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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable study report with restrictions due to limited reporting

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
A one-week acute intraperitoneal toxicity test was carried out to decide the dose level for the micronucleus test. Groups of 5-6 male mice were treated with the test material at different dose levels in 3 series of experiments, and LD50 was estimated from the number of deaths.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4,4'-methylenediphenyl diisocyanate
EC Number:
202-966-0
EC Name:
4,4'-methylenediphenyl diisocyanate
Cas Number:
101-68-8
Molecular formula:
C15H10N2O2
IUPAC Name:
1-isocyanato-4-[(4-isocyanatophenyl)methyl]benzene
Details on test material:
- Name of test material (as cited in study report): 4,4'-Diphenylmethane diisocyanate
- Analytical purity: not reported
- Impurities (identity and concentrations): not reported

Test animals

Species:
mouse
Strain:
ICR
Sex:
male

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
other: DMSO and corn oil
Details on exposure:
- Preparation of test material: MDI is insoluble in water and reacts with it to form polymers. Therefore, the test material was dissolved in a small amount of dimethylsulfoxide (DMSO), the first solvent, which does not contain water, and then it was suspended in the sterilized corn oil, the second solvent.The preparation was made separately for each test and used immediately.

Doses:
Experiment I: 10, 20, 100 and 500 mg/kg bw;
Experiment II: 133, 200, 300 and 450 mg/kg bw;
Experiment III: 89, 133 and 200 mg/kg bw
No. of animals per sex per dose:
5 in Experiment I
6 in Experiment II and III
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
ca. 100 mg/kg bw
Mortality:
see free text

Any other information on results incl. tables

Experiment No.

Dose levels (mg/kg bw)

No. of animals died/ No. of animals treated

Time of death (day)

0-1

1-3

3-5

5-7

1

500

5/5

0

3

2

0

100

0/5

0

0

0

0

20

0/5

0

0

0

0

10

0/5

0

0

0

0

2

450

4/6

0

3

1

0

300

5/6

0

2

1

2

200

5/6

0

4

1

0

133

4/6

0

2

0

2

3

200

5/6

0

2

3

0

133

4/6

0

1

1

2

89

0/6

0

0

0

0

Applicant's summary and conclusion