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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
11 to 30 June 1985
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:
1985
Report date:
1985

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
yes
Remarks:
Observation period: 7 days
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Reference substance name:
Resinoid of Canarium luzonicum (Burseraceae) obtained from the exudate by benzyl benzoate extraction.
Molecular formula:
Not applicable (UVCB)
IUPAC Name:
Resinoid of Canarium luzonicum (Burseraceae) obtained from the exudate by benzyl benzoate extraction.
Specific details on test material used for the study:
Extract of elemi gum with benzyl benzoate, containing 30% benzyl benzoate
Name of test material: Elemi resinoid P
Date of preparation: 10.9.84
Batch No: 651/84
Provider: PPF Bertrand Freres
Appearance: thick pale yellow jelly
Storage: ambiant temperature

Test animals

Species:
mouse
Strain:
not specified
Remarks:
white
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS

- Age at study initiation: 4-5 weeks
- Weight at study initiation: Females: 17-23 g; males: 21-25 g
- Fasting period before study: 4 hours
- Housing: individually
- Diet (e.g. ad libitum): commercial pelleted diet, ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period:

IN-LIFE DATES: From: 11 June 1985 To: 18 June 1985

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: groundnut oil
Details on oral exposure:
VEHICLE
- Concentration in vehicle: 20 % w/v

MAXIMUM DOSE VOLUME APPLIED: 40 mL/kg bw
Doses:
2, 5 and 10 g/kg bw
No. of animals per sex per dose:
3 at 5 g/kg bw
1 at 2 and 10 g/kg bw
Control animals:
no
Details on study design:
The animals are observed for signs of toxicity for 7 days after intubation and any animal dying during this period is autopsied. Animals are weighed before administration and before killing at the end of the observation period. Post-mortem examination is then performed.
Statistics:
None

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.
Mortality:
2/2 at 10 g/kg bw; 1/6 at 5 g/kg bw; 0/2 at 2 g/kg bw
Clinical signs:
All the mice dosed at 5 g/kg bw and 10 g/kg bw were shown signs of stress within 30 min after treatment. After 18 h, the mice dosed at 10 g/kg bw and one male dosed at 5 g/kg bw were also somnolent and showing laboured breathing. All these mice died within 22-25 h. All the surviving mice recovered within 18 h.
Body weight:
All the surviving mice gained weight during the 7-day observation.
Gross pathology:
Autopsy of the mice that died revealed:
- gaseous distension of the stomach and intestines
- pale liver
- diarrhoea
All the surviving mice presented a normal appearance at autopsy.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Under the test conditions, the LD50 of the test item is greater than 5000 mg/kg bw in mice therefore it does not require classification according to CLP and GHS criteria.
Executive summary:

3 groups of 4-5 week-old white mice were given a single dose of test item suspended in 20% w/v groundnut oil at 2, 5 and 10 g/kg bw. All the mice dosed at 5 g/kg bw and 10 g/kg bw were shown signs of stress within 30 min after treatment. After 18 h, the mice dosed at 10 g/kg bw and one male dosed at 5 g/kg bw were also somnolent and showing laboured breathing. All these mice died within 22-25 h. All the surviving mice recovered within 18 h.

Autopsy of the mice that died revealed:

- gaseous distension of the stomach and intestines

- pale liver

- diarrhoea

All the surviving mice presented a normal appearance at autopsy.

Under the test conditions, the LD50 of the test item is greater than 5000 mg/kg bw in mice therefore it does not require classification according to CLP and GHS criteria.