Item | Information |
---|---|
CAS RN | 62-73-7 |
Chemical Name | Dimethyl 2,2-dichlorovinyl phosphate; Dichlorvos |
Substance ID | 23B5502 |
Classification year (FY) | FY2011 |
Ministry who conducted the classification | Ministry of Health, Labour and Welfare (MHLW)/Ministry of the Environment (MOE) |
New/Revised | Revised |
Classification result in other fiscal year | FY2006 |
Download of Excel format | Excel file |
Item | Information |
---|---|
Guidance used for the classification (External link) | Physical Hazards & Health Hazards: GHS Classification Guidance by the Japanese Government (July, 2010) Environmental Hazards: UN GHS Document (4th revised edition) |
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 applicable |
- |
- | - | There are no chemical groups associated with explosive properties present in the molecule. |
2 | Flammable gases (including chemically unstable gases) | Not applicable |
- |
- | - | Liquid (GHS definition) |
3 | Aerosols | Not applicable |
- |
- | - | Not aerosol products. |
4 | Oxidizing gases | Not applicable |
- |
- | - | Liquid (GHS definition) |
5 | Gases under pressure | Not applicable |
- |
- | - | Liquid (GHS definition) |
6 | Flammable liquids | Not classified |
- |
- | - | From a flash point of 177 deg C (open-cup) (NFPA (14th, 2006)), it could be judged to exceed 93 deg C in the prescribed closed-cup test. Therefore, it was classified as "Not classified." |
7 | Flammable solids | Not applicable |
- |
- | - | Liquid (GHS definition) |
8 | Self-reactive substances and mixtures | Classification not possible |
- |
- | - | It contains no chemical groups associated with explosive properties but contains a chemical group associated with self-reactive properties (unsaturated bond), but there are no data. |
9 | Pyrophoric liquids | Not classified |
- |
- | - | It was classified as "Not classified" from the description of being practically non-flammable (Merck (14th, 2006)). |
10 | Pyrophoric solids | Not applicable |
- |
- | - | Liquid (GHS definition) |
11 | Self-heating substances and mixtures | Not classified |
- |
- | - | It was classified as "Not classified" from the description of being practically non-flammable (Merck (14th, 2006)). |
12 | Substances and mixtures which, in contact with water, emit flammable gases | Not classified |
- |
- | - | The substance is a compound containing phosphorus (P), but from water solubility data (about 1 g/100 mL (Merck (14th, 2006))), it was thought to be stable in water. |
13 | Oxidizing liquids | Classification not possible |
- |
- | - | The substance is an organic compound containing oxygen which is chemically bonded to an element other than carbon or hydrogen, but the classification is not possible due to no data. |
14 | Oxidizing solids | Not applicable |
- |
- | - | Liquid (GHS definition) |
15 | Organic peroxides | Not applicable |
- |
- | - | Organic compounds containing no bivalent -O-O- structure. |
16 | Corrosive to metals | Classification not possible |
- |
- | - | No data available. Besides, it is described that it is corrosive to iron and mild steel (HSDB (2010)). |
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 |
Among five LD50 values for rats [17 mg/kg (Environmental Risk Assessment for Chemical Substances vol. 4 (Ministry of the Environment, 2005)), 30 and 65 mg/kg (EHC 79 (1989)), 58.8 and 97.5 mg/kg (ATSDR (1997))], two correspond to Category 2, and three correspond to Category 3. It was classified in Category 3, to which most corresponded. |
1 | Acute toxicity (Dermal) | Category 2 |
Danger |
H310 |
P302+P352
P361+P364 P262 P264 P270 P280 P310 P321 P405 P501 |
An LD50 value for rabbits [205 mg/kg (EHC 79 (1989))] corresponds to Category 3, and an LD50 value of 113 mg/kg for rats (EHC 79 (1989))] corresponds to Category 2. By adopting a category with a higher hazard for rats, it was classified in Category 2. |
1 | Acute toxicity (Inhalation: Gases) | Not applicable |
- |
- | - | Liquid (GHS definition) |
1 | Acute toxicity (Inhalation: Vapours) | Category 1 |
Danger |
H330 |
P304+P340
P403+P233 P260 P271 P284 P310 P320 P405 P501 |
Both two LC50 values by 4-hour exposure of rats [1.66 ppm (EHC 79 (1989)) and 12.2 ppm (PATTY (5th, 2001))] correspond to Category 1. Besides, because the LC50 values were lower than 90% of the saturated vapour pressure concentration (15.8 ppm), the reference value of gasses was applied as a vapour with little mist. |
1 | Acute toxicity (Inhalation: Dusts and mists) | Category 2 |
Danger |
H330 |
P304+P340
P403+P233 P260 P271 P284 P310 P320 P405 P501 |
Among four LC50 values by 4-hour exposure of rats [0.65 mg/L, 0.523 mg/L, and 0.447 mg/L (the above, PATTY (5th, 2001)), 0.34 mg/L (EHC 79 (1989))], two correspond to Category 2, and two correspond to Category 3. By adopting a category with a higher hazard, it was classified in Category 2. Besides, because the LC50 values were higher than the saturated vapour pressure concentration (0.143 mg/L), the reference value of mists was applied. |
2 | Skin corrosion/irritation | Category 2 |
Warning |
H315 |
P302+P352
P332+P313 P362+P364 P264 P280 P321 |
It was classified in Category 2 because it is reported that severe irritation was seen in a test in which 5-20% aqueous solutions of this substance were applied to the rabbit skin (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)). |
3 | Serious eye damage/eye irritation | Category 2B |
Warning |
H320 |
P305+P351+P338
P337+P313 P264 |
It was classified in Category 2B because it was a mild irritant in a primary eye irritation test with rabbits (EPA RED (2006)). |
4 | Respiratory sensitization | Classification not possible |
- |
- | - | No data available. |
4 | Skin sensitization | Category 1 |
Warning |
H317 |
P302+P352
P333+P313 P362+P364 P261 P272 P280 P321 P501 |
It was classified in Category 1 because, in a maximization test in which 0.5% of this substance was applied to guinea pigs, erythema was observed in 35% of the animals, and it was judged as moderately sensitizing (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)). |
5 | Germ cell mutagenicity | Not classified |
- |
- | - | It is reported that it was all negative in dominant lethal tests by oral, inhalation, or intraperitoneal administration to mice (in vivo heritable germ cell mutagenicity tests) (IARC 53 (1991)), and all negative in chromosomal aberration tests with spermatogonial cells or spermatocytes after oral or inhalation administration to mice (in vivo germ cell mutagenicity tests) (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)), and all negative in micronucleus tests with bone marrow or peripheral blood after intraperitoneal administration to mice (in vivo somatic cell mutagenicity tests) (IARC 53 (1991), NTP DB (Access on Aug. 2011)). Therefore, it was classified as "Not classified." Besides, it is reported that it was negative in a sister chromatid exchange test with mice, DNA damage tests and DNA-binding tests with mice or rats, which are in vivo genotoxicity tests (IARC 53 (1991), NTP DB (Access on Aug. 2011)), and it was positive in an Ames test, an in vitro test (IARC 53 (1991), NTP DB (Access on Aug. 2011)). |
6 | Carcinogenicity | Category 2 |
Warning |
H351 |
P308+P313
P201 P202 P280 P405 P501 |
It was classified in Category 2 because it was classified in Group 2B for carcinogenicity by IARC (IARC 53 (1991)), and 2B by the Japan Society for Occupational Health (JSOH) (Recommendation of Occupational Exposure Limits (Japan Society For Occupational Health (JSOH), 2010)). Besides, in 103-week oral administration tests, significant increases were reported in papilloma in the forestomach in mice, mononuclear cell leukemia and acinar cell adenoma in the pancreas in male rats, and fibroma and fibroadenoma in the mammary gland in female rats (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)). |
7 | Reproductive toxicity | Not classified |
- |
- | - | It is reported that in two-generation and three-generation reproductive toxicity tests with rats, except for erythrocyte and plasma cholinesterase inhibition observed at or above 0.488-0.577 mg/kg/day and abnormal estrous cycling in the high dose group (7.592 mg/kg/day), which was only a statistically significant effect of reproductive toxicity (EPA RED (2006)), there were no adverse effects on reproductive parameters of mating, gestation, fertility, and delivery and the development of offspring (ACGIH (2002), IARC 53 (1991)). In developmental toxicity tests by oral administration to rats, mice, or rabbits during the gestation period or organogenesis period and a developmental toxicity test by inhalation exposure of rabbits, no adverse effects on the development of offspring, including teratogenicity, were observed (IARC 53 (1991), ATSDR (1997), EPA RED (2006)). From the above, no adverse effects on sexual function/fertility were found in multiple-generation reproductive toxicity tests, and no adverse effects on the development of offspring were seen in developmental toxicity tests. Therefore, it was classified as "Not classified." |
8 | Specific target organ toxicity - Single exposure | Category 1 (nervous system) |
Danger |
H370 |
P308+P311
P260 P264 P270 P321 P405 P501 |
On oral administration to rats, decreased activity, irregular breathing, clonic convulsions, fasciculations, prostration, decreased righting reflex, and salivation were observed at 35 mg/kg, and significant cholinesterase inhibition in the brain and erythrocytes was found at or above 5 mg/kg (EPA RED (2006)). Furthermore, cholinergic signs such as restlessness, increased salivation, muscle fasciculations, and involuntary urination occurred at or above 11 mg/kg after oral administration to dogs (ACGIH (2002)). Therefore, it was classified in Category 1 (nervous system). Besides, as for humans, it is reported that irritation of the throat, rhinorrhea, and substernal chest pain were seen in a test on male volunteers exposed to dichlorvos, but no effects were seen in pupil diameter and visual acuity, and there was a relationship between the reduction in plasma cholinesterase activity and the dichlorvos level (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)). |
9 | Specific target organ toxicity - Repeated exposure | Category 1 (nervous system, liver) |
Danger |
H372 |
P260
P264 P270 P314 P501 |
In 90-day oral administration tests with rats, significant reductions in plasma and erythrocyte cholinesterase activities at or above 1.5 mg/kg/day and cholinergic signs of tremors, salivation, and exophthalmos at or above 7.5 mg/kg/day were observed (ACGIH (2002)), and also in a 90-day oral administration test with dogs, decreased plasma and erythrocyte cholinesterase activities were reported at or above 1 mg/kg/day (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)). From the above, because all the doses were within the guidance values for Category 1, it was classified in Category 1 (nervous system). Furthermore, after 2-year diet administration to rats, surviving rats in the 500 ppm (12.5 mg/kg/day) group showed focal vacuolar degeneration and fatty degeneration of hepatocytes, hepatocellular swelling, and bile stasis, and the males and females in the 100 ppm (2.5 mg/kg/day) group had focal vacuolar degeneration (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)), and in a 2-year diet administration test with dogs, enlargement and vacuolization of hepatocytes were seen at or above 0.8 mg/kg/day (JMPR 859 (1993)). Because the doses were within the guidance values for Category 1, it was classified in Category 1 (liver). Besides, as for human exposure, it is reported that plasma cholinesterase activities decreased by 40% in a test in which volunteers were given 60-day repeated oral administration at 1.5 mg/person/day (Initial Risk Assessment Report 86 (NITE, CERI, NEDO, 2008)). |
10 | Aspiration hazard | Classification not possible |
- |
- | - | No data available. |
Hazard class | Classification |
Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | |
---|---|---|---|---|---|---|
11 | Hazardous to the aquatic environment (Acute) | Category 1 |
Warning |
H400 |
P273
P391 P501 |
It was classified in Category 1 from 48-hour EC50 = 0.00007 mg/L for crustacea (Daphnia pulex) (U.S. EPA: RED, 2006, etc.). |
11 | Hazardous to the aquatic environment (Long-term) | Category 1 |
Warning |
H410 |
P273
P391 P501 |
It was classified in Category 1 due to being not rapidly degradable (BIOWIN), and 21-day NOEC = 0.0000058 mg/L for crustacea (Daphnia magna) (U.S. EPA: RED, 2006). |
12 | Hazardous to the ozone layer | Classification not possible |
- |
- | - | This substance is not listed in the Annexes to the Montreal Protocol. |
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