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Adsorption / desorption

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Reference
Endpoint:
adsorption / desorption: screening
Type of information:
experimental study
Adequacy of study:
key study
Study period:
14 April, 2014 to 02 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)
Type:
log Koc
Value:
< 1.5
Temp.:
25 °C
Validity criteria fulfilled:
yes
Conclusions:
The calculated adsorption coefficient 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 20003/K TE 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 20003/K TE eluted with a retention time of 2.00 min. The calculated adsorption coefficient 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

2.00

0.00

< 1.5 (-6.13)*

*: below determination limit of the method

Description of key information

The adsorption coefficient was 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 20003/K TE 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 availablecyanopropyl 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 / watermixture was used as mobile phase and the column temperature was 25 °C.

 FAT 20003/K TE eluted with a retention time of 2.00 min. 

The results are listed below:

Peak No.

Mean retention time of two runs

[min]

Absolute deviation

[min]

Mean log Kocof two runs

1

2.00

0.00

< 1.5 (-6.13)*

*: below determination limit of the method

[LogKoc: 1.5]