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EC number: 701-017-2 | CAS number: -
- 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

Dermal absorption
Administrative data
- Endpoint:
- dermal absorption in vivo
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study meets generally accepted scientific principles
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 007
- Report date:
- 2007
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- No guidelines exist for this kind of study. The study was performed considering parts of the OECD guideline No. 427, Percutaneous Absorption: in vivo method, 2004.
- GLP compliance:
- no
Test material
- Reference substance name:
- m-tolylidene diisocyanate
- EC Number:
- 247-722-4
- EC Name:
- m-tolylidene diisocyanate
- Cas Number:
- 26471-62-5
- IUPAC Name:
- 2,4-diisocyanato-1-methylbenzene
- Details on test material:
- 2,4-TDI
- Name of test material (as cited in study report): 2,4-TDI
- Supplier: Sigma-Aldrich
- Analytical purity: 99.7%
- Batch No.: 6124X
- Stability under test conditions: stability was guaranteed under the storage conditions until 04 May 2009
- Homogeneity: homogeneous by visual inspection and due to the high purity
2,6-TDI
- Name of test material (as cited in study report): 2,6-TDI
- Supplier: Sigma-Aldrich
- Analytical purity: 99.8%
- Batch No.: 1284332
- Stability under test conditions: stability was guaranteed under the storage conditions until 31 Aug 2007
- Homogeneity: homogeneous by visual inspection and due to the high purity
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Chales River Laboratories, Sulzfeld, Germany
- Age at study initiation: 10 - 12 weeks
- Weight at study initiation: ca. 300 g
- Fasting period before study: no
- Housing: Macrolon cages type III
- Individual metabolism cages: no
- Diet: Provimi Kliba SA, Kaiseraugust, Switzerland, ad libitum
- Water: ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 24°C
- Humidity (%): 30 - 70%
- Photoperiod: natural day/night rhythm with additional artificial light as required during working hours
Administration / exposure
- Type of coverage:
- semiocclusive
- Vehicle:
- unchanged (no vehicle)
- Duration of exposure:
- 1 min (skin sample), 1 h, 2 h, 4 h, 8 h
- Doses:
- 300 µl/kg which corresponds to 360 mg/kg
- No. of animals per group:
- 2 animals per exposure period (1 h, 2 h, 4 h, 8 h);
1 animal was sacrificed without exposur (untreated control)
1 animal for skin preparation (2 skin samples were prepared) and 1 min exposure of the preparated skin
= 10 animals in total - Control animals:
- yes
- Remarks:
- Negative control: untreated skin sites (2) of one animal; Positive control: 10 µl of the undiluted mixture of 2,6-TDI and 2,4-TDI (1:1, v:v) directly given into the reagent
- Details on study design:
- DOSE PREPARATION
undiluted 2,6-TDI and 2,4-TDI (1:1, v:v)
APPLICATION OF DOSE:
10 µl/cm2 (100µl/10 cm2)
TEST SITE
- Preparation of test site: clipping and cleaning with acetone at least 24 h before treatment
- Area of exposure: 10 cm2, difined by a rubber ring and spacer
- Type of cover / wrap used: a permeable (gauze) dressing containing a chorcoal filter and the whole was further protected by a semi-occlusive adhesive bandage
SAMPLE PREPARATION
- Preparation details: animals were sacrificed, skin samples were prepared, the skin samples were transferred into the reagent (consisting of Dibutylamine in toluene). It was guaranteed that samples remained submersed in the reagent
- Storage procedure: after reaction time of 15 min samples were stored at 4°C
ANALYSIS
The amount of free isocyanates on the skin was determined by chemical analysis
Results and discussion
- Signs and symptoms of toxicity:
- not examined
- Dermal irritation:
- not examined
Any other information on results incl. tables
- Analytical results of 2,6- and 2,4 -TDI on rat skin are shown in table 1. The negative control (0µl/10cm2) showed no background detection of isocyanate reactivity in untreated skin.
- Positive control (1:1 mixture of 2,6 -TDI and 2,4 -TDI) resulted in values of 40 and 100 mg/100 µl. Therefore the nominal ratio of 1:1 varied from the experimental ratio of 4:10 (due to preparation of stock solution or calibration of analytical equipment)
Table 1: Analytical results of 2,6 -TDI and 2,4 -TDI on rat skin after different exposure periods
Nominal dose [µl/10 cm2] | Positive control | 0 | 0 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 |
Exposure time [min] | - | - | - | 1 | 1 | 60 | 60 | 120 | 120 | 240 | 240 | 480 | 480 |
Animal no. | - | 1 | 1 | 2 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |
2,6-TDI [mg/sample] | 40 | <1 | <1 | 12 | 12 | 18 | 8 | 8 | 10 | 6 | 4 | 2 | 3 |
2,4-TDI [mg/sample] | 100 | <1 | <1 | 57 | 59 | 56 | 24 | 24 | 29 | 21 | 14 | 14 | 18 |
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