2,2'-azobis[2,4-dimethylvaleronitrile]

Endpoint summary

Description of key information

one study on acute toxicity by oral route and one study on acute toxicity by inhalative route available.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records

Reference

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

supporting study

Study period:

unknown

Reliability:

4 (not assignable)

Rationale for reliability incl. deficiencies:

documentation insufficient for assessment

Qualifier:

no guideline available

Principles of method if other than guideline:

Only abstract with species and LD50 value given.
A handwritten report is available, language japanese

GLP compliance:

no

Test type:

standard acute method

Limit test:

no

Specific details on test material used for the study:

not available

Species:

mouse

Strain:

not specified

Sex:

not specified

Details on test animals or test system and environmental conditions:

not available

Route of administration:

oral: unspecified

Vehicle:

not specified

Details on oral exposure:

not available

Doses:

not available

No. of animals per sex per dose:

not available

Control animals:

not specified

Details on study design:

not available

Statistics:

not available

Preliminary study:

not available

Key result

Sex:

not specified

Dose descriptor:

LD50

Effect level:

> 6 000 mg/kg bw

Mortality:

description not available

Clinical signs:

other: description not available

Gross pathology:

description not available

Other findings:

description not available

Interpretation of results:

GHS criteria not met

Conclusions:

An LD50 (orally in mice) is available, it is stated to be over 6000 mg/kg bw.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Acute toxicity: via inhalation route

Link to relevant study records

Reference

Endpoint:

acute toxicity: inhalation

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

comparable to guideline study

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 403 (Acute Inhalation Toxicity)

GLP compliance:

no

Test type:

acute toxic class method

Species:

rat

Strain:

Crj: CD(SD)

Sex:

male

Details on test animals or test system and environmental conditions:

Quarantine and Animal Selection
were quarantined after arrival for 6 days prior to testing. During the quarantine period rats
were weighed and observed for clinical signs of disease 3 times. Rats were obtained from the
general population of stock rats released from quarantine and were selected for use on this study fiom those rats exhibiting a normal pattern of weight gain and no overt signs of disease.
Housing
Rats were housed either singly or in pairs in suspended, stainless steel, wire-mesh cages.
Animal Room Environment
Animal rooms were maintained on a timer-controlled, 12-hour light/12-hour dark cycle.
Environmental conditions of the rooms were targeted to be within a temperature range of 23 +/- 1°C and a relative humidity range d 50 +/-10%. Excursions outside these ranges were of insufficient magnitude and/or duration to have adversely affected the validity of the study.
Identification
IEach rat was assigned a unique 6-digit identification number which corresponded to a numbered card affixed to the cage. Prior to exposure, the tail of each rat was numbered with waterinsoluble markers so that individual rats could be identified after exposure.
Feed and Water
Exkept during exposure, PMI Feeds. Lnc. Certified Rodent Diet #5002 and tap water fromUnited Water Delaware were available ad libitum.

Route of administration:

inhalation: aerosol

Type of inhalation exposure:

nose only

Vehicle:

air

Mass median aerodynamic diameter (MMAD):

4.5 µm

Geometric standard deviation (GSD):

2.2

Details on inhalation exposure:

Atmosphere Generation
Chamber atmospheres of the substance were generated by suspending the particulate test substance in
tered into the jetmill with a K-Tron model T-20 Twin Screw Volumetric Feeder. Filtered,
high-pressure air (60 Umin) introduced into the jetmill carried the resulting atmosphere into the exposure chamber. Chamber concentrations of the substance were controlled by varying the test.
Test atmospheres were exhausted through a high-capacity particle filter followed by an MSA charcoal/HEPA filter cartridge prior to discharge into the fume
hood.
Chamber Construction and Design
The exposure chamber was constructed of glass with a nominal internal volume of 34 L. A b fle positioned immediately inside the chamber inlet promoted
uniform chamber distribution ofthe test atmosphere.
Exposure Mode
During exposure, rats were individually restrained in stainless steel cylinders with conical nose pieces. The restrainers were inserted into the polymethylmethacrylate faceplate of the exposure chamber so that only the nose of each rat extended into the chamber.

Analytical verification of test atmosphere concentrations:

yes

Duration of exposure:

4 h

Concentrations:

9.3 mg/L
Range: 6.8-15 mg/L3 (SD:3.2, n=6)

No. of animals per sex per dose:

6

Control animals:

no

Key result

Sex:

male

Dose descriptor:

other: ALC

Remarks:

Approximate Lethal Concentration

Effect level:

9.3 mg/L air

Exp. duration:

4 h

Mortality:

One rat died during exposure to H-22860 at a concentration of 9.3 mgL.
All remaining animals survived the exposure and were sacrificed at the conclusion of the I4-day recovery period.

Clinical signs:

other: After the exposure, when the rats were removed from the restrainers. clinical signs included nasal and ocular discharges and stained and/or wet fur. In addition rats had test substance on their faces. These clinical signs are typically observed in rats su

Body weight:

Four of 5 surviving rats experienced slight to servere weight losses (ranging from I .8 to 15% of initial body weight ) within 1 day of exposure.
The I remaining rat gained weight. Body weights of rats began to increase by study day 3 and increased over the remainder of the 14day recovery period.

Interpretation of results:

GHS criteria not met

Conclusions:

Under the conditions of this study, the approximate lethal concentration (ALC)for the substance is 9.3 mg/L. On an acute inhalation basis. The substance is considered to have very low toxicity (ALC greater tban 2 mg/L).

Executive summary:

One group of 6 d e Cd:CD@(SD)BR rats was exposed nose-only for a single, 4-how period to the substance in air. The test atmosphere was generated by suspending the dry powder in air. The concentration of the substance

was determined by gravimetric analysis. Rats were weighed and observed far clinical signs of toxicity during a 14-day recovery period. Rats were exposed to a chamber concentration of 9.3 mg/L

the substance.

The mass median aerodynamic diameter (MMAD) of the dust generated was 4.5 pm. One rat died during the exposure to

the substance.

With the exception of 1 rat with hunched posture the day after exposure, no notable clinical signs of toxicity were evident on this study. Rats generally exhibited slight to severe body-weight losses within 1 day of exposure but began to regain weight by test day 3.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Dose descriptor:

discriminating conc.

Value:

9.3 mg/m³ air

Acute toxicity: via dermal route

Endpoint conclusion

Endpoint conclusion:

no study available

Justification for classification or non-classification

The available information is conclusive but not sufficient for classification.