Butyl chloroformate

98%

Reagent Code: #142997
label
Alias n-butyl chloroformate; butyl chloroformate
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CAS Number 592-34-7

science Other reagents with same CAS 592-34-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 136.58 g/mol
Formula ClCOOCH₂CH₂CH₂CH₃
badge Registry Numbers
EC Number 209-750-5
MDL Number MFCD00000650
thermostat Physical Properties
Melting Point -70 °C
Boiling Point 142 °C(lit.)
inventory_2 Storage & Handling
Density 1.074 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used primarily as a reagent in organic synthesis, especially in peptide synthesis where it helps in activating carboxylic acids for amide bond formation via mixed anhydrides. It is also employed to introduce the n-butoxycarbonyl protecting group to amines, allowing selective protection during multi-step reactions. This facilitates the coupling of amino acids without significant racemization. Commonly used in pharmaceutical manufacturing and research laboratories for protecting group chemistry and activation reactions. Requires careful handling due to high reactivity with moisture and nucleophiles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿580.00
inventory 100g
10-20 days ฿1,000.00
inventory 500g
10-20 days ฿4,800.00
inventory 2.5kg
10-20 days ฿23,900.00

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Butyl chloroformate
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Used primarily as a reagent in organic synthesis, especially in peptide synthesis where it helps in activating carboxylic acids for amide bond formation via mixed anhydrides. It is also employed to introduce the n-butoxycarbonyl protecting group to amines, allowing selective protection during multi-step reactions. This facilitates the coupling of amino acids without significant racemization. Commonly used in pharmaceutical manufacturing and research laboratories for protecting group chemistry and activat

Used primarily as a reagent in organic synthesis, especially in peptide synthesis where it helps in activating carboxylic acids for amide bond formation via mixed anhydrides. It is also employed to introduce the n-butoxycarbonyl protecting group to amines, allowing selective protection during multi-step reactions. This facilitates the coupling of amino acids without significant racemization. Commonly used in pharmaceutical manufacturing and research laboratories for protecting group chemistry and activation reactions. Requires careful handling due to high reactivity with moisture and nucleophiles.

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