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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1956-57 and 1981
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non GLP, but sufficient data is available for interpetation of results.
Cross-referenceopen allclose all
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1957
Reference Type:
study report
Title:
Unnamed
Year:
1981
Reference Type:
other company data
Title:
Unnamed
Year:
1956
Reference Type:
study report
Title:
Unnamed
Year:
1956

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Female rats were exposed to graded doses of 1-nitropropane vapor in a closed chamber for a periods of one hour. The LC50 concentrations were determined.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1-nitropropane
EC Number:
203-544-9
EC Name:
1-nitropropane
Cas Number:
108-03-2
Molecular formula:
C3H7NO2
IUPAC Name:
1-nitropropane
Details on test material:
1-Nitropropane :
Purity: 96.12%
Source: Sterington, Lousianna
Lot number: 9A17-7B

Test animals

Species:
rat
Strain:
Wistar
Sex:
female
Details on test animals or test system and environmental conditions:
Six female Wistar rats weighing 150 - 200 g.

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Details on inhalation exposure:
One hour inhalation exposures were conducted to determine the LD50 of the compound. The atmospheres were generated using a constant infusion pump and a vaporizer. The exposures occurred under dynamic airflow conditions.
Analytical verification of test atmosphere concentrations:
yes
Remarks:
Colormetric analysis
Duration of exposure:
1 h
Concentrations:
Actual concentrations: 8.60, 11.02, and 14.40 mg/L
No. of animals per sex per dose:
6 female rats per dose
Control animals:
not specified
Details on study design:
Female rats were exposed to graded doses of 1-nitropropane vapor in a closed chamber. One hour inhalation exposures were conducted to determine the LC50 of the compound. The atmospheres were generated using a constant infusion pump and a vaporizer. The exposures occurred under dynamic airflow conditions. Animals were observed 7 days following exposure.
Statistics:
The following endpoint was established using the Miller-Tainter method of LD50 dosage response determination.


Results and discussion

Preliminary study:
No data
Effect levels
Sex:
female
Dose descriptor:
LC50
Effect level:
11.02 mg/L air
Exp. duration:
1 h
Mortality:
Mortality observed in animals over 7 day period following exposures to 8.6, 11.02, and 14.40 mg/L where 0, 3, and 5 animals died after one hour of exposure, respectively.
Clinical signs:
other: Irritation at five minutes of exposure, no convulsant action noted except at 17 mg/L were it appeared slight. Concentration of 1-nitropropane was not sufficient for anesthetic effects. All animals exhibited ataxia following removal from the chamber. N
Body weight:
No data
Gross pathology:
No data
Other findings:
None

Any other information on results incl. tables

The acute inhalation toxicity, the LC50 was calculated from a rat LC50 at 1 hr (11.02 mg/L) by dividing by 2 as per the following guideline, "NFPA, Recommendations on the Transport of Dangerous Goods, UN Publication, 4th Ed. Section 6.4)." The calculated LC50 value of 5.5 mg/L was converted to 5500 mg/m3.

Applicant's summary and conclusion

Interpretation of results:
Toxicity Category III
Remarks:
Migrated information Criteria used for interpretation of results: other: EU GHS
Conclusions:
Following a 1 hour inhalation exposure, the LC50 is 11.02 mg/l .
Executive summary:

None