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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: other routes

Currently viewing:

Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Not sufficiently detailed study suffering severe limitations.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1947

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
In this old study (study conducted largely before the date of publication of the OECD Guidelines relevant for this endpoint), animals were exposed intraperitoneally to test substance at 6 different concentrations and were only observed for mortality.
When compared to standard acute toxicity studies, this study suffers various limitations: only males were dosed; the observation period was only 7 days; the protocol was poorly described; the equipment used was not detailed; the analytical monitoring was not performed and animals were only observed for determinig the mortality rate.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-ethylhexyl mercaptoacetate
EC Number:
231-626-4
EC Name:
2-ethylhexyl mercaptoacetate
Cas Number:
7659-86-1
Molecular formula:
C10H20O2S
IUPAC Name:
2-ethylhexyl 2-sulfanylacetate
Details on test material:
- Name of test material (as cited in study report):
Thioglycolate de 2-ethyle hexyle

Test animals

Species:
mouse
Strain:
Swiss
Sex:
male

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
arachis oil
Doses:
0.8, 1.0, 1.2, 1.4, 1.5, 1.6 mL/kg (corresponding to approximately 0.78, 0.97, 1.17, 1.36, 1.46, 1.56 g/kg bw based on a reported density of 0.972
g/mL)
No. of animals per sex per dose:
10 animals in 0.8-, 1.0- and 1.6-mL/kg treatment groups; 20 animals in the other treatment groups.
Control animals:
no

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
1.36 mL/kg bw
95% CL:
1.33 - 1.39
Remarks on result:
other: LD50 equivalent to 1320 mg/kg bw

Any other information on results incl. tables

Table of mortality

Tested concentration (mL/kg)

Mortality

Number of animals

Rate (%)

0.8

0/10

0

1.0

0/10

0

1.2

3/20

15

1.4

10/20

50

1.5

15/20

70

1.6

10/10

100

Applicant's summary and conclusion

Conclusions:
By intraperitoneal administration, the LD50 was estimated to be 1320 mg/kg bw in mouse.
Executive summary:

In this old study, groups of 10 to 20 male swiss mice were given the substance at 0.8 to 1.6 mL/kg by intraperitoneal injection. The LD50 was found to be 1.36 ml/kg bw, equivalent to 1320 mg/kg bw, based on the density of the substance of 0.972 mL/g.