Name | Quizalofop-Ethyl |
Synonyms | All-in-one Quizalofop-Ethyl Assure (Du Pont) Quinazalofop-ethyl Early Growth Response-3 Quizalofop-ethyl Standard 2-[4-(6-Chloro-2-quinoxalinyl)-phenoxy]ethyl propionate ethyl 2-[3-(6-chloroquinoxalin-2-yl)oxyphenoxy]propanoate Ethyl 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoate ethyl 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoate Quizalofop-ethyl,Ethyl 2-[4-(6-chloro-2-quinoxalinyloxy)phenoxy]propionate |
CAS | 76578-14-8 |
InChI | InChI=1/C19H17ClN2O4/c1-3-24-19(23)12(2)25-14-5-4-6-15(10-14)26-18-11-21-17-9-13(20)7-8-16(17)22-18/h4-12H,3H2,1-2H3 |
Molecular Formula | C19H17ClN2O4 |
Molar Mass | 372.8 |
Density | 1.2671 (rough estimate) |
Melting Point | 92-93° |
Boling Point | bp0.2 220° |
Flash Point | 100°C |
Water Solubility | 303ug/L(temperature not stated) |
Vapor Presure | 3.05E-10mmHg at 25°C |
Appearance | neat |
Merck | 13,8178 |
BRN | 7145610 |
pKa | -1.39±0.48(Predicted) |
Storage Condition | 0-6°C |
Refractive Index | 1.6800 (estimate) |
Hazard Symbols | Xn - Harmful |
Risk Codes | 21/22 - Harmful in contact with skin and if swallowed. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
UN IDs | UN3077 9/PG 3 |
WGK Germany | 3 |
RTECS | UA2458255 |
HS Code | 29333990 |
Toxicity | LD50 in male, female rats, male, female mice (mg/kg): 1670, 1480, 2350, 2360 orally; all 10,000 dermally; LC50 (96 hr) in rainbow trout: 10.7 mg/l (Sakata) |
The original drug was white or gray-brown powder. mp92 ~ 93 deg C; bpo.2 220. Solubility at 20 °c (g/L): Water 0003, acetone 111, ethanol 9, hexane 2.6, xylene 120. Storage Stability under normal conditions.
from 4-chloro-2-nitroaniline in benzene or toluene solvent, in the presence of pyridine catalyst reaction with diketene, to produce the corresponding open acetylation, the product is treated with an aqueous alkaline solution to form the corresponding quinoxalinone nitrogen oxide. Quinoxalinone nitrogen oxide in the presence of sodium hydroxide (or potassium hydroxide), toluene water as solvent, reaction at 60~70 deg C, the formation of ammonia oxide in aqueous alkali solution, at room temperature, with a certain amount of sodium borohydride reaction, get 6 chlorine 2 (1H)-quinoxalinone. 6 A chlorine 2 (1H)-quinoxalinone in DMF solution with thionyl chloride, 2,6-= chloroquinoxaline. 2,6-= chloroquinoxaline is then condensed with hydroquinone in DMF under nitrogen to give 4-(6-chloro-2-quinoxalinyloxy) phenol. 4-(-6-chloro -2-quinoxalinoxy) phenol and a-halogenated propionic acid ethyl ester in acetonitrile solution, with potassium carbonate as acid binding agent, condensation to obtain quetiapine. Quetiapine can also be prepared by direct action of 2,6-= chloroquinoxaline and ethyl p-hydroxyphenoxypropionate in the presence of potassium carbonate in an acetonitrile solution under reflux.
as a post-emergence herbicide, annual and perennial weeds can be selectively controlled. It has excellent herbicidal activity on gramineous weeds, and is highly selective between gramineous weeds and dicotyledonous crops. The stems and leaves can complete the absorption of the chemicals in a few hours, and the annual weeds can spread throughout the whole plant in 24 hours. Suitable for cotton, soybean, rape, peanut, flax, apple, grape, sugar beet and a variety of wide leaf vegetable crops, control of monocotyledonous weeds, dog tooth root, perennial weeds such as reeds also have a role. In the mixed field of single-and double-leaf weeds, it can be used together with the herbicides for controlling broad-leaved weeds such as sugarbeet tannin, Huwei, broad-leaved litter and weed burning.
male and female rats, male and female mice oral LD50 (mg/kg): 1670, 1480,2350, 2360. Both rat and mouse percutaneous LD50> lOOOmg/ kg. No irritation to the skin, mild irritation to the eyes. There was no teratogenic, mutagenic and carcinogenic effect on animals in the test dose. Carp LC50 was 0. 6mg/L(48h), 10.7mg/L (9h) for rainbow trout, 2.8mg/L (96h) for blue gill bionics and 2.1mg/L (96h) for Daphnia. The Wild Duck LD50 is 2000mg/kg.
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Application | dry field herbicide, suitable for soybean, peanut, cotton, potato, mung bean, watermelon, control of grass weeds in broad-leaved crop fields such as rapeseed. |
category | pesticide |
toxicity grade | poisoning |
Acute toxicity | oral-rat LD50: 1480 mg/kg; Oral-mouse LD50: 2350 mg/kg |
flammability hazard characteristics | toxic nitrogen oxides and chloride gases from combustion |
storage and transportation characteristics | The warehouse is ventilated and dried at low temperature; It is stored and transported separately from food raw materials |
extinguishing agent | dry powder, foam, sand |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |