Alcohols C13-15 (branched and linear, odd numbered), reaction product with 1-chloro-2,3-epoxypropane

Acute Toxicity: oral

Administrative data

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: detailed information to fulfill the basic scientific principle

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1974

Report date:

1974

Materials and methods

Test guideline

Qualifier:

no guideline available

Principles of method if other than guideline:

Four groups each of 10 male rats and one group of 20 male rats were treated with the undiluted substance. The application volume was 17.8 mL/kg, 23.7 mL/kg, 27.4 mL/kg and 31.6 mL/kg, respectively. One control group with 10 male rats was treated with demineralized water at 31.6 mL/kg.

GLP compliance:

no

Test type:

standard acute method

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

Alcohols, C13-15 (odd numbered, branched and linear)

Molecular formula:

C13H28O and C15H32O

IUPAC Name:

Alcohols, C13-15 (odd numbered, branched and linear)

Constituent 2

Reference substance name:

Alcohols, C13, branched glycidyl ethers

Molecular formula:

C16H32O2

IUPAC Name:

Alcohols, C13, branched glycidyl ethers

Constituent 3

Reference substance name:

[(tridecyloxy)methyl]oxirane

EC Number:

276-765-1

EC Name:

[(tridecyloxy)methyl]oxirane

Cas Number:

72689-40-8

Molecular formula:

C16H32O2

IUPAC Name:

2-[(tridecyloxy)methyl]oxirane

Constituent 4

Reference substance name:

Alcohols, C15, branched glycidyl ethers

Molecular formula:

C18H36O2

IUPAC Name:

Alcohols, C15, branched glycidyl ethers

Constituent 5

Reference substance name:

[(pentadecyloxy)methyl]oxirane

EC Number:

302-058-5

EC Name:

[(pentadecyloxy)methyl]oxirane

Cas Number:

94088-56-9

Molecular formula:

C18H36O2

IUPAC Name:

2-[(pentadecyloxy)methyl]oxirane

Constituent 6

Reference substance name:

secondary reaction products of Oxirane, mono{[C13-15 (odd numbered, linear and branched)-alkyloxy)methyl] derivs.

Molecular formula:

UVCB, not applicable

IUPAC Name:

secondary reaction products of Oxirane, mono{[C13-15 (odd numbered, linear and branched)-alkyloxy)methyl] derivs.

Constituent 7

Reference substance name:

unknown constituents

IUPAC Name:

unknown constituents

Test material form:

liquid

Specific details on test material used for the study:

C13-15 glycidylether
Grilonit Epoxid-Resin
Clear colorless liquid with high viscosity
storage at room temperature protected from light
density: 0.89 g/cm3

Test animals

Species:

rat

Strain:

Sprague-Dawley

Sex:

male

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Willi Gassner (WIGA) SPF breeding CH-8741 Sulzfeld Switzerland
- Weight at study initiation: between 110 g and 178 g (mean 133 g)
- Fasting period before study: overnight
- Housing: in groups of 10 or 20 animals in Makrolon (55 x 33 x 20 cm) cages during acclimatization and in groups of 5 animals in Makrolon cages (38 x 22 x 15 cm) after treatment and during observation.
- Diet: ad libitum except overnight before treatment
- Water: ad libitum
- Acclimation period: 3 to 7 days


ENVIRONMENTAL CONDITIONS
- Temperature (°C): approx. 22 °C
- Humidity (%): approx. 57%

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

unchanged (no vehicle)

Details on oral exposure:

MAXIMUM DOSE VOLUME APPLIED: 31.6 mL/kg

Doses:

control group: 31.6 mL/kg demineralized water
Test group 1: 17.8 mL/kg
Test group 2: 23.7 mL/kg
Test group 3: 27.4 mL/kg
Test group 4: 31.6 mL/kg

No. of animals per sex per dose:

Control group: 10 males
Test group 1: 10 males
Test group 2: 10 males
Test group 3: 10 males
Test group 4: 20 males

Control animals:

yes

Details on study design:

Four groups each of 10 male rats and one group of 20 male rats were treated with the undiluted substance. The single-application volume was 17.8 mL/kg, 23.7 mL/kg, 27.4 mL/kg and 31.6 mL/kg, respectively. One control group with 10 male rats was treated with demineralized water at 31.6 mL/kg.
All animals were examined for mortality and clinical signs at 10, 18 and 33 minutes, 1, 1.8, 3.3, 6 and 24 hours after treatment and at least once daily up to day 14, the end of the observation period. Body weights were recorded on the day of treatment prior to application and on days 7 and 14. All animals that died spontaneously during the course of the study were necropsied and examined as soon as they were found dead.

Results and discussion

Preliminary study:

None

Effect levels

Sex:

male

Dose descriptor:

LD50

Effect level:

ca. 30.1 mL/kg bw

Mortality:

No deaths occurred in the control group and test group treated with 17.8 mL/kg, 23.7 mL/kg and 27.4 mL/kg.
16 out of 20 rats died in the highest treated group (31.6 mL/kg) during the course of the study. All animals died between day 3 and 8.

Clinical signs:

other: Systemic toxicity was observed in all test item treated groups. All clinical signs disapeared in the lowest treated group (17.8 mL/kg) after day 4, whereas the animals treated with 23.7 mL/kg, 27.4 mL/kg and the surviving animals treated with 31.6 mL/kg s

Gross pathology:

For the 31.6 mL/kg treated animals, red discoloration of the stomach with hemmorhage was noted at the unscheduled necropsy in 12 out of 16 animals. Blood in the stomach was observed in 5 animals. Red discoloration of the small intestine with hemmorhage was observed in 10 animals and blood in the small intestine was seen in 12 animals.

Applicant's summary and conclusion

Interpretation of results:

GHS criteria not met

Conclusions:

Oral LD50 male rats > 27.4 and < 31.6 ml/kg
Oral LD50 male rats = 30.1 ml/kg (26.8 g/kg)
density = 0.89 g/cm3

Executive summary:

Four groups each of 10 male rats and one group of 20 male rats were treated with the undiluted substance. The single-application volume was 17.8 mL/kg, 23.7 mL/kg, 27.4 mL/kg and 31.6 mL/kg, respectively. One control group with 10 male rats was treated with demineralized water at 31.6 mL/kg.

Mortality and clinical signs were observed during 14 days after treatment.

No deaths occurred in the control group and test groups treated with 17.8 mL/kg, 23.7 mL/kg and 27.4 mL/kg.

16 out of 20 rats died in the highest treated group (31.6 mL/kg) during the course of the study.

Systemic toxicity was observed in all test item treated groups. All clinical signs disappeared in the lowest treated group (17.8 mL/kg) after day 4 whereas the animals treated with 23.7 mL/kg, 27.4 mL/kg and the surviving animals treated with 31.6 mL/kg still showed clinical signs at the end of the observation period.

Loss of body weight was noted in the 31.6 mL/kg treated group during the first week of observation but the surviving animals did not recover completly at the end of the observation period compared with the control animals. Body weight increased in the other treated groups was comparable to the control group.

For the 31.6 mL/kg treated animals, red discoloration of the stomach with hemmorhage was noted at the unscheduled necropsy in 12 out of 16 animals. Blood in the stomach was observed in 5 animals. Red discoloration of the small intestine with hemmorhage was observed in 10 animals and blood in the small intestine was seen in 12 animals.