Registration Dossier
Registration Dossier
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EC number: 412-420-5 | CAS number: 133909-99-6 TRITYL-LOSARTAN; TRITYL-MK0954
Short-term toxicity to fish
Administrative data
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- GLP compliance:
- no
Test material
- Reference substance name:
- 2-butyl-4-chloro-4,5-dihydro-5-hydroxymethyl-1-[2'-(2-triphenylmethyl-1,2,3,4-2H-tetrazol-5-yl)-1,1'-biphenyl-4-methyl]-1H-imidazole
- EC Number:
- 412-420-5
- EC Name:
- 2-butyl-4-chloro-4,5-dihydro-5-hydroxymethyl-1-[2'-(2-triphenylmethyl-1,2,3,4-2H-tetrazol-5-yl)-1,1'-biphenyl-4-methyl]-1H-imidazole
- Cas Number:
- 133909-99-6
- Molecular formula:
- C41H37ClN6O
- IUPAC Name:
- [2-butyl-4-chloro-1-({2'-[2-(triphenylmethyl)-2H-1,2,3,4-tetrazol-5-yl]-[1,1'-biphenyl]-4-yl}methyl)-1H-imidazol-5-yl]methanol
Constituent 1
Test organisms
- Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
Study design
- Test type:
- semi-static
- Water media type:
- freshwater
- Total exposure duration:
- 96 h
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 24 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.073 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.073 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Duration:
- 72 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.073 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 0.073 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Duration:
- 96 h
- Dose descriptor:
- LC100
- Effect conc.:
- >= 0.073 mg/L
- Nominal / measured:
- meas. (arithm. mean)
Any other information on results incl. tables
- Sublethal observations / clinical signs:
No observed effect concentration after 96 h : >=0.073mg/l
Applicant's summary and conclusion
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
