1708-35-6

Basic information

• Product Name: 1,3-Dioxolane-4-methanol, 2-hexyl-
• Synonyms: 2-Hexyl-1,3-dioxolane-4-methanol; 4-19-00-00680 (Beilstein Handbook Reference); BRN 0108185; EINECS 216-960-0; FEMA No. 2542; Heptanal glyceryl acetal; Heptanal glyceryl acetal (1,2 acetal); Heptanal, 1,2-glyceryl acetal; Heptanal, cyclic (hydroxymethyl)ethylene acetal; (2-hexyl-1,3-dioxolan-4-yl)methanol
• CAS NO: 1708-35-6
• Molecular Formula: C₁₀H₂₀O₃
• Molecular Weight: 188.264
• EINECS: 216-960-0
• Mol File: 1708-35-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 271.9°C at 760 mmHg
• Flash Point: 132.4°C
• Density: 0.975g/cm³
• Vapor Pressure: 0.000813mmHg at 25°C
• Refractive Index: 1.442
• CAS DataBase Reference: 1,3-Dioxolane-4-methanol, 2-hexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane-4-methanol, 2-hexyl-(1708-35-6)
• EPA Substance Registry System: 1,3-Dioxolane-4-methanol, 2-hexyl-(1708-35-6)

Safety Data

• Hazardous Substances Data: 1708-35-6(Hazardous Substances Data)

Usage

General Description

1,3-Dioxolane-4-methanol, 2-hexyl- is an organic compound with the chemical formula C10H20O3. It is a clear, colorless liquid with a mild, pleasant odor. This chemical is commonly used as a solvent in various industrial applications such as paints, coatings, and adhesives. It is also used as a precursor in the production of other chemicals and pharmaceuticals. Due to its low toxicity and favorable chemical properties, 1,3-Dioxolane-4-methanol, 2-hexyl- is considered a versatile and useful compound in the manufacturing industry. However, it should be handled with care and proper safety measures in place to prevent exposure and potential adverse effects.

Upstream product

• 111-71-7 heptanal 
• 854844-09-0 4-(3,5-dinitro-benzoyloximethyl)-2-hexyl-[1,3]dioxolane 
• 56-81-5 glycerol 

Relevant articles and documents

Method for the Synthesis of Cyclic Acetals by the Reactive Extraction of a Polyol in a Concentrated Solution

A method for the synthesis of cyclic acetals comprises reacting at least one carbonyl-function compound selected from aldehydes, ketones, and/or linear acetals, on a polyol in a concentrated aqueous solution exceeding 20 wt % in a reactor containing an acidic catalyst. The carbonyl-function compound is selected so that the cyclic acetal obtained has a water solubility lower than 20000 mg/kg. During the catalytic reaction for the cyclic acetal synthesis, at least one portion of the organic phase containing the cyclic acetal is separated. The acidic catalysis is either homogeneous when using a water-soluble strong acid, or heterogeneous when using a solid acid such as a resin, a zeolite, or any appropriately acidified solid. The extractive reaction method can be used for obtaining high conversions and selectivity.