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EC number: 442-080-3 | 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
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- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
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- 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

Carcinogenicity
Administrative data
- Endpoint:
- carcinogenicity: oral
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Study period:
- From August 1978 to September 1980
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Test procedure is not following a guideline, nevertheless the report is scientifically acceptable. Justification for read across approach is explained in the endpoint summary of repeated dose/reproductive toxicity.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 984
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 983
Materials and methods
- Principles of method if other than guideline:
- test item was administered in the diet to F344 rats for 103 weeks (chronic) to determine its carcinogenic potential. The dose levels were 2250 or 4500 ppm for male rats and 4500 or 9000 ppm for female rats.
- GLP compliance:
- not specified
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Breeding Laboratories, Portage, MI.
- Age at study initiation: 6 weeks old.
- Housing: five per Polycarbonate cage, changed twice per week.
- Bedding: Absorb-Dri@ hardwood chips (Lab Products, Inc.); changed twice per week.
- Diet: ad libitum, Purina Laboratory Chow.
- Water: ad libitum, acidified with hydrochloric acid to pH 2.5.
- Acclimation period: approximately 2 weeks before the test began.
ENVIRONMENTAL CONDITIONS
- Temperature: 22 - 26 °C
- Humidity: 30 - 70 %
- Air changes: 12-1 5 times per hour
- Photoperiod: 12 hours of fluorescent light per day
Administration / exposure
- Route of administration:
- oral: feed
- Details on exposure:
- DIET PREPARATION
- Preparation: test diets were prepared by first mixing a small amount of PurinaB Lab Chow and the required amount of test item with a mortar and pestle and then adding this premix to the required amount of animal meal and mixing for 10 to 30 minutes in a Patterson-Kelly@ twin- shell blender equipped with an intensifier bar.
- Maximum Storage Time: 3 weeks
- Storage Conditions: -20 °C
- Analysis: dosed feed samples were analyzed periodically by ultraviolet spectroscopy. The results obtained indicate that only one of the formulations analyzed was slightly (+10.6 %) out of specifications (> ± 10 %). Results from three separate standard analyses at MRI verified the accuracy of the formulations. - Duration of treatment / exposure:
- 103 weeks
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
Female rats: 0, 4500 and 9000 ppm
Basis:
nominal in diet
- Remarks:
- Doses / Concentrations:
Male rats: 0, 2250 and 4500 ppm
Basis:
nominal in diet
- No. of animals per sex per dose:
- 50 males and 50 females, except for only 49 control male rats
- Control animals:
- yes, plain diet
Examinations
- Observations and examinations performed and frequency:
- DETAILED CLINICAL OBSERVATION
Observed twice daily for mortality and signs of morbidity.
Clinical signs were recorded monthly.
BODY WEIGHT
Body weight data collected weekly for the first 13 weeks, monthly until week 91, and every 2 weeks thereafter.
FOOD CONSUMPTION AND COMPOUND INTAKE
Feed consumption data collected every 4 weeks. - Sacrifice and pathology:
- All animals necropsied and examined histologically.
GROSS PATHOLOGY: Yes.
Tissues examined: gross lesions, skin (with mammary gland), mandibular lymph nodes, salivary gland, sternum (with bone marrow), larynx or anterior trachea, oesophagus, thyroid, parathyroid, lungs with mainstream bronchi, heart, stomach (glandular and nonglandular), duodenum, large intestine, liver, pancreas, spleen, kidneys, adrenal glands, urinary bladder, gonads, prostate or uterus, brain, and pituitary.
Tissue preservation: tissues were preserved in 10 % neutral buffered formalin embedded in paraffin, sectioned, and stained with haematoxylin and eosin.
HISTOPATHOLOGY: Yes - Statistics:
- Statistical analyses for a possible dose-related effect on survival used the method of Cox (1972) for testing two groups for equality and Tarone's (1975) extensions of Cox's meth ods for testing for a dose-related trend.
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Description (incidence and severity):
- no compound-related clinical signs were observed
- Mortality:
- no mortality observed
- Description (incidence):
- no compound-related clinical signs were observed
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- after week 20 lower than those of the controls
- Food consumption and compound intake (if feeding study):
- no effects observed
- Description (incidence and severity):
- 97 % and 99 % that of the controls for males and 99 % and 99 % for females
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- statistically significant between bladder stones and bladder tumours in male
- Histopathological findings: neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- transitional-cell carcinomas in the urinary bladder of males
- Details on results:
- CLINICAL SIGNS AND MORTALITY
Survival of high-dose male rats was significantly lower (P < 0.05) than that of the controls. Survival of all other dosed rat groups was comparable with that of the respective controls.
No compound-related clinical signs were observed.
BODY WEIGHT AND WEIGHT GAIN
After week 20, mean body weights of dosed rats of each sex were lower than those of the controls.
FOOD CONSUMPTION AND COMPOUND INTAKE
The average daily feed consumption per rat by low-and high-dose rats was 97 % and 99 % that of the controls for males and 99 % and 99 % for females.
HISTOPATHOLOGY: NEOPLASTIC
Urinary Bladder: transitional-cell carcinomas in the urinary bladder of male rats occurred with a statistically significant (P ≤ 0.002) positive trend (controls, 0/45; low-dose, 0/50; high- dose, 8/49, 16 %) and the incidence in the high-dose group was significantly higher (P ≤ 0.016) than that in the controls. The combined incidence of transitional-cell carcinomas and papillomas showed a statistically significant (P < 0.001) positive trend (controls, 0/45; low-dose, 0/50; high-dose, 9/49, 18 %) and the incidence in high dose rats was significantly higher (P ≤ 0.008) than that in the controls. These tumours were not observed in statistically significant proportions in female rats (0/49, 1/49, 1/47).
The transitional-cell carcinomas were visualized grossly as 1- to 1.5-cm masses attached to the mucosal surface of the urinary bladder. Seven of the eight high-dose male rats with transitional-cell carcinomas also had bladder stones (calculi). Microscopically, most of the carcinomas had transitional-like cells that formed protrusions into the bladder lumens. Some had papillary areas. The carcinomas had moderate numbers of mitoses and some nuclear pleomorphism. Discrete invasions through the bladder wall occurred in one male rat, but no metastases were evident in the lungs or other tissues.
Kidney: chronic inflammation was observed in significantly (P ≤ 0.01) increased incidence in dosed female rats . The dose relationship and intensity of the increased interstitial lymphoplasmocytic infiltrates and cortical fibrosis clearly set these changes apart from the minor inflammatory component that may accompany the progressive nephropathy normally encountered in aging rats. The changes in the high-dose females were often observed grossly as pitted or roughened renal cortical surfaces. Chronic inflammation of the kidney was not significant in dosed male rats. In those animals in which this lesion was observed, there was no correlation with urinary bladder stones.
Pancreas: pancreatic islet-cell carcinomas in male rats occurred with a statistically significant (P = 0.034) negative trend (control, 3/44, 7 %; low-dose, 0/48; high-dose, 0/45) by the Cochran-Armitage test. The incidences were not significant in pair-wise comparisons between the dosed groups and the controls, and these tumours were not observed in female rats. Total pancreatic islet-cell tumours (adenomas or carcinomas) were not significantly different for either sex of rats.
Thyroid: C-cell carcinoma in the thyroid was observed in female rats with a statistically significant (P ≤.0.038) positive trend (controls, 0/50; low-dose, 0149; high-dose, 3/ 50, 6 %). Neither the pair-wise comparisons of the high-dose group with the controls nor the combination of C-cell adenomas or carcinomas was statistically significant in any of the tests. These tumours were not observed in statistically significant proportions in male rats.
Uterus: endometrial stromal polyps were observed in statistically significant (P ≤ 0.017) negative trend (controls, 11/50, 22 %; low-dose, 7/50, 14 %; high-dose, 2/50, 4 %) and in decreased incidence (P ≤ 0.022) in the high-dose group in a pair-wise comparison with the controls. The combined incidence of endometrial stromal polyps and sarcomas was statistically significant (P ≤ 0.017) in the negative direction (controls, 14/50, 28 %; low-dose, 7/50, 14 %; high-dose, 4/50, 8 %). A significantly lower (P ≤ 0.029) incidence in the high-dose group was observed in the pair-wise comparisons with the controls. The combined incidence of endometrial stromal polyps and sarcomas in the high-dose group was not significantly different from the historical rate of this tumour in untreated female at the same laboratory (117/759, 15.4 %). - Relevance of carcinogenic effects / potential:
- Under the conditions of the bioassay, test item was carcinogenic for male F344 rats, causing transitional-cell carcinomas in the urinary bladder.
Effect levels
open allclose all
- Dose descriptor:
- dose level: urinary bladder tumours
- Effect level:
- 4 500 ppm
- Based on:
- test mat.
- Sex:
- male
- Basis for effect level:
- other: Transitional-cell carcinomas of the urinary bladder and bladder stones; there was a statistically significant association (p ≤ 0.001) between bladder stones and bladder tumours.
- Remarks on result:
- other: Effect type: carcinogenicity (migrated information)
- Dose descriptor:
- dose level: bladder stones
- Effect level:
- 2 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: Urinary bladder tumours were not observed.
Any other information on results incl. tables
Incidence of urinary bladder and kidney lesions in rats in the 2 years study
Males | Females | |||||
Control | Low Dose (2250 ppm) | High Dose (4500 ppm) | Control | Low Dose (4500 ppm) | High Dose (9000 ppm) | |
Urinary Bladder | ||||||
No. of animals with tissues examined microscopically | 45 | 50 | 49 | 49 | 49 | 47 |
Transitional-cell carcinoma | 0 | 0 | 8 (16 %)* | 0 | 0 | 0 |
Transitional-cell papilloma | 0 | 0 | 1 (2 %) | 0 | 1 (2 %) | 1 (2 %) |
Transitional-cell hyperplasia | 0 | 1 (2 %) | 2 (4 %) | 0 | 0 | 0 |
Stones (calculi) (*) | 0 | 1 (2 %) | 10 (20 %) | 0 | 0 | 0 |
Kidney | ||||||
No. of animals with tissues examined microscopically | 49 | 50 | 49 | 50 | 50 | 50 |
Chronic inflammation | 2 (4 %) | 3 (6 %) | 6 (12 %) | 4 (8 %) | 17 (34 %) | 41 (82 %)*** |
Nephropathy | 32 (65 %) | 36 (72 %) | 30 (61 %) | 19 (38 %) | 23 (46 %) | 28 (56 %) |
*P ≤ 0.016, relative to controls
**Observed at necropsy or by microscopic examination.
***P ≤ 0.01, relative to controls
Applicant's summary and conclusion
- Conclusions:
- Under the conditions of the bioassay, test item was carcinogenic for male F344 rats, causing transitional-cell carcinomas in the urinary bladder. With one exception, bladder stones were observed in all rats having transitional-cell carcinoma. There was no evidence of test item induced carcinogenicity in female F344 rats. There was an increased incidence of chronic inflammation of the kidney in treated female rats.
- Executive summary:
test item was administered in the diet to F344 rats for 103 weeks (chronic) to determine its carcinogenic potential. The dose levels were 2250 or 4500 ppm for male rats and 4500 or 9000 ppm for female rats. Compound-related lesions were observed in the urinary tract. Most noticeable was the development of uroliths (urinary bladder stones), which occurred at a greater frequency in males than females. Transitional-cell carcinomas in the urinary bladder of male rats occurred at a significantly (p ≤ 0.016) higher incidence in the 4500 ppm (high dose) group (8/49) than in the controls (0/45). Seven of the eight male rats with transitional-cell carcinomas of the urinary bladder also had bladder stones. There was a statistically significant association (p ≤ 0.001) between bladder stones and bladder tumours in male rats fed melamine (4500 ppm). Urinary bladder tumours were not observed in the low-dose (2250 ppm) male rat group, while bladder stones were observed in one rat in this group. In the female rat chronic inflammation of the kidney was observed at an increased incidence (relative to controls) in both the low (4500 ppm) and high (9000 ppm) dose groups. Thus, test item resulted to be not carcinogenic for female rats
Conclusion
Under the conditions of the bioassay, test item was carcinogenic for male F344 rats, causing transitional-cell carcinomas in the urinary bladder. With one exception, bladder stones were observed in all rats having transitional-cell carcinoma. There was no evidence of induced carcinogenicity in female F344 rats. There was an increased incidence of chronic inflammation of the kidney in treated female rats.
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