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 | Intention |
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Submitter | Austria |
Regulatory programme |
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CLP Annex VI Index Number |
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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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Intention timeline
Date of intention | 2019-06-04 |
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Expected date of submission | 2019-09-30 |
Documents
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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.
Oct. 8, 2019
- Harmonised classification at the time of the proposal: Acute Tox. 4*, H302
- Harmonised classification at the time of the proposal: Acute Tox. 4*, H312
- Harmonised classification at the time of the proposal: Acute Tox. 4, H302
- Harmonised classification at the time of the proposal: Acute Tox. 4, H312
- Specific concentration limits at the time of the proposal: STOT SE 3; H335: C >= 1%
- Proposed harmonised classification by the dossier submitter: To be further specified → Acute Tox. 3, H311
- Proposed harmonised classification by the dossier submitter: Acute Tox. 3, H331
- Proposed harmonised classification by the dossier submitter: Acute Tox. 4, H302
- Proposed harmonised classification by the dossier submitter: Flam. Liq. 2, H225
- Proposed harmonised classification by the dossier submitter: Skin Corr. 1A, H314
- Proposed specific concentration limits by the dossier submitter: Oral: ATE = 500 mg/kg Dermal: ATE = 420 mg/kg Inhal: ATE = 7.2 mg/L STOT SE 3; H335: C >= 1%
- Status: Intention → Submitted
- Submitted for accordance check: 2019-10-03
Jan. 14, 2020
- Proposed harmonised classification by the dossier submitter: Eye Dam. 1, H318
Feb. 4, 2020
- CLH report: https://echa.europa.eu/documents/10162/a3a82182-ac99-3103-b2cf-913dfaf07636
- Deadline for commenting: 2020-04-03
- Final submission date: 2019-12-19
- Hazard classes open for commenting: Acute Toxicity - inhalation Acute Toxicity - dermal Acute Toxicity - oral Serious eye damage/eye irritation
- Legal deadline for opinion adoption: 2021-06-19
- Status: Submitted → Opinion Development
- Start of consultation: 2020-02-03
May 7, 2020
- Comments received: https://echa.europa.eu/documents/10162/9944ccf4-d285-ffe9-1c6f-8829568481da
March 27, 2021
- Name: Triethylamine → triethylamine
April 9, 2021
- Name: triethylamine → Triethylamine
July 1, 2021
- CLH report: https://echa.europa.eu/documents/10162/a3a82182-ac99-3103-b2cf-913dfaf07636
- Comments received: https://echa.europa.eu/documents/10162/9944ccf4-d285-ffe9-1c6f-8829568481da
- Date of opinion: 2021-06-10
- Status: Opinion Development → Opinion Adopted
Oct. 8, 2021
- Background document: https://echa.europa.eu/documents/10162/361a4c0a-5d21-cc49-5415-f4596d5f2821
- Comments received: https://echa.europa.eu/documents/10162/c1373904-4066-4cf6-cb31-b6f793862fe7
- Proposed specific concentration limits by the dossier submitter: Oral: ATE = 500 mg/kg Dermal: ATE = 420 mg/kg Inhal: ATE = 7.2 mg/L STOT SE 3; H335: C >= 1% → Oral: ATE = 500 mg/kg Dermal: ATE = 420 mg/kg Inhal: ATE = 7.2 mg/L STOT SE 3; H335: C => 1%
- RAC opinion: https://echa.europa.eu/documents/10162/db19f23b-9d4a-afb4-37da-587b2cfbee4e
This version
Sept. 24, 2019
- Expected date of submission: 2019-10-31 → 2019-09-30
July 26, 2019
- Regulatory programme: Chemical registered under REACH
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