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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Diss Factsheets

Administrative data

Endpoint:
hydrolysis
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1992
Report date:
1992
Reference Type:
other: FOCUS calculation
Title:
Unnamed
Year:
2008
Report date:
2008

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EPA Guideline Subdivision N 161-1 (Hydrolysis)
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
methyl (2E)-2-methoxyimino-2-[2-[(2-methylphenoxy)methyl]phenyl]acetate
EC Number:
604-351-6
Cas Number:
143390-89-0
Molecular formula:
C18 H19 N O4
IUPAC Name:
methyl (2E)-2-methoxyimino-2-[2-[(2-methylphenoxy)methyl]phenyl]acetate
Details on test material:
- Name of test material (as cited in study report): [14C]242009; also denominated [14C]BAS 490 F
- Lot No.: 39/149-1 and L48/92 (Z-isomer)
- Radiochemical purity: > 98% (incl. Z-isomer 242010)
- Specific activity: 3.578 MBq/mg
- Locations of the label: (E)-2-[2-(2-Methylphenoxy)-methyl]-[ring-U-14C]phenyl-2-(methoxyimido)=acetic acid methyl ester ("ring-B-14C-labelled BAS 490 F")
Radiolabelling:
yes

Study design

Analytical monitoring:
yes
Buffers:
- pH: 5.0
- Type and final molarity of buffer: <= 0.05 M
- Composition of buffer: Citrate sodium hydroxide

- pH: 7.0
- Type and final molarity of buffer: <= 0.05 M
- Composition of buffer: Phosphate

- pH: 9.0
- Type and final molarity of buffer: <= 0.05 M
- Composition of buffer: Boric acid, potassium chloride sodium hydroxide
Details on test conditions:
STOCK SOLUTION
- Preparation: 2.4 mg radio labelled test substance were dissolved in 10 ml acetonitril
- Storage: under nitrogen conditions

SAMPLES PREPARATION
- Preparation: 0.5 ml stock solution were added to buffer solution and sterilized through a filter (pore-diameter 0.22 µm). 20 ml aliquots of the sterilized solution were transferred in 25 ml tubes with ground joint and stored in the dark at 25 ± 1 °C.
- Sterility check: after sterile filtration, 15 and 30 days
Duration of testopen allclose all
Duration:
30 d
pH:
5
Temp.:
25 °C
Initial conc. measured:
0.23 mg/L
Duration:
30 d
pH:
7
Temp.:
25 °C
Initial conc. measured:
0.23 mg/L
Duration:
30 d
pH:
9
Temp.:
25 °C
Initial conc. measured:
0.23 mg/L
Number of replicates:
2

Results and discussion

Total recovery of test substance (in %)open allclose all
% Recovery:
97
pH:
5
Temp.:
25 °C
Duration:
30 d
% Recovery:
54
pH:
7
Temp.:
25 °C
Duration:
30 d
% Recovery:
0
pH:
9
Temp.:
25 °C
Duration:
4 d
Dissipation DT50 of parent compoundopen allclose all
pH:
5
Temp.:
25 °C
DT50:
ca. 821.8 d
Type:
(pseudo-)first order (= half-life)
Remarks on result:
other: DT50 values estimated by FOCUS modelling
pH:
7
Temp.:
25 °C
DT50:
ca. 35 d
Type:
(pseudo-)first order (= half-life)
Remarks on result:
other: DT50 values estimated by FOCUS modelling
pH:
9
Temp.:
25 °C
DT50:
ca. 0.38 d
Type:
(pseudo-)first order (= half-life)
Remarks on result:
other: DT50 values estimated by FOCUS modelling
Details on results:
Half-lifes of BAS 490 F based on measurements:
at pH 5 (25 °C) = ca. 875 d
at pH 7 (25 °C) = ca. 34 d
at pH 9 (25 °C) = ca. 0.29 d

Applicant's summary and conclusion