TEPRALOXYDIM Chemical Properties

Melting point:

71.5°

Boiling point:

469.1±55.0 °C(Predicted)

Density 

1.26±0.1 g/cm3(Predicted)

vapor pressure 

2.7 X 10-5 Pa

Flash point:

93℃

storage temp. 

0-6°C

pka

4.24±0.25(Predicted)

color 

white

Odor

moderate aromatic

Appearance

Clear dark yellow liquid

PH

3.9

Major Application

agriculture
environmental

InChI

1S/C17H24ClNO4/c1-2-14(19-23-7-3-6-18)17-15(20)10-13(11-16(17)21)12-4-8-22-9-5-12/h3,6,12-13,20H,2,4-5,7-11H2,1H3/b6-3+,19-14+

InChIKey

IOYNQIMAUDJVEI-BMVIKAAMSA-N

SMILES

CC\C(=N/OC\C=C\Cl)C1=C(O)CC(CC1=O)C2CCOCC2

LogP

2.880 (est)

EPA Substance Registry System

Tepraloxydim (149979-41-9)

Safety Information

Hazard Codes 

Xn,N

Risk Statements 

61-52

Safety Statements 

53-26-36/39

WGK Germany 

3

Storage Class

11 - Combustible Solids

Hazard Classifications

Carc. 2
Repr. 2

Toxicity

LD50 in rats (mg/kg): > 2200 orally; > 2000 dermally; LC50 in rats (mg/l): 5.1 by inhalation; LC50 (96 hr) in trout: > 100 mg/l (Kibler)

TEPRALOXYDIM Usage And Synthesis

Uses

Tepraloxydim is a pesticide or a pesticide residue.

Uses

Herbicide.

Application

NOHSC supports the registration of tepraloxydim at 200 g/L in ARAMO HERBICIDE, as an emulsifiable concentrate, for the control of grass weeds in canola, chickpeas, field peas, lupins, faba beans, lentils, subclover and vetch.

Definition

ChEBI: Tepraloxydim is a member of oxanes.

Synthesis

The synthesis of TEPRALOXYDIM involves first constructing a substituted cyclohexenone ring, followed by the introduction of hydroxyl and tetrahydropyran substituents to enhance solubility and stability. The final key step in the synthesis lies in the formation of the oxime ether bond.

TEPRALOXYDIM(149979-41-9)Related Product Information

• Furan
• Sebacic acid
• TEPRALOXYDIM-5-HYDROXY
• TEPRALOXYDIM