847682-00-2

Usage

Type of compound

Ether alcohol

Common uses

Solvent
Stabilizer
Additive in industrial and consumer products

Ability

Dissolves a wide range of substances

Applications

Formulation of coatings, adhesives, and sealants
Coupling agent in the production of polymers and resins

Characteristics

Low volatility
High solvency

Considered

Versatile and efficient chemical in various manufacturing processes

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 1043468-88-7 6,12-bis(allyloxymethyl)-4,7,11,14-tetraoxaheptadeca-1,16-dien-9-ol 
• 3391-30-8 2,2-dimethyl-[1,3]dioxan-5-ol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 1392500-13-8 (E)-1-(1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl)-4-((3-(3,4-bis(methoxymethoxy)styryl)-5-(methoxymethoxy)phenoxy)methyl)-1H-1,2,3-triazole 
• 1392500-17-2 (E)-1-(1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl)-4-((3-(methoxymethoxy)-5-(4-(methoxymethoxy)styryl)phenoxy)methyl)-1H-1,2,3-triazole 
• 1392500-18-3 (E)-4-((3-(2-(benzo[d][1,3]dioxol-5-yl)vinyl)-5-(methoxymethoxy)phenoxy)methyl)-1-(1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl)-1H-1,2,3-triazole 
• 1392500-07-0 5,5'-(2-azidopropane-1,3-diyl)bis(oxy)bis(2,2-dimethyl-1,3-dioxane) 
• 1392500-11-6 C₂₂H₃₄O₉S 
• 1043468-87-6 1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl 2-(4-(4-chlorobenzoyl)phenoxy)-2-methylpropanoate 
• 1043468-82-1 1,3-bis(1,3-dihydroxypropan-2-yloxy)propan-2-yl 2-(4-(4-chlorobenzoyl)phenoxy)-2-methylpropanoate 
• 1043468-91-2 1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl 2-(4-(2-(4-chlorobenzamido)ethyl)phenoxy)-2-methylpropanoate 
• 1043468-83-2 1,3-bis(1,3-dihydroxypropan-2-yloxy)propan-2-yl 2-(4-(2-(4-chlorobenzamido)ethyl)phenoxy)-2-methylpropanoate 
• 1043468-93-4 1,3-bis(2,2-dimethyl-1,3-dioxan-5-yloxy)propan-2-yl 2-(4-chlorophenoxy)-2-methylpropanoate 
• 1043468-84-3 1,3-bis(1,3-dihydroxypropan-2-yloxy)propan-2-yl 2-(4-chlorophenoxy)-2-methylpropanoate 

Relevant academic research and scientific papers

An efficient method for the refinement of 1,3-methyleneglycerol via bridged acetal exchange and the synthesis of a symmetrically branched glycerol trimer

Acid-catalyzed equilibrium of a mixture of 1,2- and 1,3-methyleneglycerol in 1,4-dioxane affords predominantly the 1,3-isomer via bridged acetal exchange. The minor 1,2-isomer is removed via sequential pivaloylation and tritylation to afford the desired 1,3-isomer in >99.5% purity. A symmetrically branched triglycerol is efficiently synthesized starting from the purified 1,3-isomer. Georg Thieme Verlag Stuttgart · New York.

An efficient and practical method for the preparation of a branched oligoglycerol with acetonide protection groups

A novel method for the preparation of l,3-bis(2,2-dimethyl1,3-dioxan-5- yloxy)propan-2-ol, a branched oligoglycerols (BGL), was developed from 1,3-diallylated glycerol in excellent yield.

Synthesis of branched heptaglycerol bearing eight hydroxyl groups with four cyclic protecting groups

A large series of branched oligoglycerols, BGL07 (heptamer) with cyclic protecting groups, was synthesized. Georg Thieme Verlag Stuttgart.