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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP, non-guideline study, available as unpublished report, limitations in design and/or reporting but otherwise adequate for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Principles of method if other than guideline:
Six rats per sex per dose were exposed to the saturated vapour of the test substance. After an observation period of 7 days, animals were necropsied.
GLP compliance:
no
Test type:
other: Inhalation risk test
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-(diethoxyphosphinyl)-2-methyl-2-butenoic acid ethyl ester
EC Number:
601-818-6
Cas Number:
122009-11-4
Molecular formula:
C11 H21 O5 P
IUPAC Name:
4-(diethoxyphosphinyl)-2-methyl-2-butenoic acid ethyl ester
Details on test material:
- Name of test material (as cited in study report): C-5-Phosphonester

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 206.3 g for males, 165.7 g for females

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
air
Details on inhalation exposure:
- An air stream was conducted through a 5-cm layer of the test substance at 20°C to achieve an atmosphere that was saturated with the vapour of the test substance.
- Rate of air: 200 L/h
Analytical verification of test atmosphere concentrations:
not specified
Duration of exposure:
8 h
Concentrations:
Saturated vapour: 0.09 mg/L
No. of animals per sex per dose:
2 groups of 6 animals (3 males and 3 females each)
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 0.09 mg/L air
Based on:
test mat.
Exp. duration:
8 h
Mortality:
No mortality was observed in all exposed rats.
Clinical signs:
other: No clinical signs of toxicity findings were observed.
Body weight:
see Table 1 in "any other information on results incl. tables"
Gross pathology:
No pathological effects were observed.

Any other information on results incl. tables

Table 1: Body weight

 Days after  Males     Females   
 treatment  First group  Second group  First group  Second group
 0  192.0 187.3  168.7  162.7
 7  234.0 240.7  175.3  169.0

Applicant's summary and conclusion

Conclusions:
Exposure to the saturated vapour pressure for 8 hours to the test substance does not result in mortality.
Executive summary:

Six rats per sex were exposed to the saturated vapour (0.09 mg/L air) of the test substance for 8 hours. After an observation period of 7 days, animals were necropsied. No clinical signs, pathological effects or mortality was observed in all exposed animals.