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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term repeated dose toxicity: oral
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: does not meet important criteria of today standard methods; poor documentation

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1961
Report date:
1961

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Oral gavage study with 6 male rats over 2 weeks.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Hexamethylene diisocyanate
EC Number:
212-485-8
EC Name:
Hexamethylene diisocyanate
Cas Number:
822-06-0
Molecular formula:
C8H12N2O2
IUPAC Name:
1,6-diisocyanatohexane

Test animals

Species:
rat
Strain:
other: albino ChR-CD
Sex:
male
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
peanut oil
Details on oral exposure:
no data
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
10 administrations over a 2-week period
Frequency of treatment:
daily
Doses / concentrations
Remarks:
Doses / Concentrations:
300 mg/kg
Basis:
actual ingested
No. of animals per sex per dose:
6
Control animals:
no
Details on study design:
3 rats were chosen at random for sacrifice 4 hours after the tenth treatment and 3 rats were kept for a 10-day observation period

Results and discussion

Effect levels

open allclose all
Dose descriptor:
NOAEL
Sex:
male
Remarks on result:
not determinable
Remarks:
no NOAEL identified
Dose descriptor:
LOEL
Effect level:
300 mg/kg bw/day (actual dose received)
Sex:
male

Target system / organ toxicity

Critical effects observed:
not specified

Any other information on results incl. tables

HDI as a five per cent solution in peanut oil was administered by stomach tube daily for ten days over a two-week period at a dose level of 300 ma/kg to six male albino ChR-CD rats. Although the rats showed diarrhea and salivation, and appeared uncomfortable after most treatments, they survived. During the first week, weight losses were observed consistently in all animals. During the second week, there were sporadic weight losses, but most animals gained weight. High water eonsumption was also noted in the treated rats during the second week. No clinical signs of toxicity were observed during the 10-days recovery period. Gross and microscopic examination of tissues revealed an ulcerative gastritis in rats sacrificed the tenth treatment day, and healing gastritis in rats sacrificed ten days later.

Applicant's summary and conclusion