GC-NIC-MS measurement method for penflufen residual amount

A GC-NCI-MS and flufenapyroxamide technology, which is applied in the field of GC-NCI-MS determination of flufenapyroxad residues, can solve the problems of low sensitivity of anti-interference ability, avoid matrix interference, and have good repeatability , the effect of high sensitivity

Inactive Publication Date: 2016-06-29
崔淑华
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Now various testing institutions and enterprises have purchased gas chromatography-mass spectrometers (GC-MS), and are generally equipped with negative chemical ion sources (NCI). Now many types of pesticides contain electronegative groups, organochlorines and pseudo Pyrethrin pesticide molecules mostly contain strong electronegative groups such as -F, -Cl, -Br or -COO-; organophosphorus pesticide molecules mostly contain =S, -OR, -P, -O-, -Cl, or -P=O and other electronegative groups; and most of the new pesticides developed in recent years contain -F groups. Therefore, the use of GC-NCI-MS can facilitate the multi-residue analysis of various pesticides. Compared with MS, it can obtain better anti-interference ability, lower s

Method used

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  • GC-NIC-MS measurement method for penflufen residual amount
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  • GC-NIC-MS measurement method for penflufen residual amount

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Example 1: Detection of flufenapyramide residues in wheat

[0035] (1) Sample pretreatment

[0036] extract

[0037] Weigh 5g of wheat sample (ground into flour) that has been thoroughly mixed into a 50mL centrifuge tube, add 20mL of water to resuscitate for 30min, then accurately add 20mL of acetonitrile solution containing 1% acetic acid, shake and extract for 20min, ultrasonically extract for 5min, add 3g of anhydrous Magnesium sulfate and 2g sodium acetate, after vortexing for 1min, centrifuge at 7000r / min for 5min. After centrifugation, take 8 mL of acetonitrile extract and rotate it at 40 °C or blow it with nitrogen until it is nearly dry, add 1 mL of acetonitrile and vortex it, and wait for purification.

[0038] purify

[0039] Pre-wash C with 5 mL of acetonitrile 18 / PSA solid phase extraction column, when the liquid level reaches the top of the adsorbent, transfer the above extraction solution into the column, wash the test tube with 2mL acetonitrile, and ...

Embodiment 2

[0065] Example 2: Detection of flufenapyroxamide residues in pork

[0066] (1) Sample pretreatment

[0067] extract

[0068] Weigh 5g of fully mixed pork sample into a 50mL centrifuge tube, add 5mL of water to mix, let it stand for 30min, add 20mL of acetonitrile accurately, extract homogeneously for 2min, add 3g of anhydrous magnesium sulfate and 2g of sodium chloride, and vortex for 1min , 7000r / min centrifugal 5min. After centrifugation, take 8 mL of the acetonitrile extract at 40°C for rotary steaming or nitrogen blowing to about 1 mL for purification.

[0069] purify

[0070] Pre-wash C with 5 mL of acetonitrile 18 / PSA solid phase extraction column, when the liquid level reaches the top of the adsorbent, transfer the above extraction solution into the column, wash the test tube with 2mL acetonitrile, and transfer the washing liquid into the SPE column, when the solution reaches the top of the adsorbent, add Add 4mL of acetonitrile to the column for elution, all the ...

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Abstract

The invention discloses a GC-NCI-MS method for determining the residual amount of flufenapyroxamide, which is mainly used for measuring the residual flufenapyroxystrobale content in complex matrix food and agricultural products such as grains and animal-derived foods. Use acetonitrile or an acetonitrile solution containing 1% acetic acid to homogeneously extract the residual flufenapyramide in the sample, C 18 After purification and concentration of the /PSA solid phase extraction column, gas chromatography-negative chemical ion source-mass spectrometry (GC-NCI-MS) detection, a calibration standard working curve is established using a blank matrix solution that does not contain the pesticide to be tested, and the external standard method is used for quantification. The average recovery rate of this method is 88.9%-104.7%, the average relative standard deviation (RSD) is 4.2%-7.5%, and the detection limit is lower than 1.09 μg/kg. Strong characteristics, good repeatability, and accurate qualitative and quantitative advantages. It can meet the technical requirements of the United States, the European Union, Japan and other countries for corresponding product safety testing, and provide strong technical support for ensuring the food safety of our people and the healthy development of foreign export trade.

Description

technical field [0001] The present invention relates to a kind of GC-NCI-MS determination method of flufenapyramide residual amount, more specifically adopt gas chromatography-negative chemical ion source-mass spectrometry (GC-NCI-MS) to qualitatively and quantitatively measure grain, pork, The invention relates to a method for residual flufenapyroxamide content in animal and plant-derived foods with complex matrices such as beef, mutton, chicken and other animal muscles and products, and belongs to the technical field of determination of pesticide residues. Background technique [0002] Fluxapyroxad is a succinate dehydrogenase inhibitor fungicide developed by BASF. Chemical name: 3-difluoromethyl-1-methyl-N-(3',4',5'-trifluorobiphenyl-2-yl)-1H-pyrazole-4-carboxamide; molecular formula: C18H12F5N3O ; Relative molecular mass: 381.3; Melting point: 157°C; Relative density: 1.42. Solubility in solvents (g / L, 20°C): acetone > 250, acetonitrile 168, ethyl acetate 123, metha...

Claims

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Application Information

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IPC IPC(8): G01N30/02G01N30/06
CPCG01N30/02G01N30/06
Inventor 崔淑华
Owner 崔淑华
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