110-68-9 | N-Methylbutylamine

Packsize	Purity	Availability	Price	Discounted Price
250mg	93%	in stock	$79.00	$55.00
1g	93%	in stock	$96.00	$67.00
5g	93%	in stock	$133.00	$93.00

Description

• Catalog Number: AB77611
• Chemical Name: N-Methylbutylamine
• CAS Number: 110-68-9
• Molecular Formula: C5H13N
• Molecular Weight: 87.1634
• MDL Number: MFCD00009426
• SMILES: CCCCNC

Computed Properties

• Complexity: 19.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.3

Upstream Synthesis Route

Methylbutylamine, also known as N-methylbutan-1-amine, is a versatile chemical compound commonly used in chemical synthesis processes. Its primary application lies in its role as a building block for the synthesis of various organic compounds and pharmaceuticals. In particular, methylbutylamine is a crucial intermediate in the production of numerous chemicals due to its unique chemical properties and functional groups. It serves as a valuable precursor in the creation of amine-based compounds, which are essential in the pharmaceutical, agrochemical, and material science industries. Additionally, methylbutylamine plays a vital role in the synthesis of polymers and other complex organic molecules, making it a fundamental component in modern chemical research and development. With its diverse applications and reactivity, methylbutylamine is a cornerstone in the world of chemical synthesis.

Literature

• (2,2'-Bipyridyl-κN,N')bis-(N-butyl-N-methyl-dithio-carbamato-κS,S')cadmium(II).

  Acta crystallographica. Section E, Structure reports online 20110301

• Anti-inflammatory and antinociceptive evaluation of newly synthesized 4-(substituted ethanoyl) amino-3-mercapto-5-(4-methoxy) phenyl-1,2,4-triazoles.

  Journal of pharmacy & bioallied sciences 20110101

• DNA interactions of new antitumor platinum complexes with trans geometry activated by a 2-metylbutylamine or sec-butylamine ligand.

  Biochemical pharmacology 20040315