19037-58-2

Basic information

• Product Name: (3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE
• Synonyms: (3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE;Isopropiosyringone;1-(4-Hydroxy-3,5-diMethoxyphenyl)propan-2-one
• CAS NO: 19037-58-2
• Molecular Formula: C₁₁H₁₄O₄
• Molecular Weight: 210.23
• Product Categories: Aromatic Ketones (substituted)
• Mol File: 19037-58-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 340°Cat760mmHg
• Flash Point: 130.1°C
• Appearance: /
• Density: 1.153g/cm³
• Vapor Pressure: 4.49E-05mmHg at 25°C
• Refractive Index: 1.523
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE(19037-58-2)
• EPA Substance Registry System: (3,5-DIMETHOXY-4-HYDROXYPHENYL)ACETONE(19037-58-2)

Safety Data

• Hazardous Substances Data: 19037-58-2(Hazardous Substances Data)

Usage

Uses

Syringylacetone can be used for thermal decomposition of biomass wastes derived from palm oil production.

InChI:InChI=1/C11H14O4/c1-7(12)4-8-5-9(14-2)11(13)10(6-8)15-3/h5-6,13H,4H2,1-3H3

Upstream product

• 148123-59-5 3-(4-benzyloxy-3,5-dimethoxyphenyl)-2-methylpropene 
• 148123-58-4 2,6-dimethoxy-4-(2-methylprop-2-enyl)phenol 
• 148123-56-2 1,3-dimethoxy-2-(2-methylprop-2-enyloxy)benzene 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 64-17-5 ethanol 
• 148123-60-8 1-(4-benzyloxy-3,5-dimethoxyphenyl)propan-2-one 

Downstream Products

• 101664-64-6 (E)-1,4-bis(3,4,5-trimethoxyphenyl)-2,3-dimethyl-2-butene 
• 101664-65-7 (Z)-1,4-bis(3,4,5-trimethoxyphenyl)-2,3-dimethyl-2-butene 
• 50544-08-6 5,5'-(2,3-dimethylbutane-1,4-diyl)bis(1,2,3-trimethoxybenzene) 
• 16603-18-2 (3,4,5-trimethoxyphenyl)acetone 
• 129308-27-6 (4-acetoxy-3,5-dimethoxy-phenyl)-acetone 

Relevant articles and documents

Methoxyphenols from burning of Scandinavian forest plant materials

Semivolatile compounds in smoke from gram-scale incomplete burning of plant materials were assessed by gas chromatography and mass spectrometry. Gas syringe sampling was shown to be adequate by comparison with adsorbent sampling. Methoxyphenols as well as 1,6-anhydroglucose were released in amounts as large as 10 mg kg-1 of dry biomass at 90% combustion efficiency. Wood, twigs, bark and needles from the conifers Norway spruce and Scots pine emitted 12 reported 2-methoxyphenols in similar proportions. Grass, heather and birchwood released the same 2-methoxyphenols but also the corresponding 2,6-dimethoxyphenols which are characteristic of angiosperms. The methoxyphenols are formed from lignin and differ in structure by the group in para position relative to the phenolic OH group. Prominent phenols were those with trans-l-propenyl and ethenyl groups in that position. Vanillin, 4- hydroxy-3-methoxybenzaldehyde, was a prominent carbonyl compound from the conifer materials. (C) 2000 Elsevier Science Ltd.