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54672-38-7

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  • 3,5,9-Trioxa-4-phosphaundecan-1-aminium,7-(acetyloxy)-4-hydroxy-N,N,N-trimethyl-10-oxo-, inner salt, 4-oxide, (7R)-(9CI)

    Cas No: 54672-38-7

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54672-38-7 Usage

General Description

Diacetyl-L-Glycerophosphorylcholine, also known as choline alfoscerate or alpha-GPC, is a chemical compound derived from lecithin. It is a natural source of choline, an essential nutrient that is important for brain function and overall health. Diacetyl-L-Glycerophosphorylcholine is commonly used as a dietary supplement to support cognitive function, memory, and learning. It has been studied for its potential benefits in improving symptoms of age-related cognitive decline, Alzheimer's disease, and other neurological disorders. Additionally, it may also have potential benefits for physical performance and athletic training. Overall, diacetyl-L-Glycerophosphorylcholine is a promising compound with potential applications in both brain health and sports nutrition.

Check Digit Verification of cas no

The CAS Registry Mumber 54672-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54672-38:
(7*5)+(6*4)+(5*6)+(4*7)+(3*2)+(2*3)+(1*8)=137
137 % 10 = 7
So 54672-38-7 is a valid CAS Registry Number.

54672-38-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1,2-diacetoxy glycerylphosphoryl choline

1.2 Other means of identification

Product number -
Other names DIACETYL-L-GLYCEROPHOSPHORYLCHOLINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54672-38-7 SDS

54672-38-7Downstream Products

54672-38-7Relevant articles and documents

Oxygenation reactions catalyzed by the F557V mutant of soybean lipoxygenase-1: Evidence for two orientations of substrate binding

Hershelman, Dillon,Kahler, Kirsten M.,Price, Morgan J.,Lu, Iris,Fu,Plumeri, Patricia A.,Karaisz, Fred,Bassett, Natasha F.,Findeis, Peter M.,Clapp, Charles H.

, (2019/09/10)

Plant lipoxygenases oxygenate linoleic acid to produce 13(S)-hydroperoxy-9Z,11E-octadecadienoic acid (13(S)-HPOD) or 9-hydroperoxy-10E,12Z-octadecadienoic acid (9(S)-HPOD). The manner in which these enzymes bind substrates and the mechanisms by which they control regiospecificity are uncertain. Hornung et al. (Proc. Natl. Acad. Sci. USA 96 (1999) 4192–4197) have identified an important residue, corresponding to phe-557 in soybean lipoxygenase-1 (SBLO-1). These authors proposed that large residues in this position favored binding of linoleate with the carboxylate group near the surface of the enzyme (tail-first binding), resulting in formation of 13(S)-HPOD. They also proposed that smaller residues in this position facilitate binding of linoleate in a head-first manner with its carboxylate group interacting with a conserved arginine residue (arg-707 in SBLO-1), which leads to 9(S)-HPOD. In the present work, we have tested these proposals on SBLO-1. The F557V mutant produced 33% 9-HPOD (S:R = 87:13) from linoleic acid at pH 7.5, compared with 8% for the wild-type enzyme and 12% with the F557V,R707L double mutant. Experiments with 11(S)-deuteriolinoleic acid indicated that the 9(S)-HPOD produced by the F557V mutant involves removal of hydrogen from the pro-R position on C-11 of linoleic acid, as expected if 9(S)-HPOD results from binding in an orientation that is inverted relative to that leading to 13(S)-HPOD. The product distributions obtained by oxygenation of 10Z,13Z-nonadecadienoic acid and arachidonic acid by the F557V mutant support the hypothesis that ω6 oxygenation results from tail-first binding and ω10 oxygenation from head-first binding. The results demonstrate that the regiospecificity of SBLO-1 can be altered by a mutation that facilitates an alternative mode of substrate binding and adds to the body of evidence that 13(S)-HPOD arises from tail-first binding.

Facile syntheses of L-α-glycerophosphorylcholine

Park, Jong Moon,De Castro, Kathlia A.,Ahn, Hyunseok,Rhee, Hakjune

experimental part, p. 2689 - 2691 (2010/12/19)

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