Date: 2016-10-14Category: Not ApplicableState: Union GovernmentCountry: Europe
Commission Regulation (EU) 2016/1814 of 13 October 2016 amending the Annex to Regulation (EU) No 231/2012 laying down specifications for food additives listed in Annexes II and III to Regulation (EC) No 1333/2008 of the European Parliament and of the Council as regards specifications for steviol glycosides (E 960) (Text with EEA relevance)
Executive Summary:
Commission Regulation (EU) 2016/1814 amends Regulation (EU) No 231/2012, updating specifications for steviol glycosides (E 960) used as food additives. This amendment includes adding rebaudioside M to the list of permitted steviol glycosides and modifying the definition to allow for varying ratios of glycosides. The regulation is effective twenty days after its publication in the Official Journal of the European Union, 14 October 2016.
Key Points / Main Content:
* **Amendment Purpose:** To update specifications for the food additive steviol glycosides (E 960).
* **Regulation Amended:** Commission Regulation (EU) No 231/2012.
Specifications Update:
* **Steviol Glycoside Composition:** Preparations must contain not less than 95% of eleven named steviol glycosides (stevioside, rebaudiosides A, B, C, D, E, F, and M, steviolbioside, rubusoside, and dulcoside) on a dried basis, in any combination and ratio.
* **Rebaudioside M Inclusion:** Rebaudioside M is added to the list of permitted steviol glycosides.
* **Manufacturing Process:** The manufacturing process involves water extraction of Stevia rebaudiana Bertoni leaves, purification via ion-exchange chromatography, and recrystallization from methanol or aqueous ethanol.
* **Purity Criteria:** The additive must meet specific purity criteria, including limits for total ash, loss on drying, residual solvents (methanol and ethanol), arsenic, and lead.
* **Identification:** Specifications detail solubility and pH levels for identification.
Impact Analysis:
European Commission:
* Impact: Responsible for implementing and enforcing the updated regulations regarding steviol glycosides.
* Action Required: Ensure the amended regulation is applied and monitored across member states.
Food Manufacturers:
* Impact: Need to comply with the new specifications for steviol glycosides (E 960) in their food products.
* Action Required: Adjust manufacturing processes and product formulations to meet the updated standards, including the inclusion of rebaudioside M and revised purity criteria.
Member States:
* Impact: Must ensure the regulation is binding and directly applicable within their jurisdictions.
* Action Required: Incorporate the amended specifications into national regulations and oversee compliance by food manufacturers.
Food Safety Authority:
* Impact: Evaluated the safety of the proposed changes to the specifications for steviol glycosides E 960
* Action Required: Continue to monitor and provide scientific opinions on the safety of food additives.
Key Entities Referenced
European Union: A political and economic union of member states located primarily in Europe.
European Commission: The executive branch of the European Union responsible for proposing legislation, implementing decisions, and managing the EU's day-to-day operations.
Regulation (EC) No 1333/2008: A regulation of the European Parliament and of the Council on food additives.
Regulation (EC) No 1331/2008: A regulation of the European Parliament and of the Council establishing a common authorisation procedure for food additives, food enzymes and food flavourings.
Regulation (EU) No 231/2012: A Commission Regulation laying down specifications for food additives listed in Annexes II and III to Regulation (EC) No 1333/2008.
Steviol Glycosides E 960: A food additive, a sweetener extracted from the Stevia rebaudiana Bertoni plant.
Stevia rebaudiana Bertoni: A plant species from which steviol glycosides are extracted.
European Food Safety Authority (EFSA): The agency of the European Union that provides independent scientific advice and communicates on existing and emerging risks associated with the food chain.
14.10.2016 EN Official Journal of the European Union L 278/37
COMMISSION REGULATION (EU) 2016/1814
of 13 October 2016
amending the Annex to Regulation (EU) No 231/2012 laying down specifications for food
additives listed in Annexes II and III to Regulation (EC) No 1333/2008 of the European Parliament
and of the Council as regards specifications for steviol glycosides (E 960)
(Text with EEA relevance)
THE EUROPEAN COMMISSION,
Having regard to the Treaty on the Functioning of the European Union,
Having regard to Regulation (EC) No 1333/2008 of the European Parliament and of the Council of 16 December 2008
on food additives (1), and in particular Article 14 thereof,
Having regard to Regulation (EC) No 1331/2008 of the European Parliament and of the Council of 16 December 2008
establishing a common authorisation procedure for food additives, food enzymes and food flavourings (2), and in
particular Article 7(5) thereof,
Whereas:
(1) Commission Regulation (EU) No 231/2012 (3) lays down specifications for food additives listed in Annexes II
and III to Regulation (EC) No 1333/2008.
(2) Those specifications may be updated in accordance with the common procedure referred to in Article 3(1) of
Regulation (EC) No 1331/2008, either on the initiative of the Commission or following an application.
(3) On 13 November 2013 an application was submitted for the amendment of specifications concerning the food
additive steviol glycosides (E 960). The application was made available to the Member States pursuant to Article 4
of Regulation (EC) No 1331/2008.
(4) The current specifications stipulate that steviol glycosides (E 960) preparations contain not less than 95 % of ten
named steviol glycosides: stevioside, rebaudiosides A, B, C, D, E and F, steviolbioside, rubusoside and dulcoside,
on a dried basis. The specifications further define the preparations/final product consisting mainly (at least 75 %)
of stevioside and/or rebaudioside A.
(5) The applicant requests that rebaudioside M is added to the list of permitted steviol glycosides as an additional
glycoside that may comprise the assay value of not less than 95 % (total steviol glycoside content). The applicant
also requests that the minimum amount of 75 % of stevioside and/or rebaudioside A is deleted, i.e., to change the
‘Definition’ of steviol glycosides.
(6) The applicant further requests to expand the lists of chemical names and molecular weights and CAS numbers to
include, in addition to stevioside and rebaudioside A, the other nine steviol glycosides. Rebaudioside M should
also be added to the listing of molecular formulas. To account for the greater sweetness potency of
rebaudioside M, the ‘Description’ of steviol glycosides should be amended.
(7) Since stevioside and rebaudioside A may not necessarily be the principal steviol glycosides, the stevioside and
rebaudioside A criterion under the ‘Identification’ of steviol glycosides should be removed from the specifications.
(8) According to information provided by the applicant, a production process has been developed which allows for
the selective isolation of rebaudioside M resulting in the production of steviol glycosides preparations enriched in
(1) OJ L 354, 31.12.2008, p. 16.
(2) OJ L 354, 31.12.2008, p. 1.
(3) Commission Regulation (EU) No 231/2012 of 9 March 2012 laying down specifications for food additives listed in Annexes II and III to
Regulation (EC) No 1333/2008 of the European Parliament and of the Council (OJ L 83, 22.3.2012, p. 1).L 278/38 EN Official Journal of the European Union 14.10.2016
rebaudioside M specifically, at a range of concentrations (from 50 % up to nearly 100 %). According to the
applicant, only leaves of the Stevia rebaudiana Bertoni plant comprise the starting material for the production of
steviol glycoside extracts containing at least 50 % rebaudioside M. Its manufacturing process is similar to the
general method of extracting steviol glycosides from the leaves of S. rebaudiana which has been previously
reviewed by EFSA in 2010 (1).
(9) In the new production process, the crushed stevia leaves are extracted with hot water and the resulting extract is
subjected to isolation and purification (by use of ion-exchange chromatography). This initial stage is followed by
additional purification steps, including further and repeated recrystallisation and separation steps. Through the
manipulation of these purification steps (i.e. specific number of crystallisation steps, solvent concentration, as
well as temperature and duration of the process) the manufacturer is able to selectively crystallise a preparation
high in rebaudioside M. Also, the production process involves use of solvents (ethanol and methanol) that are
currently recognised for use in the manufacture of steviol glycoside preparations.
(10) That production process results in a preparation that contains 95 % of steviol glycosides with rebaudioside M
representing more than 50 % of the finished product and the remainder comprising the following ten related
steviol glycosides in any combination and ratio: stevioside, rebaudiosides A, B, C, D, E, F, dulcoside, steviolbioside
and rubusoside. While extracts characterised by a ≥ 95 % content of rebaudioside M contain < 5 % of
rebaudiosides D, A and B combined, extracts with a lower rebaudioside M content (approximately 50 %) may
comprise close to 40 % rebaudioside D and 7 % rebaudioside A.
(11) In its opinion (2) of 8 December 2015 the European Food Safety Authority (‘the Authority’) concluded that
extending the current specifications to include rebaudiosides D and M as alternatives to rebaudioside A in the
predominant components of steviol glycosides would not be of a safety concern. The Authority also concluded
that provided that the total amount of steviol glycosides (stevioside; rebaudiosides A, B, C, D, E, F and M; steviol
bioside; rubusoside and dulcoside) were greater than 95 %, which are all converted to steviol, and given that
there was no evidence of absorption for intact glycosides at realistic use levels, the specific steviol glycosides
(E 960) composition would not be of a safety concern. It was also considered that the ADI of 4 mg/kg bw/day
(expressed as steviol equivalents) can also be applied where total steviol glycosides (stevioside; rebaudiosides A, B,
C, D, E, F and M; steviolbioside; rubusoside and dulcoside) comprise more than 95 % of the material.
(12) Taking into account the submitted application and the evaluation made by the Authority, it is appropriate to
amend the specifications of the food additive E 960.
(13) Regulation (EU) No 231/2012 should therefore be amended accordingly.
(14) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on
Plants, Animals, Food and Feed,
HAS ADOPTED THIS REGULATION:
Article 1
The Annex to Regulation (EU) No 231/2012 is amended in accordance with the Annex to this Regulation.
Article 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the
European Union.
(1) EFSA Panel on Food Additives and Nutrient Sources (ANS); Scientific Opinion on safety of steviol glycosides for the proposed uses as
a food additive. EFSA Journal 2010;8(4):1537. [85 pp.]. doi:10.2903/j.efsa.2010.1537
(2) EFSA ANS Panel (EFSA Panel on Food Additives and Nutrient Sources added to food), 2015. Scientific opinion on the safety of the
proposed amendment of the specifications for steviol glycosides (E 960) as a food additive. EFSA Journal 2015;13(12):4316, 29 pp.
doi:10.2903/j.efsa.2015.431614.10.2016 EN Official Journal of the European Union L 278/39
This Regulation shall be binding in its entirety and directly applicable in all Members States.
Done at Brussels, 13 October 2016.
For the Commission
The President
Jean-Claude JUNCKERL 278/40 EN Official Journal of the European Union 14.10.2016
ANNEX
In the Annex to Regulation (EU) No 231/2012, the entry for E 960 steviol glycosides is replaced by the following:
‘E 960 STEVIOL GLYCOSIDES
Synonyms
Definition The manufacturing process comprises two main phases: the first involving water extrac
tion of the leaves of the Stevia rebaudiana Bertoni plant and preliminary purification of
the extract by employing ion exchange chromatography to yield a steviol glycoside pri
mary extract, and the second involving recrystallisation of the steviol glycosides from
methanol or aqueous ethanol resulting in a final product containing not less than 95 %
of the below identified 11 related steviol glycosides, in any combination and ratio.
The additive may contain residues of ion-exchange resins used in the manufacturing pro
cess. Several other related steviol glycosides that may be generated as a result of the pro
duction process, but do not occur naturally in the Stevia rebaudiana plant have been ident
ified in small amounts (0,10 to 0,37 % w/w).
Chemical name Steviolbioside: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic
acid
Rubusoside: 13-β-D-glucopyranosyloxykaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Dulcoside A: 13-[(2-O-α–L-rhamnopyranosyl-β–D-glucopyranosyl)oxy]kaur-16-en-18-oic
acid, β-D-glucopyranosyl ester
Stevioside: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic acid,
β-D-glucopyranosyl ester
Rebaudioside A: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid, β-D- glucopyranosyl ester
Rebaudioside B: 13-[(2-O-β–D-glucopyranosyl-3-O-β–D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid
Rebaudioside C: 13-[(2-O-α–L-rhamnopyranosyl-3-O-β–D-glucopyranosyl-β-D-glucopyra
nosyl)oxy]kaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Rebaudioside D: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid, 2-O-β-D-glucopyranosyl-β-D-glucopyranosyl ester
Rebaudioside E: 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]kaur-16-en-18-oic
acid, 2-O-β-D-glucopyranosyl-β-D-glucopyranosyl ester
Rebaudioside F: 13[(2-O-β-D-xylofurananosyl-3-O-β-D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid, β-D-glucopyranosyl ester
Rebaudioside M: 13-[(2-O-β-D-glucopyranosyl-3-O-β-D-glucopyranosyl-β-D-glucopyrano
syl)oxy]kaur-16-en-18-oic acid, 2-O-β-D-glucopyranosyl-3-O-β-D-glucopyranosyl-β-D-glu
copyranosyl ester
Molecular formula Trivial name Formula Conversion factor
Steviol C H O 1,00
20 30 3
Steviolbioside C H O 0,50
32 50 13
Rubusoside C H O 0,50
32 50 13
Dulcoside A C H O 0,40
38 60 17
Stevioside C H O 0,40
38 60 18
Rebaudioside A C H O 0,33
44 70 23
Rebaudioside B C H O 0,40
38 60 18
Rebaudioside C C H O 0,34
44 70 22
Rebaudioside D C H O 0,29
50 80 2814.10.2016 EN Official Journal of the European Union L 278/41
Rebaudioside E C H O 0,33
44 70 23
Rebaudioside F C H O 0,34
43 68 22
Rebaudioside M C H O 0,25
56 90 33
Molecular weight and Trivial name CAS Number Molecular weight (g/mol)
CAS No
Steviol 318,46
Steviolbioside 41093-60-1 642,73
Rubusoside 64849-39-4 642,73
Dulcoside A 64432-06-0 788,87
Stevioside 57817-89-7 804,88
Rebaudioside A 58543-16-1 967,01
Rebaudioside B 58543-17-2 804,88
Rebaudioside C 63550-99-2 951,02
Rebaudioside D 63279-13-0 1 129,15
Rebaudioside E 63279-14-1 967,01
Rebaudioside F 438045-89-7 936,99
Rebaudioside M 1220616-44-3 1 291,30
Assay Not less than 95 % steviolbioside, rubusoside, dulcoside A, stevioside, rebaudiosides A, B,
C, D, E, F and M on the dried basis, in any combination and ratio.
Description White to light yellow powder, approximately between 200 and 350 times sweeter than
sucrose (at 5 % sucrose equivalency).
Identification
Solubility Freely soluble to slightly soluble in water
pH Between 4,5 and 7,0 (1 in 100 solution)
Purity
Total ash Not more than 1 %
Loss on drying Not more than 6 % (105 °C, 2h)
Residual solvents Not more than 200 mg/kg methanol
Not more than 5 000 mg/kg ethanol
Arsenic Not more than 1 mg/kg
Lead Not more than 1 mg/kg’