Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
screening for reproductive / developmental toxicity
Type of information:
other: collection of data
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Referenceopen allclose all

Reference Type:
other: collection of data
Title:
Query: Records containing the term 1-OCTANOL as displayed on http://toxnet.nlm.nih.gov on December 18, 2018.
Author:
Hazardous Substances Data Bank (HSDB)
Reference Type:
review article or handbook
Title:
Patty's Toxicology Volumes 1-9 5th ed.
Author:
Bingham, E.; Cohrssen, B.; Powell, C.H.
Year:
2001
Bibliographic source:
Bingham, E.; Cohrssen, B.; Powell, C.H.; Patty's Toxicology Volumes 1-9 5th ed. John Wiley & Sons. New York, N.Y. (2001)., p. V6 469

Materials and methods

GLP compliance:
not specified

Test material

Test material form:
liquid

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: gavage

Results and discussion

Any other information on results incl. tables

Developmental or Reproductive Toxicity/ In an oral gavage study, pregnant female Wistar rats were dosed with 0, 130, 650, 975, or 1300 mg/kg 1-octanol during gestational days 6 through 15. Maternal toxicity occurred with a dose-related increase in severity of clinical signs, including lateral and abdominal position, unsteady gait, salivation, piloerection, nasal discharge, and pneumonia. Food consumption and body weight gain decreased slightly in all but the lowest dose group. There was no developmental toxicity.

Applicant's summary and conclusion