Boron tribromide

99.9% metals basis

Reagent Code: #143043
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Alias Boron tribromide; boron bromide, natural alkali
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CAS Number 10294-33-4

science Other reagents with same CAS 10294-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.52 g/mol
Formula BBr₃
badge Registry Numbers
EC Number 233-657-9
MDL Number MFCD00011312
thermostat Physical Properties
Melting Point −46 °C(lit.)
Boiling Point ~90 °C
inventory_2 Storage & Handling
Density 2.60 g/mL at 20 °C(lit.)
Storage 2-8℃, avoid light, and fill with argon

description Product Description

Used primarily as a reagent in organic synthesis, especially for the cleavage of ether groups, including methyl and benzyl ethers, making it valuable in the deprotection step during the synthesis of complex organic molecules. Widely applied in the pharmaceutical industry for modifying functional groups in drug intermediates. Also serves as a catalyst in certain alkylation and isomerization reactions. Its strong Lewis acid properties make it effective in promoting various electrophilic reactions. Handles under inert conditions due to high reactivity with moisture and air.

format_list_bulleted Product Specification

Test Parameter Specification
Assay (%) 98-102.5
Purity (Based on Trace Metal Analysis)(%) 99.9-100
Trace Metal Analysis (ppm) 0-2000
APPEARANCE Colorless to amber liquid
ICP MAJOR ANALYSIS CONFIRMED Confirms boron component

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿590.00
100g
10-20 days ฿1,870.00
500g
10-20 days ฿7,400.00
2.5kg
10-20 days ฿32,200.00
Boron tribromide
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Used primarily as a reagent in organic synthesis, especially for the cleavage of ether groups, including methyl and benzyl ethers, making it valuable in the deprotection step during the synthesis of complex organic molecules. Widely applied in the pharmaceutical industry for modifying functional groups in drug intermediates. Also serves as a catalyst in certain alkylation and isomerization reactions. Its strong Lewis acid properties make it effective in promoting various electrophilic reactions. Handles

Used primarily as a reagent in organic synthesis, especially for the cleavage of ether groups, including methyl and benzyl ethers, making it valuable in the deprotection step during the synthesis of complex organic molecules. Widely applied in the pharmaceutical industry for modifying functional groups in drug intermediates. Also serves as a catalyst in certain alkylation and isomerization reactions. Its strong Lewis acid properties make it effective in promoting various electrophilic reactions. Handles under inert conditions due to high reactivity with moisture and air.

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