Di-tert-butyl carbonate

98%

Reagent Code: #176964
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CAS Number 34619-03-9

science Other reagents with same CAS 34619-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.24 g/mol
Formula C₉H₁₈O₃
badge Registry Numbers
MDL Number MFCD14560560
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a reagent in organic synthesis, particularly for introducing the tert-butoxycarbonyl (Boc) protecting group to amines. This protection is essential in peptide synthesis, where it prevents unwanted reactions at the amine group during coupling steps. It is favored for its stability under a variety of reaction conditions and ease of removal under mild acidic conditions, allowing selective deprotection without affecting other functional groups. Also employed in the preparation of carbamates and other protected intermediates in pharmaceutical and agrochemical manufacturing.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿750.00
inventory 1g
10-20 days ฿1,860.00
inventory 5g
10-20 days ฿8,280.00
inventory 25g
10-20 days ฿33,450.00

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Di-tert-butyl carbonate
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Used as a reagent in organic synthesis, particularly for introducing the tert-butoxycarbonyl (Boc) protecting group to amines. This protection is essential in peptide synthesis, where it prevents unwanted reactions at the amine group during coupling steps. It is favored for its stability under a variety of reaction conditions and ease of removal under mild acidic conditions, allowing selective deprotection without affecting other functional groups. Also employed in the preparation of carbamates and other pr
Used as a reagent in organic synthesis, particularly for introducing the tert-butoxycarbonyl (Boc) protecting group to amines. This protection is essential in peptide synthesis, where it prevents unwanted reactions at the amine group during coupling steps. It is favored for its stability under a variety of reaction conditions and ease of removal under mild acidic conditions, allowing selective deprotection without affecting other functional groups. Also employed in the preparation of carbamates and other protected intermediates in pharmaceutical and agrochemical manufacturing.
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