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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline with acceptable restrictions (no purity of test substance listed)

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1986
Report date:
1986
Reference Type:
secondary source
Title:
1,3,5-TRIOXANE, CAS Number 110-88-3, USEPA HPV Challenge Program Submission
Author:
Trioxane Manufacturers Consortium Members, BASF Performance Copolymers, LLC (Formerly Ultraform Company) and Ticona
Year:
2000
Bibliographic source:
USEPA Submission

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Version / remarks:
(adopted 1981)
GLP compliance:
yes
Remarks:
(Bio/dynamics Inc)
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
1,3,5-trioxane
EC Number:
203-812-5
EC Name:
1,3,5-trioxane
Cas Number:
110-88-3
Molecular formula:
C3H6O3
IUPAC Name:
1,3,5-trioxane
Details on test material:
- Name of test material (as cited in study report): Trioxane (C-235)
- Physical state: solid
- Lot/batch No.: 41115 AT
- Storage condition of test material: in a ventilated, temperature monitored room (15-29 °C)

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Charles River Breeding Laboratories
- Age at study initiation: males 9 weeks, females 12 weeks
- Mean weight at study initiation:
Group I - males 338 g (310 - 360) females 230 g (220 - 245);
Group II - males 329 g (315 - 342) females 226 g (219 - 239)
- Diet (e.g. ad libitum): Purina Rodent Laboratory Chow
- Water (e.g. ad libitum): automated watering system
- Acclimation period: 28-30 days


ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19-24
- Humidity (%): 30-70
- Photoperiod (hrs dark / hrs light): 12/12

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure chamber volume: 100 L
- Source and rate of air: Chamber air was drawn through 1/4" Teflon line and regulated at a flow of 1 L/min for Group I or 0.5 L/min for Group II using a calibrated Dwyer flowmeter and Nupro metering valve. Chamber air was then directed to a glass "Y" tube where it was diluted with room air at a flow of 5 L/min. The resultant 5 to 1 chamber air dilution for Group I, or 10 to 1 chamber air dilution for Group II, was drawn into the Miran using a model Thomas 107CA 183 pump.
- Method of particle size determination: Particle size distribution samples were taken using a TSI Aerodynamic Particle Sizer equiped with a TSI Diluter.
- Temperature, humidity in air chamber: 24-27 °C, 40-48 %


TEST ATMOSPHERE
- Brief description of analytical method used: exposure levels were analysed using a Miran 1A Ambient Air Analyzer and a strip chart recorder.
- Samples taken from breathing zone: yes
- nominal cancentrations were determined by weighing.

TEST ATMOSPHERE
- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.): 1.6/1.2 µm (exposure 1), 1.1/1 µm (exposure 2)

Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
4 h
Concentrations:
Initial dose: 8370 ppm, corresponding to 30.8 mg/l (measured).
Follow up dose: 10643 ppm, corresponding to 39.2 mg/l (measured), which was the maximum attainable vapour concentration.
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: All animals were observed individually, immediately prior to exposure, as a group at approximately 15-minute intervals during the first hour of exposure, and hourly thereafter. All animals were observed individually upon removal from the chamber (about one half-hour after exposure was completed) and at hours one and two post-exposure. Body weights were measured at day 1 (immediately prior to exposure), and on days 2, 3, 5, 8, and 15 (just prior to sacrifice).
- Necropsy of survivors performed: yes (including nasal passages, trachea, external surface, orifices, cranial cavity, carcass, brain, spinal chord, thoracic, abdominal and pelvic cavities and their viscera, cervical tissues and organs.
- Other examinations performed: clinical signs, body weight

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 39.2 mg/L air
Exp. duration:
4 h
Remarks on result:
other: No mortalities observed at the highest tested dose of 39.2 mg/l air.
Mortality:
No mortalities were observed.
Clinical signs:
other: Increased secretory response, respiratory distress, and general signs of poor condition were reported.
Body weight:
There was a compound-related reduction in body weight for both sexes following exposure (8 - 9%). Animals gained body weight normally during the second week of the observation period.
Gross pathology:
At necropsy, no treatment-related abnormalities were observed, and no target organs could be identified.

Any other information on results incl. tables

Summary of symptoms

Test concentration

8370 ppm ( i.e. 30.8 mg/l air)

Symptom

Onset

Duration

Affected animals/treated animals

Lacrimation

4 h

14 days

Few

Shallow breathing

4 h

Less than 24 h

6/10

Irregular breathing

4 h

2 days

9/10

Reduced activity

45 min.

Less than 24 h

Most

Nasal discharge

4 h

14 days

About the half

10643 ppm (i.e. 39.2 mg/l air)

Lacrimation

15 min.

13 days

Many

Shallow breathing

4 h

Less than 24 h

About the half

Irregular breathing

30 min.

5 days

All

Reduced activity

15 min.

Less than 24 h

All

Nasal discharge

4 h

14 days

Few to most

Summary of body weight data

Body weights (g)

Test concentration

8370 ppm ( i.e. 30.8 mg/l air)

Time point (days)

0

2

3

5

8

15

Males

338

310

319

325

342

364

Females

230

210

218

221

233

239

10643 ppm (i.e. 39.2 mg/l air)

Males

329

293

292

310

330

352

Females

226

210

216

216

224

235

Applicant's summary and conclusion