Di-tert-butyl dicarbonate

98%

Reagent Code: #60114
label
Alias Di-tert-butyl dicarbonate; Boc anhydride; Di-tert-butyl dicarbonate; Bis(tert-butoxycarbonyl) oxide; Boc Anhydride
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CAS Number 24424-99-5

science Other reagents with same CAS 24424-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.25 g/mol
Formula C₁₀H₁₈O₅
badge Registry Numbers
EC Number 246-240-1
MDL Number MFCD00008805
thermostat Physical Properties
Melting Point 23 °C(lit.)
Boiling Point 56-57 °C/0.5 mmHg(lit.)
inventory_2 Storage & Handling
Density 0.95 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used primarily as a protecting agent in organic synthesis, it safeguards amine groups during chemical reactions, particularly in peptide synthesis. Its role is crucial in preventing unwanted side reactions, ensuring the integrity of the target molecule. Additionally, it serves as a reagent in the preparation of carbamates, which are valuable intermediates in pharmaceuticals and agrochemicals. Its application extends to the modification of amino acids and proteins, aiding in the study of their structure and function. The compound's stability and ease of removal make it a preferred choice in complex organic transformations.

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Test Parameter Specification
Purity (GC) 98-100
Refractive Index (N20D) 1.4089-1.4091
Appearance White low melting point crystalline solid or liquid
Note This product is a low melting point solid and may change state in different environments (solid, liquid, or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5kg
10-20 days ฿14,200.00
inventory 500g
10-20 days ฿1,990.00
inventory 2.5kg
10-20 days ฿8,860.00
inventory 10kg
10-20 days ฿23,580.00
inventory 25g
10-20 days ฿300.00
inventory 100g
10-20 days ฿510.00

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Di-tert-butyl dicarbonate
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Used primarily as a protecting agent in organic synthesis, it safeguards amine groups during chemical reactions, particularly in peptide synthesis. Its role is crucial in preventing unwanted side reactions, ensuring the integrity of the target molecule. Additionally, it serves as a reagent in the preparation of carbamates, which are valuable intermediates in pharmaceuticals and agrochemicals. Its application extends to the modification of amino acids and proteins, aiding in the study of their structure and function. The compound's stability and ease of removal make it a preferred choice in complex organic transformations.
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