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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1986
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: No OECD guideline or GLP defined.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1986

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: EG-Richtlinie 84/449 (Amtsblatt der Europäischen Gemeinschaften 27, 1984, L 251, 96)
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Tributyl phosphate
EC Number:
204-800-2
EC Name:
Tributyl phosphate
Cas Number:
126-73-8
Molecular formula:
C12H27O4P
IUPAC Name:
tributyl phosphate

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Winkelmann, Borchen, Germany
- Age at study initiation: 9 (males) to 14 (females) weeks
- Weight at study initiation: 165 g for males and 163 g for females
- Fasting period before study: 16 h
- Housing: 5 animals per cage
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +- 2
- Humidity (%): 50 +- 10
- Photoperiod (hrs dark / hrs light): 12/12

IN-LIFE DATES: From: 1986-14-01 To: 1986-02-24

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Doses:
1.3; 1.5; 1.8; 2,.0; 3.1 mL/kg bw
No. of animals per sex per dose:
5/sex/dose
Control animals:
not specified
Details on study design:
body weight was determined before application, one week later and at the end of the 14-day observation period
Statistics:
after Rosiello et al., J. Tox. Environ. Health 3, 797, 1977

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
1 552 mg/kg bw
Mortality:
1,5 ml/kg bw: 2 male/ 2 female
1,8 ml/kg bw: 3 male/ 4 female
2,0 ml/kg bw: 4 male/ 4 female
3,1 ml/kg bw: 5 male/ 5 female
Clinical signs:
other: Clinical signs were observed in dose groups: 1,5; 1,8; 2,0; 3,1 ml/kg bw.
Gross pathology:
No findings in dose group 1,3 ml/kg.
In dose group 1,5 ml/kg 4 rats (2 male/2 female) showed effects on gastric mucosa.
In the 1,8 ml/kg dose group 3 male animals showed effects on gastric mucosa and 4 female animals had effects on gastric mucosa, inflated intestine and reddened stomach.
In the 2,0 ml/kg dose group 4 male and 4 female animals showed effects on gastric mucosa, inflated intestines and a reddened lung. In the dose group of 3,1 ml/kg all animals (5male/ 5 female) showed effects on gastric mucosa, inflated intestines and a reddened lung.

Any other information on results incl. tables

After a single oral dose of 1,5 up to 3,1 ml/kg bw following symptoms could be observed in the test animals:

Diminished general condition; narcosis, bloody eye margins, face down position or lateral position, ruffled fur.

Applicant's summary and conclusion

Executive summary:

Tributyl phosphate was tested in a single dose experiment in male and female Wistar rats.

The doses tested were: 1,3; 1,5; 1,8; 2,0; 3,1 ml/kg bw.

Signs of intoxication were: diminuated general condition; narcose, bloody eye margins, face down position or lateral position, ruffled fur.

The LD50 was: 1,6 ml/kg bw for male and female rats.