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Diss Factsheets
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EC number: 200-624-5 | CAS number: 66-25-1
- 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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics in vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 993
Materials and methods
- Objective of study:
- distribution
- excretion
- toxicokinetics
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- - Short description of test conditions:
n-Hexanal was dissolved in physiological saline containing 1 % bovine serum albumin and administered to mice at a dose of 6.8 µmol/10g body weight by i.v. injection into the tail vein. Mice administered the aldehyde were dissected under ether anesthesia at 0, 5, 10, 30, 60, and 120 min after the treatments. Blood was drawn from the heart and the plasma was prepared by centrifugation.
- Parameters analysed / observed: The content of n-hexanal in the plasma and liver and lung homogenates was determined. - GLP compliance:
- no
Test material
- Reference substance name:
- Hexanal
- EC Number:
- 200-624-5
- EC Name:
- Hexanal
- Cas Number:
- 66-25-1
- Molecular formula:
- C6H12O
- IUPAC Name:
- hexanal
- Test material form:
- liquid
- Details on test material:
- purchased from Wako Pure Chemicals
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- mouse
- Strain:
- other: ddY
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Clea Japan Inc.
- Age at study initiation: 6 weeks
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
Administration / exposure
- Route of administration:
- intravenous
- Vehicle:
- physiological saline
- Remarks:
- containing 1 % bovine serum albumin
- Details on exposure:
- n-Hexanal was dissolved in physiological saline containing 1 % bovine serum albumin and administered to mice at a dose of 6.8 µmol/10g body weight by i.v. injection into the tail vein.
- Duration and frequency of treatment / exposure:
- once
Doses / concentrations
- Dose / conc.:
- 6.8 other: µmol/10 g bw
- No. of animals per sex per dose / concentration:
- not specified
- Control animals:
- yes
- Positive control reference chemical:
- no
- Details on study design:
- no details given
- Details on dosing and sampling:
- TOXICOKINETIC / PHARMACOKINETIC STUDY (Absorption, distribution, excretion)
- Tissues and body fluids sampled (delete / add / specify): blood, plasma, liver, lung
- Time and frequency of sampling: 0, 5, 10, 30, 60 and 120 min after treatment
Results and discussion
Main ADME resultsopen allclose all
- Type:
- distribution
- Results:
- After injection n-hexanal is transported to the lung and the liver.
- Type:
- excretion
- Results:
- It is thought that n-hexanal could be either metabolized by the enzymes and/or transferred into the lung as such and excreted into expired gas easily.
Toxicokinetic / pharmacokinetic studies
- Details on absorption:
- not examined
- Details on distribution in tissues:
- After the injection of n-hexanal, the plasma content reached to ca. 500 nmol/ml at 5 min and decreased to less than half at 10 min. In the lung, the content of n-hexanal increased immediately and reached ca. 150 nmol/g in 30 min. From the mean of lung weight being ca. 0.17 g, the amount of n-hexanal in whole lung was ca. 26 nmol. This value corresponded to ca. 0.080 % of the whole injected aldehyde. After 30 min, the content of n-hexanal decreased significantly. The amount of n-hexanal at 120 min was ca. 20 % of that seen at 30 min. In the liver, the content of n-hexanal increased slightly 10 min after the injection. The content at 30 min decreased to the level of the untreated group.
- Details on excretion:
- It is thought that n-hexanal could be either metabolized by the enzymes and/or transferred into the lung as such and excreted into expired gas easily.
Metabolite characterisation studies
- Metabolites identified:
- not measured
Any other information on results incl. tables
no effect on the activities of GSH-Px and GSSGR and the content of GSH was observed
Applicant's summary and conclusion
- Conclusions:
- After the injection of n-hexanal, the plasma content reached to ca. 500 nmol/ml at 5 min and decreased to less than half at 10 min. In the lung, the content of n-hexanal increased immediately and reached ca. 150 nmol/g in 30 min. From the mean of lung weight being ca. 0.17 g, the amount of n-hexanal in whole lung was ca. 26 nmol. This value corresponded to ca. 0.080 % of the whole injected aldehyde. After 30 min, the content of n-hexanal decreased significantly. The amount of n-hexanal at 120 min was ca. 20 % of that seen at 30 min. In the liver, the content of n-hexanal increased slightly 10 min after the injection. The content at 30 min decreased to the level of the untreated group. It is thought that n-hexanal could be either metabolized by the enzymes and/or transferred into the lung as such and excreted into expired gas easily.
- Executive summary:
n-Hexanal was dissolved in physiological saline containing 1 % bovine serum albumin and administered to mice at a dose of 6.8 µmol/10g body weight by i.v. injection into the tail vein. Mice administered the aldehyde were dissected under ether anesthesia at 0, 5, 10, 30, 60, and 120 min after the treatments. Blood was drawn from the heart and the plasma was prepared by centrifugation. The content of n-hexanal in the plasma and liver and lung homogenates was determined. After the injection of n-hexanal, the plasma content reached to ca. 500 nmol/ml at 5 min and decreased to less than half at 10 min. In the lung, the content of n-hexanal increased immediately and reached ca. 150 nmol/g in 30 min. From the mean of lung weight being ca. 0.17 g, the amount of n-hexanal in whole lung was ca. 26 nmol. This value corresponded to ca. 0.080 % of the whole injected aldehyde. After 30 min, the content of n-hexanal decreased significantly. The amount of n-hexanal at 120 min was ca. 20 % of that seen at 30 min. In the liver, the content of n-hexanal increased slightly 10 min after the injection. The content at 30 min decreased to the level of the untreated group. It is thought that n-hexanal could be either metabolized by the enzymes and/or transferred into the lung as such and excreted into expired gas easily.
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