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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
05 June 2000 - 24 July 2000
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: According to OECD Guideline 203 and GLP.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2000
Report date:
2000

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 203 (Fish, Acute Toxicity Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium dicyanoamide
EC Number:
217-703-5
EC Name:
Sodium dicyanoamide
Cas Number:
1934-75-4
Molecular formula:
C2HN3.Na
IUPAC Name:
sodium dicyanoazanide
Constituent 2
Reference substance name:
Sodiumdicyanamide
IUPAC Name:
Sodiumdicyanamide
Test material form:
other: solid
Details on test material:
Appearance: solid, white
Purity: 98.1%
Lot-No.: 62/3727
Storage: RT
Expiry date: January 2002

Sampling and analysis

Analytical monitoring:
yes

Test solutions

Vehicle:
yes

Test organisms

Test organisms (species):
Danio rerio (previous name: Brachydanio rerio)

Study design

Test type:
static
Water media type:
freshwater
Limit test:
yes
Total exposure duration:
96 h

Results and discussion

Effect concentrationsopen allclose all
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
400 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
160 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)

Any other information on results incl. tables

Sublethal observations / clinical signs:

As a result of the supporting analyses, it could be shown that the test substance was sufficiently (103% recovery on the basis of t0) stable during the period of incubation. Thus, the inhibition values obtained within this study are based on the nominal concentrations.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The concentration where no toxic effect occured (NOEC after 96h) was calculated as being 160 mg/L test substance. The LC50 (96h) was calculated as 400 mg/L.
Executive summary:

The study was performed in year 2000 according to OECD-Test Guideline 203 and GLP. In order to investigate the influence of the test substance towards the fish, the animals were exposed to different concentrations of the test substance for 96h. Daily the test solutions were examined for dead animals.The concentration where no toxic effect occured (NOEC after 96h) was calculated as being 160 mg/L test substance. The LC50 (96h) was calculated as 400 mg/L. The concentration where all test animals died (LC100) was calculated as 1000 mg/L.