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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1959
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: limited number of endpoints investigated (only clinical signs and hematogogy)

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1959
Report date:
1959

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
10 rats were orally exposed to 0.25 mL/kg bw/day (201.5 mg/kg bw/day, being the density = 0.806 g/m³) of TDM for a period of 21 days
GLP compliance:
no
Remarks:
GLP was not mandatory at the time of the study

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2,4,6,6-pentamethylheptane-4-thiol
EC Number:
296-714-7
EC Name:
2,2,4,6,6-pentamethylheptane-4-thiol
Cas Number:
93002-38-1
Molecular formula:
C12H26S
IUPAC Name:
2,2,4,6,6-pentamethylheptane-4-thiol
Details on test material:
- Name of test material (as cited in study report): TDM (tertiar dodecylmercaptan)
- Analytical purity: not reported

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
not reported

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: oil
Details on oral exposure:
VEHICLE
- Concentration in vehicle: 2.5%
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
21 days
Frequency of treatment:
daily
Doses / concentrations
Remarks:
Doses / Concentrations:
0.25 mL/kg bw
Basis:
actual ingested
No. of animals per sex per dose:
10 (sex not reported)
Control animals:
not specified
Details on study design:
no further data reported
Positive control:
No

Examinations

Observations and examinations performed and frequency:
HAEMATOLOGY: Yes
Sacrifice and pathology:
Not reported
Other examinations:
No further data
Statistics:
Not reported

Results and discussion

Results of examinations

Details on results:
Animals´ blood count was normal.

Effect levels

Dose descriptor:
NOAEL
Remarks on result:
not determinable
Remarks:
no NOAEL identified

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion