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 Development |
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Submitter | Sweden |
Regulatory programme |
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Classification
Harmonised classification at the time of the proposal |
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Proposed harmonised classification by the dossier submitter |
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Hazard classes open for commenting | Acute toxicity Reproductive toxicity |
Proposed specific concentration limits by the dossier submitter | Oral: ATE = 530 mg/kg |
Intention timeline
Date of intention | 2016-02-10 |
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Expected date of submission | 2018-12-28 |
Submitted for accordance check | 2019-04-17 |
Final submission date | 2019-08-09 |
Start of consultation | 2019-10-14 |
Deadline for commenting | 2019-12-13 |
Legal deadline for opinion adoption | 2021-02-07 |
Documents
CLH report |
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Annexes to the CLH Report |
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Comments received |
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Related substances
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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. 30, 2020
- Date of opinion: 2020-09-17
Dec. 7, 2020
- Background document: https://echa.europa.eu/documents/10162/ec52cbd3-b176-9428-f317-b1962f39be9f
- Comments received: https://echa.europa.eu/documents/10162/5dea8600-71fd-9789-b14f-1998080091c4
- RAC opinion: https://echa.europa.eu/documents/10162/19507471-2f49-9564-d788-0452b1e124ab
Dec. 10, 2020
- Status: Opinion Development → Opinion Adopted
Dec. 14, 2020
- Comments received: https://echa.europa.eu/documents/10162/47bc9fa7-3a49-ed45-a641-7a714a1fd277
Jan. 18, 2023
- ATP number and date: ATP18 - (16/02/2022), 23/11/2023
- Link to ATP / File Title: Official Journal
- Link to ATP / Full Path: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32022R0692&qid=1667995782196
This version
Jan. 20, 2020
- Comments received: https://echa.europa.eu/documents/10162/47bc9fa7-3a49-ed45-a641-7a714a1fd277
Jan. 14, 2020
- Status: Public Consultation → Opinion Development
Oct. 21, 2019
- Annexes to the CLH Report: https://echa.europa.eu/documents/10162/70a6674a-5c10-4124-c3fd-e12a59fe6ff1
- CLH report: https://echa.europa.eu/documents/10162/7e8c4cd4-3259-27ff-0588-7fcdbc513b41
- Harmonised classification at the time of the proposal: Repr. 1B, H360FD
- Deadline for commenting: 2019-12-13
- Final submission date: 2019-08-09
- Hazard classes open for commenting: Acute toxicity Reproductive toxicity
- Legal deadline for opinion adoption: 2021-02-07
- Proposed harmonised classification by the dossier submitter: Acute Tox. 4, H332
- Proposed specific concentration limits by the dossier submitter: Oral: ATE = 530 mg/kg
- Status: Submitted → Public Consultation
- Start of consultation: 2019-10-14
May 7, 2019
- Harmonised classification at the time of the proposal: Acute Tox. 4, H302 → Acute Tox. 4*, H302
- Harmonised classification at the time of the proposal: Acute Tox. 4, H332 → Acute Tox. 4*, H332
- Harmonised classification at the time of the proposal: Repr. 1B, H360FD
- Status: Intention → Submitted
- Submitted for accordance check: 2019-04-17
April 4, 2019
- Regulatory programme: Other substance → Chemical registered under REACH
- Submitter email: kemi@kemi.se
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