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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Physical & Chemical properties

Water solubility

Currently viewing:

Administrative data

Link to relevant study record(s)

Reference
Endpoint:
water solubility
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because the substance is hydrolytically unstable at pH 4, 7 and 9 (half-life less than 12 hours)

Description of key information

Water solubility [3-(trimethoxysilyl)propylamine]: 5.7E+05 mg/L at 20°C (QSAR)


 


Water solubility [3-aminopropylsilanetriol]: Above approximately 1000 mg/L condensation reactions can occur over time, limiting the concentration dissolved in water. The calculated solubility is 1.0E+06 mg/L at 20°C (QSAR)


 


Water Solubility [methanol]: miscible at 20°C

Key value for chemical safety assessment

Water solubility:
570 000 mg/L
at the temperature of:
20 °C

Additional information

The requirement to conduct a water solubility study for the submission substance is waived on the basis that it hydrolyses rapidly to form 3-aminopropylsilanetriol and methanol.


 


However, the water solubility of 3-(trimethoxysilyl)propylamine has been calculated using a validated QSAR method to be 5.7E+05 mg/L at 20°C.


 


The silanol hydrolysis product, 3-aminopropylsilanetriol, exists only in dilute aqueous solutions and readily condenses at concentrations above approximately 1000 mg/L. The overall rate of condensation is dependent on nominal loading, temperature, and pH of the system, as well as what else is present in solution.


 


The condensation reactions of silanetriols may be modelled as an equilibrium between monomer, dimer, trimer and tetramer, with the linear tetramer cyclising to the thermodynamically stable cyclic tetramer. The reaction is reversible unless the tetramer concentration exceeds its solubility; in this case, the tetramer forms a separate phase, driving the equilibrium towards the tetramer. For 3-aminopropylsilanetriol, a solution at 100 mg/L (the highest concentration often used in ecotoxicity tests) is predicted to contain > 99 % monomer. At loadings above about 1000 mg/L the concentration of the tetramer is predicted to exceed its solubility, resulting in formation of a separate phase. Further information is given in a supporting report (PFA 2016am) attached in Section 13.


 


The hydrolysis product, 3-aminopropylsilanetriol, is very hydrophilic and hence the calculated solubility is 1.0E+06 mg/L at 20°C using a QSAR method. This QSAR method for water solubility cannot be validated for silanetriols because the saturation concentration of silanetriols in water is limited by condensation reaction rather than lack of true solubility as discussed above. A prediction of 1E+06 mg/L at 20°C is indicative but has no practical meaning. The prediction is however considered valid for use in environmental exposure modelling and toxicokinetics modelling because it is considered to adequately describe the hydrophilicity of the substance and hence the partitioning behaviour.


 


Methanol is reported to be miscible in water at 20°C (OECD 2004).


 


 


Reference:


 


OECD (2004): SIDS Initial Assessment Report for SIAM 19, Berlin, Germany, 18-20 October 2004, Methanol, CAS 67-56-1.


 


PFA (2016am). Peter Fisk Associates, Analogue Report - Silanols and aquatic systems. Reference:404.105.003