Food additive#bulking

To regulate these additives and inform consumers each additive is assigned a unique number called an "E number", which is used in Europe for all approved additives. This numbering scheme has been adopted and extended by the Codex Alimentarius Commission as the International Numbering System for Food Additives (INS) to internationally identify all additives (INS number.,

{{Cite web| publisher = United Nations, World Health Organization| title = Codex Alimentarius, Codex General Standard for Food Additives (GSFA) Online Database| url = https://www.fao.org/fao-who-codexalimentarius/codex-texts/dbs/gsfa/en/|date=2025|access-date=4 January 2025}}

E numbers are all prefixed by "E", but countries outside Europe use only the number, whether the additive is approved in Europe or not.

For example, acetic acid is written as E260 on products sold in Europe, but is simply known as additive 260 in some countries. Additive 103, alkannin, is not approved for use in Europe, so does not have an E number, although it is approved for use in Australia and New Zealand. Since 1987, Australia has had an approved system of labelling for additives in packaged foods. Each food additive has to be named or numbered. The numbers are the same as in Europe, but without the prefix "E".{{cn|date=March 2023}}

The United States Food and Drug Administration (FDA) lists these items as GRAS;{{cite web |title=GRAS Notices |url=https://www.hfpappexternal.fda.gov/scripts/fdcc/index.cfm?set=GRASNotices|publisher=US Food and Drug Administration |access-date=4 January 2025 |date=2 January 2025}} they are listed under both their Chemical Abstracts Service number and FDA regulation under the United States Code of Federal Regulations.{{cite web |title=Determining the Regulatory Status of a Food Ingredient |url=https://www.fda.gov/food/food-ingredients-packaging/determining-regulatory-status-food-ingredient |publisher=US Food and Drug Administration |access-date=4 January 2025 |date=20 September 2018}}{{cite web |title=Understanding How the FDA Regulates Food Additives and GRAS Ingredients |url=https://www.fda.gov/food/food-additives-and-gras-ingredients-information-consumers/understanding-how-fda-regulates-food-additives-and-gras-ingredients |publisher=US Food and Drug Administration |access-date=4 January 2025 |date=6 June 2024}}

The FDA publishes a list of food additives for all approved ingredients.{{cite web |title=Final Rules: Food Additives and Color Additives |url=https://www.hfpappexternal.fda.gov/scripts/fdcc/index.cfm?set=FinalRules |publisher=US Food and Drug Administration |access-date=4 January 2025 |date=25 October 2024}}

Food additives can be divided into several groups, although there is some overlap because some additives exert more than one effect. For example, salt is both a preservative as well as a flavor.Erich Lück and Gert-Wolfhard von Rymon Lipinski "Foods, 3. Food Additives" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. {{doi| 10.1002/14356007.a11_561}}{{cite web |title=Food Additives and GRAS Ingredients – Information for Consumers |url=https://www.fda.gov/food/food-ingredients-packaging/food-additives-and-gras-ingredients-information-consumers |publisher=US Food and Drug Administration |access-date=4 January 2025 |date=24 May 2024}}

• Acidulants confer sour or acid taste. Common acidulants include vinegar, citric acid, tartaric acid, malic acid, fumaric acid, and lactic acid.
• Acidity regulators are used for controlling the pH of foods for stability or to affect activity of enzymes.
• Anticaking agents keep powders such as milk powder from caking or sticking.
• Antifoaming agents reduce or prevent foaming in foods. Foaming agents do the reverse.
• Antioxidants such as vitamin C are preservatives by inhibiting the degradation of food by oxygen.
• {{anchor|bulking}}Bulking agents such as starch are additives that increase the bulk of a food without affecting its taste.
• Colorings are added to food to replace colors lost during preparation or to make food look more attractive.
• Fortifying agents: Vitamins and minerals may be added to increase the nutritional value
• In contrast to colorings, color retention agents are used to preserve a food's existing color.
• Emulsifiers allow water and oils to remain mixed together in an emulsion, as in mayonnaise, ice cream, and homogenized milk.
• Flavorings are additives that give food a particular taste or smell, and may be derived from natural ingredients or created artificially.

In Europe, flavorings do not have an E-code and they are not considered as food additives.

• Flavor enhancers enhance a food's existing flavors. A popular example is monosodium glutamate. Some flavor enhancers have their own flavors that are independent of the food.
• Flour treatment agents are added to flour to improve its color or its use in baking.
• Glazing agents provide a shiny appearance or protective coating to foods.
• Humectants prevent foods from drying out.
• Tracer gas allows for package integrity testing to prevent foods from being exposed to atmosphere, thus guaranteeing shelf life.
• Preservatives prevent or inhibit spoilage of food due to fungi, bacteria and other microorganisms.
• Stabilizers, thickening and gelling agents, like agar or pectin (used in jam for example) give foods a firmer texture. While they are not true emulsifiers, they help to stabilize emulsions.
• Sweeteners are added to foods for flavoring. Sweeteners other than sugar are added to keep the food energy (calories) low.
• Thickening agents are substances which, when added to the mixture, increase its viscosity without substantially modifying its other properties.
• Bisphenols, phthalates, and perfluoroalkyl chemicals (PFCs) are indirect additives used in manufacturing or packaging. In July 2018 the American Academy of Pediatrics called for more careful study of those three substances, along with nitrates and food coloring, as they might harm children during development.{{cite news |title=Press release: Some Common Food Additives May Pose Health Risks to Children |url=https://www.aap.org/en-us/about-the-aap/aap-press-room/Pages/AAP-Says-Some-Common-Food-Additives-May-Pose-Health-Risks-to-Children.aspx |work=American Academy of Pediatrics |date=July 23, 2018}}

With the increasing use of processed foods since the 19th century, food additives are more widely used. Many countries regulate their use. For example, boric acid was widely used as a food preservative from the 1870s to the 1920s,{{cite book |author=Bucci, Luke |title=Nutrition applied to injury rehabilitation and sports medicine |url=https://archive.org/details/nutritionapplied0000bucc |url-access=registration |publisher=CRC Press |location=Boca Raton |year=1995 |pages=[https://archive.org/details/nutritionapplied0000bucc/page/151 151] |isbn=0-8493-7913-X }}{{cite book | editor=Rev. Lyman Abbott | title = The Outlook (Vol. 65)|url=https://books.google.com/books?id=__bt37n7ncQC&q=boric+acid+outlook| publisher = Outlook Co. | year = 1900 | pages = 403}} but was banned after World War I due to its toxicity, as demonstrated in animal and human studies. During World War II, the urgent need for cheap, available food preservatives led to boric acid being used again, but it was finally banned in the 1950s. Such cases led to a general mistrust of food additives, and an application of the precautionary principle led to the conclusion that only additives that are known to be safe should be used in foods. In the United States, this induced adoption of the Delaney clause, an amendment to the Federal Food, Drug, and Cosmetic Act of 1938, stating that no carcinogenic substances may be used as food additives.{{Cite journal|last=Epstein|first=S|date=March 1973|title=The Delaney Amendment|url=https://linkinghub.elsevier.com/retrieve/pii/0091743573900169|journal=Preventive Medicine|language=en|volume=2|issue=1|pages=140–149|doi=10.1016/0091-7435(73)90016-9|pmid=4803324}} However, after the banning of cyclamates in the United States and Britain in 1969, saccharin, the only remaining legal artificial sweetener at the time, was found to cause cancer in rats.{{Cite journal|last=Reuber|first=M D|date=August 1978|title=Carcinogenicity of saccharin.|journal=Environmental Health Perspectives|language=en|volume=25|pages=173–200|doi=10.1289/ehp.7825173|issn=0091-6765|pmc=1637197|pmid=363408}} Widespread public outcry in the United States, partly communicated to Congress by postage-paid postcards supplied in the packaging of sweetened soft drinks, led to the retention of saccharin, despite its violation of the Delaney clause.{{cite book | title = Assessment of technologies for determining cancer risks from the environment | publisher = DIANE publishing | year = 1981 | location = Darby, Pennsylvania, USA | pages = 177 | isbn = 1-4289-2437-X }} However, in 2000, saccharin was found to be carcinogenic in rats due only to their unique urine chemistry.{{Cite journal | last1 = Whysner | first1 = J. | last2 = Williams | first2 = GM. | title = Saccharin mechanistic data and risk assessment: urine composition, enhanced cell proliferation, and tumor promotion | journal = Pharmacol Ther | volume = 71 | issue = 1–2 | pages = 225–52 | year = 1996 | doi = 10.1016/0163-7258(96)00069-1| pmid = 8910956 }}{{Cite journal | last1 = Dybing | first1 = E. | title = Development and implementation of the IPCS conceptual framework for evaluating mode of action of chemical carcinogens | journal = Toxicology | volume = 181–182 | pages = 121–5 |date=December 2002 | doi = 10.1016/S0300-483X(02)00266-4| pmid = 12505296 | bibcode = 2002Toxgy.181..121D }}

In 2007, Food Standards Australia New Zealand published an official shoppers' guidance with which the concerns of food additives and their labeling are mediated.{{cite web| last =Food Standards Australia New Zealand| author-link =Food Standards Australia New Zealand| title =Choosing the Right Stuff – the official shoppers' guide to food additives and labels, kilojoules and fat content| year =2007| url =http://www.foodstandards.gov.au/newsroom/publications/choosingtherightstuff/| access-date =3 May 2009| url-status =dead| archive-url =https://web.archive.org/web/20090514070251/http://www.foodstandards.gov.au/newsroom/publications/choosingtherightstuff/| archive-date =14 May 2009}} In the EU, it can take 10 years or more to obtain approval for a new food additive. This includes five years of safety testing, followed by two years for evaluation by the European Food Safety Authority (EFSA) and another three years before the additive receives an EU-wide approval for use in every country in the European Union.{{cite web |title=Food additives |url=https://www.efsa.europa.eu/en/topics/topic/food-additives |publisher=European Food Safety Authority |access-date=4 January 2025 |date=3 January 2025}} Apart from testing and analyzing food products during the whole production process to ensure safety and compliance with regulatory standards, Trading Standards officers (in the UK) protect the public from any illegal use or potentially dangerous mis-use of food additives by performing random testing of food products.{{cite web |title=Food additives |url=https://www.food.gov.uk/safety-hygiene/food-additives |publisher=UK Food Standards Agency |access-date=4 January 2025 |date=13 December 2024}}

There has been controversy associated with the risks and benefits of food additives. Natural additives may be similarly harmful or be the cause of allergic reactions in certain individuals. For example, safrole was used to flavor root beer until it was shown to be carcinogenic. Due to the application of the Delaney clause, it may not be added to foods, even though it occurs naturally in sassafras and sweet basil.{{cite book |author=Fennema, Owen R. |title=Food chemistry |url=https://archive.org/details/foodchemistry00fenn |url-access=limited |publisher=Marcel Dekker |location=New York, N.Y |year=1996 |pages=[https://archive.org/details/foodchemistry00fenn/page/n940 827] |isbn=0-8247-9691-8 }}

Although concerns have been expressed about a linkage between additives and hyperactivity, there is no clear evidence of a cause-and-effect relationship.{{cite journal |vauthors=Amchova P, Kotolova H, Ruda-Kucerova J |title=Health safety issues of synthetic food colorants |journal=Regulatory Toxicology and Pharmacology|volume=73 |issue=3 |pages=914–22 |date=December 2015 |pmid=26404013 |doi=10.1016/j.yrtph.2015.09.026 |url= https://www.sciencedirect.com/science/article/abs/pii/S0273230015300751}}

In 2012, the EFSA proposed the tier approach to evaluate the potential toxicity of food additives. It is based on four dimensions: toxicokinetics (absorption, distribution, metabolism and excretion); genotoxicity; subchronic (at least 90 data) and chronic toxicity and carcinogenity; reproductive and developmental toxicity.

A subset of food additives, micronutrients added in food fortification processes preserve nutrient value by providing vitamins and minerals to foods such as flour, cereal, margarine and milk which normally would not retain such high levels.{{cite journal | last1=Weaver | first1=Connie M | last2=Dwyer | first2=Johanna | last3=Fulgoni | first3=Victor L | last4=King | first4=Janet C | last5=Leveille | first5=Gilbert A | last6=MacDonald | first6=Ruth S | last7=Ordovas | first7=Jose | last8=Schnakenberg | first8=David | title=Processed foods: contributions to nutrition | journal=American Journal of Clinical Nutrition | volume=99 | issue=6 | date=23 April 2014 | issn=0002-9165 | doi=10.3945/ajcn.114.089284 | pages=1525–1542|pmid=24760975|pmc=6410904}} Added ingredients, such as air, bacteria, fungi, and yeast, also contribute manufacturing and flavor qualities, and reduce spoilage.{{cite web | title=Food processing: The advantages of processed foods| date=1 May 2010 | url=https://www.eufic.org/en/food-production/article/the-greatest-thing-since-sliced-bread-a-review-of-the-benefits-of-processed | access-date=5 August 2019|publisher=The European Food Information Council}}

The United States Food and Drug Administration defines a food additive as "any substance the intended use of which results or may reasonably be expected to result directly or indirectly in its becoming a component or otherwise affecting the characteristics of any food". For a novel food additive to be approved, a food additive approval petition must be submitted to the FDA.{{cite web |title=Guidance for Industry: Questions and Answers About the Food Additive or Color Additive Petition Process |url=https://www.fda.gov/regulatory-information/search-fda-guidance-documents/guidance-industry-questions-and-answers-about-food-additive-or-color-additive-petition-process |publisher=US Food and Drug Administration |access-date=4 January 2025 |date=20 September 2018}} The identity of the ingredient, the proposed use in the food system, the technical effect of the ingredient, a method of analysis for the ingredient in foods, information on the manufacturing process, and full safety reports must be defined in a food additive petition. The FDA evaluates the chemical composition of the ingredient, the quantities that would be typically consumed, acute and chronic health impacts, and other safety factors. The FDA reviews the petition prior to market approval of the additive.

ISO has published a series of standards regarding the topic and these standards are covered by ICS 67.220.{{cite web

| last = International Organization for Standardization

| author-link = International Organization for Standardization

| title = 67.220: Spices and condiments. Food additives

| url = http://www.iso.org/iso/iso_catalogue/catalogue_ics/catalogue_ics_browse.htm?ICS1=67&ICS2=220

| access-date = 23 April 2009

}}

{{portal|Food}}

• Food Chemicals Codex
• Joint FAO/WHO Expert Committee on Food Additives
• List of food labeling regulations

{{Reflist}}

• [https://www.who.int/news-room/fact-sheets/detail/food-additives WHO fact sheet on food additives], 16 November 2023

{{Food chemistry}}

{{Public health}}

{{Authority control}}

Category:European Union food law

Category:Food science