4756-11-0

Usage

General Description

1,2,3-Propanetriol,1-(3,4-dimethoxyphenyl)- is a chemical compound that is also known as vanillylpropyl alcohol. It is a derivative of propanetriol, also known as glycerol, and contains a 3,4-dimethoxyphenyl group. 1,2,3-Propanetriol,1-(3,4-dimethoxyphenyl)- is commonly used in the production of cosmetic and personal care products, as well as in the synthesis of pharmaceuticals. It has antioxidant and moisturizing properties, making it a popular ingredient in skincare products. Additionally, it is used as a flavoring agent in food and beverages due to its pleasant aroma and taste.

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 31706-95-3 1'-Hydroxymethyleugenol 
• 93160-12-4 (2RS,3RS)-2,3-diacetoxy-3-(3,4-dimethoxy-phenyl)-propionic acid methyl ester 
• 186581-53-3 diazomethane 
• 1208-42-0 threo-guaiacylglycerol 
• 30461-78-0 cis-3-(3,4-dimethoxyphenyl)-3-propenoic acid methyl ester 
• 14737-88-3 (Z)-3,4-dimethoxycinnamic acid 
• 22511-06-4 3,4-dimethoxyphenylpropiolic acid 
• 5396-67-8 2-bromo-3-(3,4-dimethoxy-phenyl)-3-hydroxy-propionic acid methyl ester 
• 5401-66-1 (2RS,3SR)-2,3-dibromo-3-(3,4-dimethoxy-phenyl)-propionic acid methyl ester 
• 5396-64-5 methyl (E)-3-(3,4-dimethoxyphenyl)acrylate 
• 14737-89-4 3,4-dimethoxy-trans-cinnamic acid 
• 31337-58-3 (E)-3-(3,4-dimethoxyphenyl)allyl acetate 
• 5396-69-0 3-acetoxy-2-bromo-3-(3,4-dimethoxy-phenyl)-propionic acid methyl ester 

Downstream Products

• 54844-36-9 3-(3,4-dimethoxyphenyl)propane-1,2-diol 
• 78886-14-3 3-<3,4-dimethoxyphenyl>-2-oxo propanol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 141-46-8 Glycolaldehyde 

Relevant academic research and scientific papers

The synthesis and analysis of lignin-bound Hibbert ketone structures in technical lignins

Understanding the structure of technical lignins resulting from acid-catalysed treatment of lignocellulosic biomass is important for their future applications. Here we report an investigation into the fate of lignin under acidic aqueous organosolv conditions. In particular we examine in detail the formation and reactivity of non-native Hibbert ketone structures found in isolated organosolv lignins from both Douglas fir and beech woods. Through the use of model compounds combined with HSQC, HMBC and HSQC-TOCSY NMR experiments we demonstrate that, depending on the lignin source, both S and G lignin-bound Hibbert ketone units can be present. We also show that these units can serve as a source of novel mono-aromatic compounds following an additional lignin depolymerisation reaction.