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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study with acceptable restrictions
Justification for type of information:
The study is well documented following general scientific practice.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1974
Report date:
1974

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Animals were fasted for 24 hours, then given a single calcuated dose and placed in a cage for a two week observation period.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium tetrahydroborate
EC Number:
241-004-4
EC Name:
Sodium tetrahydroborate
Cas Number:
16940-66-2
Molecular formula:
BH4.Na
IUPAC Name:
Sodium tetrahydridoborate(1–)
Details on test material:
- Name of test material (as cited in study report): Sodium borohydride powder
- Physical state: powder
- Lot/batch No.: 3-97

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: not reported
- Age at study initiation: not reported
- Weight at study initiation: 150-250 g
- Fasting period before study: 24 hours
- Housing: screen bottom cages
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: not reported


ENVIRONMENTAL CONDITIONS: not reported


Administration / exposure

Route of administration:
oral: gavage
Vehicle:
corn oil
Details on oral exposure:
VEHICLE
- Concentration in vehicle: 250 mg/ml
Doses:
50, 100 and 1000 mg/kg
No. of animals per sex per dose:
6
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: not reported
- Necropsy of survivors performed: no
Statistics:
not reported

Results and discussion

Effect levels
Key result
Sex:
male
Dose descriptor:
LD50
Effect level:
100 mg/kg bw
Remarks on result:
other: LD50 for sodium tetrahydroborate
Mortality:
No animals died at 50 mg/kg; 3/6 animals died at 100 mg/kg within one hour; 6/6 animals died at 1000 mg/kg within one minute.
Clinical signs:
no data
Body weight:
no data
Gross pathology:
not applicable
Other findings:
not reported

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
The acute oral LD50 for sodium tetrahydroborate was determined to be 100 mg/kg.