| Identification | Back Directory | [Name]
CYCLOATE | [CAS]
1134-23-2 | [Synonyms]
EUREX
SABET
Ronit
etsan
R-2063
RO-NEET
CYCLOATE
Cycolate
ro-neete
AGRO-NET
HSDB 1712
HSDB-1712
ro-neet10g
ro-neet6-e
hexylthiocarbam
Cycloate Standard
CYCLOATE, 1GM, NEAT
hexylthiocarbam (jmaf)
cycloate (bsi,iso,wssa)
5-Ethylcyclohexylehtylcarbatate
Cycloate@1000 μg/mL in Methanol
Cycloate @100 μg/mL in Methanol
S-ethyl N-cyclohexylthiocarbamate
s-ethylethylcyclohexylthiocarbamate
s-ethylcyclohexylethylcarbamothioate
s-ethyln-ethylthiocyclohexanecarbamate
S-ETHYL CYCLOHEXYL(ETHYL)THIOCARBAMATE
S-ETHYLN-ETHYLCYCLOHEXANECARBAMOTHIOATE
CYCLOATE PESTANAL (S-ETHYL N-CYCLO- HEXY
S-Ethyl N-ethyl-N-cyclohexylthiocarbamate
S-ethyl N-cyclohexyl-N-ethylcarbamothioate
5-ETHYL N-CYCLOHEXYL N-ETHYL THIOCARBAMATE
s-ethyln-cyclohexyl-n-ethyl(thiocarbamate)
cyclohexylethylthio-carbamicacis-ethylester
S-ethyl N-cyclohexyl-N-ethyl-carbamothioate
S-ETHYL-N-ETHYL-N-CYCLOHEXYLTHIOL-CARBAMATE
Cycloate Solution in Acetonitrile, 100μg/mL
cyclohexylethyl-carbamothioicacis-ethylester
n-ethylthio-cyclohexanecarbamicacis-ethylester
Cyclohexylethylcarbamothioic acid, S-Ethyl ester
Carbamic acid, cyclohexylethylthio-, S-ethyl ester
Carbamothioic acid, cyclohexylethyl-, S-ethyl ester
N-cyclohexyl-N-ethyl-thiocarbamic acid S-ethyl ester
Cyclohexanecarbamic acid, N-ethylthio-, S-ethyl ester
Carbamothioic acid, N-cyclohexyl-N-ethyl-, S-ethyl ester | [EINECS(EC#)]
214-482-7 | [Molecular Formula]
C11H21NOS | [MDL Number]
MFCD00055341 | [MOL File]
1134-23-2.mol | [Molecular Weight]
215.36 |
| Chemical Properties | Back Directory | [Appearance]
Cycolate is an oily, clear, or amber to yellow
liquid. Aromatic odor; | [Melting point ]
11.5°C | [Boiling point ]
145 °C(Press: 10 Torr) | [density ]
1.0156 | [vapor pressure ]
0.002Pa at 25℃ | [refractive index ]
1.5500 (estimate) | [Fp ]
>100 °C | [storage temp. ]
0-6°C | [form ]
Liquid | [pka]
-1.30±0.20(Predicted) | [Water Solubility ]
85mg/L(22 ºC) | [BRN ]
2937178 | [LogP]
3.88 at 20℃ | [CAS DataBase Reference]
1134-23-2 | [EPA Substance Registry System]
Cycloate (1134-23-2) |
| Hazard Information | Back Directory | [Chemical Properties]
Cycolate is an oily, clear, or amber to yellow
liquid. Aromatic odor; | [General Description]
Colorless liquid with an aromatic odor. Used as a selective systemic herbicide. | [Air & Water Reactions]
Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids or alkalis. | [Reactivity Profile]
CYCLOATE is a thiocarbamate ester. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides. | [Agricultural Uses]
Herbicide: Used to control broadleaf weeds, annual and perennial grasses and nutgrass in spinach, beets, and sugar
beets. Not approved for use in EU countries. Actively
registered in the U.S. | [Trade name]
ETSAN®; EUREX®; R-2063®; RO-
NEET®; RO-NEET®-6E; RO-NEET® 10G; RONIT®;
SABET® | [Potential Exposure]
Cycolate is a thiocarbamate herbicide
used to control broad leaf weeds, annual and perennial
grasses and nutgrass in spinach, beets, and sugar beets. | [First aid]
Eyes: If this chemical gets into the eyes, remove
any contact lenses at once and irrigate immediately for at
least 15 minutes, occasionally lifting upper and lower lids.
Seek medical attention immediately. If this chemical contacts
the skin, remove contaminated clothing and wash immedi-
ately with soap and water. Seek medical attention immedi-
ately. If this chemical has been inhaled, remove from
exposure, begin rescue breathing (using universal precau-
tions) if breathing has stopped, and CPR if heart action has
stopped. Transfer promptly to a medical facility. When this
chemical has been swallowed, get medical attention. If victim
is conscious and able to swallow, have victim drink 4 to 8 oz
of water. Do not induce vomiting. | [Shipping]
UN3082 Environmentally Hazardous substances,
liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous haz-
ardous material, Technical Name Required | [Incompatibilities]
Cycolate reacts violently with powerful
oxidizers such as calcium hypochlorite. Thiocarbamate
esters are combustible. Poisonous gases are generated by
the thermal decomposition of thiocarbamate compounds,
including carbon disulfide, oxides of sulfur, oxides of nitro-
gen, hydrogen sulfide, ammonia, and methylamine. Thio
and dithiocarbamates slowly decompose in aqueous solu-
tion to form carbon disulfide and methylamine or other
amines. Such decompositions are accelerated by acids.
Flammable gases are generated by the combination of thio-
carbamates with aldehydes, nitrides, and hydrides.
Thiocarbamates are incompatible with acids, peroxides, and
acid halides. | [Waste Disposal]
Do not discharge into drains
or sewers. Dispose of waste material as hazardous waste
using a licensed disposal contractor to an approved landfill.
Consult with environmental regulatory agencies for guid-
ance on acceptable disposal practices. Incineration with
effluent gas scrubbing is recommended. Containers must be
disposed of properly by following package label directions
or by contacting your local or federal environmental control
agency, or by contacting your regional EPA office. | [Uses]
Herbicide used to control several broad-leaved weeds and many annual grasses in
sugar beets, table beets and spinach | [Definition]
ChEBI:Cycloate is a primary aliphatic amine. | [Flammability and Explosibility]
Nonflammable | [Environmental Fate]
Soil. The reported half-life in soil is approximately 4–8 weeks (Hartley and Kidd,
1987)
Groundwater. According to the U.S. EPA (1986) cycloate has a high potential to leach
to groundwater
Plant. Cycloate is rapidly metabolized in sugarbeets to carbon dioxide, ethylcyclohexylamine, sugars, amino acids and other natural constituents (Humburg et al., 1989)
Chemical/Physical. In the gas phase, cycloate reacts with hydroxyl and NO3 radicals
but not with ozone. With hydroxy radicals, cleavage of the cyclohexyl ring was suggested
leading to the formation of a compound tentatively identified as C2H5(CHO)NC(O)SC2H5.
The calculated photolysis lifetimes of cycloate in the troposphere with hydroxyl and NO3
radicals are 5.2 hours and 1.4 days, respectively (Kwok et al., 1992). |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,N | [Risk Statements ]
22-51/53 | [Safety Statements ]
61 | [RIDADR ]
UN3082 9/PG 3 | [WGK Germany ]
2 | [RTECS ]
GU7200000 | [Hazardous Substances Data]
1134-23-2(Hazardous Substances Data) | [Toxicity]
LC50 (96-hour) for rainbow trout 4.5 mg/L (Hartley and Kidd, 1987), for mosquito fish 10 ppm (Humburg et al., 1989); acute oral LD50 of technical cycloate for male
and female rats 2,000–3,190 and 3,160–4,100 mg/kg, respectively (Hartley and Kidd,
1987), 1,678 mg/kg (RTECS, 1985) |
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