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132767-86-3

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132767-86-3 Usage

Description

Diisooctylthiophosphinic Acid, also known as Cyanex 302, is an application-specific reagent that possesses unique properties. It is a metal complex with antibacterial and antifungal activities, making it a versatile compound for various applications.

Uses

Used in Chemical Industry:
Diisooctylthiophosphinic Acid is used as a metal complexing agent for the separation and purification of metal ions in chemical processes. Its ability to form stable complexes with metals allows for efficient extraction and recovery of valuable metal resources.
Used in Pharmaceutical Industry:
Diisooctylthiophosphinic Acid is used as an antimicrobial agent for its antibacterial and antifungal properties. It can be incorporated into pharmaceutical formulations to combat infections caused by various pathogens, contributing to the development of effective treatments and preventive measures.
Used in Agriculture:
In the agricultural sector, Diisooctylthiophosphinic Acid is used as a biocidal agent to protect crops from harmful microorganisms. Its application helps in maintaining crop health and increasing yield by reducing the impact of diseases caused by bacteria and fungi.
Used in Water Treatment:
Diisooctylthiophosphinic Acid is used in water treatment processes as a metal ion sequestering agent. It helps in removing metal ions from water, which can cause corrosion, staining, and other issues. This contributes to the production of clean and safe water for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 132767-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132767-86:
(8*1)+(7*3)+(6*2)+(5*7)+(4*6)+(3*7)+(2*8)+(1*6)=143
143 % 10 = 3
So 132767-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H35OPS/c1-13(9-15(3,4)5)11-18(17,19)12-14(2)10-16(6,7)8/h13-14H,9-12H2,1-8H3,(H,17,19)

132767-86-3 Well-known Company Product Price

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  • Aldrich

  • (38224)  Diisooctylthiophosphinicacid  technical, ~85% (T)

  • 132767-86-3

  • 38224-100ML-F

  • 760.50CNY

  • Detail

132767-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name hydroxy-sulfanylidene-bis(2,4,4-trimethylpentyl)-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Diisooctylmonothiophosphinic acid

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:132767-86-3 SDS

132767-86-3Downstream Products

132767-86-3Relevant articles and documents

Process for the preparation of highly purified, dialkydithiophosphinic compounds

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Page/Page column 7, (2008/06/13)

An improved process for production of dialkyldithiophosphinic acid including sulfurizing a purified dialkylphosphinic acid by: reacting a hypophosphorous acid or salt with a stoichiometric excess of an alpha olefin in the presence of a free radical initiator to form a reaction product comprising monoalkylphosphinic acid and dialkylphosphinic acid; adding sufficient aqueous base to the reaction product to i) form the salts of the phosphinic acids, and ii) establish an aqueous phase and an organic phase, wherein a monoalkylphosphinic acid solubilizes into an aqueous phase; separating the organic phase from the aqueous phase; acidifying the organic phase and removing the olefin from the organic phase; isolating the purified dialkylphosphinic acid product; and sulfurizing the purified dialkylphosphinic acid product to form a dialkydithiophosphinic acid. The present invention also provides a process for preparing purified dialkylthiophosphinic chloride, and a process for preparing purified dialkylmonothiophosphinic acids.

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