Ammonium bromide

CAS12124-97-9
EC235-183-8

List details

Basic info

Status Opinion Development
Submitter Sweden
Regulatory programme
  • Chemical registered under REACH
  • Active substance in Biocidal Products

Classification

Proposed harmonised classification by the dossier submitter
  • Eye Irrit. 2, H319
  • Repr. 1B, H360FD
  • Lact., H362
  • STOT SE 3, H336
  • STOT RE 2, H373
Hazard classes open for commenting Acute toxicity Skin corrosion/irritation Serious eye damage/eye irritation skin sensitization Germ cell mutagenicity Carcinogenicity Reproductive toxicity Specific target organ toxicity — single exposure Specific target organ toxicity — repeated exposure

Intention timeline

Date of intention 2016-01-25
Expected date of submission 2018-06-29
Submitted for accordance check 2018-10-05
Final submission date 2019-02-22
Start of consultation 2019-04-15
Deadline for commenting 2019-06-14
Legal deadline for opinion adoption 2020-08-23

Documents

CLH report
Annexes to the CLH Report
Comments received
Public consultations - received attachments

Related substances

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Related regulatory records

  • Registered substances
    Tonnage band: 1000 - 10000 tonnes per annum
  • Registrants
    Tonnage band: 1000 - 10000 tonnes per annum
  • Biocidal active substances under the name Bromide activated chloramine (BAC) generated from ammonium bromide and sodium hypochlorite
    Product type: PT11-Preservatives for liquid-cooling and processing systems
  • Biocidal active substances under the name Bromide activated chloramine (BAC) generated from ammonium bromide and sodium hypochlorite
    Product type: PT12-Slimicides

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
Aug. 7, 2019
  • Status: Public ConsultationOpinion Development
July 26, 2019
  • Comments received: https://echa.europa.eu/documents/10162/fe27992c-9579-de40-d2d7-5e29d2571a72
  • Public consultations - received attachments: https://echa.europa.eu/documents/10162/58b97314-58b4-5667-fb8c-4ece69d955bd
April 19, 2019
  • Annexes to the CLH Report: https://echa.europa.eu/documents/10162/f75e3d1d-30b0-ed98-1944-aedec189a44a
  • CLH report: https://echa.europa.eu/documents/10162/535027b8-ae49-02cd-a5a9-0c875d50242d
  • Deadline for commenting: 2019-06-072019-06-14
  • Start of consultation: 2019-04-082019-04-15
April 4, 2019
  • Deadline for commenting: 2019-06-07
  • Final submission date: 2019-02-22
  • Hazard classes open for commenting: Acute toxicity Skin corrosion/irritation Serious eye damage/eye irritation skin sensitization Germ cell mutagenicity Carcinogenicity Reproductive toxicity Specific target organ toxicity — single exposure Specific target organ toxicity — repeated exposure
  • Legal deadline for opinion adoption: 2020-08-23
  • Regulatory programme: BPDActive substance in Biocidal Products
  • Regulatory programme: Other substanceChemical registered under REACH
  • Status: SubmittedPublic Consultation
  • Start of consultation: 2019-04-08
  • Submitter email: kemi@kemi.se
Oct. 23, 2018
  • Submitter: Sweden
  • Submitter email: kemi@kemi.se
Oct. 16, 2018
  • Proposed harmonised classification by the dossier submitter: Eye Irrit. 2, H319
  • Proposed harmonised classification by the dossier submitter: Lact., H362
  • Proposed harmonised classification by the dossier submitter: STOT RE 2, H373
  • Regulatory programme: BPD
  • Status: IntentionSubmitted
  • Submitter: Sweden
  • Submitter email: kemi@kemi.se
  • Submitted for accordance check: 2018-10-05
Add the related substance to your watchlist to monitor this regulatory record.