Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 202-377-9 | CAS number: 94-96-2
- 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 microorganisms
Administrative data
Link to relevant study record(s)
Description of key information
The initial test substance concentration of 31.2 mg/L (20.5 mg/L DOC/L) used in the 28- day ready biodegradability study can be considered a presumptive No Observed Effects Concentration (NOEC) since it resulted in ready biodegradability (93% degradation at 28 d but failing the 10-day window) of the test substance in contact with microorganisms from a composite of domestic effluent, river water and soil.
Key value for chemical safety assessment
- EC10 or NOEC for microorganisms:
- 31.2 mg/L
Additional information
The results of a 28 day ready biodegradability test, performed on the test material, 2-Ethyl -1,3-Hexanediol at the Environmental Sciences Section Health and Environment Laboratories of Eastman Kodak Company, Rochester, New York (Watson, 1989) according to the OECD Guideline 301E, EEC/Annex V Guideline C.3 and U.S. EPA/TSCA 40 CFR Section 796.3240 can be used to identify a No Observed Adverse Effect Concentration (NOEC) for microorganisms in water. The test inoculum used in the study was a mixture of secondary effluent from domestic wastewater from the Van Lare Waste Treatment Plant, water from the Genesee River, and garden soil from Monroe County. The biodegradation of the test material was determined by measurement of the loss of dissolved organic carbon (DOC) from the test chemical solution. The test material in Test flask A was readily biodegradable (93% degradation at d 27) but failed the 10-day window requirement according to the definitions of OECD Guideline 301E. The test material in Test flask B showed evidence of rapid biodegradability in an enhanced biodegradability test (74% degradation at d 42) after inoculation with acclimated test organisms from Test flask A. The initial test substance concentration of 31.2 mg/L (20.5 mg DOC/L) used in the 28-day ready biodegradability study can be considered a presumptive NOEC since it resulted in ready biodegradability (93% degradation at 28 d but failing the 10 day window).
In a supporting study entitled “ Secondary Waste Treatment Compatibility of 2 -Ethyl-1,3-hexanediol: (Watson, 1989), nominal concentrations of the test chemical of 0.1 mg/L, 1 mg/L, 10 mg/L, 100 mg/L and 1,000 mg/L had no significant effect on glucose metabolism in a test with domestic sewage sludge. The study concluded that the test chemical is not expected to affect secondary waste treatment microorganisms adversely at concentrations of less than or equal to 1,000 mg/L. Therefore, the value of 1,000 mg/L is the no observed adverse effect (NOEC) level as determined by the supporting study. However, since ECHA Guidance states that glucose breakdown is not relevant for a sewage biodegradation study, the information from this supporting study is not relied upon for the final NOEC selected.
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.