Name | QUINOXYFEN |
Synonyms | Quintec QUINOXYFEN FORTRESS(R) Legend Elios Legend (fungicide) 5,7-dichloro-4-(4-fluorophenoxy)quinoline 5,7-dichloro-4-(p-fluorophenoxy)quinoline 5,7-dichloro-4-quinolyl-4-fluorophenyl ether Quinoline, 5,7-dichloro-4-(4-fluorophenoxy)- quinoline,4,5,7-trichloro-4-(4-fluorophenoxy)- (5,7-dichloro-4-quinolyl) (4-fluorophenyl) ether |
CAS | 124495-18-7 |
EINECS | 602-997-3 |
InChI | InChI=1/C15H8Cl2FNO/c16-9-7-12(17)15-13(8-9)19-6-5-14(15)20-11-3-1-10(18)2-4-11/h1-8H |
Molecular Formula | C15H8Cl2FNO |
Molar Mass | 308.13 |
Density | 1.430 |
Melting Point | 105-106° |
Boling Point | 423℃ |
Flash Point | >100°C |
Water Solubility | 0.12 mg l-1 (20 °C) |
Vapor Presure | 1.2 x 10-5 Pa (20 °C) |
Appearance | neat |
Color | White to Light yellow |
Merck | 14,8079 |
pKa | 2.87±0.50(Predicted) |
Storage Condition | 0-6°C |
Refractive Index | 1.648 |
Physical and Chemical Properties | Density: 1.43g/cm3 Boiling Point: 423°C refractive index: 1.648 vapor pressure: 5.62 E-07mmHg at 25°C |
Risk Codes | R43 - May cause sensitization by skin contact R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. |
Safety Description | S24 - Avoid contact with skin. S37 - Wear suitable gloves. S46 - If swallowed, seek medical advice immediately and show this container or label. S60 - This material and its container must be disposed of as hazardous waste. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
UN IDs | UN3077 9/PG 3 |
WGK Germany | 3 |
RTECS | VB4287500 |
HS Code | 38220090 |
Hazard Class | 9 |
Packing Group | III |
Toxicity | LD50 orally in rats: >5000 mg/kg; dermally in rabbits: >2000 mg/kg; by inhalation in rats: >3.38 mg/l (Longhurst) |
LogP | 5.1 at 20℃ |
dissociation constant | 3.56 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Overview | Quinoxyl (quinoxyfen), also known as Raphanofen, is a quinoline fungicide newly introduced by Dow Yinong in the United States in recent years. It is a phenoxyquinoline fungicide. This kind of protective fungicide, including single-component preparations and compounding agents with suspensions and emulsions, is widely used in cherry, grape, lettuce and other vegetable and fruit crops. The fungicide was first approved for use in Europe in 1997. Previous studies abroad have shown that this fungicide has a good effect on the control of powdery powder, but resistant strains have been found in Europe, and my country has not yet been used in production. |
safety information | dangerous goods transport code: UN3077 9/PG 3 dangerous category code: R43 safety instructions: S24 dangerous goods mark: Xi; N |
mainly uses | as a fungicide, mainly used for the prevention and control of powdery mildew. |
sterilization mechanism | it mainly affects the whole process of pathogen growth and pathogen infection, such as spore germination, suction device and attachment cell formation, etc. In 2003, related research studied the mechanism of action of quinoline drugs on barley powdery powder, showing that its mechanism of action is to change the accumulation of protein kinase C of barley powdery powder and catalyze the formation of protein kinase A subunit. |
main references | [1] yang Fang, Lu Shengyu, Chen Xiangming, et al. high performance liquid chromatography for the detection of residual quinol in various food matrices [J]. chromatography, 2008, 26(4):499-503. [2] yang Peng, Zhang Rong, Duan xiayu, etc. monitoring of sensitivity of powdery powdery fungi populations to triadimefon and quinoxide in major wheat regions of China in 2008 [J]. journal of plant pathology, 2010, 40(4):404-410. |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |