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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Long-term toxicity to aquatic invertebrates

Administrative data

Endpoint:
long-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Only a secondary source, but this test has been made on behalf of German Bundesumweltamt. Details given in the report are sufficient for evaluation.

Data source

Reference
Reference Type:
secondary source
Title:
Xylidine, BUA Stoffbericht 161
Year:
1994
Bibliographic source:
BUA, Beratergremium für umweltrelevante Altstoffe (BUA) der Gesellschaft Deutscher Chemiker, S.Hirzel Verlag 1995

Materials and methods

Test guidelineopen allclose all
Qualifier:
equivalent or similar to guideline
Guideline:
other: DIN 38412
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 211 (Daphnia magna Reproduction Test)
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
2,3-xylidine
EC Number:
201-755-0
EC Name:
2,3-xylidine
Cas Number:
87-59-2
Molecular formula:
C8H11N
IUPAC Name:
2,3-dimethylaniline

Sampling and analysis

Analytical monitoring:
not specified

Test organisms

Test organisms (species):
Daphnia magna

Study design

Test type:
semi-static
Water media type:
freshwater
Total exposure duration:
48
Post exposure observation period:
21 d

Test conditions

Hardness:
2.5 mmol/l
Test temperature:
25°C
pH:
8

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
EC50
Effect conc.:
10 mg/L
Nominal / measured:
nominal
Conc. based on:
not specified
Basis for effect:
immobilisation
Duration:
24 h
Dose descriptor:
NOEC
Effect conc.:
0.16 mg/L
Nominal / measured:
nominal
Conc. based on:
not specified
Basis for effect:
immobilisation

Applicant's summary and conclusion