Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1972
Report date:
1972
Reference Type:
other: method publication
Title:
A method for determining the dermal toxicity of pesticides
Author:
Noakes DN, Sanderson DM
Year:
1969
Bibliographic source:
Br J Ind Med. 1969, 26(1):59-64;

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The method according to Noakes and Sanderson was used (Noakes DN, Sanderson DM, Br J Ind Med. 1969, 26(1):59-64). Briefly, the test item was applied on a 6x8 cm area of the skin of albino rats (whose hair was previously clipped) and then occlusively covered by a double layer of plaster. Exposure time was 24 h after which the plaster was removed and the test item was washed away using water and detergent. Observation time was 7 days.
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2'-bipyridyl
EC Number:
206-674-4
EC Name:
2,2'-bipyridyl
Cas Number:
366-18-7
Molecular formula:
C10H8N2
IUPAC Name:
2,2'-bipyridine
Details on test material:
- Name of test material (as cited in study report): 2,2'-bipyridyl
- Substance type: yellowish-fawn crystalline solid
- Physical state: solid

Test animals

Species:
rat
Strain:
other: Alderley Park SPF albino
Sex:
female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 170-240 g

Administration / exposure

Type of coverage:
occlusive
Vehicle:
water
Details on dermal exposure:
TEST SITE
- Area of exposure: back
- Type of wrap if used: plaster, double-layered

REMOVAL OF TEST SUBSTANCE
- Washing (if done): yes with warm water and soap
- Time after start of exposure: 24 h

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.625 - 5 g/kg bw
- Constant volume or concentration used: no data
- For solids, paste formed: yes
Duration of exposure:
24 h
Doses:
625, 1250, 2500, 5000 mg/kg bw
No. of animals per sex per dose:
3
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Other examinations performed: clinical signs, body weight
Statistics:
In the study report at hand, only a LD50 range was given.
The here reported LD50 was calculated as arithmetic mean between the 625 and the 1250 mg/kg bw dose group.

Results and discussion

Effect levelsopen allclose all
Sex:
female
Dose descriptor:
LD50
Effect level:
> 625 - < 1 250 mg/kg bw
Based on:
test mat.
Remarks on result:
other: data as given in the study report
Sex:
female
Dose descriptor:
LD0
Effect level:
625 mg/kg bw
Based on:
test mat.
Remarks on result:
other: data as given in the study report
Sex:
female
Dose descriptor:
LD100
Effect level:
1 250 mg/kg bw
Based on:
test mat.
Remarks on result:
other: data as given in the study report
Mortality:
At all but the lowest dose (625 mg/kg bw), animals died within 24-48 h (table 1).
Clinical signs:
other: Animals in the 625 mg/kg bw dose group were hunched with piloerection but showed no tremors. In all but the lowest dose group, animals showed marked tremors and excreted orange-colored urine. The site of application showed severe erythema after removal of

Any other information on results incl. tables

Table 1: Cumulative mortality amongst rats treated dermally with 2,2’-bipyridine:

Time after application [d]

Dose [mg/kg bw] and cumulative mortality

625

1250

2500

5000

1

0/3

2/3

3/3

3/3

2

0/3

3/3

3/3

3/3

7

0/3

3/3

3/3

3/3

 

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
After dermal application of 2,2-bipyridine to rats under occlusive dressing, 0 rats died at a dose of 625 mg/kg bw (LD0) but all rats in the group died at 1250 mg/kg bw (LD100). The LD50 is therefore between 625 and 1250 mg/kg bw.
Executive summary:

Dermal toxicity of 2,2'-bipyridine to rats was assessed by applying the test item as aqueous paste to the clipped skin of female rats for 24 h under occlusive dressing. The test item was applied in concentrations of 625, 1250, 2500, and 5000 mg/kg bw to three animals per dose group. Subsequently, the dressing was removed, the application site was washed and the animals were observed for 7 d.

The study was neither performed according to a guideline nor under GLP. Also were no information on body weights/weight gain available.

In all but the lowest dose (625 mg/kg bw), all animals died within 48 h after application exhibiting orange-colored urine and marked tremor. None of the rats in the 625 mg/kg bw dose group died but hunched posture with piloerection and impaired weight gain was observed in these animals. In all rats, severe erythema were observed at the application site after removal of the dressing.

The LD50 was between 625 and 1250 mg/kg bw.