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Merck
CN

90756

CDP-ethanolamine sodium salt hydrate

≥93.0% (HPLC)

Synonym(s):

Cytidine 5′-diphosphate ethanolamine sodium salt hydrate, Cytidine 5′-diphosphoethanolamine sodium salt hydrate, Cytidine diphosphate ethanolamine sodium salt hydrate

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About This Item

Empirical Formula (Hill Notation):
C11H20N4O11P2 · xNa+ · yH2O
Molecular Weight:
446.24 (anhydrous free acid basis)
NACRES:
NA.25
UNSPSC Code:
12352201
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Quality Level

assay

≥93.0% (HPLC)

application(s)

clinical testing

format

neat

storage temp.

−20°C

Biochem/physiol Actions

Metabolite of glycerophospholipid metabolism and phosphatidylethanolamine (PE) biosynthesis.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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METABOLISM AND FUNCTION OF BACTERIAL LIPIDS. II. BIOSYNTHESIS OF PHOSPHOLIPIDS IN ESCHERICHIA COLI.
J KANFER et al.
The Journal of biological chemistry, 239, 1720-1726 (1964-06-01)
Martina Gsell et al.
Methods in molecular biology (Clifton, N.J.), 1033, 29-44 (2013-09-03)
The yeast Saccharomyces cerevisiae has become a valuable eukaryotic model organism to study biochemical and cellular processes at a molecular basis. A common strategy for such studies is the use of single and multiple mutants constructed by genetic manipulation which
L B Tijburg et al.
Biochemical and biophysical research communications, 160(3), 1275-1280 (1989-05-15)
In the present study pulse-label and pulse-chase experiments with isolated rat hepatocytes in suspension were designed to investigate the effects of the presence of either serine or ethanolamine in the medium on the rate of phosphatidylethanolamine synthesis via the CDPethanolamine



Global Trade Item Number

SKUGTIN
90756-50MG04061833458280
90756-10MG04061833423868