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D-Fructose 6-phosphate disodium salt hydrate - 95%, high purity , CAS No.26177-86-6

    Grade & Purity:
  • ≥95%
In stock
Item Number
F113774
Grouped product items
SKU Size
Availability
Price Qty
F113774-100mg
100mg
2
$79.90
F113774-500mg
500mg
2
$319.90

Glycolytic intermediate.

Basic Description

Synonyms D-Fructose, 6-(dihydrogen phosphate), sodium salt (1:2) | SCHEMBL3465198 | D-FRUCTOSE-6-PHOSPHATE DISODIUM SALT | D-Fructose-6-phosphate (disodium) salt | fructose 6-phosphate disodium salt | Sodium(2R,3R,4S)-2,3,4,6-tetrahydroxy-5-oxohexylphosphate | dis
Specifications & Purity ≥95%
Biochemical and Physiological Mechanisms Fructose-6-phosphate is a glycolytic intermediate produced by the isomerization of glucose-6-phosphate by phosphoglucoisomerase.Sugar intermediate of the glycolytic pathway produced by the isomerization of glucose-6-phosphate by phosphoglucoisomerase.
Storage Temp Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

D-Fructose 6-phosphate (F6P) is a sμgar intermediate of the glycolytic pathway that may be used to help identify, differentiate and characterize enzymes such as phosphofructokinase(s), pyrophosphate-dependent fructose-6-phosphate 1-phosphotransferase(s), D-fructose-6-phosphate aldolase(s), glutamine:fructose-6-phosphate amidotransferase(s) and glucosamine-6P synthase(s).
A glycolytic intermediate formed by the isomerization of glucose-6-phosphate.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides - Hexoses
Direct Parent Hexose phosphates
Alternative Parents Monosaccharide phosphates  Beta-hydroxy ketones  Alkyl phosphates  Acyloins  Alpha-hydroxy ketones  Secondary alcohols  1,2-diols  Primary alcohols  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Organic cations  
Molecular Framework Aliphatic acyclic compounds
Substituents Hexose phosphate - Monosaccharide phosphate - Acyloin - Beta-hydroxy ketone - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Alpha-hydroxy ketone - Secondary alcohol - Ketone - 1,2-diol - Polyol - Organic alkali metal salt - Primary alcohol - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic salt - Organic sodium salt - Organic cation - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as hexose phosphates. These are carbohydrate derivatives containing a hexose substituted by one or more phosphate groups.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 488200229
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488200229
IUPAC Name disodium;[(2R,3R,4S)-2,3,4,6-tetrahydroxy-5-oxohexyl] phosphate
INCHI InChI=1S/C6H13O9P.2Na/c7-1-3(8)5(10)6(11)4(9)2-15-16(12,13)14;;/h4-7,9-11H,1-2H2,(H2,12,13,14);;/q;2*+1/p-2/t4-,5-,6-;;/m1../s1
InChIKey WJTRLMLMSLDAPQ-CCXTYWFUSA-L
Smiles C(C(C(C(C(=O)CO)O)O)O)OP(=O)([O-])[O-].[Na+].[Na+]
Isomeric SMILES C([C@H]([C@H]([C@@H](C(=O)CO)O)O)O)OP(=O)([O-])[O-].[Na+].[Na+]
PubChem CID 22812950
Molecular Weight 304.1(anhydrous)

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

20 results found

Lot Number Certificate Type Date Item
C2513494 Certificate of Analysis Jan 08, 2025 F113774
C2513495 Certificate of Analysis Jan 08, 2025 F113774
J2412313 Certificate of Analysis Sep 19, 2024 F113774
J2412314 Certificate of Analysis Sep 19, 2024 F113774
C2427182 Certificate of Analysis Mar 21, 2024 F113774
C2427221 Certificate of Analysis Mar 21, 2024 F113774
C2404298 Certificate of Analysis Feb 28, 2024 F113774
J2325289 Certificate of Analysis Oct 10, 2023 F113774
J2325290 Certificate of Analysis Oct 10, 2023 F113774
G2301362 Certificate of Analysis Jun 06, 2023 F113774
G2301354 Certificate of Analysis Jun 06, 2023 F113774
G2301353 Certificate of Analysis Jun 06, 2023 F113774
D23081142 Certificate of Analysis Mar 21, 2023 F113774
D23081141 Certificate of Analysis Mar 21, 2023 F113774
D23081148 Certificate of Analysis Mar 21, 2023 F113774
D23081147 Certificate of Analysis Mar 21, 2023 F113774
G2212109 Certificate of Analysis Jul 15, 2022 F113774
H2217382 Certificate of Analysis Jun 11, 2022 F113774
H2217381 Certificate of Analysis Jun 11, 2022 F113774
H2217383 Certificate of Analysis Jun 11, 2022 F113774

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Chemical and Physical Properties

Solubility H2O: 250 mg/mL (822.10 mM), Need ultrasonic
Sensitivity light & moisture sensitive
Molecular Weight 304.100 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 9
Rotatable Bond Count 6
Exact Mass 303.994 Da
Monoisotopic Mass 303.994 Da
Topological Polar Surface Area 170.000 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 262.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 3
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 3

Citations of This Product

1. Ai Yuan-li, Wang Wei-jia, Liu Fan-jian, Fang Wei, Chen Hang-zi, Wu Liu-zheng, Hong Xuehui, Zhu Yuekun, Zhang Ci-xiong, Liu Long-yu, Hong Wen-bin, Zhou Bo, Chen Qi-tao, Wu Qiao.  (2023)  Mannose antagonizes GSDME-mediated pyroptosis through AMPK activated by metabolite GlcNAc-6P.  CELL RESEARCH,    (1-19). 

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