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D-Psicose

Basic information

  • Product Name:D-Psicose
  • CasNo.:551-68-8
  • MF:C6H12O6
  • MW:180.158

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:109 °C
  • Packing:Sweet syrupy liquid
  • Throughput:
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Product Details

CasNo： 551-68-8

MF： C6H12O6

Appearance： Sweet syrupy liquid

Cost-effective and customizable D-Psicose 551-68-8 factory

  • Molecular Formula:C6H12O6
  • Molecular Weight:180.158
  • Appearance/Colour:Sweet syrupy liquid 
  • Vapor Pressure:1.79E-14mmHg at 25°C 
  • Melting Point:109 °C 
  • Refractive Index:16.3 ° (C=0.94, H2O) 
  • Boiling Point:551.7 °C at 760 mmHg 
  • PKA:11.86±0.20(Predicted) 
  • Flash Point:301.5 °C 
  • PSA：118.22000 
  • Density:1.589 g/cm3 
  • LogP:-3.37720 

D-Psicose(Cas 551-68-8) Usage

Enzyme inhibitor

This ketohexose (FW = 180.16 g/mol), also known as D-ribo-2-hexulose and reportedly fpound in cane molasses, has epimers of D-psicose are Dfructose, D-sorbose, and L-tagatose. D-Psicose is an alternative substrate for fructokinase. The structural composition of D-psicose at 27°C in D2O is 22% a-pyranose, 24% b-pyranose, 39% a-furanose, and 15% bfuranose. Target(s): ketohexokinase, or hepatic fructokinase; also alternative substrate.

Definition

ChEBI: The D-enantiomer of psicose.

InChI:InChI=1/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5-,6+/m1/s1

551-68-8 Relevant articles

Few-Unit-Cell MFI Zeolite Synthesized using a Simple Di-quaternary Ammonium Structure-Directing Agent

Abeykoon, Milinda,Al-Thabaiti, Shaeel,Bell, Alexis T.,Boscoboinik, J. Anibal,Dai, Heng,Dauenhauer, Paul,Dorneles de Mello, Matheus,Duan, Xuekui,Ghosh, Supriya,Kamaluddin, Huda Sharbini,Khan, Zaheer,Kumar, Gaurav,Li, Xinyu,Lu, Peng,Luo, Tianyi,Mkhoyan, K. Andre,Narasimharao, Katabathini,Qi, Liang,Rimer, Jeffrey D.,Tsapatsis, Michael

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Synthesis of a pentasil-type zeolite wit...

Hydroxyapatite-Supported Polyoxometalates for the Highly Selective Aerobic Oxidation of 5-Hydroxymethylfurfural or Glucose to 2,5-Diformylfuran under Atmospheric Pressure

Guan, Hongyu,Li, Ying,Wang, Qiwen,Wang, Xiaohong,Yu, Hang

, p. 997 - 1005 (2021/08/06)

(NH4)5H6PV8Mo4O40 supported on hydroxyap...

PROCESSES FOR PREPARING SORBOSE FROM GLUCOSE

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Paragraph 0012-0013; 0016-0018; 0035-0037; 0038, (2020/08/25)

Processes for converting glucose to sorb...

Bi-Functional Magnesium Silicate Catalyzed Glucose and Furfural Transformations to Renewable Chemicals

Kumar, Abhinav,Srivastava, Rajendra

, p. 4807 - 4816 (2020/08/24)

Bio-refinery is attracting significant i...

551-68-8 Process route

dihydroxyacetone
96-26-4,26776-70-5

dihydroxyacetone

Glyceraldehyde
56-82-6,367-47-5,26793-98-6

Glyceraldehyde

DL-dendroketose
470-14-4

DL-dendroketose

fructose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

fructose

sorbose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

sorbose

lyxo-2-hexulose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

lyxo-2-hexulose

ribo-2-hexulose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

ribo-2-hexulose

Conditions
Conditions Yield
sodium hydroxide; In water; at 25 ℃; for 1h; Product distribution; further catalysts;
8 % Chromat.
2 % Chromat.
40 % Chromat.
32 % Chromat.
18 % Chromat.
dihydroxyacetone
96-26-4,26776-70-5

dihydroxyacetone

Glyceraldehyde
56-82-6,367-47-5,26793-98-6

Glyceraldehyde

DL-dendroketose
470-14-4

DL-dendroketose

fructose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

fructose

sorbose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

sorbose

lyxo-2-hexulose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

lyxo-2-hexulose

ribo-2-hexulose
57-48-7,87-79-6,87-81-0,551-68-8,3615-39-2,3615-56-3,6035-50-3,7776-48-9,16354-64-6,17598-81-1,17598-82-2,23140-52-5,30237-26-4,65732-90-3,73952-10-0,73952-11-1,139686-85-4,18875-34-8

ribo-2-hexulose

Conditions
Conditions Yield
sodium hydroxide; In water; at 25 ℃; for 1h; Product distribution; further catalysts;
8 % Chromat.
2 % Chromat.
40 % Chromat.
32 % Chromat.
18 % Chromat.

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