1126-78-9 | N-Butylaniline

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$19.00	$13.00
5g	95%	in stock	$22.00	$15.00
25g	95%	in stock	$47.00	$33.00
100g	95%	in stock	$145.00	$102.00

Description

• Catalog Number: AB46726
• Chemical Name: N-Butylaniline
• CAS Number: 1126-78-9
• Molecular Formula: C10H15N
• Molecular Weight: 149.2328
• MDL Number: MFCD00035798
• SMILES: CCCCNc1ccccc1
• NSC Number: 7114

Computed Properties

• Complexity: 84.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 2.8

Upstream Synthesis Route

N-Butylaniline, also known as butylphenylamine, is a versatile chemical compound commonly used in various chemical synthesis processes. One of its key applications is as a primary intermediate in the production of dyes, specifically acid dyes and reactive dyes. N-Butylaniline serves as a crucial building block in dye manufacturing due to its ability to undergo various reactions, such as diazotization and coupling, to yield a wide range of colorants with different properties.Additionally, N-Butylaniline is employed in the synthesis of antioxidants, pharmaceuticals, and rubber chemicals. Its reactivity and chemical properties enable it to participate in reactions leading to the formation of valuable products in these industries. In the production of antioxidants, N-Butylaniline acts as a key ingredient in the synthesis of hindered phenols, which are used to prevent the degradation of materials due to oxidation. In pharmaceuticals, it can be utilized in the synthesis of certain drugs and pharmaceutical intermediates. Moreover, in the rubber industry, N-Butylaniline is involved in the creation of rubber accelerators, which enhance the vulcanization process and improve the properties of rubber products.Overall, N-Butylaniline plays a significant role in chemical synthesis as a versatile compound that contributes to the creation of various products essential in different industries.

Literature

• Recognition and resolution of isomeric alkyl anilines by mass spectrometry.

  Journal of the American Society for Mass Spectrometry 20090201

• New chemical constituents of Euphorbia quinquecostata and absolute configuration assignment by a convenient Mosher ester procedure carried out in NMR tubes.

  Journal of natural products 20020901