112-59-4 | Diethylene glycol monohexyl ether

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$15.00	$10.00
25g	97%	in stock	$16.00	$11.00
100g	97%	in stock	$35.00	$24.00
500g	97%	in stock	$95.00	$66.00

Description

• Catalog Number: AI08946
• Chemical Name: Diethylene glycol monohexyl ether
• CAS Number: 112-59-4
• Molecular Formula: C10H22O3
• Molecular Weight: 190.27988000000002
• MDL Number: MFCD00010703
• SMILES: CCCCCCOCCOCCO
• NSC Number: 403666

Computed Properties

• Complexity: 86.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 10
• XLogP3: 1.7

Upstream Synthesis Route

The chemical compound 2-(2-(hexyloxy)ethoxy)ethanol, also known as $name$, plays a crucial role in chemical synthesis as a versatile solvent and reagent. Its unique chemical structure, characterized by a chain of six carbon atoms with ethylene glycol units on either end, allows for a wide range of applications in organic chemistry.One of the key uses of 2-(2-(hexyloxy)ethoxy)ethanol in chemical synthesis is as a solvent for various reactions, especially those involving organic compounds that are poorly soluble in traditional solvents. Its ability to dissolve a wide range of substances makes it a valuable tool in the preparation of pharmaceuticals, polymers, and specialty chemicals.Moreover, in the realm of organic synthesis, 2-(2-(hexyloxy)ethoxy)ethanol can act as a reagent in reactions such as esterifications, etherifications, and acetylations. Its hydroxyl groups can participate in important chemical transformations, leading to the formation of new compounds with unique properties.Furthermore, the long aliphatic chain in 2-(2-(hexyloxy)ethoxy)ethanol provides a hydrophobic component that can enhance the solubility of nonpolar substances and facilitate the extraction of desired products in organic reactions. This feature makes it particularly useful in liquid-liquid extractions and chromatographic separations.Overall, the application of 2-(2-(hexyloxy)ethoxy)ethanol in chemical synthesis showcases its utility as a versatile solvent and reagent, enabling the efficient and effective preparation of a diverse range of organic compounds.

Literature

• In vitro and in vivo genetic toxicology studies with diethylene glycol monohexyl ether.

  Journal of applied toxicology : JAT 20010101