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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: limited but acceptable documented study report which meets basic scientific principles

Data source

Reference
Reference Type:
other: microfiche
Title:
Unnamed
Year:
1977

Materials and methods

Principles of method if other than guideline:
other: acute toxicity study
GLP compliance:
no
Test type:
other: acute toxicity study

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
Details on test material:
2-mercaptobenzothiazole Dry Strain: batch 48/6/1001/0

Test animals

Species:
rat
Strain:
other: Charles River rats
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: dust
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Duration of exposure:
4 h
Concentrations:
1270 mg/m3
No. of animals per sex per dose:
5
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 1 270 mg/L air

Any other information on results incl. tables

Mortality: 0/5

Clinical symptoms: Ptosis and hypoactivity were observed after 90 minutes of exposure and lasted 55 minutes. No deaths were observed during exposure or the 14 day observation period which followed.

The average 2 -week body weight gain were within the normal limits.

Pathology: complete necropsies were done on all male and female rats used in this experiment when study was terminated at the end of the 14 -day post-exposure observation period. No gross tissue changes attributable to the effects of the test material were observed in any of the rats examined.

Particle size distribution:

A sample of airborn dust was collected from the test atmosphere for purpose of conducting a microscopic determination of particle size distribution. Particles were counted with respect to 4 size ranges, viz. 5 mircron or smaller, 6 to 10 micron, 11 to 25 microns and larger than 25 microns.

 Particle Size range(microns)  Number of particles counted  Percent of total counted
 1 -5  165  78.2
 6 -10  22  10.4
 11 -25  16  7.6
 < 25  8  3.8

Applicant's summary and conclusion