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CYCLOATE

CYCLOATE Structure
CAS No.
1134-23-2
Chemical Name:
CYCLOATE
Synonyms
SABET;EUREX;Ronit;etsan;R-2063;RO-NEET;CYCLOATE;Cycolate;ro-neete;AGRO-NET
CBNumber:
CB0134167
Molecular Formula:
C11H21NOS
Molecular Weight:
215.36
MOL File:
1134-23-2.mol
MSDS File:
SDS
Modify Date:
2024/8/4 16:55:17

CYCLOATE Properties

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)
Flash point >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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H331-H411
Precautionary statements  P261-P271-P273-P304+P340+P311-P391-P403+P233
Hazard Codes  Xn,N
Risk Statements  22-51/53
Safety Statements  61
RIDADR  UN3082 9/PG 3
WGK Germany  2
RTECS  GU7200000
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)

CYCLOATE price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 45408 Cycloate PESTANAL?, analytical standard 1134-23-2 250MG ₹5986.23 2022-06-14 Buy
Product number Packaging Price Buy
45408 250MG ₹5986.23 Buy

CYCLOATE Chemical Properties,Uses,Production

Chemical Properties

Cycolate is an oily, clear, or amber to yellow liquid. Aromatic odor;

Uses

Herbicide used to control several broad-leaved weeds and many annual grasses in sugar beets, table beets and spinach

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.

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).

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.

CYCLOATE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 79)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-29-81148696 +86-15536356810 China 2584 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
Career Henan Chemica Co +86-0371-86658258 +8613203830695 China 30253 58 Inquiry
Hebei Guanlang Biotechnology Co., Ltd. +8619930503259 China 18433 58 Inquiry
SUZHOU SENFEIDA CHEMICAL CO.,LTD +86-0512-83500002 +8615195660023 China 23053 58 Inquiry
Hebei Fengmu Trading Co., Ltd. +8613393234347 China 2986 58 Inquiry
LGC Standards +44 (0)20 8943 8480 United Kingdom 6495 0 Inquiry
Cyclohexylethylcarbamothioic acid, S-Ethyl ester Cycolate N-cyclohexyl-N-ethyl-thiocarbamic acid S-ethyl ester S-ethyl N-cyclohexyl-N-ethylcarbamothioate S-ethyl N-cyclohexyl-N-ethyl-carbamothioate CYCLOATE EUREX S-ETHYL CYCLOHEXYL(ETHYL)THIOCARBAMATE S-ETHYL-N-ETHYL-N-CYCLOHEXYLTHIOL-CARBAMATE SABET RO-NEET R-2063 Carbamic acid, cyclohexylethylthio-, S-ethyl ester Carbamothioic acid, cyclohexylethyl-, S-ethyl ester Cyclohexanecarbamic acid, N-ethylthio-, S-ethyl ester ro-neete Ronit S-Ethyl N-ethyl-N-cyclohexylthiocarbamate s-ethylcyclohexylethylcarbamothioate s-ethylethylcyclohexylthiocarbamate s-ethyln-cyclohexyl-n-ethyl(thiocarbamate) s-ethyln-ethylthiocyclohexanecarbamate 5-ETHYL N-CYCLOHEXYL N-ETHYL THIOCARBAMATE AGRO-NET S-ethyl N-cyclohexylthiocarbamate CYCLOATE, 1GM, NEAT CYCLOATE PESTANAL (S-ETHYL N-CYCLO- HEXY cycloate (bsi,iso,wssa) hexylthiocarbam (jmaf) S-ETHYLN-ETHYLCYCLOHEXANECARBAMOTHIOATE 5-Ethylcyclohexylehtylcarbatate cyclohexylethyl-carbamothioicacis-ethylester cyclohexylethylthio-carbamicacis-ethylester etsan hexylthiocarbam n-ethylthio-cyclohexanecarbamicacis-ethylester ro-neet10g ro-neet6-e Cycloate @100 μg/mL in Methanol Cycloate Standard Cycloate@1000 μg/mL in Methanol Carbamothioic acid, N-cyclohexyl-N-ethyl-, S-ethyl ester Cycloate Solution in Acetonitrile, 100μg/mL HSDB 1712 HSDB-1712 Enavogliflozin Impurity 28 1134-23-2 000134-23-3 C11H21NOS Alphabetic C CO - CZPesticides&Metabolites Herbicides Thiocarbamates