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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

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Description of key information

The test substance is estimated to be stable at pH 4, 7 and 9 at 50 °C: it analogous has a half-life period longer than one year at 25 °C at pH 4, 7 and 9.

Key value for chemical safety assessment

Half-life for hydrolysis:
1 yr
at the temperature of:
25 °C

Additional information

Hydrolysis is a common degradation route in the environment, namely the reaction of a substance with water with a net exchange of the X group with an OH at the reaction centre such that RX + H2O → ROH + HX. Hydrolysis is often dependent upon pH as the reaction is commonly driven by hydrogen or hydroxide ions. Hydrolysis kinetics are usually determined experimentally and should be used to consider the test type and whether parent or degradation product should be tested.

In the case of CAS 4193-55-9, it can be estimated that hydrolysis does not occur because there are not hydrolysable groups in any of the structures; this is also confirmed by calculation with HYDROWIN 2.0.

Hydrolysable organic groups are in fact those groups that can react with water like Esters, Anhydrides, Amides, Carbammates, Nitriles, Cyanates, Epoxides, Halomethanes, Alkylhalides, Urea and none of these groups are present within the substance or their impurities.

A test was conducted according to internationally accepted testing guidelines and performed according to GLP on an analogous substance of the Stilbene Fluorescent Whitening Agents category, group 3, CAS 16470-24-9. The analogous and the substance under registration (CAS 16470-24-9 and CAS 4193-55-9, respectively) are very similar and are constituted by the same functional groups, except for CAS 16470-24-9 is tetrasulphonated instead than disulphonated, sodium salt. The difference in sulphonation can have an influence on water solubility, but not on the hydrolysation potential, since both substances have no hydrolysable groups in the chemical structure. Quantity and chemical identity of the impurities has no influence on the possibility of Read Across for this end point. For further details refer to the Category Justification Report attached to the section 13.

Hydrolysis was determined at 50 °C at pH 4, 7 and 9 for the preliminary test in the analogous substance. The determination of residual test substance was performed by high performance liquid chromatography (HPLC) using an external standard. The test substance is stable at pH 4, 7 and 9 at 50 °C: it has a half-life period longer than one year at 25 °C at pH 4, 7 and 9.