D-Psicose - ≥98% , CAS No.551-68-8

CAS: 551-68-8 Cat. No.: P120931 Molecular Weight: 180.16 Beilstein Registry Number: 1(4)4400 EC Number: 208-999-7
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(3R,4R,5R)-1,3,4,5,6- pentahydroxyhexan-2-one | (3R,4R,5R)-1,3,4,5,6-pentahydroxyhexan-2-one, D-ribo-2-Hexulose
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100g
P120931-100g
3

$9.90

$14.90
Save $5.00 (33.56%)
500g
P120931-500g
1

$13.90

$20.90
Save $7.00 (33.49%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

D-Psicose protects and preserves pancreatic β-islets through the maintenance of hyperglycemia and by the prevention of fat accumulation in Otsuka Long-Evans Tokushima Fatty rats.

Specifications

Synonyms
(3R, 4R, 5R)-1, 3, 4, 5, 6- pentahydroxyhexan-2-one | (3R, 4R, 5R)-1, 3, 4, 5, 6-pentahydroxyhexan-2-one, D-ribo-2-Hexulose
Specifications & Purity
≥98%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504756012
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756012
Canonical SmilesC(C(C(C(C(=O)CO)O)O)O)O
IUPAC Name(3R,4R,5R)-1,3,4,5,6-pentahydroxyhexan-2-one
InChIKeyBJHIKXHVCXFQLS-PUFIMZNGSA-N
INCHI1S/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
Isomeric SMILES C([C@H]([C@H]([C@H](C(=O)CO)O)O)O)O
WGK Germany 3
Molecular Weight 180.16
Beilstein 1(4)4400
Reaxy-Rn 2207947
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2207947&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentMonosaccharides
Alternative Parents Beta-hydroxy ketones  Acyloins  Alpha-hydroxy ketones  Secondary alcohols  Polyols  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monosaccharide - Beta-hydroxy ketone - Acyloin - Alpha-hydroxy ketone - Secondary alcohol - Ketone - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as monosaccharides. These are compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn.
External Descriptors psicose
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
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.

12 results found

Lot NumberCertificate TypeDateItem
C2612709Certificate of AnalysisFeb 27, 2026 P120931
C2612710Certificate of AnalysisFeb 27, 2026 P120931
C2612711Certificate of AnalysisFeb 27, 2026 P120931
E2608040Certificate of AnalysisFeb 27, 2026 P120931
H2407473Certificate of AnalysisJul 23, 2024 P120931
H2407479Certificate of AnalysisJul 23, 2024 P120931
H2407481Certificate of AnalysisJul 23, 2024 P120931
G2426407Certificate of AnalysisJul 08, 2024 P120931
A2408024Certificate of AnalysisJul 27, 2022 P120931
K2204650Certificate of AnalysisJul 27, 2022 P120931
K2204681Certificate of AnalysisJul 27, 2022 P120931
K2204968Certificate of AnalysisJul 27, 2022 P120931

Show more ⌵

Chemical and Physical Properties
SolubilitySoluble in water; Soluble in Methanol,Ethanol; Insoluble in Acetone
Specific Rotation[α]4°(C=1,H2O)
Melt Point(°C)109°C
Molecular Weight180.160 g/mol
XLogP3-3.200
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass180.063 Da
Monoisotopic Mass180.063 Da
Topological Polar Surface Area118.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity147.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Mei-Ling Liu, Lan Hong, Yueming Zhu, Razi Epsztein, Ting Shi, Yuanxia Sun, Zhijun Xu, Shi-Peng Sun, Weihong Xing.  (2023)  Constructing biocatalytic nanochannel membranes for unidirectional isomer conversion and separation.  AICHE JOURNAL,  69  (11): (e18187).  [PMID:] [10.1002/aic.18187]
2. Shuangshuang Duan, Yonghua Chen, Guodong Wang, Zebin Li, Shitong Dong, Yingshuai Wu, Yuanwei Wang, Chunling Ma, Ruiming Wang.  (2023)  A study of targeted mutation of l-rhamnose isomerase to improve the conversion efficiency of D-allose.  ENZYME AND MICROBIAL TECHNOLOGY,      [PMID:37245327] [10.1016/j.enzmictec.2023.110259]
3. Xiaofeng Zhang, Xinqi Xu, Xuemei Yao, Rong Wang, Hengtao Tang, Xin Ju, Liangzhi Li.  (2020)  Exploring Multifunctional Residues of Ribose-5-phosphate Isomerase B from Ochrobactrum sp. CSL1 Enhancing Isomerization of d-Allose.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:32100533] [10.1021/acs.jafc.9b07855]
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.