29909-09-9

Basic information

• Product Name: (3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate
• Synonyms: (3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate;2,2-Dimethoxy-1,3-propanediol 1-dihydrogen phosphate;2,2-Dimethoxy-1,3-propanediol 1-phosphoric acid;Phosphoric acid 2,2-dimethoxy-3-hydroxypropyl ester
• CAS NO: 29909-09-9
• Molecular Formula: C₅H₁₃O₇P
• Molecular Weight: 216.126281
• EINECS: 249-947-3
• Mol File: 29909-09-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 402.4°C at 760 mmHg
• Flash Point: 197.2°C
• Appearance: /
• Density: 1.471g/cm³
• Vapor Pressure: 3.76E-08mmHg at 25°C
• Refractive Index: 1.482
• CAS DataBase Reference: (3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: (3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate(29909-09-9)
• EPA Substance Registry System: (3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate(29909-09-9)

Safety Data

• Hazardous Substances Data: 29909-09-9(Hazardous Substances Data)

Usage

Description

(3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate is an organic compound that serves as a flame retardant and plasticizer, enhancing the fire resistance and flexibility of various materials.
Used in Polymer and Resin Industry:
(3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate is used as a flame retardant and plasticizer for improving the fire resistance and flexibility of polymers and resins.
Used in Adhesive, Sealant, and Coating Production:
(3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate is used as an additive in the production of adhesives, sealants, and coatings to enhance their fire resistance and flexibility.
Used in Electrical Component Manufacturing:
(3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate is used as a component in the manufacturing of electrical components to improve their thermal stability and safety.
Used in Construction Material Industry:
(3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate is used as an additive in the production of construction materials to enhance their fire resistance and flexibility.
It is important to handle and store (3-hydroxy-2,2-dimethoxy)propyl dihydrogen phosphate with care due to its potential harmful effects if ingested, inhaled, or exposed to the skin or eyes.

InChI:InChI=1/C5H13O7P/c1-10-5(3-6,11-2)4-12-13(7,8)9/h6H,3-4H2,1-2H3,(H2,7,8,9)

Upstream product

• 36680-67-8 3-hydroxy-2,2-dimethoxypropyl acetate 
• 2524-64-3 chlorophosphoric acid diphenyl ester 
• 819862-89-0 3-hydroxy-2,2-dimethoxypropyl dibenzyl phosphate 
• 153214-82-5 2,2-dimethoxypropane-1,3-diol 
• 174648-17-0 3-acetoxy-2,2-dimethoxypropyl dibenzyl phosphate 
• 24423-98-1 3-chloro-1-hydroxypropan-2-one 
• 149-73-5 trimethyl orthoformate 
• 231280-23-2 5,5-dimethoxy-2-phenoxy-1,3,2-dioxaphosphorinane 2-oxide 

Downstream Products

• 57-04-5 dihydroxyacetone phosphate 

Relevant articles and documents

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Improved straightforward chemical synthesis of dihydroxyacetone phosphate through enzymatic desymmetrization of 2,2-dimethoxypropane-1,3-diol

Dihydroxyacetone phosphate (DHAP) was synthesized in high purity and yield in four steps starting from dihydroxyacetone dimer (DHA) (47% overall yield). DHA was converted into 2,2-dimethoxypropane-1,3-diol, which was desymmetrized by acetylation with lipase AK. The alcohol function was phosphorylated to give dibenzyl phosphate ester 4. From 4, two routes were investigated for large-scale synthesis of DHAP. First, acetate hydrolysis was performed prior to hydrogenolysis of the phosphate protective groups. The acetal hydrolysis was finally catalyzed by the phosphate group itself. Second, acetate and acetal hydrolysis were performed in one single step after hydrogenolysis.