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Diss Factsheets
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EC number: 201-100-9 | CAS number: 78-27-3
- 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
Toxicity to other aquatic organisms
Administrative data
- Endpoint:
- toxicity to other aquatic vertebrates
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Well documented publication
Data source
Reference
- Reference Type:
- publication
- Title:
- Comparative Developmental Toxicity of Acetylenic Alcohols on Embryos and Larvae of Xenopus laevis
- Author:
- Dawson D.A., Schultz T.W., Baker L.L., Wilke T.S.
- Year:
- 1 990
- Bibliographic source:
- ASTM Special Tech Publ. Vol. 1096, 1990, p. 267-277
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Xenopus laevis embryos and larvae were tested to assess the relative toxicity and teratogenicity of a series of 14 aetyknic alcohols. Tertiary propargylic alcohols and alkene-ols were expected to act as simple narcotics and not be teratogenic. However, primary and secondary propargylic and homopropargylic alcohols might be metabolically activated, by alcohol dehydrogenase, to become teratogenic Mid-to-late blastula stage embryos were exposed to graded concentrations of each alcohol for 96 h. Embryo malformation (fmECw) and lethality (EmLCw) endpoints were determined for each alcohol, and the Mortality/Malformation Index (MMI) was calculated as a measure of relative tetatogenic potential. Additionally, untreated, healthy-appearing 5-day-old tadpoles were exposed to each alcohol for 96 h, and the tadpole lethality endpoint (TdLCm) was determined. The ratio of the embryo LCw to tadpole LCn (E/T) was calculated as a measure of aloohol reactivity. The primary propargylic alcohols had teratogenic potential, producing head, eye, gut, and skeletal malformations and MMI values > 3 .0. All other alcohols caused only edema and improper gut coiling.The E/T ratios indicated that primary and secondary propargylic and homopropargylic alcohols were reactive, whereas tertiary propargylic alcohols and alkene-ols were not. In addition, quantitative strucure-activity relationships (QSARs) were explored, and comparisons of tadpole and fathead minnow lethality data indicated that toxicity in one system can be used to predict toxicity in the other.
- GLP compliance:
- no
Test material
- Reference substance name:
- 1-ethynylcyclohexanol
- EC Number:
- 201-100-9
- EC Name:
- 1-ethynylcyclohexanol
- Cas Number:
- 78-27-3
- Molecular formula:
- C8H12O
- IUPAC Name:
- 1-ethynylcyclohexanol
- Details on test material:
- Purity: >= 95 %
Constituent 1
Test organisms
- Test organisms (species):
- Xenopus laevis
Study design
- Total exposure duration:
- 96 h
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 5.41 mmol/L
- Basis for effect:
- mortality
- Remarks on result:
- other: Embryo mortality
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Effect conc.:
- 1.55 mmol/L
- Basis for effect:
- other: Teratogenetic effects on Embryos
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 1.8 mmol/L
- Basis for effect:
- mortality
- Remarks on result:
- other: Tadpole mortality
Any other information on results incl. tables
The lowest effect value of 1.55 mmol/L for teratogenic effect on tadpole embryos was recalculated by use of the substances mol weight into an effect concentration of 192.48 mg/L
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.