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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Toxicity to microorganisms

Currently viewing:

Administrative data

Link to relevant study record(s)

Reference
Endpoint:
toxicity to microorganisms, other
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Justification for type of information:
Please refer to the analogue justification attached to IUCLID section 13.
Reason / purpose for cross-reference:
other:
Duration:
14 d
Dose descriptor:
NOEC
Effect conc.:
102.7 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
other: Result of toxicity control from ready biodegradability test
Validity criteria fulfilled:
yes
Conclusions:
Test item is not inhibitory to aerobic activated sludge microorganisms since degradation was 30% after 14 days (and 46% after 28 d).
Executive summary:

Since no studies on the toxicity to aquatic microorganisms are available for p-anisic acid (CAS 100-09-4) a ready biodegradability study is used to derive a NOEC for the toxicity to aquatic microorganisms. If a compound degrades well in a ready biodegradability test, or does not inhibit the degradation of a positive control at a certain concentration, this concentration can be used as a NOEC value. This approach is in accordance with the Guidance on information requirements and chemical safety assessment (Chapter R.7b: Endpoint specific guidance, ECHA 2017).

A substance can be assumed to be not inhibitory to aquatic microorganisms, if in the toxicity control of a ready biodegradation test, more than 25% degradation based on ThOD occurred within 14 days (OECD guideline 301F). For the test item a biodegradation test according to OECD guideline 301F is available (Hammesfahr, 2017). The test includes a toxicity control, which contains 102.7 mg/L of the test item and 104.1 mg/L mg/L of sodium benzoate. The toxicity control attained 30% degradation after 14 days of incubation. Hence, the substance is not toxic to aquatic microorganisms in the toxicity control and the test item concentration of 102.7 mg/L can be used as NOEC.

Description of key information

NOEC (14 d) = 102.7 mg/L (test material, OECD 301F, nominal)

Key value for chemical safety assessment

EC10 or NOEC for microorganisms:
102.7 mg/L

Additional information

No data are available on the toxicity to microorganisms of p-anisic-acid (CAS No. 100-09-4). Therefore data from the analogue substance sodium anisate (CAS 536-45-8) were used for read across. This read-across is in accordance with Regulation (EC) No. 1907/2006 Annex XI, 1.5. In this case of read-across, the best suited (highest degree of structural similarity, nearest physico-chemical properties) read-across substance was used for the assessment. This read-across is justified in within the analogue justification in IUCLID Section 13.

Since no studies on the toxicity to aquatic microorganisms are available a ready biodegradability study is used to derive a NOEC for the toxicity to aquatic microorganisms. If a compound degrades well in a ready biodegradability test, or does not inhibit the degradation of a positive control at a certain concentration, this concentration can be used as a NOEC value. This approach is in accordance with the Guidance on information requirements and chemical safety assessment (Chapter R.7b: Endpoint specific guidance, ECHA 2017).

A substance can be assumed to be not inhibitory to aquatic microorganisms, if in the toxicity control of a ready biodegradation test, more than 25% degradation based on ThOD occurred within 14 days (OECD guideline 301F). For the test item a biodegradation test according to OECD guideline 301F is available. The test includes a toxicity control, which contains 102.7 mg/L of the test item and 104.1 mg/L mg/L of sodium benzoate. The toxicity control attained 30% degradation after 14 days of incubation. Hence, the substance is not toxic to aquatic microorganisms in the toxicity control and the test item concentration of 102.7 mg/L can be used as NOEC.