Item | Information |
---|---|
CAS RN | 65405-77-8 |
Chemical Name | cis-3-Hexenyl salicylate |
Substance ID | R02-A-010-METI, MOE |
Classification year (FY) | FY2020 |
Ministry who conducted the classification | Ministry of Economy, Trade and Industry (METI)/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) | 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) | |
Model SDS by MHLW (External link) | |
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. |
2 | Flammable gases | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition) |
3 | Aerosols | Not classified (Not applicable) |
- |
- | - | Not aerosol products. |
4 | Oxidizing gases | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition) |
5 | Gases under pressure | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition) |
6 | Flammable liquids | Not classified |
- |
- | - | A flash point was 110 deg C (closed-cup) (GESTIS (Accessed June 2020)). |
7 | Flammable solids | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition) |
8 | Self-reactive substances and mixtures | Classification not possible |
- |
- | - | There is a chemical group associated with self-reactive properties (ethylenes) present in the molecule, but the classification is not possible due to no data. |
9 | Pyrophoric liquids | Not classified |
- |
- | - | It is estimated that it does not ignite at normal temperatures from an autoignition temperature of 390 deg C (ECHA (Accessed June 2020)). |
10 | Pyrophoric solids | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition) |
11 | Self-heating substances and mixtures | Classification not possible |
- |
- | - | 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). |
13 | Oxidizing liquids | Not classified (Not applicable) |
- |
- | - | The substance is an organic compound containing oxygen (but not fluorine or chlorine) which is chemically bonded only to carbon or hydrogen. |
14 | Oxidizing solids | Not classified (Not applicable) |
- |
- | - | Liquid (GHS definition) |
15 | Organic peroxides | Not classified (Not applicable) |
- |
- | - | Organic compounds containing no bivalent -O-O- structure in the molecule. |
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. |
Hazard class | Classification | Pictogram Signal word |
Hazard statement (code) |
Precautionary statement (code) |
Rationale for the classification | |
---|---|---|---|---|---|---|
1 | Acute toxicity (Oral) | Not classified |
- |
- | - | [Rationale for the Classification] It was classified as "Not classified" (Category 5 in UN GHS classification) from (1). [Evidence Data] (1) LD50 for rats: 5,000 mg/kg (REACH registration dossier (Accessed June 2020)) |
1 | Acute toxicity (Dermal) | Not classified |
- |
- | - | [Rationale for the Classification] It was classified as "Not classified" from (1). [Evidence Data] (1) LD50 for rabbits: > 5,000 mg/kg (REACH registration dossier (Accessed June 2020)) |
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] Classification not possible due to lack of data. |
3 | Serious eye damage/eye irritation | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
4 | Respiratory sensitization | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
4 | Skin sensitization | Not classified |
- |
- | - | [Rationale for the Classification] It was classified as "Not classified" from (1) - (3). [Evidence Data] (1) It is reported that in a patch test in 50 persons, by induction by 3-week occlusive application of about 100 mg of a 15% solution of this substance and challenge by 48-hour occlusive application of about 100 mg an 8% solution at 14 days after induction, there were no skin reactions (REACH registration dossier (Accessed June 2020)). (2) It is reported that in a patch test in 25 persons, after 24-hour occlusive application of a 5% solution of sodium lauryl sulfate to the forearms followed by 48-hour application of this substance, no positive reactions were seen in any subject (REACH registration dossier (Accessed June 2020)). (3) It is reported that in a maximization test with guinea pigs (n = 20) (OECD TG 406, GLP, intradermal administration: 5% solution), a positive rate was 0% (0/20) at both 24 and 48 hours after removal of patches (REACH registration dossier (Accessed June 2020)). |
5 | Germ cell mutagenicity | Classification not possible |
- |
- | - | [Rationale for the Classification] Since there was no in vivo data, classification was not possible due to lack of data. [Evidence Data] (1) In a bacterial reverse mutation test, negative results were reported (JECDB (Accessed June 2020)). (2) In an in vitro mammalian cell (CHL/IU) chromosome aberration test, negative results were reported (JECDB (Accessed June 2020)). |
6 | Carcinogenicity | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. |
7 | Reproductive toxicity | Classification not possible |
- |
- | - | [Rationale for the Classification] Since (1) was a screening test, the concern with respect to reproductive/developmental effects could not be ruled out. Therefore, classification was not possible due to lack of data. In (1), reproductive/developmental effects were observed at 360 mg/kg/day, but since the maternal death rate exceeded 10%, classification based on (1) was considered inappropriate. At the low and intermediate doses at which there were no general toxicity effects, no reproduction/developmental toxicity was observed, but there was no data on developmental toxicity. [Reference Data, etc.] (1) It was reported that in a combined repeated dose toxicity study with the reproduction/developmental toxicity screening test with rats dosed by gavage (OECD TG422, GLP, for 14 days prior to mating and until the day before necropsy (for 42 days) (males), for 14 days prior to mating and until day 4 of lactation (for 41 to 49 days) (females)), at 360 mg/kg/day, general toxicity effects such as death of maternal rats (3/12 cases), reduced body weight gain, reduced food consumption, hematological effects (lower erythrocyte count, higher MCV/MCH/reticulocyte rates and prolonged APTT/PT (males), lower platelet count (females)), higher liver weights/higher AST/ALT (females) and reproductive effects (tendency of lower gestation index, prolonged gestation period, a lower number of implantation sites, tendency of a lower delivery index, tendency of a higher number of stillborn pups) were observed in parental rats, and a lower number of liveborn pups, increased external abnormalities (vestigial tail, complete rachischisis, exencephaly), reduced body weight gain after birth, and a lower viability index on postnatal day 4 were observed in pups (JECDB (Accessed June 2020)). |
8 | Specific target organ toxicity - Single exposure | Classification not possible |
- |
- | - | [Rationale for the Classification] Classification not possible due to lack of data. Classification was not possible based on (1) because the doses used in the test exceeded the range of Category 2. [Reference Data, etc.] (1) It was reported that in an acute dermal toxicity test with rabbits, skin irritation signs such as redness and edema were observed at 5,000 mg/kg (REACH registration dossier (Accessed June 2020)). |
9 | Specific target organ toxicity - Repeated exposure | Classification not possible |
- |
- | - | [Rationale for the Classification] Based on (1), it was considered to be classified as "Not classified" in the oral route, but there was no information on toxicity in the other route. Therefore, classification was not possible due to lack of data. [Evidence Data] (1) It was reported that in a combined repeated dose toxicity study with the reproduction/developmental toxicity screening test with rats dosed by gavage (OECD TG422, GLP) (males: for 42 days, females: for 41 to 49 days), no effects were observed at the doses of up to 120 mg/kg/day (converted guidance value: 56 mg/kg/day (males), 54.7 mg/kg/day (females), within the range for Category 2), while death and lower body weight gain (pregnant females), hematological effects (anemic findings and prolonged coagulation time, mainly in males) and increased hepatogenic enzyme activities (males and females) were observed at 360 mg/kg/day (converted guidance value: 168 mg/kg/day (males), 164 mg/kg/day (females), in the range corresponding to "Not classified") (JECDB (Accessed June 2020)). |
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) | Category 1 |
Warning |
H400 | P273 P391 P501 |
It was classified in Category 1 from 48-hour EC50 = 0.6 mg/L for crustacea (Daphnia magna) (REACH registration dossier, 2021). |
11 | Hazardous to the aquatic environment Long term (Chronic) | Category 1 |
Warning |
H410 | P273 P391 P501 |
If chronic toxicity data are used, then it is classified in Category 2 because sufficient data on rapid degradability were not obtained and due to 72-hour NOErC = 0.15 mg/L for algae (Desmodesmus subspicatus) (REACH registration dossier, 2021). 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 because sufficient data on rapid degradability were not obtained and due to 48-hour EC50 = 0.6 mg/L for crustacea (Daphnia magna) (REACH registration dossier, 2021). By drawing a comparison between 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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