93892-07-0

Basic information

• Product Name: 1,1-dibutoxyhexane
• Synonyms: 1,1-dibutoxyhexane;Hexanal dibutyl acetal
• CAS NO: 93892-07-0
• Molecular Formula: C₁₄H₃₀O₂
• Molecular Weight: 230.3868
• EINECS: 299-487-2
• Mol File: 93892-07-0.mol

Chemical Properties

• Boiling Point: 234.6°Cat760mmHg
• Flash Point: 52.3°C
• Appearance: /
• Density: 0.844g/cm³
• Vapor Pressure: 0.0802mmHg at 25°C
• Refractive Index: 1.429
• CAS DataBase Reference: 1,1-dibutoxyhexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dibutoxyhexane(93892-07-0)
• EPA Substance Registry System: 1,1-dibutoxyhexane(93892-07-0)

Safety Data

• Hazardous Substances Data: 93892-07-0(Hazardous Substances Data)

Usage

Chemical compound

1,1-Dibutoxyhexane is a chemical compound consisting of a six-carbon hydrocarbon chain with two butoxy (C4H9O) groups attached at position 1.

Color

It is a colorless liquid.

Molecular weight

The molecular weight of 1,1-Dibutoxyhexane is 258.44 g/mol.

Industrial use

1,1-Dibutoxyhexane is primarily used as a solvent in various industrial processes and applications.

Dispersing agent

It is used as a dispersing agent in paints, coatings, and adhesives.

Component in chemical reactions

1,1-Dibutoxyhexane is also used as a component in chemical reactions.

Solvent for chemical synthesis

It is used as a solvent for chemical synthesis.

Low toxicity

1,1-Dibutoxyhexane is considered to have low toxicity.

Health hazards

It is not known to have any significant health hazards associated with its use.

InChI:InChI=1/C14H30O2/c1-4-7-10-11-14(15-12-8-5-2)16-13-9-6-3/h14H,4-13H2,1-3H3

Relevant articles and documents

Method for producing enol ethers

Enol ethers of the formula I where R1is an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radical which may carry further substituents which do not react with acetylenes or allenes, and the radicals R, independently of one another, are hydrogen or aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radicals, which may be bonded to one another to form a ring, and m is 0 or 1, are prepared by reacting an acetal or ketal of the formula II with an acetylene or allene of the formula III or IV where R and R1have the abovementioned meanings, in the gas phase at elevated temperatures in the presence of a zinc- or cadmium- and silicon- and oxygen-containing heterogeneous catalyst.