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Diss Factsheets

Toxicological information

Acute Toxicity: inhalation

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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 study (OECD TG 403) with acceptable restrictions. Restriction: no analytical monitoring of the atmosphere concentration. Observation period not reported.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1968
Report date:
1968

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Deviations:
yes
Remarks:
: no analytical monitoring of the atmosphere concentration.
GLP compliance:
no
Test type:
other: Inhalation Risk Test
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Oxydiethylene bis(chloroformate)
EC Number:
203-430-9
EC Name:
Oxydiethylene bis(chloroformate)
Cas Number:
106-75-2
Molecular formula:
C6H8Cl2O5
IUPAC Name:
oxydiethane-2,1-diyl dichlorocarbonate
Details on test material:
- Name of test material (as cited in study report): Diglycoldichlorkolensäureester
- Physical state: liquid
- Analytical purity: no data
- Other: pH 1; Melting point +4 °C; Boiling point 199 °C

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: mean of 3 males and 3 females 170 g (experiment 1) 3 males and 3 females 156 g (experiment 2 same conditions)

ENVIRONMENTAL CONDITIONS
no data

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
other: inhalation chamber
Vehicle:
other: air
Details on inhalation exposure:
Animals were exposed to a saturated atmosphere in an inhalation chamber. Atmosphere generation: dynamic. Air was conducted through a 5-cm
layer of TS in a fritted wash bottle. Nominal concentration was 0.0875 mg/L
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
8 h
Concentrations:
saturated atmosphere
No. of animals per sex per dose:
6

Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 7 days
- Frequency of observations and weighing: mean body weight prior to exposure and at termination of the study
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs
Statistics:
none

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC0
Effect level:
0.087 mg/L air (nominal)
Exp. duration:
8 h
Mortality:
no deaths
Clinical signs:
other: Initially attempts to escape; slight irritation of the mucosa.
Body weight:
meaan body weight development was positive.
day 0: mean of 3 males and 3 females 170 g (experiment 1); 3 males and 3 females 156 g (experiment 2 same conditions)
day 7: mean of 3 males and 3 females 187 g (experiment 1) ; 3 males and 3 females 170 g (experiment 2 same conditions)
Gross pathology:
Necropsy findings: 2 cases of chronic bronchitis, 1 case of bronchiectasia.

Any other information on results incl. tables

Mortality:

               ---------------------------

                  Exposure         Animals

                  period        dead/exposed

                  ---------------------------

                    8 h            0/12

                   ---------------------------

Signs of toxicity: Initially attempts to escape; slight irritation of the mucosa.

Necropsy findings:

2 cases of chronic bronchitis, 1 case of bronchiectasia.

Applicant's summary and conclusion

Conclusions:
According to OECD TG 403 there is no likely inhalation hazard under normal conditions of exposure.