Processed eucheuma seaweed (PES)
E 407a · Processed euchema seaweed · PROCESSED EUCHEUMA SEAWEED (PES) · E407a · 407a · Processed euchema seaweed · Afinát řasy Eucheuma · ALGA EUCHEUMA TRANSFORMADA · ALGA EUCHEUMA TRASFORMATA · Algas Eucheuma transformadas · Alghe eucheuma trasformate · ALGUE EUCHEUMA TRANSFORMÉE · Algues Euchema transformées · ALGĂ EUCHEUMA PRELUCRATĂ · Algă marină Eucheuma prelucrată · ALKA TAL-BAĦAR EUCHEUMA PPROĊESSATA · Apdoroti raudondumbliai · APSTRĀDĀTAS EUCHEUMA JŪRASZĀLES · Bearbetad Eucheumaalg · Feldolgozott Euchema moszat · Forarbejdet eucheuma-tang · Guma Euchema · Guma Euchema / Afinát řasy Eucheuma · GUMA EUCHEUMA · GUMA EUCHEUMA / AFINÁT ŘASY EUCHEUMA · Käsitelty Eucheuma-levä · predelana morska alga eucheuma · PRERAĐENA MORSKA ALGA EUCHEUMA · Prerađena morska alga euchema · Processed euchema seaweed · PROCESSED EUCHEUMA SEAWEED · Przetworzone wodorosty morskie z gatunku Eucheuma · Pārstrādātas Euchema jūraszāles · SPRACOVANÁ CHALUHA EUCHEUMA · Spracovaná chaluha Euchema · TSELLULOOSI SISALDAV KARRAGEEN · Töödeldud Eucheuma merevetikad · Verarbeitete Euchema-Algen · Verwerkt Eucheuma-wier · Ħaxixa tal-baħar eucheuma pproċessata · Επεξεργασμένα φύκη Euchema · ΤΡΟΠΟΠΟΙΗΜΕΝΑ ΦΥΚΗ EUCHEUMA · ОБРАБОТЕНИ EUCHEUMA ВОДОРАСЛИ · Преработени „eucheuma“ водораслиE number E407aINS 407a
Listed as an emulsifier, a gelling agent and a thickener by Codex.
Listed as emulsifiers (Codex) · gelling agents (Codex) · thickeners (Codex) · stabilisers (Codex) · humectants (Codex) · glazing and surface-finishing agents (Codex) · bulking agents (Codex) · carriers (Codex)
- Codex Alimentarius: Emulsifier — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Gelling agent — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Thickener — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Stabilizer — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Humectant — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Glazing agent — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Bulking agent — CXS 192-1995 Table One, INS 407a
- Codex Alimentarius: Carrier — CXS 192-1995 Table One, INS 407a
Processed Eucheuma seaweed is a less refined relative of carrageenan, made by washing the seaweed with alkali rather than extracting the polysaccharide out of it. It is used in dairy products and processed meats.
Where it is and isn’t permitted
| Jurisdiction | Status | Scope and limits | Citation |
|---|---|---|---|
| Australia and New Zealand | Permitted, with conditions | 54 food categories no numerical limit (good manufacturing practice) Show every food category
| Food Standards Code, Schedule 15, S15—5and 53 further provisionsretrieved 2026-10-17 |
| Canada | No listing matchedHealth Canada’s lists name additives without E or INS numbers, so this site matches them by exact name. A substance listed there under a name this site does not recognise has no row here. | ||
| European Union | Permitted, with conditions | 69 food categories Show every food category
| Regulation (EC) No 1333/2008, Annex IIand 68 further provisionsretrieved 2026-10-18 |
| Great Britain | Permitted, with conditions | 67 food categories Show every food category
| Assimilated Regulation (EC) No 1333/2008and 66 further provisionsretrieved 2026-10-18 |
| Japan | No listing matchedThis site imports only Japan’s list of designated additives (Appended Table 1 to the Regulations for Enforcement of the Food Sanitation Act), matched by English name. Existing additives, natural flavouring agents and ordinary foods used as additives are permitted outside that list and are not imported, so an empty row does not show that Japan does not permit the substance. | ||
| South Korea | No listing matchedThis site imports Part III of South Korea’s Standards and Specifications for Food Additives, matched by CAS number, then INS number, then exact name. Mixed preparations and sanitisers are not imported, and an entry whose identifiers disagreed with a page’s is held for review, so an empty row does not show that South Korea does not permit the substance. | ||
| United States | Not listedDoes not appear on this jurisdiction’s permitted list. That is not the same as being prohibited. | ||
| Codex Alimentarius | Permitted, with conditions | 21 food categories no numerical limit (good manufacturing practice) Show every food category and its notes
| CXS 192-1995 Table Three, INS 407aand 21 further provisionsretrieved 2026-09-07 |
How much is permitted
A listing usually limits the quantity as well as the food. Only one of the forms that takes is a figure: quantum satis and good manufacturing practice permit the amount the technological effect requires and no more, which is a limit rather than the absence of one. Figures below are the range across every food category this page is listed in, and categories differ between regulators — see how much is permitted.
| Australia and New Zealand | — | 54 GMP |
|---|---|---|
| European Union | — | 46 several limits, 1 quantum satis, 22 no quantity stated |
| Great Britain | — | 67 quantum satis |
| Codex Alimentarius | — | 22 GMP |
No regulator sets a figure for Processed eucheuma seaweed (PES). That is not an absence of control: where the listing says quantum satis or good manufacturing practice, the quantity is limited to what the effect requires.
What it is made from
Made by treating Eucheuma seaweed with alkali and washing it, leaving the cellulose of the seaweed in place. That retained cellulose is what distinguishes it from carrageenan, and why it has its own listing.
- Vegan
- Vegetarian
Compare other additives on the dietary indexes.
The two specifications, compared
The European Union sets identity and purity by regulation; JECFA publishes its own through FAO, advisory until a country adopts it. Both documents are below in full. These are the parameters each puts a number on.
| Parameter | European Union | JECFA |
|---|---|---|
| Loss on drying | no more than 12 % | no more than 12 % |
| Lead | no more than 5 mg/kg | no more than 5 mg/kg |
| Arsenic | no more than 3 mg/kg | no more than 3 mg/kg |
| Mercury | no more than 1 mg/kg | no more than 1 mg/kg |
| Cadmium | no more than 2 mg/kg | no more than 2 mg/kg |
The two documents state the same figures for every parameter compared here.
How the EU defines it
The legal specification an additive must meet to be sold as this E number in the EU — what it is, how it may be made, and the purity it must reach. From Commission Regulation (EU) No 231/2012.
E 407a Processed eucheuma seaweed
Processed eucheuma seaweed is obtained by aqueous alkaline (KOH) treatment at high temperature of the strains of seaweeds Eucheuma cottonii and Eucheuma spinosum, of the class Rhodophyceae (red seaweeds) followed by fresh water washing to remove impurities and drying to obtain the product. Further purification may be achieved by washing with an alcohol. The alcohols authorised are restricted to methanol, ethanol or propan-2-ol. The product consists chiefly of the potassium, sodium, magnesium and calcium sulphate esters of galactose and 3,6-anhydrogalactose polysaccharide. Up to 15 % algal cellulose is also present in the product. The wording processed eucheuma seaweed is reserved to the non hydrolysed or otherwise chemically degraded polymer. Formaldehyde may be present up to a maximum of 5 mg/kg.
Synonyms: PES (acronym for processed eucheuma seaweed). The PES obtained from Euchema cottonii is generally called kappa PES and the PES from Euchema spinosum iota PES.
Assay, identification and purity criteria
Description and assay
- Description
- Tan to yellowish, coarse to fine powder which is practically odourless
Identification
- Test for galactose
- Passes test
- Test for anhydrogalactose
- Passes test
- Test for sulphate
- Passes test
- Solubility
- Forms cloudy viscous suspensions in water. Insoluble in ethanol for a 1,5 % solution.
Purity criteria
- Solvent residues
- Not more than 0,1 % of methanol, ethanol, propan-2-ol, singly or in combination
- Viscosity
- Not less than 5 mPa.s (1,5 % solution at 75 °C)
- Loss on drying
- Not more than 12 % (105 °C, 4 hours)
- Sulphate
- Not less than 15 % and not more than 40 % on the dried basis (as SO₄)
- Ash
- Not less than 15 % and not more than 40 % determined on the dried basis at 550 °C
- Acid-insoluble ash
- Not more than 1 % on the dried basis (insoluble in 10 % hydrochloric acid)
- Acid-insoluble matter
- Not less than 8 % and not more than 15 % on the dried basis (insoluble in 1 % v/v sulphuric acid)
- Low molecular weight carrageenan (Molecular weight fraction below 50 kDa)
- Not more than 5 %
- Arsenic
- Not more than 3 mg/kg
- Lead
- Not more than 5 mg/kg
- Mercury
- Not more than 1 mg/kg
- Cadmium
- Not more than 2 mg/kg
- Microbiological criteria: Total plate count
- Not more than 5 000 colonies per gram
- Microbiological criteria: Yeast and moulds
- Not more than 300 colonies per gram
- Microbiological criteria: Escherichia coli
- Absent in 5 g
- Microbiological criteria: Salmonella spp.
- Absent in 10 g
How JECFA defines it
The international specification for identity and purity, prepared by the Joint FAO/WHO Expert Committee on Food Additives and published by FAO. It is a different document from any above, written by a different body and revised on its own cycle; it is advisory, and a country adopts it or does not.
INS 407a Processed Eucheuma Seaweed
A substance with hydrocolloid properties obtained from either Eucheuma cottonii or E. spinosum (from the Rhodophyceae class of red seaweeds). In addition to carrageenan polysaccharides, processed eucheuma seaweed may contain up to 15% of insoluble algal cellulose and minor amounts of other insoluble matter. Articles of commerce may include sugars for standardization purposes or salts to obtain specific gelling or thickening characteristics. It is distinguished from carrageenan (INS No. 407) by its higher content of cellulosic matter and by the fact that it is not solubilized and precipitated during processing. The functional component of the product obtained from E. cottonii is kappa-carrageenan (a copolymer of D-galactose-4-sulfate and 3,6-anhydro-D-galactose). From E. spinosum it is iota-carrageenan (a copolymer of D-galactose-4-sulfate and 3,6-anhydro-D-galactose-2-sulfate). Processing consists of soaking the cleaned seaweed in alkali for a short time at elevated temperatures. The material is then thoroughly washed with water to remove residual salts followed by purification, drying, and milling to a powder. Alcohols that may be used during purification are restricted to methanol, ethanol, and isopropanol.
Synonyms: PES, PNG-carrageenan, semi-refined carrageenan; INS No. 407a PES; PNG-carrageenan; Semi-refined carrageenan
Assay, identification and purity criteria
Description and assay
- Specification history
- Prepared at the 68th JECFA (2007) and published in FAO JECFA Monographs 4 (2007), superseding specifications prepared at the 57th JECFA (2001)and published in the Combined Compendium of Food Additive Specifications, FAO JECFA Monographs 1 (2005). A group ADI “not specified” for carrageenan and processed Eucheuma seaweed was established at the 57th JECFA (2001).
- DESCRIPTION
- Light tan to white coarse to fine powder
- FUNCTIONAL USES
- Thickener, gelling agent, stabilizer, emulsifier
Identification
- Solubility (Vol. 4)
- Forms cloudy viscous suspensions in water; insoluble in ethanol A 1 g sample disperses and partially dissolves in 100 ml of water at 80º giving a cloudy opalescent solution. (The sample disperses in water more readily if first moistened with alcohol, glycerol, or a saturated solution of glucose or sucrose in water).
- Test for sulfate
- Dissolve a 100-mg sample in 20 ml of water. Heat to boiling, cool to room temperature, and add 3 ml of barium chloride TS and 5 ml of hydrochloric acid, dilute TS. Filter the mixture. Boil the filtrate for 5 min. A white, crystalline precipitate appears.
- Test for galactose and anhydrogalactose (Vol.4)
- Proceed as directed in Volume 4 (under "General Methods, Organic Components, Gum Constituents Identification") using the following as reference standards: galactose, rhamnose, galacturonic acid, 3,6-anhydrogalactose, mannose, arabinose and xylose. Galactose and 3,6-anhydrogalactose should be present.
- Identification of hydrocolloid and predominant type of copolymer
- Add 4 g of sample to 200 ml of water, and heat the mixture in a water bath at 80º, with constant stirring until dissolved. Replace any water lost by evaporation, and allow the solution to cool to room temperature. The solution becomes viscous and may form a gel. To 50 ml of the solution or gel, add 200 mg of potassium chloride, then reheat, mix well, and cool. A short-textured ("brittle") gel indicates a carrageenan of a predominantly kappa-type. A compliant ("elastic") gel indicates a predominantly iota-type.
- Infrared absorption
- Passes test See description under TESTS
- Test: Infrared absorption
- Prepare a 0.2% aqueous solution of the sample. Cast films of 0.5 mm thickness (when dry) on a suitable non-sticking surface such as Teflon and obtain the infrared absorption spectrum of each film. (Alternatively, the spectra may be obtained using films cast on potassium bromide plates if care is taken to avoid moisture). Iota- and kappa-carrageenan have strong, broad absorption bands, typical of all polysaccharides, in the 1000 to 1100 cm -1 region. Other characteristic absorption bands and their intensities relative to the absorbance at 1050 cm -1 are as follows: Wave number Molecular Assignment Absorbance Relative (cm -1 ) to 1050 cm -1 Kappa Iota 1220-1260 ester sulfate 0.6-1.0 0.9-1.2 928-933 3,6-anhydrogalactose 0.3-0.6 0.2-0.6 840-850 galactose-4-sulfate 0.3-0.5 0.2-0.4 800-805 3,6-anhydrogalactose- 0.0-0.2 0.2-0.4 2-sulfate
Purity criteria
- Loss on drying (Vol. 4)
- Not more than 12% (105º to constant weight)
- pH (Vol. 4)
- Between 8 and 11 (1 in 100 suspension)
- Viscosity
- Not less than 5 cp at 75º (1.5% solution) See description under TESTS
- Sulfate
- Not less than 15% and not more than 40% (as SO4 2- ) on the dried basis See description under TESTS
- Total ash
- Not less than 15% and not more than 30% on the dried basis See description under TESTS
- Acid-insoluble ash (Vol. 4)
- Not more than 1% Use the ash from the Total ash test
- Acid-insoluble matter (Vol. 4)
- Not less than 8% and not more than 15% on the dried basis Use 2 g of sample obtained from part (a) of the procedure for sulfate determination
- Residual solvents (Vol. 4)
- Not more than 0.1% of ethanol, isopropanol, or methanol, singly or in combination See description under TESTS
- Microbiological criteria
- Initially prepare a 10 -1 dilution by adding a 50 g sample to 450 ml of
- (Vol. 4)
- Butterfield's phosphate-buffered dilution water and homogenizing the mixture in a high speed blender. Total (aerobic) plate count: Not more than 5000 cfu/g Salmonella spp.: Negative per test E. coli : Negative in 1 g
- Arsenic (Vol. 4)
- Not more than 3 mg/kg Determine by the atomic absorption hydride technique. Use Method II for sample preparation.
- Lead (Vol. 4)
- Not more than 5 mg/kg Determine using an AAS/ICP-AES technique appropriate to the specified level. The selection of sample size and method of sample preparation may be based on the principles of the method described in Volume 4 (under "General Methods, Metallic Impurities").
- Cadmium (Vol.4)
- Not more than 2 mg/kg Determine using an AAS/ICP-AES technique appropriate to the specified level. The selection of sample size and method of sample preparation may be based on the principles of the method described in Volume 4 (under "General Methods, Metallic Impurities").
- Mercury (Vol.4)
- Not more than 1 mg/kg Determine by the cold vapour atomic absorption technique
- Test: Sulfate
- Principle: Hydrolysed sulfate groups are precipitated as barium sulfate. Procedure: (a) Disperse an accurately weighed 15 g sample of commercial product into 500 ml of 60% w/w isopropanol/water at room temperature. Stir gently for 4 h. Filter through ash-free filter paper. Discard the filtrate. Wash the material remaining on the filter paper with two 15-ml portions of 60% isopropanol/water. Dry the material at 105º to constant weight. Approximately 1 g of the dried matter is to be used for part (b). The remainder should be retained for determination of Total ash, Acid-insoluble matter, and viscosity. (b) Accurately weigh a 1 g sample (W1 ) obtained from part (a), Transfer the sample to a 100-ml long-neck round-bottom flask and add 50 ml of 0.2 N hydrochloric acid. Fit a condenser, preferably one with at least 5 condensing bulbs, to the flask and reflux for 1 h. Add 25 ml of a 10% (by volume) hydrogen peroxide solution and resume refluxing for about 5 h or until the solution becomes completely clear. Transfer the solution to a 600-ml beaker, bring to a boil, and add dropwise 10 ml of a 10% barium chloride solution. Heat the reaction mixture for 2 h on a boiling water bath. Filter the mixture through ash-free slow-filtration filter paper. Wash with boiling distilled water until the filtrate is free from chloride. Dry the filter paper and contents in a drying oven. Gently burn and ash the paper at 800° in a tared porcelain or silica crucible until the ash is white. Cool in a desiccator. Weigh the crucible containing the ash. Calculate the percentage sulfate from the weight in g (W2) of the ash (barium sulfate) using the formula: (W2/W1) x 100 x 0.4116.
- Test: Total ash
- Accurately weigh 2 g of the dried sample (W1) obtained from part (a) under the procedure for Sulfate determination. Transfer to a previously ignited, tared, silica or platinum crucible. Heat the sample with a suitable infrared lamp, increasing the intensity gradually, until the sample is completely charred; continue heating for an additional 30 min. Transfer the crucible with charred sample into a muffle furnace and ignite at about 550º for 1 h. Cool in a desiccator and weigh. Repeat the ignition in the muffle furnace until a constant weight (W2) is obtained. If a carbon-free ash is not obtained after the first ignition, moisten the charred spot with a 1 in 10 solution of ammonium nitrate and dry under an infrared lamp. Repeat the ignition step. Calculate the percentage of total ash of the sample: (W2/W1) x 100. Retain the ash for the Acid-insoluble ash test .
- Test: Viscosity
- Transfer 7.5 g of the dried sample obtained from part (a) under the procedure for sulfate determination into a tared, 600-ml tall-form (Berzelius) beaker, and disperse with agitation for 10 to 20 min in 450 ml of deionized water. Add sufficient water to bring the final weight to 500 g and heat in a water bath, with continuous agitation, until a temperature of 80º is reached (20-30 min). Add 7.5 g of diatomaceous earth or perlite filter aid. Stir for two minutes. Add water to adjust for loss by evaporation. Filter the solution through a Büchner funnel (pre-heated with hot water to 80º) equipped with a coarse filter paper. Place the filter assembly in a vacuum receiver bottle. Filter 200 ml of solution. Cool to 76-77º, and heat in a constant temperature bath at 75º. Pre-heat the bob and guard of a Brookfield LVF viscometer to approximately 75º in water. Dry the bob and guard and attach them to the viscometer, which should be equipped with a No. 1 spindle (19 mm in diameter, approximately 65 mm in length) and capable of rotating at 30 rpm. Adjust the height of the bob in the sample solution, start the viscometer rotating at 30 rpm and, after six complete revolutions of the viscometer, take the viscometer reading on the 0-100 scale. If the viscosity is very low, increased precision may be obtained by using the Brookfield UL (ultra low) adapter or equivalent. Record the results in centipoises, obtained by multiplying the reading on the scale by the factor given by the Brookfield manufacturer.
- Test: Residual solvents (Vol. 4)
- See Method 1 under Vol. 4. General Methods, Organic Components, Residual Solvents. Prepare standard, blank, and calibration solutions as directed under Method1. Sample Preparation Disperse 1 ml of a suitable antifoam emulsion, such as Dow-Corning G-10 or equivalent, in 200 ml of water contained in a 1000-ml 24/40 round-bottom distilling flask. Add about 5 g of the sample, accurately weighed, and shake for 1 h on a wrist -action mechanical shaker. Connect the flask to a fractionating column and distil about 100 ml, adjusting the heat so that the foam does not enter the column. Quantitatively transfer the distillate to a 200-ml volumetric flask, fill to the mark with water and shake the flask to mix. Weigh accurately 8.0 g of this solution into an injection vial. Add 1.0 ml of the internal standard solution. Heat at 60º for 10 min and shake vigorously for 10 sec.
Authorised in other additives, enzymes, flavourings and nutrients
These authorisations are not for use in food. They let this substance be used inside another additive, a food enzyme, a flavouring or a nutrient preparation — often as a carrier — and it reaches food only as part of that product. Annex III to Regulation (EC) No 1333/2008.
| Part | May be used in | Maximum level | Citation |
|---|---|---|---|
| Annex III, Part 2: Food additives other than carriers in food additives | All food additive preparationsAuthorised as a member of Table 1 of Part 6, listed as "Table 1" Note (1): Except enzymes authorised as food additives. | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 2, via Table 1 of Part 6 |
| Annex III, Part 3: Food additives including carriers in food enzymes | Food enzymesNote (1): Including enzymes authorised as food additives. | In enzyme preparation: quantum satis In final food except beverages: quantum satis In beverages: quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 3 |
| Annex III, Part 4: Food additives including carriers in food flavourings | All flavouringsAuthorised as a member of Table 1 of Part 6, listed as "Table 1" | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 4, via Table 1 of Part 6 |
| Annex III, Part 5, Section A: Food additives added in nutrients except in nutrients intended to be used in foodstuffs listed in Part E, point 01.10, of Annex II and foodstuffs for infants and young children listed in Part E, point 13.1, of Annex II | All nutrientsCan be used as a carrier: Yes | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 5, Section A |
Every name it appears under
44 recorded names. A label may use any of them.
E number
- E407a
INS number
- 407a
As it appears in regulation
- Processed euchema seaweed
Other names
- E 407a
- Processed euchema seaweed
- PROCESSED EUCHEUMA SEAWEED (PES)
Hazard reference values
EFSA and JECFA have both assessed Processed eucheuma seaweed (PES) and their conclusions are not two comparable figures — EFSA records 75 mg/kg bw/day, JECFA not specified. An acceptable daily intake is a reference value set by a committee, not a threshold above which harm begins. “Not specified”, “not limited” and “not allocated” are conclusions, not missing data, and they are shown in the words each body used rather than reduced to a number. See where the two committees differ.
Evidence and how bodies read it
What assessing bodies concluded
Each conclusion is paraphrased in the body's own framing, from the published opinion linked beneath it. Where bodies differ, both stand; this site does not adjudicate between them or add a view of its own.
EFSA 2018
The ANS Panel found no concern for genotoxicity or carcinogenicity for carrageenan (E 407) and processed Eucheuma seaweed (E 407a), but noted uncertainties in the chemistry, exposure and toxicological data. It concluded that the group ADI of 75 mg/kg bw/day should be considered temporary while the database is improved within five years.
Common questions
Assembled from what is above, in the words the questions are usually asked in. Each answer is the same statement the relevant section makes, with the same citations behind it.
- What is E 407a?
- E 407a is Processed eucheuma seaweed (PES). Processed Eucheuma seaweed is a less refined relative of carrageenan, made by washing the seaweed with alkali rather than extracting the polysaccharide out of it. It is used in dairy products and processed meats.
- What is Processed eucheuma seaweed (PES) used for in food?
- It is listed as an emulsifier, a gelling agent and a thickener — the role Codex assigns it. This page shows every function each regulator records, with the citation for each.
- Where is Processed eucheuma seaweed (PES) permitted?
- Of the seven regulators this site reads, Australia and New Zealand, the EU, Great Britain and the Codex standard permit it. Each permission is for named foods at named levels, not a blanket one; the table on this page gives them with citations.
- Is Processed eucheuma seaweed (PES) vegan?
- Yes. Processed eucheuma seaweed (PES) is not derived from animals, and is suitable for vegetarians. This page says what it is made from and how.
Sources for this page
- anz retrieved 2026-10-17
- eu retrieved 2026-10-18
- gb retrieved 2026-10-18
- gsfa retrieved 2026-09-07
- euspecs retrieved 2026-10-18
- jecfaspecs retrieved 2026-09-23
Full licence terms and publisher details on Sources. How this page is built and updated: Method.
Machine-readable: a JSON record of this additive is given on request —how to ask for access.
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