Fmoc-Sec(Trt)-OH

97%

Reagent Code: #229198
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CAS Number 1639843-37-0

science Other reagents with same CAS 1639843-37-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 632.61 g/mol
Formula C₃₇H₃₁NO₄Se
badge Registry Numbers
MDL Number MFCD11041250
thermostat Physical Properties
Boiling Point 798.1±60.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in solid-phase peptide synthesis to incorporate selenocysteine, the 21st amino acid, into peptides. The Fmoc group allows for mild base deprotection, while the Trt (trityl) group protects the reactive selenol side chain during synthesis. This protection scheme is essential for preventing oxidation and unwanted side reactions. After chain assembly, the Trt group can be selectively removed under mild acidic conditions, enabling further modifications or formation of selenyl-sulfide bonds. Commonly applied in the preparation of selenopeptides for studies in redox biology, enzyme mimicry, and structural analysis using techniques like X-ray crystallography or NMR.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,540.00
250mg
10-20 days ฿25,930.00
1g
10-20 days ฿69,950.00
5g
10-20 days ฿209,810.00
Fmoc-Sec(Trt)-OH
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Used in solid-phase peptide synthesis to incorporate selenocysteine, the 21st amino acid, into peptides. The Fmoc group allows for mild base deprotection, while the Trt (trityl) group protects the reactive selenol side chain during synthesis. This protection scheme is essential for preventing oxidation and unwanted side reactions. After chain assembly, the Trt group can be selectively removed under mild acidic conditions, enabling further modifications or formation of selenyl-sulfide bonds. Commonly appl

Used in solid-phase peptide synthesis to incorporate selenocysteine, the 21st amino acid, into peptides. The Fmoc group allows for mild base deprotection, while the Trt (trityl) group protects the reactive selenol side chain during synthesis. This protection scheme is essential for preventing oxidation and unwanted side reactions. After chain assembly, the Trt group can be selectively removed under mild acidic conditions, enabling further modifications or formation of selenyl-sulfide bonds. Commonly applied in the preparation of selenopeptides for studies in redox biology, enzyme mimicry, and structural analysis using techniques like X-ray crystallography or NMR.

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