8003-45-0

Basic information

• Product Name: THIOLIX
• Synonyms: THIOLIX
• CAS NO: 8003-45-0
• Molecular Weight: 0
• Mol File: 8003-45-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: THIOLIX(CAS DataBase Reference)
• NIST Chemistry Reference: THIOLIX(8003-45-0)
• EPA Substance Registry System: THIOLIX(8003-45-0)

Safety Data

• Hazardous Substances Data: 8003-45-0(Hazardous Substances Data)

Upstream product

• 959-98-8 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide 
• 2157-19-9 1,2,3,4,7,7-hexachloro-5,6-bis(hydroxymethyl)bicyclo<2.2.1>hept-2-ene 
• 33213-65-9 beta-endosulfan 
• 959-98-8 alpha-endosulfan 
• 17378-23-3 1,2,3,4,7,7-hexachloro-5,6-di(hydroxymethyl)bicyclo<2.2.1>hept-2-ene 

Downstream Products

• 33213-65-9 endosulfan II 
• 52854-33-8 (1R,2R,5S,8S,9S)-1,9,10,11-Tetrachloro-4,6-dioxa-5-thia-tricyclo[7.2.1.0^2,8]dodec-10-ene 5-oxide 
• 33213-65-9 beta-endosulfan 
• 3868-61-9 endosulfan lactone 
• 3369-52-6 endosulfan ether 

Relevant articles and documents

NOXIOUS ARTHROPOD CONTROL AGENT CONTAINING AMIDE COMPOUND

An object of the present invention is to provide a compound having the controlling activity on a noxious arthropod, and a noxious arthropod controlling agent containing an amide compound of formula (I): wherein X represents a nitrogen atom or a CH group, p represents 0 or 1, A represents a tetrahydrofuranyl group or the like, R1, R2, R3, R4, R5, R6 and R7 represent a hydrogen atom or the like, n represents 1 or 2, Y represents an oxygen atom or the like, m represents any integer of 0 to 7, and Q represents a C1-8 chain hydrocarbon group optionally having a phenyl group or the like, has the excellent noxious arthropod controlling effect.

Use of citric acid derivatives as pesticidal adjuvants

The invention provides the use as a pesticidal adjuvant of at least one citric acid derivative and compositions containing the derivative, which has a log octanol-water coefficient (log P) of 2.6 to 11 and an equivalent hydrocarbon (EH) value of 29 to 47. The invention has been shown to enhance the efficacy of a range of pesticides.

Triplet Sensibilized Isomers of the Insecticide Thiodane

The photoisomerization reactions of cyclodiene insecticide Thiodane were investigated in different solvent systems, with wavelengths above 290 nm.The results show that β-isomer (2) can be converted in the presence of acetone into the α-isomer (1).Photokinetic experiments give sufficient information on the character of the excited state of these compounds. - Key words: Thiodane, Photochemical Reactions, Isomerization