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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study with acceptable restrictions (exposure concentrations in the test and the stability of the test substance were not confirmed by analysis).

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1987
Report date:
1987

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: DIN 38412 part 15
Principles of method if other than guideline:
Method: other: DIN 38412, Part 15
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
N-methylformamide
EC Number:
204-624-6
EC Name:
N-methylformamide
Cas Number:
123-39-7
Molecular formula:
C2H5NO
IUPAC Name:
N-methylformamide
Details on test material:
- Name of test material (as cited in study report): Monomethylformamide
- Analytical purity: 99.7%

Sampling and analysis

Analytical monitoring:
no

Test organisms

Test organisms (species):
Leuciscus idus
Details on test organisms:
TEST ORGANISM
- Common name: golden orfe
- Source: Fish farm P. Eggers, 2354 Hohenwestedt, FRG
- Length at study initiation: 5.3 cm (range: 4.7 - 5.7)
- Weight at study initiation: 3.7 g ( range: 2.1 - 4.9 cm)
- Feeding during test: no food


ACCLIMATION
- Acclimation period: about 7 weeks
- Acclimation conditions: same as test
- Type and amount of food: growing feed F/B 50; SSNIFF Spezialdiaeten GmbH
- Feeding frequency: daily, ad libitum
- Health during acclimation (any mortality observed): during the last 2 weeks 0.04% mortality
- Medical treatment: twice with 0.05 mg/L malachite green chloride; once with 10 mg/L tetracycline hydrochloride

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
96 h

Test conditions

Hardness:
2.5 mmol/L
Test temperature:
20 ±1 °C
Dissolved oxygen:
> 60% of max. saturation
Details on test conditions:
TEST SYSTEM
- Test vessel:
- Material, size, headspace, fill volume: all glass aquarium (30 x 22 x 24 cm)
- Aeration: yes
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- Biomass loading rate: 3.7 g fish/L test water


TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: reconstituted freshwater according to DIN 38412 part 11
- Alkalinity: 5.5 mmol/L
- Ca/Mg ratio: 4:1
- Na/K ions: 10:1
Reference substance (positive control):
yes
Remarks:
chloroacetamide

Results and discussion

Effect concentrationsopen allclose all
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
10 000 mg/L
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
> 10 000 mg/L

Any other information on results incl. tables

Sublethal observations / clinical signs:

Effects:

- no observable effect concentration (NOEC; 96 h):  10000 mg/L 

- maximum concentration causing no mortality:  10000 mg/L 

- minimum concentration causing 100 % mortality:  >10000 mg/L (effects related to nominal concentrations) 

 

Symptoms:

- no abnormalities

Applicant's summary and conclusion