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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Dermal absorption

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Administrative data

Endpoint:
dermal absorption in vivo
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Although rather limited documentation most important information is available

Data source

Reference
Reference Type:
publication
Title:
Toxicological evaluation of Dihydroxynaphthalene , important components of oxidation hair dyes
Author:
Wallat S, Bartnik F, Kästner W, Maak N, Potokar M.
Year:
1985
Bibliographic source:
Aerztl.Kosmetol. 15, 356-364

Materials and methods

Principles of method if other than guideline:
The test substance was formulated into a so-called basic-cream with a ph about 9.5. the formulations were applied to the back skin of the test rat - shaved 24 hours before applicaion. To prevent oral uptake of the applied radioactivity the treated skin area was covered with a specially designed perforated glass capsule; treatment time: 48 hours
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Naphthalene-1,5-diol
EC Number:
201-487-4
EC Name:
Naphthalene-1,5-diol
Cas Number:
83-56-7
Molecular formula:
C10H8O2
IUPAC Name:
naphthalene-1,5-diol
Test material form:
other: cristalline powder
Details on test material:
HPLC: no impurities
Radiolabelling:
yes

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
other: a so-called basic cream with a pH of about 9.5
Duration of exposure:
48 hours
Doses:
no data
No. of animals per group:
no data
Control animals:
no
Details on study design:
The test substance was formulated into a so-called basic-cream with a ph about 9.5. the formulations were applied to the back skin of the test rat - shaved 24 hours before applicaion. To prevent oral uptake of the applied radioactivity the treated skin area was covered with a specially designed perforated glass capsule; treatment time: 48 hours

Results and discussion

Signs and symptoms of toxicity:
not specified
Dermal irritation:
not specified
Absorption in different matrices:
no data
Total recovery:
no data
Percutaneous absorption
Dose:
no data
Parameter:
percentage
Absorption:
>= 7.7 - <= 9.5 %
Remarks on result:
other: 48 hours

Applicant's summary and conclusion

Executive summary:

The test substance was formulated into a so-called basic-cream with a ph about 9.5. the formulations were applied to the back skin of the test rat - shaved 24 hours before application. To prevent oral uptake of the applied radioactivity the treated skin area was covered with a specially designed perforated glass capsule; treatment time: 48 hours. The absorption rate ranges between 7.7 and 9.5 %