Item | Information |
---|---|
CAS RN | 12789-03-6 |
Chemical Name | Chlordane |
Substance ID | R02-A-006-MHLW |
Classification year (FY) | FY2020 |
Ministry who conducted the classification | Ministry of Health, Labour and Welfare (MHLW) |
New/Revised | New |
Classification result in other fiscal year | |
Download of Excel format | Excel file |
Item | Information |
---|---|
Guidance used for the classification (External link) | GHS Classification Guidance for the Japanese Government (FY2019 revised edition (Ver. 2.0)) |
UN GHS document (External link) | UN GHS document |
Definitions/Abbreviations (Excel file) | Definitions/Abbreviations |
Model Label by MHLW (External link) | MHLW Website (in Japanese Only) |
Model SDS by MHLW (External link) | MHLW Website (in Japanese Only) |
OECD/eChemPortal (External link) | eChemPortal |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | |
---|---|---|---|---|---|---|
1 | Explosives | Not classified (Not applicable) |
- |
- | - | There are no chemical groups associated with explosive properties present in the molecule. It was classified as "Not classified." |
2 | Flammable gases | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition). It was classified as "Not classified." |
3 | Aerosols | Not classified (Not applicable) |
- |
- | - | Not aerosol products. It was classified as "Not classified." |
4 | Oxidizing gases | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition). It was classified as "Not classified." |
5 | Gases under pressure | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition). It was classified as "Not classified." |
6 | Flammable liquids | Classification not possible |
- |
- | - | No data available. There is information that a pure substance is not combustible (GESTIS (Access on May 2020)), but for industrial use, there are solutions in an organic solvent, some of which are combustible. |
7 | Flammable solids | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition). It was classified as "Not classified." |
8 | Self-reactive substances and mixtures | Not classified (Not applicable) |
- |
- | - | There are no chemical groups present in the molecule associated with explosive or self-reactive properties. It was classified as "Not classified." |
9 | Pyrophoric liquids | Classification not possible |
- |
- | - | No data available. There is information that a pure substance is not combustible (GESTIS (Access on May 2020)), but for industrial use, there are solutions in an organic solvent, some of which are combustible. |
10 | Pyrophoric solids | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition). It was classified as "Not classified." |
11 | Self-heating substances and mixtures | Classification not possible |
- |
- | - | Classification is not possible because test methods applicable to liquid substances are not available. |
12 | Substances and mixtures which, in contact with water, emit flammable gases | Not classified (Not applicable) |
- |
- | - | The chemical structure of the substance does not contain metals or metalloids (B, Si, P, Ge, As, Se, Sn, Sb, Te, Bi, Po, At). It was classified as "Not classified." |
13 | Oxidizing liquids | Not classified (Not applicable) |
- |
- | - | The substance is an organic compound containing chlorine (but not fluorine or oxygen) which is chemically bonded only to carbon or hydrogen. It was classified as "Not classified." |
14 | Oxidizing solids | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition). It was classified as "Not classified." |
15 | Organic peroxides | Not classified (Not applicable) |
- |
- | - | Organic compounds containing no bivalent -O-O- structure in the molecule. It was classified as "Not classified." |
16 | Corrosive to metals | Classification not possible |
- |
- | - | No data available. |
17 | Desensitized explosives | Not classified (Not applicable) |
- |
- | - | There are no chemical groups associated with explosive properties present in the molecule. It was classified as "Not classified." |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | |
---|---|---|---|---|---|---|
1 | Acute toxicity (Oral) | Category 3 |
Danger |
H301 | P301+P310 P264 P270 P321 P330 P405 P501 |
[Rationale for the Classification] It was classified in Category 3 from (1) - (3). [Evidence Data] (1) LD50 for rats: 137-590 mg/kg (ATSDR (2018)) (2) LD50 for rats: 500 mg/kg (Patty (6th, 2012)) (3) LD50 for rats: 570 mg/kg (Patty (6th, 2012)) |
1 | Acute toxicity (Dermal) | Category 3 |
Danger |
H311 | P302+P352 P361+P364 P280 P312 P321 P405 P501 |
[Rationale for the Classification] It was classified in Category 3 from (1), (2). [Evidence Data] (1) LD50 for rats: 530-840 mg/kg (ATSDR (2018)) (2) LD50 for rabbits: 1,150 mg/kg (ATSDR (2018)) |
1 | Acute toxicity (Inhalation: Gases) | Not classified |
- |
- | - | [Rationale for the Classification] Liquid (GHS definition). It was classified as "Not classified." |
1 | Acute toxicity (Inhalation: Vapours) | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
1 | Acute toxicity (Inhalation: Dusts and mists) | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
2 | Skin corrosion/irritation | Classification not possible |
- |
- | - | [Rationale for the Classification] There is a description of (1), but the classification is not possible due to lack of data. [Reference Data, etc.] (1) Early use of this substance resulted in irritation of the eye and skin of industrial and agricultural workers, but this does not appear to have been a problem (Patty (6th, 2012)). |
3 | Serious eye damage/eye irritation | Classification not possible |
- |
- | - | [Rationale for the Classification] There is a description of (1), but the classification is not possible due to lack of data. [Reference Data, etc.] (1) Early use of this substance resulted in irritation of the eye and skin of industrial and agricultural workers, but this does not appear to have been a problem (Patty (6th, 2012)). |
4 | Respiratory sensitization | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
4 | Skin sensitization | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
5 | Germ cell mutagenicity | Classification not possible |
- |
- | - | [Rationale for the Classification] Based on (1) and (2), although there were findings indicating concerns about genotoxicity, there were no relevant findings. Based on weight of evidence, it was classified as "Classification not possible." [Evidence Data] (1) As for in vivo, in a dominant lethal test using the bone marrow cells after intraperitoneal injection to mice, negative results were reported, but in a chromosomal aberration test and a micronucleus test using the bone marrow cells of mice, and in a DNA damage test using rat liver, positive results were reported (ATSDR (2018), IRIS Tox Review (1998)). (2) As for in vitro, in a bacterial reverse mutation test and in a mammalian cell chromosome aberration test, positive and negative results were reported. In a sister chromatid exchange analysis with the cultured mammalian cells, positive results were reported (ATSDR (2018), IRIS Tox Review (1998), CEBS (Access on August 2020)). |
6 | Carcinogenicity | Category 2 |
Warning |
H351 | P308+P313 P201 P202 P280 P405 P501 |
[Rationale for the Classification] Based on (1) to (3), it was classified in Category 2. [Evidence Data] (1) As for the classification results by domestic and international organizations, the IARC classified chlordane (CAS RN 57-74-9) in Group 2B (IARC 79 (2001)) and the EPA classified this substance in L (likely carcinogen in humans) (IRIS Tox Review (1998)). (2) In most of epidemiology studies, no significant associations were observed between occupational exposure to, and serum levels of, this substance or its components and/or metabolites and risk of cancer. Some studies, however, reported significant associations between serum levels of this substance or its components and/or metabolites and risk of cancer of the male reproductive organs, non-Hodgkin's lymphoma, and pancreatic cancer. In case-control studies, significant associations between self-reported use of this substance and risk of rectal cancer and between usage in pesticide application of this substance and risk of breast cancer were observed (ATSDR (2018)). (3) In carcinogenicity studies with mice dosed by feeding, an increase in hepatocellular tumors was observed in males (ATSDR (2018)). |
7 | Reproductive toxicity | Category 2 |
Warning |
H361 | P308+P313 P201 P202 P280 P405 P501 |
[Rationale for the Classification] Based on (1) and (2), it was classified in Category 2. [Evidence Data] (1) In developmental toxicity studies with female rats dosed by gavage on days 6 to 19 of gestation, at doses at which a decrease in body weight gain was observed in dams, a decrease in viable fetuses was observed (IRIS Tox Review (1998), ATSDR (2018)). (2) In a seven-day oral administration study using female mice during late gestation (doses: 0, 1, 2.5 mg/kg), neurobehavioral effects in neonates (depressed acquisition of conditioned avoidance response (mean responses: 13.1/16 in the control group, 9.7/16 in the low-dose group, and 9.7/16 in the high-dose group), an increase in seizure threshold (mean responses: 90.1 volts in the control group, 108.6 volts in the low-dose group, 134.9 volts in the high-dose group), and an increase in exploratory activity (mean responses: 93.9 times in the control group, 88.4 times in the low-dose group, 137.7 times in the high-dose group)) were observed (IRIS Tox Review (1998), Al-Hachim, G.M. and A. Al-Baker. 1973.. Br. J. Pharmacol. 49: 480-483.). |
8 | Specific target organ toxicity - Single exposure | Category 1 (central nervous system) |
Danger |
H370 | P308+P311 P260 P264 P270 P321 P405 P501 |
[Rationale for the Classification] Based on (1) and (2), it was classified in Category 1 (central nervous system). [Evidence Data] (1) In acute exposure of humans and experimental animals to this substance, neurotoxicity was a principal endpoint and tremors and convulsions were observed in both humans and experimental animals (IRIS (1998)). (2) As for the cases of humans exposed to this substance, it was reported that convulsions were observed in oral exposure, and effects on the central nervous system including chest pains, dyspnea, shortness of breath, ataxia, headache, dizziness, irritability, excitability, confusion, incoordination, tremors, convulsions, and coma were observed in inhalation exposure (ATSDR (2018)). |
9 | Specific target organ toxicity - Repeated exposure | Category 1 (liver, kidney) |
Danger |
H372 | P260 P264 P270 P314 P501 |
[Rationale for the Classification] There was no reliable report about repeated exposure of humans to this substance. In experimental animals, based on (1) to (3), at doses for Category 1, effects on the liver and kidney were observed. Therefore, it was classified in Category 1 (liver, kidney). [Evidence Data] (1) It was reported that in a 2- to 9-month oral toxicity study with rats dosed by feeding, at or above 0.125 mg/kg/day (within the range for Category 1), centrilobular hypertrophy and cytoplasmic inclusions of hepatocytes were observed (ATSDR (2018)). (2) It was reported that in a 28-day oral toxicity study with rats, at or above 0.25 mg/kg/day (within the range for Category 1), histopathologic kidney lesions were observed in males; and at 25 mg/kg/day (within the range for Category 2), hypertrophy of the liver in males and females, an increase in absolute kidney weight, an increase in blood urea nitrogen (BUN), and a decrease in serum creatine kinase in males, and anisokaryosis of hepatocytes and histopathologic kidney lesions in females were observed (ATSDR (2018)). (3) It was reported that in a 13-week inhalation exposure test with rats (8 hours/day, 5 days/week), at or above 0.001 mg/L (converted guidance value (6 hours/day): 0.00096 mg/L, within the range for Category 1), hepatocellular enlargement or vacuolization was observed (ATSDR (2018)). [Reference Data, etc.] (4) In several studies on occupational exposure of humans to this substance at low levels, there was no report indicating that the liver was the target organ of this substance (IRIS (1998)). On the other hand, there was a report suggesting that jaundice was associated with continued exposure such as living in a house in which this substance had been used to control termites (ATSDR (2018)). (5) As for humans who had been exposed to aerosols of this substance at home or in the workplace for a period ranging from 3 days to 15 months (for 5.84 months on average), it was reported that in a test conducted after 4 months to 10 years (for 2.4 years on average) from the exposure, impaired proliferative responses to plant mitogens were observed, which suggested that the exposure to this substance was associated with immune deficiency (ATSDR (2018)). (6) An increased risk of diabetes among people engaged in agriculture who used this substance (372 diabetics, 7,365 nondiabetics) was reported (ATSDR (2018)) (7) It was reported that in a chronic and acute exposure of humans to this substance, neurological toxicity could be a potential toxicological endpoint (IRIS (1998)). |
10 | Aspiration hazard | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | |
---|---|---|---|---|---|---|
11 | Hazardous to the aquatic environment Short term (Acute) | - |
- |
- | - | - |
11 | Hazardous to the aquatic environment Long term (Chronic) | - |
- |
- | - | - |
12 | Hazardous to the ozone layer | - |
- |
- | - | - |
|