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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
dissociation constant
Type of information:
experimental study
Adequacy of study:
other information
Study period:
1977
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data from handbook or collection of data

Data source

Reference
Reference Type:
review article or handbook
Title:
CRC Handbook of Chemistry and Physics
Author:
Weast RC
Year:
1977
Bibliographic source:
CRC Handbook of Chemistry and Physics, 58th edn. CRC Press, Inc., West Palm Beach, Florida, USA

Materials and methods

GLP compliance:
no

Test material

Constituent 1
Reference substance name:
Thiazole
EC Number:
206-021-3
EC Name:
Thiazole
Cas Number:
288-47-1
IUPAC Name:
1,3-thiazole
Constituent 2
Reference substance name:
Imidazole
EC Number:
206-019-2
EC Name:
Imidazole
Cas Number:
288-32-4
IUPAC Name:
1H-imidazole
Constituent 3
Reference substance name:
Benzimidazole
EC Number:
200-081-4
EC Name:
Benzimidazole
Cas Number:
51-17-2
IUPAC Name:
1H-benzimidazole

Results and discussion

Dissociating properties:
yes
Dissociation constantopen allclose all
No.:
#1
pKa:
2.44
Remarks on result:
other: Thiazole (corresponding acid)
No.:
#2
pKa:
6.95
Remarks on result:
other: Imidazole (corresponding acid)
No.:
#3
pKa:
5.53
Remarks on result:
other: Benzimidazole (corresponding acid)

Any other information on results incl. tables

From the pKa vaules of the corresponding acids of the above mentioned substances it is deduced that 2 -Chlorobenzothiazole is a weak base. In neutral media, 2 -Chlorobenzothiazole is predominantly in the non-charged molecular form.

Applicant's summary and conclusion

Conclusions:
From the pKa vaules of the corresponding acids of the above mentioned substances it is derived that 2 -Chlorobenzothiazole is a weak base. In neutral media, 2 -Chlorobenzothiazole is predominantly in the non-charged molecular form.