Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: No OECD guideline or GLP defined. No doses defined.

Data source

Reference
Reference Type:
publication
Title:
Evaluation of the toxicity of polyvinylacetate phthalate in experimental animals
Author:
Schoneker D.R. et al.
Year:
2002
Bibliographic source:
Food and Chemical Toxicology 41 (2003) 405-413

Materials and methods

Principles of method if other than guideline:
male and female albino mice weighing 18-20 g, were used. The animals were fasted for a period of 4-16 h prior to treatment. Range-finding tests of the acute toxicity were conducted initially. 5% gum acacia was used as the vehicle. All surviving animals were maintained for a subsequent 14-day period. The LD50 was calculated from the mortality data.
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Phthalic acid
EC Number:
201-873-2
EC Name:
Phthalic acid
Cas Number:
88-99-3
Molecular formula:
C8H6O4
IUPAC Name:
benzene-1,2-dicarboxylic acid
Details on test material:
no data

Test animals

Species:
mouse
Strain:
other: albino
Sex:
male/female
Details on test animals or test system and environmental conditions:
Breeder: Canadian Breeding Laboratories and Charles River Laboratories
weight at study initiation: 18-20g
fasting period: 4 to 16 hours prior to treatment

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
other: 5% gum acacia
Details on oral exposure:
All surviving animals were maintained for a subsequent 14-day period. The LD50 was calculated from the mortality data according to Lichfield and Wilcoxan (1949).
Doses:
no data
No. of animals per sex per dose:
10
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

Phthalic acid, Mouse,LD50= >5000 mg/kg bw

Applicant's summary and conclusion

Executive summary:

In an acute oral toxicity study in male and female albino mice the LD50 was >5000 mg/kg bw.