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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1959
Report date:
1959

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
yes
Remarks:
only 7-day observation period
Principles of method if other than guideline:
BASF test was generally performed as described in OECD guideline 401
GLP compliance:
no
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
Diisobutyl phthalate
EC Number:
201-553-2
EC Name:
Diisobutyl phthalate
Cas Number:
84-69-5
Molecular formula:
C16H22O4
IUPAC Name:
diisobutyl phthalate
Details on test material:
- Name of test material (as cited in study report): Palatinol IC (di-iso-butylphthalate; test substance number: IX/418)
- Molecular weight (if other than submission substance): 278
- Physical state: clear fluid
- Analytical purity: no data
No additional data provided

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Gassner
- Age at study initiation: no data
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
No additional data

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
olive oil
Details on oral exposure:
VEHICLE
- Concentration in vehicle: 10% (in the 207.8 and 1662.7 mg/kg dose groups) and 60%) (in the 1662.7, 3325.4, 6650.9, 8313.6 and 10392.0 mg/kg dose groups)
- Amount of vehicle (if gavage): 12, 16, 5.33, 10.7, 13.3 and 16.7 ml, respectively in the 207.8, 1662.7, 3325.4, 6650.9, 8313.6 and 10392.0 mg/kg dose groups

MAXIMUM DOSE VOLUME APPLIED: 16.7 ml/kg
Doses:
ca. 0, 207.8, 1662.7, 3325.4, 6650.9, 8313.6 and 10392.0 mg/kg bw (calculated from 0, 0.2, 1.6, 3.2, 6.4, 8.0 and 10.0 ml/kg bw bw considering test substance density of 1.0392g/cm3 at 20°C)
No. of animals per sex per dose:
3 (only males) in the 207.8 and 1662.7 mg/kg dose groups, 5 (only females) in the 3325.4, 6650.9 and 8313.6 mg/kg dose groups and 10 (only females) in the 10392.0 mg/kg dose group
Control animals:
yes
Details on study design:
- The test substance was administered via single dose gavage to groups of five animals per sex and dose level.
- Body weight was determined before the start of the study for determination of dose.
- Animals were observed approximately 1-3 hours after dosing and then daily over a period of 7 days.
- At necropsy, all rats were examined for gross pathological changes. No further details available.
Statistics:
none necessary

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 10 392 mg/kg bw
Based on:
test mat.
Remarks on result:
other: 5/10 animals died at this dose level
Mortality:
see below (Table 1)
Clinical signs:
1) Clinical signs in dose groups 10392.0 - 6650.9 mg/kg bw: directly after application rats showed signs of Dyspnea, 24h later test animals were apathic and some of the animals had diarrhea. After 4-6 days animals showed no clinical signs any more - but in some cases horrent fur.

2) Clinical signs in dose groups 3200 mg/kg bw: 1 hour after application of test substance rats showed signs of Dyspnea.
Body weight:
no data
Gross pathology:
Gross pathology: 10392.0 showed signs of lobular pattern of the liver.
Other findings:
- Histopathology: 10392.0 2/2 animals showed signs of diffuse fatty degeneration of the liver.
- Potential target organs: liver

Any other information on results incl. tables

Table 1: Mortality

Dose level (mg/kg bw)

Total mortality/total animals in the group after

1 hour

24 hours

48 hours

7 days

10392.0

0/10

2/10

4/10

5/10

8313.6

0/5

0/5

1/5

1/5

6650.9

0/5

0/5

1/5

1/5

3325.4

0/5

0/5

0/5

0/5

1662.7

0/3

0/3

0/3

0/3

207.8

0/3

0/3

0/3

0/3

0

0/10

0/10

0/10

0/10

Applicant's summary and conclusion