Polydextrose
68424-04-4 · POLYDEXTROSES · E1200 · 1200 · Polydextrose · Polydextroses · Polidekstroza · Polidekstrozė · Polidestrosio · Polidestrożju · Polidextrosa · Polidextrose · Polidextroză · Polidextróz · Polydekstroosi · Polydextros · Polydextrosa · Polydextrose · Polydextróza · Polüdekstroos · Πολυδεξτρόζη · ПолидекстрозаE number E1200INS 1200CAS 68424-04-4
Listed as a thickener, a stabiliser and a humectant by Codex and the US.
Listed as thickeners (US, Codex) · stabilisers (US, Codex) · humectants (US, Codex) · texturisers (CA, US) · glazing and surface-finishing agents (Codex) · bulking agents (Codex) · nutrient supplements (US) · formulation aids (US)
- United States: Stabilizer or thickener — FDA, Substances Added to Food: POLYDEXTROSE
- Codex Alimentarius: Thickener — CXS 192-1995 Table One, INS 1200
- United States: Stabilizer or thickener — FDA, Substances Added to Food: POLYDEXTROSE
- Codex Alimentarius: Stabilizer — CXS 192-1995 Table One, INS 1200
- United States: Humectant — FDA, Substances Added to Food: POLYDEXTROSE
- Codex Alimentarius: Humectant — CXS 192-1995 Table One, INS 1200
- Canada: Bodying and texturizing agent — Health Canada, List of Permitted Food Additives with Other Purposes of Use (List 8)
- United States: Texturizer — FDA, Substances Added to Food: POLYDEXTROSE
- Codex Alimentarius: Glazing agent — CXS 192-1995 Table One, INS 1200
- Codex Alimentarius: Bulking agent — CXS 192-1995 Table One, INS 1200
- United States: Nutrient supplement — FDA, Substances Added to Food: POLYDEXTROSE
- United States: Formulation aid — FDA, Substances Added to Food: POLYDEXTROSE
Polydextrose is a bulking agent and soluble fibre, used to replace sugar and fat while keeping the body of the food. It contributes about a quarter of the calories of sugar because the body digests only part of it.
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 | Permitted | no numerical limit (good manufacturing practice) In: Unstandardized foods. Purpose: Bodying and texturizing agent. Limit: Good Manufacturing Practice. | Health Canada, List of Permitted Food Additives with Other Purposes of Use (List 8), item P.4retrieved 2026-10-17 |
| European Union | Permitted, with conditions | 71 food categories Show every food category
| Regulation (EC) No 1333/2008, Annex IIand 70 further provisionsretrieved 2026-10-18 |
| Great Britain | Permitted, with conditions | 69 food categories Show every food category
| Assimilated Regulation (EC) No 1333/2008and 68 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 | Permitted, with conditions | Designated food additive: Standards and Specifications for Food Additives, Part III, 1. …Designated food additive: Standards and Specifications for Food Additives, Part III, 1. 일반식품첨가물 (general food additives), 폴리덱스트로스 (“Polydextrose”, the English the Code prints beside it). Main use (주용도) of 폴리덱스트로스: 습윤제, 안정제, 증점제. Standard for use (사용기준) of 폴리덱스트로스: (1) [to be used under the general standard for use in II. 2. 1), the minimum amount that achieves the technical effect, with no limit set for this additive in particular] “II. 2. 1)의 규정에 따라 사용하여야 한다.” The Korean is the standard as published. There is no official English translation of the current Code (the English version on MFDS’s website is the 2020 edition and has no legal effect); the English in square brackets is this site’s description of what each sentence does, not a translation of the foods or the levels. Compositional specifications (Part IV) are not imported, nor are the general standards in Part II, which apply to every additive. | Standards and Specifications for Food Additives (식품첨가물의 기준 및 규격), MFDS Notification, Part III (Standards for use, by item)retrieved 2026-10-18 |
| United States | Permitted, with conditions | 21 CFR 172.841retrieved 2026-10-17 | |
| Codex Alimentarius | Permitted, with conditions | 11 food categories no numerical limit (good manufacturing practice) Show every food category and its notes
| CXS 192-1995 Table Three, INS 1200and 11 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 |
|---|---|---|
| Canada | — | 1 GMP |
| European Union | — | 46 several limits, 3 quantum satis, 22 no quantity stated |
| Great Britain | — | 69 quantum satis |
| South Korea | — | 1 no quantity stated |
| United States | — | 1 no quantity stated |
| Codex Alimentarius | — | 12 GMP |
No regulator sets a figure for Polydextrose. 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.
GRAS notices to the FDA
A GRAS notice is a company’s conclusion that a substance is generally recognised as safe for the use it describes. FDA’s letter responds to that conclusion, for that notifier and that use. It is not a listing in 21 CFR, and it is not counted as a US permission above. The substance and use are as FDA’s inventory words them; this site matched the notice to this page by exact name.
GRN No. 107 · Polydextrose · Danisco Cultor America
Intended use: Use in non-sweet baked goods, breading and batter coatings, flavor bits on crackers, snack chips, ready-to-eat breakfast cereals, surimi (minced fish and meat), ready-to-drink nutritional beverages, noncarbonated beverages and dry beverage mixes for multiple technical effects at varying levels
FDA’s response (2002-10-17): At the notifier's request, FDA ceased to evaluate this notice
What it is made from
Made by heating glucose with a small amount of sorbitol and an acid catalyst, which links the sugar into randomly branched chains that human enzymes cannot fully break down.
- Vegan
- Vegetarian
Compare other additives on the dietary indexes.
- CAS registry number
- 68424-04-4
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 |
|---|---|---|
| Assay | no less than 90 % | no less than 90 % |
| Sulphated ash | no more than 0.3 % | no more than 0.3 % |
| Lead | no more than 0.5 mg/kg | no more than 0.5 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 1200 Polydextrose
Randomly bonded glucose polymers with some sorbitol end-groups, and with citric acid or phosphoric acid residues attached to the polymers by mono or diester bonds. They are obtained by melting and condensation of the ingredients and consist of approximately 90 parts D-glucose, 10 parts sorbitol and 1 part citric acid and/or 0,1 part phosphoric acid. The 1,6-glucosidic linkage predominates in the polymers but other linkages are present. The products contain small quantities of free glucose, sorbitol, levoglucosan (1,6-anhydro-D-glucose) and citric acid and may be neutralised with any food grade base and/or decolourised and deionised for further purification. The products may also be partially hydrogenated with Raney nickel catalyst to reduce residual glucose. Polydextrose-N is neutralised polydextrose
Synonyms: Modified polydextroses
Assay, identification and purity criteria
Description and assay
- Assay
- Content not less than 90 % of polymer on the ash free and anhydrous basis
- Description
- White to light tan-coloured solid. Polydextroses dissolve in water to give a clear, colourless to straw coloured solution
Identification
- Test for sugar
- Passes test
- Test for reducing sugar
- Passes test
- pH
- Between 2,5 and 7,0 for polydextrose (10 % solution) Between 5,0 and 6,0 for polydextrose-N (10 % solution)
Purity criteria
- Water content
- Not more than 4,0 % (Karl Fischer method)
- Sulphated ash
- Not more than 0,3 % (polydextrose) Not more than 2,0 % (polydextrose N)
- Nickel
- Not more than 2 mg/kg for hydrogenated polydextroses
- 1,6-Anhydro-D-glucose
- Not more than 4,0 % on the ash-free and the dried basis
- Glucose and sorbitol
- Not more than 6,0 % combined on the ash-free and the dried basis; glucose and sorbitol are determined separately
- Molecular weight limit
- Negative test for polymers of molecular weight greater than 22 000
- 5-Hydroxy-methylfurfural
- Not more than 0,1 % (polydextrose) Not more than 0,05 % (polydextrose-N)
- Lead
- Not more than 0,5 mg/kg
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 1200 Polydextroses
Randomly bonded condensation polymers of glucose with some sorbitol end-groups, and with citric acid or phosphoric acid residues attached to the polymers by mono or diester bonds. They are obtained by melting and condensation of the ingredients which consist of approximately 90 parts D-glucose, 10 parts sorbitol and up to 1 part citric acid or 0.1 part phosphoric acid. The 1,6-glucosidic linkage predominates in the polymers but other linkages are present. The products contain small quantities of free glucose, sorbitol, levoglucosan (1,6-anhydro-D-glucose) and citric acid and may be neutralized with any food-grade base and/or decolourized and deionized for further purification. The products may also be partially hydrogenated with Raney nickel catalyst to reduce residual glucose. Polydextrose-N is neutralized Polydextrose.
Synonyms: Modified polydextroses; INS No. 1200
Assay, identification and purity criteria
Description and assay
- Specification history
- Prepared at the 51st JECFA (1998) and published in FNP 52 Add 6 (1998) superseding specifications prepared at the 44th JECFA (1995), published in FNP 52 Add 3 (1995). An ADI "not specified" was established at the 31st JECFA in 1987.
- C.A.S. number
- 68424-04-4
- Assay
- Not less than 90.0% of polymer on the ash-free and water-free bases
- DESCRIPTION
- White to light tan-coloured solid. Polydextroses dissolve in water to give clear, colourless to straw-coloured solutions
- FUNCTIONAL USES
- Bulking agent, humectant, stabilizer, thickener
- METHOD OF ASSAY
- Phenol Solution Add 20 ml of water to 80 g of phenol. Glucose Standard Solutions Weigh accurately 100 mg of alpha-D-glucose (minimum 97% purity) into a 500-ml volumetric flask and make up to volume with distilled water. Dilute five aliquots of the solution with distilled water to obtain the following concentrations of standard: 50, 40, 20, 10 and 5 μg/ml. Standard Curve Run each analysis in triplicate. On a daily basis, pipet 2.0 ml of each of the Glucose Standard Solutions into 4-dram (14.8 ml) acetone-free screw-cap vials. Add 0.12 ml of the phenol solution and mix gently. Uncap vials and add rapidly 5 ml of sulfuric acid TS. Immediately recap the vials and shake vigorously. CAUTION : Rubber gloves and safety shield should be used in the sulfuric acid addition step. Let the vials stand at room temperature for 45 min. Determine absorbances at 490 nm in a suitable spectrophotometer, using a Phenol Solution-sulfuric acid mixture as a blank in the reference cell. Plot mean absorbances versus concentrations in μg/ml. Procedure In triplicate, weigh accurately about 250 mg of the sample into a 250-ml volumetric flask and make up to volume with distilled water. Transfer a 10 ml aliquot to a 250-ml volumetric flask and make up to volume with distilled water. Proceed as in Standard Curve. Calculate the percentage of polymer by the formula: where A = the sample absorbance S = the slope of absorbance versus glucose concentration in μg/ml obtained from the Standard Curve C = the concentration of the sample solution in μg/ml (adjusted for ash and moisture) P G and P 1 = the percentages of glucose and 1,6-anhydro-D-glucose, respectively, determined by the tests for monomers (see Purity tests for 1,6-Anhydro-D-glucose, glucose and sorbitol as described above).
Identification
- Solubility (Vol. 4)
- Very soluble in water
- Test for sugar
- To 1 drop of 1 in 10 solution of the sample, add 4 drops of 5% phenol solution, then rapidly add 15 drops of sulfuric acid TS. A deep yellow to orange colour is produced.
- Solubility in acetone
- With vigorous swirling add 1 ml of acetone to 1 ml of a 1 in 10 solution of the sample. The solution remains clear. With vigorous swirling add 2 ml of acetone to the solution. A heavy, milky turbidity develops immediately.
- Test for reducing sugar
- To 1 ml of a 1 in 50 solution of the sample, add 4 ml of alkaline cupric citrate TS. Boil vigorously 2-4 min. Remove from heat and let precipitate (if any) settle. The supernatant is blue or blue-green.
Purity criteria
- Water (Vol. 4)
- Not more than 4.0% (Karl Fischer Method)
- pH (Vol. 4)
- 2.5 - 7.0 (for Polydextrose) (1 in 10 soln) 5.0 - 6.0 (for Polydextrose-N) (1 in 10 soln)
- Sulfated ash (Vol. 4)
- Not more than 0.3% (for Polydextrose) Not more than 2.0% (for Polydextrose-N)
- Nickel (Vol. 4)
- Not more than 2 mg/kg for hydrogenated polydextroses Use method Nickel for polyols
- 1,6-Anhydro-D-glucose
- Not more than 4.0% on the ash-free and the dried bases See description under TESTS
- Glucose and sorbitol
- Not more than 6.0% combined on the ash-free and the dried bases; glucose and sorbitol are determined separately See description under TESTS
- Molecular weight limit
- Negative to test for polymer of molecular weight greater than 22,000 See description under TESTS
- 5-Hydroxymethylfurfural
- Not more than 0.1% in Polydextrose Not more than 0.05% in Polydextrose-N See description under TESTS
- Lead (Vol. 4)
- Not more than 0.5 mg/kg Determine using an atomic absorption 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, “Instrumental Methods.”
- Test: Lead (Vol. 4)
- Apparatus: Use a suitable atomic absorption spectrophotometer (Perkin-Elmer Model 6000, or equivalent), a graphite furnace containing a L'vov platform (Perkin-Elmer Model HGA-500, or equivalent), and an autosampler (Perkin-Elmer Model AS-40, or equivalent). Use a lead hollow cathode lamp (lamp current of 10 mA), a slit width of 0.7 mm (set low), the wavelength set at 283.3 nm, and a deuterium arc lamp for background correction. Use argon as the carrier gas. (Note: For this test use reagent-grade chemicals with as low a lead content as practicable, as well as high-purity water and gases. Before use, rinse all glassware and plasticware twice with 10% nitric acid and twice with 10% hydrochloric acid, and then rinse thoroughly with high-purity water.) Lead Nitrate Stock Solution: Dissolve 159.8 mg of reagent-grade lead nitrate in 1000.0 ml of water. Prepare and store this solution in glass containers that are free from lead salts. Each ml of this solution contains the equivalent of 100 μg of lead ion. Standard Lead Solution: On the day of use, dilute 10.0 ml of Lead Nitrate Stock Solution with water to 100.0 ml, and mix. Each ml of Standard Lead Solution contains the equivalent of 10 μg of lead ion. Standard Solutions: Prepare a series of lead standard solutions serially diluted from the Standard Lead Solution. Into separate 100 ml volumetric flasks, pipet 0.2, 0.5, 1, 2 ml, and 5 ml, respectively, of Standard Lead Solution, dilute to volume with water, and mix. The Standard Solutions contain, respectively, 0.02, 0.05, 0.1, 0.2, and 0.5 μg of lead per ml. Matrix Modifier: Transfer 100.0 mg of ammonium phosphate, dibasic ((NH 4 ) 2 HPO 4 ) to a 10 ml volumetric flask, dilute to volume with water, and mix. Sample Solution: Transfer about 1 g of the sample, accurately weighed, to a 10 ml volumetric flask, add 5 ml of water, and mix. Dilute to volume with water, and mix. Spiked (fortified) Sample Solution: Prepare a solution as directed under Sample Solution, but add 100 μl of the Standard Lead Solution, dilute to volume with water, and mix. This solution contains 0.1 μg/ml of added lead. Procedure: With the use of an autosampler, atomize 10-μl aliquots of the five Standard Solutions, using the following sequence of conditions: step (1) dry at 130 o with a 20-sec ramp period, a 40-sec hold time, and a 300 ml/min argon flow rate; step (2) char at 800 o with a 20-sec ramp period, a 40-sec hold time, and a 300 ml/min argon flow rate; step (3) atomize at 2400 o for 6 sec with a 50 ml/min argon flow rate, and read; step (4) clean at 2600 o with a 1-sec ramp period, a 5-sec hold time, and a 300 ml/min argon flow rate; and step (5) recharge at 20 o with a 2-sec ramp period, a 20-sec hold time, and a 300 ml/min argon flow rate. Atomize 10 μl of the Matrix Modifier in combination with 10 μl of the Sample Solution under identical conditions used for the Standard Solutions. Repeat with 10 μl of the Matrix Modifier in combination with 10 μl of the Spiked Sample Solution. Plot a standard curve using the concentration, in μg/ml, of each Standard Solution versus its maximum absorbance value compensated for background correction, and draw the best straight line. From the Standard Curve, determine the concentrations C S and C A in μg/ml, of the Sample Solution and the Spiked Sample Solution, respectively. Calculate the quantity, in mg/kg, of lead in the sample by the formula: where W = the weight, in g, of the sample taken. Calculate the recovery by the formula: where 0.1 = the amount of lead, in μg/ml, added to the Spiked Sample Solution.
- Test: 1,6-Anhydro-D-glucose, glucose and sorbitol
- Gas chromatography - Octadecane Solution: Accurately weigh 50 mg of n-octadecane into a 100-ml volumetric flask and make up to volume with pyridine. - Monomer Standard Solution: Weigh accurately 50 mg reagent grade alpha-D-glucose, 40 mg anhydrous D-sorbitol (min. 97% purity), and 35 mg of reagent grade (1,6-anhydro-D-glucose), into a 100-ml volumetric flask and make up to volume with pyridine. Silylation of Monomer Standard Solution Transfer 1.0 ml of Monomer Standard Solution to a screw-cap vial and add 1 ml of Octadecane Solution and 0.5 ml of N-trimethylsilylimidazole. Cap the vial and immerse in an ultrasonic bath at 70 o for 60 min. Gas Chromatograph conditions Glass column, 2.44 m by 2 mm i.d. packed with 3% OV-1 on Gas Chrom Q 100/120 mesh. Flame ionization detector. Temperatures: column 175 o ; injection port 210 o ; detector 230 o . Retention times (min): 1,6-anhydro-D-glucose, pyranose form 3.7; 1,6-anhydro-D-glucose furanose form (not present in standard) 4.3; n-octadecane 5.1; alpha-D-glucose 8.7; D-sorbitol 11.3; beta-D-glucose 13.3. Procedure Accurately weigh 20 mg of the sample into a screw-cap vial and add 1.0 ml of Octadecane Solution, 1 ml of pyridine, and 0.5 ml of N-trimethylsilylimidazole. Cap the vial and immerse in an ultrasonic bath at 70 o for 60 min. Prior to sample analysis, inject 3 μl of the silylated Monomer Standard Solution into the gas chromatograph. Repeat two times, then inject 3 μl of the sample solution. Calculate the percentage of each monomer by the formula: where W = the weight of the sample in mg, adjusted for ash and moisture W S = the weight in mg of the monomer in the Monomer Standard Solution R = the ratio of the area of the monomer peak to the area of the octadecane peak in the sample injection R S = the mean ratio of the area of the monomer peak to the area of the octadecane peak in the standard injections. In the case of glucose, the peak areas for the alpha- and beta-epimers and in the case of 1,6-anhydro-D-glucose the peak areas for the pyranose form and furanose form are combined.
- Test: Molecular weight limit
- Apparatus Use a suitable high-pressure liquid chromatograph (HPLC) equipped with a differential refractometer, either a loop injector or suitable autosampler, a column heating block or oven and a computing integrator, or computer data handling system with molecular weight determination capabilities. Use a Waters Ultrahydrogel 250 A size exclusion column, or equivalent. The column is maintained at 45 o , and the HPLC pump supplies eluent to it at 0.8 ml/min reproducible to 0.5%. The differential refractometer should be set at a sensitivity of 4 x 10 -6 refractive index units full scale, and the plotter of the integrator should be set to 64 millivolts full scale. Maintain the detector cell at 35±0.1 o . Noise attributable to the detector and electronics should be less than 0.1% full scale. Eluent The eluent is 0.1 N sodium nitrate containing 0.025% sodium azide. Dissolve 35.0 g of sodium nitrate and 1.0 g of sodium azide in 100 ml of HPLC-grade water. Filter through a 0.45-μm filter into a 4-l flask. Dilute to volume with HPLC-grade water. De-gas by applying an aspirator vacuum for 30 min. Standard Solution Transfer 20 mg each of dextrose, stachyose, 5800, 23,700, and 100,000 MW pullulan standards into a 10-ml volumetric flask. Dissolve in and dilute to volume with Eluent. Filter through a 0.45 μm syringe filter into a suitable autosampler vial, and seal (All components of the Standard Solution are available from Polymer Laboratories, Inc., Technical Center, Amherst Fields Research Park, 160 Old Farm Road, Amherst, MA 01002, USA). Column Equilibration After installation of a new column in the HPLC, pump Eluent through it overnight at 0.3 ml/min. Before calibration or analysis, increase the flow slowly to 0.8 ml/min over a 1-min period, then pump at 0.8 ml/min for at least 1 h before the first injection. Check the flow gravimetrically, and adjust it if necessary. Reduce the flow to 0.1 ml/min when the system is not in use. Data System Setup Set the integrator or computerized data handling system as their respective manuals instruct for normal gel permeation chromatographic determinations. Set the integration time to 15 min. Column Standardization After the HPLC system has been equilibrated at a flow rate of 0.8 ml/min for at least 1 h, inject 50 μl of the Standard Solution five times, allowing 15 min between injections. Record the retention times of the various components in the Standard Solution. Retention times for each component should agree within ± 2 sec. Insert the average retention time along with the molecular weight of each component into the calibration table of the molecular weight distribution software. System Suitability Check the regression results for a cubic fit of the calibration points. They should have an R 2 value of 0.9999+. Dextrose and stachyose should be baseline-resolved from one another and from the 5800 MW pullulan standard. Elevated valleys are usually observed between the 5800, 23,700 and 100,000 MW pullulan standards. Sample Preparation Transfer 50 mg of sample, accurately weighed, into a 10-ml volumetric flask. Dissolve in and dilute to volume with Eluent. Filter through a 0.45-μm syringe filter into a suitable autosampler vial. Procedure Inject 50 μl of the Sample Preparation, following the same conditions and procedure as described under Column Standardization. Using the Formula weight Distribution software of the data reduction system, generate a molecular weight distribution curve of the sample. There is no measurable peak above a molecular weight of 22,000.
- Test: 5-Hydroxymethylfurfural (HMF)
- Principle HMF solutions absorb light in the ultraviolet region. The maximum absorption occurs at 283 nm and the molar extinction coefficient is 16,830 at that wavelength. The HMF concentration in polydextrose solutions is determined from the optical density at 283 nm and the application of the Beer-Lambert law. Apparatus - Standard laboratory equipment - Ultraviolet spectrophotometer - Spectrophotometer cells (quartz), 1.00 cm path length Procedure Accurately weigh 1.00±0.01 g of the sample into a 100-ml volumetric flask and make up to volume with distilled water (for polydextrose-N 70% solution use 1.43 ± 0.01 g sample). Read the optical density of this solution against a water blank at 283 nm in a 1.00 cm quartz cell in the spectrophotometer according to the directions supplied with the instrument. Under these conditions, the % HMF in the original sample is 0.0749 x optical density, on the dried basis. Calculation where C = % HMF in the original polydextrose sample M = HMF molecular weight D = optical density of the solution L = the path length of the spectrophotometer cell E = the molar extinction coefficient for HMF The numbers 100 and 10 are factors to convert solution concentration in mg/l to % HMF in the original sample, on the dried basis.
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 1: Carriers in food additives | All food additives | quantum satis | Regulation (EC) No 1333/2008, Annex III, Part 1 |
| 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 enzymesCan be used as a carrier: Yes Note (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
22 recorded names. A label may use any of them.
E number
- E1200
INS number
- 1200
CAS registry number
- 68424-04-4
As it appears in regulation
- Polydextrose
- Polydextroses
Other names
- POLYDEXTROSES
Hazard reference values
| Type | Value | Population | Assessed by | Opinion |
|---|---|---|---|---|
| ADI | not specified | — | JECFA | 1987 |
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 2021
The FAF Panel found no genotoxicity concern and no adverse effects at the highest doses tested for polydextrose (E 1200), and concluded that no numerical ADI is needed and there is no safety concern at reported uses and use levels. It recommended lowering the limit for lead and adding limits for arsenic, cadmium and mercury in the specifications.
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 1200?
- E 1200 is Polydextrose. Polydextrose is a bulking agent and soluble fibre, used to replace sugar and fat while keeping the body of the food. It contributes about a quarter of the calories of sugar because the body digests only part of it.
- What is Polydextrose used for in food?
- It is listed as a thickener, a stabiliser and a humectant — the role Codex and the US assign it. This page shows every function each regulator records, with the citation for each.
- Where is Polydextrose permitted?
- Of the seven regulators this site reads, Australia and New Zealand, Canada, the EU, Great Britain, South Korea, the US 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 Polydextrose vegan?
- Yes. Polydextrose 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
- ca retrieved 2026-10-17
- eu retrieved 2026-10-18
- gb retrieved 2026-10-18
- kr retrieved 2026-10-18
- ecfr retrieved 2026-10-17
- 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.
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