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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term repeated dose toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Study period:
1964
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Non-GLP non-guideline study, available as unpublished report, notable limitations in design and/or reporting.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1964
Report date:
1964

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
In a repeated dose toxicity study 10 rats (5/sex) were exposed daily, during 4 weeks (Saturdays and Sundays excluded), to Irgazingelb 2 GLT: 5% suspension with Arabic gum (application volume 0.4 cm³/animal). To prevent licking, the animals were kept in a narrow grating cage during 3 hours after application, subsequently the application site (ca. 20 cm²) was wiped with a wet sponge.
GLP compliance:
not specified
Remarks:
prior to GLP implementation
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Mixture of octachloro, monomethoxy-heptachloro and bismethoxy-hexachloro derivatives of 3,3'-[(2-methyl-1,3-phenylene)diimino]bis[2,3-dihydro-1H-isoindol-1-one]
EC Number:
600-735-2
Cas Number:
106276-79-3
Molecular formula:
Mixture of C23H8Cl8N4O2, C24H11Cl7N4O3, C25H14Cl6N4O4
IUPAC Name:
Mixture of octachloro, monomethoxy-heptachloro and bismethoxy-hexachloro derivatives of 3,3'-[(2-methyl-1,3-phenylene)diimino]bis[2,3-dihydro-1H-isoindol-1-one]

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 124 - 139 g, average 133 g

Administration / exposure

Type of coverage:
not specified
Vehicle:
other: aqueous suspension with Arabic gum
Details on exposure:
TEST SITE
- Area of exposure: ca. 20 cm²
- Amount(s) applied (volume or weight with unit): 0.4 cm³/animal
- Application: 1 x per day, durning 4 weeks, always on the same skin area (saturdays and sundays excluded)
- Shavings or clipplings: depilated back skin

REMOVAL OF TEST SUBSTANCE
- Washing (if done): wiped with a wet sponge
- Time after start of exposure: 3 hours

TEST MATERIAL / VEHICLE
- Concentration (if solution): 5% suspension with Arabic gum

USE OF RESTRAINERS FOR PREVENTING INGESTION: yes
To prevent licking, the animals were kept during 3 hours after administration in a narrow grating cage.
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
4 weeks
Frequency of treatment:
Daily, excluding saturdays and sundays.
No. of animals per sex per dose:
5/sex
Control animals:
not specified

Examinations

Observations and examinations performed and frequency:
SKIN OBSERVATIONS: Yes
Assessment of skin observations checked respectively 24 h after or before the next application.

BODY WEIGHT: Yes
At start and termination of the experiment

RESORPTIVE TOXICITY: Yes

Results and discussion

Results of examinations

Details on results:
- Body weight at termination of experiment: 183 - 246 g, average 221g
- 10/10 without without findings
- No local Irritation
- No resorptive toxicity

Effect levels

Dose descriptor:
NOAEL
Remarks on result:
not determinable
Remarks:
no NOAEL identified

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion