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Physical & Chemical properties

Dissociation constant

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Reference
Endpoint:
dissociation constant
Type of information:
experimental study
Adequacy of study:
key study
Study period:
12 December 2011 to 09 March 2012
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 112 (Dissociation Constants in Water)
Version / remarks:
(1981)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EPA OPPTS 830.7370 (Dissociation constants in water)
Version / remarks:
(1996)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Specific details on test material used for the study:
Identification FAT 40854/A TE
Description Reddish-brown powder (determined at NOTOX)
Batch TZ 5719 / BOP 02-11
Content 46.2% (4 main constituants)
Test substance storage At room temperature in the dark
Stability under storage conditions Stable
Expiry date 01 April 2016
Dissociating properties:
no
Conclusions:
No accurate pKa value of the test substance could be determined (OECD 112: titration method).
Executive summary:

The dissociation constant of FAT 40854/A TE was determined according to OECD 112, EPA OPPTS 830.7370 and GLP.

With both test samples of the preliminary test two equivalence points were observed. With a titration run on a corresponding blank it was demonstrated that one of the equivalence points was related to the background of HCl.

Although an equivalence point of the test substance was found, the value was very close to the equivalence point of HCl and fell in its background. Therefore it was concluded that the main study could not be adequately performed and no accurate pKa value of the test substance could be determined.

Description of key information

 No accurate pKa value of the test substance could be determined.

Key value for chemical safety assessment

Additional information

The dissociation constant of FAT 40854/A TE was determined according to OECD 112, EPA OPPTS 830.7370 and GLP.

With both test samples of the preliminary test two equivalence points were observed. With a titration run on a corresponding blank it was demonstrated that one of the equivalence points was related to the background of HCl.

Although an equivalence point of the test substance was found, the value was very close to the equivalence point of HCl and fell in its background. Therefore it was concluded that the main study could not be adequately performed and no accurate pKa value of the test substance could be determined.

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