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Product Name
L-Ascorbic acid 2-phosphate sesquimagnesium salt hydrate, ≥95%
SMILES string
O=C1O[C@@]([C@@H](O)CO)([H])C([O-])=C1OP([O-])([O-])=O.O=C2O[C@@]([C@@H](O)CO)([H])C([O-])=C2OP([O-])([O-])=O.O.[Mg+2].[Mg+2].[Mg+2]
InChI
1S/2C6H9O9P.3Mg.H2O/c2*7-1-2(8)4-3(9)5(6(10)14-4)15-16(11,12)13;;;;/h2*2,4,7-9H,1H2,(H2,11,12,13);;;;1H2/q;;3*+2;/p-6/t2*2-,4+;;;;/m00..../s1
InChI key
HKRNHMZODRSAPN-IXNKEUJHSA-H
biological source
synthetic (organic)
assay
≥95%
form
powder
technique(s)
HPLC: suitable
color
white to off-white
solubility
water: 50 mg/mL
storage temp.
room temp
Quality Level
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Application
Biochem/physiol Actions
Features and Benefits
- Can be used in Cell Biology, Metabolomics and Biochemical research
- High-quality compound suitable for multiple research applications
General description
Moreover, MAP plays a pivotal role in metabolomics and biochemical research. Acting as an antioxidant, it effectively scavenges free radicals, offering protection against oxidative damage. Its anti-inflammatory properties contribute to the reduction of inflammation, and studies have indicated its ability to stimulate collagen production. Additionally, MAP serves as a chelating agent, further expanding its applications in various research studies. The multifaceted nature of MAP makes it a valuable tool in scientific investigations, contributing to advancements in cell biology, metabolomics, and biochemical research.
Other Notes
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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