N,N-Dimethylformamide Dibutyl Acetal

98%

Reagent Code: #217798
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CAS Number 18503-90-7

science Other reagents with same CAS 18503-90-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.33 g/mol
Formula C₁₁H₂₅NO₂
badge Registry Numbers
MDL Number MFCD00015249
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a versatile solvent and reagent in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a butylating agent, enabling the introduction of butyl groups into molecules under mild conditions. Its stability and solubility properties make it suitable for reactions involving sensitive intermediates, including those in the manufacture of agrochemicals and dyes. Additionally, it functions as a protecting group carrier in multi-step syntheses due to its selective deprotection characteristics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1ml
10-20 days ฿1,070.00
5ml
10-20 days ฿1,510.00
N,N-Dimethylformamide Dibutyl Acetal
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Used as a versatile solvent and reagent in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a butylating agent, enabling the introduction of butyl groups into molecules under mild conditions. Its stability and solubility properties make it suitable for reactions involving sensitive intermediates, including those in the manufacture of agrochemicals and dyes. Additionally, it functions as a protecting group carrier in multi-step syntheses due to its sel

Used as a versatile solvent and reagent in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a butylating agent, enabling the introduction of butyl groups into molecules under mild conditions. Its stability and solubility properties make it suitable for reactions involving sensitive intermediates, including those in the manufacture of agrochemicals and dyes. Additionally, it functions as a protecting group carrier in multi-step syntheses due to its selective deprotection characteristics.

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