Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term repeated dose toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: study data do not give sufficient experimental details

Data source

Reference
Reference Type:
publication
Title:
N, N-dicyclohexyl-2-benzothiazolesulfenamide
Author:
Vorobeva, R.S.,
Year:
1968
Bibliographic source:
Toksikol. Nov. Khim. Veshchestv,|Vnedryaemykh Reszin. Shinnuyu Prom. 1968, 89-93, cited in:|Chem. Abstr. 71: 20566h

Materials and methods

Principles of method if other than guideline:
other: subacute inhalation study
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
N,N-dicyclohexylbenzothiazole-2-sulphenamide
EC Number:
225-625-8
EC Name:
N,N-dicyclohexylbenzothiazole-2-sulphenamide
Cas Number:
4979-32-2
Molecular formula:
C19H26N2S2
IUPAC Name:
N-(1,3-benzothiazol-2-ylsulfanyl)-N-cyclohexylcyclohexanamine
Details on test material:
no data

Test animals

Species:
rat
Strain:
not specified
Sex:
male

Administration / exposure

Route of administration:
inhalation
Duration of treatment / exposure:
15 d
Frequency of treatment:
2h/d
Doses / concentrations
Remarks:
Doses / Concentrations:
340-400 mg/m3
Basis:

No. of animals per sex per dose:
no data
Control animals:
not specified
Details on study design:
Post-exposure period: no data

Results and discussion

Target system / organ toxicity

Critical effects observed:
not specified

Any other information on results incl. tables

No effect except mucous membrane irritation were observed. No pronounced liver or kidney changes were observed.

Applicant's summary and conclusion