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S-butyl O-ethyl carbonodithioate, also known as S-butyl ethyl xanthate, is an organic compound with the chemical formula C6H12S2. It is a colorless to pale yellow liquid that is soluble in organic solvents and slightly soluble in water. S-butyl O-ethyl carbonodithioate is primarily used as an extractant in the hydrometallurgical industry, particularly in the extraction of precious metals such as gold and silver from their ores. It functions by forming complexes with metal ions, allowing for their separation from other components in the ore. S-butyl O-ethyl carbonodithioate is also used as a flotation collector in the mining industry to promote the separation of valuable minerals from waste rock. Due to its reactivity with metal ions, it is essential to handle this chemical with care, adhering to proper safety protocols to minimize potential health and environmental risks.

2594-90-3

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2594-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2594-90-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2594-90:
(6*2)+(5*5)+(4*9)+(3*4)+(2*9)+(1*0)=103
103 % 10 = 3
So 2594-90-3 is a valid CAS Registry Number.

2594-90-3SDS

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 O-ethyl butylsulfanylmethanethioate

1.2 Other means of identification

Product number -
Other names O-Ethyl-S-n-butyldithiocarbonat

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:2594-90-3 SDS

2594-90-3Relevant academic research and scientific papers

Expeditious synthesis of 1-substituted taurines with diverse functionalized side-chains

Kakaei, Saeed,Chen, Ning,Xu, Jiaxi

supporting information, p. 302 - 309 (2013/01/15)

A radical addition reaction and subsequent performic acid oxidation were used for the synthesis of 1-substituted taurines with diverse functionalized side-chains from N-allylphthalimide and various xanthates. The current approach shows high yields and short synthetic route and reaction time. Moreover, the current method is a convenient and practical method for the synthesis of 1-substituted taurines with different functionalized side-chains.

S-alkyl chlorothioformates from xanthates

Gade, Alexandra M.,Abelt, Christopher J.

, p. 2097 - 2099 (2008/02/12)

Reaction of S-alkyl O-ethyl xanthates (S-alkyl O-ethyl dithiocarbonates) with catalytic Vilsmeier reagent generated in situ from N-formylmorpholine (morpholine-4-carbaldehyde) gives S-alkyl chlorothioformates in good yields. Georg Thieme Verlag Stuttgart.

Pesticidal compositions containing phosphoric esters and divalent sulphur compounds

-

, (2008/06/13)

Pesticidal composition comprising: a pesticidal, phosphoric ester the molecule of which has at least one alkyl group of 1 to 3 carbon atoms, 0.05 to 10% of an agent stabilizing the said ester against decomposition by protonisation, together with adjuvants characterized in that the stabilizing agent comprises at least one sulphur compound containing per molecule at least one divalent sulphur atom of which one valence is bonded to an atom chosen from sulphur, carbon, nitrogen, hydrogen, and metals capable of giving a salt, the other valence being bonded to an atom chosen from hydrogen, the carbon atom already noted, a second carbon atom, the nitrogen atom already noted, a second nitrogen atom, the metal atom already noted in the case of a metal of valence greater than one, a second atom of metal and oxygen when the first valence is not attached to an atom of hydrogen, the proportion of sulphur calculated with reference to the weight of the sulphur compound being between 5 and 99%. Process for stabilizing a phosphoric ester of which the molecule possesses at least one alkyl group containing 1 to 3 carbon atoms characterized in that there is added to the phosphoric ester or to a mixture which contains it, 0.05 to 10% calculated on the weight of the phosphoric acid ester of an agent capable of stabilizing the said phosphoric ester against protonisation and comprising at least one sulphur compound such as that defined thereupon.

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