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O,O-dipentyl hydrogen phosphorodithioate, also known as di-sec-pentyl hydrogen phosphorodithioate, is an organophosphorus compound with the chemical formula C10H23O2PS2. It is a colorless to pale yellow liquid with a pungent odor and is used as a pesticide, specifically as an acaricide and miticide, to control mites and ticks in agriculture. The compound is also known for its potential to inhibit acetylcholinesterase, an enzyme involved in nerve impulse transmission, which can lead to its pesticidal effects. Due to its chemical structure, it is considered a hazardous substance and requires careful handling to prevent environmental and health risks.

2253-54-5

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2253-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2253-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2253-54:
(6*2)+(5*2)+(4*5)+(3*3)+(2*5)+(1*4)=65
65 % 10 = 5
So 2253-54-5 is a valid CAS Registry Number.

2253-54-5Relevant academic research and scientific papers

Microwave irradiation technique for synthesis of dialkyl dithiophosphoric acids

Guemguem, Bahattin,Biricik, Nermin,Baysal, Akin

, p. 2507 - 2512 (2007/10/03)

Microwave heating technique was applied to the preparation of dialkyl dithiophosphoric acids from the reaction of alcohol with phosphorus pentasulphide. A microwave oven (CEM-MDS 2000) was utilized to determine the preparation conditions for the best yield of dialkyl dithiophosphoric acids under atmospheric pressure at various times and power. Six different (C4-C9) chain-length of dialkyl dithiophosphoric acids were studied. All experiments were performed in an open Teflon (poly-tetrafluoroethylene) vessel. The results obtained showed that the reaction of dialkyl dithiophosphoric acids can be achieved more rapidly using microwave heating than using conventional procedures.

REDOX REACTIONS OF ANTIMONY(III) O,O-DISUBSTITUTED PHOSPHORODITHIOATES WITH FERRIC CHLORIDE

Woo, Edward J.,Kalbacher, Barbara J.,McEwen, William E.

, p. 269 - 278 (2007/10/02)

The reaction of antimony(III) tris-(O,O-diethylphosphorodithioate) with three equivalents of ferric chloride in ether solution has been found to give ferrous chloride, bis-(O,O-diethylthiophosphoryl) disulfide and dichloroantimony O,O-diethyl phosphorodithioate as the major products.However, a relatively low yield of bis-(O,O-diethylthiophosphoryl) trisulfide was also obtained.The structures of these products were established by independent syntheses.Several additional antimony(III) tris-(O,O-disubstituted phosphorodithioates) were prepared, and the major organic product obtained by reaction of each of these compounds with three equiva lents of ferric chloride was the corresponding bis-(O,O-disubstituted thiophosphoryl) disulfide.A mechanism for this reaction has been suggested, and evidence in support of the mechanism has been presented.The various antimony(III) tris-(O,O-dialkyl phosphorodithioates) are passivating agents in petroleum refining.The results reported in this and in our previous papers indicate that such compounds undergo a variety of reactions with components of crude petroleum prior to the ultimate pyrolysis reactions which occur in the fluid catalytic cracking process.

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