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GB/T 39878-2021 English PDF

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GB/T 39878-2021: Examination methods for estazolam in suspected drugs - Gas chromatography and gas chromatography-mass spectrometry
Status: Valid
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GB/T 39878-2021English209 Add to Cart 3 days [Need to translate] Examination methods for estazolam in suspected drugs - Gas chromatography and gas chromatography-mass spectrometry Valid GB/T 39878-2021

PDF similar to GB/T 39878-2021


Standard similar to GB/T 39878-2021

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Basic data

Standard ID GB/T 39878-2021 (GB/T39878-2021)
Description (Translated English) Examination methods for estazolam in suspected drugs - Gas chromatography and gas chromatography-mass spectrometry
Sector / Industry National Standard (Recommended)
Classification of Chinese Standard A92
Word Count Estimation 11,121
Issuing agency(ies) State Administration for Market Regulation, China National Standardization Administration

GB/T 39878-2021: Examination methods for estazolam in suspected drugs - Gas chromatography and gas chromatography-mass spectrometry


---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.
Examination methods for estazolam in suspected drugs-Gas chromatography and gas chromatography-mass spectrometry ICS 13.310 A92 National Standards of People's Republic of China Estazolam test in suspected drugs Gas chromatography and gas chromatography-mass spectrometry Released on 2021-04-30 2021-08-01 implementation State Administration of Market Supervision and Administration Issued by the National Standardization Management Committee

Table of contents

Foreword Ⅲ 1 Scope 1 2 Normative references 1 3 Terms and definitions 1 4 Principle 1 5 Reagent 1 6 Instruments and equipment 2 7 Operation method 2 7.1 Qualitative analysis 2 7.2 Quantitative analysis 3 8 Evaluation and presentation of results 5 8.1 Evaluation of qualitative results 5 8.2 Evaluation of quantitative results 5 8.3 Presentation of results 6 8.4 Evaluation and expression of measurement uncertainty 6 9 Detection limit 6 Appendix A (informative appendix) Internal standard method standard solution and external standard method sample extraction operating parameters 7 Appendix B (informative appendix) Eszolam related information 8

Foreword

This standard was drafted in accordance with the rules given in GB/T 1.1-2009. Please note that some of the contents of this document may involve patents. The issuing agency of this document is not responsible for identifying these patents. This standard was proposed by the Ministry of Public Security of the People's Republic of China. This standard is under the jurisdiction of the National Criminal Technology Standardization Technical Committee (SAC/TC179). This standard was drafted by. Material Evidence Identification Center of the Ministry of Public Security. The main drafters of this standard. Gao Lisheng, Zhang Chunshui, Zheng Hui, Zhao Yang, Qian Zhenhua, Chang Ying, Zhai Wanfeng, Li Peng, Zhao Yanbiao, Yang Hongxian, Zheng Xiaoyu, Wen Wu, Liu Klin, Huang Xing, Wang Yi, Wang Weixin. Estazolam test in suspected drugs Gas chromatography and gas chromatography-mass spectrometry

1 Scope

This standard specifies the gas chromatography-mass spectrometry (GC-MS) qualitative inspection method and gas chromatography (GC) quantitative inspection method of Estazolam Principles, reagents and materials, instruments and equipment, operating methods, and result evaluation and presentation. This standard applies to the qualitative and quantitative analysis of estazolam in solid samples of suspected drugs.

2 Normative references

The following documents are indispensable for the application of this document. For dated reference documents, only the dated version applies to this article Pieces. For undated reference documents, the latest version (including all amendments) is applicable to this document. GB/T 27418 Evaluation and Expression of Uncertainty in Measurement GA/T 122 Terminology for toxicological analysis

3 Terms and definitions

The terms and definitions defined in GA/T 122 are applicable to this document.

4 Principle

Extract estazolam from solid samples of suspected drugs. Use gas chromatography-mass spectrometry to detect with retention time, characteristic ion fragmentation The ratio of slice and ion abundance is used as the basis for qualitative judgment; gas chromatographic detection is used, and the chromatographic peak area is used as the quantitative basis. The internal standard standard curve method is used for quantitative analysis.

5 Reagents

Unless otherwise specified, the reagents used in the analysis are chromatographically pure. 5.1 Methanol. 5.2 Internal standard. Propyl spasmolytic (SKF525A) (purity not less than 95%). 5.3 Standard material stock solution. 1.0mg/mL estazolam standard material stock solution, stored at 0℃~4℃, valid for 12 months. 5.4 Internal standard stock solution for quantitative internal standard curve method. Weigh 500 mg of SKF525A, dilute it with methanol to a 50 mL volumetric flask, and prepare it 10.0mg/mL SKF525A internal standard stock solution. Keep refrigerated at 0℃~4℃, valid for 12 months. 5.5 Standard working solution for qualitative use. Pipette an appropriate amount of estazolam standard substance stock solution, dilute it with methanol, and prepare a 0.1 mg/mL moxa solution. Stazolam standard working solution. Store at 0℃~4℃, the validity period is 3 months. 5.6 Qualitative control standard working solution. pipette an appropriate amount of estazolam standard substance stock solution, dilute with methanol, and prepare 0.005mg/mL The standard working solution of estazolam. Store under refrigeration at 0℃~4℃, valid for 1 month. 5.7 Standard working solution for external standard single-point method quantification. pipette an appropriate amount of estazolam standard substance stock solution, dilute with methanol, and prepare 0.1mg/mL estazolam standard working solution. Store at 0℃~4℃, the validity period is 3 months.

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