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GB 7912-2010 English PDF

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GB 7912-2010: Gardenia yellow of the national food safety standards of food additives
Status: Valid

GB 7912: Evolution and historical versions

Standard ID	Contents [version]	USD	STEP2	[PDF] delivered in	Standard Title (Description)	Status	PDF
GB 7912-2010	English	189	Add to Cart	3 days [Need to translate]	Gardenia yellow of the national food safety standards of food additives	Valid	GB 7912-2010
GB 7912-1987	English	239	Add to Cart	2 days [Need to translate]	Food additive--Gardenia yellow, crocin	Obsolete	GB 7912-1987

PDF similar to GB 7912-2010

Standard similar to GB 7912-2010

GB 8817 GB 1987 GB 1886.64 GB 1886.41 GB 1886.169 GB 1886.173

Basic data

Standard ID	GB 7912-2010 (GB7912-2010)
Description (Translated English)	Gardenia yellow of the national food safety standards of food additives
Sector / Industry	National Standard
Classification of Chinese Standard	X41
Classification of International Standard	67.220.20
Word Count Estimation	8,816
Date of Issue	2010-12-21
Date of Implementation	2011-02-21
Older Standard (superseded by this standard)	GB 7912-1987
Regulation (derived from)	Ministry of Health Bulletin No. 19 of 2010
Issuing agency(ies)	Ministry of Health of the People's Republic of China
Summary	This Chinese standard applies to the Rubiaceae Gardenia (Gardenia jasminoides Ellis) fruit as raw material, extraction, refining, available dextrin diluted powder, extract or liquid food additives gardenia yellow.

GB 7912-2010: Gardenia yellow of the national food safety standards of food additives

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Gardenia yellow of the national food safety standards of food additives National Food Safety Standard Food additives Gardenia yellow Issued on. 2010-12-21 2011-02-21 implementation National Standards of People's Republic of China People's Republic of China Ministry of Health issued

Foreword

This standard replaces GB 7912-1987 "Food additives Gardenia yellow (powder, extract)." This standard compared with GB 7912-1987, the main changes are as follows. - Modify the color value, loss on drying, arsenic, lead indicators; - Added Geniposide indicators; - Cancel the heavy metals and residue on ignition requirements. Appendix A of this standard is a normative appendix. This standard replaces the standards previously issued as follows. --GB 7912-1987. National Food Safety Standard Food additives Gardenia yellow

1 Scope

This standard applies to the Rubiaceae Gardenia (Gardenia jasminoides Ellis) fruit as raw material, extraction, refining and Become available dextrin diluted powder, liquid extract or food additives gardenia yellow.

2 Normative references

The standard file referenced in the application of this standard is essential. For cited documents with dates, only the date of Version applies to this standard. For undated references, the latest edition (including any amendments) applies to this standard.

3 formula and relative molecular mass

Formula 3.1 Crocin. C44H64O24 Crocetin. C20H24O4 3.2 relative molecular mass Crocin. 977.21 (according to 2007 international relative atomic mass) Crocetin. 328.35 (according to 2007 international relative atomic mass) 4. Technical Requirements 4.1 Sensory requirements. comply with Table 1. Table 1 Sensory requirements Project requires test methods Color Powder product was orange and yellow to orange, cinnamon extract the product was Color, liquid product was brown to orange Take appropriate sample is placed in a clean, dry white porcelain plate or burning Cup, under natural light, observe its color and texture status. State organization powders, or liquid extract 4.2 Physical indicators. to comply with Table 2. Table 2. Physical and chemical indicators project index Testing method Extract powder, liquid Color value) 5440 (nmnmE cm ± ≥ 10 Appendix A A.3 Geniposide, w /% ≤ 1 (with the color value of 10 dollars for conversion) Appendix A A.4 Loss on drying, w /% ≤ 7 - GB 5009.3 direct drying Arsenic (As)/(mg/kg) ≤ 2 2 GB/T 5009.11 Lead (Pb)/(mg/kg) ≤ 3 3 GB 5009.12

Appendix A

(Normative) Testing method A.1 General Provisions Unless otherwise indicated in the analysis using only recognized as analytical reagents and GB/T 6682-2008 specified in the water. In the analysis Standard titration solution, impurities measured by standard solution, preparations and products, did not indicate when the other requirements, according to GB/T 601, GB/T 602, the provisions of preparation GB/T 603's. This solution was used in the test does not indicate what is formulated with solvent, it refers to an aqueous solution. A.2 Identification Test A.2.1 maximum absorption wavelength Take A.3.2 color value determination of gardenia yellow liquid sample using a spectrophotometer, a wavelength of 440nm should be in the vicinity of the maximum absorption peak. A.2.2 color reaction 0.5 g of sample, add 2 mL of sulfuric acid, which slowly from deep blue to purple and finally to brown. A.2.3 TLC A.2.3.1 Test Method Stationary phase micro-crystalline cellulose lamina, lamina Method. Weigh 10 g microcrystalline cellulose SF 35 mL water was added to a suspension Turbid liquid, smooth and evenly coated on a glass plate of uniform thickness, coating thickness of 0.35 mm or less, at 60 ℃ ~ 80 ℃, bake 20 min. Isoamyl alcohol mobile phase. acetone. water = 5. 6. 5 (by volume). A.2.3.2 Preparation of test solution spotting Weigh a certain amount of the sample, dubbed the concentration of 50g/L solution as spotting the test solution. A.2.3.3 spotting Dried microcrystalline cellulose TLC plate using capillary spotting. Distance from the lower end plate 2 cm, between points 1 cm, dot diameter of about 3 mm, drying with cold air when spotted. A.2.3.4 expand and observation When spotted TLC plate into the expansion slot expansion, to be launched height of 15 cm, removed, air-dried. Observation should be two yellow Spot. Rf is approximately 0.6 crocin; Rf is about 0.9 crocetin. A.3 Determination of Color Value A.3.1 Instruments and Equipment Spectrophotometer. A.3.2 Analysis step Weigh about 0.15g powder sample (accurate to 0.000 2 g) or Weigh about 1g extract or liquid sample (accurate to 0.000 2 g), Dissolved in water, transferred to a 100 mL volumetric flask, add water to volume, shake. Then draw 10 mL sample solution, transferred to 100 mL volumetric flask, add water to volume, shake. Take this sample was placed in a 1 cm cuvette with water blank control, with Measuring absorbance in a spectrophotometer (440nm ± 5nm) the maximum absorption wavelength range. (Absorbance should be controlled at 0.3 to 0.7 of Room otherwise adjust the concentration of the sample should be re-measured absorbance. ) A.3.3 Calculation Results Color value according to the formula (A.1) Calculated. 1) 5440 (× = ± c AnmE cm (A.1) Where. ) 5440 (nmnmE cm ± - sample concentration of 1%, with a 1 cm cuvette at (440nm ± 5nm) in the range of most Great absorption wavelength measured color value; Absorbance of the sample solution A-- actually measured; c-- concentration of the sample solution to be tested, in grams per milliliter (g/mL). The results parallel arithmetic mean of the measurement results shall prevail. Twice in the same condition absolutely independent determination results The difference is not more than 5% of the arithmetic mean. A.4 Determination Geniposide A.4.1 Reagents and materials a) acetonitrile. chromatography. b) Geniposide standard. the mass fraction of ≥99%. A.4.2 Instruments and Equipment High performance liquid chromatograph. with UV detector (detection wavelength 238 nm). A.4.3 reference chromatographic conditions a) Column. ODS C18,4.6mm × 25cm, particle size 5μm; or other equivalent column. b) Mobile phase. acetonitrile. water = 15.85; the 150mL and 850mL acetonitrile HPLC grade water after mixing with 0.45μm filter After filtration and degassing ultrasonic standby. c) Column temperature. 40 ℃. d) flow rate. 0.7 mL/min. e) Injection volume. 10 μL. A.4.4 Analysis step A.4.4.1 Preparation of standard curve Geniposide Weigh about 0.01g Geniposide standard (accurate to 0.0001g), with the mobile phase (aqueous acetonitrile) was dissolved and set the volume to 50mL, Obtain standard stock solution A. Draw 0.25mL, 0.75 mL, 1.25mL, 2.0mL, 2.5mL stock solution A, respectively, with the mobile phase (B Nitrile diluted aqueous solution) and set the volume to 50mL, to give 5 standard. In A.4.3 reference chromatographic conditions, the concentration gradient of standard samples Determination, the experiment was repeated twice, to obtain the average standard peak area. In standard peak area for the vertical axis, the standard Geniposide mass concentration (g/mL) Abscissa, the standard curve. A.4.4.2 Preparation of sample solution Weigh the amount of sample (accurate to 0.0001g), phase (aqueous acetonitrile) were dissolved in mobile and set the volume to 25mL, the resulting solution 0.45μm membrane filter, the filtrate was set aside. A.4.4.3 Determination In A.4.3 reference chromatographic conditions, the sample was measured according to standard Geniposide retention time qualitative. A repeat injection Times to give Geniposide average peak area value. The linear relationship between the peak area of the standard sample and standard samples Geniposide concentration between obtained test The concentration of the sample solution Geniposide (g/mL). If the concentration of the sample solution Geniposide (g/mL) is not within the scope of the standard curve should be adjusted Concentration of the sample solution or the entire redesign of the standard curve. A.4.5 Calculation Results The content of the sample Geniposide X1 according to formula (A.2) Calculated. 1 × = c cX% (A.2) Where. Content Geniposide X1-- sample,%; c1-- according jasminoidin concentration standard curve obtained in grams per milliliter (g/mL); C2-- concentration of the sample solution, in grams per milliliter (g/mL). Finally, and converting the results into a color value to 10 meter Geniposide content. The results parallel arithmetic mean of the measurement results shall prevail. Twice in the same condition absolutely independent determination results The difference is not more than 0.1%.

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