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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: dermal
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:
study report
Title:
Unnamed
Year:
1967
Report date:
1967

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Diethyl [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]phosphonate
EC Number:
213-551-9
EC Name:
Diethyl [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]phosphonate
Cas Number:
976-56-7
Molecular formula:
C19H33O4P
IUPAC Name:
diethyl (3,5-di-tert-butyl-4-hydroxybenzyl)phosphonate

Test animals

Species:
rabbit
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Age at study initiation: young adult animals
- Weight at study initiation: average body weight of about 3 kg
- Housing: single housing
- Diet: standard rabbit food ad libitum
- Water: ad libitum
- Acclimation period: 7 days

Administration / exposure

Type of coverage:
occlusive
Vehicle:
water
Remarks:
50% aqueous suspension
Details on dermal exposure:
TEST SITE
- Area of exposure: about 10 % of the total body surface area
- Type of wrap if used: impervious plastic sheeting
- Preparation of test site: The backs of the rabbits were shaved free of hair with electric clippers, the shaved area constituting about 10 % of the total body surface-area. Additionally, epidermal abrasions were made every 2 or 3 centimeters longitudinally over the area of exposure on one female and one male animal.

REMOVAL OF TEST SUBSTANCE
- Washing: yes
- Time after start of exposure: after removing of the wrap

TEST MATERIAL
- Amount applied: 5 g/ kg bw
- Concentration: 50 % (w/v) aqueous suspension
- Constant volume or concentration used: yes
Duration of exposure:
24 hours
Doses:
5000 mg/kg body weight
No. of animals per sex per dose:
2
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: weighing: before application, on day 8 and on day 14
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight,organ weights, histopathology
Statistics:
not required

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.
Mortality:
none
Clinical signs:
other: none
Gross pathology:
no findings

Any other information on results incl. tables

Scarified and unscarified rabbits gave indistinguishable results.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met