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Diss Factsheets
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EC number: 201-297-1 | CAS number: 80-62-6
- 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
Specific investigations: other studies
Administrative data
- Endpoint:
- specific investigations: other studies
- Type of information:
- experimental study
- Adequacy of study:
- disregarded due to major methodological deficiencies
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- significant methodological deficiencies
- Remarks:
- static inhalation exposure with unclear exposure; extremely high exposure; partially no dose relationship; Chinese publication with English summary
Data source
Reference
- Reference Type:
- publication
- Title:
- Toxic effect of MMA to the reproductive system of male mice
- Author:
- Wang C., Chen X, Cao S.
- Year:
- 2 011
- Bibliographic source:
- Zhiye Yu Jiankang (2011), 27(9), 970-972
Materials and methods
- Principles of method if other than guideline:
- To study the toxic effect of methylmethacrylate (MMA) to reproductive system of the male mammals.Through sperm shape abnormality test of the rats mice and the examinations of the testicular and seminal vesicle's viscera coefficient in the male mice, the experimental data were analyzed by the methods of χ2 test and variance analysis.
- GLP compliance:
- not specified
- Type of method:
- in vivo
- Endpoint addressed:
- toxicity to reproduction / fertility
Test material
- Reference substance name:
- Methyl methacrylate
- EC Number:
- 201-297-1
- EC Name:
- Methyl methacrylate
- Cas Number:
- 80-62-6
- Molecular formula:
- C5H8O2
- IUPAC Name:
- methyl 2-methylprop-2-enoate
- Test material form:
- liquid
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- other: Kunming
- Sex:
- male
Administration / exposure
- Route of administration:
- inhalation: vapour
- Vehicle:
- not specified
- Details on exposure:
- static inhalative exposure in a 50 L chamber
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- 2 h
- Frequency of treatment:
- daily on 5 consecutive days
- Post exposure period:
- 30 days since the 1st treatment
Doses / concentrationsopen allclose all
- Dose / conc.:
- 6.55 mg/L air
- Remarks:
- corresponds to 50% of the LC50
- Dose / conc.:
- 13.1 mg/L air
- Remarks:
- corresponds to 100% of the LC50
- Dose / conc.:
- 26.2 mg/L air
- Remarks:
- corresponds to 200% of the LC50
- No. of animals per sex per dose:
- 5
- Control animals:
- yes
Examinations
- Positive control:
- cyclophosphamide 30 mg/kg administered by intraperitoneal injection
Results and discussion
- Details on results:
- Clinical signs: Severe clinical signs were observed; Low dose = 50% LC50: commotion, fleeing, jumping, grasping at the walls; Mid dose = 100% LC50: decreased movement, hobbling gait or even lateral lying, occasional tumultuous jumping; high dose = 200% LC50: Appearance of fluffy and unclean dorsal hairs, significantly reduced activity, aggregation lateral laying with reduced breathing
Sperm deformity rates were 1.80%, 2.46 and 2.58%, respectively, for the treatment groups and 1.42% in the for negative control group and 3.72% in the positive control group. Medium and high dose groups: the rate of sperm deformity in mice was significantly higher than that in the negative control group, with a uniform difference of (P<0.01); while the sperm deformity rate in mice in the low-dose group compared with the negative control group, the difference was not statistically significant (P>0.05).
Sperm deformities due to MMA are predominantly head deformities.
Testicular organ weight coefficients were comparable to the negative control.
Seminal vesicle gland organ weight coefficient of the high dose group was significantly different to the negative control group (P<0.05).
Applicant's summary and conclusion
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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