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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP-study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1996

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
Deviations:
yes
Remarks:
minor deviations e.g. dose level
GLP compliance:
yes
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4,6-dichloropyrimidine
EC Number:
214-770-2
EC Name:
4,6-dichloropyrimidine
Cas Number:
1193-21-1
Molecular formula:
C4H2Cl2N2
IUPAC Name:
4,6-dichloropyrimidine

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
polyethylene glycol
Doses:
2000 mg/kg/b.w.
200 mg/kg/b.w.
No. of animals per sex per dose:
3 females 2000 mg/kg/b.w.
3 females 200 mg/kg/b.w.
3 males 200 mg/kg/b.w.
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 200 mg/kg bw
Based on:
test mat.
Remarks on result:
other: The LD50 value for male and female rats is greater than 200 mg/kg and was not exactly determined.

Any other information on results incl. tables

Animals employed as well as mortality

dose (mg/kg b.w)       sex       number of animals*       time of deaths       mortality %

200                            m            0/3                                                         0

200                            f             0/3                                                         0

2000                          f              2/3                            3 hours                  67   

* number of animals dying/number of animals employed

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The LD50 value for male and female rats is greater than 200 mg/kg and was not exactly determined.
Based on the investigations, the test substance has to be regarded as harmful if swallowed.
Executive summary:

Toxicological investigations in male and female rats were conducted after single oral administration of 4,6 -dichloropyrimidine. The LD50 was greater than 200 mg for the male and female rats.

After administration of 2000 mg/kg body weight the following clinical signs were observed in female rats: dazed condition and apathy. Two of three animals died.

After a single doese of 200 mg/kg no signs were observed in male rats, females showed piloerection up to 8 hours after application.

Body weight development was not significantly affected in both sexes after 200 mg/kg.

At necroscopy of the two intercurrent deaths females (2000 mg/kg) showed the following gross pathological findings: strong reddening of the muscosa in stomach and small intestine, liver mottled.

None of the animals sacrified at the end of study showed any noticeable gross pathological findings.