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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicity to birds

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Administrative data

Endpoint:
short-term toxicity to birds: acute oral toxicity test
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP study according to a FIFRA guideline.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1991
Report date:
1991

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EPA OPP 71-1 (Avian Acute Oral Toxicity Test)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium N-(hydroxymethyl)glycinate
EC Number:
274-357-8
EC Name:
Sodium N-(hydroxymethyl)glycinate
Cas Number:
70161-44-3
Molecular formula:
C3H7NO3.Na
IUPAC Name:
sodium N-(hydroxymethyl)glycinate
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
Suttocide A (Powder}; Lot No. J15-150D with a purity of 97%.
Dose method:
other: a single dose of the test substance in diluent was orally intubated directly into the crop or proventriculus of each bird using a stainless steel cannula.
Analytical monitoring:
yes
Vehicle:
yes

Test organisms

Test organisms (species):
Colinus virginianus

Study design

Limit test:
no
Remarks:
1. Acclimation - 16 days. 2. Fasting - At least 15 hours prior to dosing. 3. Dosing - Experimental Start Date - October 12, 1990. 4. Post-dosing observation - 14 days.
No. of animals per sex per dose and/or stage:
5
Control animals:
yes

Results and discussion

Effect levels
Duration (if not single dose):
14 d
Dose descriptor:
LD50
Effect level:
> 2 250 mg/kg bw
Conc. / dose based on:
test mat.
Basis for effect:
mortality

Any other information on results incl. tables

There were no mortalities at the 486, 810 or 1350 mg/kg dosages. There was a single, incidental mortality at 292 mg/kg. There was 40% mortality (4 of 10) at 2250 mg/kg. Treatment related effectswere seen at 810 mg/kg and higher dosages. These effects were reversible even at the highest dosage. Signs of toxicity typical of intoxication with Suttocide A included ruffled appearance, lethargy, reduced reaction to external stimuli (sound and movement), lower limb weakness, depression, wing droop and coma.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The acute oral LD5O value for northern bobwhite exposed to Suttocide A as a single oral dosage was determined to be greater than 2250 mg/kg, the highest dosage tested. The no mortality level was 1350 mg/kg. The no observed effect level was 486 mg/kg based on signs of toxicity and a loss in body weight at 810 mg/kg.