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O-isopropyl xanthate, also known as isopropyl xanthogen carbonate, is an organic compound with the chemical formula C4H10O2S2. It is a colorless liquid that is soluble in water and is widely used as a flotation reagent in the mining industry, particularly for the separation of sulfide minerals. The compound is formed by the reaction of isopropyl alcohol with carbon disulfide in the presence of a base, resulting in a xanthate ester. O-isopropyl xanthate is known for its effectiveness in promoting the selective flotation of certain minerals, making it a valuable chemical in the mineral processing sector.

108-25-8

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108-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108-25-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108-25:
(5*1)+(4*0)+(3*8)+(2*2)+(1*5)=38
38 % 10 = 8
So 108-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H8OS2/c1-3(2)5-4(6)7/h3H,1-2H3,(H,6,7)

108-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name proxan

1.2 Other means of identification

Product number -
Other names IPX

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:108-25-8 SDS

108-25-8Relevant academic research and scientific papers

Bifunctional 2-(alkoxycarbonothioylthio)acetic acids for the synthesis of TiO2-poly(vinyl acetate) nanocomposites via RAFT polymerization

Xiao, Shude,Xu, William Z.,Charpentier, Paul A.

, p. 606 - 618 (2014)

Reversible addition-fragmentation chain-transfer (RAFT) polymerization has been known as a convenient method for the synthesis of polymers of designed molecular structures. Of particular interest are bifunctional or multifunctional chain-transfer agents (CTAs) which could be employed in the development of advanced materials via RAFT polymerization. In the present study, four bifunctional 2-(alkoxycarbonothioylthio) RAFT CTAs with i£ COOH functionalities containing methoxy, ethoxy, isopropoxy, and octyloxy groups, respectively, were synthesized and characterized by FTIR and NMR spectroscopy. Polymerizations of vinyl acetate using these CTAs exhibited increased molecular weight with consumption of monomer and relatively narrow dispersities, indicative of living polymerization behavior. The effect of the concentration of 2-(ethoxycarbonothioylthio) acetic acid on the polymerization was examined, revealing that higher concentration of CTA led to lower molecular weight and narrower dispersity. As an example of the application of the synthesized bifunctional CTAs, TiO2-poly(vinyl acetate) (PVAc) nanocomposites were synthesized via a one-pot process and characterized by TGA, DSC, TEM, and affinity test, suggesting attachment of PVAc onto the nano-TiO2 particles. Copyright

Facile one pot synthesis of a range of reversible addition-fragmentation chain transfer (RAFT) agents

Skey, Jared,O'Reilly, Rachel K.

supporting information; experimental part, p. 4183 - 4185 (2009/03/11)

The application of a universal synthetic strategy for the high yielding and facile synthesis of a wide range of functional RAFT agents including trithiocarbonates, xanthates and dithiocarbamates is described. The Royal Society of Chemistry.

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