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EC number: 700-618-7 | CAS number: 39202-17-0
- 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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- weight of evidence
- Study period:
- not applicable
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The metabolism of fatty acids and their methyl esters are well documented in the scientific literature
Data source
Reference
- Reference Type:
- grey literature
- Title:
- Summary of fatty acid methyl ester metabolism
- Author:
- Strother DE
- Year:
- 2 013
- Bibliographic source:
- unpublished
Materials and methods
- Principles of method if other than guideline:
- Summary of fatty acid methyl ester metabolism
Test material
- Reference substance name:
- methyl dodec-9-enoate
- EC Number:
- 700-618-7
- Cas Number:
- 39202-17-0
- Molecular formula:
- C13H24O2
- IUPAC Name:
- methyl dodec-9-enoate
Constituent 1
Results and discussion
Any other information on results incl. tables
Metabolism of short chain fatty acid methyl esters
Hydrolysis
Esters of methanol and fatty acids have a common metabolic fate that begins with hydrolysis (both enzymatic and non-enzymatic), resulting in the carboxylic (e.g. fatty) acids and methanol.
Metabolism of methanol
Methanol is polar/hydrophilic (log P < -0.5) and thus distributed in the aqueous compartments of the organism. However, direct urinary excretion is known to be low (<3% in humans); unchanged methanol is excreted to some extent via exhalation.
Predominating is the metabolism of methanol: initially, methanol is slowly oxidized by the enzyme alcohol dehydrogenase to formaldehyde, which itself is oxidized very rapidly by the aldehyde dehydrogenase and other enzymes to formic acid. Finally, formic acid is metabolized to CO2 and H2O by means of a folate-dependent one-carbon pool pathway. The rate of formate oxidation is regulated by the hepatic concentrations of tetrahydrofolate. CO2and H2O are excreted via exhalation and urinary excretion; urinary excretion of formaldehyde and formic acid is possible to a limited extent.
The rate of methanol metabolism is independent of the plasma concentration, is slow, and is approximately one-seventh that of ethanol. Complete oxidation and excretion of methanol can require several days.
Metabolism of fatty acids
Fatty acids are an important source of energy and adenosine triphosphate (ATP) for many cellular organisms. Linear fatty acids feed into physiological pathways like the citric acid cycle, sugar synthesis, and lipid synthesis. The metabolic pathway of unsaturated fatty acids differs from that of saturated fatty acids in that it contains an additional step for rearrangement of the double bond (isomerisation cis → trans) leading to the correct trans-intermediate for β-Oxidation.
Fatty acid metabolism involves three major steps:
1. Fatty acids are transported across the outer mitochondrial membrane by carnitine-palmitoyl transferase I (CPT-I), and then couriered across the inner mitochondrial membrane by carnitine. Once inside the mitochondrial matrix, the fatty acyl-carnitine reacts with coenzyme A to release the fatty acid and produce acetyl-CoA. CPT-I is believed to be the rate-limiting step in fatty acid oxidation.
2. Once inside the mitochondrial matrix, fatty acids undergo β-oxidation. During this process, two-carbon molecules acetyl-CoA are repeatedly cleaved from the fatty acid. Acetyl-CoA can then enter the citric acid cycle, which produces NADH and FADH2. NADH and FADH2 are subsequently used in the electron transport chain to produce ATP, the energy currency of the cell.
3. Besides β-oxidation, other oxidative pathways are sometimes employed. The smooth ER of the liver can perform ω-oxidation, which is primarily for detoxification but can become much more prevalent in cases of defective β-oxidation. Fatty acids with very long chains (20 or more carbons) are first broken down to a manageable size in peroxisomes.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): no bioaccumulation potential based on study results
- Executive summary:
9-dodecenoic acid, methyl ester is a fatty acid methyl ester. Metabolism of fatty acid methyl esters begins with hydrolysis of the ester, resulting in the carboxylic (e.g. fatty) acids and methanol. Methanol is oxidized to formaldehyde, which itself is oxidized to formic acid. Finally, formic acid is metabolized to CO2and H2O. Fatty acids are an important source of energy and adenosine triphosphate (ATP) for many cellular organisms. Fatty acids undergo β-oxidation, and the products enter physiological pathways like the citric acid cycle, sugar synthesis, and lipid synthesis.
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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