Tocopherols

Acute Toxicity: dermal

Administrative data

Endpoint:

acute toxicity: dermal

Type of information:

migrated information: read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

weight of evidence

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Limited information on test item, please refer to IUCLID section 13 for read across justification.

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 402 (Acute Dermal Toxicity)

GLP compliance:

yes

Test type:

standard acute method

Limit test:

yes

Test material

Test material information

Constituent 1

Reference substance name:

α-tocopherol

EC Number:

200-412-2

EC Name:

α-tocopherol

Cas Number:

59-02-9

Molecular formula:

C29H50O2

IUPAC Name:

(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol

Test material form:

liquid: viscous

Details on test material:

Name in test report: 82-0146, MX-6059, D-alpha-Tocopherol concentrate

Test animals

Species:

rabbit

Strain:

New Zealand White

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: H.A.R.E. - Rabbits for research, Hewitt, N.J.
- Weight at study initiation: 2 - 4 kg
- Housing: housed individually in wire mesh bottom cages
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: at least 5 days

Administration / exposure

Type of coverage:

occlusive

Vehicle:

unchanged (no vehicle)

Details on dermal exposure:

TEST SITE
- clipped with electric clippers
- prior to administration abrasion of the skin was performed on the exposure sites of 3 males and 2 females. The skin of the remaining 2 male and 3 female rabbits was left intact. Abrasions were made with the point of a 22 gauge disposable hypodermic needle. The abrasions were minor incisions through the stratum corneum that were not sufficiently deep to disturb the derma or to produce bleeding.
- Area of exposure:
- % coverage: occlusive
- Type of wrap if used: layer of plastic wrap, a protective cloth and stockinette binder, all securely held in place with masking tape

REMOVAL OF TEST SUBSTANCE
- Washing (if done): gently wipped with clean gauze to remove as mucg non-absorbed test article as possible
- Time after start of exposure: 24 h

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): approximately 5ml
- Concentration (if solution): undiluted
- Constant volume or concentration used: yes constant concentration

Duration of exposure:

24 h

Doses:

5000 mg/kg

No. of animals per sex per dose:

5

Control animals:

not required

Details on study design:

- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Observations for mortality, local reactions, and toxicological findings were recorded for a total of 14 days. Body weights were recorded on the initial day of testing and at the study termination or day of death.
- Necropsy of survivors performed: no
- Other examinations performed: body weight

Results and discussion

Effect levels

Sex:

male/female

Dose descriptor:

LD50

Effect level:

> 5 000 mg/kg bw

Based on:

test mat.

Mortality:

One animal was found dead on day 14.

Clinical signs:

other: Some animals showed decreased acitivity, loss of appetite, nasal discharge and diarrhea.

Gross pathology:

Left lung almost totally dark red in color. Stomach and intestines are gas filled. Both kidneys pale yellow. Urinary bladder full of urine.

Other findings:

None

Applicant's summary and conclusion

Interpretation of results:

not classified

Remarks:

Migrated information Criteria used for interpretation of results: EU

Conclusions:

The acute dermal mediam lethal dose (LD50) of the test item in the rabbit was estimated to be greater than 5000 mg/kg body weight.

Executive summary:

The acute dermal toxicity of the test item was investigated in five female and 5 male New Zealand White rabbits.

Prior to administration abrasion of the skin was performed on the exposure sites of 3 males and 2 females. The skin of the remaining 2 male and 3 female rabbits was left intact. Abrasions were made with the point of a 22 gauge disposable hypodermic needle. The abrasions were minor incisions through the stratum corneum that were not sufficiently deep to disturb the derma or to produce bleeding.

One animal was found dead on day 14. Some animals showed decreased acitivity, loss of appetite, nasal discharge and diarrhea. Three animals showed weight loss.

The acute dermal median lethal dose (LD50) of the test item in the rabbit was estimated to be greater than 5000 mg/kg body weight.