Item | Information |
---|---|
CAS RN | 7173-51-5 |
Chemical Name | Didecyldimethylammonium chloride |
Substance ID | 24A6134 |
Classification year (FY) | FY2012 |
Ministry who conducted the classification | Ministry of Health, Labour and Welfare (MHLW)/Ministry of the Environment (MOE) |
New/Revised | New |
Classification result in other fiscal year | |
Download of Excel format | Excel file |
Item | Information |
---|---|
Guidance used for the classification (External link) | Physical Hazards and 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 |
- |
- | - | Solid (GHS definition) |
3 | Aerosols | Not applicable |
- |
- | - | Not aerosol products. |
4 | Oxidizing gases | Not applicable |
- |
- | - | Solid (GHS definition) |
5 | Gases under pressure | Not applicable |
- |
- | - | Solid (GHS definition) |
6 | Flammable liquids | Not applicable |
- |
- | - | Solid (GHS definition) |
7 | Flammable solids | Classification not possible |
- |
- | - | No data available. |
8 | Self-reactive substances and mixtures | Not applicable |
- |
- | - | There are no chemical groups present in the molecule associated with explosive or self-reactive properties. |
9 | Pyrophoric liquids | Not applicable |
- |
- | - | Solid (GHS definition) |
10 | Pyrophoric solids | Classification not possible |
- |
- | - | No data available. |
11 | Self-heating substances and mixtures | Classification not possible |
- |
- | - | No data available. |
12 | Substances and mixtures which, in contact with water, emit flammable gases | 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). |
13 | Oxidizing liquids | Not applicable |
- |
- | - | Solid (GHS definition) |
14 | Oxidizing solids | Not applicable |
- |
- | - | The substance is an organic compound containing chlorine which is a chlorine ion ionically bonded to quaternary ammonium and does not contribute to oxidization. |
15 | Organic peroxides | Not applicable |
- |
- | - | Organic compounds containing no bivalent -O-O- structure. |
16 | Corrosive to metals | Classification not possible |
- |
- | - | Test methods applicable to solid substances are not available. |
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 |
It was classified in Category 3 based on LD50 values of 238 mg/kg and 262 mg/kg for rats (EPA RED (2006)). |
1 | Acute toxicity (Dermal) | Not classified |
- |
- | - | It was classified as "Not classified" in the Classification JIS (corresponding to Category 5 in UN GHS classification) based on an LD50 value of 2,930 mg/kg for rabbits (EPA RED (2006)). |
1 | Acute toxicity (Inhalation: Gases) | Not applicable |
- |
- | - | Solid (GHS definition) |
1 | Acute toxicity (Inhalation: Vapours) | Classification not possible |
- |
- | - | No data available. |
1 | Acute toxicity (Inhalation: Dusts and mists) | Category 2 |
Danger |
H330 |
P304+P340
P403+P233 P260 P271 P284 P310 P320 P405 P501 |
It was classified in Category 2 based on an LC50 value of 0.07 mg/L by 4-hour exposure in rats (HPVIS (2009), corresponding to List 2). Besides, because the LC50 value was higher than the saturated vapour pressure concentration (4.54E-10 mg/L), it was regarded as an inhalation test on dust. |
2 | Skin corrosion/irritation | Category 1C |
Danger |
H314 |
P301+P330+P331
P303+P361+P353 P305+P351+P338 P304+P340 P260 P264 P280 P310 P321 P363 P405 P501 |
In a test by a 4-hour application to the skin of one rabbit, severe irritation symptoms continued for 24 hours, becoming leathery, decoloration, and necrosis were observed in the skin, and the test was ended because corrosivity was found on observation at 24 hours after the application. As a result, this substance was assessed to be corrosive to the rabbit skin (HPVIS (2009)). Therefore, it was classified in Category 1C. Besides, it was classified in C; R34 in EU classification (EC-JRC (ESIS) (Access on Oct. 2012)). |
3 | Serious eye damage/eye irritation | Category 1 |
Danger |
H318 |
P305+P351+P338
P280 P310 |
Extreme corneal opacity, iritis, and conjunctival irritation occurred, and the eye looked out of shape 1 hour after an application to the eye of one rabbit, and the total irritation score was 94 (maximum 110). The test was ended after 1 hour due to evidence of corrosivity obtained, and this substance was assessed to be corrosive to the rabbit eye (HPVIS (2009)). Therefore, it was classified in Category 1. |
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 it is listed as a contact allergen in Contact Dermatitis (5th, 2011) (corresponding to List 1). Besides, it is reported that the positive rate was 0% (0/20) in a skin sensitization test with guinea pigs (a Buehler test), and this substance was not a sensitizer (HPVIS (2009)). |
5 | Germ cell mutagenicity | Not classified |
- |
- | - | It was classified as "Not classified" based on a negative result in a chromosomal aberration test with bone marrow cells after oral administration to rats (in vivo somatic cell mutagenicity test) (USEPA/HPV (2005)). Besides, as for in vitro tests, it is reported that it was negative in all of an Ames test (HPVIS (2009)), a chromosomal aberration test with CHO cells (USEPA/HPV (2005)), and an HGPRT test with CHO cells (USEPA/HPV (2005)). |
6 | Carcinogenicity | Not classified |
- |
- | - | In a 104-week diet administration test with male and female rats (USEPA/HPV (2005)) and a 78-week diet administration test with male and female mice (HPVIS (2009)), reduced weight gain was observed as treatment-related effects in the high dose groups (rats: 1,500 ppm, mice: 1,000 ppm) in both tests, but no oncogenicity was found. Because there was no evidence of carcinogenicity in long-term administration tests with two animal species, it was classified as "Not classified." |
7 | Reproductive toxicity | Classification not possible |
- |
- | - | In a developmental toxicity test by oral administration to pregnant rats during the organogenesis period, maternal animals showed general toxicity such as decreases in body weights and food consumption, audible respiration, and gasping at the dose above 37.5 mg/kg/day, and a significant increase in late resorptions was observed at the dose of 50 mg/kg/day, but the effect was regarded to be due to maternal toxicity (HSDB (2010)). And in a developmental toxicity test by oral administration to pregnant rabbits during the organogenesis period, maternal animals showed general toxicity such as audible respiration, decreased weight gain, and hypoactivity at the dose of 3 mg/kg/day or above, and an increased number of dead fetuses/litter was found at 10 mg/kg/day where deaths were seen (USEPA/HPV (2005)). Adverse developmental effects were observed in both the tests, but because there were also deaths of maternal animals, they were estimated to be caused by severe maternal toxicity. Therefore, it was classified as "Classification not possible" due to lack of data. Besides, it is reported that in a two-generation reproductive test by diet administration to rats, reduced weight gain and decreased food consumption were found in the high dose group (1,000 ppm), but no reproductive toxicity was seen (USEPA/HPV (2005)). |
8 | Specific target organ toxicity - Single exposure | Category 2 (systemic toxicity) |
Warning |
H371 |
P308+P311
P260 P264 P270 P405 P501 |
In an acute oral toxicity test with rats (doses: 100-400 mg/kg, LD50 value, 262 mg/kg), there were signs such as inanimation, lacrimation, and diarrhea, and necropsy revealed discoloration and hemorrhage in the stomach and red-brown contents in the intestine in dead animals, but no marked changes in surviving animals (HPVIS (2009)). And in another acute oral toxicity test with rats (doses: 100-500 mg/kg, LD50 value, 238 mg/kg), primary signs were reported to include discoloration of urine, feces, and saliva, strabismus, ataxia, body tremors, labored respiration, slight to severe depression, and abdominal spasm (HPVIS (2009)). The above findings occurred at doses corresponding to the guidance value range for Category 1, but because it was hard to specify the target organ, and they were List 2 information, it was classified in Category 2 (systemic toxicity). |
9 | Specific target organ toxicity - Repeated exposure | Category 2 (systemic toxicity) |
Warning |
H373 |
P260
P314 P501 |
Almost no findings of adverse effects were seen at doses within the guidance value range in tests by 13-week or 104-week diet administration to rats, or 13-week or 78-week diet administration to mice, but blood-filled sinuses, hemosiderosis, and histiocytosis in the mesentery lymph node were observed at 1,500 ppm (75 mg/kg/day) corresponding to the guidance values for Category 2 only in a 104-week administration test with rats (USEPA/HPV (2005)). And it is reported that in an 8-week oral administration test with dogs, at 60 mg/kg/day (converted guidance value: 37 mg/kg/day), decreases in weight gain and food consumption as well as signs such as increased emesis, salivation, soft feces, and thin appearance were found, and mortality increased (HSDB (2010)). Because it was hard to specify the target organ for the above findings, it was classified in Category 2 (systemic toxicity). |
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 24-hour LC50 = 0.018 mg/L for crustacea (Daphnia magna) (AQUIRE, 2013). |
11 | Hazardous to the aquatic environment (Long-term) | Category 1 |
Warning |
H410 |
P273
P391 P501 |
If chronic toxicity data are used, then it is classified in Category 1 due to being not rapidly degradable (not readily degradable, a degradation rate by BOD: -3, -2, -2% (Biodegradation and Bioconcentration Results of Existing Chemical Substances under the Chemical Substances Control Law, 2008)), and 72-hour NOEC = 0.025 mg/L for algae (Pseudokirchneriella subcapitata) (AQUIRE, 2013). If acute toxicity data are used for a trophic level for which chronic toxicity data are not obtained, then it is classified in Category 1 due to being not rapidly degradable (not readily degradable, a degradation rate by BOD: -3, -2, -2% (Biodegradation and Bioconcentration Results of Existing Chemical Substances under the Chemical Substances Control Law, 2008)), and 96-hour LC50 = 0.39 mg/L for fish (Oncorhynchus kisutch) (AQUIRE, 2013). From the above results, it was classified in Category 1. |
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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