Welcome to LookChem.com Sign In|Join Free
  • or
Tripropan-2-yl phosphorotetrathioate, commonly known as DEF, is a potent organophosphate insecticide and acaricide. It is characterized by its ability to control a broad spectrum of pests on various crops by inhibiting the activity of acetylcholinesterase in the nervous system of insects and mites, resulting in paralysis and death. However, its high toxicity to humans and other mammals, along with potential environmental harm, necessitates strict regulation of its use in many countries.

2386-41-6

Post Buying Request

2386-41-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2386-41-6 Usage

Uses

Used in Agricultural Industry:
Tripropan-2-yl phosphorotetrathioate is used as an insecticide and acaricide for the control of a wide range of pests on various crops. Its application is aimed at protecting crops from damage caused by insects and mites, thereby ensuring higher yields and quality produce.
Used in Pest Management:
Tripropan-2-yl phosphorotetrathioate is used as a key component in integrated pest management strategies to control and reduce the populations of harmful insects and mites. Its effectiveness in targeting a broad spectrum of pests makes it a valuable tool in maintaining the health and productivity of agricultural ecosystems.

Check Digit Verification of cas no

The CAS Registry Mumber 2386-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2386-41:
(6*2)+(5*3)+(4*8)+(3*6)+(2*4)+(1*1)=86
86 % 10 = 6
So 2386-41-6 is a valid CAS Registry Number.

2386-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(propan-2-ylsulfanyl)-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names tripropan-2-yl phosphorotetrathioate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:2386-41-6 SDS

2386-41-6Downstream Products

2386-41-6Relevant academic research and scientific papers

Effect of iodine on the reaction of tetraphosphorus decasulfide with dialkyl disulfides

Nizamov,Garifzyanova,Batyeva

, p. 222 - 223 (1996)

Elemental iodine decreases the temperature of the reaction of P4S10 with disulfides, which results in the formation of trialkyl tetrathiolothionophosphates, from 100-110°C to 20-60°C. The latter decompose to trialkyl tetrathiophosphates.

REACTIONS OF PHOSPHORUS SULFIDES (P4S5, P4S7 AND P4S10) AND 2,4-BIS(ALKYLTHIO)-2,4-DITHIOXO-1,3,2λ5,4λ5-DITHIADIPHOSPHETANES WITH DIALKYLDISULFIDES AND THIOACETALS IN THE PRESENCE OF IODINE

Nizamov, Il'yas S.,Al'methina, Lyubov' A.,Garifzyanova, Gyuzel' G.,Sergeenko, Gul'nur G.,Batyeva, Elvira S.

, p. 71 - 82 (2007/10/02)

The reactions of P4S5 and P4S7 with dialkyl disulfides and thioacetals were studied.The use of iodine results in the reactivity enhancement of P4S5, P4S7, P4S10, homologues of Davy's reagent, and red phosphporus in the presence of elemental sulfur in the

INFLUENCE OF IODINE ON THE REACTIVITY OF TETRAPHOSPHORUS TRISULFIDE IN ORGANIC REACTIONS

Nizamov, Il'Yas S.,Garifzyanova, Gyuzel G.,Al'Metkina, Lyubov' A.,Sergeenko, Gul'Nur G.,Batyeva, Elvira S.

, p. 173 - 182 (2007/10/02)

The reactivity of β-tetraphosphorus trisulfide is increased through involvement of elemental iodine in the reactions with dialkyl disulfides, thioacetals and aminals.The reactions of β- and α-diiodotetraphosphorus trisulfides with disulfides, thioacetals

REACTIONS OF TETRAPHOSPHORUS DECASULFIDE AND 2,4-BIS(ALKYLTHIO)-2,4-DITHIOXO-1,3,2λ5,4λ5-DITHIADIPHOSPHETANES WITH DISULFIDES AND THIOACETALS

Nizamov, Il'Yas S.,Al'Metkina, Lyubov' A.,Garifzyanova, Gyuzel' G.,Batyeva, Elvira S.,Al'Fonsov, Vladimir A.,Pudovik, Arkady N.

, p. 191 - 202 (2007/10/02)

The reactions of tetraphosphorus decasulfide and 2,4-bis(4-alkylthio)-2,4-dithioxo-1,3,2λ5,4λ5-dithiadiphosphetanes with disulfides and thioacetals were studied.The reactions were found to give some novel organothiophosphorus compoun

TETRAPHOSPHORUS TRISULFIDE IN REACTIONS WITH THIOACETALS, AMINALS, SULFENAMIDES AND DISULFIDES. INFLUENCE OF AMINES AND BENZOYL PEROXIDE

Nizamov, Il'yas S.,Batyeva, Elvira S.,Al'fonsov, Vladimir A.,Musin, Rashid Z.,Pudovik, Arkady N.

, p. 229 - 237 (2007/10/02)

The reactions of tetraphosphorus trisulfide with thioacetals, aminals, sulfenamides and disulfides were studied.The reactions were found to give organothiophosphorus compounds and to be facilitated by organic amines and benzoyl peroxide.Key words: Tetraphosphorus trisulfide; thioacetals; aminals; sulfenamides; disulfides; organothiophosphorus compounds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2386-41-6