ISO 22992-2:2020
Textiles — Determination of certain preservatives — Part 2: Determination of triclosan residues method using LC-MS/MS
Textiles — Determination of certain preservatives — Part 2: Determination of triclosan residues method using LC-MS/MS
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 6
- Дата публикации:
- 30 октября 2020 г.
- Издание:
- ISO IS 22992 edition 1 version 1
- ICS:
- 59.060.01
This document specifies a method for determination of triclosan residues in textiles by high performance liquid chromatography — tandem mass spectrometry (HPLC-MS/MS). This method is applicable to all kinds of textile products.
Abstract
Overview
ISO 22992-2:2020 specifies a validated laboratory method for the determination of triclosan residues in textiles using liquid chromatography coupled with tandem mass spectrometry (HPLC‑/LC‑MS/MS). The procedure covers sample preparation, ultrasonic extraction with methanol, concentration and cleanup, instrumental analysis by LC‑MS/MS (electrospray ionization, MRM), calibration, blank control and result calculation. The method is applicable to all kinds of textile products.
Key topics and technical requirements
- Scope: Determination of triclosan (CAS 3380‑34‑5) in textile samples; applicable to all textile types.
- Sample preparation: Representative specimen cut to <5 mm pieces; typical test mass (1.00 ± 0.01) g.
- Extraction: Two-step ultrasonic extraction with methanol (25 mL each) at ≈40 °C for (30 ± 2) min; combined extracts concentrated with rotary evaporator to ≈1 mL, dried with nitrogen, reconstituted to 2 mL and filtered (0.22 µm).
- Standards & calibration: Stock standard 1 000 mg/L in methanol; working solutions prepared into at least five calibration levels; quantification by external standard method. Stock stored 0–4 °C up to 6 months; working solutions up to 3 months.
- LC‑MS/MS parameters (Annex A examples): C18 reversed‑phase column (150×2.1 mm, 3.5 µm); mobile phase methanol:water (90:10 v/v); flow 0.25 mL/min; injection 20 µL. ESI negative ion mode, MRM detection; typical precursor m/z 286.7 with transitions to m/z 35.0 (quant) and 142.1. Typical detection limit shown as 0.5 mg/kg.
- Quality control: Blank test to check contamination; dilution or increased sample mass recommended if analyte is outside linear range.
- Reporting & calculation: Results expressed as mg/kg (mass ratio triclosan/test specimen); report must reference ISO 22992‑2:2020 and note any deviations.
Practical applications and users
- Textile testing laboratories implementing regulatory or customer-driven chemical safety checks for triclosan in garments, home textiles and technical textiles.
- Manufacturers and suppliers verifying compliance, screening incoming materials or validating finishing processes that may use preservatives.
- Regulatory bodies and compliance auditors assessing conformity with chemical-restriction requirements.
- Research labs studying triclosan occurrence, migration or treatment effects in textile matrices.
Keywords: ISO 22992-2:2020, triclosan residues, textiles, HPLC‑MS/MS, LC‑MS/MS, ultrasonic extraction, MRM.
Related standards
Технические детали
- Технический комитет
- ISO/TC 38 - Textiles
- SKU
- ISO 22992-2:2020
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