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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Exposure related observations in humans: other data

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Administrative data

Endpoint:
exposure-related observations in humans: other data
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Article in foreign language (Japanese). Basic information obtained from the english translated summary and tables.

Data source

Reference
Reference Type:
publication
Title:
Studies on Compoxinded Perfumes for Toilet Goods. On the Non-irritative Compounded Perfumes for Soaps
Author:
Tetsuya Fujii , Saburö Furukawa and Seiji Suzuki
Year:
1972
Bibliographic source:
Yukugaku 21(12), 904-908

Materials and methods

Endpoint addressed:
skin irritation / corrosion
Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Two different closed patch test were conducted on healthy male and female subjects. For the first closed patch test, the small of back of 34 subjects were treated with 20% test substance in vaselinum aldum or unguentum hydrophilicum for 48 hours. In the second closed patch test, 2% test substance was applied on the upper inside of arm of 30 subjects for 24-72 hours. Unguentum simplex and unguentum hydrophilicum served as vehicle.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Benzyl propionate
EC Number:
204-559-3
EC Name:
Benzyl propionate
Cas Number:
122-63-4
Molecular formula:
C10H12O2
IUPAC Name:
benzyl propanoate

Method

Ethical approval:
not specified
Details on study design:
- 34 humans (first test) and 30 humans (second test)
- SCORING SYSTEM:
Reactions were recorded according to the following criteria: (-) = No reaction [negative reaction]; (+/- ) = Slight Erythema [suspected positive reaction]; (+) = Erythema [positive reaction]; (++) = Erythema and Dropsical swelling [positive reaction]; (+++) = Erythema, Papules and Vesicles [positive reaction].
Details on exposure:
TYPE OF EXPOSURE: closed

EXPOSURE LEVELS: 20% or 2%

EXPOSURE PERIOD: 24-72 hours (first test), 48 hours (second test)

Results and discussion

Results:
No reactions (erythema) were observed at 20% and 2% of the test substance.

Applicant's summary and conclusion

Conclusions:
No irritant reactions were produced neither at concentration of 20% test substance nor at a dose of 2% test substance.
Executive summary:

The publication described two closed patch tests which were conducted on healthy male and female subjects. For the 48 hour closed patch test, 34 subjects were treated with 20% test substance in vaselinum aldum or unguentum hydrophilicum on the small back. In addition, a 24- to 72 -hour closed patch test was conducted on 30 male and female subjects, with the test item at 2% in unguentum simplex or unguentum hydrophilicum. In both tests, no irritant reactions were produced in the subjects.