octhilinone (ISO); 2-octyl-2H-isothiazol-3-one

CAS26530-20-1
EC247-761-7

List details

Basic info

Status Opinion Adopted
Submitter United Kingdom
Regulatory programme
  • Active substance in Biocidal Products
CLP Annex VI Index Number
  • 613-112-00-5
Remarks OIT was originally included in Annex I to Directive 67/548/EEC following a proposal submitted by the Danish Toxicology Centre In March 1993. The harmonised classification in Annex VI of CLP was translated from the DSD classification. This CLH proposal includes a reassessment of studies used at that time and also more recent studies carried out after the preparation of the original C&L document.

Classification

Harmonised classification at the time of the proposal
  • Acute Tox. 4*, H302
  • Acute Tox. 3*, H311
  • Acute Tox. 3*, H331
  • Skin Corr. 1B, H314
  • Skin Sens. 1, H317
  • Aquatic Acute 1, H400
  • Aquatic Chronic 1, H410
Proposed harmonised classification by the dossier submitter
  • Acute Tox. 3, H301
  • Acute Tox. 3, H311
  • Acute Tox. 2, H330
  • Skin Corr. 1B, H314
  • Eye Dam. 1, H318
  • Skin Sens. 1A, H317
  • Aquatic Acute 1, H400
  • Aquatic Acute 1, M-factor=100
  • Aquatic Chronic 1, H410
  • Aquatic Chronic 1, M-factor=10
Hazard classes open for commenting Acute toxicity Skin corrosion/irritation Serious eye damage/eye irritation Skin sensitization Specific target organ toxicity - single exposure Hazardous to the aquatic environment
Proposed specific concentration limits by the dossier submitter Skin Sens. 1A, H317; C ≥ 0.005 %

Intention timeline

Date of intention 2015-06-18
Expected date of submission 2017-01-31
Submitted for accordance check 2017-02-01
Final submission date 2018-01-17
Start of consultation 2018-03-12
Deadline for commenting 2018-05-11
Date of opinion 2018-11-30
Legal deadline for opinion adoption 2019-07-19

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

  • Harmonised classification and labelling (CLP Annex VI) under the name 2-octyl-2H-isothiazol-3-one (octhilinone (ISO))
    Hazard Class and Category Codes: Acute Tox. 3 *: Acute toxicity; Acute Tox. 3 *: Acute toxicity; Acute Tox. 4 *: Acute toxicity; Skin Corr. 1B: Skin corrosion/irritation; Skin Sens. 1: ; Aquatic Acute 1: Hazardous to the aquatic environment; Aquatic Chronic 1: Hazardous to the aquatic environment
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT08-Wood preservatives
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT06-Preservatives for products during storage
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT07-Film preservatives
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT09-Fibre, leather, rubber and polymerised materials preservatives
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT10-Construction material preservatives
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT11-Preservatives for liquid-cooling and processing systems
  • Biocidal active substances under the name 2-octyl-2H-isothiazol-3-one (OIT)
    Product type: PT13-Working or cutting fluid preservatives
  • Registered substances
    Tonnage band: 0 - 10 tonnes per annum
  • Registrants
    Tonnage band: 0 - 10 tonnes per annum

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
April 4, 2019
  • Regulatory programme: BPDActive substance in Biocidal Products
Feb. 18, 2019
  • RAC opinion: https://echa.europa.eu/documents/10162/c008c675-3c11-39b3-1bf3-688e86a4b4e1https://echa.europa.eu/documents/10162/4f2ebbc7-d814-f967-12bb-223c17b9aeec
Feb. 6, 2019
  • Background document: https://echa.europa.eu/documents/10162/68ef9768-a4f4-3a4d-c692-3c1aa766a674
  • Comments received: https://echa.europa.eu/documents/10162/c01f6198-6a45-18e2-fd6e-d9f4771c1536https://echa.europa.eu/documents/10162/ae01374e-1d6e-9e6d-1d2c-3c60bbcd6ae0
  • RAC opinion: https://echa.europa.eu/documents/10162/c008c675-3c11-39b3-1bf3-688e86a4b4e1
Dec. 11, 2018
  • Date of opinion: 2018-11-30
  • Status: Opinion DevelopmentOpinion Adopted
Add the related substance to your watchlist to monitor this regulatory record.