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EC number: 406-550-1 | CAS number: - MDI
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 16 August 1989 - 30 September 1989
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study has been performed according to OECD guidelines but without GLP principles.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 989
- Report date:
- 1989
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- 1981
- Deviations:
- no
- GLP compliance:
- not specified
Test material
- Reference substance name:
- A mixture (1:2:1) of: bis(N-cyclohexyl-N'-phenyleneureido)methylene; bis(N-octadecyl-N'-phenyleneureido)methylene; bis(N-dicyclohexyl-N'-phenyleneureido)methylene
- EC Number:
- 406-550-1
- EC Name:
- A mixture (1:2:1) of: bis(N-cyclohexyl-N'-phenyleneureido)methylene; bis(N-octadecyl-N'-phenyleneureido)methylene; bis(N-dicyclohexyl-N'-phenyleneureido)methylene
- IUPAC Name:
- Reaction mass (1:2:1) of bis(N-cyclohexyl-N'-phenyleneureido)methylene and bis(N-octadecyl-N'-phenyleneureido)methylene and bis(N-dicyclohexyl-N'-phenyleneureido)methylene
- Test material form:
- solid: particulate/powder
- Details on test material:
- Description: White yellowish solid
Test substance storage: At room temperature in the dark
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- other: Japanese white albino
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Inoue Laboratory Animal Center
- Age at study initiation: 11-12 weeks old
- Weight at study initiation: 2.32 - 2.59 kg.
- Housing: Animals were housed individually in aluminium cages.
- Diet: Free access to diet for rabbits (RC4, Oriental Yeast Co., Ltd.). Animals were deprived of food during the 4 hours treatment.
- Water: Free access to tap water.
- Acclimation period: At least 7 days
ENVIRONMENTAL CONDITIONS
set to maintain:
- Temperature (°C): 18 – 26
- Humidity (%): 40 - 70
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 29 August 1989 to 02 September 1989
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- other: The test substance was dampened with 0.5 mL liquid paraffin.
- Controls:
- other: Adjacent areas of the untreated skin of each animal served as controls.
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 grams - Duration of treatment / exposure:
- 4 hours, single application.
- Observation period:
- 72 hours.
- Number of animals:
- 6
- Details on study design:
- TEST SUBSTANCE PREPARATION
The test substance was dampened with 0.5 mL liquid paraffin.
TEST SITE
Approximately 24 hours before treatment, electric clippers for animal use were used to shear their fur, and using an electric razor to shave the 6 rabbits' backs, the left and right sites were prepared. The test substance was applied to the skin of one flank, using a patch of 2x3 cm.
REMOVAL OF TEST SUBSTANCE
Four hours after the application, the dressing was removed and the skin cleaned of residual test substance using absorbent cotton and acetone.
OBSERVATIONS
- Mortality/Viability: One daily.
- Toxicity: Once daily.
- Body Weight: Once daily
- Necropsy: Not performed.
- Irritation:
The skin reactions were assessed at approximately 1, 24, 48 and 72 hours after the removal of the dressings and test substance. The irritation scores and a description of all other (local) effects were recorded.
SCORING SYSTEM:
The irritation was assessed according to the numerical scoring system according to OECD 404.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animal #1, #2, #3, #4, #5 and #6
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animal #1, #2, #3, #4, #5 and #6
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- No skin reaction such as erythema (red spots) or edema (swelling) was observed throughout the observation period.
- Other effects:
- None of the tested animals were found affected by the test substance and there were no significant changes in general condition and body weight.
Applicant's summary and conclusion
- Interpretation of results:
- other: Not irritating.
- Remarks:
- According to Regulation (EC) No. 1272/2008.
- Conclusions:
- In an skin irritation study with rabbits, performed according to OECD 404 test guidelines, no irritation was observed.
- Executive summary:
A skin irritation study with six rabbits was performed (4 hours application) with the substance according to OECD 404 test guideline.
No skin reaction such as erythema (red spots) or edema (swelling) was observed throughout the observation period of 72 hours.
None of the tested animals were found affected by the test substance and there were no significant changes in general condition and body weight.
Based on the results of the study it is concluded that MDI/CHA/ODA/DCHA does not need to be classified according to Regulation (EC) No. 1272/2008.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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