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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: scientifically acceptable and sufficient documented - but only 2 doses applied

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Principles of method if other than guideline:
Two groups of 5 male and 5 female rats were dosed once by oral gavage at dose levels of 500 or 5000 mg/kg bw. The animals were observed for mortality, body weight and clinical signs through day 14. After 14 days, the surviving animals were killed and discarded.
GLP compliance:
not specified
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
Bis(2-ethylhexyl) hydrogen phosphate
EC Number:
206-056-4
EC Name:
Bis(2-ethylhexyl) hydrogen phosphate
Cas Number:
298-07-7
Molecular formula:
C16H35O4P
IUPAC Name:
bis(2-ethylhexyl) hydrogen phosphate
Test material form:
other: liquid
Details on test material:
no data

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Doses:
500 or 5000 mg/kg bw
No. of animals per sex per dose:
5 male and 5 female rats/dose
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 500 - < 5 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

All animals doses at 5000 mg/kg bw died within 24 hours after application of bis(2-ethylhexyl) hydrogen phosphate and were necropsied. Severly redness abdominal walls, enlarged blood vessels, reddened liningof the gastrointestinal tract were found at necrosy. The stomach lining had a dark red clour. Adrenals and pancreas were reddened. Lungs in most instances were found to be scarlet red, kidneys were pale and thymus darkened.

All animals dosed with 500 mg/kg bw survived 14 days and gained weight through the study. Clinically, the animals exhibited oral/nasal discharge and diarrhea on the day of dosing only.

Applicant's summary and conclusion

Executive summary:

Two groups of 5 male and 5 female rats were dosed once by oral gavage of bis(2-ethylhexyl) hydrogen phosphate at dose levels of 500 or 5000 mg/kg bw. The animals were observed for mortality, body weight and clinical signs through day 14. After 14 days, the surviving animals were killed and discarded.

All animals doses at 5000 mg/kg bw died within 24 hours after application of bis(2-ethylhexyl) hydrogen phosphate and were necropsied. Severly redness abdominal walls, enlarged blood vessels, reddened liningof the gastrointestinal tract were found at necrosy. The stomach lining had a dark red clour. Adrenals and pancreas were reddened. Lungs in most instances were found to be scarlet red, kidneys were pale and thymus darkened.

All animals dosed with 500 mg/kg bw survived 14 days and gained weight through the study. Clinically, the animals exhibited oral/nasal discharge and diarrhea on the day of dosing only.

An oral LD50 > 500 and < 5000 mg/kg bw was determined.