623-69-8

Basic information

• Product Name: 1,3-Dimethoxy-2-propanol
• Synonyms: 1,3-DIMETHOXY-2-PROPANOL;1,3-dimethoxy-2-propano;Glycerol 1,3-dimethyl ether;glycerol,1,3-dimethylether;Glyceryl-1,3-dimethyl ether;1,3-Dimethoxypropan-2-ol;Glycerol α,γ-dimethyl ether;1,3-DiMethoxy-2-prop
• CAS NO: 623-69-8
• Molecular Formula: C₅H₁₂O₃
• Molecular Weight: 120.15
• Product Categories: pharmacetical
• Mol File: 623-69-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 169°C (estimate)
• Flash Point: 58.2 °C
• Appearance: /
• Density: 1.0085
• Vapor Pressure: 0.415mmHg at 25°C
• Refractive Index: 1.4192
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 13.68±0.20(Predicted)
• CAS DataBase Reference: 1,3-Dimethoxy-2-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dimethoxy-2-propanol(623-69-8)
• EPA Substance Registry System: 1,3-Dimethoxy-2-propanol(623-69-8)

Safety Data

• Statements: 10
• Safety Statements: 16
• RIDADR: 1987
• Hazardous Substances Data: 623-69-8(Hazardous Substances Data)

Usage

Uses

1,3-Dimethoxy-2-propanol is a possbile antiknock additive for gasoline and diesel fuel. It is also used to prepare heteroarylcarbamoylbenzene derivatives as glucokinase activators.

InChI:InChI=1/C5H12O3/c1-7-3-5(6)4-8-2/h5-6H,3-4H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 56-81-5 glycerol 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 34680-57-4 2-Chlor-1,3-dimethoxy-propane 
• 18664-32-9 1,3-dimethoxypropan-2-one 
• 85608-70-4 [2-methoxy-1-(methoxymethyl)ethyl]-4-methylbenzenesulfonate 
• 1642888-08-1 C₅₈H₈₉N₃O₂₂S 
• 1642888-07-0 C₅₂H₇₅NO₂₁S 
• 1642888-06-9 C₅₀H₇₁NO₁₈ 
• 1307864-34-1 NSP-2,7-DMG-DMAE-Z-NHS 
• 1307864-33-0 C₅₁H₇₂N₄O₁₈S₂ 
• 1307864-32-9 C₄₆H₆₆N₄O₁₅S₂ 

Relevant articles and documents

Thermodynamic characteristics of the sorption of glycerol ethers on stationary phase OV-101

Retention characteristics, temperature dependences of the retention characteristics, and thermodynamic characteristics of sorption on the nonpolar OV-101 phase are determined for 33 glycerol mono-, di-, and triethers with linear and branched monobasic alc

Cyclopentadienyl and pentamethylcyclopentadienyl ruthenium complexes as catalysts for the total deoxygenation of 1,2-hexanediol and glycerol

The ruthenium aqua complexes [cp*Ru(OH2)(N-N)](OTf) (cp* = η5-pentamethylcyclopentadienyl, N-N = 2,2′-bipyridine, phen = 1,10-phenanthroline, OTf- = trifluoromethanesulfonate) and the acetonitrile complex [cpRu(CH 3CN)(bipy)](OTf) (cp = η5-cyclopentadienyl) are water-, acid-, and thermally stable (>200°C) catalysts for the hydrogenation of aldehydes and ketones in sulfolane solution. In the presence of HOTf as a co-catalyst, they effect the deoxygenation of 1,2-hexanediol to 1-hexanol and hexane. Glycerol is deoxygenated to 1-propanol in up to 18% yield and under more forcing conditions completely deoxygenated to propene. The structure of the acetonitrile pro-catalyst [cpRu(CH3CN)(bipy)](OTf) has been determined by X-ray crystallography (space group P1 (a = 9.3778(10) A; b = 10.7852(10) A; c = 11.1818(13) A; α = 101.718(5)°; β = 114.717(4)°; γ = 102.712(5)°; R = 3.95%).