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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
16 October - 10 December 2015
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2015
Report date:
2015

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 420 (Acute Oral Toxicity - Fixed Dose Method)
GLP compliance:
yes (incl. QA statement)
Test type:
fixed dose procedure
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
(2Z)-3-(3-chloro-2-fluorophenyl)-2-(4-chloro-2-fluorophenyl)prop-2-enenitrile
EC Number:
806-533-2
Cas Number:
1219086-87-9
Molecular formula:
C15 H7 Cl2 F2 N
IUPAC Name:
(2Z)-3-(3-chloro-2-fluorophenyl)-2-(4-chloro-2-fluorophenyl)prop-2-enenitrile
Test material form:
other: white solid
Details on test material:
IUPAC Name : (Z)-3-(3-chloro-2-fluorophenyl)-2-(4-chloro-2-fluorophenyl)-acrylonitrile
Roche number : RO5463921-000
Formula : C15H7Cl2F2N
Molecular weight : 310,13 g/mol
Batch : FIS201405080058
Purity : 101,2 % (m/m)
Expiry date : 11 June 2016
Storage conditions : room temperature in the dark under nitrogen

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
arachis oil
Doses:
2000 mg/kg
No. of animals per sex per dose:
5 animals per dose
Control animals:
no

Results and discussion

Any other information on results incl. tables

A single animal was treated at 2000 mg/kg. In the absence of mortality at a dose of 2000 mg/kg, an additional group of 4 animals was treated at 2000 mg/kg.

There were no deaths.

No signs of systemic toxicity were noted during the observation period.

All animals showed expected gains in body weight over the observation period.

No abnormalities were noted at necropsy.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: other: CLP
Conclusions:
The acute oral median dose LD50 of PAC-Ethenenitrile (CAS Nr 1219086-87-9) in the female Wistar strain rat was estimated to be greater than 2000 mg/kg body weight.
Executive summary:

The acute oral median dose LD50 of PAC-Ethenenitrile (CAS Nr 1219086-87-9) in the female Wistar strain rat was estimated to be greater than 2000 mg/kg body weight (Globally Harmonized Classification System : unclassified).