2-phenoxyethanol

CAS122-99-6
EC204-589-7

List details

Basic info

Status Opinion Adopted
Submitter United Kingdom
Regulatory programme
  • Active substance in Biocidal Products
CLP Annex VI Index Number
  • 603-098-00-9

Classification

Harmonised classification at the time of the proposal
  • Acute Tox. 4*, H302
  • Eye Irrit. 2, H319
Proposed harmonised classification by the dossier submitter
  • Acute Tox. 4, H302
  • Eye Dam. 1, H318
  • STOT SE 3, H335
Hazard classes open for commenting Acute toxicity Serious eye damage/eye irritation Specific target organ toxicity — single exposure Specific target organ toxicity — repeated exposure
Proposed specific concentration limits by the dossier submitter Oral: ATE = 1394 mg/kg bw

Intention timeline

Date of intention 2016-09-28
Expected date of submission 2018-05-31
Submitted for accordance check 2018-06-14
Final submission date 2018-08-07
Start of consultation 2018-09-17
Deadline for commenting 2018-11-16
Date of opinion 2019-06-13
Legal deadline for opinion adoption 2020-02-06

Documents

CLH report
Comments received
Public consultations - received attachments
RAC opinion
Background document external link [echa.europa.eu]

Related substances

By adding any of the following substances to your watchlist, you would be monitoring this regulatory record and all possible new regulatory records related to that substance.

Related regulatory records

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.

This version
Sept. 6, 2019
  • Background document: https://echa.europa.eu/documents/10162/73d19972-51ab-e5d8-9cbd-1b8858f1a1c7
  • Comments received: https://echa.europa.eu/documents/10162/43258793-cb57-2ec9-1581-8e5afa5c1f89https://echa.europa.eu/documents/10162/daa0accf-7806-373a-fd2e-ebc506e7d32f
  • Date of opinion: 2019-06-142019-06-13
  • RAC opinion: https://echa.europa.eu/documents/10162/941f0bdf-7147-51a6-11cf-9250038b760c
July 26, 2019
  • Date of opinion: 2019-06-14
  • Status: Opinion DevelopmentOpinion 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
  • Submitter email: UKREACHCA@hse.gov.uk
Dec. 4, 2018
  • Comments received: https://echa.europa.eu/documents/10162/43258793-cb57-2ec9-1581-8e5afa5c1f89
  • Public consultations - received attachments: https://echa.europa.eu/documents/10162/e81ce8c4-c9c2-e484-9fca-54a820c424c0
  • Status: SubmittedOpinion Development
Add the related substance to your watchlist to monitor this regulatory record.