n-Butyl bromide

Standard for GC,>99.5%(GC)

Reagent Code: #143060
label
Alias Bromo n-butane; 1-bromobutane, bromobutane, butyl bromo, bromobutane, n-butyl bromo, n-butyl bromo, n-butyl bromo
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CAS Number 109-65-9

science Other reagents with same CAS 109-65-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.02 g/mol
Formula C₄H₉Br
badge Registry Numbers
EC Number 203-691-9
MDL Number MFCD00000260
thermostat Physical Properties
Melting Point -112 °C
Boiling Point 100-104 °C(lit.)
inventory_2 Storage & Handling
Density 1.276 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used primarily as an alkylating agent in organic synthesis, enabling the introduction of the butyl group into various molecules. Commonly employed in the production of pharmaceuticals, agrochemicals, and dyes. Serves as a key intermediate in the preparation of quaternary ammonium compounds, which are used as surfactants and disinfectants. Also utilized in the synthesis of flavors and fragrances due to its ability to form esters. In laboratories, it acts as a reagent for converting alcohols to bromides and in the formation of Grignard reagents when reacted with magnesium in anhydrous ether.

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inventory 5ml
10-20 days ฿480.00

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n-Butyl bromide
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Used primarily as an alkylating agent in organic synthesis, enabling the introduction of the butyl group into various molecules. Commonly employed in the production of pharmaceuticals, agrochemicals, and dyes. Serves as a key intermediate in the preparation of quaternary ammonium compounds, which are used as surfactants and disinfectants. Also utilized in the synthesis of flavors and fragrances due to its ability to form esters. In laboratories, it acts as a reagent for converting alcohols to bromides an

Used primarily as an alkylating agent in organic synthesis, enabling the introduction of the butyl group into various molecules. Commonly employed in the production of pharmaceuticals, agrochemicals, and dyes. Serves as a key intermediate in the preparation of quaternary ammonium compounds, which are used as surfactants and disinfectants. Also utilized in the synthesis of flavors and fragrances due to its ability to form esters. In laboratories, it acts as a reagent for converting alcohols to bromides and in the formation of Grignard reagents when reacted with magnesium in anhydrous ether.

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