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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
publication
Title:
Phenol Studies VI: The acute and comparative toxicity of phenol and o-, m-, and p-cresols for experimental animals.
Author:
Deichmann, W.M,; Witherup, S.
Year:
1944
Bibliographic source:
J. Pharmacol. Exp. Ther. 80, 233-240

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
yes
Remarks:
post exposure observation period 7 days, no necropsy
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Phenol
EC Number:
203-632-7
EC Name:
Phenol
Cas Number:
108-95-2
Molecular formula:
C6H6O
IUPAC Name:
phenol

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: reared in the very same institute where study was conducted
- Diet ad libitum
- Water ad libitum:

ENVIRONMENTAL CONDITIONS: no details
:

Administration / exposure

Route of administration:
oral: gavage
Doses:
300-800 mg/kg bw: Different amounts of aqueous solutions/emulsions containing 2, 5, 10 or 20% of phenol were orally administered.
No. of animals per sex per dose:
5-15 (number sof males and females equal in each group)
Control animals:
no
Statistics:
No data

Results and discussion

Effect levelsopen allclose all
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
340 mg/kg bw
Based on:
test mat.
Remarks:
20% Phenol in solution
Sex:
male/female
Dose descriptor:
LD50
Effect level:
>= 530 - <= 540 mg/kg bw
Based on:
test mat.
Remarks:
Phenol 2%, 5%, and 10% in solution
Mortality:
All rats died within 3 to 150 minutes.
Clinical signs:
other: Twitching across the body (from eyes/eyelids to extremities being last affected); body temperature (irregular, mostly subnormal), pulse and respiration rate increasing, then decxreasing, irregular and weak; pupils finally dilated; salivation, marked dyspn
Gross pathology:
no data

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
After acute oral application in rats the LD50 of phenol varied between 340 and 540 mg/kg bw.