Part No: PPS392.V.2Issued year: 2016File size: 1.1mbFile type: pdf
Biotage® MP-Cyanoborohydride is a macroporous polymer-supported cyanoborohydride which is a solid-supported equivalent of tetraalkylammonium cyanoborohydride. The bound cyanoborohydride can be utilized as a versatile reducing agent for the reductive amination of carbonyl compounds and reduction of imines.
Part No: PPS391.V.1Issued year: 2016File size: 1.79mbFile type: pdf
Biotage® MP-Triacetoxyborohydryde is a macroporous polystyrene-supported equivalent of tetraalkylammonium triacetoxyborohydride. MP-Triacetoxyborohydride has primary applications in the reductive amination of aldehydes and ketones under neutral or mildly acidic reaction conditions.
Part No: PPS404.V.1Issued year: 2016File size: 1.41mbFile type: pdf
PS-Benzaldehyde is the resin-bound equivalent of benzaldehyde. This resin is useful for scavenging various nucleophiles, including primary amines (selectively compared with secondary amines), hydrazines and also carbon-based nucleophiles such as Meldrum’s acid and organometallics.
Part No: PPS402.V.1Issued year: 2016File size: 0.95mbFile type: pdf
PS-Carbodiimide is a neutral, bound carbodiimide that can be used for the synthesis of amides and esters. PS-Carbodiimide may also be used for the synthesis of pentafluorophenyl (PFP) activated esters (Table 3) and N-hydroxysuccinimidyl esters
Part No: PPS393.V.1Issued year: 2016File size: 0.98mbFile type: pdf
Biotage® PS-HOBt(HL) is a sulfonamide-linked, polymersupported
equivalent of 1-hydroxybenzotriazole (HOBt). PS-HOBt(HL) is used to generate bound HOBt active esters, which can either be made and used in situ, or isolated and stored as stable intermediates.
Part No: PPS400.V.1Issued year: 2016File size: 1.3mbFile type: pdf
Biotage®PS-Isocyanate is a 1% cross-linked poly(styreneco-divinylbenzene) which has pendent benzylisocyanate functionality. The resin can readily scavenge excess nucleophiles, which are often used to drive reactions to completion.
Part No: PPS401.V.1Issued year: 2016File size: 2.11mbFile type: pdf
PS-PPh3-Pd resin is a polystyrene-supported equivalent of the small molecule catalyst tetrakis(triphenylphosphine) palladium(0) [Pd(Ph3P)4]. The primary application for the resin is as a catalyst for Suzuki-Miyaura coupling reactions between arylboronic acids and aryl halides.
Part No: PPS382.V.1Issued year: 2016File size: 1.63mbFile type: pdf
Biotage® PS-TBD is a polymer-supported base, which applications are Alkylation of phenols and amines; esterification of carboxylic acids using alkyl halides; alkylation of activated methylene compounds; dehalogenation of organic halides; high throughput synthesis of aryl triflates and aryl nonaflates; Williamson ether synthesis
Part No: PPS389.V.1Issued year: 2016File size: 2.64mbFile type: pdf
Biotage® PS-Triphenylphosphine is a diphenylphosphinated polystyrene resin that is a solid-supported equivalent of triphenylphosphine. The resin can readily convert alcohols or carboxylic acids to the corresponding chlorides or acid chlorides in carbon tetrachloride.
Part No: PPS437Issued year: 2016File size: 0.19mbFile type: pdf
Biotage® SNAP Bio flash cartridges were developed with a small
particle size (20 μm) and large pore size (300 Å) to provide
increased resolution and effective separation of complex
peptide mixtures. Depending on the quality of the peptides
synthesized, flash chromatography can be used either as the
sole method of purification or as a front end clean-up prior to
SNAP Bio offers close to prep-HPLC performance in a flash
format at a fraction of the cost
Part No: TN-0016.0108Issued year: 2008File size: 0.4mbFile type: pdf
Biotage SNAP cartridges can be used on any flash system.
The easy-to-use Luer-lok® connections do not need a
compression module to operate at 100 psi. Made from USP
Class VI materials, Biotage SNAP cartridges offer 7 types of
loading techniques including 3 internal dry loading options.
Packed to provide the highest plate count of any 50μm particle
cartridge on the market, SNAP provides increased loading
capacity and better compound separations.