1-Iodobutane

>98%(GC), copper-containing as stabilizer

Reagent Code: #200514
label
Alias 1-iodobutane, iodide, butyl iodide, iodide, n-butyl iodide
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CAS Number 542-69-8

science Other reagents with same CAS 542-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.02 g/mol
Formula C₄H₉I
badge Registry Numbers
EC Number 208-824-4
MDL Number MFCD00001098
thermostat Physical Properties
Melting Point −103 °C(lit.)
Boiling Point 130-131 °C(lit.)
inventory_2 Storage & Handling
Density 1.617 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area, dry

description Product Description

Used as an alkylating agent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It introduces the butyl group into molecules, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Commonly employed in the synthesis of ketones, esters, and ethers through reactions with nucleophiles such as enolates, alkoxides, and amines. Also utilized in the production of specialty chemicals including surfactants and plasticizers. Its reactivity makes it valuable in research laboratories for constructing complex organic frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿740.00
inventory 100g
10-20 days ฿2,360.00
inventory 500g
10-20 days ฿9,990.00

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1-Iodobutane
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Used as an alkylating agent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It introduces the butyl group into molecules, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Commonly employed in the synthesis of ketones, esters, and ethers through reactions with nucleophiles such as enolates, alkoxides, and amines. Also utilized in the production of specialty chemicals including surfactants and plasticizers. Its reactivity makes it valuable

Used as an alkylating agent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It introduces the butyl group into molecules, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Commonly employed in the synthesis of ketones, esters, and ethers through reactions with nucleophiles such as enolates, alkoxides, and amines. Also utilized in the production of specialty chemicals including surfactants and plasticizers. Its reactivity makes it valuable in research laboratories for constructing complex organic frameworks.

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