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GB 31622-2014: National Food Safety Standard -- Food Additives -- Myrica rubra red
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| GB 31622-2014 | English | 169 |
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National Food Safety Standard -- Food Additives -- Myrica rubra red
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GB 31622-2014
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Basic data | Standard ID | GB 31622-2014 (GB31622-2014) | | Description (Translated English) | National Food Safety Standard -- Food Additives -- Myrica rubra red | | Sector / Industry | National Standard | | Classification of Chinese Standard | C53 | | Classification of International Standard | 67.020 | | Word Count Estimation | 7,773 | | Date of Issue | 1/28/2015 | | Date of Implementation | 7/28/2015 | | Regulation (derived from) | National Health and Family Planning Committee Announcement 2015 No. 2 | | Issuing agency(ies) | National Health and Family Planning Commission of the People's Republic of China | | Summary | This Standard applies to Yangmei (Mynica rubra Sied.et Zucc) of mature fruit as raw material, through ethanol extraction, food industry adsorption resin purification, and then concentrated and dried to obtain a food additive Yangmei Hong. | GB 31622-2014: National Food Safety Standard -- Food Additives -- Myrica rubra red---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.
(National food safety standards for food additives Yangmei Hong)
National Standards of People's Republic of China
National Food Safety Standard
Yangmei Hong food additives
Published 2015-01-28
2015-07-28 implementation
People's Republic of China
National Health and Family Planning Commission issued
National Food Safety Standard
Yangmei Hong food additives
1 Scope
This standard applies to Yang Mei (MynicarubraSied.etZucc) ripe fruit as a raw material, an ethanol solution by extraction, food industry
The resin adsorption purification, and then concentrated, dried to obtain a food additive Yangmei Hong.
Formula 2, Structure and molecular weight
Formula 2.1
Cyanidin -3-O- glucoside. C21H21O11
2.2 Structure
2.3 Molecular Weight
Cyanidin-3-glucoside. 449.38 (2007 international relative atomic mass press)
3 Technical requirements
3.1 Sensory requirements
Shall comply with the requirements in Table 1.
Table 1 Sensory requirements
Project requires test methods
Color purple to red and black
Status powder
Proper amount of sample is placed in a clean, dry porcelain dish, from the
Under natural light, the color observed and the state
3.2 Physical and Chemical Indicators
Shall be in accordance with Table 2.
Table 2. Physical and chemical indicators
Item Index Test Method
Color value E1 m (525 ± 5) nm ≥ 40 Appendix A A.4
pH (10g/L solution) 3.0 ~ 4.5 GB/T 9724
Cyanidin -3-O- glucoside (w) /% ≥ 5 A.4
Loss on drying (w) /% ≤ 18 GB 5009.3 a direct drying method
Residue on ignition (w) /% ≤ 6 GB 5009.4
Total arsenic (As)/(mg/kg) ≤ 2 GB 5009.11
Lead (Pb)/(mg/kg) ≤ 3 GB 5009.12
a drying temperature and time were 105 ℃ ± 2 ℃ and 4h.
Appendix A
Testing method
A.1 General Provisions
Unless otherwise specified in this standard, the reagents were of analytical grade, standard titration solution used, the impurity determined by standard solution, and made preparations
Product, should GB/T 601, GB/T 602, GB/T 603 provisions prepared test water shall comply with GB/T 6682's. The test
When the solution does not indicate what formulated with a solvent, refer to the aqueous solution.
A.2 Identification Test
A.2.1 maximum absorption peak
Sample taken 0.1g, with ethanol - hydrochloric acid solution is dissolved (A.3.1.2) and diluted to 100mL, 525nm ± 5nm in the scope of the sample liquid
Within a maximum absorption peak.
A.2.2 color reaction
Sample taken 0.1g, was dissolved in 50mL of water, the solution was purple red ~, the solution was added sodium hydroxide solution (4.3g sodium hydroxide
It was dissolved in 100mL of water), or blue color of the solution turned dark green.
A.3 Color Value Determination
A.3.1 Reagents and materials
A.3.1.1 ethanol.
A.3.1.2 ethanol - hydrochloric acid solution. Take 4mL hydrochloric acid solution (14), placed in 1000mL volumetric flask with 40% ethanol solution was diluted
To volume, shake.
A.3.2 Instruments and Equipment
Spectrophotometer.
A.3.3 Analysis step
Sample weighed 0.1g, accurate to 0.0001g, with ethanol - hydrochloric acid to dissolve and dilute to 100mL, shake, and then draw 10mL,
Transferred to a 100mL volumetric flask, add ethanol - hydrochloric acid solution to volume, shake. This sample was placed taken 1cm cuvette, to B
Alcohol - hydrochloric acid solution as a blank, the absorbance was measured with a spectrophotometer at the wavelength of maximum absorption of 525nm ± 5nm (control absorbance should
Made between 0.2 and 0.8, the sample concentration should be adjusted or re-measuring the absorbance).
A.3.4 calculation results
Color value at the concentration of 1% test sample, a 1cm cuvette, the absorbance measured at the maximum absorption wavelength at 525nm ± 5nm of
E1 m (525 ± 5) nm meter, according to formula (A.1) is calculated.
E1 m (525 ± 5) nm =
c ×
(A.1)
Where.
A --- absorbance of the sample solution measured;
--- C concentration in the sample solution to be tested, expressed in grams per milliliter (g/mL);
100 --- concentration conversion coefficient.
The test result to the arithmetic mean of replicates results. Obtained in two independent determination results under repeatability conditions of absolute difference
Value is not more than 10% of the arithmetic mean.
Determination -3-O- glucoside prime A.4 cornflower
A.4.1 Reagents and materials
A.4.1.1 Acetonitrile. chromatographically pure.
A.4.1.2 hydrochloric acid.
A.4.1.3 formic acid.
A.4.1.4 cyanidin -3-O- glucoside reference substance. purity ≥98%.
A.4.1.5 methanol. 50%. HPLC grade methanol and an equal volume of water were mixed to homogeneity.
Hydrochloric acid solution A.4.1.6. 1499.
A.4.2 Instruments and Equipment
HPLC with UV detector.
A.4.3 Reference chromatographic conditions
A.4.3.1 Column. acid type C18 column, 4.6 mm (inner diameter) × 250mm (length), particle size 5μm. Or other equivalent column.
A.4.3.2 mobile phase. acetonitrile = water-carboxylic acid (151100).
A.4.3.3 Column temperature. 25 ℃.
A.4.3.4 flow rate. 1.0mL/min.
A.4.3.5 injection volume. 20μL.
A.4.3.6 Detection wavelength. 515nm.
A.4.4 Analysis step
Preparation of the control solution A.4.4.1
Weighed amount cyanidin -3-O- glucoside reference substance, the nearest 0.0001g, was dissolved with methanol formulated in a concentration of about
0.06mg/mL of cyanidin -3-O- glucoside control solution stored frozen. Prior to assay, this solution was diluted 3-fold with a control solution of hydrochloric acid
After backup.
Preparation of sample solution A.4.4.2
Sample weighed 0.1g, accurate to 0.0001g, placed in stoppered Erlenmeyer flask, methanol was added 100mL, sonicated for 10min, with
Microporous membrane (0.45μm) filtration, frozen. Before and after the measurement, the sample solution was diluted 3-fold with a solution of hydrochloric acid, the standby.
A.4.4.3 system suitability test
In reference A.4.3 chromatographic conditions, multiple injections of a control solution was chromatographed separation R should be greater than 1.5, the number of theoretical plates
-3-O- cyanidin glucoside calculated to be not less than 2000.
A.4.4.4 Determination
In reference A.4.3 chromatographic conditions, respectively, sample solution and control solution for chromatography. Record the chromatogram and a sample solution of
According solution chromatogram cyanidin -3-O- glucoside peak area value.
A.4.5 calculation results
Cyanidin -3-O- glucoside mass fraction w according to equation (A.2) is calculated.
w =
A1 × c × 3 × 100
A2 × m ×
100% (A.2)
Where.
Peak area A1 --- cyanidin -3-O- glucoside chromatogram of the sample solution;
C --- Control solution concentration, in milligrams per milliliter (mg/mL);
3 --- dilution;
100 --- solution volume in milliliters (mL);
Peak area A2 --- control cyanidin -3-O- glucoside solution chromatogram;
--- m sample mass, in milligrams (mg).
The test result to the arithmetic mean of replicates results. Obtained in two independent determination results under repeatability conditions of absolute difference
Value is not more than 5% of the arithmetic mean.
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