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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1979
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1979
Report date:
1979

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Five groups of five male albino rats of the Sherman-Wistar
Strain weighing between 200 and 300 gm were employed in
this study. The rats were deprived of food but not water
for 24 hours prior to dosing. Each animal was weighed and
dosed by direct administration of the experimental material
into the stomach by means of a syringe and dosing needle.
GLP compliance:
not specified
Remarks:
test done before GLP was established
Test type:
fixed dose procedure
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,5,8,11-tetramethyldodec-6-yne-5,8-diol
EC Number:
269-348-0
EC Name:
2,5,8,11-tetramethyldodec-6-yne-5,8-diol
Cas Number:
68227-33-8
Molecular formula:
C16H30O2
IUPAC Name:
2,5,8,11-tetramethyldodec-6-yne-5,8-diol
Constituent 2
Reference substance name:
2,5,8,11-tetramethyl-5,8-dodecanediol
IUPAC Name:
2,5,8,11-tetramethyl-5,8-dodecanediol
Test material form:
liquid: viscous

Test animals

Species:
rat
Strain:
other: Sherman-Wistar
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
Each animal was dosed by direct administration of the experimental material
into the stomach by means of a syringe and dosing needle.
Doses:
1 g/kg
2 g/kg
4 g/kg
8 g/kg
16 g/kg
No. of animals per sex per dose:
five animals (males) per dose
Control animals:
no
Details on study design:
Five groups of five male albino rats of the Sherman-Wistar
Strain weighing between 200 and 300 gm were employed in
this study. The rats were deprived of food but not water
for 24 hours prior to dosing. Each animal was weighed and
dosed by direct administration of the experimental material
into the stomach by means of a syringe and dosing needle.
Statistics:
The subject material when studied in male albino rats has
an acute oral LD of 12.9 gm/kg. with 19/20 Confidence
limits of from 8?8 to 20.1 gm/kg

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
12 900 mg/kg bw
Based on:
test mat.
95% CL:
> 8 400 - < 20 100
Mortality:
one animal within 24 hours in the 8 g group
one animal within 24 hours and two within 48 hours in the 16 g group
Clinical signs:
other: At the dosage levels of 1.0 and 2.0 gm/kg. the animals were ruffled, dirty and slightly depressed after 24 hours. They appeared recovered and normal after 48 hours. At the dosage level of 4.0 gm/kg. the animals were depressed after 4-6 hours. Within 24 ho
Gross pathology:
In the gross pathologic examination, slight hemorrrhaging of the GI tract was evident in those animals dying during
the course of the study. Gross pathologic examination of the animals sacrificed a t the conclusion of the observation
period revealed nothing remarkable.

Any other information on results incl. tables

 Dosage Level g/kg Number of Animals Dosed   3  5 10  11  12  13  14  Total Dead 14 Days  Total Survived 14 Days  Average Initial Weight [g]  Average Final Weight [g]
 1.0  0 235  280 
 2.0  5  0 5 220  250
 4.0  5  0 240 275 
 8.0  5  1 210  235 
 16.0  5  1 3 220  245 
                                       
                                       

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The subject material when studied in male albino rats has
an acute oral LD50 of 12.9 gm/kg. with 19/20 Confidence
limits of from 8.4 to 20.1 gm/kg.
Executive summary:

The subject material when studied in male albino rats has an acute oral LD50 of 12.9 gm/kg. with 19/20 Confidence limits of from 8.4 to 20.1 gm/kg.