts occurring in under two hours; the majority of an oral dose (80 to 90%) is excreted unchanged in the within 24 hours.


Safety
In 2023, the European Food Safety Authority reassessed the safety of erythritol and lowered the recommended daily intake limit to 0.5 grams per kg body weight, which equates to 35 g for an average adult (70 kg). The lower limit was set to "safeguard against its laxative effect and to mitigate against long-term effects, such as electrolyte imbalance arising from prolonged exposure to erythritol-induced diarrhea."

Previously, in 2015, scientists assessed doses for erythritol where symptoms of mild gastrointestinal upset occurred, such as nausea, excess , abdominal bloating or pain, and frequency. At a content of 1.6% in beverages, it was not considered to have a effect. The upper limit of tolerance was 0.78 and 0.71g/kg body weight in adults and children respectively.

In the United States, erythritol is among several sugar alcohols that are generally recognized as safe (GRAS) for food manufacturing.


Dietary and metabolic aspects

Caloric value and labeling
Nutritional labeling of erythritol in food products varies from country to country. Some places, such as and the (EU), label it as zero-calorie.(2008) European Commission Directive 2008/100/EC. Quote: "Erythritol is a polyol, and according to the current rules as provided for in Article 5(1) of Directive 90/496/EEC, its energy would be calculated using the conversion factor for polyols, namely 10 kJ/g (2,4 kcal/g). Using this energy conversion factor would not fully inform the consumer about the reduced energy value of a product achieved by the use of erythritol in its manufacture. The Scientific Committee on Food in its opinion on erythritol, expressed on March 5, 2003, noted that the energy provided by erythritol was less than 0,9 kJ/g (less than 0,2 kcal/g). Therefore it is appropriate to adopt a suitable energy conversion factor for erythritol. Current regulations (Reg. (EC) 1169/2011) preserve this conversion factor at 0 kcal/g for energy value calculation purposes."

Under Food and Drug Administration (FDA) labeling requirements in the United States, erythritol has a caloric value of zero.


Human digestion
In the body, most erythritol is absorbed into the bloodstream in the and then for the most part excreted unchanged in the . About 10% enters the colon.

In small doses, erythritol does not normally cause effects and gas or bloating, as are often experienced after consumption of other sugar alcohols (such as , , , and ). About 90% is absorbed before it enters the , and since erythritol is not digested by intestinal bacteria, the remaining 10% is excreted in the .

Large doses can cause , , and watery feces. Doses greater than 0.66 g/kg body weight in males and greater than 0.8 g/kg body weight in females cause , and doses over cause diarrhea. Rarely, erythritol can cause allergic hives ().


Blood sugar and insulin levels
Erythritol has no effect on blood sugar or blood levels, and therefore may be used as a sugar substitute by people with type 2 diabetes.
(2026). 9781118373941
The (GI) of erythritol is 0% of the GI for glucose and the (II) is 2% of the II for glucose.


Oral bacteria
Erythritol is ; since it cannot be by oral , it does not contribute to . In addition, erythritol, like , has antibacterial effects against bacteria, reduces , and may be protective against tooth decay.


Manufacturing
Erythritol is manufactured by using enzymatic of the starch from corn to generate . Glucose is then fermented with yeast or another fungus to produce erythritol. A genetically engineered form of the yeast Yarrowia lipolytica has been optimized for erythritol production by fermentation by using as a carbon source and high to increase yields up to 62%.


Chemical properties

Heat of solution
Erythritol has a strong cooling effect (, or positive heat of solution)
(2026). 9780849393617, CRC / Taylor & Francis. .
when it dissolves in water, which is often compared with the cooling effect of flavors. The cooling effect is present only when erythritol is not already dissolved in water, a situation that might be experienced in an erythritol-sweetened frosting, chocolate bar, chewing gum, or hard candy. The cooling effect of erythritol is very similar to that of and among the strongest cooling effects of all sugar alcohols. Erythritol has a p Ka of 13.903 at 18 °C.


Biological properties
According to a 2014 study, erythritol functions as an insecticide toxic to the fruit fly Drosophila melanogaster, impairing motor ability and reducing longevity even when nutritive sugars were available.

Erythritol is preferentially used by the . The presence of erythritol in the placentas of goats, cattle, and pigs has been proposed as an explanation for the accumulation of Brucella bacteria found at these sites.


Synonyms
In the 19th and the early 20th centuries, several synonyms were in use for erythritol: erythrol, erythrite, erythroglucin, eryglucin, erythromannite and phycite. Zerose is a for erythritol.


See also

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