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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
biochemical or cellular interactions
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: only short summary available; too few data for assessment

Data source

Reference
Reference Type:
publication
Title:
Effect of Chlorinated Alkanes on Hepatic Triglyceride Secretion
Author:
Selan, F. M. and Evans, M. A.
Year:
1987
Bibliographic source:
Res. Commun. Chem. in Pathol. Pharmacol. 55, 249- 269

Materials and methods

Principles of method if other than guideline:
The effect of a series of monochloroalkanes on hepatic triglyceride secretion was investigated in male Swiss Webster mice and Spague Dawley rats in vitro and in vivo.
GLP compliance:
not specified
Type of method:
other: in vivo and in vitro
Endpoint addressed:
basic toxicokinetics

Test material

Constituent 1
Chemical structure
Reference substance name:
1-chlorobutane
EC Number:
203-696-6
EC Name:
1-chlorobutane
Cas Number:
109-69-3
Molecular formula:
C4H9Cl
IUPAC Name:
1-chlorobutane
Details on test material:
- Name of test material (as cited in study report): 1-chlorobutane

Test animals

Species:
other: rat and mouse
Strain:
other: SD rats and Swiss Webster mice
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
corn oil
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
single treatment
Frequency of treatment:
once
Post exposure period:
no data
No. of animals per sex per dose:
no data
Control animals:
yes, concurrent vehicle

Results and discussion

Details on results:
1-Chlorobutane produced a dose-related decrease in serum triglyceride levels at 2 hours after administration of different doses in corn oil (0.1 ml/kg bw). The dose necessary to produce a 50% decrease in in vivo triglyceride secretion was 43.9 mmol/kg (4.1 g/kg). The n-buyl chloride concentration required to produce a 50% decrease in triglyceride secretion by isolated hepatocytes was 24.7 mM (23 mg/mL).

Applicant's summary and conclusion