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GB 30608-2014 English PDF

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GB 30608-2014: National Food Safety Standard -- Food Additives -- DL-Sodium Malate
Status: Valid

Standard ID	Contents [version]	USD	STEP2	[PDF] delivered in	Standard Title (Description)	Status	PDF
GB 30608-2014	English	189	Add to Cart	3 days [Need to translate]	National Food Safety Standard -- Food Additives -- DL-Sodium Malate	Valid	GB 30608-2014

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Basic data

Standard ID	GB 30608-2014 (GB30608-2014)
Description (Translated English)	National Food Safety Standard -- Food Additives -- DL-Sodium Malate
Sector / Industry	National Standard
Classification of Chinese Standard	C53
Classification of International Standard	67.020
Word Count Estimation	8,897
Date of Issue	4/29/2014
Date of Implementation	11/1/2014
Regulation (derived from)	National Health and Family Planning Commission Bulletin No. 7, 2014
Issuing agency(ies)	National Health and Family Planning Commission of the People's Republic of China
Summary	This Standard specifies the order of malic acid and sodium hydroxide reaction, crystallization, drying food additive sodium malate DL- obtained.

GB 30608-2014: National Food Safety Standard -- Food Additives -- DL-Sodium Malate

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
(Food additives DL-malate) National Standards of People's Republic of China National standards for food safety Food Additives DL-Malate Sodium Released.2014-04-29 2014-11-01 implementation People's Republic of China National Health and Family Planning Commission released National standards for food safety Food Additives DL-Malate Sodium

1 Scope

This standard applies to malic acid and sodium hydroxide reaction, the crystallization, drying the food additive DL-sodium malate. 2 molecular formula, structural formula and relative molecular mass 2.1 Molecular formula C4H4Na2O5nH2O (n = 3 or n = 1/2). 2.2 Structural formula HO-CH-COONa │ · nH2O CH2-COONa 2.3 Relative molecular mass Sanshui crystalline material 232.10 (according to.2011 international relative atomic mass). Semi - crystalline products 187.06 (according to.2011 international relative atomic mass).

3 request

3.1 sensory requirements Sensory requirements shall comply with the requirements of Table 1. Table 1 sensory requirements The project requires a test method Color white State crystalline powder or massive Take appropriate sample and place it in a clean, dry white porcelain dish In the natural light, observe the color and state 3.2 Physical and chemical indicators Physical and chemical indicators should be consistent with the provisions of Table 2. Table 2 Physical and chemical indicators project index Sanshui crystal products of semi - water crystal products Testing method DL-sodium malate (based on C4H4Na2O5) Content (mass fraction) /% 98.0 to 102.0 Appendix A A.3 Table 2 (continued) project index Sanshui crystal products of semi - water crystal products Testing method Alkalinity (in terms of Na2CO3) (mass fraction) /% ≤ 0.2 GB/T 9736 Drying reduction (mass fraction) /% 20.5 ~ 23.5 ≤7.0 A.4 Lead (Pb)/(mg/kg) ≤ 2.0 GB 5009.12 Fumaric acid (mass fraction) /% ≤ 1.0 A.5 Maleic acid (mass fraction) /% ≤ 0.05 A.5

Appendix A

Testing method A.1 General provisions Unless otherwise stated, only the reagents identified as analytical reagents and the tertiary water specified in GB/T 6682 were used in the analysis. Standard titration solution used in the test method, standard solution for the determination of impurities, preparations and articles, in the absence of other requirements, GB/T 601, GB/T 602 and GB/T 603. The solution used refers to an aqueous solution when it is not specified with any solvent formulation. A.2 Identification test A.2.1 Reagents and materials A.2.1.1 p-Aminobenzenesulfonic acid. A.2.1.2 Hydrochloric acid solution. 1 1. A.2.1.3 Cobalt Acetate - Uranium Oxide Solution. Weigh 4g of uranyl acetate, placed in 50mL acetic acid solution (60g/L), heated to dissolve; weighed 20g cobalt acetate, also placed in 50 mL of acetic acid solution (60 g/L); the two solutions were mixed in a warm state, cooled to about 20 ° C and held for 2 h, filtered to give. A.2.1.4 sodium nitrite solution..200 g/L. A.2.1.5 Sodium hydroxide solution. 40 g/L. A.2.2 Solubility test Weigh 1g sample, accurate to 0.01g, dissolved in water and diluted to 10mL, the solution should be clear. A.2.3 Sodium salt test Platinum wire with hydrochloric acid solution after wet, dipped in the sample, burning in a colorless flame, the flame should be bright yellow. Weigh 1g sample, accurate to 0.01g, with the appropriate amount of water dissolved, add 1mL hydrochloric acid solution, diluted with water to 20mL. Take 1mL of the Solution, add 5mL cobalt acetate - uranyl uranium solution, shake, yellow precipitate produced. A.2.4 Malate test Weigh 1g sample, accurate to 0.01g, add appropriate amount of water dissolved and diluted to 20mL. Take the sample solution 5mL into the porcelain evaporate dish 10mg of p-aminobenzenesulfonic acid, heated in water bath for several minutes, add sodium nitrite solution 5mL, slightly heated, dropping sodium hydroxide solution Alkaline, should be red. A.3 Determination of DL-sodium malate (based on C4H4Na2O5) A.3.1 Reagents and materials A.3.1.1 Glacial acetic acid. A.3.1.2 Standard titration solution for perchloric acid. c (HClO4) = 0.1 mol/L. A.3.1.3 Crystal violet indicator solution. 2g/L. A.3.2 Analysis steps Weigh 0.15g of the dried sample, accurate to 0.0001g, add 30mL glacial acetic acid dissolved, titration with titanate titration. Use the potentiometer to indicate the end point. When using the indicator to determine the end point, add a few drops of crystal violet indicator solution, the solution from purple to blue is green end. At the same time as the measurement, the same amount of reagent solution was used as a blank test in the same procedure as in the measurement. A.3.3 Calculation of results The mass fraction w1 (%) of DL-sodium malate (calculated as C4H4Na2O5) is calculated according to formula (A.1) w1 = (V1-V0) × c × M m × 1000 × 100% (A.1) Where. V1 --- sample consumption Perchloric acid standard drop solution volume, in milliliters (mL); V0 --- blank test consumption perchloric acid standard titration solution volume, in milliliters (mL); c - the exact value of the perchloric acid standard drop solution concentration in moles per liter (mol/L); M - the molar mass of sodium malate in grams per mole (g/mol) [M (C4H4Na2O5) = 89.03]; m --- the quality of the sample, in grams (g); 1000 --- conversion factor. A.4 Determination of dry reduction A.4.1 Analysis steps Weigh 4g sample, accurate to 0.0002g, placed in the already heated to the constant quality of the bottle, at 120 ℃ ± 2 ℃ constant temperature oven Dry for 2h, adjust the temperature to 160 ℃ ± 2 ℃, and then dry 2h, remove, placed in a dryer to cool to room temperature, weighing. A.4.2 Result calculation The mass fraction w2 (%) for drying reduction is calculated according to formula (A.2) w2 = m-m1 m x 100% (A.2) Where. m - the mass of the sample before drying, in grams (g); m1 --- the quality of the sample after drying, in grams (g). A.5 Determination of fumaric acid and maleic acid content A.5.1 Methodological Summary Using high performance liquid chromatography, under the selected working conditions, the diammonium hydrogen phosphate solution as the mobile phase, with high pressure infusion pump mobile phase pump Into the C18 column to separate the components of the sample solution, with UV detector for detection, by the data processing system recording and processing chromatography signal. A.5.2 Reagents and materials A.5.2.1 Water. Class I water in accordance with GB/T 6682-2008. A.5.2.2 Fumaric acid. Chromatographic pure. A.5.2.3 Maleic acid. Chromatographic pure. A.5.3 Instruments and equipment High performance liquid chromatograph with degasser, equipped with UV detector. A.5.4 Reference chromatographic conditions A.5.4.1 mobile phase. take diammonium phosphate 20g, add about 900mL water dissolved, with phosphoric acid to adjust the pH of the solution 2, and then use 0.45μm filter filter, and then set to 1000mL. A.5.4.2 Column. C18, filler pore size 12 nm, filler particle size 5 m, column length 250 mm, column inner diameter 4.6 mm, or other equivalent color Column. A.5.4.3 Flow rate. 0.8 mL/min. A.5.4.4 Column temperature. 40 ° C. A.5.4.5 Wavelength. 210 nm. A.5.4.6 Injection volume. 20 μL. A.5.5 Analysis steps A.5.5.1 Drawing of working curves According to Table A.1 DL-malic acid, maleic acid and fumaric acid concentration standard series, the preparation of two different concentrations of mixed standard solution, according to The working curve was plotted against the concentration and peak area. The retention time of each substance was given in Table A.2. Table A.1 Criteria for the concentration of each substance Name DL-malic acid maleic acid fumaric acid Standard concentration 1/(mg/L) about 50 about 0.5 to about 1.5 Standard concentration 2/(mg/L) about 100 about 1 about 3 Standard concentration 3/(mg/L) about 250 about 2.5 about 7.5 Standard concentration 4/(mg/L) about 500 about 5 about 15 Standard concentration 5/(mg/L) about 1000 about 10 about 30 Standard concentration 6/(mg/L) about.2000 about 20 about 60 Table A.2 Retention time of each substance Name DL-malic acid maleic acid fumaric acid Retention time/min 3.06 4.50 5.32 A.5.5.2 Preparation of sample solution Weigh 0.5g sample, accurate to 0.0002g, 100mL volumetric flask, add a small amount of water dissolved and diluted to the mark, mix. Chromatographic points Before filtration with 0.45μm microporous membrane. A.5.5.3 Determination Under the specified chromatographic conditions, take the standard solution and sample solution 20μL were injected into the liquid chromatograph, in the work curve on the test The concentration of fumaric acid or maleic acid in the solution. A.5.6 Calculation of results The mass fraction of fumaric acid or maleic acid is calculated as w3 (%) according to formula (A.3) w3 = c x 100 1000 × m × 100% (A.3) Where. c - Determination of the concentration of fumaric acid or maleic acid in the resulting sample in milligrams per liter (mg/L); m --- the quality of the sample, in grams (g); 100 --- volume of the sample volume, in milliliters (mL); 1000 --- conversion factor. The results of the test are based on the arithmetic mean of the parallel measurement results. The absolute difference between the two independent determinations obtained under repeatability conditions The value is not greater than 10% of its arithmetic mean. 4102-

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