Twitter LinkedIn

Comparing Silica And Polymer Supported Products

The use of solid supported scavengers has become a common method for post-synthesis purification. Polystyrene or PS based scavengers are the most widely available form of solid supported scavengers due to low cost of manufacturing. However, the PS backbone greatly influences the behavior of the scavenger in terms of solvent compatibility and reaction rate. Silica-bound ( SiliaBond®) scavengers have the advantage of a rigid non-swelling backbone that eliminates solvent compatibility and kinetic issues. Additionally, SiliaBond scavengers are easier to handle due to the absence of static.

Bound amine and isocyanate are two very popular scavenger due to their ability to remove a wide range of electrophiles and nucleophiles and therefore are the basis of our study. Here is a collection of internal data and an external study completed by the chemists at Hoffman La-Roche.

Full Text PDF

20 Item(s)

Set Descending Direction
per page

List  Grid 

  1. SiliaBond® Carboxylic Acid (WCX)

    SiliaBond® Carboxylic Acid (WCX)

    SiliaBond® Carboxylic Acid (Si-CAA) can be used as a scavenger for amines or carbonates, and for the quench of alkoxides and organometallic reagents. SiliaBond Carboxylic Acid is primarily used as a weak cation exchanger (WCX) in solid phase extraction (SPE) and in HPLC.

  2. SiliaBond® Carbodiimide (DCC)

    SiliaBond® Carbodiimide (DCC)

    SiliaBond® Carbodiimide (Si-DCC) is a bound neutral carbodiimide that may be used for the synthesis of amides, esters, and activated esters.

  3. SiliaBond® Ethyl Carbodiimide (EDC)

    SiliaBond® Ethyl Carbodiimide (EDC)

    SiliaBond® Ethyl-Dimethylaminopropyl Carbodiimide (Si-EDC) reacts in a similar fashion to SiliaBond Carbodiimide (Si-DCC). The advantage of Si-EDC is this new reagent greatly simplifies the work up procedure of the reactions since a simple filtration is all that takes to remove the unwanted side product of the amides formation (urea).

  4. SiliaBond® Maleimide

    SiliaBond® Maleimide

    SiliaBond® Maleimide (Si-MAL) has been designed to scavenge thiols. 90% of mercaptoethanol was removed with 4 eq. after 15 minutes in an aqueous environment. Complete scavenging was observed after 3 hours. SiliaBond Maleimide can also be used to immobilize peptides and proteins through the cysteine residues. 95% of L-cysteine was immobilized after only 15 minutes in a pH 4.5 buffered solution using 4 eq. of SiliaBond Maleimide.

  5. SiliaBond® Piperidine

    SiliaBond® Piperidine

    SiliaBond® Piperidine (Si-PIP) is a general purpose tertiary amine base to scavenge acids, thereby avoiding salt elimination problems. Also used as a base catalyst for Knoevenagel condensation.

  6. SiliaBond® Aluminum Chloride

    SiliaBond® Aluminum Chloride

    SiliaBond® Aluminium Chloride (Si-AlClx) is the silica supported version of the most widely used Lewis acid, aluminium chloride. It is an effective catalyst for Friedel-Crafts alkylations and acylations. It also catalyzes the formation of ethers.

  7. SiliaBond® DMAP

    SiliaBond® DMAP

    SiliaBond® DMAP (Si-DMAP) is the supported equivalent of 4-dimethylaminopyridine commonly used as a nucleophilic catalyst in a wide variety of reactions such as acylation, amidation or acetylation.

  8. SiliaBond® Diethylamine

    SiliaBond® Diethylamine

    SiliaBond® Diethylamine (SiliaBond WAX-2) is a silica bound tertiary amine base and can be used in most applications requiring a tertiary amine, particularly as a HCl sponge. Silica bound ammonium salt by-products are easily separated by filtration. This diethylamine immobilized on silica gel can be used for the same applications as SiliaBond Dimethylamine. It is a very common supported tertiary amine.

  9. SiliaBond® Nucleophile Scavenger Kit

    SiliaBond® Nucleophile Scavenger Kit

    Isocyanate - Tosic Acid - Tosyl Chloride
  10. SiliaBond® Base Kit

    SiliaBond® Base Kit

    Amine - Carbonate - Dimethylamine - Diethylamine - Morpholine - Pyridine - TBD
  11. SiliaBond® Oxidant Kit

    SiliaBond® Oxidant Kit

    Potassium Permanganate - TEMPO - Pyridinium Chlrorochromate - Pyridinium dichromate
  12. SiliaBond® Reagent Kit

    SiliaBond® Reagent Kit

    Carbodiimide - Cyanoborohydride - Dichlorotriazine - DMAP - EDC - HOBt
  13. SiliaBond® Reversed-Phase Kit

    SiliaBond® Reversed-Phase Kit

    C8 monomeric - C18 (17%) polymeric - C18 (17%) monomeric - C18 (23%) - Cyano - Phenyl
  14. SiliaBond® Acid Kit

    SiliaBond® Acid Kit

    Carboxylic Acid - Propylsulfonic Acid - TAAcOH - Tosic Acid
  15. SiliaBond® Ion Exchanger Kit

    SiliaBond® Ion Exchanger Kit

    WAX - WCX -SCX-2 -SCX -SAX - TMA Acetate
  16. SiliaBond® Electrophile Scavenger Kit

    SiliaBond® Electrophile Scavenger Kit

    Amine - Diamine - Triamine - DMAP - Piperazine - Tosyl Hydrazine
  17. SiliaMetS® Triamine

    SiliaMetS® Triamine

    SiliaMetS® Triamine (SiliaMetS WAX-3, Si-TRI) is effective for scavenging metals such as Pb, Co, Ru and Pd. Our screening studies have shown it to be the preferred scavenger for Pb. It can also be used as a scavenger for acid chlorides, isocyanates and other electrophiles.

  18. SiliaMetS® Diamine

    SiliaMetS® Diamine

    SiliaMetS® Diamine (Si-DIA) is a proven scavenger for metals and electrophiles. It scavenges acids, acid chlorides, anhydrides, aldehydes, isocyanates, and chloroformates as well as Pb, Ni, and Cd.

  19. SiliaBond® Amine

    SiliaBond® Amine

    SiliaBond® Amine (Si-NH2) is an effective scavenger of acid chlorides, sulfonyl chlorides, isocyanates and other electrophiles. Si-NH2 has been shown to be effective metal scavenger and catalyst for Knoevenagel reactions. SiliaBond Amine is also used in chromatography as normal phase sorbent.

  20. SiliaBond® TBD

    SiliaBond® TBD

    SiliaBond® TBD (1,5,7-Triazabicyclo[4.4.0]dec-5-ene, Si-TBD) is a silica bound bicyclic guanidine moiety that is sufficiently basic to deprotonate moderately acidic hydrogens. It is most commonly used for the alkylation of phenols (Williamson ether synthesis) and amines, and the esterification of carboxylic acids using alkyl halides. It may also be used to scavenge boronic acids such as phenylboronic acid: 98% removal with 1 equivalent in DCM at room temperature after 1 h.

20 Item(s)

Set Descending Direction
per page

List  Grid