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§184.1063 食品添加剂酶改性卵磷脂(Enzyme-modified lecithin)

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放大字体  缩小字体 2011-07-19 08:21:51  来源:GPO  浏览次数:3397
核心提示:   按照§184.1(b)(1)规定,食品添加剂酶改性卵磷脂加入食品中除应符合现行良好生产操作规程外,无限制性规定,用做§170.3(o)(8)中的乳化剂,用量以不超过现行良好生产操作规程为限。
发布单位
FDA
FDA
发布文号 61 FR 45889
发布日期 1996-08-30 生效日期 暂无
有效性状态 废止日期 暂无
备注 按照§184.1(b)(1)规定,食品添加剂酶改性卵磷脂加入食品中除应符合现行良好生产操作规程外,无限制性规定,用做§170.3(o)(8)中的乳化剂,用量以不超过现行良好生产操作规程为限。

    更多关于已证实属于一般公认为安全(GRAS)的可直接加入食品中的物质种类,请点击美国FDA 21 CFR 第184部分已证实属于一般公认为安全(GRAS)的可直接加入食品中的物质种类汇总

  § 184.1063   Enzyme-modified lecithin.

  (a) Enzyme-modified lecithin is prepared by treating lecithin with either phospholipase A2(EC 3.1.1.4) or pancreatin.

  (b) The ingredient meets the specifications in paragraphs (b)(1) through (b)(8) of this section. Unless otherwise noted, compliance with the specifications listed below is determined according to the methods set forth for lecithin in the Food Chemicals Codex, 4th ed. (1996), pp. 220–221, which are incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are available from the National Academy Press, 2101 Constitution Ave. NW., Washington DC 20418, or may be examined at the Center for Food Safety and Applied Nutrition's Library, 5100 Paint Branch Pkwy., College Park, MD 20740, or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202–741–6030, or go to: http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.

  (1) Acetone-insoluble matter (phosphatides), not less than 50.0 percent.

  (2) Acid value, not more than 40.

  (3) Lead, not more than 1.0 part per million, as determined by atomic absorption spectroscopy.

  (4) Heavy metals (as Pb), not more than 20 parts per million.

  (5) Hexane-insoluble matter, not more than 0.3 percent.

  (6) Peroxide value, not more than 20.

  (7) Water, not more than 4.0 percent.

  (8) Lysolecithin, 50 to 80 mole percent of total phosphatides as determined by “Determination of Lysolecithin Content of Enzyme-Modified Lecithin: Method I,” dated 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are available from the Division of Petition Control, Center for Food Safety and Applied Nutrition (HFS–215), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, or may be examined at the Center for Food Safety and Applied Nutrition's Library, 5100 Paint Branch Pkwy., College Park, MD 20740, or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202–741–6030, or go to: http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.

  (c) In accordance with §184.1(b)(1), the ingredient is used in food with no limitation other than current good manufacturing practice. The affirmation of this ingredient as generally recognized as safe as a direct human food ingredient is based upon the following current good manufacturing practice conditions of use:

  (1) The ingredient is used as an emulsifier as defined in §170.3(o)(8) of this chapter.

  (2) The ingredient is used at levels not to exceed current good manufacturing practice.

  [61 FR 45889, Aug. 30, 1996]

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