Rink Amide AM resin
0.3~0.8mmol/g, 100~200 mesh, 1% DVB
- Product Code: 96213
CAS:
183599-10-2
Molecular Weight: | 627.71 g./mol | Molecular Formula: | C₃₉H₃₅N₂O₆R |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Rink Amide AM resin is widely used in solid-phase peptide synthesis (SPPS) as a versatile support material. It is particularly valuable for synthesizing C-terminal amidated peptides, which are common in biologically active compounds. The resin facilitates the attachment of the first amino acid through its amide linker, allowing for the stepwise addition of subsequent amino acids. After synthesis, the peptide can be cleaved from the resin while retaining the amide group at the C-terminus. This makes it a preferred choice for producing peptides used in pharmaceutical research, drug development, and biochemical studies. Its compatibility with Fmoc (fluorenylmethyloxycarbonyl) chemistry further enhances its utility in automated peptide synthesizers.
Product Specification:
Test | Specification |
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APPEARANCE | solid |
PARTICLE SIZE | 100mesh 200mesh |
LOADING | 0.3mmolg 0.8mmol/g |
Matrixcrosslinked with 1 DVB | Conforms |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $105.83 |
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5.000 | 10-20 days | $316.06 |
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25.000 | 10-20 days | $1,054.02 |
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Rink Amide AM resin
Rink Amide AM resin is widely used in solid-phase peptide synthesis (SPPS) as a versatile support material. It is particularly valuable for synthesizing C-terminal amidated peptides, which are common in biologically active compounds. The resin facilitates the attachment of the first amino acid through its amide linker, allowing for the stepwise addition of subsequent amino acids. After synthesis, the peptide can be cleaved from the resin while retaining the amide group at the C-terminus. This makes it a preferred choice for producing peptides used in pharmaceutical research, drug development, and biochemical studies. Its compatibility with Fmoc (fluorenylmethyloxycarbonyl) chemistry further enhances its utility in automated peptide synthesizers.
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