29909-09-9 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.
Check Digit Verification of cas no
The CAS Registry Mumber 29909-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,0 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29909-09:
(7*2)+(6*9)+(5*9)+(4*0)+(3*9)+(2*0)+(1*9)=149
149 % 10 = 9
So 29909-09-9 is a valid CAS Registry Number.
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)
29909-09-9Relevant articles and documents
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Ballou,Fischer
, p. 1659 (1956)
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Improved straightforward chemical synthesis of dihydroxyacetone phosphate through enzymatic desymmetrization of 2,2-dimethoxypropane-1,3-diol
Charmantray, Franck,El Blidi, Lahssen,Gefflaut, Thierry,Hecquet, Laurence,Bolte, Jean,Lemaire, Marielle
, p. 9310 - 9312 (2007/10/03)
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.