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EC number: 243-814-3 | CAS number: 20427-58-1
- 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

Genetic toxicity: in vivo
Administrative data
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- data not available
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
- Remarks:
- Used in EU risk assessment report for zinc metal.
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
- GLP compliance:
- not specified
- Remarks:
- information on GLP not available
- Type of assay:
- mammalian erythrocyte micronucleus test
Test material
- Reference substance name:
- 87189-24-0
- Cas Number:
- 87189-24-0
- IUPAC Name:
- 87189-24-0
- Reference substance name:
- zinc monoglycerolate
- IUPAC Name:
- zinc monoglycerolate
- Test material form:
- other: data not available
- Details on test material:
- - Name of test material (as cited in study report): zinc monoglycerolate
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- data not available
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- data not available
- Duration of treatment / exposure:
- 13 weeks
- Frequency of treatment:
- continous
- Post exposure period:
- data not available
Doses / concentrationsopen allclose all
- Dose / conc.:
- 0.05 other: %
- Dose / conc.:
- 0.2 other: %
- Dose / conc.:
- 1 other: %
- No. of animals per sex per dose:
- data not available
- Control animals:
- yes
- Positive control(s):
- data not available
Examinations
- Tissues and cell types examined:
- Bone marrow cells examined for all types of chromosome and chromatid-type aberrations and hyperdiploid cells.
- Details of tissue and slide preparation:
- data not available
- Evaluation criteria:
- data not available
- Statistics:
- data not available
Results and discussion
Test results
- Sex:
- not specified
- Vehicle controls validity:
- not specified
- Negative controls validity:
- not specified
- Positive controls validity:
- not specified
- Remarks on result:
- not determinable
- Additional information on results:
- - Zinc monoglycerolate was negative in this assay.
Applicant's summary and conclusion
- Conclusions:
- The information summarised in this study record was taken from the EU Risk Assessment report for zinc (EU RAR 2004) where it has been thoroughly reviewed. Due to the unavailability of the primary reference, the study was rated with reliability 4 for formal reasons. However, the results of this study will be used in the hazard assessment of the zinc category substances in a weight of evidence approach.
In a micronucleus study (Windebank et al., 1995) comparable to OECD guideline study 474, rats were fed 0.05, 0.2 and 1% zinc monoglycerolate in a purified diet. Zinc monoglycerolate was negative in this assay.
No conclusion can be drawn due to the insufficient documentation.
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