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EC number: 218-267-9 | CAS number: 2100-42-7
- 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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1976-10-13 to 1976-10-27
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: Insufficient description of effect doses.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 977
- Report date:
- 1977
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: company guideline
- Deviations:
- not applicable
- Principles of method if other than guideline:
- Acute inhalation toxicity of the liquid test substance was tested in the inhalation risk assay. Six male SPF-Wistar-rats served as testing animals. The mean body weight was 121g (ranging from 115-124g). Exposure takes place at a room temperature of 23.3°C and a barometric pressure of 738.4Torr. Animal were placed in a glass vessel of 39L and exposed to the generated mixture of air and the gaseous substance. The exposure time was 8hrs.
On order to generate a mixture of air and the gaseous test substance the testing compound was transferred into a gas wash bottle equipped with a glass frit. Before and after testing the bottle was weighed. Using a rotameter the airflow through the gas wash bottle was adjusted to 400L per h.
During inhalation and 14d thereafter the behaviour of the test animals was observed. During this time the body weight was determined on a daily basis. Within the observation period access to food (Altromin 1324, Company Altromin GmbH, Lage/Lippe) and tap water was ad libitum. Housing of the rats were plastic cages filled with wood shavings. At the end of the observation period all animals were euthanised after narcotization, and than dissected and macroscopically evaluated. - GLP compliance:
- no
- Remarks:
- - Performed prior to GLP implementation
- Test type:
- other: inhalation risk assay
- Limit test:
- yes
Test material
- Reference substance name:
- 1-chloro-2,5-dimethoxybenzene
- EC Number:
- 218-267-9
- EC Name:
- 1-chloro-2,5-dimethoxybenzene
- Cas Number:
- 2100-42-7
- Molecular formula:
- C8H9ClO2
- IUPAC Name:
- 2-chloro-1,4-dimethoxybenzene
- Details on test material:
- - Name of test material (as cited in study report): CME = Chlorhydrochinondimethyläther (2-Chlor-1,4-dimethoxybenzol)
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- - Ambient temperature: 23.3°C
- Barometric pressure: 738,4 Torr
- Housing: Plastic cages filled with wood shavings
- Food and tap water: ad libitum, food (ALtromina 1324) supplier: Altromina GmbH, Lage/Lippe
- Mean body weight: 121g, ranging from 115-124g
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: air
- Details on inhalation exposure:
- - Exposure time was one time for 8hrs
- The testing compound was transferred to a gas wash bottle equipped with a glass frit
- Before and after testing the bottle was weighed
- Using a rotameter the airflow was adjusted to 400L per h
- During inhalation and 14d thereafter behaviour of the test animals was observed - Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- gravimetric determination of the substance mass spent for generation of exposure atmosphere
- Duration of exposure:
- 8 h
- Concentrations:
- see table 1
- No. of animals per sex per dose:
- 6 male Wistar-rats
- Control animals:
- no
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- discriminating conc.
- Effect level:
- ca. 600 other: mg of gaseous test substance within 8hrs of exposure. Air flow was 400L per h of a mixture of air and the gaseous test substance. Volume of the exposure chamber (galss veesel) was 39L.
- Exp. duration:
- 8 h
- Remarks on result:
- other: No lethality
- Mortality:
- none
- Clinical signs:
- other: - 3mins after beginn of exposure: restlessness - 6mins after beginn of exposure: increased breathing rate, prone position - 36mins after beginn exposure: closed eyes, squatting posture, increased breathing rate - 1d after treatment: slightly increase bre
- Body weight:
- normal body weight gain
- Gross pathology:
- dirty red coloured lungs
Applicant's summary and conclusion
- Interpretation of results:
- other: Not classified. Insufficient description of effect doses. No relevant data that can be compared to classification criteria.
- Remarks:
- Criteria used for interpretation of results: expert judgment
- Conclusions:
- No lethality at the concentration tested.
- Executive summary:
In the present inhalation toxicity study all animals survived a single 8hrs exposure to CME. During inhalation the following symptoms were observed: restlessness, increased breathing rate, closed eyes. Dissection revealed a dirty red coloration of the lung.
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