G6626
Glycerol phosphate calcium salt
>98% (TLC)
Synonym(s):
Calcium glycerophosphate
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All Photos(3)
About This Item
Linear Formula:
C3H7O6PCa
CAS Number:
Molecular Weight:
210.14
EC Number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
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Quality Level
Assay
>98% (TLC)
form
powder
color
white to off-white
solubility
0.5 M HCl: 50 mg/mL, clear, colorless to faintly yellow
cation traces
Ca: 15.0-22.8% (Dry basis)
SMILES string
OCC(OP(O)(O)=O)CO.[Ca]
InChI
1S/C3H9O6P.Ca.2H/c4-1-3(2-5)9-10(6,7)8;;;/h3-5H,1-2H2,(H2,6,7,8);;;
InChI key
DVIIMTRPWRJOMF-UHFFFAOYSA-N
Related Categories
General description
Usually contains 80% β-isomer and 20% rac-α-isomer.
Application
β-glycerol phosphate can be used as part of a mineralization medium to aid in the differentiation of osteoblasts.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Dentinogenesis is a necessary prerequisite for dental tissue engineering. One of the steps for dentinogenesis is to obtain large quantities of highly purified odontoblasts. Therefore, we have undertaken an experiment applying different concentrations of β-glycerophosphate (β-GP) to induce the differentiation
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Effect of phosphorus on the production of microcystin was researched. The effects of soluble reactive phosphorus (SRP) on the growth of cells and on the production of Microcystin were studied. In addition, the efficiency of four different phosphorus compounds was
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For bone regeneration therapy using stem cells, well-defined ex vivo protocols to expand mesenchymal stromal cells (MSC), as well as assays to show their potential differentiation into the osteogenic lineage, are needed. Aim of this study was to analyze the
N Z Sun et al.
The Journal of international medical research, 40(2), 761-767 (2012-05-23)
To investigate the capability of human placenta-derived adherent cells to differentiate into osteocytes and adipocytes. Placenta-derived adherent cells were isolated by type IV collagenase digestion of a single freshly obtained human placenta and cultured under standard conditions. Cell surface markers
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