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GB 1886.241-2016: National Food Safety Standard -- Food Additives -- Glycyrrhizic Acid Tripotassium
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National Food Safety Standard -- Food Additives -- Glycyrrhizic Acid Tripotassium
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GB 1886.241-2016
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Basic data | Standard ID | GB 1886.241-2016 (GB1886.241-2016) | | Description (Translated English) | National Food Safety Standard -- Food Additives -- Glycyrrhizic Acid Tripotassium | | Sector / Industry | National Standard | | Classification of Chinese Standard | X40 | | Word Count Estimation | 6,662 | | Date of Issue | 2016-08-31 | | Date of Implementation | 2017-01-01 | | Regulation (derived from) | Announcement of the State Administration of Public Health and Family Planning 2016 No.11 | | Issuing agency(ies) | National Health and Family Planning Commission of the People's Republic of China, State Food and Drug Administration | GB 1886.241-2016: National Food Safety Standard -- Food Additives -- Glycyrrhizic Acid Tripotassium
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(Food safety national standard - Food additive - Three potassium glycyrrhizinate)
National Standards of People's Republic of China
National standards for food safety
Food additives
2016-08-31 released
2017-01-01 Implementation
People's Republic of China
National Health and Family Planning Commission released
National standards for food safety
Food additives
1 Scope
This standard is based on Glycyrrhizauralensis Fisch, Glycyrrhizain flate,
(GlycyrrhizaglabraL.) Dried roots and rhizomes as raw materials, after extraction, concentration, potash and drying process
The food additive is three potassium glycyrrhizinate.
2 Chemical name, structural formula, molecular formula and relative molecular mass
2.1 Chemical name
Three potassium
2.2 Structural formula
2.3 Molecular formula
C42H59K3O16
2.4 Relative molecular mass
937.20 (according to.2007 international relative atomic mass)
3 technical requirements
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
status
Yellow to brown
powder
Take the appropriate amount of sample in a clean, dry white porcelain dish
Under the 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
Item Index Test Method
(In dry basis), w /% ≥ 10.0 Appendix A, A.3
pH (1% aqueous solution) 6 to 8 GB/T 9724
Dry reduction, w /% ≤ 8 GB 5009.3 direct drying method
Burning residue, w /% ≤ 27 GB/T 9741a
Total arsenic (in As)/(mg/kg) ≤ 2.0 GB 5009.11
Lead (Pb)/(mg/kg) ≤ 2.0 GB 5009.12
a 700 ° C to 800 ° C.
Appendix A
Testing method
A.1 General provisions
The reagents and water used in this standard, when not specified in other requirements, refer to the analysis of pure reagents and GB/T 6682 provides three levels of water. test
The standard solution, impurity standard solution, preparation and preparation used in the test shall be classified according to GB/T 601, GB/T 602,
GB/T 603. The solution used in the test refers to the aqueous solution when it is not specified in the formulation of the solvent.
A.2 Identification test
A.2.1 Reagents and materials
hydrochloric acid.
A.2.2 Identification of potassium ions
Take platinum wire, wet with hydrochloric acid, dipped in the sample, in the colorless flame burning, blue glass glass perspective, the flame was purple.
A.3 Determination of the content of tripotassium glycyrrhizinate (calculated as the dry basis)
A.3.1 Methodological Summary
The sample was dissolved into glycyrrhizic by dissolving, filtered and determined by liquid chromatography (UV detector), external standard method. When calculating the results, try
The mass of the sample is the mass of the sample minus the mass of the drying reduction in the sample. As a result, the 18-β-potassium trihydrate
(C42H59K3O16).
A.3.2 Reagents and materials
A.3.2.1 Methanol. liquid chromatography grade.
A.3.2.2 glacial acetic acid. excellent grade pure.
A.3.2.3 Water. Level 1 water specified in GB/T 6682.
A.3.2.4 Mobile phase solution. Methanol glacial acetic acid (71 1 28), mix well and filter through 0.45 μm filter (organic)
Degassed.
A.3.2.5 Glycyrrhizic acid monoammonium reference substance. purity ≥95% (determined by liquid chromatography).
A.3.3 Instruments and equipment
High performance liquid chromatograph with UV detector.
A.3.4 Analysis steps
A.3.4.1 Preparation of reference solution
Weigh about 20mg (accurate to 0.01mg) glycyrrhizic acid monoammonium reference substance, dissolved with mobile phase solution, and constant volume to 100mL, shake.
A.3.4.2 Preparation of sample solution
Approximately 100 mg (accurate to 0.01 mg) of the potassium triphosphate sample was weighed and placed in a 100 mL volumetric flask and dissolved in a mobile phase solution.
To the scale, the 0.45μm filter (organic) filter, to be measured.
A.3.4.3 Reference chromatographic conditions
A.3.4.3.1 Column. 250 mm long, 4.6 mm in inner diameter, 5 μm in diameter, and C18 column. Or the equivalent separation effect of the column.
A.3.4.3.2 mobile phase. methanol acetic acid aqueous solution.
A.3.4.3.3 Flow rate. 1.0 mL/min.
A.3.4.3.4 Column temperature. room temperature.
A.3.4.3.5 Detection wavelength. 250 nm.
A.3.4.3.6 Injection volume. 10 μL.
A.3.4.4 Determination
Followed by injection of reference substance solution and sample solution, external standard method quantitative. The high performance liquid chromatogram of glycyrrhizic acid is shown in Appendix B.
A.3.5 Calculation of results
The mass fraction w1 of the contents of tripotassium glycyrrhizinate (calculated as the dry basis) is calculated according to formula (A.1)
w1 =
1.12 × V × cs × A
m × (1 - w2) × As ×
100% (A.1)
Where.
1.12 --- conversion of glycyrrhizic acid monoammonium salt into the conversion factor of potassium trihydrate;
V --- sample volume, in milliliters (mL);
cs - the concentration of monoammonium glycyrrhizinate in the reference solution, in milligrams per milliliter (mg/mL);
A - the peak area of glycyrrhizic acid in sample solution;
m --- the quality of the sample in milligrams (mg);
w2 --- sample dry reduction of the content,%;
As - the peak area of glycyrrhizic acid in the reference solution.
The results of the test are based on the arithmetic mean of the parallel measurement results (1 decimal place is reserved). Two independent tests obtained under repetitive conditions
The absolute difference of the result is not more than 5% of the arithmetic mean.
Appendix B
Glycyrrhetinic acid for liquid chromatography and the reference retention time for each component
B.1 Schematic diagram of glycyrrhizic acid by liquid chromatography
The schematic diagram of liquid chromatography of glycyrrhizic acid is shown in Figure B.1.
Description.
1 - 24 - hydroxy glycyrrhizic acid;
2 --- 18-β glycyrrhizic acid;
3 --- 18-α Glycyrrhizic acid.
Figure B.1 Schematic representation of glycyrrhizic acid by liquid chromatography
B.2 Glycyrrhizic acid components for reference retention time
Table B.1 Reference retention time for each component of glycyrrhizic acid
Finger number Component name Retention time a/min
1 24-Hydroxy Glycyrrhizic Acid 7.0
2 18-beta glycyrrhizic acid 8.1
3 18-α Glycyrrhizic acid 10.0
The retention times of the components of different instruments, different separation columns, and even at different times are different, but the elution order of each component is constant.
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