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Adsorption / desorption

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Link to relevant study record(s)

Reference
Endpoint:
adsorption / desorption: screening
Type of information:
experimental study
Adequacy of study:
key study
Study period:
15 April 2014 to 04 September 2014
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 121 (Estimation of the Adsorption Coefficient (Koc) on Soil and on Sewage Sludge using High Performance Liquid Chromatography (HPLC))
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method C.19 (Estimation of the Adsorption Coefficient (KOC) on Soil and Sewage Sludge Using High Performance Liquid Chromatography (HPLC))
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Type of method:
HPLC estimation method
Media:
other: HPLC-column
Radiolabelling:
no
Test temperature:
25 °C
Details on study design: HPLC method:
HPLC-system:
Agilent Technologies 1260 Infinity
Quaternary pump G1311B
Autosampler ALS G1367E
Column oven G1316A
Detector DAD G4212B

Column specification: EC 150/4.6 Nucleodur 100-5 CN-RP 150 x 5
Column temperature: 25 °C
Detection wavelength standard solutions: 220 nm
Detection wavelength test item: 220 nm
Mobile phase: Methanol/water (55/45,v/v)
Flow rate: 0.5 mL/min
Injection volume: 2 µL (reference items); 2 µL (test item)
Key result
Type:
log Koc
Value:
< 1.5
Temp.:
25 °C
Details on results (HPLC method):
The aim of this study was the determination of the adsorption coefficient of the test item FAT 20060/F by high performance liquid chromatography (HPLC) method according to EC method C.19 and OECD guideline 121. The analysis was performed on an analytical column packed with a commercially available cyanopropyl solid phase containing lipophilic and polar moieties. A moderately polar stationary phase based on a silica matrix was used (Nucleodur 100-5 CN-RP). A 55/45 (v/v) methanol/ water mixture was used as mobile phase and the column temperature was 25 °C. FAT 20060/F eluted with a retention time of 1.82 min. Since this retention time is lower than the determined dead time of the HPLC, the adsorption coefficient could not be calculated and is therefore below the determination limit of the method (<1.5).

None

Validity criteria fulfilled:
yes
Conclusions:
FAT 20060/F eluted with a retention time of 1.82 min. Since this retention time is lower than the determined dead time of the HPLC, the adsorption coefficient could not be calculated and is therefore below the determination limit of the method.
Executive summary:

The aim of this study was the determination of the adsorption coefficient of the test item FAT 20060/F by high performance liquid chromatography (HPLC) method according to EC method C.19 and OECD guideline 121. The analysis was performed on an analytical column packed with a commercially available cyanopropyl solid phase containing lipophilic and polar moieties. A moderately polar stationary phase based on a silica matrix was used (Nucleodur 100-5 CN-RP). A 55/45 (v/v) methanol/water mixture was used as mobile phase and the column temperature was 25 °C. FAT 20060/F eluted with a retention time of 1.82 min. Since this retention time is lower than the determined dead time of the HPLC, the adsorption coefficient could not be calculated and is therefore below the determination limit of the method. The results are listed below:


 


















Peak No.



Mean retention time of two runs


[min]



Absolute deviation


[min]



Mean log Kocof two runs



1



1.82



0.00



<1.5*



*: below determination limit of the method

Description of key information

FAT 20060/F eluated with a retention time of 1.82 min. Since this retention time is lower than the determined dead time of the HPLC, the adsorption coefficient could not be calculated and is therefore below the determination limit of the method.

Key value for chemical safety assessment

Koc at 20 °C:
31.6

Additional information

The aim of this study was the determination of the adsorption coefficient of the test item FAT 20060/F by high performance liquid chromatography (HPLC) method according to EC method C.19 and OECD guideline 121.The analysis was performed on an analytical columnpacked with a commercially available cyanopropyl solid phase containing lipophilic and polar moieties. A moderately polar stationary phase based on a silica matrix was used (Nucleodur 100-5 CN-RP). A 55/45 (v/v) methanol/water mixture was used as mobile phase and the column temperature was 25 °C. FAT 20060/F eluted with a retention time of 1.82 min. Since this retention time is lower than the determined dead time of the HPLC, the adsorption coefficient could not be calculated and is therefore below the determination limit of the method. The results are listed below:


 


















Peak No.



Mean retention time of two runs


[min]



Absolute deviation


[min]



Mean log Koc of two runs



1



1.82



0.00



<1.5*



*: below determination limit of the method


 


[LogKoc: 1.5]