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EC number: 201-188-9 | CAS number: 79-24-3
- 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
Description of key information
OECD considered nitromethane, nitroethane and 1-nitropropane to be a category at SIAM. Therefore data from the analogue 1-nitropropane is used.
Oral administration of the analogue, 1-Nitropropane, to rats for a period of twenty-eight consecutive days at dose levels of up to 100 mg active ingredient/kg/day resulted in toxicologically significant effects at 100 mg active ingredient/kg/day. No such effects were detected at 30 or 10 mg active ingredient/kg/day and, the "No Observed Effect, Level " (NOEL) is, therefore, considered to be 30 mg active ingredient/kg/day.
Groups of male and female rats and mice were exposed to 0, 100, 350, or 1000 ppm (0, 0.3, 1.0 or 3.0 mg/L) of nitroethane for 6 hr/day, 5 days/wk for a total of 64-65 exposures with an interim sacrifice of rats and mice after 20-21 exposures. Parameters monitored were clinical observations, body weights, organ weights, hematologic characteristics including methemoglobin (MetHb) determination, clinical chemistries, urinalysis, gross pathology and histopathology. Minimal changes in MetHb, spleen and salivary glands were observed in rats exposed to 100 ppm. Mice exposed to 100 ppm nitroethane showed minimal changes in the nasal turbinates and transient (even after continued exposure) effects on salivary gland epithelium only. The 100 ppm nitroethane exposure concentration was judged to be a minimal effect level under the conditions of this study.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Link to relevant study records
- Endpoint:
- short-term repeated dose toxicity: oral
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 1994
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP, guideline study (Note- The exposure period was only 28 days.)
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
- Qualifier:
- according to guideline
- Guideline:
- other: Japanese Ministry of Health and Welfare Guidelines (1986)
- Deviations:
- no
- Remarks:
- Not specified in report
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes
- Limit test:
- no
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Animals: Animals (male and female Sprague-Dawley CD rats) were acclimated for 8 days before use. A total of 30/sex were accepted into the study. At the beginning of the study, males weighed 121 - 161 g and females weighed 121-159 g, and were approximately 5-6 weeks old. The animals were allowed free access to food (except for the night prior to urine collection, when it was withdrawn) and water. The diet and drinking water did not contain any contaminants that might have influenced the study. Rats were maintained on a 12 hour light/dark cycle. Animals were randonly allocated to 6 groups (5/sex/group).
- Route of administration:
- oral: gavage
- Vehicle:
- arachis oil
- Details on oral exposure:
- The test material was administered daily, for up to twenty-eight consecutive days, by gavage using a stainless steel cannula attached to a disposable plastic syringe. Control animals were treated in an identical manner with 2 ml/kg/day of Arachis oil B.P. Animals from satellite groups 5 and 6 were maintained for a further fourteen days treatment-free period following termination of treatment. The volume of test and control material administered to each animal was based on the most recent bodyweight and was adjusted at weekly intervals.
- Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- The stability and homogeneity of the test material formulations were determined by Safepharm Analytical Laboratory. Samples were taken of each test material formulation and were analysed for concentration of 1 -Nitropropane at Safepharm Analytical Laboratory.
- Duration of treatment / exposure:
- 28 days, post exposure 14 days
- Frequency of treatment:
- daily
- Remarks:
- Doses / Concentrations:0, 10, 30, 100 mg/kg/dayBasis:other: nominal
- No. of animals per sex per dose:
- 5/sex/group
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- Test conduct: Four groups of animals were dosed with 0 (control), 10, 30 or 100 mg/kg/day active material for 28 consecutive days by gavage, and then were terminated. Controls were dosed with 2 ml/kg/day Arachis oil BP. The two additional groups (satellite animals) were dosed with 0 or 100 mg/kg/day test material for 28 days and then were allowed to recover for 14 days before termination.
- Positive control:
- No
- Observations and examinations performed and frequency:
- All animals were examined for signs of toxicity before dosing and 1 and 5 hours after dosing on weekdays and before dosing and 1 hour after treatment on weekends. During the treatment-free period, satellite animals were observed twice daily on weekdays and once daily on weekends.Body weights were recorded on day 0 and on days 7, 14, 21 and 28. Satellite animals also were weighed on days 35 and 42 (at termination). Food consumption was recorded for each cage (5 animals) at weekly intervals. Water intake was visually inspected. Clinical chemistry (urea, total protein, albumin, albumin/globulin ratio, sodium , potassium, chloride, calcium, inorganic phosphorus, alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, glucose, gamma glutamyl transpeptidase, triglycerides, total chloesterol, total bilirubin and creatinine) and hematological analyses (hematocrit, hemoglobin, erythrocyte count, total and differential leukocyte count, platelet count, mean corpuscular hemoglobin, mean corpuscular volume, mean corpuscular hemoglobin concentration, methemoglobin concentration, reticulocyte count and clotting time) were performed on blood collected from the lateral tail vein of all survivors from the control and high dose groups (both main study and satellite animals) at termination. Blood for hematological and blood chemistry analyses was collected into tubes containing potassium EDTA or lithium heparin, respectively (with the exception of blood for clotting time analysis, which was collected into sodium citrate). Animals were not fasted prior to blood collection. Urinalysis (volume, specific gravity, pH, protein, glucose, ketones, bilirubin, urobilinogen, reducing substances and blood) was performed on control and high dose main study animals during week 4 and from satellite animals during the final week of the study. Urine samples were collected over a period of approximately 16 hours, by housing the rats in metabolism cages. Animals did not have access to food during the collection period.
- Sacrifice and pathology:
- At termination, all surving animals were euthanized and were subjected to a full external and internal examination. The adrenals, brain, testes, ovaries, heart, kidneys, liver, pituitary and spleen were weighed. The organs, plus the aorta (thoracic), bone and bone marrow (femur and sternum), cecum, colon, duodenum, eyes, gross lesions, ileum, jejunum, lungs, lymph nodes (cervial and mesenteric), muscle (skeletal), esophagus, pancreas, prostate, rectum, salivary glands, sciatic nerve, seminal vesicles, skin (hind limb), stomach, thymus, thyroid/parathyroid, trachea, urinary bladder and uterus were fixed in 10% buffered formalin. Microscopic examinations were performed on tissues from control and high dose animals. All lesions from other groups were also examined microscopically.
- Other examinations:
- None
- Statistics:
- Statistical analyses: Absolute and relative organ weights, hematological, blood chemistry, weekly body weight gain and quantitative urinalysis data were analyzed by one was analysis of variance (ANOVA) incorporating the Fmax test for homogeneity of variance. Data with heterogenous variances were analyzed with the Kruskal Wallis non-parametric analysis of variance and the Mann Whitney U-Test. The critical level of significance was P < 0.05.
- Clinical signs:
- effects observed, treatment-related
- Mortality:
- mortality observed, treatment-related
- Body weight and weight changes:
- effects observed, treatment-related
- Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Food efficiency:
- not examined
- Water consumption and compound intake (if drinking water study):
- no effects observed
- Ophthalmological findings:
- not examined
- Haematological findings:
- no effects observed
- Clinical biochemistry findings:
- no effects observed
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- no effects observed
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Gross pathological findings:
- effects observed, treatment-related
- Histopathological findings: non-neoplastic:
- no effects observed
- Histopathological findings: neoplastic:
- no effects observed
- Details on results:
- Effects at 100 mg/kg: One high dose male was killed in extremis on day 27. This animal had exhibited hunched posture, lethargy and ataxia on day 16. This animal exhibited dark kidneys, thickening of the forestomach and sloughing of the glandular gastric epithelium at necropsy. Animals showed signs of increased salivation one hour after dosing on day 15. Sporadic incidents were then noted approximately 5 minutes after dosing from day 16 on. This lasted for up to one hour after dosing. Red/brown staining around the mouth was apparent from day 15 on. Two females developed hunched posture on day 28. Body weight gain was reduced in main study males during weeks 2 and 4. This was not observed in females or satellite males. Food consumption of main study males was reduced by 13% during the last week of the study. A reduction in food intake was not observed in satellite males. Water consumption did not appear to be altered. Hemoglobin, hematocrit and erythrocyte counts were reduced and white blood cells (lymphocytes) and clotting time were increased in main study females (with respect to the study control). However, hemoglobin, hematocrit and erythrocyte counts were within the normal ranges for rats of the same strain and age. Mean corpuscular hemoglobin concentration was reduced in main study males. Methemoglobin and lymphocyte counts were increased in satellite males and hematocrit was decreased in satellite females. Plasma urea was increased in main study males with respect to study controls, but not to historical controls. The albumin/globulin ratio and triglycerides were elevated and alkaline phosphatase was less than control in main study females. Urine volume was increased and urine specific gravity was decreased in main study females. Absolute and relative brain weights were increased in main study animals, with only female relative weights not achieving statistical significance. Main study females also had increased absolute and relative kidney weights and decreased relative ovary weights. The absolute weight of the pituitary was decreased and the relative heart weight was increased in main study males with respect to the study control (but not historical controls). There was no pathological evidence of brain toxicity. The incidences of all morphological changes in the organs that were examined were similar to control. Effects at 30 mg/kg: There were no deaths or clinical signs of toxicity. Males had increased body weight gains during weeks 2 and 4. There was no effect of treatment on food consumption. Water consumption did not appear to be altered. Urine volume was increased and urine specific gravity was decreased in main study females. Changes in these parameters were dose-dependent. Absolute brain and liver weights were increased in main study females and males, respectively. Effects at 10 mg/kg: There were no deaths or clinical signs of toxicity. Body weight gains and food consumption were unaffected by treatment. Water consumption did not appear to be altered. There was an increase in methemoglobin in main study males. Alkaline phosphatase was less than control in main study females. Urine specific gravity was decreased in main study females. The absolute weights of the adrenals and heart were increased in main study females. Controls: A dark accessory lobe of the liver was found in one female at necropsy.
- Dose descriptor:
- NOEL
- Effect level:
- 30 mg/kg bw/day (nominal)
- Sex:
- male/female
- Basis for effect level:
- body weight and weight gain
- clinical signs
- food consumption and compound intake
- gross pathology
- mortality
- organ weights and organ / body weight ratios
- Dose descriptor:
- LOAEL
- Effect level:
- 100 mg/kg bw/day (nominal)
- Sex:
- male/female
- Basis for effect level:
- body weight and weight gain
- clinical signs
- food consumption and compound intake
- gross pathology
- mortality
- organ weights and organ / body weight ratios
- Critical effects observed:
- not specified
- Conclusions:
- Clinical findings in a few animals dosed with 100 mg/kg were consistent with toxicity to the nervous system. Organ weight data revealed significant increases in brain weights in high dose animals. However, there were no treatment-related morphologic changes in the brain. Kidney weights were increased in high dose animals and urinalyses suggested that females treated with 30 and 100 mg/kg produced increased amounts of dilute urine. However, blood chemistries and histopathology revealed no evidence of kidney toxicity. Therefore, there was "no convincing evidence of treatment-related renal effects." None of the other changes observed were considered to be related to treatment since they were not dose-dependent.Oral administration of the test material, 1-Nitropropane, to rats for a period of twenty-eight consecutive days at dose levels of up to 100 mg active ingredient/kg/day resulted in toxicologically significant effects at 100 mg active ingredient/kg/day. No such effects were detected at 30 or 10 mg active ingredient/kg/day and, the "No Observed Effect, Level " (NOEL) is, therefore, considered to be 30 mg active ingredient/kg/day.
- Executive summary:
None
Reference
The dose levels were chosen based on a 14-day study with 10, 50, 150 and 250 mg/kg test material. All animals treated with 250 mg/kg and one animal treated with 150 mg/kg were killed in extremis. No effects were noted at 10 mg/kg.
A detailed justification for setting the NOAEL (actually a NOEL) at 30 mg/kg was provided by the investigators. Effects considered to be related to treatment with 100 mg/kg/day were hunched posture, lethargy, ataxia and death. Effects considered possibly related to treatment with 100 mg/kg/day were reduced body weight gain and increased brain weight. The increase in the absolute brain weight of females treated with 30 mg/kg/day was not considered to be biologically significant since an increase in the relative weight was not observed.
Changes in clincial chemistries, hematologies, urinalysis and weights of organs other than the brain were not considered to be related to treatment since there were no corresponding morphologic changes and/or the changes were not dose-dependent.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 30 mg/kg bw/day
- Study duration:
- subacute
- Species:
- rat
- Quality of whole database:
- Good
Repeated dose toxicity: inhalation - systemic effects
Link to relevant study records
- Endpoint:
- sub-chronic toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- circa 1982
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Essentially a GLP/Guideline study
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 413 (Subchronic Inhalation Toxicity: 90-Day Study)
- Deviations:
- yes
- Remarks:
- feed consumption was not measured.
- GLP compliance:
- yes
- Remarks:
- Study was initiated prior to GLP and completed with GLP.
- Limit test:
- no
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Fischer 344 rats (15/sex), 9 weeks old, from Charles River Laboratory, Wilmington, MA were used in this study. Each rat was uniquely identified with a numbered metal ear tag. All animals were housed in stainless steel cages with wire bottoms (2 rats/cage) and were acclimated for 14 days prior to exposure in an animal holding room designed to maintain a temperature of 70°F, relative humidity of 50%, and a light cycle of 12 hours light and dark. A standard diet (Purina Laboratory Chow, Ralston Purina Co., St. Louis, MO) and water were removed during the exposure period, but were available ad libitum at all other times. Rats were assigned to control or treatment groups by a statistical randomization procedure using a computer program.
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Remarks on MMAD:
- MMAD / GSD: Not applicable.
- Details on inhalation exposure:
- Exposures were conducted in 1 cubic meter stainless steel and glass Rochester-type chambers under dynamic airflow conditions. Airflow was approximately 175 i/min. Temperature and relative humidity in the animal holding room and in the chambers were controlled by a system designed to maintain temperature at approximately 70°F and relative humidity at approximately 50%.The NE vapor was generated by metering the test material at a controlled rate with a precision pump into a warmed vaporization flask (100-130°C). The vapor was swept with compressed air into the air inlet of the exposure chamber and then diluted to the desired concentration.
- Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Analysis for NE in the exposure chamber atmosphere was performed by an infrared spectrophotometer equipped with a variable path1ength gas cell (Miran I, Foxboro, Norwalk, CT). The wavelength used for the analYSis was 11.5 microns. The analysis was performed 1-2 times per hour for each exposure concentration. Standards for the analysis were prepared by injecting a measured volume of NE into aU-tube connected to a SARAN gas sampling bag. The U-tube was gently heated with an air gun to improve evaporation of NE. The analytical concentration of NE in the exposure chamber was determined by interpolation from a standard curve derived from vapor standards of known concentrations. Complete standard curves were run prior to the first exposure and weekly thereafter. One standard bag was run before every exposure day to check the analytical system. The nominal concentration of NE in the exposure chamber was the ratio of the rate at which the test material was dispensed to the rate of total airflow through the chamber.
- Duration of treatment / exposure:
- 6 hours/day
- Frequency of treatment:
- 5 days/week (excluding holidays) for a 92 day period. (an interim group of 5 rats/sex/concentration were exposed for a 30 day period).
- Remarks:
- Doses / Concentrations:0, 100, 350 or 1000 ppmBasis:nominal conc.
- No. of animals per sex per dose:
- 15 rats/sex/concentration (an interim group of 5 rats/sex/concentration were exposed for a 30 day period).
- Control animals:
- yes, sham-exposed
- Details on study design:
- Four groups of Fischer 344 rats (15/sex), 9 weeks old were exposed to 0, 100, 350 or 1000 ppm (0, 0.3, 1.0, and 3.0 mg/L) of NE. Five rats/sex/exposure concentration were exposed for 6 hours/day, 5 days/week for a 30-day period, respectively, at which times they were necropsied, i.e. the interim kill. The remaining rats (10/sex) were exposed for 6 hours/day, 5 days/week (excluding holidays) for a 92-day period until they were necropsied, i.e. the terminal kill of the l3-week study.
- Positive control:
- No data
- Observations and examinations performed and frequency:
- Body weights were obtained prior to the first exposure, twice weekly for the first two weeks and once weekly thereafter.
- Sacrifice and pathology:
- Clinical Observations: Blood was collected for hematology analysis and clinical chemistry studies from the tail vein and from the cervical vessels of rats, respectively. Urine was collected for urinalysis from rats only. The hematologic parameters included red blood cell (RBC) counts, total and differential white blood cell (WBC) counts, hemoglobin (Hgb) concentration and packed cell volume (PCV)[a]. Reticulocytes were determined as described by Wintrobe (1961); and Heinz bodies were determined by a method developed in this laboratory.[b] Urinalysis included pH, glucose, protein, ketones, bilirubin, occult blood, and urobilinogen[c] as well as specific gravity.[d] The clinical chemistry studies included the determination of blood urea nitrogen (BUN), serum glutamic pyruvic transaminase (SGPT), serum glutamic oxaloacetic transaminase (SGOT), serum alkaline phosphatase (AP), glucose, bilirubin, serum creatinine, phosphorus (P), and calcium (Ca)[e]. Blood for methemoglobin determination was collected by orbital sinus puncture from rats and mice and was analyzed by the method described by Hainline (1965) .Pathology: Gross necropsy was performed on all animals. All rats were fasted overnight. All animals were weighed prior to necropsy to determine organ to body weight ratios for the liver, kidney, brain, heart, thymus, and testes (male) which were obtained at necropsy. All animals were anesthetized with methoxyflurane and decapitated after the trachea was clamped. Blood samples were co11ected from the severed ,cervical vessels for clinical chemistry determinations as previously mentioned. A complete gross pathologic examination was performed, including examination of the eyes by pressing a wet microscope slide against the cornea and examining it under bright fluorescent illumination. The eyes from 5 rats/sex/concentration for both the interim and terminal kills were preserved in Zenker's solution. The eyes of the 'remaining rats of the terminal kill were preserved in 10% neutral phosphate-buffered formalin. The lungs were distended to approximately their normal inspiratory volume with 10% neutral phosphate-buffered formalin.Representative specimens of approximately 40 tissues were retained and preserved in 10% neutral phosphate-buffered formalin. A complete set of tissues (except sternum) was prepared and histologically evaluated from rats that died spontaneously and that were selected for the interim and terminal kills. Of the terminal kill, only 5/sex/species of the 0 and 1000 ppm exposure groups were evaluated. As a minimum, sections of liver, lungs, kidneys, heart, thymus, spleen, and nasal turbinates were prepared and evaluated from all spontaneous dead, all interim kill, and 5/sex of the terminal kill rats from the 100 and 350 ppm exposure groups. These tissues were processed for microscopic examination by conventional histologic methods, stained with hematoxylin and eosin and evaluated by light microscopy. In a few cases, a tissue specimen was not obtained at necropsy or was lost during the processing, and tissues such as the parathyroid glands were evaluated only to the extent that they were included in theroutine sections of the thyroid glands.[a] RBC , WBC-Coulter Counter Model ZBI; Hgb-Hemoglobinometer, Coulter Electronics, Hialeah, FL; PCV-Microhematocrit Centrifuge, Clay-Adams Co., New York, NY.[b] Standard Operating Procedures of Pathology Group, Toxicology Research, Dow Chemical USA.[c] Multistix, Ames Co., Elkhart, IN.[d] T. S. Meter American Optical Co., Buffalo, NY[e] CentrifiChem System 400, Methods File, Union Carbide Corp., Rye, NY.ReferencesHainline Jr., A. (1965). in Standard Methods of Clinical Chemistry, Academic Press, New York and London, Vol. 5, pp 143-157.
- Other examinations:
- No additional information available.
- Statistics:
- Hematology, methemoglobin, specific gravity of urine, clinical chemistry, body weights, organ weights, and organ to body weight values were evaluated by analysis of variance and Dunnett's test using a level of significance of p <0.05.
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- Cyanotic skin color, dull and dark red eyes in males and females and unkept appearance in females
- Mortality:
- mortality observed, treatment-related
- Description (incidence):
- Cyanotic skin color, dull and dark red eyes in males and females and unkept appearance in females
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- decreased body weight
- Food consumption and compound intake (if feeding study):
- not specified
- Food efficiency:
- not specified
- Water consumption and compound intake (if drinking water study):
- not specified
- Ophthalmological findings:
- not specified
- Haematological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- Increased reticulocytes and Heinz bodies. Methemoglobin levels elevated at all concentrations
- Clinical biochemistry findings:
- effects observed, treatment-related
- Description (incidence and severity):
- Increased bilirubin levels in 1000 ppm females. Decreased glucose levels of males and females exposed to 350 or 1000 ppm.
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- not specified
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Description (incidence and severity):
- Due to decreased body weights a number of absolute and/or relative organ weights were affected.
- Gross pathological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- Increased spleen size
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- Nasal turbinates exhibited chronic active inflammation of the olfactory epithelium, salivary gland changes, spleen exhibited extramedullary hematopoiesis, liver had fatty change and kidneys had decreased cytoplasmic granularity of proximal tubular cells.
- Histopathological findings: neoplastic:
- not specified
- Details on results:
- For each exposure chamber the mean daily time-weighted average (TWA) analytical concentration was very close to the intended target concentrationand the mean daily calculated nominal concentration. The close agreement between the analytical and nominal'concentrations for each exposure chamber indicates that the test material losses were minimal in the vapor generation and exposure system. Also, the temperature and relative humidity values were compatible between the chambers. Clinical observations: Two clinical findings consistent with the grossly observable treatment-induced methemoglobinemia were (1) dull, dark red eyes and (2) grayish or bluish colored skin of the extremities (cyanosis). The dull, dark red eye color was not very distinctive in the 350 ppm group and was not noticed until after 4 weeks of exposure. However, this eye color was very pronounced in the 1000 ppm group and was noted after the firstexposure and thereafter. The gray color of the hairless skin of the extremities was noted in the 350 ppm rats after 9 weeks of exposure, whereas a more perceptible bluish-gray color was seen in the 1000 ppm group after 4 exposures and continued to the end of the study. These color changes were visible after exposure and were not visible in the morning prior to the 'next exposure, approximately 19 hours later. Swelling in the salivary gland region was found in some rats of the 100 and 350 ppm groups after the 5th and 6th exposures and in the 1000 ppm group after exposures 2 through 6. This observation is consistent with a mild transient viral infection (sialodacryoadenitis) which commonly occurs in this laboratory, since there were no histopathological changes in the salivary glands or vicinity thereof in the interim kill rats. Increased amounts of porphyrin pigment around the nares were observed in the rats of the 1000 ppm exposure group during the 1st and 3rd exposure weeks. This transient clinical sign was possibly another indication of the sialodacryoadenitis infection suggested by the swelling in thesalivary gland region, stated previously, and was not judged to be a treatment-related effect.During this study female rats of the 100, 350, and 1000 ppm exposure groups had an unkempt appearance which was an expression of their general weakened condition secondary to the toxicity of the test material.Body Weights: The animal randomization procedure used in this study did not assure equal group mean body weight at the beginning of the study.Despite the fact that the 1000 ppm female rats weighed statistically significantly less than their controls prior to the start of the study, there was obvious growth retardation of this group along with the males of the 1000 ppm group and the male and female rats of the 350 ppm group. All of these treatment groups had statistically significant body weight decreases when compared to controls during the last month of the study, clearly a treatment-related effect. Group mean body weights for both sexes of the 100 ppm group were comparable to their controls. Organ Weights: No toxicologically significant changes were found in any of these mean weights. However, at both kills the fasted mean body weights of the females of the 350 ppm exposure group and of the males and females of the 1000 ppm exposure group were statistically significantly decreased. Their decreased body weights were responsible for the secondary decreases and increases in the absolute and/or relative weights, respectively, of the liver, kidney, heart, brain, thymus, and testes. No toxicological importance was attributed to the statistically significant increases in the absolute heart weight of the 1000 ppm females of the terminal kill or in the absolute testes weight of the 100 ppm males of the terminal kill.Hematology: Hematology parameters of male and female rats were obtained prior to the interim kill and twice before the terminal kill to examine the reproducibility of the packed cell volume (PCV), red blood cell (RBC), hemoglobin (Hgb), and white blood cell (WBC) results obtained at the first analysis before the terminal kill. Prior to the interim kill the statistically significant increases of the WBC counts of the 1000 ppm exposure group may have been a treatment-related effect, possibly a result of the chronic active inflammation seen histologically in the nasal turbinates. However, due to the variability in the mean WBC counts obtained prior to the terminal kill, this was considered a sporadic finding and of no toxicologic significance.Of the two hematological analyses prior to the terminal kill, the following are the only results considered to have any possible toxicological significance. In the second analysis prior to the terminal kill, the 1000 ppm female rats had a statistically significantly increased PCV with a decreased (though not statistically significant) RBC count. This data may have been indicative of the increased number of reticulocytes present, approximately 4 times greater than the controls. At the interim and second terminal analyses the statistically significantly lowered hemoglobin values of the 1000 ppm male rats was a possible exposure-related effect.In addition, the appearance of reticulocytes and Heinz bodies found prior to the interim and terminal kills showed: the 100 ppm exposure group was comparable to the controls, whereas the 350 ppm and 1000 ppm exposure groups showed increases in these parameters over control. The increased emergence of these reticu10cytes and Heinz bodies was probably associated with the methemoglobinemia observed in these two treatment groups.Urinalysis: All parameters of both time periods were interpreted to be unaffected by exposures to NE.Clinical Chemistry Studies: Statistically significant changes in alkaline phosphatase activity (AP) of the 1000 ppm females and in the serum phosphorus levels of the male and/or female NE exposed rats which occurred at the interim and/or terminal kills were not associated with gross or histopathologic exposure-related changes in livers or kidneys and thus were not diagnostic of adverse treatment-related effects on those tissues.At the terminal kill, the 1000 ppm female rats had statistically significantly increased bilirubin levels which could have been a result of exposure to the test material. At the terminal kill, glucose levels of the male and female rats of the 350 and/or 1000 ppm exposure groups that were statistically significantly decreased were indicative of the poor nutritional state of the rats of these groups, a general response to the toxicity of NE. There was a statistically significant increase in the glucose level of the 350 ppm females of the interim kill. However this was considered to be of no toxicological importance because of its isolated occurrence and lack of dose-response.Methemoglobin: Prior to the interim kill on exposure day 20, experiment day 29, methemoglobin (MetHb) analysis was performed approximately 15 hours after exposure; the MetHb levels of all NE exposed rats were comparable to their controls. However, further MetHb analysis was prompted by the clinical observation of dull dark red eyes and bluish skin of the 1000 ppm rats' extremities which were found only after exposure and would disappear by morning (~l9 hrs later). Because female rats exposed to 1000 ppm NE visually appeared to be affected more than the males, the analysis was performed on the 1000 ppm females and the control group right after exposure. The statistically significantly increased amount of MetHb found in the 1000 ppm females clearly demonstrated that time was the essential factor for the determination of MetHb. Subsequent evaluation of the other exposure groups (both sexes) showed a concentration-related increased amount of MetHb in the male and female rats of all treatment groups. To more completely characterize the time-dependent MetHb effect, a timed sequence of analyses was performed the day before the terminal kill. The determinations were performed. right after exposure (<1/2 hr), 4 and 19 hours later, on rats and mice (only the 1000 ppm NE exposure groups were sampled at approximately 4 hours after exposure). By morning (19 hrs after exposure) the MetHb levels of the 100 and 350 ppm exposure groups of ratswere comparable to the controls, and only the 1000 ppm exposure groups of rats were statistically significantly increased. The data indicate initially higher concentrations of MetHb in rats than in mice, but a faster rate of MetHb disappearance in mice than in rats.Gross Pathology and HistopathologyMany gross pathology and histopathology observations were typical of naturally-occurring spontaneous lesions, conmonly seen in this age and strain of rats and mice used in this study and will not be discussed. Interim Kill-Rats: Treatment-related effects specifically attributed to the test material occurred at all 3 exposure groups which involved either the spleen, nasal turbinates, liver or kidneys. Upon gross examination, the spleen appeared enlarged in a few of the 350 ppm males and 1000 ppm females and in all of the 1000 ppm males. It was also dark colored in all 350 and 1000 ppm males and in most 1000 ppm females. At histopathologic examination, the spleen showed increased congestion of the red pulp in all 350 ppm males and in all 1000 ppm rats as well as an increase in extramedullary hematopoieSis in a few 350 ppm male rats, inmost 1000 ppm female rats and in all 1000 ppm male rats. These alterations in the spleen were considered to be consistent with the methemoglobinemia induced by exposure to NE.Nasal turbinate lesions found only by histopathological inspection were (1) chronic active inflammation in the region of the olfactory epithelium found in one female of the 100 ppm group, all males and a single female of the 350 ppm group, and all rats of the 1000 ppm group, and (2) degeneration in the olfactory epithelium observed in all males and most females of the 350 ppm exposure group and in all of the 1000 ppm group. The degeneration consisted of a flattening of the olfactory mucosal epithelium and intercellular mucosal edema of the olfactory epithelium in the dorsal medial portion of the nasal turbinates. These responses of inflammation and degeneration were the result of exposure to NE.Only histopathological changes were found in the liver and kidneys. The liver effects observed were described as vacuolization, consistent with fatty change, seen in most male rats exposed to 1000 ppm HE. Decreased cytoplasmic granularity of predominantly the proximal tubular cells of the kidneys was observed in a few male rats of the 1000 ppm group. Three findings that were secondary to the toxicity of the test material and occurred only in the 1000 ppm treatment group were (1) a gross observation in two female rats of thickened stomach walls histopathologically described as submucosal gastric edema and was probably the result of not eating and/or stress, (2) a decrease in adipose tissue reserves of both sexes that represented a decreased food intake, and (3) perineal soiling of most females that was viewed as a nonspecific expression of the sickened condition of the animals. There was no effect noted in the salivary gland of female rats exposed to 1000 ppm. In males, the slight effect noted (salivary gland acini vacuolization) was observed in both control and 1000 ppm exposed rats.Terminal Kill-Rats: Exposure associated changes caused directly by NE were found in the spleen, nasal turbinates, salivary glands, liver, or kidneys of all 3 exposure groups. The spleen was grossly observed to be dark in most of the 350 ppm males and dark and enlarged in all male and female rats of the 1000 ppm group. Microscopic changes included (1) an increase in congestion of all male rats exposed to NE and in the majority of the females of the 350 and 1000 ppm groups, and (2) an increase in extramedullary hematopoiesis in all treated males and in a single or a few female rats of each NE exposure group. All of these changes were considered the result of NE induced methemoglobinemia.Treatment-related effects in the nasal turbinates were not observed on gross inspection but were evident upon histopathologic examination. Chronic active inflammation and degeneration were observed in the region of the olfactory epithelium of a few males and females exposed to 350 ppm NE and of most exposed to 1000 ppm NE. Degeneration was characterized by a flattening of the epithelium and intercellular mucosal edema of the olfactory region in the dorsal medial portion of the nasal turbinates and was moderate in severity in rats exposed to 1000 ppm but slight in those at 350 ppm.Salivary gland alterations associated with treatment were limited to histopathologic observations. A decreased cytoplasmic granularity and decreased eosinophilic staining of the ductal epithelial cells was seen in all treated male and female rats. The severity varied from very slight in rats exposed to 100 ppm to slight in those exposed to 350 and 1000 ppm. In addition. vacuolization of the salivary gland acini was seen in most females exposed to 1000 ppm of NE.Histopathologic changes in the liver were characterized by vacuolization consistent with fatty change and were present in rats of all exposure levels excluding 100 ppm males and control females. The severity of the vacuolization varied from very slight in the control males to slight in the others. This observation was believed to be related to exposure to NE. Several alterations specific to the rats of the 1000 ppm exposure group occurred in the kidney, thymus, adipose tissue, and haircoat. Renal changes consisted of a dark appearance upon gross inspection of a few males. Histologically the kidney lesions were observed as a decreased cytoplasmic granularity of the renal cortical (predominantly proximal) tubular epithelial cells of all males in the 1000 ppm exposure group. Such changes were the result of treatment. Decreased thymic size was noted at necropsy in a few males of the 1000 ppm group but no microscopic alterations were recognized. thus this was judged to be a secondary (nonspecific) treatment-related effect. The decrease in adipose tissue in a few of. the 1000 ppm males and the perineal soiling of a few 1000 ppm females were also considered to be nonspecific changes secondary to the toxicity of the test material.
- Dose descriptor:
- NOAEC
- Effect level:
- 100 ppm
- Based on:
- test mat.
- Sex:
- male
- Basis for effect level:
- other: Local effects; Histopathologic changes noted in nasal turbinates following 6 hr/day, 5 days/week for 13 weeks exposure to 350 ppm
- Dose descriptor:
- NOAEC
- Effect level:
- ca. 100 ppm
- Based on:
- test mat.
- Sex:
- female
- Basis for effect level:
- other: Local effects; Histopathologic changes noted in one of 10 nasal turbinates following 6 hr/day, 5 days/week for 4 weeks but not 13 weeks exposure to 100 ppm
- Dose descriptor:
- LOAEC
- Effect level:
- 100 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: Systemic effects; Histopathologic changes noted in salivary gland following 6 hr/day, 5 days/week for 13 weeks exposure to 100 ppm.
- Critical effects observed:
- not specified
- Conclusions:
- Exposure of rats to 1000 ppm NE resulted in decreased body weight gain, elevated MetHb levels with cyanosis, increased reticulocytes and Heinz bodies in peripheral blood and associated splenic congestion and extramedullary hematopoiesis. Other major target organ effects in these animals included degenerative and inflammatory changes in the olfactory nasal epithelium, hepatocellular vacuolization, decreased cytoplasmic granularity of renal cortical tubular epithelium and ductal epithelial cells of the salivary glands. Rats exposed to 350 ppm NE showed similar but less severe changes in MetHb, spleen, nasal turbinates and salivary glands. Minimal changes in MetHb, spleen and salivary glands were observed in rats :xposed to 100 ppm.
- Executive summary:
The subchronic toxicity of nitroethane was examined in rats. Groups of rats were exposed to 0, 100, 350, or 1000 ppm (0, 0.3, 1.0 or 3.0 mg/l) of NE for 6 hr/day, 5 days/wk for a total of 64-65 exposures with an interim sacrifice of rats after 20-21 exposures. Parameters monitored were clinical observations, body weights, organ weights, hematologic characteristics including methemoglobin (MetHb) determination, clinical chemistries, urinalysis, gross pathology and histopathology.
Exposure of rats to 1000 ppm NE resulted in decreased body weight gain, elevated MetHb levels with cyanosis, increased reticulocytes and Heinz bodies in peripheral blood and associated splenic congestion and extramedullary hematopoiesis. Other major target organ effects in these animals included degenerative and inflammatory changes in the olfactory nasal epithelium, hepatocellular vacuolization, decreased cytoplasmic granularity of renal cortical tubular epithelium and ductal epithelial cells of the salivary glands. Rats exposed to 350 ppm NE showed similar but less severe changes in MetHb, spleen, nasal turbinates and salivary glands. Minimal changes in MetHb, spleen and salivary glands were observed in rats exposed to 100 ppm.
Reference
Table 1 Mean Methemoglobin (MetHb) Values for Rats Prior to the 93-Day Terminal Kill 13-Week Study
Exposure | % MetHb (Mean + S.D.) | |||
Level, ppm | N | Immediately After Last (64th) Exposure | 4 hrs After Last Exposure | 19 hrs After Last Exposure |
Males | ||||
0 | 5 | 0.4 + 0.4 | N.D. | 0.5 + 0.3 |
100 | 5 | 2.4 + 0.5 | N.D. | 0.4 + 0.3 |
350 | 5 | 12.9 + 1.5* | N.D. | 0.6 + 0.2 |
1000 | 5 | 50.7 + 5.4* | 58.6 + 6.1 a | 1.5 + 0.8* |
Females | ||||
0 | 5 | 0.5 + 0.3 | N.D. | 0.5 + 0.3 |
100 | 5 | 5.3 + 1.7 | N.D. | 0.8 + 0.8 |
350 | 5 | 30.7 + 3.9* | N.D. | 0.8 + 0.5 |
1000 | 5 | 61.8 + 6.0* | 64.1 + 4.6a | 1.9 + 0.3 |
*Statistically significant deviation from control mean using Dunnett's test, p <0.05.
aNo statistical analysis was performed on this data since no control data was determined at this time period.
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LOAEC
- 300 mg/m³
- Study duration:
- subchronic
- Species:
- rat
- Quality of whole database:
- Good
Additional information
Oral Exposure
No reliable animal studies were found for nitromethane exposure through the oral route. Instead 1 -nitropropane was used as a surrogate for read across. In a 28 -day (sub acute) oral gavage study in male and female Spraque-Dawley rats exposed to 0, 10, 30 and 100 mg/kg/day of 1 -nitropropane, no treatment related effects were seen at the 10 and 30 mg/kg/d dose levels (NOEL = 30 mg/kg/d). At the 100 mg/kg/day level (LOAEL), the treatment related effects were hunched posture, lethargy, and axatia. Death occurred in one high dose male. Also, observed in the high dose group was a slight decrease in body weight gain in males and an increased in brain weight.
The subchronic toxicity of nitroethane was examined in rats and mice. Groups of male and female rats and mice were exposed to 0, 100, 350, or 1000 ppm (0, 0.3, 1.0 or 3.0 mg/L) of nitroethane for 6 hr/day, 5 days/wk for a total of 64-65 exposures with an interim sacrifice of rats and mice after 20-21 exposures. Parameters monitored were clinical observations, body weights, organ weights, hematologic characteristics including methemoglobin (MetHb) determination, clinical chemistries, urinalysis, gross pathology and histopathology.
Exposure of rats to 1000 ppm nitroethane resulted in decreased body weight gain, elevated MetHb levels with cyanosis, increased reticulocytes and Heinz bodies in peripheral blood and associated splenic congestion and extramedullary hematopoiesis. Other major target organ effects in these animals included degenerative and inflammatory changes in the olfactory nasal epithelium, hepatocellular vacuolization, decreased cytoplasmic granularity of renal cortical tubular epithelium and ductal epithelial cells of the salivary glands. Rats exposed to 350 ppm nitroethane showed similar but less severe changes in MetHb, spleen, nasal turbinates and salivary glands. Minimal changes in MetHb, spleen and salivary glands were observed in rats exposed to 100 ppm.
Mice exposed to 1000 ppm nitroethane showed increased MetHb, evidence of toxicity in the salivary glands, liver, olfactory nasal epithelium and multinucleated spermatids in the testes. Overall these changes were less severe than those observed in rats. Less extensive toxicity was observed in mice exposed to 350 ppm and only MetHb, liver, salivary glands and nasal turbinates were affected. Mice exposed to 100 ppm nitroethane showed minimal changes in the nasal turbinates and transient (even after continued exposure) effects on salivary gland epithelium only. The 100 ppm nitroethane exposure concentration was judged to be a minimal effect level under the conditions of this study.
Justification for selection of repeated dose toxicity via oral route - systemic effects endpoint:
Read Across: Conducted similar to a GLP/Guideline study
Justification for selection of repeated dose toxicity inhalation - systemic effects endpoint:
Conducted similar to a GLP/Guideline study
Justification for classification or non-classification
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