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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
circa 1965
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: This study was conducted prior to GLP and test guidelines, but sufficient data is available for interpretation of results

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1965
Report date:
1965

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Groups of 5 rats received 0.5, 1.0 or 2.0 ml/kg and were observed for 14 days.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Propane-1,2-diyl diacetate
EC Number:
210-817-6
EC Name:
Propane-1,2-diyl diacetate
Cas Number:
623-84-7
Molecular formula:
C7H12O4
IUPAC Name:
propane-1,2-diyl diacetate
Details on test material:
A liquid sample was obtained from the R&D group, South Charleston, West Virginia Lot 22_DS-60-2; RD-6884

Test animals

Species:
rat
Strain:
other: Albino rats were used. In other sections of report, Wistar rats were used
Sex:
male

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
unchanged (no vehicle)
Doses:
0.5, 1.0 or 2.0 ml/kg
No. of animals per sex per dose:
5 male rats/dose
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
1.41 mL/kg bw
Based on:
test mat.

Any other information on results incl. tables

Rats dosed with 2.0 ml/kg died on the day of dosing. Signs and/or symptoms were very sluggish behavior with rapid breathing.

Rasts dosed with 0.5 or 1.0 ml/kg survived the 14 day observation period. Rats gained weight during the observation period.

Applicant's summary and conclusion

Conclusions:
The ip LD50 in rats was 1.41 ml/kg.
Executive summary:

The acute toxicity following ip administration was examined. The ip LD50 in rats was 1.41 ml/kg.