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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
developmental toxicity
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Original data not available

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1978
Reference Type:
secondary source
Title:
No information
Author:
!SIDSP*
Year:
1993
Bibliographic source:
OECD/SIDS. Screening Information Data Set (SIDS) of OECD High Production Volume Chemicals Programme, 19, (1993)

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 414 (Prenatal Developmental Toxicity Study)
Principles of method if other than guideline:
Developmental toxicity and teratogenicity were analyzed
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,3,4-trichlorobut-1-ene
EC Number:
219-397-9
EC Name:
2,3,4-trichlorobut-1-ene
Cas Number:
2431-50-7
Molecular formula:
C4H5Cl3
IUPAC Name:
2,3,4-trichlorobut-1-ene
Details on test material:
- Name of test material (as cited in study report): 1-Butene, 2,3,4-trichloro

Test animals

Species:
rat
Strain:
Wistar

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure (if applicable):
not specified
Vehicle:
not specified
Analytical verification of doses or concentrations:
not specified
Details on mating procedure:
no data
Duration of treatment / exposure:
6th to 16th day of gestation
Frequency of treatment:
6h/d
Duration of test:
10 d
Doses / concentrations
Remarks:
Doses / Concentrations:
0, 0.0007, 0.003, 0.017 mg/L (0, 0.1, 0.5, 2.5 ppm)
Basis:

No. of animals per sex per dose:
no data
Control animals:
yes
Details on study design:
Post observation period: until 21st day of gestation

Results and discussion

Results: maternal animals

Maternal developmental toxicity

Details on maternal toxic effects:
Maternal toxic effects:yes

Details on maternal toxic effects:
At 2.5 ppm: decreased food consumption and bodyweights

Effect levels (maternal animals)

open allclose all
Dose descriptor:
NOAEC
Effect level:
0.003 other: mg/L
Basis for effect level:
other: maternal toxicity
Dose descriptor:
LOAEC
Effect level:
0.017 other: mg/L
Basis for effect level:
other: maternal toxicity

Results (fetuses)

Details on embryotoxic / teratogenic effects:
Embryotoxic / teratogenic effects:no data

Details on embryotoxic / teratogenic effects:
At 2.5 ppm: decreased foetal weight, no teratogenicity

Effect levels (fetuses)

open allclose all
Dose descriptor:
NOAEC
Effect level:
0.003 other: mg/L
Basis for effect level:
other: teratogenicity
Dose descriptor:
LOAEC
Effect level:
0.017 other: mg/L
Basis for effect level:
other: fetotoxicity

Fetal abnormalities

Abnormalities:
not specified

Overall developmental toxicity

Developmental effects observed:
not specified

Any other information on results incl. tables

Freetext:
NOEL for maternal animals: 0.5 ppm
NOEL for offspring: 0.5 ppm
Maternal general toxicity: decreased food consumption and
bodyweights in the 2.5 ppm-group
Pregnancy and litter data: decreased foetal weight in the
2.5 ppm-group, no teratogenicity

Applicant's summary and conclusion