Welcome to LookChem.com Sign In|Join Free

CAS

  • or

115-90-2

Post Buying Request

115-90-2 Suppliers

Recommended suppliersmore

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

115-90-2 Usage

Description

Fensulfothion is a systemic previously but not currently registered for insecticidal and nematicidal activity in the United States.

Chemical Properties

Different sources of media describe the Chemical Properties of 115-90-2 differently. You can refer to the following data:
1. Fensulfothion is a yellow oil.
2. Liquid.

Uses

Different sources of media describe the Uses of 115-90-2 differently. You can refer to the following data:
1. Fensulfothion is a highly toxic insecticide used for agriculture purposes.
2. Nematocide, insecticide.
3. Nematocide and pesticide used to control free-living, cyst-forming and root-knot nematotodes and soil insects in vegetable and fruit crops.

General Description

Oily yellow or brown liquid. Used as an insecticide, nematocide and mosquito larvicide.

Air & Water Reactions

Incompatible with alkali chemicals. Hydrolyzes in alkali, isomerize in air [EPA, 1998]. Slightly soluble in water.

Reactivity Profile

Organothiophosphates, such as FENSULFOTHION, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Hazard

Cholinesterase inhibitor. Questionable carcinogen.

Health Hazard

FENSULFOTHION displays cholinesterase inhibiting properties. Death results primarily from respiratory arrest stemming from failure of the respiratory center, paralysis of respiratory muscles and intense bronchoconstriction.

Fire Hazard

(Non-Specific -- Organophosphorus Pesticide, Liquid, n.o.s.) FENSULFOTHION may burn but may not ignite readily. Containers may explode in heat of fire. When heated highly toxic fumes of phosphorus and sulfur oxides are emitted. Incompatible with alkali chemicals. Hydrolyzes in alkali, isomerizes in air.

Safety Profile

A poison by ingestion, inhalation, and skin contact. Experimental reproductive effects. A pesticide. When heated to decomposition it emits very toxic fumes of SOx and POx.

Potential Exposure

A potential danger to those involved in the manufacture, formulation, or application of this insecticide used to control parasitic, sedentary, and freeliving nematodes.

Environmental Fate

Soil. In soils, the bacterium Klebsiella pneumoniae degraded fensulfothion to fensulfothion sul?de (Timms and MacRae, 1982, 1983). The following microorganisms were also capable of degrading the parent compound to the corresponding sul?de: Escherichia coli, Pseudomonas ?uorescens, Nocardia opaca, Lactobacillus plantarum and Leuconostoc mesenteroides (Timms and MacRae, 1983).Plant. Readily oxidized in plants to the corresponding sulfone (Hartley and Kidd, 1987).Chemical/Physical. Emits toxic fumes of phosphorus and sulfur oxides when heated to decomposition (Sax and Lewis, 1987; Lewis, 1990).Isomerizes readily to the O,S-diethyl isomer (Worthing and Hance, 1991). The hydrolysis half-lives of fensulfothion in a sterile 1% ethanol/water solution at 25°C and pH values of 4.5, 6.0, 7.0 and 8.0, were 69, 77, 87 and 58 weeks, respectively (Chapman and Cole, 1982).

Shipping

UN3018 Organophosphorus pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the presence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials.

Waste Disposal

Alkaline hydrolysis. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Check Digit Verification of cas no

The CAS Registry Mumber 115-90-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115-90:
(5*1)+(4*1)+(3*5)+(2*9)+(1*0)=42
42 % 10 = 2
So 115-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H17O4PS2/c1-4-13-16(17,14-5-2)15-10-6-8-11(9-7-10)18(3)12/h6-9H,4-5H2,1-3H3

115-90-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name fensulfothion

1.2 Other means of identification

Product number -
Other names Diethyl 4-(methylthio)phenyl phosphate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Insecticide
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:115-90-2 SDS

115-90-2Upstream product

115-90-2Related news

Influence of continuous light and FENSULFOTHION (cas 115-90-2) treatment on acetylcholinesterase in roots of Pisum sativum08/26/2019

Fensulfothion, O,O-diethyl O-[p-(methylsulfinyl)phenyl] phosphorothioate, an organophosphorus pesticide, inhibits the activity but not the de novo synthesis of acetylcholinesterase in pea (Pisum sativum) roots. The rate of incorporation of labeled amino acids from 14C-labeled chlorella protein h...detailed

Enhanced microbial degradation of carbofuran and FENSULFOTHION (cas 115-90-2) after repeated applications to acid mineral soil☆08/25/2019

Carbofuran added to soil samples from fields previously treated with this insecticide for soil insect control broke down much faster than in soil from fields with no history of carbofuran use. In experimental field plots, a second annual application of carbofuran or fensulfothion broke down much...detailed

Toxicity of methyl parathion and FENSULFOTHION (cas 115-90-2) to the fish Mystus cavasius08/24/2019

The 96-h LC50 values of methyl parathion and fensulfothion (with the 95% confidence limits in parentheses), to the freshwater fish Mystus cavasius were, respectively, 5·9 (5·4 to 6·5) and 16·5 (14·8 to 17·8) ppm. Both the pesticides induced severe morpho-anatomical deformities and behaviou...detailed

Oxidative degradation of FENSULFOTHION (cas 115-90-2) by hydroxyl radical in aqueous medium08/22/2019

Oxidative degradation of fensulfothion, a model organophosphorus compound, has been investigated by pulse radiolysis and H2O2/UV photolysis. A nearly complete transformation of fensulfothion was observed within 4 min of irradiation. Very little Total Organic Carbon (TOC) reduction was obtained a...detailed

115-90-2Relevant articles and documents

Agents for combating pests

-

, (2008/06/13)

The present invention relates to the use of the sulphenic acid amides of the general formula (I) STR1 in which X represents identical or different halogen atoms, Y1 and Y2 are identical or different and represent hydrogen, halogen, alkyl, alkoxy, halogenoalkyl or NO2 and Z represents halogen, --OH, --NHOH or the group --OR1, in which R1 denotes optionally substituted radicals from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl, aryl, aralkyl and heterocyclyl, or Z represents the group STR2 in which R2 and R3 are identical or different and denote hydrogen or a heterocyclic radical, or Z represents the group --OM in which M denotes ammonium or the equivalent of an alkali metal, alkaline earth metal or heavy metal cation, for prolonging the duration of a high activity in agents for combating soil pests.