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Diss Factsheets
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EC number: 204-289-6 | CAS number: 118-96-7
- 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
Endpoint summary
Administrative data
Link to relevant study record(s)
- Endpoint:
- basic toxicokinetics
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1 Apr 1974 - 31 May 1975
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Objective of study:
- absorption
- metabolism
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 417 (Toxicokinetics)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.36 (Toxicokinetics)
- GLP compliance:
- no
- Remarks:
- no (The study was conducted in 1975 whereas OECD and EU Guidelines as well as GLP Principles were implemented in 1981 and 1988)
- Radiolabelling:
- yes
- Remarks:
- 14C-labeled nitrotoluenes
- Species:
- rat
- Strain:
- other: Charles River CD
- Sex:
- female
- Route of administration:
- oral: gavage
- Vehicle:
- peanut oil
- Duration and frequency of treatment / exposure:
- 24 hours/ administered once
- Remarks:
- Doses / Concentrations:
test material suspended in peanut oil was administered in volume of 1 ml/100g bw (approx. 1/10 of the LD50) - Control animals:
- not specified
- Details on absorption:
- The nitrotoluenes were readily absorbed after oral administration in the rat. The absorption was essentially completed in 24 hours with approximately 60 to 90% of the aministered doses. The extents of absorption were in the fillowing order: 2,4-DNT, 3,4-DNT > TNT, 2,5-DNT > 2,3-DNT, 2,6-DNT.
- Details on distribution in tissues:
- The liver and kidney contained small but significant amounts of radioactivity. Very small amounts of radioactivity were also found in the other tissue including brain, lungs, skeletal muscle, and/or spleen.The tissue to plasma radioactivity ratios indicated that the nitrotoluenesand/or their metabolites were, in general, readily taken into most tissues.
- Details on excretion:
- Most of the absorbed radioactivity from oral administration of nitrotoluenes were excreted in the urine. It indicated that these compounts were extensively metabolised in the body since nitrotoluenes are water insoluble. The aromatic ring of these nitrotoluenes remained intact.
- Details on metabolites:
- TLC analysis of the urine from treated rats indicated that the nitrotoluenes were metabolised extensively. Unchanged parent compunds were not present in the urine.The urinary metabolites consisted of one or two classes of polar metabolites. TLC analysis of brain extracts from TNT treated rats revealed a radioactive nonpolar metabolite. However this did not correspond to TNT.
- Conclusions:
- Interpretation of results: low bioaccumulation potential based on study results.
The absorption in 24 hours is 60 to 90% of the aministered doses. Nitrotoluenes are extensively metabolised in the body since they are water insoluble
Reference
Description of key information
The absorption in 24 hours is 60 to 90% of the aministered doses. Nitrotoluenes are extensively metabolised in the body since they are water insoluble.
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
- Absorption rate - oral (%):
- 60
Additional information
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