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(EU) 2015/649:就L-亮氨酸作為藥片餐桌甜味劑載體的使用,修訂歐洲議會和理事會條例(EC) No 1333/2008附錄II和委員會條例 (EU) No 231/2012附錄(amending Annex II to Regulation (EC) No 1333/2008 of the European

嘉峪檢測網        2015-09-17 22:30

【發布單位】 EUROPEAN COMMISSION
【發布文號】 (EU) 2015/649
【發布日期】 2015-04-24
【生效日期】
【廢止日期】
【替代法規】
【效  力】
【食品伙伴網解讀】 2015年4月25,歐盟發布委員會條例(EU) 2015/649,就L-亮氨酸作為藥片中餐桌甜味劑載體的使用,修訂歐洲議會和理事會條例(EC) No 1333/2008附錄Ⅱ和委員會條例 (EU) No 231/2012附錄。具體內容詳見本法規附件。
  COMMISSION REGULATION (EU) 2015/649
 
  of 24 April 2015
 
  amending Annex II to Regulation (EC) No 1333/2008 of the European Parliament and of the
 
  Council and the Annex to Commission Regulation (EU) No 231/2012 as regards the use of
 
  L-leucine as a carrier for table-top sweeteners in tablets
 
  (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 Articles 10(3), 14 and 30(5) 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) Annex II to Regulation (EC) No 1333/2008 lays down a Union list of food additives approved for use in foods
 
  and their conditions of use.
 
  (2) Commission Regulation (EU) No 231/2012 (
 
  3
 
  ) lays down specifications for food additives that are listed in
 
  Annexes II and III to Regulation (EC) No 1333/2008.
 
  (3) Those lists 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.
 
  (4) On 9 September 2010 an application for authorisation of the use of L-leucine as a carrier (tableting aid) for
 
  table-top sweeteners in tablets was submitted by Germany where such use was authorised. That application has
 
  been made available to the Member States pursuant to Article 4 of Regulation (EC) No 1331/2008.
 
  (5) There is a technological function and need for the use of L-leucine in table-top sweeteners in tablets. L-leucine is
 
  homogeneously mixed with sweeteners before pressing tablets from the mixture and it aids tableting by ensuring
 
  that the tablets do not remain stuck to the pressing tools.
 
  (6) The European Food Safety Authority (‘the Authority’) evaluated the safety of amino acids and related substances
 
  when used as flavouring substances and expressed its opinion on 29 November 2007 (
 
  4
 
  ). The Authority
 
  concluded that the human exposure to amino acids through food is in orders of magnitude higher than the
 
  anticipated levels of exposure from their use as flavouring substances and that nine of the substances, including
 
  L-leucine, were not of safety concern at their estimated levels of intake as flavouring substances.
 
  (7) It was demonstrated in the application that even a high consumption of sweetener tablets would not exceed 4 %
 
  of the intake quantity recommended for L-leucine.
 
  (8) Therefore, it is appropriate to authorise the use of L-leucine as a carrier for table-top sweeteners in tablets as
 
  specified in Annex I to this Regulation and to assign E 641 as an E-number to that food additive.
 
  (9) The specifications for L-leucine should be included in Regulation (EU) No 231/2012 when it is included in the
 
  Union lists in Annex II to Regulation (EC) No 1333/2008 for the first time. In this regard it is appropriate to take
 
  into account the purity criteria of the European Pharmacopoeia for L-leucine.
 
  25.4.2015 EN Official Journal of the European Union L 107/17
 
  (
 
  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).
 
  (
 
  4
 
  ) EFSA Journal (2008) 870, 1-46. (10) Regulations (EC) No 1333/2008 and (EU) No 231/2012 should therefore be amended accordingly.
 
  (11) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on
 
  Plant, Animals, Food and Feed,
 
  HAS ADOPTED THIS REGULATION:
 
  Article 1
 
  Annex II to Regulation (EC) No 1333/2008 is amended in accordance with Annex I to this Regulation.
 
  Article 2
 
  The Annex to Regulation (EU) No 231/2012 is amended in accordance with Annex II to this Regulation.
 
  Article 3
 
  This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the
 
  European Union.
 
  This Regulation shall be binding in its entirety and directly applicable in all Member States.
 
  Done at Brussels, 24 April 2015.
 
  For the Commission
 
  The President
 
  Jean-Claude JUNCKER
 
  L 107/18 EN Official Journal of the European Union 25.4.2015 ANNEX I
 
  Annex II to Regulation (EC) No 1333/2008 is amended as follows:
 
  (1) In Part B, in Section 3 ‘Additives other than colours and sweeteners’, the following new entry is inserted after the
 
  entry for food additive E 640:
 
  ‘E 641 L-leucine’
 
  (2) In part E, in food category 11.4.3 ‘Table-top sweeteners in tablets’, the following new entry is inserted after the entry
 
  for food additive E 640:
 
  ‘E 641 L-leucine 50 000’
 
  25.4.2015 EN Official Journal of the European Union L 107/19 ANNEX II
 
  In the Annex to Regulation (EU) No 231/2012, the following new entry is inserted after the entry for E 640:
 
  ‘E 641 L-LEUCINE
 
  Synonyms 2-Aminoisobutylacetic acid; L-2-Amino-4-methylvaleric acid; alpha-Ami-
 
  noisocaproic acid; (S)-2-Amino-4-methylpentanoic acid; L-Leu
 
  Definition
 
  Einecs 200-522-0
 
  CAS number 61-90-5
 
  Chemical name L-Leucine; L-2-Amino-4-methylpentanoic acid
 
  Chemical formula C6H13NO2
 
  Molecular Weight 131,17
 
  Assay Content not less than 98,5 % and not more than 101,0 % on the
 
  anhydrous basis
 
  Description White or almost white crystalline powder or shiny flakes
 
  Identification
 
  Solubility Soluble in water, acetic acid, dilute HCl and alkaline hydroxides and
 
  carbonates; slightly soluble in ethanol
 
  Specific rotation [α]D
 
  20 between + 14,5° and + 16,5°
 
  (4 % solution (anhydrous basis) in 6N HCl)
 
  Purity
 
  Loss on drying Not more than 0,5 % (100 °C – 105 °C)
 
  Sulphated Ash Not more than 0,1 %
 
  Chlorides Not more than 200 mg/kg
 
  Sulphates Not more than 300 mg/kg
 
  Ammonium Not more than 200 mg/kg
 
  Iron Not more than 10 mg/kg
 
  Arsenic Not more than 3 mg/kg
 
  Lead Not more than 5 mg/kg
 
  Mercury Not more than 1 mg/kg’
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