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EC number: 252-405-9 | CAS number: 35155-28-3
- 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
Endpoint summary
Administrative data
Description of key information
Oral:
The oral LD50 value of test item in Wistar rats was established to be within the range of 300-2000 mg/kg body weight.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 300 mg/kg bw
- Quality of whole database:
- 1
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Oral:
One in vivo study is available. According to the OECD 423 test guideline, initially, the test substacne was administered by oral gavage to three female Wistar rats at 2000 mg/kg body weight. In a stepwise procedure three additional groups of three females were dosed at 300 mg/kg body weight.
Initially, test item was administered by oral gavage to three female Wistar rats at 2000 mg/kg body weight. In a stepwise procedure two additional groups of three females were dosed at 300 mg/kg body weight.
At 2000 mg/kg, two animals were found dead on Day 1 and one animal was found dead on Day 2. At 300 mg/kg, one animal was found dead on Day 2. No further mortality occurred.
At 2000 mg/kg, lethargy, clonic spasms, lateral recumbency, hunched posture, uncoordinated movements, slow breathing, shallow respiration, piloerection, salivation, watery discharge from both eyes, pale appearance and/or ptosis were noted for all animals on Day 1. At 300 mg/kg, lethargy, flat posture, hunched posture, laboured respiration, gasping, piloerection, chromodacryorrhoea (mouth and nose) and/or ptosis were noted on Days 1 and/or 2.
The mean body weight gain shown by the surviving animals over the study period was considered to be normal.
Abnormalities of the lungs (swollen and several dark red foci) were found in the animal dosed at 300 mg/kg that died during the study, at macroscopic post mortem examination.
Macroscopic post mortem examination of the other animals that died during the study and of the surviving animals at termination did not reveal any abnormalities.
The oral LD50 value of test item in Wistar rats was established to be within the range of 300-2000 mg/kg body weight, the LD50 cut-off value was considered to be 500 mg/kg body weight.
Justification for classification or non-classification
Oral LD50: 300-2000 mg/kg body weight
Therefore in accordance with Regulation (EC) No. 1272/2008 (amended by 286/2011) Table 3.1.1 , this substance should be classified as Category 4.
Specific target organ toxicity-single exposure:
Death: At 2000 mg/kg, two animals were found dead on Day 1 and one animal was found dead on Day 2. At 300 mg/kg, one animal was found dead on Day 2.
Clinical observation: At 2000 mg/kg, lethargy, clonic spasms, lateral recumbency, hunched posture, uncoordinated movements, slow breathing, shallow respiration, piloerection, salivation, watery discharge from both eyes, pale appearance and/or ptosis were noted for all animals on Day 1. At 300 mg/kg, lethargy, flat posture, hunched posture, laboured respiration, gasping, piloerection, chromodacryorrhoea (mouth and nose) and/or ptosis were noted on Days 1 and/or 2.
Macroscopic Findings:Abnormalities of the lungs (swollen and several dark red foci) were found in the animal dosed at 300 mg/kg that died during the study, at macroscopic post mortem examination.
Therefore in accordance with Regulation (EC) No. 1272/2008 Table 3.8.1 and 3.8.2, this substance should be classified as Category 2.
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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