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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2002
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study without detailed documentation

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2002
Report date:
2002

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
not specified
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Reaction product of 2-hydroxybenzoic acid, styrene and oxozinc
Molecular formula:
not applicable for UVCB substance
IUPAC Name:
Reaction product of 2-hydroxybenzoic acid, styrene and oxozinc
Test material form:
liquid - solid: mixture of
Remarks:
water and Reaction products of 2-hydroxybenzoic acid and styrene and zinc oxide

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Doses:
5000 mg/kg bw
No. of animals per sex per dose:
10
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.
Mortality:
no mortality observed
Clinical signs:
other: no clinical sign observed
Body weight:
other body weight observations
Remarks:
Body weight increased
Gross pathology:
No pathological changes were observed at necropsy.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Oral LD50 was greater than 5000 mg/kg bw for both mele and female Wistar rats.
Executive summary:

In the acute oral toxicity study according to OECD TG 401, 10/sex/group of rats were administrated with test item (5000 mg/kg/bw) by oral gavage. No toxic signs were observed after application of test item, and no death occurred within two weeks.No pathological changes were observed at necropsy.Oral LD50 was greater than 5000 mg/kg bw for both male and female Wistar rats.