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GB 1886.76-2015 English PDF

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GB 1886.76-2015: National Food Safety Standard -- Food Additives -- Curcumin
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GB 1886.76-2015English189 Add to Cart 3 days [Need to translate] National Food Safety Standard -- Food Additives -- Curcumin Valid GB 1886.76-2015

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Basic data

Standard ID GB 1886.76-2015 (GB1886.76-2015)
Description (Translated English) National Food Safety Standard -- Food Additives -- Curcumin
Sector / Industry National Standard
Classification of Chinese Standard X40
Classification of International Standard 67.220.20
Word Count Estimation 9,939
Date of Issue 2015-11-13
Date of Implementation 2016-05-13
Regulation (derived from) National Health and Family Planning Commission Announcement No
Issuing agency(ies) National Health and Family Planning Commission of the People's Republic of China
Summary This standard applies to Curcuma longa (Curcuma longa L.) as the raw material of rhizome, the organic solvent extraction, and then refined by the physical method derived from the food additive curcumin.

GB 1886.76-2015: National Food Safety Standard -- Food Additives -- Curcumin

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(National food safety standards for food additives curcumin) National Standards of People's Republic of China National Food Safety Standard Food additives curcumin Issued on. 2015-11-13 2016-05-13 implementation People's Republic of China National Health and Family Planning Commission released National Food Safety Standard Food additives curcumin

1 Scope

This standard applies to Zingiberaceae turmeric (CurcumalongaL.) Roots as raw material, organic solvent extraction, and then by physical methods Refining derived food additives curcumin. 2 chemical name, molecular formula, molecular mass and structural formula 2.1 Chemical Name Curcumin. 1,7-bis (4-hydroxy-3-methoxyphenyl) hept-1,6-diene-3,5-dione Bisdemethoxycurcumin. 1- (4-hydroxyphenyl) -7- (4-hydroxy-3-methoxyphenyl) hept-1,6-diene-3,5-dione Bis Bisdemethoxycurcumin. 1,7-bis (4-hydroxyphenyl) hept-1,6-diene-dione Formula 2.2 Curcumin. C21H20O6 Bisdemethoxycurcumin. C20H18O5 Double Bisdemethoxycurcumin. C19H16O4 2.3 formula Curcumin. R1 = R2 = OCH3 Bisdemethoxycurcumin. R1 = OCH3, R2 = H Double Bisdemethoxycurcumin. R1 = R2 = H 2.4 relative molecular mass Curcumin. 368.39 (according to 2011 international relative atomic mass) Bisdemethoxycurcumin. 338.39 (according to 2011 international relative atomic mass) Double Bisdemethoxycurcumin. 308.39 (according to 2011 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 Project requires test methods Color orange State crystal or crystalline powder With turmeric smell peculiar smell Take the right amount of sample is placed in a white porcelain dish, under natural light, observed Color, state, smell the smell 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 Total curcumin content /% ≥ 90.0 Appendix A A.3 Residual solvent (hexane, ethyl acetate and isopropanol) a/(mg/kg) ≤ 50.0 Appendix A A.4 Total arsenic (As)/(mg/kg) ≤ 3.0 GB 5009.11 Lead (Pb)/(mg/kg) ≤ 2.0 GB 5009.12 a extraction solvent is ethanol, acetone, isopropyl alcohol, n-hexane and/or ethyl acetate.

Appendix A

Testing method A.1 General Provisions This standard reagents and water in the absence of other requirements specified, refers to three analytical reagent water and GB/T 6682 stipulated. test Test used in the determination of impurities standard solution, the reagent solution and the sample solution, in the absence of other specified requirements, according to GB/T 601, GB/T 602 and GB/T 603 provisions prepared. Solution was used in the tests did not indicate what is formulated with solvent, it refers to an aqueous solution. A.2 Identification Test A.2.1 Reagents and materials A.2.1.1 ether. A.2.1.2 glacial acetic acid. A.2.1.3 sodium hydroxide solution. 0.05mol/L. A.2.1.4 Hydrochloride. 1mol/L. A.2.1.5 ethanol. 95%. A.2.1.6 sulfuric acid. A.2.1.7 silica gel thin layer plate. silica gel weighed 10g, add water, 20mL, placed ground in a mortar into a thin slurry suitable thick, uniform coating On the glass, the coating thickness of 0.5mm. 100 ℃ activation 30min. A.2.1.8 developing solvent. chloroform. methanol = 99. A.2.2 Identification method A.2.2.1 solubility Insoluble in water and ether, soluble in ethanol and glacial acetic acid. A.2.2.2 color reaction A.2.2.2.1 Weigh 0.1g sample was dissolved in 5mL sodium hydroxide solution, then red roses, a solution of hydrochloric acid to the acid, the solution that is It rose from the red to bright yellow. A.2.2.2.2 Weigh 10mg sample was dissolved in 5mL ethanol solution, the color is pure microstrip yellow green fluorescence, plus a small amount of sulfuric acid becomes Of red roses. A.2.2.3 TLC A.2.2.3.1 Preparation of sample solution. Weigh the sample 0.1g, dissolved in 10mL ethanol. When using the supernatant. A.2.2.3.2 spotted. The activated silica gel plates, using a micro syringe 2μL sample solution spotted. Spacing of 1.5cm. A.2.2.3.3 expand the observation. Good point will advance into the sheet is expanded when (expansion room temperature with developing solvent saturated chromatography tank uplink law Is 17 ℃ ~ 20 ℃). When the solvent front to be reached 15cm, removed, air-dried. Observation should have three yellow spots, Rf values were 0.11 ~ 0.12,0.23 ~ 0.25,0.41 ~ 0.43. A.3 Determination of the total content of curcumin A.3.1 Method summary According to calculate the total content of curcumin curcumin ethanol absorbance intensity at a particular wavelength. A.3.2 Reagents and materials 95% ethanol. A.3.3 Instruments and Equipment Spectrophotometer. A.3.4 Analysis step Take about 0.1g sample (accurate to 0.0002g), placed in 100mL flask, add 95% ethanol, dissolved by shaking shake. With 95% Ethanol volume mix. Pipette 1.0mL solution to 250mL volumetric flask, constant volume with 95% ethanol. With a 1cm cuvette, measuring 425nm Absorbance under. A.3.5 Calculation Results Curcumin content of total mass fraction w1, according to equation (A.1) Calculated. w1 = A × 250 × 100 m × 1607 (A.1) Where. A --- absorbance of the sample; 250 --- volume conversion factor; 100 --- capacity conversion factor; M --- the quality of the sample, in grams (g); 1607 --- 425nm at the specific absorption coefficient of ethanol solution of curcumin standard products. A.4 Determination of residual solvents (n-hexane, ethyl acetate and isopropanol) of A.4.1 Principle When the balance of the sample in a sealed vial, at a certain temperature, the residual solvent vaporization equilibrium, the upper layer of gas injected into the gas Chromatograph determination, quantitative comparison with a standard curve. A.4.2 Reagents and materials Note. Unless otherwise noted, all reagents were HPLC grade. A.4.2.1 N, N- dimethylformamide (HPLC grade). A.4.2.2 standard stock solution. Weigh isopropyl alcohol (HPLC grade) and hexane (HPLC grade), ethyl acetate (HPLC grade) each 0.05g (nearest 0.0001g), was dissolved in N, N- dimethylformamide and treated with N, N- dimethylformamide was diluted to 50mL volumetric flask, constant volume. this Equivalent to 1.0mg solution 1mL isopropanol, n-hexane and ethyl acetate. Placed in 4 ℃ refrigerator. A.4.3 Instruments and Equipment A.4.3.1 Gas chromatograph. with flame ionization detector (FID). A.4.3.2 analytical balance, a sense of the amount of 0.1mg. A.4.3.3 flask. 50mL. A.4.3.4 Vial. 100mL small infusion bottle mouth. A.4.3.5 sealing jaws. A.4.3.6 airtight needle. 100μL. A.4.3.7 pipettes. 500μL, 5mL. A.4.3.8 headspace autosampler (automatic headspace method). A.4.3.9 Vial. 20mL headspace vial (automatic headspace method). A.4.4 Analysis step A.4.4.1 manual headspace method A.4.4.1.1 standard curve drawing Take vial (A.4.3.4), along the sides of the bottle to the micropipette injecting 500μL stock standard solution, quickly stuffed back on the rubber stopper, aluminum cap sealing After opening at 80 ℃ ± 2 ℃ oven heating 2h, then cool to room temperature, 100μL micro-injector, according to 20μL, 40μL, 60μL, 80μL and 100μL take headspace were injected into the chromatograph, with its peak height (peak area) on the vertical axis, corresponding to the amount of sample solvent Horizontal, standard curve or standard curve linear regression equation. A.4.4.1.2 GC reference conditions A.4.4.1.2.1 Column. 6% cyanopropyl/phenyl and 94% dimethyl polysiloxane capillary column 60.0m × 0.32mm (within Diameter) × 1.8μm, or equivalent person. A.4.4.1.2.2 Column temperature. 40 ℃ maintained 3min, at a rate of 2 ℃/min the temperature was raised to 70 ℃, then at a rate of 20 ℃/min the temperature was raised to 180 ℃ holding 4min, then at a rate of 30 ℃/min heating to 280 ℃. A.4.4.1.2.3 vaporization chamber temperature.200 ℃. A.4.4.1.2.4 detector temperature. 300 ℃. A.4.4.1.2.5 carrier gas. nitrogen, purity ≥99.99%. A.4.4.1.2.6 gas. hydrogen, purity ≥99.99%. A.4.4.1.2.7 carrier gas flow rate. 2.0mL/min. A.4.4.1.2.8 hydrogen flow rate. 40mL/min. A.4.4.1.2.9 air flow rate. 450mL/min. A.4.4.1.2.10 makeup flow. 20.0mL/min. A.4.4.1.2.11 Injection mode. split injection, split ratio of 1. A.4.4.1.2.12 Running time. 28.17min. A.4.4.1.3 Determination Take vial (A.4.3.4), weighed 2g (accurate to 0.0001g) sample, placed in the bottom, add 5mLN, N- dimethylformamide, Li That anti-stoppered rubber gag, aluminum lid sealed, and then heated in an oven at 80 ℃ ± 2 ℃ 2h, vial upon heating gasification, cooling to room temperature, With micro sample taken 100μL headspace, chromatographic analysis, the resulting sample chromatogram peak height (peak area), based on the standard curve was dissolved Agent content of each sample was calculated residual amount of the solvent. A.4.4.2 automatic headspace method A.4.4.2.1 standard curve drawing Draw stock standard solution 0.25mL, 0.5mL, 1.0mL, 2.5mL and 5.0mL vial respectively in N, N- dimethylformamide Amides volume to 5.0mL, with aluminum coating containing PTFE gasket cover seal. Add automatic headspace analyzer, the sample after a good balance, self Fixed import gas chromatograph for analysis. Its peak height (peak area) as the vertical axis and corresponding to a solvent content of samples horizontal, label production Standard curve or standard curve linear regression equation. A.4.4.2.2 GC reference conditions With A.4.4.1.2. A.4.4.2.3 headspace autosampler reference conditions A.4.4.2.3.1 equilibrium temperature. 80 ℃. A.4.4.2.3.2 equilibration time. 40min. A.4.4.2.3.3 loop temperature. 100 ℃. A.4.4.2.3.4 loop volume. 0.5mL. A.4.4.2.3.5 transmission line temperature. 120 ℃. A.4.4.2.4 Determination Weigh sample 0.5g (accurate to 0.0001g) in the headspace vial (A.4.3.9) added 5mLN, N- dimethylformamide, containing PTFE Vinyl-coated aluminum cover gasket seal. Add automatic headspace analyzer, the sample is a good balance after the auto-import gas chromatograph for analysis. Chromatographic solvent residue in Appendix B in Figure B.1. A.4.5 Calculation Results The quality of each solvent fraction wi, in milligrams per kilogram (mg/kg), according to equation (A.2) Calculated. wi = mi (A.2) Where. Quality mi --- derived from the standard curve for each solvent in micrograms (μg); M --- the quality of the sample, in grams (g). The results to three significant figures. Two independent determination results under the absolute difference in repetition condition must not exceed the arithmetic 20% of the mean.

Appendix B

Residual solvent chromatogram GC residual solvent schematic B.1 Solvent residue gas chromatography is shown in Figure B.1. GC residual solvent schematic diagram B.1 With reference to the residual solvent component B.2 retention time Reference of each component solvent residue retention time shown in Table B.1. Table B.1 residual solvent components reference Retention time Peak No. Ingredient name Retention time a/min 1 isopropanol 8.526 2 hexane 11.216 3 ethyl acetate 13.735 a different instrument, different separation column, and even different time injection retention time of each component will be different, but the elution order of the components is constant.

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