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Supplier: Supra Sciences
Description: Common reagent utilized for peptide synthesis on solid support.

SDS

Supplier: Ambeed
Description: Rink Amide MBHA resin 0.3-0.8 mmol/g, resin 100-200 mesh, 1% DVB

New Product

Supplier: Bachem Americas
Description: Fmoc-Rink amide-AM resin, a standard resin for the Fmoc-SPPS of peptide amides. Cleavage was performed with 50 % TFA in CH₂Cl₂ or 95% aqueous TFA. Scavengers may be required. Bachem additionally offers the Rink amide (RAM) linker (Q-1660).

Supplier: Bachem Americas
Description: Resin for the Fmoc-SPPS of peptide amides. Cleavage was achieved with 50 % TFA in CH₂Cl₂. or 95% TFA Scavengers may be required. (EP 0 285 562 B1 licensed to Bachem)

Supplier: Chem Impex International
Description: It is used for the synthesis of the solid phase peptide synthesis of peptide amines utilizing Fmoc-protected amino acids.

Supplier: Ambeed
Description: 4-[(2,4-Dimethoxyphenyl)-(fmoc-amino)methyl]phenoxyacetic acid 98%

Supplier: Thermo Scientific Chemicals
Description: 5g CAS: 145069-56-3, MDL: MFCD00153509
Supplier: Bachem Americas
Description: Ramage resin is highly suitable for the preparation of peptide amides by the Fmoc-strategy and is recommended for C-terminal Phe, Tyr and Ile. Cleavage has been performed with 50 % TFA in CH₂Cl₂ or 95% aqueous TFA. Scavengers may be required. Tricyclic amide linker resin has been used for the synthesis of fluorogenic substrates for continuous assay of aminopeptidase P. Bachem additionally offers the Ramage amide linker (Q-2745) to be coupled to other types of carrier resin.

Supplier: Bachem Americas
Description: For Fmoc solid phase synthesis of N-alkyl peptide amides by reductive amination.

Supplier: Bachem Americas
Description: Useful for the synthesis of peptide amides using Fmoc strategy. Cleavage has been performed with 50 % TFA in CH₂Cl₂ or 95% aqueous TFA. Scavengers may be required.

Supplier: Bachem Americas
Description: Sieber amide resin has been developed for the Fmoc-SPPS of fully t-butyl protected peptide amides. Cleavage can be achieved with 1% TFA in methylene chloride. Scavengers may be required. As N-methylation increases the acid-lability of the peptide bond, Malakoutikhah et al. employed Sieber resin for obtaining short peptide amides containing multiple MePhe residues.

Supplier: Supra Sciences
Description: Common reagent utilized for peptide synthesis on solid support.

SDS

Supplier: Supra Sciences
Description: Solid supported primary amine utilized in solid phase synthesis for coupling amino acids at carboxyl terminus.

SDS

Supplier: Thermo Scientific Chemicals
Description: Powder
Catalog Number: (97067-756)
Supplier: Cytiva
Description: NHS-activated Sepharose™ 4 Fast Flow is composed of cross-linked 4% agarose beads, NHS activated for coupling amino-containing proteins and peptides in process-scale applications. NHS (N-hydroxysuccinimide) coupling forms a chemically stable amide bond with ligands containing primary amino groups. The resin provides a spacer arm to the coupled ligand and suitable for immobilising smaller protein and peptide ligands.

Supplier: Bachem Americas
Description: The Wang support, p-benzyloxybenzyl alcohol resin, is the most widely used resin for attaching carboxylic acids for further functionalization. Cleavage conditions for the ester anchor involve concentrated TFA or TFA/CH₂Cl₂ to provide carboxylic acids or cyclization-cleavage under acidic or basic conditions. Release of an amide function by treatment with an amine in the presence of a Lewis acid was also reported. Wang resin was used to add vinyl and iodobenzoic acids via carbodiimide coupling and the products subjected to Heck conditions with alkenes or with alkynes or to Suzuki coupling with boron reagents. The Ugi multicomponent condensation reaction was conducted on Wang resin with the carboxylic acid, amine or isonitrile as the anchored functional group. Solid-phase lactam syntheses were also achieved by reaction of the resin-bound isonitrile with an amine and an ω-keto-acid as well as other synthetic transformations such as the Biginelli reaction and construction of heterocycles such as quinolones, imidazoles, hydantoins, and 1,4-benzodiazepine-2,5-diones. On a Wang resin primary, secondary, and tertiary alcohols have been converted to 4-methoxybenzyl ethers. As well as anchoring carboxylic acids to Wang resin, phenols were attached under Mitsunobu conditions, subjected to further transformations and cleaved under acidic conditions.

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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