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

  • ≥95%
Item Number
F113774
Grouped product items
SKUSizeAvailabilityPrice Qty
F113774-100mg
100mg
In stock
$79.90
F113774-500mg
500mg
In stock
$319.90

Glycolytic intermediate.

Basic Description

SynonymsD-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 MechanismsFructose-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 TempProtected from light,Store at -20°C
Shipped InIce chest + Ice pads
NoteWherever 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.

Names and Identifiers

Pubchem Sid488200229
Pubchem Sid Urlhttps://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
InChi Key WJTRLMLMSLDAPQ-CCXTYWFUSA-L
Canonical 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

Certificate of Analysis(COA)

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18 results found

Lot NumberCertificate TypeDateItem
J2412314Certificate of AnalysisSep 19, 2024 F113774
J2412313Certificate of AnalysisSep 19, 2024 F113774
C2427182Certificate of AnalysisMar 21, 2024 F113774
C2427221Certificate of AnalysisMar 21, 2024 F113774
C2404298Certificate of AnalysisFeb 28, 2024 F113774
J2325289Certificate of AnalysisOct 10, 2023 F113774
J2325290Certificate of AnalysisOct 10, 2023 F113774
G2301353Certificate of AnalysisJun 06, 2023 F113774
G2301354Certificate of AnalysisJun 06, 2023 F113774
G2301362Certificate of AnalysisJun 06, 2023 F113774
D23081141Certificate of AnalysisMar 21, 2023 F113774
D23081142Certificate of AnalysisMar 21, 2023 F113774
D23081147Certificate of AnalysisMar 21, 2023 F113774
D23081148Certificate of AnalysisMar 21, 2023 F113774
G2212109Certificate of AnalysisJul 15, 2022 F113774
H2217381Certificate of AnalysisJun 11, 2022 F113774
H2217382Certificate of AnalysisJun 11, 2022 F113774
H2217383Certificate of AnalysisJun 11, 2022 F113774

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Chemical and Physical Properties

SolubilityH2O: 250 mg/mL (822.10 mM), Need ultrasonic
Sensitivitylight & moisture sensitive

Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS07
Hazard Statements

H302:Harmful if swallowed

H371:May cause damage to organs

Precautionary Statements

P260:Do not breathe dust/fume/gas/mist/vapors/spray.

Related Documents

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).  [PMID:37460805] [10.1038/s41422-023-00848-6]

References

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).  [PMID:37460805] [10.1038/s41422-023-00848-6]

Solution Calculators