Reaction mass of cobalt and copper and iron

Acute Toxicity: oral

Administrative data

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

2001

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

guideline study with acceptable restrictions

Remarks:

GLP study according to OECD Guideline 423 and EU Method B.1 trisConsidering the lack of information on purity and particle size, a reliablility of 2 is assigned

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2001

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)

Test guideline 2

Qualifier:

according to guideline

Guideline:

EU Method B.1 tris (Acute Oral Toxicity - Acute Toxic Class Method)

GLP compliance:

yes

Test type:

acute toxic class method

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

Coated copper flakes

IUPAC Name:

Coated copper flakes

Details on test material:

Lot/batch number: not provided
Specification: no information was provided on the specification of the sample used in this study
Purity: not provided
Stability: Test substance: not provided. Test preparations: Not assessed, however, test substance preparations were freshly prepared.

Test animals

Species:

rat

Strain:

Sprague-Dawley

Sex:

male/female

Details on test animals or test system and environmental conditions:

Source: charles river (UK) Ltd, Margate, Kent, UK
At the start of the study the males weighed 271 to 299 g and the females weighed 198 to 218g, and were approximately eight weeks of age.
3 animals per group

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

arachis oil

Details on oral exposure:

the test material was administered orally as a suspension inarachis oil BP.

Doses:

200 and 2000 mg/kg bw
concentration in vehicle: 20 and 200 mg/ml at 200 and 2000 mg/kg bw, respectively
Total volume applied: 10 ml/kg

No. of animals per sex per dose:

A group of three fasted females was treated with 2000 mg/kg bw.
Further groups of 3 male and 3 female fasted animals were treated at a dose level of 200 mg/kg bw.

Control animals:

no

Results and discussion

Effect levels

Sex:

male/female

Dose descriptor:

LD50

Effect level:

>= 300 - <= 500 mg/kg bw

Mortality:

Two animals treated with 2000 mg/kg bw were found dead five days after dosing.
One animal treated with 2000 mg/kg bw was killed in extremis eight days after dosing.
There were no deaths noted at a dose level of 200 mg/kg bw.

Clinical signs:

other: Signs of systemic toxicity noted in animals treated with 2000 mg/kg bw were hunched posture, lethargy, pilo-erection, diarrhoea, decreased respiration rate, laboured respiration, ataxia, pallor of the extremities, emaciation, tiptoe gait and faeces staine

Gross pathology:

abnormalities noted at necropsy of the animals treated with 2000 mg/kg bw that died during the study were abnormally red lungs, dark liver, dark kidneys, copper-coloured material present in the stomach, haemorrhagic gastric mucosa, sloughing of the non-glandular epithelium of the stomach and haemorrhagic small and large intestines.

No abnormalities were noted at necropsy of animals treated with 200 mg/kg bw.

Other findings:

The LD50 of the test material was estimated to be in the range of 300-500 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:

harmful

Conclusions:

The test material from the manufacturere corresponds to the composition of “ coated copper flakes” .
The acute oral LD50 of the test material in the rat was estimated to be in the range of 300 - 500 mg/kg bw. Coated copper flakes therefore meet the criteria for classification as harmful according to Annex VI of Commission Directive 2001/59/EC. Copper coated flakes should be attributed the symbol Xn: harmful and the Risk Phrase R22: Harmful if swallowed.
The results are considered as applicable to the "coated copper flakes" .

Executive summary:

The test material identity was not provided in details. Considering the information from the reports on the same material, the tested material falls in the composition category of "coated copper flakes" (see– section 1.2), consistent with a biocidal product use (PBD notification was the reason for doing the test).

The acute oral LD50 of the test material in the rat was estimated to be in the range of 300 - 500 mg/kg bw.

The test material meets the criteria for classification as harmful according to Annex VI of Commission Directive 2001/59/EC. The test substance should be attributed the symbol Xn: harmful and the Risk Phrase R22: Harmful if swallowed.