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About This Item
Empirical Formula (Hill Notation):
C5H8Na5O14P3
CAS Number:
Molecular Weight:
499.98
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6043637
Quality Segment
assay
≥75% (HPLC)
form
powder
impurities
<18% water (Karl Fischer)
color
white
solubility
water: 50 mg/mL, clear to slightly hazy, colorless to very faintly yellow
shipped in
dry ice
storage temp.
−20°C
SMILES string
[Na+].[Na+].[Na+].[Na+].O[C@H]1[C@@H](O)[C@H](O[C@@H]1COP(O)([O-])=O)OP([O-])(=O)OP([O-])([O-])=O
InChI
1S/C5H13O14P3.4Na/c6-3-2(1-16-20(8,9)10)17-5(4(3)7)18-22(14,15)19-21(11,12)13;;;;/h2-7H,1H2,(H,14,15)(H2,8,9,10)(H2,11,12,13);;;;/q;4*+1/p-4/t2-,3-,4-,5?;;;;/m1..../s1
InChI key
QZAPPJHVNYCTAX-CKJQBBATSA-J
General description
Substrate for phosphoribosyltransferases in the synthesis of nucleotides.
Application
Pentasodium salt has been used in a study to assess the relationship between the muscarinic receptor cationic current and internal calcium in guinea-pig jejunal smooth muscle cells. It has also been used in a study to investigate inhibitors of the bacterial cell wall biosynthesis of the enzyme Mur D.
Analysis Note
Purity ≥ 75% based on an assay system using orotidine-5′-phosphate pyrophosphorylase and orotidine-5′-phosphate decarboxylase mixed enzymes.
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.
Signal Word
Warning
Hazard Codes
Precautionary Statements
Hazard Classifications
STOT SE 2
Storage Class
11 - Combustible Solids
WGK
WGK 3
PPE (personal protective equipment)
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Flash Point (°C)
Not applicable
Flash Point (°F)
Not applicable
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