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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1990
Report date:
1990

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Principles of method if other than guideline:
Four groups of 5 male and 5 female Wistar rats were nose/head-only exposed to an aerosol concentration of 1,8-naphthylendiamine at an analytical concentration of 0, 156, 413 or 877 mg/m³ (highest technical feasible concentration) for 4 hours. The animals were observed for mortality, weight and clinical signs through day 14. A gross necropsy was performed.
GLP compliance:
yes
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
1,8-naphthylenediamine
EC Number:
207-529-8
EC Name:
1,8-naphthylenediamine
Cas Number:
479-27-6
Molecular formula:
C10H10N2
IUPAC Name:
naphthalene-1,8-diamine
Details on test material:
purity: 99.5%

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
nose/head only
Vehicle:
other: acetone-polyethylenglycol 400 in air
Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
4 h
Concentrations:
0. 156, 413 or 877 mg 1,8-naphthylendiamine/m³ air
No. of animals per sex per dose:
5 male and 5 female rats/concentration
Control animals:
yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 877 mg/m³ air (analytical)
Based on:
test mat.
Exp. duration:
4 h
Remarks on result:
other: highest technical feasible concentration

Any other information on results incl. tables

An exposition up to 877 mg/m³ 1,8-naphtylenediamine (highest technical feasible concentration) was tolerated without mortality. All animals exposed to 413 and 877 mg/m³ and revealed at the first exposition day a reduced motility and a bloody nose, additional one rat exposed to 413 mg/m³ a reduced respiration rate. All rats had no clinical symptoms at the first post-observation day. At the 3rd post-observation day in all rats exposed to 413 mg/m³ and in female rats exposed to 877 mg/m³ a reduction of weight gain was observed.

Applicant's summary and conclusion

Executive summary:

Four groups of 5 male and 5 female Wistar rats were nose/head-only exposed to an aerosol concentration of 1,8-naphthylendiamine at an analytical concentration of 0, 156, 413 or 877 mg/m³ (highest technical feasible concentration) for 4 hours. The animals were

observed for mortality, weight and clinical signs through day 14. A gross necropsy was performed.

An exposition up to 877 mg/m³ 1,8-naphtylenediamine (highest technical feasible concentration) was tolerated without mortality. All animals exposed to 413 and 877 mg/m³ and revealed at the first exposition day a reduced motility and a bloody nose, additional one rat exposed to 413 mg/m³ a reduced respiration rate. All rats had no clinical symptoms at the first post-observation day. At the 3rd post-observation day in all rats exposed to 413 mg/m³ and in female rats exposed to 877 mg/m³ a reduction of weight gain was observed. Therefore the LC50 is > 877 mg/kg bw for male and female rats