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Registry of CLH intentions until outcome

Registry of CLH intentions until outcome

The registry of classification and labelling (CLH) intentions until outcome lists the intentions and proposals received by ECHA for a new or revised harmonised classification and labelling of a substance. The proposals are submitted by Member State competent authorities, manufacturers, importers or downstream users.  

Interested parties can follow the progress of a proposal through the CLH process, from the notification of the intention to the adoption of the opinion of the Committee for Risk Assessment (RAC). The advance notice enables interested parties to plan and prepare for commenting later on.

Anyone with relevant information on the identity or hazard properties of a substance is encouraged to provide this information to the dossier submitter during the early stages of the process, or at the latest during the public consultation.

Where an opinion has been adopted by RAC, the status is indicated as ‘Opinion Adopted’.

Note: The classification tables for those substances that have been reviewed are listed in the ‘Corrigenda to the RAC opinions’ document.

difethialone (ISO);3-[3-(4′-bromobiphenyl-4-yl)-1,2,3,4-tetrahydronaphthalen-1-yl]-4-hydroxy-2H-1-benzothiopyran-2-one

EC / List no: 600-594-7 CAS no: 104653-34-1
CLP Annex VI Index number
607-717-00-3
Further substance information
Status
Opinion Adopted
Date of intention
04/12/2008
Expected date of submission
31/08/2010
Submitted for accordance check
01/09/2010
Final submission date
28/09/2012
Withdrawal date
Legal deadline for opinion adoption
04/09/2014
Submitter
Norway
Submitter's email
Harmonised classification at the time of the proposal
-
Specific concentration limits at the time of the proposal
Proposed harmonised classification by the dossier submitter
Acute Tox. 1, H300
Acute Tox. 1, H310
Acute Tox. 1, H330
Repr. 1A, H360D
STOT RE 1, H372
Aquatic Acute 1, H400
Aquatic Acute 1, M-factor=100
Aquatic Chronic 1, H410
Aquatic Chronic 1, M-factor=100
Proposed specific concentration limits by the dossier submitter
STOT RE 1; H372: C ≥ 0,02 %
STOT RE 2; H373: 0,002 % ≤ C < 0,02 %
Regulatory programme
Active substance in Biocidal Products
Remarks
Start of consultation
05/03/2013
Deadline for commenting
19/04/2013
Hazard classes open for commenting
CLH report
Annexes to the CLH report
Date of opinion
14/03/2014
RAC Opinion
Background document
RCOM (Comments received)
Attachments received during public consultation (excluding journal articles)
Minority opinion(s)
Other annexes
ATP number and date
ATP09 - (19/07/2016), 01/03/2018
Link to ATP
Latest update
02/04/2019

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