A Guide to Food Additives

The best way to be sure that what you eat has been produced without any cruelty to animals is to plant it, watch it grow and then harvest it yourself. But only a small proportion of UK residents are in a position to obtain an optimum fresh and varied Vegan diet exclusively from home-grown or otherwise locally produced food. Added to which, not all people who are in this position are Vegans. Therefore, mass produced, preserved and packaged food, gathered from diverse and distant places, will be relied upon to some extent by nearly all Vegans in the UK. So, Vegans need to be able to trust, read and understand the food labelling information available on packaging, as well as to evaluate the acceptability of products with regard to cruelty to animals.

The article is intended to help.



FOOD ADDITIVES

The food we eat is chemically complex. Many different chemicals exist within a given foodstuff, and we do not know how one ingredient reacts with others over time or within a recipe. Scientists are making incredibly clever discoveries about food and body chemistry, but this knowledge is not widely broadcast, easily acted upon nor very extensive. Much of our culinary knowledge is passed on by ancient traditions of practice, or we follow recipe books, and glean principles from these through experimentation, which gradually metamorphose into our own style of artistry.

We rely upon our ‘senses’, ‘memories’ and ‘manual skills’ to obtain the food we need, whether this involves growing it ourselves from seeds, or buying it ready-made from a shop. But nutrients are used by our bodies on a molecular level, which is more distant in scale to the senses we rely upon than humans are small in contrast to the Galaxy which surrounds us. If we change what we eat, and the environments in which it is produced, the lessons of trial and error passed on through history can no longer serve us. We do not really know what we eat at the best of times: our requirement for food is a very mysterious thing, although central to our health, happiness and survival.

Food additives compound the problem. Food producers add them to their products because they react chemically with the foodstuffs in ways that increase their commercial usefulness. Edible things decay and have limited shelf-life. Best eaten fresh, their appearance, taste and nutritional value deteriorates with time. Additives benefit food producers by making their foods’ look more appealing, taste pleasing and pass nutritional tests for as long a time as possible. In this way, they remain marketable following journeys through a wide a variety of environmental conditions to the plates of potential customers. Foods with additives can never be as healthy as fresh foods without them, and the side-effects of their chemical reactions are still not known. Their purpose is primarily to deceive.

The reason we eat is so that we may have health, happiness and life. If we eat the wrong things, or don’t eat anything at all, we become miserable, sick and die. “Health” is now understood as the body’s capacity to fight against disease rather than the absence of any threats to its wellbeing, and our bodies have incredible mechanisms for resisting illness. . Added to which, different species of creature, and different individual creatures within each species (including humans), also have slightly different nutritional requirements and chemical defences. Our digestive needs and self-defence mechanisms also change during the different stages of each life. Generally, we can say that some things are good for us, and some things are bad for us, and that each thing whether good or bad has thresholds within which it may do good, be survived, or cause grievous bodily harm, or even fatality. There are also numerous good and bad things within each identifiable food.

The art of successful eating would therefore seem to be to maximise the variety of good things digested in optimum quantities, whilst minimising the range of bad things consumed without ever exceeding the body’s capacities for self-defence. Food is an everyday matter of life and death even where only plants are considered as being suitable for food.

To help safeguard life in dubious circumstances, we have a useful tendency to formulate dietary laws. To use a USA term, legally permitted ingredients added to food by producers are “Generally Regarded As Safe” (or “GRAS” for short). This does not mean that they are known to be safe, only that there is no firm knowledge yet available to prove that they are harmful. In the kitchen we know that as a general rule it is healthy to eat fruits and vegetables, but in the Pharmacist’s laboratory we are also aware that there are plants which are poisonous or ought only be consumed or applied carefully to our body surfaces in small quantity by prescription. These plants may grow side by side in the same gardens, fields and hedgerows or even be different parts of the same plants. In recreational gardens, they may just seem to be bursts of colour and patterns of similar botanical forms, and the only perceived consequence of touching them or subjecting our olfactory senses to them may be a reprimand or explanation from a watchful gardener. The knowledge we receive about our food is very compartmentalised and disconnected.

For example, from the Flax plant we obtain decorative blooms for flower displays, linnen fibre to make our clothes and furnishings, oil to make our paints and clean our paint brushes, and seed to supply essential nutrition and properties to our baking and breakfast cereals, and more besides. These different products are from the same plant but do not have interchangeable uses. Processing each of these distinct products differently can bring about an even wider variety of results. Similarly, one single food additive will result in a different chemical change when used for different purposes, in different foodstuffs, and as a result of different conditions and processes. Furthermore, the same chemical may be obtained from a variety of sources, wider than even the same family of plants. We do not yet have the ability to predict the chemical changes that can occur, let alone to assess them on a level appropriate to establishing what they do within our bodies when we consume them as food.

Where quite a lot is known about an ingredient, standard amounts have been agreed to define a “GRAS” level. This falls between a Minimum Tolerable Daily intake, and a Maximum Tolerable Daily intake (MTDI) with a Recommended Daily Allowance (RDA) somewhere in between. This knowledge may have been obtained through experimentation on other species. What is known about an ingredient does not usually include information about the long-term effects of toxins upon human health amongst different groups of people living in different lands and climates, or amongst those at different stages of bodily or mental development. (The other foodstuffs that it may react with in the bowels after consumption are not considered in advance of serious illness resulting. How often do you see health warnings on foods saying “Not to be eaten with” an incompatible product?)

All the countries in the European Union share a common list of additives. They are preceded with an ‘E’ to show that they have been approved for use within the Union, and they must be displayed on the labels of foods containing them. Some additives, which do not have E numbers, do not need to be declared. These include solvents used to dilute other additives (such as colourings) and to extract flavours. Flavourings constitute the largest group of non-E additives. Additives permitted in the EU can be known to give rise to illnesses such as eczema, hyperactivity, nausea, allergies, asthma and migraine in some people.

In children, the effects of toxins may not become noticeable until undeveloped tissues and organs ought to be effective. It may then be impossible to associate the malformation with the particular chemical responsible, or to identify its source. That being said, sufficient evidence does continue to arise and continues to result in many GRAS substances being reclassified as toxic and prohibited. But more new, untested additives find their way onto the shelves each year.


Uses for Food Additives fall into 12 broad categories:

1. Preservatives or antimicrobials


These are substances (or processes) which are used to prevent foods being spoiled by bacteria, fungus and mould, so that they maintain appetising appearance and edibility for a longer period of time.


EXAMPLES:

Benzoic Acid and its sodium (Na) salts.

These are bacteriostatic or germicidal agents. Benzoic Acid is found naturally in berries such as raspberries.
As an acid, it can only be used in foods with a ph value of less than 4.5.
Apparently, the human body can excrete Benzoic Acid completely through urination within 9 to 15 hours of eating food containing it. It may be problematic for people who have ineffective immune systems if total elimination is necessary.

Sulfur Dioxide (HSO3 etc) and Sulphites.

These are the most effective inhibitors of deterioration of dried fruits and fruit juices, and were used by the ancient Egyptians and Romans.
However, it destroys thiamine and foods preserved in this way cannot be used as sources of this essential vitamin.
They are also toxic and ought to be consumed in small quantities only.

Nisin

Sorbic Acid and Salts.

Naturally present in some fruits, this can inhibit growth of some moulds, yeasts and bacteria whilst leaving others to break down foods into a more stable state, such as cheeses, pickles and some drinks.
(2,4-hexadienoic acid, CH3-CH=CHCH=CHCOOH)

Propionic Acid and Salts.

Calcium and Sodium salts of propionic acid are used in bread to inhibit the growth of micro-organisms which are not susceptible to high baking temperatures, and would otherwise cause ‘Rope’ under summer conditions.

CH3CH2COOH

Antioxidants.

Prevent oxidation which causes fatty products and oils to go rancid.

Ascorbic Acid (Vitamin C).

Can be used to preserve water-soluble products.

Salt.

Pickling in salt and fermentation processes resulting in the production of lactic acid, alcohol or acetic acid are methods of food preservation that date from ancient times. For example, human droppings falling on floors of salt caves near the Dead Sea resulted in sodium nitrate and sodium nitrite, which were then used to preserve corpses, or parts thereof for later consumption. The nitrite also prevents development of the Clostridium botulinum bacterium, which causes the most deadly botulism poisoning when affected decaying flesh it eaten. However, nitrites can react with secondary amines in the human digestive system to form nitrosamines, which are highly carcinogenic.

Saltpetre (nitrates) and Nitrites.

These occur naturally in many foods, especially vegetables, and are increased during digestion in the human gut. The metabolism of infants is not able to deal with these efficiently, because they cannot deal with the modifications they make to blood haemoglobin, and so its use should be restricted.

Acetic Acid (vinegar)

Alcohol

Diethyl pyrocarbonate

This preservative decomposes rapidly in water to form ethyl alcohol and carbon dioxide. It is useful in the preparation of wines, beer and other drinks. It apparently produces urethane when reacting with some foods, and so is no longer GRAS.
C2H5OCOOCOOC2H5

Sodium diacetate.

Another Rope inhibitor used in breads and other baking.

Hexamethylenetetramine.

Used to preserve some fish products in some parts of the world (though not Australia).

Sugars

Glycerol

Herbs

Hop Extract

Spices and condiments.

Contain antioxidants which help to preserve food when refrigeration is unavailable.

Essential Oils

Materials formed during process smoking

Food Irradiation

Materials from Preservative Packaging:

“Biphenyl” is a fungistatic ingredient of citric fruit wrappers, which is intended to migrate to the fruit to inhibit mould growth.

Careful, contamination-free handling, storage and transit.

Refrigeration.

Freezing.

Other Historic Food Preservatives

Ethylene and Propene:

Produced by incomplete combustion of oil shale; was used by the Chinese to ripen bananas and peas many thousands of years ago.

2. Antioxidants

These preserve fatty products and oils. They prevent oxidation occurring, which would cause fats and oils to turn rancid.

EXAMPLES:

Esters of gallic acid


BHA (butylated hydroxyanisole)

Has similar properties to the natural oxidant, Vitamin E (alpha-tocopherol). Usually associated with the poisonous cresol and phenol groups, but these are safe, and so are given the name ‘butylated’. Various esters (propyl, acetyl and dodecyl) of gallic acid (3,4,5-trihydroxy-benzoic acid) are used in margarine, oils, cream cheese and instant mashed potatoes to give them longer shelf life.

BHT (butylated hydroxytoluene)

Has similar properties to the natural oxidant, Vitamin E (alpha-tocopherol). Usually associated with the poisonous cresol and phenol groups, but these are safe, and so are given the name ‘butylated’. Various esters (propyl, acetyl and dodecyl) of gallic acid (3,4,5-trihydroxy-benzoic acid) are used in margarine, oils, cream cheese and instant mashed potatoes to give them longer shelf life.

Phospholipids

Vitamin C

(Used in some water-soluble products.)

Tocopherols (Vitamin E)

TBHQ



3. Sequesterants


Substances which react with traces of metal ions, tying them up in a manner that prevents their normal reactions, such as catalysing the decomposition of food. They are used in shortenings, mayonnaise, lard, soup, margarine, cheese, etc.

EXAMPLES:

Citric Acid

This is the chief acid in citrus fruit (6-7% in lemon juice), which acts as a helping agent of synergist for antioxidants.

Phosphates.

Used in detergents to bind up metal ions in water.

4. Colourings

Substances used to colour food differently to its natural appearance.

EXAMPLES:

Synthetic colours

are mainly coal-tar dyes, many of which have been found to be carcinogenic. The list of GRAS dyes are growing shorter. In Australia all fat-soluble dyes have been banned since 1955, but when SO3-Na+ is added, they become water-soluble, and these have gradually lost their GRAS status as their safety has been disproven. Canada were first to ban butter yellow (11020-p-dimethylaminoazosudan I) in 1934 for being notoriously carcinogenic.

Aromatic hydrocarbon rings

are taken from coal tar (mainly benzene and naphthalene), and the colour is then introduced by one or more diazo (dinitrogen) groups –N=N-. So that the dye becomes water soluble, one or more sulfonic acid groups are attached (SO3-), with Sodium (Na+) or NH4+ providing the other ion.
The dyes are generally made by joining two halves of the desired molecule in a diazo coupling reaction between Nitrogen atoms. This can be problematic within a human or other animal gut, where it is broken in half again by bacteria, one half is then no longer sulfonated, and it can be absorbed by the gut. (This was first discovered in 1935, when the first antibacterial sulfa drug called Prontosil was found to form ‘sulphanilamide’, an active drug, in the bowel.) When the chemical bonding between the two halves are such that both parts remain sulfonated upon breaking, the chemicals will hopefully not be absorbed but pass through the body without poisoning it. Tar was medically observed to cause cancer in humans in 1775, even though animal experiments only suggested similar results through cross-species comparison in 1918.

Triphenylmethane colours

are all “sulfonated” and highly water soluble. They do not break up metabolically and are poorly absorbed, therefore remaining non-toxic. All of the synthetic colours are members of the same azo group but are not formed in the same way, therefore incurring different health risks. Two of the basic materials for their manufacture are naphthylamines, one of these being 2-naphthylamine which is very carcinogenic, and can sometimes pollute the other less harmful variety. 2-napthylamine was medically observed as carcinogenic in humans in 1895; experiments upon other species of animal suggested that this might be the case 43 years later in 1938
. In 1960 there were 14 permitted food dyes in the USA compared to 30 in the UK, but 9 of the US dyes were banned in the UK. The gold colour used in pre-1977 UK kippers was abandoned upon entry into the EU, along with British pork sausage pink. One of the big problems associated with repeated LD50 testing of these substances is that their long term effects are not even considered. By administering doses sufficient only to kill half of the animals used in trials, and soon afterwards destroying the animals which manage to survive the quantities fed to them, dyes which are then GRAS may actually inflict unobserved injury, generate slow-forming cancers and have cumulative toxicity in the subject species as well as humans.
Although people prefer brightly coloured foods, which stimulate appetite and salivation (and even affect the way we experience their taste) there are no health reasons in favour of their inclusion.

E100 to E109 – yellow (E102 tartrazine)

E110 to E119 – orange

E120 to E129 – red

Erythrosine, used to colour some cereals. Is mostly excreted through the faeces, and therefore not regarded as toxic.

E130 to E139 – blue

E140 to E149 – green

E150 to E159 – brown and black (E150 ammoniacal caramel)

E160 to E169 – unclassified

E170 to E189 – unique surface colourants

E190 to E199

E200 to E209

E210 benzoic acid

E211 sodium benzoate

E212 potassium benzoate

E213 calcium benzoate

E405 propylene glycol alginate



5. Flavourings and Flavour Enhancers

Aromatic substances, both natural and synthetic, which are used as components of food flavours, or directly in foods, and in artificial sweetening agents. In 1991, there were estimated to be between 1100 and 1400 natural or synthetic flavours available. It has not been possible to check them all for health risks.

The industry divides flavourings into five main groups: 1. Aromatic raw materials of vegetable and animal origin, such as pepper or meat extract. 2. Natural flavours such as concentrates prepared from aromatic raw materials by extraction and concentration. (The flavour of Tarragon vinegar is, for example, extracted from Tarragon.) 3. Natural flavouring substances that are isolated from aromatic raw materials by physical means. Lemon oil bought in a bottle, for example, contains the same chemicals as the zest of lemon, which can be collected by rubbing a sugar cube over a lemon. 4. Natural substances that are isolated by chemical processes but are identical with the natural substance. For example, monosodium glutamate prepared synthetically is the same as monosodium glutamate found naturally in tomatoes, mushrooms, parmesan cheese and sweet corn. 5. Artificial flavouring substances that have not been identified in natural products but that stimulate natural flavours.

It is hard to identify flavourings in food products, due to the wide variety of sources and mixtures and the small quantities that are present. The technique of gas chromatography can identify quite sensitive differences when comparing different sources of nominally similar compounds, which may have distinctly different taste. As plants with distinctive flavours ripen, their flavour may not change but the quantity of distinctive flavourings may rise and fall. If fatty acids are in a food, they may oxidise and the resultant rancid taste may override the desired flavour even though it is still present.
The smell of rotting potatoes is caused by bacterium which break down the two amino acids tryptophan and tyrosine to produce compounds found in human faeces and horse dung, which can contaminate potatoes which are not themselves rotting. The flavours of some fungicides and other preservatives used in foods can be picked up by humans at incredibly low levels, placing highly toxic substances in a realm of aesthetic concern only.


EXAMPLES:

2-methoxypyrazines,

including 3-isopropyl derivative, responsible for the aroma and flavour of green capsicums, which is also in pea pods, with a far smaller quantity in the pea seed.

Monosodium glutamate (MSG)

This is the most common flavour enhancer. It is the monosodium salt of glutamic acid, one of the natural amino acids. Eaten in excess it can cause illness, and it is now banned from baby foods. It is used generously by cooks in South East Asia, especially in complex dishes to bring out many subtle flavours. It is efficiently manufactured through fermentation of glucose or sucrose produced by the acid hydrolysis of any inexpensive, marginally available carobydrate. In Thailand, it might be made from molasses and tapioca in a nutrient medium containing nitrogen (such as available in urea). The organism Corynebacterium glutanicum sets to work until short, needle-like, dull-appearance crystals form, which smell like sauerkraut whilst tasting both sweet and salty. They can easily be mistaken for borax, sodium metaphosphate, table sugar or table salt, which are common illegal additives – borax especially may be placed in flesh food dishes, being highly poisonous. The presence of borax in MSG can be identified by dissolving the crystals in a solution of Turmeric powder extracted into ethanolor methylated spirits. If borax is present, newspaper strips will turn pink in the solution. If the crystals are dissolved directly into Hydrochloric Acid, a similar result will be obtained.

Disodium 5’-guanylate and disodium 5’-inosinate

Ethyl maltol

Thaumatin



6. Sweeteners


EXAMPLES:

Honey

.The sweetener used most usually in the ancient Roman Empire, providing for the sweet tooth of St John the Baptist whilst living in the wilderness. It is an animal product, cultivated by bees for their own nutritional needs. Whilst the Vegan Society has sympathised in the past with back-garden bee-keepers who care for the bees in the hives they provide, most honey is obtained without concern for the creatures on a factory-farming basis. Because taking honey from even the best-kept bees is depriving them of at least a proportion of the fruits of their labour (perhaps replacing it with an inferior good such as sucrose), Vegans now avoid eating honey. It is widely used in many pre-packaged products such as fruit bars, muesli and breakfast cereals, and there are many varieties available in jars.

Sugar:

Sucrose (Cane sugar – Saccharum officinarum)

Sucrose is a chemical combination of glucose and fructose. When sucrose is ‘inverted’ it breaks up into glucose plus fructose, which are both then sweeter than the sucrose they came from. It has a relative sweetness of 1.0. Cane sugar is used as the standard against which to measure other sweeteners, by dissolving it in a 4% water solution and comparing its taste.
This was not cultivated in Europe until AD800, and sugar beet (Beta vulgaris) was not cultivated until AD 1800. It gained popularity as a luxury good, made available through slave plantations in the tropics. Food producers use it for various reasons; it preserves the flavour and substance of animal flesh and fruits, it tastes sweet and refreshing, and it degreases the palate after eating oils. It does also have nutritional value, providing proteins, minerals and carbohydrate. It also keeps indefinitely without refrigeration. In solution with salt, it can also save the lives of children suffering from diarrhoea when used as a medicine. Sugar can contribute to dental caries because it feeds the bacterium Spectrococcus mutans which converts it into an acid which attacks the teeth and gums, but more sticky sweet substances have a worse effect. Consuming sugars in their natural state in plants is more beneficial to health though because they are accompanied with more nutrients. Therefore, obtaining nutrition from refined sucrose can cause nutritional imbalances and give rise to obesity and/or nutritional deficiencies.

Sucrose Octoacetate

This is a derivative of sugar which obtained the opposite of the desired effect. It is so bitter that it has found a use as an additive in methylated spirits to deter drinking and resultant blindness).

Ethylene glycol

This serves as an anti-freeze, and is toxic, although it has occurred as a food additive. It has a relative sweetness of 1.3.

Fructose

Glycerol (glycerine)

This sugar has a relative sweetness of 0.6.

Lactose

Lactose is a chemical combination of galactose and maltose.

Lead Sugar and Defrutum.

The ancient Romans boiled down grape juice in lead pans to give a concentrated sweet syrup. (When other fruits were used it was called defrutum.) The syrup consequently contained lead salts such as lead acetate (sugar of lead), which is equivalent to sucrose for sweetness. It has a relative sweetness of 1.0. This sugar was added to wine as a sweetener and preservative because lead kills microbes. Lead has adverse health effects upon the human brain and this use of lead in wine, along with lead plumbing and other uses of the metal, has been suggested as the cause of the downfall of the Roman Empire.

Artificial Sweetening Substances:

Saccharin

In tests of high concentrations, potent carcinogenic impurities were found to be present. Otherwise known as ortho-tolenesulfonamide, it was patented and first manufactured in 1894 along with concerns about its safety, it having been discovered in a laboratory by a European called Fahlberg whilst working in the US. It can be used in foods without adding calories, because it is passed through the body unchanged. It does not survive cooking, and animal experimentation suggests that it might be a very mild carcinogen. It has a relative sweetness of 500 to 700.

Sorbitol

Cyclamate (Sodium cyclohexylsulfamate)

Dominated the US market in the mid-60s until it was banned. This sweetener survives cooking. It is mildly carcinogenic. It has a relative sweetness of 30 to 80.

Acesulfame K

Similarly structured to Cyclamate and Saccharin, with a sweetness comparable to Aspartame, but it is stable in water and heat. It is not metabolised, but excreted from the body. It has a relative sweetness of 150.

Dulcin – sucrol (4-ethoxyphenyl)urea

Made at the University of Bern by Joseph Berlinerblau during synthetic chemistry research. It tasted sweet, and he patented it 7 years later. One of the workers testing it for toxicity named it because of its sweet taste in 1893, when animal tests gave inconclusive results. It has a relative sweetness of 250. Considered better than Saccharin because it lacked the bitter aftertaste, its benefits were considered to outweigh its risks. In 1951 the US declared it to be unsafe after further studies, and it was removed from the US market.

D-tryptophan

This has a relative sweetness of 35.

Aspartame (NutraSweet and Equal)

A sweetener of different type to other synthetic sweeteners, it is made of two amino acids joined together to give a dipeptide (aspatyl phenylalanine or methyl ester). Although an essential amino acid, this chemical must be avoided by one person in 15,000 who has a genetic condition called phenylketonuria (PKU). Aspartame decomposes at a rate of 10% per month at ambient temperature, making it useful only for foods with a fast turnover (soft drinks and fruit yoghurts, for example). It cannot be used in cooked foods because this escalates its decomposition. It is alleged that it may break down into methanol which could cause drunken human behaviour, but the small quantities are unlikely to ever be greater than found naturally in fruit juices, and are unlikely to have a serious effect. If present in permitted foods, it must be included on the ingredients list with a warning of risk to PKU sufferers. It is not recommended for pregnant women for whom the equivalent of one measure to sweeten a hot drink is twice the RDA. It has a relative sweetness of 100 to 200.

Methyl fenchyl L-aspartylaminomalonate

A derivative of Aspartame, is has a relative sweetness to sugar of 25,000.

Thaumatin (Talin)

A peptide molecule larger than Aspartame, derived from the West African plant called the ketemfe (Thaumatococcus danielli). Its sweetness is not experienced instantaneously, but has a long and lingering effect 3,000 times sweeter than sugar, with potential as a flavour enhancer. It has been used in pet foods, and it increases weight gain in pigs. It is GRAS.

Hernandulcin

It has a relative sweetness of 1,000.

Sucralose – 4,1’,6’-trichloro-4,1’,6’-trideoxygalactosucrose

It has a relative sweetness of 650. Experiments have been carried out by adding chlorine to sucrose, and where the substitution is made causes different effect. A Tetrachloro substitution in the right place can give an increase in sweetness by 2200. In the wrong place, a chemical as bitter as quinine arises. Sucralose is considered GRAS.

7. Acids and Bases


Acids are used to create a tart taste in foods or to alter the acidity of the medium to prevent chemical processes such as crystallisation occurring. Bases are used as baking powder ingredients, and powders in effervescent beverages.



8. Gelling Agents, Stabilisers, Emulsifiers and Thickeners

Substances used to produce or maintain desirable consistencies in foodstuffs. Stabilisers and thickeners are added to improve the texture and blends of foods. Emulsifying (surface-active) agents are food soaps, used to stabilise emulsions of oil and water components in foods.

EXAMPLES:

Modifying Agents

Group I – Vegetable gums
Agar
Alginic Acid (salts and esters)
Gums of larch
Carrageenan:
This is a polymer made from edible seaweed, belonging to a group of chemicals called polysaccharides (carbohydrates of high molecular mass, including sugars, cellulose and starch). Polysaccharides are particularly effective in icings, frozen desserts, salad dressing, whipped cream, confectionery and cheeses.
Acacia
Guar
Karaya
Locust Bean
Tragacanth
Hydroxypropylmethylcellulose
Methylcellulose
Pectin
Sodium carboxymethylcellulose
Sodium actenyl succinate starch
Xantham gum

Group II – Mineral Salts
Sodium Phosphate:
Is also a water retention agent responsible, in excess quantities, for stunting development of bones in children and reducing adult height. Also being a Mineral Salt, its prevalence is further increased.
CO3(2-)
HCO3(-) of Na+, K+, NH4+, CA2+, Mg2+
CaCl2
CaO
KH tartrate
PO4(3+) of (Na+, K+, Ca2+) including meta, poly and pyrophosphates

Group III – Food Acids
Acetic
Citric
Fumaric
Lactic
Malic
Tartaric (and NH4(+), Ca(2+), K(+), Na(+), salts)

Group IV – Emulsifiers (Surface Active Agents)
Food surficants (soaps) used to stabilise emulsions of oil and water components in foods.
NH4(+)
Salts of phosphatidic acids
Diacetyltartaric acid of ester of mono- and diglycerides,
Glycerol lactostearate
Partially esterified fatty acids (with glycerol or sucrose)
Various polysorbates
Sorbitan monostearate
Phospholipids from natural sources

Group V – Humectants
These prevent foods drying out.

Polyhydric alcohols are additives used as humectants in foods, and tobacco. They tend to be sweet. They are also added to sugarless chewing gum to sweeten it. They have the same energy (calorific) value as cane sugar (16.5 kJ/g).

Glycerol
Mannitol
Sorbitol
Polydextrose
Xylitol

Water Retention Agents: Phosphates are essential minerals, but they are used in soft drinks and production of modified starches, as well as for water retention, and other processed foods. Polyphosphates are used in processing fish, poultry and mammalian flesh to bind water and reduce ‘drip’, and as an aid to yet further processing.
When children consume excessive quantities of phosphates, as when taken as additives in many different foodstuffs, is thought to result in bone growth termination and reduction in their adult height.


Group VI – Thickeners

Starch: Variety of chemically, physically and enzymatically modified starches (with some chemical restrictions on the product formed

.

9. Improving Agents

Chemical compounds that enhance pre-existing qualities within foods, polishing and glazing, taste, consistency, appearance, shelf-life, and so on.


10. Nutritional Supplements


Vitamins and Minerals


A
B1
B2
B12
Niacin (nicotinamide)
C (Ascorbic Acid)
D2
D3
Calcium
Iodine
Iron
Phosphorus

11. Chemicals from Packaging

EXAMPLES:

Reagents

Atomisers/Vaporising Agents

Antibiotics

Release Agents

Propellants (for canisters)

Nitrous oxides E942 (a potent greenhouse gas, also known as laughing gas in a medical context, which has been observed to immobilise the body’s ability to absorb Vitamin B12).

12. Naturally Occurring Toxins

EXAMPLES:

Glycoalkaloids.

Potentially toxic compounds found in plants of the Solanaceae family, which include potatoes, tomatoes, capsicum, tobacco &c (native to the Americas). Only those present in potatoes have been recorded as causing human death, but others cause less extreme conditions.
Humans have greater adverse reactions to potato glycoalkaloids than do other animals, although it can cause foetal death or foetal reabsorption in other species. Bruising and greening of potatoes indicates glycoalkaloid presence, and the worse the bruising and greening the higher the concentration of toxins.
Warning: radiation treatment to preserve potatoes inhibits bruising and greening, but has no effect upon glycoalkaloid build-up. Therefore, in irradiated potatoes (and other members of the Solanaceae family) there is no visible indicator of glycoalkaloid presence, but the vegetables are available for a longer period of time for the toxins to accumulate.

Rhododendrons, snakeweed, deadly nightshade:

When animals or products of their making (milk, honey, etc) are eaten by humans, after these animals have been feeding on plants which may not affect them but are highly toxic to humans, the poisons are passed on to the humans.

Cassava.

Widely eaten in Nigeria, the Cassava root contains compounds which form cyanide during cooking. The toxins pass out of the root when soaked in water, and the traditional preparation involves much soaking, but build-up over time is thought to be responsible for deafness and walking difficulties.


SOME FOODS HARMFUL TO OTHER SPECIES:

Canines:

Grapes, fresh and dried (raisins, sultanas, currants) Chocolate

Rats:

Lysinoalanine: a compound formed in foodstuffs which have been treated with alkali as a preparation for isolating proteins, or in a preparation of maize as eaten by primitive Middle Americans. Saccharin (ortho-toluenesulfonamide): this concentrates urine very highly in their bladders, and may have a mild carcinogenic effect upon them.


For more detailed information about particular ingredients, and whether they are suitable for Vegans, the following website has been formulated by the University of Wageningen in the Netherlands, for your consultation. However, this site is still in the process of construction and does not include information about food additives obtained from analysis outside of the specific dietary field (excluding information gained through medical uses, for example):



Wageningen University Food Information Website



(http://www.food-info.net/uk/index.htm)



References:



The Animal Free Shopper, by the Vegan Society.

Much of the above information has been taken from theConsumer Guide - Chemistry in the Marketplace, by Ben Selinger. This book is no longer in print, and was written for the benefit of Australians. It is possible that some of the details about particular chemicals are now out of date, but it is still the only book of its kind to draw such useful information from. Therefore, for more than a general guide, please research particular chemicals further on the above website, along with other reference sources.


Author: Eleisha C Newman (Show email address.)