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ChemicalBook--->CAS DataBase List--->153233-91-1

153233-91-1

153233-91-1 Structure

153233-91-1 Structure
IdentificationBack Directory
[Name]

ETOXAZOLE
[CAS]

153233-91-1
[Synonyms]

yi-5301
etoxazol
ETOXAZOLE
Etoxazole-D5
ETOXAZOLE STANDARD
etoxazole (bsi, pa iso)
2-(2,6-Difluorophenyl)-4-...
Etoxazole@100 μg/mL in Methanol
Etoxazole@1000 μg/mL in Acetone
4-(4-(tert-Butyl)-2-ethoxyphenyl)-2-(2,6-difluorophenyl)-4,5-dihydrooxazole
2-(2,6-Difluorophenyl)-4-[4-(tert-butyl)-2-ethoxyphenyl]-4,5-dihydrooxazole
4-(4-tert-butyl-2-ethoxyphenyl)-2-(2,6-difluorophenyl)-4,5-dihydro-1,3-oxazole
Oxazole, 2-(2,6-difluorophenyl)-4-4-(1,1-dimethylethyl)-2-ethoxyphenyl-4,5-dihydro-
2-(2,6-Difluorophenyl)-4-(4-(1,1-dimethylethyl)-2-ethoxyphenyl)-4,5-di hydrooxazole
[EINECS(EC#)]

201-167-4
[Molecular Formula]

C21H23F2NO2
[MDL Number]

MFCD07363987
[MOL File]

153233-91-1.mol
[Molecular Weight]

359.41
Chemical PropertiesBack Directory
[Appearance]

Pale-yellow liquid when pure or reddish-brown liquid or semisolid as a technical product. Mild odor.
[Melting point ]

101-102°
[Boiling point ]

449.1±45.0 °C(Predicted)
[density ]

1.15±0.1 g/cm3(Predicted)
[Fp ]

457℃
[storage temp. ]

0-6°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

neat
[pka]

2.04±0.70(Predicted)
[color ]

White to Off-White
[BRN ]

8930214
[Stability:]

Hygroscopic
[InChI]

InChI=1S/C21H23F2NO2/c1-5-25-18-11-13(21(2,3)4)9-10-14(18)17-12-26-20(24-17)19-15(22)7-6-8-16(19)23/h6-11,17H,5,12H2,1-4H3
[InChIKey]

IXSZQYVWNJNRAL-UHFFFAOYSA-N
[SMILES]

O1CC(C2=CC=C(C(C)(C)C)C=C2OCC)N=C1C1=C(F)C=CC=C1F
[EPA Substance Registry System]

Etoxazole (153233-91-1)
Hazard InformationBack Directory
[Chemical Properties]

Pale-yellow liquid when pure or reddish-brown liquid or semisolid as a technical product. Mild odor.
[Uses]

Etoxazole is a acaricide/insecticide that works via chitin biosynthesis inhibition for the control of mites.
[Uses]

Acaricide.
[Potential Exposure]

Aromatic hydrocarbon; Thiazole fungicide Etridiazole is a fungicide used in some countries as a seed treatment on barley, beans, corn, cotton, peanuts, peas, sorghum, soybeans, safflower, and wheat. It is also used on cotton for in-furrow application at planting, on ornamental plants and shrubs by horticultural nurseries, on nonbearing citrus and nonbearing coffee, and for golf course fairways, tees and greens. Some states hold Special Local Need registrations for use on tobacco transplants
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions) if breathing has stopped, and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit. Do not induce vomiting when formulations containing petroleum solvents are ingested
[Shipping]

UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. Military driver shall be given full and complete information regarding shipment and conditions in case of emergency. AR 50-6 deals specifically with the shipment of chemical agents. Shipments of agent will be escorted in accordance with AR 740-32.
[Incompatibilities]

Diazo compounds can detonate. This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids. Toxic gases are formed by mixing materials of this class with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents. Flammable gases are formed by mixing materials in this group with alkali metals. Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides. This chemical is sensitive to prolonged exposure to heat. This chemical is incompatible with strong oxidizing agents
[Description]

Etoxazole is an organofluorine acaricide. It induces toxicity in two-spotted spider mite (T. urticae) larvae (LC50 = 0.036 mg/L for the London reference strain) through inhibition of chitin synthase 1. It reduces acetylcholinesterase (AChE) activity in the freshwater fish O. niloticus in a concentration-dependent manner. Etoxazole (2.2-22 mg/kg per day) inhibits the activity of catalase, glutathione peroxidase (GPX), and AChE in the liver and kidneys of rats in a dose-dependent manner. Formulations containing etoxazole have been used for the control of mites in agriculture.
[Waste Disposal]

Incineration would be an effective disposal procedure where permitted. If an efficient incinerator is not available, the product should be mixed with large amounts of combustible material and contact with the smoke should be avoided. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers
[Definition]

ChEBI: Etoxazole is an organofluorine acaricide.
[storage]

Store at -20°C
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
[RTECS ]

RP6795100
[Hazardous Substances Data]

153233-91-1(Hazardous Substances Data)
[Toxicity]

LD50 in rats (mg/kg): >5000 orally; >2000 dermally; LC50 (96 hr) in Japanese carp: 0.89 mg/l (Ishida)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2,6-Difluorobenzamide-->Chloroacetaldehyde dimethyl acetal-->1-tert-butyl-3-ethoxybenzene
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