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EC number: 295-458-3 | CAS number: 92045-76-6 A complex combination of hydrocarbons obtained from residual oils by solvent crystallisation and treated with hydrogen in the presence of a catalyst. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C25.
- 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:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- Not reported
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: This study was classified as reliable with restrictions. The study is an acceptable, well-documented study report that followedsound scientific principles.
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 996
Materials and methods
- Principles of method if other than guideline:
- The method did not strictly follow the guideline but is deemed appropriate as utilized in this report.
Fischer-344 rats of each sex were fed control diet or diet containing one of 5 waxes for 90 days at a dietary concentration of 2.0%. Extra groups of rats (5 of each sex) were fed control diet or one of the 5 waxes for 90 days followed by exposure to control diet only for an additional 28 or 85 days. These extra groups were used to determine whether effects were reversible. - GLP compliance:
- not specified
Test material
- Reference substance name:
- 8002-74-2, 92045-74-4, 63231-60-7
- IUPAC Name:
- 8002-74-2, 92045-74-4, 63231-60-7
- Reference substance name:
- low melting point wax, paraffin (LMPW)
- IUPAC Name:
- low melting point wax, paraffin (LMPW)
- Reference substance name:
- intermediate and high melting point paraffin wax
- IUPAC Name:
- intermediate and high melting point paraffin wax
- Reference substance name:
- microcrystalline paraffin and hydrocarbon wax
- IUPAC Name:
- microcrystalline paraffin and hydrocarbon wax
- Test material form:
- other: waxy solid
- Details on test material:
- - Name of test material (as cited in study report): low melting point paraffin wax
- Substance type: paraffin wax
- Physical state: solid
- Viscosity at 100°C: 3.3 cSta
- Average molecular weight: 375
-Average carbon number distribution: 19-42
- Name of test material (as cited in study report): 1:1 mix of low melting point wax, paraffin and high melting point wax, microcrystalline
- Substance type: paraffin wax and microcrystalline wax mix
- Physical state: solid
- Viscosity at 100°C: 7.2 cSta
- Average molecular weight: 305
-Average carbon number distribution: 19-72
- Name of test material (as cited in study report): intermediate melting point wax, paraffin
- Substance type: paraffin wax
- Physical state: solid
- Viscosity at 100°C: 6.3 cSta
- Average molecular weight: 450
-Average carbon number distribution: 21-49
- Name of test material (as cited in study report): high sulphur wax
- Substance type: microcrystalline wax
- Physical state: solid
- Viscosity at 100°C: 13.7 cSta
- Average molecular weight: 600
-Average carbon number distribution: 20-74
- Name of test material (as cited in study report): high melting point wax
- Substance type: microcrystalline wax
- Physical state: solid
- Viscosity at 100°C: 15.4 cSta
- Average molecular weight: 630
-Average carbon number distribution: 22-80
The following applies to all five waxes:
- Analytical purity: not provided
- Impurities (identity and concentrations): no provided
- Composition of test material, percentage of components: not provided
- Isomers composition: not provided
- Purity test date: not provided
- Lot/batch No.: not provided
- Expiration date of the lot/batch: not provided
- Stability under test conditions: not provided
- Storage condition of test material: all test materials were stored in the dark at room temperature under an atmosphere of nitrogen
Constituent 1
Constituent 2
Constituent 3
Constituent 4
- Radiolabelling:
- no
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan sprague-dawley, Inc.
- Age at study initiation: 4 weeks
- Weight at study initiation: not provided
- Fasting period before study: no information provided
- Housing: five rats of each sex per cage
- Individual metabolism cages: no
- Diet (e.g. ad libitum): powered diet of rat and mouse no. 1 maintenance diet was provided ad libitum
- Water (e.g. ad libitum): tap water was provided ad libitum
- Acclimation period: seven days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 to 24°C
- Humidity (%): 45 to 70%
- Air changes (per hr): not provided
- Photoperiod (hrs dark / hrs light): 12 hours light and 12 hours dark
IN-LIFE DATES: not provided
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- unchanged (no vehicle)
- Details on exposure:
- PREPARATION OF DOSING SOLUTIONS: test diets of 20,000 ppm were prepared by serial dilution from 10% (100,00 ppm) premix. The samples of wax were solid and were first converted to a sprayed powder by drawing molten wax through an atomizer with a stream of liquid nitrogen.
DIET PREPARATION
- Rate of preparation of diet (frequency): fresh diets were prepared weekly
- Mixing appropriate amounts with (Type of food): rat and mouse No. 1 maintenance diet, Special Diet Services Limited, Witham, Essex
- Storage temperature of food: stored at room temperature and sealed in metal containers prior to use.
VEHICLE
- Justification for use and choice of vehicle (if other than water): none
- Concentration in vehicle: none
- Amount of vehicle (if gavage): none
- Lot/batch no. (if required): none
- Purity: none
HOMOGENEITY AND STABILITY OF TEST MATERIAL: confirmed analytically in study report - Duration and frequency of treatment / exposure:
- Fischer-344 rats were fed control diet or diet containing one of 5 waxes for 90 days followed by exposure to control diet only for an additional 28 to 58 days. These extra groups were used to determine whether effects were reversible.
Doses / concentrations
- Remarks:
- Doses / Concentrations:
Rats were dosed 20,000 ppm of each of five waxes in their diet, equivalent to a dietary concentration of 2.0%.
- No. of animals per sex per dose / concentration:
- five animals per sex per dose
- Control animals:
- yes
- Positive control reference chemical:
- none
- Details on study design:
- - Dose selection rationale: not provided
- Rationale for animal assignment (if not random): random - Details on dosing and sampling:
- PHARMACOKINETIC STUDY (Absorption, distribution, excretion)
- Tissues and body fluids sampled: perirenal fat, kidney, liver, mesenteric lymph nodes, and spleen
- Time and frequency of sampling: not provided
Metabolite characterization studies were not preformed
Results and discussion
Toxicokinetic / pharmacokinetic studies
- Details on distribution in tissues:
- Mineral hydrocarbons (MHC) were found in the livers, mesenteric lymph nodes (MLNs), and perirenal fat of all groups fed waxes; levels in the spleen and kidney were much less and did not exceed 0.1 mg/g tissue. Statistically significant increases of saturated hydrocarbon content in the liver were observed in groups fed waxes (LMPW, MP, and IMPW) except animals fed microcrystalline waxes (HSW and HMPW). Accumulation in the liver was greater in females than males. After a reversal period during which time the animals were fed control diet only, there was a lowering of MHC levels in both sexes with a greater reduction after the 85-day reversal period (80-90% reduction in females for the LMPW, IMPW, and MP waxes; not measured in males). The MLNs contained statistically significant increases of mineral hydrocarbons in the same treatment groups as for the liver. The MHC content in the MLNs was higher in females than males. There was little indication of any reduction in MHC of the MLNs after the 28-day reversal period. Data were not available for the 85 day-reversal groups. In samples of perirenal fat, the MHC content was increased to a similar extent in males and females fed LMPW. Although there was some evidence of a reduction in MHC levels after a 28-day reversal period, elevated levels nevertheless still remained.
Applicant's summary and conclusion
- Conclusions:
- MHCs were found in the livers, mesenteric lymph nodes (MLNs), and perirenal fat of all groups fed waxes; levels in the spleen and kidney were much less and did not exceed 0.1 mg/g tissue. Statistically significant increases of saturated hydrocarbon content in the liver were observed in groups fed waxes (LMPW, MP, and IMPW) except animals fed microcrystalline waxes (HSW and HMPW). Accumulation in the liver was greater in females than males. After a reversal period during which time the animals were fed control diet only, there was a lowering of MHC levels in both sexes with a greater reduction after the 85-day reversal period (80-90% reduction in females for the LMPW, IMPW, and MP waxes; not measured in males). The MLNs contained statistically significant increases of mineral hydrocarbons in the same treatment groups as for the liver. The MHC content in the MLNs was higher in females than males. There was little indication of any reduction in MHC of the MLNs after the 28-day reversal period. Data were not available for the 85 day-reversal groups. In samples of perirenal fat, the MHC content was increased to a similar extent in males and females fedLMPW. Although there was some evidence of a reduction in MHC levels after a 28-day reversal period, elevated levels nevertheless still remained.
- Executive summary:
- In a toxicokinetic study, five Fischer-344 rats of each sex were fed control diet or diet containing one of five microcrystalline or paraffin waxes (LMPW, HMPW, MP, HSW, IMPW) for 90 days at a dietary concentration of 2.0% or 20,000 ppm. Extra groups of rats (five of each sex) were fed control diet or one of the 5 waxes for 90 days followed by exposure to control diet only for an additional 28 or 85 days. These extra groups were used to determine whether effects were reversible.
MHCs were found in the livers, mesenteric lymph nodes (MLNs), and perirenal fat of all groups fed waxes; levels in the spleen and kidney were much less and did not exceed 0.1 mg/g tissue. Statistically significant increases of saturated hydrocarbon content in the liver were observed in groups fed waxes (LMPW, MP, and IMPW) except animals fed microcrystalline waxes (HSW and HMPW). Accumulation in the liver was greater in females than males. After a reversal period during which time the animals were fed control diet only, there was a lowering of MHC levels in both sexes with a greater reduction after the 85-day reversal period (80-90% reduction in females for the LMPW, IMPW, and MP waxes; not measured in males). The MLNs contained statistically significant increases of mineral hydrocarbons in the same treatment groups as for the liver. The MHC content in the MLNs was higher in females than males. There was little indication of any reduction in MHC of the MLNs after the 28-day reversal period. Data were not available for the 85 day-reversal groups. In samples of perirenal fat, the MHC content was increased to a similar extent in males and females fedLMPW. Although there was some evidence of a reduction in MHC levels after a 28-day reversal period, elevated levels nevertheless still remained.
This study received a Klimisch score of 2 and is classified as reliable with restrictions.
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