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28319-77-9

  • Product NameCholine glycerophosphate
  • Molecular FormulaC8H20NO6P
  • Molecular Weight257.224
  • Purity99%
  • AppearanceWhite waxy solid
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Product Details

Quick Details

  • CasNo: 28319-77-9
  • Molecular Formula: C8H20NO6P
  • Appearance: White waxy solid
  • Purity: 99%

Quality Manufacturer Supply  Factory Sells Choline glycerophosphate 28319-77-9 Customized Supply

  • Molecular Formula:C8H20NO6P
  • Molecular Weight:257.224
  • Appearance/Colour:White waxy solid 
  • Vapor Pressure:0Pa at 25℃ 
  • Melting Point:-98oC 
  • Boiling Point:480℃[at 101 325 Pa] 
  • Flash Point:11 °C 
  • PSA:108.86000 
  • LogP:-0.38240 

Choline glycerophosphate(Cas 28319-77-9) Usage

Description

Choline alfoscerate is a nootropic reportedly effective in the treatment of age-associated memory impairment. In man, it decreased and prevented scopolamine-induced amnesia. In vitro studies suggest that choline alfoscerate acts indirectly on cholinergic transmission by elevating the synthesis of acetylcholine.

Chemical Properties

White waxy solid

Originator

Sandoz; Italfarmaco (Italy)

Uses

sn-Glycero-3-phosphocholine (Choline Alfoscerate) is a phospholipid; precursor in choline biosynthesis. sn-Glycero-3-phosphocholine is an intermediate in catabolic pathway of phosphatidylcholine. sn-Glycero-3-phosphocholine is used as an Nootropic.

Definition

ChEBI: A member of the class of phosphocholines that is the choline ester of sn-glycero-3-phosphate. It is one of the major osmolyte in the renal medullary cells.

Brand name

Delecit

General Description

L-α-Glycerophosphorylcholine is a phospholipid, which is a derivative of phosphatidylcholine.

Flammability and Explosibility

Notclassified

Biochem/physiol Actions

Increases inositol phosphate formation.

InChI:InChI=1/C8H20NO6P/c1-9(2,3)4-5-14-16(12,13)15-7-8(11)6-10/h8,10-11H,4-7H2,1-3H3/t8-/m1/s1

28319-77-9 Relevant articles

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Baer,Kates

, p. 1394,1396 (1948)

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Preparation method of glycerophosphocholine

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Paragraph 0028-0032; 0033-0037; 0038-0042; 0043-0047, (2021/09/08)

The invention discloses a preparation me...

METHOD OF PREPARING CHOLINE ALFOSCERATE AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Paragraph 0113-0141, (2020/10/27)

The present invention relates to a metho...

Synthesis method for compound choline alfoscerate for promoting brain functions

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Paragraph 0025, (2019/11/21)

The invention discloses a synthesis meth...

Method of preparing L-alpha-glycerol phosphatidylcholine

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Paragraph 0087; 0089; 0091; 0093, (2018/06/26)

The invention provides a method of prepa...

28319-77-9 Process route

(2R)-3-chloro-1,2-propanediol
57090-45-6

(2R)-3-chloro-1,2-propanediol

phosphorylcholine chloride
107-73-3

phosphorylcholine chloride

L-glycero-3-phosphorylcholine
28319-77-9,563-24-6

L-glycero-3-phosphorylcholine

Conditions
Conditions Yield
phosphorylcholine chloride; With potassium hydroxide; In methanol; for 1h;
(2R)-3-chloro-1,2-propanediol; In methanol; at 65 ℃; for 16h; Temperature;
99%
phosphorylcholine chloride; With potassium hydroxide; In ethanol; for 0.5h;
(2R)-3-chloro-1,2-propanediol; In ethanol; at 75 - 85 ℃; for 6h;
79.6%
C<sub>8</sub>H<sub>21</sub>NO<sub>6</sub>P<sup>(1+)</sup>*Cl<sup>(1-)</sup>

C8H21NO6P(1+)*Cl(1-)

L-glycero-3-phosphorylcholine
28319-77-9,563-24-6

L-glycero-3-phosphorylcholine

Conditions
Conditions Yield
With 717 type ion exchange resin; In ethanol; water; at 0 ℃; for 4h;
77%

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;

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