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GB 8817-2001 PDF English

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GB 8817-2001: Food additive Caramel (Sulfite ammonia caramel, ammonia caramel, plain caramel)
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Status: Obsolete

GB 8817: Historical versions

Standard IDUSDBUY PDFDeliveryStandard Title (Description)Status
GB 8817-2001210 Add to Cart Auto, 9 seconds. Food additive Caramel (Sulfite ammonia caramel, ammonia caramel, plain caramel) Obsolete
GB 8817-1988199 Add to Cart 2 days Food additive--Caramel Obsolete

Similar standards

GB 1886.64   GB 1886.29   GB 1886.41   GB 1886.173   

GB 8817-2001: Food additive Caramel (Sulfite ammonia caramel, ammonia caramel, plain caramel)

---This is an excerpt. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.), auto-downloaded/delivered in 9 seconds, can be purchased online: https://www.ChineseStandard.net/PDF.aspx/GB8817-2001
NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 67.220.20 X 41 Replacing GB 8817-1998 Food additive - Caramel (Sulfite ammonia caramel, ammonia caramel, plain caramel) ISSUED ON: AUGUST 06, 2001 IMPLEMENTED ON: FEBRUARY 01, 2002 Issued by: General Administration of Quality Supervision, Inspection and Quarantine of the PRC.

Table of Contents

Foreword ... 3 1 Scope ... 4 2 Normative references ... 4 3 Requirements ... 4 4 Test method ... 5 5 Inspection rules ... 11 6 Marking, packaging, transportation, storage ... 11 Food additive - Caramel (Sulfite ammonia caramel, ammonia caramel, plain caramel)

1 Scope

This standard specifies the technical requirements, test methods, inspection rules, packaging, marking, storage, transportation requirements for liquid and powdered caramel made by ammonium sulfite method, ammonia method, plain method. This standard applies to liquid and powdered caramel made by ammonium sulfite method, ammonia method, plain method, using sucrose, starch syrup, xylose mother liquor, etc. as raw materials. It is used as colorants in food.

2 Normative references

The provisions contained in the following standards constitute the provisions of this standard through reference in this standard. When this standard was published, the versions shown were all valid. All standards are subject to revision. Parties using this standard should explore the possibility of using the latest version of the following standards. GB/T 602-1988 Chemical reagent - Preparations of stock standard solutions GB/T 5009.5-1985 Method for determination of protein in foods GB/T 5009.17-1996 Method for determination of total mercury in foods GB/T 5009.34-1996 Method for determination of sulfite in foods GB/T 8449-1987 Method for determination of lead in food additives GB/T 8450-1987 Method for determination of arsenic in food additives GB/T 8451-1987 Method for limit test of heavy metals in food additives

3 Requirements

3.1 Sensory indicators 3.1.1 Color and appearance: Dark brown, thick liquid or powdery. 4.2 Determination of absorbance Weigh 0.5 g of sample (accurate to 0.002 g). Use water to make the volume reach to the mark in a 500 mL volumetric flask; use a 1 cm cuvette to measure its absorbance at 610 nm with a spectrophotometer. 4.3 Determination of loss on drying 4.3.1 Determination method Weigh 2 g of sample (accurate to 0.0002 g) in a weighing bottle that has been weighed constant. Dry at 105 °C for 2 h. Cool it. Weigh it. 4.3.2 Expression of analysis results Where: X1 - Loss on drying, %; m1 - Mass of weighing bottle and sample before drying, g; m2 - Mass of weighing bottle and sample after drying, g; m - Mass of sample, g. 4.4 Determination of ammonia nitrogen 4.4.1 Reagents and solutions 4.4.1.1 Boric acid (GB/T 628): 2% solution. 4.4.1.2 Methyl red-bromocresol green mixed indicator solution: Mix 5 parts of 0.2% bromocresol green ethanol solution and 1 part of 0.2% methyl red ethanol solution. 4.4.1.3 Magnesium oxide (HGB 1294). 4.4.1.4 Hydrochloric acid (GB/T 622): 0.1 mol/L solution, which is prepared and calibrated according to GB/T 602. 4.4.2 Determination method Weigh 5g of sample (accurate to 0.01 g). Place it in a 500 mL distillation flask. Add 2 g of magnesium oxide and 200 mL of water. Distill by direct fire. The distillate is absorbed in 5 mL of 2% boric acid solution with 5 drops of mixed indicator solution. When the distillate reaches about 100 mL, stop distillation and titrate the distillate with 0.1 mol/L hydrochloric acid, until it turns gray-red. A and B are mixed in equal amounts before use. 4.6.1.9 4-Methylimidazole standard solution Weigh the sample 4-methylimidazole (accurate to 0.1000 g). Place it in a 100 mL volumetric flask. Add 95% ethanol to the mark. Each 1 mL of this solution is equivalent to 1.0 mg of 4-methylimidazole. Before use, use 95% ethanol to dilute it, to the level that each 1 mL is equivalent to 0.1 mg of 4-methylimidazole standard solution. 4.6.2 Method and steps 4.6.2.1 Extraction Weigh 5 g of sample (accurate to 0.01 g). Add 15 mL of water to dissolve. Add 15 mL of 10% sodium carbonate. Add 80 mL of chloroform-anhydrous ethanol mixed solution to a 250 mL separatory funnel. Shake vigorously for 4 min ~ 5 min. After complete layering, collect the chloroform-anhydrous ethanol extract in a 250 mL stoppered conical flask. Use 70 mL of chloroform-anhydrous ethanol mixed solution to extract the above water layer once. Combine the extracts. Add 20 mL of 0.05 mol/L sulfuric acid to the extract. Shake vigorously 60 times. Separate the water layer. Concentrate this solution to 2 mL ~ 3 mL in a 60 °C ~ 70 °C water bath. Slowly add about 0.2 g of sodium bicarbonate fine powder, until no bubbles are generated. Use ethanol to dissolve it to 5 mL. 4.6.2.2 Plate preparation Weigh 3 g of silica gel (GF 254). Add 1 mL of 80% sodium bicarbonate solution and 6 mL of distilled water. Mix well and apply on a 125 mm×85 mm thin plate. Dry naturally in the air. Put it in an oven at 120 °C for 2 minutes. After taking it out, put it in a dryer for use. 4.6.2.3 Spotting Spot 10 μL, 20 μL, 30 μL of 4-methylimidazole standard solution and 100 μL of sample diluent on the thin plate, respectively. Develop the thin plate in the developing agent until the solvent front reaches 10 cm. Take out the thin plate. Blow dry it. Spray it with a newly prepared color developer. Within 5 min ~ 10 min, the yellow spot of 4-methylimidazole can reach the deepest depth and remain stable for several hours. According to the size and color depth of the spot compared with the standard spot, determine the content of 4-methylimidazole in the sample. 4.6.3 Expression of analysis results Where: X3 - 4-methylimidazole content, %; c - Amount of sample spot equivalent to standard spot, µg; m - Sample mass, g; V1 - Spot volume, μL; V2 - Total volume of sample solution, μL; A610 - Absorbance of sample at 610 nm; 0.1/A610 - Content converted to chromaticity of 0.1. 4.7 Determination of arsenic It is determined by arsenic spot method after wet digestion in accordance with GB/T 8450-1987. 4.8 Determination of lead It is determined by wet digestion in accordance with GB/T 8449-1987. 4.9 Determination of heavy metals It is determined by wet digestion in accordance with GB/T 8451-1987. 4.10 Determination of total nitrogen It is determined according to GB/T 5009.5. 4.11 Determination of total sulfur 4.11.1 Reagents and solutions 4.11.1.1 Magnesium oxide (HGB 1294). 4.11.1.2 Magnesium nitrate [Mg(NO3)2·6H2O] (HG 3-1077). 4.11.1.3 Sucrose (HG 3-1001). 4.11.1.4 Nitric acid (GB/T 626). 4.11.1.5 Hydrochloric acid (1:1) (GB/T 622).

5 Inspection rules

5.1 The same type of products with intact packaging produced by the same equipment by the same shift are considered as a batch. 5.2 Randomly select samples from each batch of products. Select small samples of 5% of the number of pieces or barrels of liquid products in each batch (at least 3 pieces or 3 barrels). Take not less than 500 mL of samples from each piece (or barrel), or 2 bags for powder product (250 g sample from each bag). The sampled samples shall be mixed quickly and evenly; respectively contained in two clean, dry large-mouth bottles, labeled with the manufacturer's name, batch and sampling date. One copy shall be sent to the laboratory for testing, whilst the other copy shall be kept for future reference. 5.3 Drying loss (solid) and absorbance are mandatory inspection items. Arsenic, lead, heavy metals, ammonia nitrogen, sulfur dioxide, 4-methylimidazole, total nitrogen, total sulfur are type spot inspection items. 5.4 If one of the indicators in the inspection does not meet this indicator, double the number of products from the same batch shall be performed for re-inspection. If there is still one item in the re-inspection result that does not meet this standard, the batch of products shall be judged as unqualified. 5.5 If the supplier and the purchaser have objections to the product quality, the two parties may negotiate and select the relevant statutory arbitration department to proceed, in accordance with the relevant provisions of this standard.

6 Marking, packaging, transportation, storage

6.1 Marking The product packaging shall be firmly marked with the product name, manufacturer name, address, trademark, model, standard number, production date, net content, storage period, production license, batch number, etc. The words "food additives" shall also be marked. 6.2 Packaging Plastic packaging made of packaging materials that meet food hygiene standards shall be used. The liquid specifications are 2, 10, 20, 30 kg; the powder specifications are 0.5, 1, 2.5, 10 kg, or packaged according to the specifications required by the buyer. The sealing shall be tight; the liquid and powder are all packaged with corrugated paper. 6.3 Storage The product shall be stacked in a ventilated, clean, dry place; it shall not be mixed with ......

Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.
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