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QUINOXYFEN

CAS No.
124495-18-7
Chemical Name:
QUINOXYFEN
Synonyms
Quinoxyphen;Quintec;QUINOXYFEN;FORTRESS(R);Legend Elios;Quinoxyfen 0.1;Quinoxyfen >Legend (fungicide);Quinoxyfen Standard;Gestrinone Impurity 11
CBNumber:
CB7757516
Molecular Formula:
C15H8Cl2FNO
Molecular Weight:
308.13
MDL Number:
MFCD03265638
MOL File:
124495-18-7.mol
MSDS File:
SDS
Last updated:2023-05-15 10:42:50

QUINOXYFEN Properties

Melting point 105-106°
Boiling point 423℃
Density 1.430
vapor pressure 1.2 x 10-5 Pa (20 °C)
Flash point >100 °C
storage temp. 0-6°C
solubility Chloroform (Slightly), Methanol (Slightly)
Water Solubility 0.12 mg l-1 (20 °C)
pka 2.87±0.50(Predicted)
color White to Light yellow
Merck 14,8079
LogP 5.1 at 20℃
Dissociation constant 3.56
EWG's Food Scores 1-2
FDA UNII PPC78J1VCW
EPA Substance Registry System Quinoxyfen (124495-18-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09
Signal word  Warning
Hazard statements  H317-H410
Precautionary statements  P261-P272-P273-P280-P302+P352-P333+P313
Hazard Codes  Xi,N
Risk Statements  43-50/53
Safety Statements  24-37-46-60-61
RIDADR  UN3077 9/PG 3
WGK Germany  3
RTECS  VB4287500
HazardClass  9
PackingGroup  III
HS Code  38220090
Toxicity LD50 orally in rats: >5000 mg/kg; dermally in rabbits: >2000 mg/kg; by inhalation in rats: >3.38 mg/l (Longhurst)

QUINOXYFEN price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 46439 Quinoxyfen PESTANAL 124495-18-7 100mg $202 2024-03-01 Buy
TCI Chemical Q0093 Quinoxyfen >98.0%(GC) 124495-18-7 200mg $151 2024-03-01 Buy
TRC Q765500 Quinoxyfen 124495-18-7 500mg $95 2021-12-16 Buy
Chem-Impex 38419 Quinoxyfen,98%(GC) 98%(GC) 124495-18-7 200MG $141.12 2021-12-16 Buy
American Custom Chemicals Corporation AGR0000260 QUINOXYFEN 95.00% 124495-18-7 200MG $684 2021-12-16 Buy
Product number Packaging Price Buy
46439 100mg $202 Buy
Q0093 200mg $151 Buy
Q765500 500mg $95 Buy
38419 200MG $141.12 Buy
AGR0000260 200MG $684 Buy

QUINOXYFEN Chemical Properties,Uses,Production

Chemical Properties

Off-White Solid

Uses

Quinoxyfen is under development for the control of powdery mildew in cereals and grapes.

Uses

Agricultural fungicide.

Definition

ChEBI: A member of the class of quinolines carrying two chloro substituents at positions 5 and 7 together with a 4-fluorophenoxy substituent at position 4. A fungicide used mainly to control powdery mildew in cereals.

Environmental Fate

The stability of quinoxyfen in the soil has been shown to vary depending on soil type and source. DT50 values obtained in the field varied from 5 to 454 days for a range of soil types. The strong adsorptive properties of quinoxyfen reduce its soil dissipation rate, but result in no leaching potential of this fungicide into waterways or groundwater. The primary metabolite formed in the soil is 3-hydroxyquinoxyfen . A secondary soil metabolite is 5,7-dichloro-4-hydroxyquinoline (DCHQ). DCHQ was also found not to leach, even in sandy soils. Under acidic aqueous conditions, DCHQ was the primary metabolite found, and this was produced in greater quantities at acidic pHs. An additional metabolite was isolated from both water and the sediment in an aqueous clay loam system. Although not positively identified, it is suspected to be 6-hydroxyquinoxyfen.
A similar hydrolysis profile is observed in water as in soil (3). The primary product produced under acidic conditions in the absence of light was DCHQ. However, in the presence of light, photolysis was greatly increased and dose dependent on the amount of sunlight received. The primary photolysis product was 2-chloro-10- fluoro[1]benzopyrano[2,3,4-de]quinoline (CFBPQ).

Metabolic pathway

Quinoxyfen is a novel fungicide for the control of powdery mildew in cereals. Its mode of action is unknown but it appears to differ from those of current fungicides and thus may be novel (Longhurst et al., 1996). Quinoxyfen is tightly bound to soil components and is somewhat persistent in this medium but in aqueous solution it is subject to rapid photodecomposition. Photodegradation is therefore likely to be an important process in its immediate removal from the environment. Plant metabolites have not been reported but unchanged quinoxyfen has been confirmed as the major residue.
The compound is rapidly metabolised and eliminated following ingestion by rats and goats. Metabolism involves mainly hydroxylation of the intact quinoxyfen, cleavage at the ether bond and conjugation of the resulting metabolites. The information presented below was obtained from two sources (DowElanco, 1996; Reeves et al., 1996).

Degradation

Quinoxyfen is stable in the dark at 25 °C and it is stable in aqueous solution at pH 7 and 9. Its DT50 at pH 4 was 16 days (40°C) but it was degraded more rapidly than this in light. Aqueous photolysis of dilute solutions occurs with DT50 values of 1.7 and 22.8 hours in June and December (Europe), respectively. The main degradation product was 2-chloro-10-fluoro[1]benzopyrano[2,3,4-de]quinoline (2, up to 30%); a second product (up to 11%) was probably 5,7-dichloro-4-hydroxyquinoline (3) (see Scheme 1).

Toxicity evaluation

The specificity of quinoxyfen to fungi may account for its relatively safe toxicological profile. Quinoxyfen has no demonstrable effect in any genotoxicity tests, and the rat oral LD50 is >5000 mg/kg. Quinoxyfen was not shown to cause skin irritation, but studies with rabbit indicated it might cause mild eye irritation and it has the potential to cause skin sensitization, as shown in guinea pigs with repeated exposure. A NOEL of 20 mg/kg bw/day was established through 1-year and 2-year rat chronic feeding studies. The aquatic precautions with quinoxyfen may be due to its high logP. The rainbow trout LD50 is 0.27 mg/L; however, this is well above its water solubility of 0.116 mg/L. In addition, the Daphnia 48h EC50 is 0.08 mg/kg and the Selenastrum capricornutum 72 h EbC50 is 0.03 mg/kg. With the exception of some aquatic species, quinoxyfen has a very desirable toxicological profile toward nontarget species in the environment. Its toxicity toward birds, honeybees, and earthworms is low.

23834-01-7
30008-10-7
124495-18-7
Synthesis of QUINOXYFEN from 4,5,7-Trichloro Quinoline and Sodium 4-hydroxyphenolate

QUINOXYFEN Preparation Products And Raw materials

Global( 135)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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Zhejiang ZETian Fine Chemicals Co. LTD
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Nanjing Dolon Biotechnology Co.,Ltd.
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SIMAGCHEM CORP
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TargetMol Chemicals Inc.
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AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
CR Corporation Lomited
fred.wen@crcorporation.cn CHINA 12069 58

View Lastest Price from QUINOXYFEN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
QUINOXYFEN pictures 2023-03-24 QUINOXYFEN
124495-18-7
US $50.00 / kg 1kg 98% 20 tons Hebei Duling International Trade Co. LTD
  • QUINOXYFEN pictures
  • QUINOXYFEN
    124495-18-7
  • US $50.00 / kg
  • 98%
  • Hebei Duling International Trade Co. LTD
QUINOXYFEN FORTRESS(R) Quinoline, 5,7-dichloro-4-(4-fluorophenoxy)- (5,7-dichloro-4-quinolyl) (4-fluorophenyl) ether Quinoxyfen 100mg [124495-18-7] Legend (fungicide) Legend Elios Quinoxyfen 0.1 Quinoxyphen Solution, 1000ppm Quinoxyfen Standard FlufenoxuronSolution,100mg/L,5x1ml Quinoxyfen @100 μg/mL in Methanol TriflumuronSolution,100mg/L,5x1ml Quinoxyfen@1000 μg/mL in Methanol QuinoxyfenSolution,100mg/L,1ml QuinoxyfenSolution,1,000mg/L,1ml TefluthrinSolution,100mg/L,5x1ml TefluthrinSolution,1000mg/L,5x1ml Quinoxyfen > Quintec Quinoxyphen Gestrinone Impurity 11 124495-18-7 C15H8Cl2FNO Agro-Products Aromatics Intermediates & Fine Chemicals Pharmaceuticals API