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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: A scientific study.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1988

Materials and methods

Principles of method if other than guideline:
A study with 2 guinea pigswith 0.5, 2.0, 5.0, 10.0% substance. 24h of application. Readings at 1, 24, 48h.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Benzothiazole-2-thiol
EC Number:
205-736-8
EC Name:
Benzothiazole-2-thiol
Cas Number:
149-30-4
Molecular formula:
C7H5NS2
IUPAC Name:
1,3-benzothiazole-2-thiol
Constituent 2
Reference substance name:
Mercaptobenzothiazole
IUPAC Name:
Mercaptobenzothiazole
Details on test material:
- Name of test material (as cited in study report):Mercaptobenzothiazole

Test animals

Species:
guinea pig
Strain:
Hartley
Details on test animals or test system and environmental conditions:
350-420 g, 5-6 weeks, from Charles River Breeding Laboratories, Inc. Massachusetts.
They were housed in individual cages and fed on a pellet diet.
The housing conditions were a room temperature set at 70+/-2ºF, a relative humidity of 45%, 10 air changes per hour, and a 12/12 hour light cycle.

Test system

Amount / concentration applied:
0.5, 2,5, 10 % w/w
Duration of treatment / exposure:
24h
Observation period:
1, 24 and 48h after removal of the test material
Number of animals:
2

Results and discussion

In vivo

Results
Irritation parameter:
other: Thereshold irritation concentration
Basis:
mean
Reversibility:
no data
Remarks on result:
other: 5% concentration resulted in at least a minimal amount of erythema.

Applicant's summary and conclusion

Conclusions:
5% and 10% concentrations of the test material produced slight irritant reactions.
Executive summary:

The aim of the study was to determine the irritant potential of the test material. Concentrations of the test material: 0.5, 2,5, 10 % w/w. The result was: 5% and 10% concentrations of the test material produced slight irritant reactions.