Di-tert-butyl dicarbonate

99%

Reagent Code: #60115
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 complex chemical reactions, ensuring they remain unaffected while other transformations occur. This is particularly crucial in peptide synthesis, where it helps in the stepwise construction of peptide chains. Additionally, it serves as a reagent in the preparation of carbamates, which are valuable intermediates in pharmaceuticals and agrochemicals. Its role in the synthesis of various bioactive molecules and fine chemicals underscores its importance in research and industrial applications.

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Test Parameter Specification
Purity 99-100
Refractive Index (n20D) 1.4075-1.4095
Oxygen (Elemental Analysis) 35.8-36.9
Hydrogen (Elemental Analysis) 7.9-8.5
Appearance White solid or colorless liquid
Note Low melting point solid; 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 ฿27,500.00
inventory 25g
10-20 days ฿470.00
inventory 100g
10-20 days ฿1,160.00
inventory 1kg
10-20 days ฿5,700.00

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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 complex chemical reactions, ensuring they remain unaffected while other transformations occur. This is particularly crucial in peptide synthesis, where it helps in the stepwise construction of peptide chains. Additionally, it serves as a reagent in the preparation of carbamates, which are valuable intermediates in pharmaceuticals and agrochemicals. Its role in the synthesis of various bioactive molecules and fine chemicals underscores its importance in research and industrial applications.
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