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Diss Factsheets
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EC number: 700-762-0 | CAS number: -
- 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
Hydrolysis
Administrative data
- Endpoint:
- hydrolysis
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Data are from a peer reviewed source.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
Cross-reference
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- hydrolysis
- Type of information:
- other: Technical Discussion
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Data are from a peer reviewed source.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in IUCLID Section 13.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Principles of method if other than guideline:
- Technical discussion
- GLP compliance:
- not specified
- Conclusions:
- Hydrolysis is not expected to be a significant mechanism of degradation in the environment because hydrocarbons, C14-20 Aliphatics (≤2% aromatics) lack a hydrotically reactive functional group. Therefore, hydrocarbons are not subject to hydrolysis and this fate process will not contribute to the degradative loss of the substance from the environment.
- Executive summary:
Hydrolysis is a reaction in which a water molecule of hydroxide ion substitutes for another atom of group of atoms present in a chemical resulting in a structural change of that chemical. Potentially hydrolysable groups include alkyl halides, amides, carbamates, carboxylic acid esters and lactone epoxides, phosphate esters, and sulfonic acid esters. The lack of a suitable leaving group renders compounds resistant to hydrolysis.
The chemical constituents that comprise hydrocarbons, C14-20 Aliphatics (≤2% aromatics) consist entirely of carbon and hydrogen and do not contain hydrolysable groups. As such, they have a very low potential to hydrolyze. Therefore this degradative process will not contribute to their removal from the environment.
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Hydrolysis
- Author:
- Neely, W.B.
- Year:
- 1 985
- Bibliographic source:
- In: Environmental exposure from chemicals" (Neely, W.B. & Blau, G.E., Eds), Vol. I, Academic Press, Boca Raton, FL, USA: 157-173
- Reference Type:
- other: Handbook
- Title:
- Chapter 8. Rate of Aqueous Photolysis.
- Author:
- Harris
- Year:
- 1 982
- Bibliographic source:
- In: Handbook of Chemical Property Estimation Methods. W. J. Lyman, W. F. Reehl and D. H. Rosenblatt, eds. McGraw-Hill Book Company, New York, USA.
- Reference Type:
- publication
- Title:
- No information
- Author:
- Gould
- Year:
- 1 959
Materials and methods
- Principles of method if other than guideline:
- Technical discussion
- GLP compliance:
- not specified
Test material
- Reference substance name:
- C14-16 (even numbered) and C16 (branched) saturated and unsaturated aliphatic hydrocarbons
- EC Number:
- 700-762-0
- Molecular formula:
- All molecules present in the mixture have the general molecular formula CnH2n for olefins or CnH2n+2 for the paraffin’s with n being an even number
- IUPAC Name:
- C14-16 (even numbered) and C16 (branched) saturated and unsaturated aliphatic hydrocarbons
- Test material form:
- liquid: viscous
Constituent 1
Results and discussion
Applicant's summary and conclusion
- Conclusions:
- Hydrolysis is not expected to be a significant mechanism of degradation in the environment because hydrocarbons, C14-20 Aliphatics (≤2% aromatics) lack a hydrotically reactive functional group. Therefore, hydrocarbons are not subject to hydrolysis and this fate process will not contribute to the degradative loss of the substance from the environment.
- Executive summary:
Hydrolysis is a reaction in which a water molecule of hydroxide ion substitutes for another atom of group of atoms present in a chemical resulting in a structural change of that chemical. Potentially hydrolysable groups include alkyl halides, amides, carbamates, carboxylic acid esters and lactone epoxides, phosphate esters, and sulfonic acid esters. The lack of a suitable leaving group renders compounds resistant to hydrolysis.
The chemical constituents that comprise hydrocarbons, C14-20 Aliphatics (≤2% aromatics) consist entirely of carbon and hydrogen and do not contain hydrolysable groups. As such, they have a very low potential to hydrolyze. Therefore this degradative process will not contribute to their removal from the environment.
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.