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GB 29226-2012 English PDF

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GB 29226-2012: Food additive calcium aspartate
Status: Valid
Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
GB 29226-2012179 Add to Cart 2 days Food additive calcium aspartate Valid

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Basic data

Standard ID: GB 29226-2012 (GB29226-2012)
Description (Translated English): Food additive calcium aspartate
Sector / Industry: National Standard
Classification of Chinese Standard: X40
Classification of International Standard: 67.220.20
Word Count Estimation: 7,724
Regulation (derived from): Ministry of Health Bulletin No. 23 of 2012
Issuing agency(ies): Ministry of Health of the People's Republic of China
Summary: This Chinese standard applies to L- aspartic acid with calcium hydroxide or calcium oxide or calcium carbonate as raw material, chelation reaction obtained a food additive calcium aspartate.

GB 29226-2012: Food additive calcium aspartate

---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 additive calcium aspartate National Standards of People's Republic of China National standards for food safety Food Additives Calcium aspartate 2012-12-25 release 2013-01-25 Implementation Issued by the Ministry of Health of the People's Republic of China National standards for food safety Food Additives Calcium aspartate

1 Scope

This standard applies to L-aspartic acid and calcium hydroxide or calcium oxide or calcium carbonate as raw material, the chelating reaction prepared by the food Tim Addition of calcium aspartate. 2 chemical name, molecular formula, structural formula and relative molecular mass 2.1 Chemical name Calcium aspartate 2.2 Molecular formula C8H12O8N2Ca 2.3 Structural formula 2.4 Relative molecular mass 304.2 (according to the.2007 international relative atomic mass)

3 technical requirements

3.1 sensory requirements Shall comply with the provisions of Table 1. Table 1 sensory requirements The project requires a test method Color white State powder Take the appropriate sample in a clean, dry white porcelain dish, in the natural light, observe its color and status 3.2 Physical and chemical indicators Shall comply with the provisions of Table 2. Table 2 Physical and chemical indicators Item Index Test Method Calcium (in terms of Ca), w /% 12.0 to 13.8 Appendix A, A.3 L-aspartic acid content, w /% ≥ 79.0 Appendix A A.4 Specific rotation αm (20 ° C, D)/[(°) · dm2 · kg-1] 19.0 to 23.0 GB/T 613 Moisture, w /% ≤ 6.0 GB 5009.3 Direct drying method pH 6.0 to 7.5 GB/T 9724 Lead (Pb)/(mg/kg) ≤ 2 GB 5009.12 Total arsenic (in As)/(mg/kg) ≤ 1 GB/T 5009.11

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 6682-2008 are used in the analysis. test Method used in the standard titration solution, impurity determination standard solution, preparation and products, without any other requirements, according to GB/T 601, GB/T 602 and GB/T 603; the solution used in the absence of specified solvent, refers to the aqueous solution. A.2 Identification test A.2.1 Reagents and materials A.2.1.1 Indanetone solution. 20 g/L. A.2.1.2 Platinum wire. A.2.2 Identification method A.2.2.1 Indanone test Weigh about 1g sample, accurate to 0.1g, dissolved in 1000mL water, take this solution 5mL, add 1mL indanetrione solution, heating To boiling, about 3min after the purple. A.2.2.2 Calcium salt reaction Take platinum wire dipped in a little sample, burning on a colorless flame, the flame was brick red. A.3 Determination of calcium content A.3.1 Methodological Summary This method uses a small amount of magnesium as a co-indicator, that is, magnesium ions and chromium black T to produce a stable complex to indicate color changes, with ethylenediamine (EDTA) standard titration solution titration, according to ethylenediamine tetraacetic acid disodium (EDTA) standard titration solution consumption of the amount of calculation Calcium content. A.3.2 Reagents and materials A.3.2.1 Triethanolamine. A.3.2.2 Magnesium Sulfate Solution. 120 g/L. A.3.2.3 Ammonia-Ammonium Chloride Buffer. pH = 10.0. A.3.2.4 Ethylenediamine tetraacetic acid disodium (EDTA) standard titration solution. c (EDTA) = 0.05 mol/L. A.3.2.5 Chromium Black T Indicator. 5 g/L. A.3.3 Analysis steps 2 drops of magnesium sulfate solution, add ammonia - ammonium chloride buffer 15mL, plus chromium black T indicator solution 2 drops, with EDTA standard solution titration to Pure blue; another sample 0.35g, accurate to 0.0002g, add water 30mL to dissolve, add triethanolamine 5 drops, and with the above titration Of magnesium sulfate solution, and then EDTA standard solution titration, to the color from purple to pure blue is the end. While doing blank experiment. A.3.4 Calculation of results Calcium (in terms of Ca) content of the mass fraction w, according to formula (A.1) calculation. w = (V-V0) × c × M 1000 × m × 100% (A.1) Where. V --- sample consumption EDTA standard solution titration solution volume value in milliliters (mL); V0 --- blank test consumption EDTA standard solution titration solution volume value in milliliters (mL); c - the concentration of EDTA standard solution in moles per liter (mol/L); M - the molar mass of calcium in grams per mole (g/mol) [M (Ca) = 40.1]; m - the mass of the sample, in grams (g); 1000 --- conversion factor. The arithmetic mean of the results of two parallel measurements is the result of the report. The absolute difference between the two parallel determinations is not more than 0.3%. A.4 Determination of L-aspartic acid content A.4.1 Methodological Summary Calcium aspartate reacts with excess copper sulphate to form soluble calcium aspartate, which reacts with potassium iodide and is labeled with sodium thiosulfate Quasi-solution titration, according to sodium thiosulfate standard titration solution consumption, calculate the L-aspartic acid content. A.4.2 Reagents and materials A.4.2.1 Potassium iodide. A.4.2.2 Glacial acetic acid. A.4.2.3 Copper sulfate solution. 0.1 mol/L. A.4.2.4 Sodium hydroxide solution. 1 mol/L. A.4.2.5 Sodium hydroxide solution. 0.1 mol/L. A.4.2.6 sodium thiosulfate standard titration solution. c (Na2S2O3) = 0.02mol/L. A.4.2.7 Boric acid - potassium chloride buffer solution (pH 9.0). Weigh 3.09 g of boric acid, add 0.1mol/L potassium chloride 500mL, add 210mL 0.1 mol/L sodium hydroxide. A.4.2.8 Starch indicator. 1 g/L. A.4.2.9 phenolphthalein indicator solution. 5g/L. A.4.3 Analysis steps Weigh the appropriate amount of sample (about aspartic acid ≤ 100mg), accurate to 0.0002g, add water and set capacity of 30mL volume. will The sample solution was placed in a 150 mL Erlenmeyer flask, 5 mL of copper sulfate solution was added, 2 drops of phenolphthalein indicator solution, and adjusted with 1 mol/L sodium hydroxide solution Section to the solution was blue and purple, add boric acid - potassium chloride buffer solution 30mL, shake. After standing for 1 h, filter with 30 mL boric acid-potassium chloride Buffer solution Wash the filter and precipitate, combine the lotion. Add 1.5mL glacial acetic acid and potassium iodide 7.0g, shaking dissolved, with sodium thiosulfate standard Solution titration, near the end of the point, add starch indicator solution 2mL, continue to titration to blue disappear. While doing blank experiments. A.4.4 Calculation of results L-aspartic acid content of the mass fraction w1, according to formula (A.2) calculation. w1 = (V-V0) c × M 1000 × m × 100% (A.2) Where. V - sample consumption of sodium thiosulfate standard titration solution volume in milliliters (mL); V0 --- blank test consumption of sodium thiosulfate standard titration solution volume, in milliliters (mL); c - sodium thiosulfate standard solution concentration in moles per liter (mol/L); M-L-aspartic acid molar mass in grams per mole (g/mol) [M (C4H7O4N) = 133.1]; m - the mass of the sample, in grams (g); 1000 --- conversion factor. The arithmetic mean of the results of two parallel measurements is the result of the report. The absolute difference between the two parallel determinations is not more than 0.3%. No. 1 amendment This amendment is approved by the National Health and Family Planning Commission of the People's Republic of China on December 1,.2014, No. 19 The date of approval. The formula (A.2) of A.4.4 in Appendix A is amended to read as follows. w1 = 2 × (V - V0) × c × M 1000 × m × 100% (A.2) Where. 2 --- conversion factor; V - sample consumption of sodium thiosulfate standard titration solution volume in milliliters (mL); V0 --- blank test consumption of sodium thiosulfate standard titration solution volume, in milliliters (mL); c - sodium thiosulfate standard solution concentration in moles per liter (mol/L); M-L-aspartic acid molar mass in grams per mole (g/mol) [M (C4H7O4N) = 133.1]; 1000 --- conversion factor; m - the mass of the sample, in grams (g).
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