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Eradicane

Eradicane Structure
CAS No.
759-94-4
Chemical Name:
Eradicane
Synonyms
EPTC;Genep;Witox;EPTAM;ALIROX;R-1608;Niptan;Torbin;fda1541;eptam6e
CBNumber:
CB4169538
Molecular Formula:
C9H19NOS
Molecular Weight:
189.32
MOL File:
759-94-4.mol
MSDS File:
SDS
Modify Date:
2023/5/4 17:34:42

Eradicane Properties

Melting point 25°C
Boiling point 127°C (20 torr)
Density 0.95
vapor pressure 3.192Pa at 25℃
refractive index nD30 1.4750
Flash point 116 °C
storage temp. 0-6°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka -1.22±0.70(Predicted)
form Liquid
color Clear colorless
Water Solubility 0.375 g/100 mL
Merck 13,3669
BRN 1762751
Stability Stable. Incompatible with strong oxidizing agents.
LogP 3.21 at 20℃
NIST Chemistry Reference Carbamothioic acid, dipropyl-, s-ethyl ester(759-94-4)
EPA Substance Registry System S-Ethyl dipropylthiocarbamate (759-94-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H302+H312-H315-H317-H319-H331-H411
Precautionary statements  P273-P280-P301+P312-P302+P352+P312-P304+P340+P311-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22
Safety Statements  2-23
RIDADR  2902
WGK Germany  1
RTECS  FA4550000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29302000
Toxicity LD50 orally in rats: 1631 mg/kg (Antognini)

Eradicane price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 45469 EPTC PESTANAL?, analytical standard 759-94-4 250MG ₹6516.65 2022-06-14 Buy
Product number Packaging Price Buy
45469 250MG ₹6516.65 Buy

Eradicane Chemical Properties,Uses,Production

Chemical Properties

Light yellow liquid or yellow granular material. Commercial products may be in the form of dusts, sprays, solutions, wettable powder suspensions or emulsions.

Uses

A preemergence herbicide.

General Description

S-Ethyl dipropylthiocarbamate (EPTC) is a pale to dark yellow liquid with an aromatic odour/pleasant scent characteristic to thiocarbamates. EPTC is a commonly used herbicide. EPTC has a pleasant scent and at 20°C is miscible with most organic solvents, including acetone, ethyl alcohol, kerosene, methyl isobutyl ketone (MIBK), and xylene.
EPTC was the first thiocarbamate herbicide developed. EPTC formulations are used for the control of preemergent weeds, especially grasses. EPTC inhibits photosynthesis, respiration, and the synthesis of lipids, proteins, and RNA in these seedlings. Resistant plants are less sensitive to the herbicidal action apparently due to their ability to rapidly metabolise EPTC.

Air & Water Reactions

Water insoluble. Slowly decomposes in water to form carbon disulfide and propyl amine. Such decompositions are accelerated by acids.

Reactivity Profile

Eradicane may generate flammable gases with aldehydes, nitrides, and hydrides. Incompatible with acids, peroxides, and acid halides.

Health Hazard

SYMPTOMS: Symptoms of exposure to Eradicane may include headache, giddiness, nervousness, blurred vision, weakness, nausea, cramps, diarrhea, sweating, miosis, tearing, salivation, vomiting and cyanosis.

Fire Hazard

Flash point data are not available for Eradicane, but Eradicane is probably combustible.

Agricultural Uses

Herbicide: Some formulations are Restricted Group Pesticides (RUP). EPTC is a pre-emergence and early post-emergence herbicide used to control the growth of germinating annual weeds, including broadleaves, grasses, and sedges. It is used in every region of the United States in the production of a wide variety of food crops. The heaviest usage is in the Corn Belt, Northeastern and Mid-Atlantic states, Coastal and Northern Great Plains and in the Pacific Northwest on corn, potatoes, sweet potatoes, dry beans, peas, alfalfa, and snap beans. EPTC is also used on home-grown vegetables and ornamentals. Not approved for use in EU countries. Registered for use in the U.S. and other countries

Trade name

ALIROX®; EPTAM®; EPTAM® 6E; EPTAM 2.3G (granular, 2.3% by weight); EPTAM 10G (granular, 10% by weight); ERADICANE®; GENEP® EPTC; R-1608®; SHORTSTOP®; STAUFFER® R 1608; TORBIN®

Safety Profile

Poison by ingestion, inhalation, and intravenous routes. Moderately toxic by skin contact route. Mutation data reported. An herbicide. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also CARBAMATES

Potential Exposure

EPTC is a pre-emergence and early postemergence thiocarbamate herbicide used to control the growth of germinating annual weeds, including broadleaves, grasses, and sedges. It is used in every region of the United States in the production of a wide variety of food crops. The heaviest usage is in the Corn Belt, Northeastern and Mid-Atlantic states, Coastal and Northern Great Plains and in the Pacific Northwest on corn, potatoes, sweet potatoes, dry beans, peas, alfalfa, and snap beans. EPTC is also used on home-grown vegetables and ornamentals. Some formulations are Restricted Group Pesticides (RUP)

Metabolic pathway

A new class of xenobiotic metabolite derived from the glutathione conjugate is produced by corn, cotton, and corn cell suspension cultures treated with 14C-EPTC (S-ethyl dipropylthiocarbamate). This metabolite is characterized as S-(N,N-dipropylcarbamoyl)-O- malonyl-3-thiolactic acid and is not detected in soybean plants or peanut cell suspension cultures. A second major metabolite of EPTC, S-(N,N- dipropylcarbamoyl)-N-malonylcysteine, is present in all tissues.

Shipping

UN2902 Pesticides, liquid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required

Incompatibilities

Thiocarbamate esters are combustible. They react violently with powerful oxidizers such as calcium hypochlorite. Thermal decomposition of thiocarbamate compounds include carbon disulfide, oxides of sulfur, oxides of nitrogen, hydrogen sulfide, ammonia, andmethylamine. Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. Flammable gases are generated by the combination of thiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates are incompatible with acids, peroxides, and acid halides.

Waste Disposal

Land burial is acceptable for small quantities. Larger quantities can be incinerated. (EPTC is combustible and could be incinerated. Recommendable method: Incineration. Peer-review: Incineration in a unit witheffluent gas scrubbing is recommendable for large amount. 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. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal

Eradicane Preparation Products And Raw materials

Global( 109)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
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s-ethyln,n-di-n-propylthiocarbamate Stauffer R 1608 staufferr1608 eptc (bsi,iso,wssa,jmaf) EPTC(Eptam) ETHYLDIPROPYLTHIOCARBAMATE S-ETHYLDIISOPROPYLTHIOCARBAMATE S-ETHYL DIPROPYLTHIOCARBAMATE, 1GM, NEAT EPTAM (EPTC), 250MG, NEAT EPTC PESTANAL (S-ETHYL N,N-DIPROPYL-THIO ALIROX safener eptc S-ETHYL N N-DI-N-PROPYLTHIOLCARBAMATE S-Ethyl-N,N-dipropylthiocarbamate S-Ethyl dipropylcarbamothioate S-ETHYL DIPROPYLTHIOCARBAMATE R-1608 ethyln,n-di-n-propylthiolcarbamate ethyl-n,n-dipropylthiolcarbamate fda1541 Genep Genep eptc genepeptc Knoxweed N,N-Dipropylthiocarbamic acid S-ethyl ester n,n-dipropylthiocarbamicacids-ethylester Niptan S-Aethyl-N,N-dipropylthiolcarbamat s-aethyl-n,n-dipropylthiolcarbamat[german] S-Ethyl N,N-di-n-propylthiocarbamate Carbamothioic acid, dipropyl-, S-ethyl ester EPTC (ISO) S-ethyl dipropylthiocarbamate EPTC Standard S-ethyl N,N-dipropylcarbamothioate S-Ethyl dipropylthiocarbamate 500mg [759-94-4] Torbin Witox HARVISIT ERADICANE EPTAM(R) EPTAM EPTC dichlormid eptc Carbamic acid, dipropylthio-, S-ethyl ester Dipropylcarbamothioic acid S-ethyl ester dipropylcarbamothioicacids-ethylester dipropyl-carbamothioicacis-ethylester dipropylthiocarbamicacids-ethylester dipropylthio-carbamicacis-ethylester Eptam 6E eptam6e EPTC (pesticide, MW 189) Ethyl di-n-propylthiolcarbamate Ethyl N,N-di-n-propylthiolcarbamate Ethyl N,N-dipropylthiolcarbamate ethyldi-n-propylthiolcarbamate Carbamothioic acid, N,N-dipropyl-, S-ethyl ester EPTC@1000 μg/mL in Methanol