A more recent version of this regulatory record is available. This version is kept only as a historical record. Please see the Record history section for link to the most recent version.



List details

Basic info

Status Opinion Adopted
Submitter Denmark
Regulatory programme
  • Active substance in Biocidal Products


Proposed harmonised classification by the dossier submitter
  • Acute Tox. 3, H301
  • Acute Tox. 2, H330
  • Skin Irrit. 2, H315
  • Eye Dam. 1, H318
  • Skin Sens. 1, H317
  • Aquatic Acute 1, H400
  • Aquatic Acute 1, M-factor=1
  • Aquatic Chronic 2, H411
Hazard classes open for commenting Explosive Flammable solid Self-reactive substance or mixture Pyrophoric solid Self-heating substance or mixture Substance or mixture which in contact with water emits flammable gas Oxidising solid Substance or mixture corrosive to metals Acute toxicity Skin corrosion/irritation Serious eye damage/eye irritation Skin sensitization Germ cell mutagenicity Carcinogenicity Reproductive toxicity Specific target organ toxicity — single exposure Specific target organ toxicity — repeated exposure Hazardous to the aquatic environment Hazardous for the ozone layer

Intention timeline

Date of intention 2015-07-15
Expected date of submission 2017-03-15
Submitted for accordance check 2017-03-10
Final submission date 2018-05-23
Start of consultation 2018-07-18
Deadline for commenting 2018-09-18
Date of opinion 2019-06-14
Legal deadline for opinion adoption 2019-11-22


CLH report
Annexes to the CLH Report
Comments received
RAC opinion
Background document external link [echa.europa.eu]

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Record history

The following timeline shows when we detected changes of this regulatory record (the date might slightly differ from the date of the actual change). Additions between versions are hightlighted in green color, red color shows data removed between versions.

Sept. 24, 2019
  • Date of opinion: 2019-06-142019-06-13
  • Proposed harmonised classification by the dossier submitter: STOT RE 1, H372
This version
Sept. 10, 2019
  • Background document: https://echa.europa.eu/documents/10162/5429b66a-a0cd-36c5-e99d-fa13abd928f8
  • Comments received: https://echa.europa.eu/documents/10162/3a984a45-fee1-b79e-b897-be996c31e9fehttps://echa.europa.eu/documents/10162/18fb0dbe-5f32-0b51-4d59-0e5bc1f819f2
  • RAC opinion: https://echa.europa.eu/documents/10162/71a363a5-d374-c9d7-28df-289b7a26c646
July 26, 2019
  • Date of opinion: 2019-06-14
  • Status: Public ConsultationOpinion Adopted
April 4, 2019
  • Regulatory programme: BPDActive substance in Biocidal Products
Feb. 18, 2019
  • Regulatory programme: Existing active substance in Biocidal Products (in the meaning of Directive 98/8/EC)BPD
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