Eradicane Property

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

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

Hazardous Substances Data

759-94-4(Hazardous Substances Data)

Toxicity

LD50 orally in rats: 1631 mg/kg (Antognini)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H331Toxic if inhaled

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Eradicane Chemical Properties,Usage,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

Selective systemic herbicide used for preemergence control of perennial and annual grasses such as johnsongrass, nutgrass and quackgrass. Also for control of some broadleaved weeds such as chickweed, henbit, lambsquarters, pigweed and purslane. EPTC is also used in vegetable crops, alfalfa, cotton, flax, pineapple, almonds and walnuts.

Uses

EPTC is a pesticide, S-Ethyl-N,N-dipropylthiocarbamate.

Uses

A preemergence herbicide.

Definition

ChEBI: EPTC is a tertiary amine.

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 714, 1959 DOI: 10.1021/ja01512a052

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.

Flammability and Explosibility

Non flammable

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)

Environmental Fate

Soil. EPTC is rapidly degraded by soil microbes and fungi yielding carbon dioxide, ethyl mercaptan and amino residues (Kaufman, 1967; Lee, 1984; Hartley and Kidd, 1987). Degradation occurs via hydrolysis of the ester linkage forming the corresponding mercaptan, alkylamine (n-dipropylamine) and carbon dioxide. Transthiolation and oxidation of the mercaptan forms the alcohol which is further oxidized to afford a metabolic pool (Kaufman, 1967). EPTC partially degraded in both sterile and nonsterile clay soils. Mineralization was not observed since carbon dioxide was not detected (MacRae and Alex- ander, 1965). EPTC sulfoxide was also reported as a metabolite identified in soil (Somasundaram and Coats, 1991) and in corn plants (Casida et al., 1974). The rapid formation of carbon dioxide was also observed from the microbial degradation of EPTC by a microbial metabolite isolated from Jimtown loam soil and designated JE1 (Dick et al., 1990). These researchers proposed that EPTC hydroxylated at the a-propyl carbon forming the unstable a-hydroxypropyl EPTC which degrades to N-depropyl EPTC and propionaldehyde. Metabolization of N-depropyl EPTC yields s-ethyl formic acid and propylamine. Demethylation of s-ethyl formic acid gives s-methyl formic acid. Propylamine and smethyl formic acid probably degrades to ammonia and methyl mercaptan, respectively and carbon dioxide (Dick et al., 1990). The reported half-lives in soil ranged from 2 to 4 weeks in two agricultural soils (Regina heavy clay and Weyburn loam) (Smith and Fitzpatrick, 1970) to 30 days (Jury et al., 1987). Rajagopal et al. (1989) reported that the persistence of EPTC in soil ranged from <4 to 6 weeks when applied at recommended rates.
Plant. EPTC is rapidly metabolized by plants to carbon dioxide and naturally occurring plants constituents (Humburg et al., 1989).
Chemical/Physical. Emits toxic fumes of phosphorus and sulfur oxides when heated to decomposition (Sax and Lewis, 1987).
In the gas phase, EPTC reacts with hydroxyl and/or NO3 radicals but not with ozone. With hydroxy radicals in the presence of NO3, S-ethyl N-formyl-N-propylthiocarbamate formed as the major product. With NO3 radicals only, the major product was C3H7(CHO)NC(O)SC2H5. In addition, a minor product formed tentatively identified as CH3CH2CH2(CH3CH2C(O))NC(O)SCH2CH3. The calculated photolysis lifetimes of EPTC in the troposphere with hydroxyl and NO3 radicals are 5.8 hours and 5.0 days, respectively (Kwok et al., 1992).

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