Sucroglycerides
E 474 · Sucroglycerides · Sugar glycerides · E474 · 474 · Sucroglycerides · SACARIDOGLICÉRIDOS · Sacaroglicéridos · Saccharoseestere i blanding med mono- og diglycerider af fedtsyrer · Sacharoglicerydy · Sacharoglyceridy · Sacharozės gliceridai · Sackarosestrar i blandning med mono- och diglycerider av fettsyror · Saharogliceridi · Saharozes glicerīdi · saharozni gliceridi · Sahharoglütseriidid · Sokeriglyseridit · Sucrogliceridi · Sucroglicéridos · Sucroglyceriden · Sucroglycerides · SUKROGLIĊERIDI · Sukrogliċeruri · Szaharózgliceridek · Zaharogliceride · Zuckerglyceride · Σακχαρογλυκερίδια · ЗахароглицеридиE number E474INS 474
Listed as an emulsifier by Codex.
Listed as emulsifiers (Codex)
- Codex Alimentarius: Emulsifier — CXS 192-1995 Table One, INS 474
Sucroglycerides are a mixture of sucrose esters and mono- and diglycerides, produced in one step rather than blended. They are used in dairy products, baked goods and drinks.
Where it is and isn’t permitted
| Jurisdiction | Status | Scope and limits | Citation |
|---|---|---|---|
| Australia and New Zealand | No listed food uses foundThis site has not matched this substance to any food use on this jurisdiction’s list of authorised food additives. A food additive may be used only in foods that list names. Flavourings, enzymes, processing aids and added nutrients are regulated separately and do not appear on it. | ||
| 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 | 29 food categories highest permitted level 50,000 mg/l Show every food category
| Regulation (EC) No 1333/2008, Annex IIand 28 further provisionsretrieved 2026-10-18 |
| Great Britain | Permitted, with conditions | 28 food categories highest permitted level 10,000 mg/kg or mg/l Show every food category
| Assimilated Regulation (EC) No 1333/2008, Annex II (as at 28 June 2024), via E 473–474: Sucrose esters of fatty acidsand 27 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 | 55 food categories highest permitted level 20,000 mg/kg Show every food category and its notes
| CXS 192-1995 Table One, INS 474and 54 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.
| European Union | 1,000 mg/kg – 50,000 mg/kg | 26 numeric limit, 3 quantum satis |
|---|---|---|
| Great Britain | 2,000 mg/kg – 10,000 mg/kg | 22 numeric limit, 3 several limits, 3 quantum satis |
| Codex Alimentarius | 200 mg/kg – 20,000 mg/kg | 55 numeric limit |
What it is made from
Made by reacting sucrose directly with an edible fat or oil, which yields both sucrose esters and glycerides together. The fat may be plant or animal.
- Vegan status depends on the source
- Vegetarian status depends on the source
- May raise a halal question
- May raise a kosher question
This is not an omission. What this additive is made from is not fixed — depending on the manufacturer it may be plant, animal or microbial in origin, nobody is required to say which, and the same product can change source between production runs. Ask the manufacturer if it matters to you; a label cannot answer it.
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 |
|---|---|---|
| Assay | no less than 40 % | no less than 40 % |
| Sulphated ash | no more than 2 % | no more than 2 % |
| Lead | no more than 2 mg/kg | no more than 2 mg/kg |
| Arsenic | no more than 3 mg/kg | — |
| Mercury | no more than 1 mg/kg | — |
| Cadmium | no more than 1 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 474 Sucroglycerides
Sucroglycerides are produced by reacting sucrose with an edible fat or oil to produce a mixture of essentially mono-, di- and triesters of sucrose and fatty acids (including lauric acid) together with residual mono-, di- and triglycerides from fat or oil. No organic solvents shall be used in their preparation other than cyclohexane, dimethylformamide, ethyl acetate, 2-methyl-1-propanol and propan-2-ol
Synonyms: Sugar glycerides
Assay, identification and purity criteria
Description and assay
- Assay
- Content not less than 40 % and not more than 60 % of sucrose fatty acid esters
- Description
- Soft solid masses, stiff gels or white to off-white powders
Identification
- Test for sugar
- Passes test
- Test for fatty acids
- Passes test
- Solubility
- Insoluble in cold water, soluble in ethanol
Purity criteria
- Sulphated ash
- Not more than 2 % (800 ± 25 °C)
- Free sugar
- Not more than 5 %
- Free fatty acids
- Not more than 3 % (estimated as oleic acid)
- Arsenic
- Not more than 3 mg/kg
- Lead
- Not more than 2 mg/kg
- Mercury
- Not more than 1 mg/kg
- Cadmium
- Not more than 1 mg/kg
- Methanol
- Not more than 10 mg/kg
- Dimethylformamide
- Not more than 1 mg/kg
- 2-Methyl-1-propanol
- [image] | Not more than 10 mg/kg, single or in combination Cyclohexane
- Ethyl acetate
- [image] | Not more than 350 mg/kg, single or in combination Propan-2-ol
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 474 Sucroglycerides
Sucroglycerides are obtained by reacting sucrose with an edible fat or oil with or without the presence of a solvent. They consist of a mixture of mono- and di-esters of sucrose and fatty acids together with mono-, di- and triglycerides from the fat or oil. Only the following solvents may be used in the production: dimethyl formamide, cyclohexane, isobutanol, isopropanol and ethyl acetate.
Synonyms: INS No. 474
Assay, identification and purity criteria
Description and assay
- Specification history
- Prepared at the 49 th JECFA (1997) and published in the Combined Compendium of Food Additive Specifications, FAO JECFA Monographs 1 (2005). A group ADI of 0 - 30 mg/kg bw for this substance and sucrose esters of fatty acids, sucrose oligoesters type I and type II and sucrose monoesters of lauric, palmitic or stearic acid was established at the 73 rd JECFA (2010).
- Assay
- Not less than 40% and not more than 60% of sucrose esters
- DESCRIPTION
- Odourless, soft, solid masses, white to off-white powders, or stiff gels
- FUNCTIONAL USES
- Emulsifier
- METHOD OF ASSAY
- Determine by high pressure liquid chromatography (see Volume 4) using the following conditions: Sample preparation Add about 250 mg of the sample, accurately weighed to a 50 ml volumetric flask. Dilute to volume with tetrahydrofuran, and mix. Filter through a 0.5-μm membrane filter. Procedure Inject 100 μl of the sample into the pre-stabilized high pressure liquid chromatograph. Conditions Column: Styrene-divinylbenzene copolymer for gel permeation chromatography (TSK-GEL G2000 (Supelco) or equivalent) Mobile phase: HPLC-grade degassed tetrahydrofuran Flow rate: 0.7 ml/min Detector: Refractive index detector Temperatures: Column: 38° Detector: 38° Record the chromatogram for about 90 min. Calculate the percentage of sucrose ester content in the sample taken by the formula: 100 A/T where A is the the sum of peak areas for the three main components, the mono-, di- and triesters, eluting at about 65, 68 and 73 min, respectively; and T is the sum of all peak areas eluting within 90 min. Appendix
Identification
- Solubility (Vol. 4)
- Insoluble in cold water; soluble in ethanol
- Test for fatty acids
- Add 1 ml of ethanol to 0.1 g of the sample, dissolve by warming, add 5 ml of dilute sulfuric acid TS, heat in a water bath for 30 min and cool. A yellowish white solid or oil is formed, which is soluble in 3 ml of ether.
- Test for sugar
- To 2 ml of the solution separated from the solid or oil in the Test for fatty acids add 1 ml of anthrone TS carefully down the inside of the test tube. The boundary surface of the two layers turns to blue or green.
Purity criteria
- Sulfated ash (Vol. 4)
- Not more than 2% Test 2 g of the sample (Method I)
- Acid value (Vol. 4)
- Not more than 6
- Free sucrose
- Not more than 5% See description under TESTS
- Dimethyl formamide
- Not more than 1 mg/kg See description under TESTS
- Cyclohexane and isobutanol
- Not more than 10 mg/kg, singly or in combination See description under TESTS
- Ethyl acetate and isopropanol
- Not more than 350 mg/kg, singly or in combination
- Lead (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 principles of methods described in Volume 4 (under “General Methods, Metallic Impurities”).
- Test: Free sucrose
- Determine by gas liquid chromatography (see Volume 4) using the following conditions: Reagents - Internal Standard: 5 mg/ml cholesterol in chloroform or 10 mg/ml tetracosane in chloroform - Pyridine (dried over molecular sieve) - N,O-Bis-(Trimethylsilyl)-acetamide (BSA) - Trimethylchlorosilane (TMCS) Procedure Weigh accurately 20-50 mg of the sample into a silylation vial, add 1 ml internal standard solution, 1 ml pyridine, and 0.5 ml each of BSA and TMCS. Seal vial, and heat at 70° for 30 min. Inject 1 μl into the gas liquid chromatograph. Conditions Column: - length: 0.3 m - diameter: 4 mm (i.d.) - material: glass - packing: Dexil Carrier gas: Nitrogen Flow rate: 40 ml/min Detector: FID Temperature programme: Hold for 1 min at 160°, then 160-375° at 15°/min. Measure peak areas for sucrose and internal standard. The response factor (RF) is calculated from a number of gas liquid chromatography runs with standard solutions of sucrose containing internal standard. Calculation mg of internal standard × area sucrose RF = area internal standard × mg sucrose and mg internal standard × area sucrose × 100 % free sucrose = RF × area internal standard × mg sample
- Test: Dimethyl formamide
- Determine by hydrolysis to dimethylamine and analysis by gas liquid chromatography ( see Volume 4) using the following conditions: Reagents - Dimethyl formamide - Dimethylamine hydrochloride - Methanol - Ethanol - Hydrochloric acid - Sodium hydroxide Standard solutions Prepare 4.47 mg/ml (equivalent to 4.0 mg/ml of dimethyl formamide) stock solution of dimethylamine hydrochloride in ethanol, and prepare standard solutions equivalent to 4, 2 and 1 μg/ml of dimethyl formamide, respectively, by dilution of the stock solution with 0.1% sodium hydroxide solution in ethanol. Sample preparation The apparatus for the hydrolysis is shown in the Appendix. Weigh accurately about 40 g of the sample into a 1000-ml round-bottomed flask. Add 500 ml of 5% methanolic solution of sodium hydroxide, and attach the flask to the apparatus. Set an Erlenmeyer flask containing 10 ml of 1% methanolic solution of hydrochloric acid to the apparatus. Heat the round-bottomed flask and let the content reflux for 1 hour, then distil to collect about 50 ml of the distillate while cooling water of the reflux condenser is stopped. Evaporate the distillate to almost dryness on a boiling water bath. Dissolve the residue with a small amount of ethanol, add 2.5 ml of 5% ethanolic solution of sodium hydroxide, and dilute to 25 ml with ethanol to prepare a sample solution. Procedure Inject 2 μl of the sample solution into the gas liquid chromatograph under the conditions below. Calibration curve Prepare a calibration curve by injecting each 2 μl of the standard solutions into the gas chromatograph. Conditions Column: - length: 2 m - diameter: 2 mm (i.d.) - material: glass - packing: 10% amine 220 and 10% KOH on 80/100 weak acid washed Chromosorb W - conditioning: Heat to 130° overnight with 5 ml/min of nitrogen flow rate Carrier gas: Nitrogen Flow rate: 17 ml/min Detector: FID Temperatures - injection port: 198±5° - column: 60° Calculation C ( μ g/ml) x 25 (ml) CDFA (mg/kg) = W (g) where CDFA is the Concentration of dimethyl formamide; C is the Concentration of dimethyl formamide detected; and W is the weight of sample taken.
- Test: Cyclohexane and isobutanol
- Determine by gas liquid chromatography (see Volume 4) using the following conditions: Reagents - Dimethylformamide (GLC purity grade) - Cyclohexane (UV spectrophotometric grade) - Isobutanol (analytical grade) Standard solutions Prepare a 0.1% stock solution of cyclohexane and isobutanol in dimethylformamide by pipetting 130 μl of cyclohexane and 125 μl of isobutanol into dimethylformamide and making up the volume to 10 ml. Prepare by dilution a range of solutions containing 5, 10 and 20 mg/kg of cyclohexane and isobutanol. Prepare a response curve by injecting 5 μl of these diluted standard solutions into the gas chromatograph under the conditions below. Sample preparation Weigh 5 g of sample to the nearest 10 mg into a flask with a ground glass stopper, add 5 g of dimethylformamide and warm to dissolve. Cool and inject 5 μl into the gas chromatograph under the conditions below. Column - length: 3 m - diameter: 4.5 mm - material: stainless steel - packing: 20% Carbowax 20 M on Chromosorb G 60/80 Carrier gas: Helium (1.6 bar) Detector: Flame ionization Temperatures - injection port: 130° - column: 130° - detector: 200° Determine the concentration of cyclohexane and isobutanol in the sample solution (50%) by comparison with the standard solutions and multiply the concentration by two to convert the results to correspond to the original sucroglycerides.
- Test: Isopropanol and ethyl acetate Determine by
- gas chromatography (see Volume 4) with a head space sampler using the following conditions: Reagents - Isopropanol - Ethyl acetate Standard solutions Take each 1 g of isopropanol and ethyl acetate in a volumetric flask and add water to total volume of 100 ml, and prepare 0.02-0.4 g/100 ml solutions by dilution of this solution. If necessary, prepare standard solutions containing up to 7 g/100 ml of isopropanol and ethyl acetate. Procedure Place 1 g (1.0 ± 0.1 g) of powdered sample in a sample vial. Add 5 μl of water to the sample vial and seal it quickly with a septum. Set the sample vial in a pre-conditioned gas chromatograph and start the analysis under the below-mentioned conditions. Calibration curve Take 1 g of powdered sucrose esters of fatty acids, solvent free or known residual solvent contents, in a sample vial, add 5 μl of the standard solution and seal it quickly with a septum. Set the sample vial in a pre-conditioned gas chromatograph and start the analysis under the following conditions and obtain calibration curves for each solvent. Column: - length: 30 m - diameter: 0.53 mm (i.d.) - material: Silica capillary - film: 100% methyl polysiloxane - conditioning: Heat to 60° for 2-3 h with approximately 10 ml/min of nitrogen Carrier gas: Nitrogen Flow rate: 5 ml/min Detector: Flame ionization Temperatures: - injection port: 110° - column: 40° - detector: 110° Head space sampler: - Sample volume: 1.0 g ± 0.1 g + 5 μl - Sample heating temp.: 80° - Sample heating time: 40 min - Syringe temperature: 85° - Sample gas injection: 0.4 ml Calculation Ci = Ai x Cfi x 1000 where Ci is the Concentration of solvent i (mg/kg); Ai is the Peak area of solvent i (μv.sec.); and Cfi is the Conversion coefficient for solvent i (slope of the calibration curve) (μg/μv.sec).
Every name it appears under
29 recorded names. A label may use any of them.
E number
- E474
INS number
- 474
As it appears in regulation
- Sucroglycerides
Other names
- E 474
- Sucroglycerides
- Sugar glycerides
The EU re-evaluation programme
Every additive authorised in the EU before 20 January 2009 was put back through EFSA by Commission Regulation (EU) No 257/2010, and this one is named in it. What the Regulation required is below; whether the opinion has since been published is not something this site records.
- Already re-evaluated when the programme began. Listed in Annex I as “Sucroglycerides”, against the words “Re-evaluation completed on 23 November 2004; revised on 26 January 2006”, and therefore not re-evaluated again under it.
Hazard reference values
The two committees set different figures. EFSA's acceptable daily intake is 40 mg/kg bw/day; JECFA's is 30 mg/kg bw/day (1997). An acceptable daily intake is a reference value set by a committee, not a threshold above which harm begins. The lower figure is not a finding that the other body was wrong: the two work to different terms of reference, on their own timetables, and sometimes from different data. This site states both and chooses between them nowhere. See where the two committees differ.
| Type | Value | Population | Assessed by | Opinion |
|---|---|---|---|---|
| ADI | 30 mg/kg bw/day | — | JECFA | 1997 |
| ADI | 40 mg/kg bw/day | consumers | EFSA | not identified in the dataset |
Evidence and how bodies read it
Studies, and the differing conclusions regulators drew from them, are curated rather than machine-read, and none has been written for this substance yet.
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 474?
- E 474 is Sucroglycerides. Sucroglycerides are a mixture of sucrose esters and mono- and diglycerides, produced in one step rather than blended. They are used in dairy products, baked goods and drinks.
- What is Sucroglycerides used for in food?
- It is listed as an emulsifier — the role Codex assigns it. This page shows every function each regulator records, with the citation for each.
- Where is Sucroglycerides permitted?
- Of the seven regulators this site reads, 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 Sucroglycerides vegan?
- It depends on the source, and a label will not tell you. Sucroglycerides can be made from plant or animal material, manufacturers are not obliged to say which, and the same product can change between production runs. Anyone who needs to know has to ask the manufacturer.
Sources for this page
- 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
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