Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
from 1986-07-23 to 1986-08-13
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Guideline study without deviations.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1986
Report date:
1986

Materials and methods

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

Test material

Constituent 1
Chemical structure
Reference substance name:
N-butyl acetate
EC Number:
204-658-1
EC Name:
N-butyl acetate
Cas Number:
123-86-4
Molecular formula:
C6H12O2
IUPAC Name:
butyl acetate
Details on test material:
- Name of test material (as cited in study report): n-butyl acetate, T-3916
- Physical state: clear liquid
- Analytical purity: "pure"
- compound code: T-3916
- Stability under test conditions: stable at storage conditions
- Storage condition of test material: at ambient temperature in the dark

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Iffa-Credo, Brussels, Belgium
- Age at study initiation: 8 -12 weeks
- Weight at study initiation: males 196 to 294 g, females 209 to 250 g
- Fasting period before study: no; food and water were withheld during exposure
- Housing: individually in Macrolon cages with purified sawdust (Woody Clean from The Broekman Institute, Someren, The Netherlands) as bedding material
- Diet (e.g. ad libitum): standard laboratory animal diet (RMH-B, pellet diameter 10 mm, Hope Farms, Woerden, The Netherlands)
- Water (e.g. ad libitum): tap-water
- Acclimation period: 7 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 - 22
- Humidity (%): 60 - 90
- Air changes (per hr):
- Photoperiod (hrs dark / hrs light): 12 /12


IN-LIFE DATES: From: 1986-07-16 To: death

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
head only
Vehicle:
other: unchanged (no vehicle)
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: dynamic spraying head-only inhalation system (cylindrical inhalation chamber, made of chrome-nickel steel) as discribed by Niessen et al (1963, Archiv für Toxicologie 20, 44-60), with some modifications
- Exposure chamber volume: 12 L
- Method of holding animals in test chamber: radially mounted cylindrical Perspex animal confinement cages
- Source and rate of air: compressed air; 10 L/min
- Method of conditioning air: temperature controlled room
- System of generating particulates/aerosols: spraying nozzle with an exit hole diameter of 0.4 mm, air flow 10 L/min, test substance delivered by a high precision infusion syringe pump (UNITA Ib, Braun-Melsungen, FRG) at constant rates of 2, 4.5, and 9 mL/h
- Method of particle size determination: low-pressure cascade impactor (type LPI 4/0, 06/2) from Hauke, Gmunden, Austria
- Treatment of exhaust air: air is routed through washing bottles with 80%-ethanol and water
- Temperature, humidity, pressure in air chamber: 18 - 21°C; 20 - 55%

TEST ATMOSPHERE
- Brief description of analytical method used: absorption on charcoal, Gaschromatography (Hewlett Packard GC 5880 with FID detection)
- Samples taken from breathing zone: yes
- Particle size distribution: only 0.09% of the total test substance content in the breathing atmosphere was present as aerosol (combined weight of impactor fractions compared with the total content (analytically measured concentration) of the sampled air)
- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.): 1.01 µm / 3.30 (high dose group; test substance vaporized completely at lower concentrations)

CLASS METHOD (if applicable)
- Rationale for the selection of the starting concentration: suitable test substance concentrations were estimated by pretests. Pretests were performed from higher to lower Test substance concentrations (52.9 and 26.5 mg/L, analytically verified)
Analytical verification of test atmosphere concentrations:
yes
Remarks:
samples are taken hourly / GC
Duration of exposure:
4 h
Concentrations:
analytical (mean of 4 measurements for each dose): 0.8, 2.2, 5.2 mg/L
nominal: 3.1, 7.1, 14.1 mg/L
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, histopathology (lungs)
Statistics:
no data

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
0.74 mg/L air
Exp. duration:
4 h
Mortality:
low-dose: 6/10, mid-dose: 10/10, high-dose: 10/10
All deaths occurred within 24 h of exposure.

Any other information on results incl. tables

Mortality rates:

low-dose: 6/10, mid-dose: 10/10, high-dose: 10/10

All deaths occurred within 24 h of exposure.

Major signs of toxicity: lethargy, hyperpnea, tremors, ataxia.

Macroscopic examination at necropsy revealed bloody nose
and/or mouth and hyperaemic lungs in animals of all exposure
groups. Histopathology of lung tissue revealed vesicular emphysema in all animal

Applicant's summary and conclusion

Conclusions:
The LC50 value in this study with male and female rats was 0.74 mg/L.
Executive summary:

In an acute inhalation toxicity study, young adult male and female wistar rats (5 animals of each sex per group) were exposed by inhalation route (head only) to vapors/aerosols of n-butyl acetate for 4 hours at concentrations of 0.8, 2.2, and 5.2 mg/L. Animals were then observed for 14 days.

 

LC50Combined =  0.74  mg/L

6 of 10 animals died in the low dose group. In the mid-dos and high-dose group 10 of 10 animals died. All deaths occured within 24 h of exposure (Debets, 1986).