59068-03-0

Basic information

• Product Name: 1,3-bis[(2-ethylhexyl)oxy]propan-2-ol
• Synonyms: 1,3-bis[(2-ethylhexyl)oxy]propan-2-ol;1,3-Bis[(2-ethylhexyl)oxy]-2-propanol
• CAS NO: 59068-03-0
• Molecular Formula: C₁₉H₄₀O₃
• Molecular Weight: 316.5191
• EINECS: 261-587-9
• Mol File: 59068-03-0.mol

Chemical Properties

• Boiling Point: 402.5°C at 760 mmHg
• Flash Point: 197.2°C
• Appearance: /
• Density: 0.895g/cm³
• Vapor Pressure: 3.73E-08mmHg at 25°C
• Refractive Index: 1.449
• CAS DataBase Reference: 1,3-bis[(2-ethylhexyl)oxy]propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis[(2-ethylhexyl)oxy]propan-2-ol(59068-03-0)
• EPA Substance Registry System: 1,3-bis[(2-ethylhexyl)oxy]propan-2-ol(59068-03-0)

Safety Data

• Hazardous Substances Data: 59068-03-0(Hazardous Substances Data)

Usage

Physical state

Clear, colorless liquid

Odor

Mild

Solubility

Highly soluble in organic solvents

Uses

Plasticizer in the production of plastics, adhesives, and sealants
Solvent in various industries
Ingredient in personal care products such as lotions and creams
Surfactant and emulsifier in industrial processes

Properties

Improves flexibility and durability of materials

Safety precautions

Can be harmful if ingested or inhaled
Can cause skin and eye irritation upon contact
Should be handled with care

InChI:InChI=1/C19H40O3/c1-5-9-11-17(7-3)13-21-15-19(20)16-22-14-18(8-4)12-10-6-2/h17-20H,5-16H2,1-4H3

Upstream product

• 104-76-7 2-Ethylhexyl alcohol 
• 106-89-8 epichlorohydrin 
• 123-05-7 d,l-2-ethylhexanal 
• 56-81-5 glycerol 
• 2461-15-6 2-ethyl-hexyl glycidyl ether 
• 96-23-1 1,3-Dichloro-2-propanol 

Relevant articles and documents

NEW COMPOUND, VISCOSITY INDEX IMPROVER, AND LUBRICANT COMPOSITION

PROBLEM TO BE SOLVED: To provide a viscosity index improver excellent in shear stability, and a lubricant composition containing the viscosity index improver. SOLUTION: The invention provides a compound represented by the general formula (1) in the figure, and a polymer comprising a constitutional unit (a) derived from the general formula (1). (In the general formula (1), R1 represents a hydrogen atom or methyl group; R2, R3, R4 and R5 each independently represent a C2-18 alkyl group; and m and n each independently represent an integer from 1 to 10.) SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Method for producing ethylhexylglycerin

The present invention provides a producing method of ethylhexylglycerin, comprising the steps of (A) agitating 2-ethylhexylglycidyl ether, water, an organic solvent and a catalyst; (B) reacting the mixture at 80-120anddeg;C for 15-25 hours after the agitation, and then synthesizing ethylhexylglycerin; (C) adding ethylacetate after the synthesis; (D) removing a water layer in the step (C) and washing an organic layer with water; and (E) distilling the washed organic layer, and accordingly obtaining ethylhexylglycerin.(AA) Temperature(anddeg;C)COPYRIGHT KIPO 2015

Coalescent for aqueous compositions

A coalescent composition selected from 1,3-(C6-C12alkyloxy)-2-propanol, 1,1'-oxybis[3-(C6-C12alkyloxy)]-2-propanol, and mixtures thereof is provided. Preferred coalescents are 1,3-(decyloxy)-2-propanol and 1,1'-oxybis[3-(heptyloxy)]-2-propanol. A method for forming glycerol diethers and diglycerol diethers, an aqueous coating composition including the coalescent compositions and a method for forming a coating are also provided.

PROCESS FOR PRODUCING ETHER COMPOUND

The present invention relates to a process for producing an ether compound in a simplified, efficient manner, including the step of reacting a hydroxyl group-containing compound with an epoxy compound in the presence of an oxide of a metal of Group 4 of the Periodic Table on which a sulfate ion is supported, wherein a sum of a diffraction intensity of a (111) crystal lattice plane and a diffraction intensity of a (?111) crystal lattice place of the metal oxide is 2000 cps or larger as measured by subjecting the metal oxide to powder X-ray diffraction analysis.

POLYOL ETHERS AND PROCESS FOR MAKING THEM

New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol to carbonyl compound in the process is greater than 5:1.

Selective synthesis of aliphatic ethylene glycol sulfonate surfactants

The selective synthesis of a series of components in a commercial surfactant mixture was studied. The general structure of the surfactant was a glycerol-based double chain monosulfonate molecule, with a C8-Guerbert alcohol, 2-ethylhexanol, at C-1, a pentyloxy group at C-3 and a 3-oxypropane-1-sulfonic acid or an ethoxylated 3-oxypropane-1-sulfonic acid side chain at the C-2 position. The main chain alcohol was obtained by a base catalyzed reaction of 2-ethylhexyl glycidyl ether with a pentyl alcohol. High C-3 selectivity was obtained. Two methods were used for the construction of the ethoxylated side chain at the C-2. A sequence consisting of O-allylation followed by ozonolysis and sodium borohydride work-up gave good yields of the desired ethoxylated homologs. A shorter, more efficient method involved the reaction with 1,2-ethylene sulfate. This method gave the ethoxylated bomologs with high selectivity and in high yields. O-Propane sulfonation was accomplished by the reaction of the appropriate alkoxides with 1,3-propane sulfone. The pure sodium sulfonates were isolated in good overall yields by continuous extraction with hexane or diethyl ether. Acta Chemica Scandinavica 1996.