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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1993
Report date:
1993

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Reference substance name:
Creosote - US type P1/P13
IUPAC Name:
Creosote - US type P1/P13
Test material form:
aerosol dispenser: not specified
Remarks:
migrated information: aerosol
Details on test material:
Creosote [CAS No. 8001-58-9]: US Type P1/13 based on GC/MS
(Selection of Key Compounds)
(see RTI Study 6939 Project ID 70C-6939-001)

Name CAS-No. [%]
========================================
[US P1/13]
Naphthalene 91-20-3 9.0
1-Methylnaphthalene 90-12-0 2.3
2-Methylnaphthalene 91-57-6 5.1
Indene 95-13-6 0.9
Fluorene 86-73-7 4.2
Acenaphthylene 208-96-8 0.3
Acenaphthene 83-32-9 6.1
Phenanthrene 85-01-8 12.2
Anthracene 120-12-7 2.2
Fluoranthene 206-44-0 6.8
Pyrene 129-00-0 6.0
Benz[a]anthracene 56-55-3 0.5
Chrysene 218-01-9 1.5
Benzo(a)pyrene 50-32-8 0.5
Total of 5 remaining EPA-PAH: ca. 1.4

Test animals

Species:
rat
Strain:
other: Sprague-Dawley derived Crl:CD® BR VAF/Plus®
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source:
- Age at study initiation: 53 – 75 days
- Weight at study initiation: males: 234 – 283 g, females: 192 – 216 g

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
whole body
Vehicle:
air
Details on inhalation exposure:
MMAD +-GSD [µm]:
5000 mg/m³: 3.4 +-1.89 (2.5% of particles ≤ 1 µm diameter)
600 mg/m³: 1.3 +-1.64 (29% of particles ≤ 1 µm diameter)
Analytical verification of test atmosphere concentrations:
yes
Remarks:
GC-FID after sampling (9 key aromatics quantified (approx. 50 % of creosote), then result extrapolated to total creosote by using a factor of 1.64.
Duration of exposure:
4 h
Concentrations:
600, 5000 mg/m^3 (analytical)
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight
Statistics:
--

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
discriminating conc.
Effect level:
5 000 mg/m³ air
Based on:
test mat.
Remarks:
analytical (gravimetric)
Exp. duration:
4 h
Mortality:
No deaths occurred at maximum dose.
Clinical signs:
other: 5000 mg/kg: Directly after exposure, 9/10 animals with reduced activity. Three males and one female showed increased salivation. During the 14-day post-exposure period, five males and four females exhibited decreased activity. 60
Body weight:
5000 and 600 mg/kg: bw gain depressed, persisted for 14 days post exposure.
Gross pathology:
No significant macroscopic abnormalities were found at necropsy.

Any other information on results incl. tables

Table A6_1-1.               Table for Acute Toxicity (inhalation)

Dose[mg/m3air]

Toxicological results*

Duration of clinical signs

Time of death

Mortality (%)

Particles£5mm

(%)

males

600

0/2/5

4h – 14d

-

-

99

5000

0/5/5

4h – 14d

-

-

53

LC50value > 5000 mg/m3air (aerosol)

 

females

600

0/0/5

4h – 14d

-

-

99

5000

0/4/5

4h – 14d

-

-

53

LC50value > 5000 mg/m3air (aerosol)

 

*number of dead animals / number of animals with clinical signs of toxicity / total number of animals

Applicant's summary and conclusion

Conclusions:
Based on the results of this study, the four-hour LC50 for Creosote P1/P13 was greater than 5000 mg/m³.