Item | Information |
---|---|
CAS RN | 10141-05-6 |
Chemical Name | Cobalt(II) bis(nitrate) |
Substance ID | m-nite-10141-05-6_v1 |
Download of Excel format | Excel file |
Item | Information |
---|---|
Guidance used for the classification (External link) | To Guidance List |
UN GHS document (External link) | To UN GHS document |
FAQ(GHS classification results by the Japanese Government) | To FAQ |
List of Information Sources (Excel file) | List of Information Sources |
List of Definitions/Abbreviations | Definitions/Abbreviations |
Sample Label by MHLW (External link) | MHLW Website (in Japanese Only) |
Sample SDS by MHLW (External link) | MHLW Website (in Japanese Only) |
OECD/eChemPortal (External link) | To OECD/eChemPortal (External link) |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | Classification year (FY) | GHS Classification Guidance for the Japanese Government | |
---|---|---|---|---|---|---|---|---|
1 | Explosives | Classification not possible |
- |
- | - | There is a chemical group associated with explosive properties (nitrates) present in the molecule, but the classification is not possible due to no data. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
2 | Flammable gases | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
3 | Aerosols | Not classified (Not applicable) |
- |
- | - | Not aerosol products. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
4 | Oxidizing gases | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
5 | Gases under pressure | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
6 | Flammable liquids | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
7 | Flammable solids | Not classified |
- |
- | - | It is not combustible (ICSC (J) (2013)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
8 | Self-reactive substances and mixtures | Classification not possible |
- |
- | - | There is a chemical group associated with explosive properties (nitrates) present in the molecule, but the classification is not possible due to no data. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
9 | Pyrophoric liquids | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
10 | Pyrophoric solids | Not classified |
- |
- | - | It is not combustible (ICSC (J) (2013)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
11 | Self-heating substances and mixtures | Not classified |
- |
- | - | It is not combustible (ICSC (J) (2013)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
12 | Substances and mixtures which, in contact with water, emit flammable gases | Not classified |
- |
- | - | It contains a metal (Co), but it is estimated that it does not react vigorously with water because the measured water solubility data of 103 g/100 g was obtained (R.Lide (2010)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
13 | Oxidizing liquids | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
14 | Oxidizing solids | Classification not possible |
- |
- | - | It is estimated to be oxidizing due to a nitrate, but the classification is not possible due to no data. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
15 | Organic peroxides | Not classified (Not applicable) |
- |
- | - | It is an inorganic compound. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
16 | Corrosive to metals | Classification not possible |
- |
- | - | Test methods applicable to solid substances are not available. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
17 | Desensitized explosives | - |
- |
- | - | - | - | - |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | Classification year (FY) | GHS Classification Guidance for the Japanese Government | |
---|---|---|---|---|---|---|---|---|
1 | Acute toxicity (Oral) | Category 4 |
Warning |
H302 | P301+P312 P264 P270 P330 P501 |
This substance was classified in Category 4, based on a report of an LD50 value (OECD TG 401) of 434 mg/kg (SIAP (2014), HSDB (Access on July 2016)) for rats. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
1 | Acute toxicity (Dermal) | Classification not possible |
- |
- | - | Classification not possible due to lack of data. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
1 | Acute toxicity (Inhalation: Gases) | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition) | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
1 | Acute toxicity (Inhalation: Vapours) | Not classified (Not applicable) |
- |
- | - | Solid (GHS definition) | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
1 | Acute toxicity (Inhalation: Dusts and mists) | Classification not possible |
- |
- | - | Classification not possible due to lack of data. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
2 | Skin corrosion/irritation | Not classified |
- |
- | - | It is described that, in a skin irritation test (OECD TG 404) in rabbits, because the values of erythema and oedema were below the threshold irritation score of ≥ 2.3 and the effects were fully recovered within 48 hours, the substance was not irritating (SIAP (2014)). Therefore, this substance was classified as "Not classified." | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
3 | Serious eye damage/eye irritation | Category 1 |
Danger |
H318 | P305+P351+P338 P280 P310 |
It is described in SIAP that "The soluble cobalt salts present a hazard for human health, based on the bioaccessibility of cobalt ions (acute oral toxicity, respiratory and eye irritation, skin sensitization, repeated dose toxicity, carcinogenicity and reproduction)." (SIAP (2014)). Also it is reported that irreversible effects were observed in an eye irritation test (OECD TG 405) in rabbits. Therefore, this substance was classified in Category 1. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
4 | Respiratory sensitization | Category 1A |
Danger |
H334 | P304+P340 P342+P311 P261 P284 P501 |
According to the Recommendation of Occupational Exposure Limits (Japan Society For Occupational Health (JSOH), 2015), cobalt and its compounds are listed in Group 1 of occupational sensitizers to the airways. Also, it is shown that IgA and IgE antibodies against cobalt were generated in workers who had engaged in metalworking for a long time and had developed symptoms of asthma, and cobalt functions as a hapten (ATSDR (2004)). From the above, this substance was classified in Category 1. In addition, this substance is classified in "Resp. Sense 1 H334" in the EU CLP Classification (ECHA C&L Inventory (Access on September 2016)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
4 | Skin sensitization | Category 1A |
Warning |
H317 | P302+P352 P333+P313 P362+P364 P261 P272 P280 P321 P501 |
According to the Recommendation of Occupational Exposure Limits (Japan Society For Occupational Health (JSOH), 2015), cobalt and its compounds are listed in Group 1 of occupational sensitizers to the skin. Also, there are many reports that cobalt causes dermatitis in humans, and that cobalt chloride and cobalt sulfate are skin sensitizers in experimental animals (ATSDR (2004)) and it was suggested that this substance had skin sensitization similar to cobalt chloride and cobalt sulfate (SIAP (2014)). Therefore, this substance was classified in Category 1A. In addition, this substance is classified as "Skin Sense 1 H317" in the EU CLP Classification (ECHA C&L Inventory (Access on September 2016)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
5 | Germ cell mutagenicity | Classification not possible |
- |
- | - | There are no data available for this substance itself. However, as for in vivo tests, it was reported that the results were positive in micronucleus tests and chromosomal aberration tests using mouse bone marrow cells for cobalt dichloride, a soluble cobalt(II) compound (ATSDR (2004), CICAD 69 (2009), The Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013)), but these data are not fully reliable or valid. It is reported that significant increases in micronuclei or DNA damage in peripheral blood were not detected in exposure to workers (SIAP (2014)). As for in vitro tests, both positive and negative results were reported for bacterial reverse mutation tests. A micronucleus test, a chromosomal aberration test, and a gene mutation test in cultured mammalian cells were positive (ATSDR (2004), CICAD 69 (2009), The Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), IARC 52 (1991)), but in in vitro micronucleus tests performed using mouse bone marrow cells isolated from the in vivo micronucleus tests described above, the result was negative regardless of the presence or absence of "S9." In SIAP (2014), it was described that soluble cobalt does not show mutagenicity (mutations) to bacteria and cells, but does show chromosomal damage in vitro, and that this is presumed to be due to reactive oxygen species (ROS). According to the weight of evidence, based on negative findings in in vivo chromosomal damage tests and negative findings in human occupational exposure, it was said that protective processes are effective in vivo. From the above, because it was assumed that soluble cobalt compounds have no in vivo effect, this substance was classified as "Classification not possible." |
FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
6 | Carcinogenicity | Category 2 |
Warning |
H351 | P308+P313 P201 P202 P280 P405 P501 |
There are no test results for this substance itself. As for cobalt sulfate and other soluble divalent cobalt salts, IARC classified them in Group 2B (IARC 52 (1991)). As for cobalt and cobalt salts, NTP classified them in R (NTP RoC (14th, 2016)), the Japan Society For Occupational Health (JSOH) classified them in Group 2B (Recommendation of Occupational Exposure Limits (2016)). Therefore, this substance was classified in Category 2. Moreover, EU classified this substance in Carc. 1B and designated this substance as SVHC (ECHA (2011)). | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
7 | Reproductive toxicity | Category 1B |
Danger |
H360 | P308+P313 P201 P202 P280 P405 P501 |
There is information that this substance is soluble in water (CICAD 69 (2006)). Although there is no information on the reproductive effects of this substance itself, it is considered that the information on soluble cobalt compounds was considered available for the classification. In a test in which cobalt chloride hexahydrate was fed to male rats (265 ppm: 20 mg Co/kg/day), moderate to severe congestion appeared in the testes after administration for 35 days; and significant effects on spermatogonial cells, spermatocytes and sperm cells were observed in addition to degenerative or necrotic changes in the germinal epithelium of the testes and Sertoli cells after administration for 70 days (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013)). In a test where male mice administered cobalt(II) chloride in drinking water for 12 weeks were mated with unexposed females, decreases were observed in the epididymal sperm count and in the survival of newborn pups at doses of 200 mg/L or higher. At doses of 400 mg/L or higher, the number of pregnant animals was reduced (declining fertility of males), testis weights decreased, and testicular sperm counts and daily sperm production decreased. Also in a tissue observation of the testes, hypertrophy of the interstitial Leydig cells, congested blood vessels, degeneration of the spermatogonial cells, and necrosis of seminiferous tubules and interstitial tissue were observed at doses of 400 mg/L or higher (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), CICAD 69 (2006)). In another study in which pregnant rats were given cobalt sulfate by gavage (gestation day 1 to 21), from the 50 mg/kg/day dose level, which is lower than the level of maternal toxicity expression at 100 mg/kg/day, relative weight decrease of liver, adrenal gland, or spleen were observed), fetuses were reported to have malformations (malformations of the cranium, spinal column, renal pelvis, renal tubule, ovary, and testis). It was also reported that in orally administered pregnant mice (gestation days 6 to 15), at 50 mg/kg/day, malformations of eyelids, kidneys, cranium, and spine occurred in fetuses (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013)). From the above, for soluble cobalt compounds, harmful effects on male genetic organs and consequent reduction in fertility by the oral route, and teratogenicity observed at dose levels without the maternal toxicity were reported. This substance is also a soluble cobalt compound, and it is considered that similar reproductive and developmental toxicities are likely to occur. Therefore, this substance was classified in Category 1B. Moreover, EU had classified this substance in Repr. 1B along with other soluble cobalt compounds such as cobalt sulfate and cobalt dichloride, and designated this substance as SVHC (ECHA (2011)). |
FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
8 | Specific target organ toxicity - Single exposure | Category 2 (central nervous system, gastrointestinal tract), Category 3 (respiratory tract irritation) |
Warning |
H371 H335 |
P308+P311 P260 P264 P270 P405 P501 P304+P340 P403+P233 P261 P271 P312 |
There is information that this substance is soluble in water (CICAD 69 (2006)). This substance and other soluble cobalt salts, cobalt (II) chloride (CAS RN 7646-79-9), cobalt (II) sulfate (CAS RN 10124-43-3), and cobalt (II) acetate (CAS RN 71-48-7) caused sedation, diarrhoea, tremors and convulsions prior to death, decrease in body temperature, increased heart rate, and piloerection at the highest dose (equivalent amount to Category 2) in acute oral toxicity tests in rats. However, no macroscopic alterations were observed in the most significant organs, and most effects disappeared after 72 hours (SIAP (2014)). Furthermore, it is also described that cobalt compounds caused hypothermia in rats by single oral administration (ATSDR (2004)), however, it is reported in the original literature (Speijers et al., Food Chem Toxicol. 20: 311 (1982)) that in the single oral dose test using rats with cobalt nitrate hexahydrate (CAS RN 10026-22-9), a hexahydrate of this substance, dose-related hypothermia, and at highest doses of 2,250 mg/kg (equivalent anhydrate amount: 1,413 mg/kg) sedation and diarrhea, were observed (ATSDR (2004)). Also, in a single oral dose test using rats of cobalt (II) dichloride, depression of spontaneous activity, muscle tone, and respiration and effects on the gastrointestinal tract were reported at doses equivalent to Category 1 (ATSDR (2004)). Therefore, it was classified in Category 1 (central nervous system, gastrointestinal tract) in the GHS Classification (FY 2015). Taking the above information together, this substance, as with other soluble cobalt salts, may also have effects on the central nervous system and the gastrointestinal tract. Since the symptoms described in SIAP and ATSDR were seen at doses equivalent to Category 2, this substance was classified in Category 2 (Central nervous system, gastrointestinal tract). Furthermore, there is a description that the dust of this substance irritates the nose and throat, and inhalation of this substance causes coughs and dyspnea in humans (HSDB (Access on September 2016)). Therefore, this substance was classified in Category 2 (central nervous system, gastrointestinal tract), and Category 3 (respiratory tract irritation). |
FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
9 | Specific target organ toxicity - Repeated exposure | Category 1 (nervous system, respiratory organs, cardiovascular system, thyroid, blood system), Category 2 (reproductive organs (male)) |
Danger Warning |
H372 H373 |
P260 P264 P270 P314 P501 |
There is information that this substance is soluble in water (CICAD 69 (2006)). No data on this substance with regard to humans or experimental animals is available. As information for soluble cobalt compounds, in humans, the following was reported as overdose symptoms from cobalt chloride or cobalt sulfate administered for the treatment of anemia: effects on the nervous system (anorexia, nausea, tinnitus, hearing loss, neuropathy) and the thyroid (goiter and inhibition of thyroid iodine uptake). As a result of oral administration of cobalt chloride to volunteers, it was reported that erythroid haematopoiesis was enhanced and there were many complaints of headaches and abdominal discomfort as subjective symptoms (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), CICAD 69 (2006)). Also, as cobalt sulfate had been added for the purpose of stabilizing the foam on beer, deaths due to cardiomyopathy were reported among heavy beer drinkers and myocardial damage action of cobalt was a concern (CICAD 69 (2006), ACGIH (7th, 2001)). By restricting the addition of cobalt, it is said that the occurrence of cardiomyopathy and resulting death disappeared (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013)). From the above, the nervous system, cardiovascular system, thyroid, and haemal system could be cited as target organs for repeated exposures of soluble cobalt compounds, including this substance, in humans. As for experimental animals, in tests using rats dosed with cobalt dichloride by gavage for 7 months, increases in red blood cell numbers and hemoglobin levels were observed at doses of 0.5 mg Co/kg/day or more (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), ATSDR (2004)). Blood effects were also observed in tests in which cobalt chloride hexahydrate was orally administered to rats for 8 weeks (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), ATSDR (2004)). In addition, in inhalation exposure tests of cobalt sulfate heptahydrate using rats or mice for 13 weeks or 2 years, inflammatory tissue changes were observed in the respiratory organs in both rats and mice from the low concentration of 0.3 mg/m3 (0.11 mg/m3 as cobalt). Additionally, in the 13-week exposure test using rats, an influence in the blood (polycythemia, platelet count reduction, increased reticulocyte counts) was observed (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), CICAD 69 (2006)). Furthermore, it was reported that in a test in which cobalt dichloride was administered in the drinking water for 12 weeks at concentrations of 200 to 800 ppm to male mice, a decrease in the weight of the testes, a decrease in the epididymal sperm count, reduced daily sperm production and necrosis of seminiferous tubules and interstitial tissue were observed at doses of 400 to 800 ppm (47 to 93 mg/kg/day, 21 to 42 mg/kg/day as cobalt) (converted guidance value: 19.6 to 39.2 mg/kg/day) (Environmental Risk Assessment for Chemical Substances Vol.11 (Ministry of the Environment, 2013), CICAD 69 (2006)). From the above, it was considered that the target organs of soluble cobalt compounds are the respiratory organs, haemal system, testes; and the effects on testes and that on others correspond to Category 2 and category 1, respectively. Therefore, based on the information regarding the effects of repeated exposure to soluble cobalt compounds on humans and experimental animals, this substance was classified in Category 1 (nervous system, respiratory organs, cardiovascular system, thyroid, haemal system) and Category 2 (genetic organs (men)). |
FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
10 | Aspiration hazard | Classification not possible |
- |
- | - | Classification not possible due to lack of data. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | Classification year (FY) | GHS Classification Guidance for the Japanese Government | |
---|---|---|---|---|---|---|---|---|
11 | Hazardous to the aquatic environment Short term (Acute) | Not classified |
- |
- | - | From 48-hour LC50 = 172 mg/L for crustacea (Artemia salina) (CICAD 69, 2006), it was classified as "Not classified." | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
11 | Hazardous to the aquatic environment Long term (Chronic) | Not classified |
- |
- | - | Reliable chronic toxicity data were not obtained. Because it is poorly water soluble (water solubility = 103 g/100 g water, R.Lide, 2010), and classified as "Not classified" for acute toxicity, it was classified as "Not classified." | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
12 | Hazardous to the ozone layer | Classification not possible |
- |
- | - | No data available. | FY2016 | GHS Classification Guidance for the Japanese Government (FY2013 revised edition (Ver. 1.1)) |
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