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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Phototransformation in air is not expected to be a significant removal process for reaction mass containing six benzylated amine silanes or its hydrolysis products. The substance is not expected to evaporate into the atmosphere from the water surface due to the low vapour pressure of the substance and its hydrolysis products.

The AOPWIN model (v 1.92) was used to estimate the rate constant kOH for reaction of the hydrolysis products of reaction mass containing six benzylated amine silanes with hydroxyl radicals. However, since this prediction method has not been validated to assess applicability to silanes and silanols, results should be treated with caution.

The overall half-life in air under default conditions of hydroxyl radical concentration was calculated using the following expressions:

kdegair(d-1) = kOH(cm3/molecule. sec) x OH Concair(molecules/cm3) x 24 x 3600

DT50(d) = ln 2/ kdegair(d-1)

Where:

kdegair= total rate constant for degradation in air

kOH= rate constant for reaction with hydroxyl radicals

OH Concair= concentration of hydroxyl radicals in air =5 x 105OH molecules/ cm3

DT50= half-life

The results are presented in the following table.

Table 4.1.2 Results of photodegradation in air calculations.

 Constituent

 

 

SMILES neutral

SMILES hp neutral

Parent:

kOH(cm3/ molecule. sec)

HP:

kOH(cm3/ molecule. sec)

Parent:

kdegair (d-1)

HP:

 

kdegair (d-1)

Parent:DT50(days)

HP:

DT50(days)

1

 

 

NCCNCCC[Si](OC)(OC)OC

O([Si](O)(O)CCCNCC[N])

121.21 E-12

129.078 E-12

5.2

5.5

0.13

0.12

2

 

 

NCCN(Cc1ccccc1)CCC[Si](OC)(OC)OC

N(Cc1ccccc1)(CCC[Si](O)(O)O)CC[N]

137.748 E-12

145.610 E-12

5.9

6.2

0.11

0.11

3

 

 

c1ccccc1CNCCNCCC[Si](OC)(OC)OC

O([Si](O)(O)CCC[N]CCNCc1ccccc1)

176.748 E-12

184.61 E-12

7.6

7.9

0.09

0.087

4

 

 

c1ccccc1CNCCN(Cc1ccccc1)CCC[Si](OC)(OC)OC

N(Cc1ccccc1)(CCC[Si](O)(O)O)CC[N]Cc2ccccc2

193.280 E-12

201.141 E-12

8.3

8.6

0.083

0.080

5

 

 

N(Cc1ccccc1)(Cc2ccccc2)CCNCCC[Si](OC)(OC)OC

N(Cc1ccccc1)(Cc2ccccc2)CC[N]CCC[Si](O)(O)O

193.280 E-12

201.141 E-12

8.3

8.6

0.083

0.080

6

 

 

N(Cc1ccccc1)(Cc2ccccc2)CCN(Cc3ccccc3)CCC[Si](OC)(OC)OC

N(Cc1ccccc1)(Cc2ccccc2)CC[N](Cc3ccccc3)CCC[Si](O)(O)O

209.811 E-12

217.672 E-12

9.06

9.4

0.076

0.074