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EC number: 210-676-0 | CAS number: 621-29-4
- 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

Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Study period:
- From 12 November 1979 to 20 October 1980
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: well documented and scientifically acceptable
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
- Report date:
- 1980
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- no
- Test type:
- standard acute method
Test material
- Reference substance name:
- m-tolyl isocyanate
- EC Number:
- 210-676-0
- EC Name:
- m-tolyl isocyanate
- Cas Number:
- 621-29-4
- Molecular formula:
- C8H7NO
- IUPAC Name:
- 1-isocyanato-3-methylbenzene
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Rationale for alternative/additional species to rat n/a
- Source: Winkelmann, Borchen)
- Females (if applicable) nulliparous and non-pregnant: [yes, 5]
- Rationale for use of males (if applicable) n/a
- Age at study initiation:
- Weight at study initiation: 179 g
- Fasting period before study: n/a
- Housing: Mkrolonkafugen Type III cage.
- Historical data: n/a
- Diet (e.g. ad libitum): n/a
- Water (e.g. ad libitum):n/a
- Acclimation period: n/a
- Microbiological status when known n/a
- Method of randomisation in assigning animals to test and control groups :n/a
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ± 1.5
- Humidity (%): 60 ± 5
- Air changes (per hr): 12 hours , from 7 am to 7 pm
- Photoperiod (hrs dark / hrs light): n/a
IN-LIFE DATES: From: To: n/a
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- unchanged (no vehicle)
- Doses:
- 1000, 1500, 2000, 2500, 3100, 4000 or 5000 µl/kg bw (= ca. 1060, 1590, 2120, 2650, 3286, 4240, 5300 mg/kg bw)
- No. of animals per sex per dose:
- 5 male and 5 female rats/group
- Control animals:
- no
- Details on study design:
- Five male and 5 female young adult male Wistar rats (160 -180 g) per group reveived per gavage a single dose of 1000, 1500, 2000, 2500, 3100, 4000 or 5000 µl/kg bw m-tolylisocyanate. The animals were observed for mortality body weights and clinical signs through day 14.
- Statistics:
- calculation of LD50 according Fink and Hund, Arzneim Forsch 15, 624 (1965)
Results and discussion
Effect levels
- Key result
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 2 926 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- 2 380 - 3 210
- Mortality:
- Males:
none for male rats at 1000 µl/kg bw, 1500 µg/kg bw doses.
20% at 2000 µl/kg bw dose
40% 2500 µg/kg bw dose
40 % 3100 µl/kg bw dose
100% 4000 µl/kg bw dose
100% 5000 µl/kg bw dose.
Females:
0% 1000 µl/kg bw dose
20% 1500 µg/kg bw dose
20% 2000 µl/kg bw dose
20% 2500 µg/kg bw dose
60 % at 3100 µl/kg bw dose
80% 4000 µl/kg bw dose
100% 5000 µl/kg bw dose respectively. - Body weight:
- lower than 10% body weight loss
- Remarks:
- body weight reduction at 1500 µl/kg bw and above.
- Other findings:
- Signs of intoxication: Sedation, reduction of gerneral condition. Female rats showed a body weight reduction at 1500 µl/kg bw and above. A dose of 1000 µl/kg bw was tolerated by male and female rats without symptoms.
Any other information on results incl. tables
Dose mg/kg | Sex | Symptoms |
1.0 | M | - |
1.5 | M | Worsening General well-being; Sedation. |
2.0 | M | Worsening General well-being; Sedation. |
2.5 | M | Worsening General well-being; Sedation. |
3.1 | M | Worsening General well-being; Sedation. |
4.0 | M | Worsening General well-being; Sedation. |
5.0 | M | Worsening General well-being; Sedation. |
1.0 | F | - |
1.5 | F | Worsening General well-being; Sedation; Weight lost. |
2.0 | F | Worsening General well-being; Sedation. |
2.5 | F | Worsening General well-being; Sedation. |
3.1 | F | Worsening General well-being; Sedation; Weight lost. |
4.0 | F | Worsening General well-being; Sedation; Weight lost. |
5.0 | F | Worsening General well-being; Sedation. |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Moderately Toxic. No symptoms at 1000 µl/kg bw was tolerated by male and female rats without symptoms.
- Executive summary:
Five male and 5 female young adult male Wistar rats (160 -180 g) per group were dosed undiluted at 1000, 1500, 2000, 2500, 3100, 4000 or 5000 µl/kg bw m-tolylisocyanate. The animals were observed for mortality body weights and clinical signs through day 14.
Signs of intoxication: Sedation, reduction of gerneral condition. Fermale rats showed a body weight reduction at 1500 µl/kg bw and above. A dose of 1000 µl/kg bw was tolerated by male and female rats without symptoms.
The symptoms appeared 1 hour after application low to moderately pronounced and partially held until the last test day. The deaths were recorded from the 4th hour to the 4th day of the experiment. There were none between males and females significant differences in the nature and intensity of the symptoms and the number of deaths. The acute oral LD50 for male rats is 2760 µl/kg bw (= ca. 2926 mg/kg bw).
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