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WTO notification · TBT

European UnionProposed measure, not in force yet

Chemical products – European Union

Official title

Draft Commission Implementing Decision (EU) on the non-approval of active bromine generated from sodium bromide by electrolysis, alkyl (C12-C14) dimethylbenzylammonium chloride (ADBAC (C12-C14)) and hydrogen peroxide as active substances for use in biocidal products of the respective product-types 11, 12, 22 and 12 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council

The European Union notified this proposed TBT measure to the WTO on 6 August 2026. The comment period closed on 5 October 2026.

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Source: WTO ePing (opens in a new tab). Summaries by Expodite, which is independent of the WTO.

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At a glance

Products

Biocidal products and treated articles treated with or incorporating biocidal products

Notifying member
European Union
Status
Proposed measure, not in force yet
Objectives
  • Protection of human health or safety
  • Protection of the environment
  • Harmonization
Area
TBT: Technical product rulesTechnical barriers to trade
Notification type
Regular notification
Document symbol
G/TBT/N/EU/1228
ICS classification
  • 71.100 Products of the chemical industry

Key dates

Distributed by the WTO
Comment deadline
Closed on 5 October 2026
Proposed adoption
December 2026
Proposed entry into force
20 days from publication in the Official Journal of the EU (Application 12 months after adoption)

How to comment

The comment period closed on 5 October 2026. You can still raise concerns about the measure with your country's WTO TBT enquiry point, quoting the document symbol G/TBT/N/EU/1228; it can take them up with the European Union.

Find your country's enquiry point on WTO ePing (opens in a new tab)

What the notification says

This draft Commission Implementing Decision does not approve certain active substances in biocidal products pursuant to Regulation (EU) No 528/2012 of the European Parliament and of the Council. For these active substance/product-type combinations included in the review programme of existing active substances listed in Annex II to Regulation (EU) No 1062/2014, all the participants have withdrawn or are considered to have withdrawn their support. For these active substances either the role of participant had been previously taken over or not. For those that the role of participant had not previously been taken over, no notification has been submitted to the European Chemicals Agency. Therefore, all these active substance/product-type combinations should not be approved for use in biocidal products. As a consequence, also treated articles treated with or incorporating those active substances cannot be placed on the market in the Union 180 days after the decision.

Sources

Expodite writes its summary from the official record. The notification and the documents it notifies are on the WTO's own websites.

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