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G6014

Sigma-Aldrich

rac-Glycerol 1-phosphate disodium salt hydrate

≥75% (enzymatic)

Synonym(s):

DL-α-Glycerophosphate disodium salt hydrate

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About This Item

Empirical Formula (Hill Notation):
C3H7Na2O6P · xH2O
CAS Number:
1555-56-2
Molecular Weight:
216.04 (anhydrous basis)
Beilstein:
5177716
MDL number:
MFCD00150339
UNSPSC Code:
12352201
PubChem Substance ID:
24895242

Assay

≥75% (enzymatic)

impurities

~6 mol/mol water

storage temp.

2-8°C

SMILES string

O.[Na+].[Na+].OCC(O)COP([O-])([O-])=O

InChI

1S/C3H9O6P.2Na.H2O/c4-1-3(5)2-9-10(6,7)8;;;/h3-5H,1-2H2,(H2,6,7,8);;;1H2/q;2*+1;/p-2

InChI key

OFNNKPAERNWEDD-UHFFFAOYSA-L

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Application

rac-Glycerol 1-phosphate does not affect the growth and metabolism of E. coli at concentrations of 5-100μm.

Biochem/physiol Actions

rac-Glycerol 1-phosphate was shown to be produced in mammalian tissues by the hydrolysis of rac-glycerol 1:2-cyclic phosphate by a soluble phosphodiesterase.

Quality

The main impurity is β-glycerophosphate.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Jiangwei Yao et al.
Biochimica et biophysica acta, 1831(3), 495-502 (2012-09-18)
Membrane phospholipid synthesis is a vital facet of bacterial physiology. Although the spectrum of phospholipid headgroup structures produced by bacteria is large, the key precursor to all of these molecules is phosphatidic acid (PtdOH). Glycerol-3-phosphate derived from the glycolysis via
Kyung Ok Yu et al.
Biotechnology and bioengineering, 110(1), 343-347 (2012-08-14)
Triacylglycerol (TAG) is a microbial oil feedstock for biodiesel production that uses an inexpensive substrate, such as glycerol. Here, we demonstrated the overproduction of TAG from glycerol in engineered Saccharomyces cerevisiae via the glycerol-3-phosphate (G3P) pathway by overexpressing the major
Ryuichiro Shinohara et al.
Environmental science & technology, 46(19), 10572-10578 (2012-09-22)
Differences in biogenic phosphorus (P) compounds between sediment and suspended particles in aquatic environments are important for understanding the mechanisms of internal P loading, but these differences are still unknown. We used solution-state (31)P-nuclear magnetic resonance spectroscopy ((31)P NMR) with
Michele Alves-Bezerra et al.
Biochimica et biophysica acta, 1821(12), 1462-1471 (2012-08-21)
Although triacylglycerol (TAG) stores play a critical role in organisms, mechanisms underlying TAG synthesis are poorly understood in invertebrates. In mammals, the synthesis of glycerolipids, including TAG, diacylglycerol (DAG) and phospholipids (PL), occurs predominantly by the glycerol-3-phosphate (G3P) pathway in
Valéria E Chaves et al.
Lipids, 47(8), 773-780 (2012-06-12)
We have previously shown that a high-protein, carbohydrate-free diet can decrease the production of glycerol-3-phosphate (G3P) from glucose and increase glyceroneogenesis in both brown (BAT) and epididymal (EAT) adipose tissue. Here, we utilized an in-vivo approach to examine the hypothesis
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