2255-17-6

Basic information

• Product Name: FENITROTHION-O-ANALOG
• Synonyms: 3-Methyl-4-nitrophenyl dimethyl phosphate;3-methyl-4-nitrophenyldimethylphosphate;4-nitro-m-cresodimethylphosphate;Accothion O-analog;accothiono-analog;BAY 42247;bay42247;Dimethyl 3-methyl-4-nitrophenyl phosphate
• CAS NO: 2255-17-6
• Molecular Formula: C₉H₁₂NO₆P
• Molecular Weight: 261.17
• Mol File: 2255-17-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 330.4°C at 760 mmHg
• Flash Point: 153.6°C
• Appearance: /
• Density: 1.339g/cm³
• Vapor Pressure: 0.000319mmHg at 25°C
• Refractive Index: 1.52
• Storage Temp.: 0-6°C
• CAS DataBase Reference: FENITROTHION-O-ANALOG(CAS DataBase Reference)
• NIST Chemistry Reference: FENITROTHION-O-ANALOG(2255-17-6)
• EPA Substance Registry System: FENITROTHION-O-ANALOG(2255-17-6)

Safety Data

• RIDADR: 3018
• HazardClass: 6.1(a)
• PackingGroup: II
• Hazardous Substances Data: 2255-17-6(Hazardous Substances Data)

Usage

General Description

Fenitrothion-o-analog is a derivative of the organic compound, fenitrothion, which is an organophosphate insecticide primarily used in the agricultural sector for pest control. Due to its organophosphate structure, it acts as a powerful neurotoxin that inhibits cholinesterase enzymes in insects, leading to their eventual death. Its chemical formula may vary depending on the specific form or analog used. However, like all organophosphates, exposure to fenitrothion-o-analog may lead to harmful side effects in non-target organisms, including humans. These risks make careful handling and appropriate use essential.

InChI:InChI=1/C9H12NO6P/c1-7-6-8(4-5-9(7)10(11)12)16-17(13,14-2)15-3/h4-6H,1-3H3

Upstream product

• 122-14-5 MEP 

Relevant articles and documents

Metabolism of an Insecticide Fenitrothion by Cunninghamella elegans ATCC36112

In this study, the detailed metabolic pathways of fenitrothion (FNT), an organophosphorus insecticide by Cunninghamella elegans, were investigated. Approximately 81% of FNT was degraded within 5 days after treatment with concomitant accumulation of four m

Oxidation of organophosphorus pesticides for the sensitive detection by a cholinesterase-based biosensor

A potentiometric flow injection-type biosensor developed in our laboratory was used for the determination of organophosphorus pesticides (OPs). The principle of the biosensor is that the degree of inhibition of a sensor enzyme by an OP is dependent on the concentration of the pesticide. The sensor system consisted of a reactor with acetylcholinesterase (AChE) immobilized on a controlled pore glass and a detector with a tubular H+-selective membrane electrode. In order to examine the possibility of enhancing the sensitivity of the sensor by converting OPs to oxidized forms (stronger inhibitors), a comparison of the degree of enzyme inhibition by OPs at 10-6 M before and after their oxidation was made. All of the ten pesticides tested exhibited greater inhibitory power toward the sensor enzyme following oxidation. All of the oxidized pesticides at 10-6 M inhibited the sensor enzyme to a considerable degree, demonstrating the utility of the developed method for the class-specific determination of OPs. A calibration curve for diazinon, over the concentration range of 10-11-10-4 M, was obtained. The lower detection limit was 2 × 10-10 M. Treatment of the inhibited enzyme with pyridine-2-aldoxime restored the enzyme to near full activity, allowing repeated use of the sensor,

Kinetic study on the interactions of cyclodextrins with organic phosphates and thiophosphates

α-Cyclodextrin (α-CD) and 6-O-α-D-glucopyranosyl-β- cyclodextrin (G1-β-CD) affected the rates of phenol release from a few dimethyl(nitrophenyl) phosphates and the corresponding thiophosphates in aqueous alkaline solutions. Curvefitting analysis of change