SS-EN-ISO-21676 Water quality - Determination of the dissolved fraction of selected active pharmaceutical ingredients, transformation products and other organic substances in water and treated waste water - Method using high performance liquid chromatography and mass spectrometric detection (HPLC-MS/MS or -HRMS) after direct injection (ISO 21676:2018)

SS-EN-ISO-21676 - 2021 EDITION - CURRENT


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This document specifies a method for the determination of the dissolved fraction of selected active pharmaceutical ingredients and transformation products, as well as other organic substances (see Table 1 of the document) in drinking water, ground water, surface water and treated waste water. The lower application range of this method can vary depending on the sensitivity of the equipment used and the matrix of the sample. For most compounds to which this document applies, the range is = 0,025 µg/l for drinking water, ground water and surface water, and = 0,050 µg/l for treated waste water. The method can be used to determine further organic substances or in other types of water (e.g. process water) provided that accuracy has been tested and verified for each case, and that storage conditions of both samples and reference solutions have been validated.

To find similar documents by classification:

13.060.50 (Examination of water for chemical substances)


Directive 2000/60/EC of the European Parliament and of the Council of 23 October 2000 establishing a framework for Community action in the field of water policy (substitutes Directive Reference 01/991 - Common Position on WFD)

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Designation Name

SS-EN ISO 21676:2021

Revision Level

2021 EDITION

Status

Current

Publication Date

Aug. 9, 2021

Language(s)

English

Page Count

48

International Equivalent

EN ISO 21676:2021(IDT); ISO 21676:2018(IDT)