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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
Not specified
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study was based on EEC methodology and performed at a reputable testing facility, however no information on GLP was provided in the test report.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1997

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Report states study in accordance with EEC Methodology however no specific guideline was cited.
GLP compliance:
not specified
Remarks:
No information on GLP was provided in the test report.
Test type:
fixed dose procedure
Limit test:
yes

Test material

Constituent 1
Reference substance name:
2-Chloropropionic acid methyl ester.
IUPAC Name:
2-Chloropropionic acid methyl ester.
Details on test material:
- Name of test material (as cited in study report): Methyl ACPA / 2-Chloropropionic acid methyl ester
- Physical state: Liquid
- Analytical purity: 99.4%

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
not specified
Doses:
2000 mg/kg/bw
No. of animals per sex per dose:
2 animals per sex per dose
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
not specified

Any other information on results incl. tables

A summary of the clinical signs observed during the course of the study is shown in Table 1.

 

Table1.

Signs

No of rats in group showing signs

Male

Female

Piloerection

2/2

2/2

Hunched Posture

2/2

2/2

Waddling gait

2/2

2/2

Lethargy

2/2

2/2

Pallor of the extremities

2/2

2/2

Increased salivation

2/2

2/2

Gasping/noisy respiration

0/2

1/2

Unsteadiness

2/2

2/2

Increased respiration

2/2

2/2

Protruding eyes

1/2

1/2

Temporary loss of hind limb function

1/2

2/2

 

Applicant's summary and conclusion

Interpretation of results:
not classified
Conclusions:
The acute lethal oral dose of Methyl ACPA to rats was shown to be greater than 2000 mg/kg/bw.
Executive summary:

The oral effect of Methyl-2-chloropropionate on rats was evaluated in a study in accordance with EEC methodology. Two male and two female Sprague-Dawley rats were dosed by oral gavage at 2000 mg/kg/bw. The animals were observed and clinical signs recorded for a period of 14 days after which the animals were sacrificed.

No deaths occurred. There was evidence of systemic toxicity in all animals which persisted throughout the study. Body weight gains were considered normal for this type of study. No abnormalities were evident at the macroscopic examination.

In conclusion, the acute lethal oral dose for Methyl-2-chloropropionate was shown to be > 2000 mg/kg/bw.

The toxicity end point for the oral route of exposure is above the 2000 mg/kg/bw threshold for classification under the CLP regulation; therefore no classification relating to oral toxicity is required.