16083-20-8 Usage
Description
N,N,N-Tributyl-1-butanaminium·propenoic acidanion is a versatile chemical compound composed of a quaternary ammonium cation (N,N,N-Tributyl-1-butanaminium) and a propenoic acid anion. The cation features four butyl groups attached to a central nitrogen atom, while the anion contains a carboxyl group and a double bond, endowing it with acidic and reactive properties. N,N,N-Tributyl-1-butanaminium·propenoic acidanion is widely used in various industrial processes due to its unique characteristics.
Uses
Used in Organic Synthesis:
N,N,N-Tributyl-1-butanaminium·propenoic acidanion is used as a phase transfer catalyst in organic synthesis reactions. It facilitates the transfer of reactants between two immiscible phases, enhancing the efficiency and selectivity of the reactions.
Used in Metal Ion Extraction:
In the field of metal ion extraction, N,N,N-Tributyl-1-butanaminium·propenoic acidanion plays a crucial role in the selective extraction of metal ions. Its unique structure allows it to selectively bind and separate specific metal ions from complex mixtures, making it a valuable tool in various industries.
Used in Material Surface Modification:
N,N,N-Tributyl-1-butanaminium·propenoic acidanion is also employed in the modification of surface properties of materials. Its reactive nature enables it to alter the surface characteristics of various materials, improving their performance in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16083-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,8 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16083-20:
(7*1)+(6*6)+(5*0)+(4*8)+(3*3)+(2*2)+(1*0)=88
88 % 10 = 8
So 16083-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H36N.C3H4O2/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-2-3(4)5/h5-16H2,1-4H3;2H,1H2,(H,4,5)/q+1;/p-1
16083-20-8Relevant articles and documents
Isobutylene-rich macromonomers: Dynamics and yields of peroxide-initiated crosslinking
Dakin, Jackson M.,Shanmugam, Karthik Vikram Siva,Twigg, Christopher,Whitney, Ralph A.,Parent, J. Scott
, p. 123 - 132 (2015)
New isobutylene-rich elastomers bearing multiple pendant styrenic, acrylic, maleimidic, vinylic, and allylic functional groups have been prepared and examined in the context of peroxide-initiated crosslinking. Halide displacement from brominated poly(isobutylene-co-isoprene) (BIIR) by the requisite carboxylate nucleophiles in homogeneous toluene solutions provide the desired esters in quantitative yield without complications from dehydrohalogenation or premature crosslinking. Heating the resulting macromonomers with dicumyl peroxide to 160 °C under solvent-free conditions gives thermoset derivatives, with reaction rates and yields depending markedly on functional group structure. In general, high cure extents can only be achieved using highly reactive pendant functional groups, owing to the competitive balance between crosslinking through C=C oligomerization, and degradation through β-scission of backbone macroradical intermediates. Independent control of crosslinking rates and cure extents is gained through the use of nitroxyl radical traps bearing acrylate functionality.
