≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
D-Panose has been used in a study to determine the composition and sequence of glucan containing mixed linkages by carbon-13 nuclear magnetic resonance. It has also been used in a study to characterize electrophoretic behavior of sugar isomers.
| Pubchem Sid | 504756222 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504756222 |
| Canonical Smiles | C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C(CO)O)C(C(C=O)O)O)O)O)O)O)O)O)O |
| IUPAC Name | (2R,3R,4R,5R)-2,3,5,6-tetrahydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyhexanal |
| InChIKey | ZCLAHGAZPPEVDX-MQHGYYCBSA-N |
| INCHI | 1S/C18H32O16/c19-1-5(22)9(24)16(6(23)2-20)34-18-15(30)13(28)11(26)8(33-18)4-31-17-14(29)12(27)10(25)7(3-21)32-17/h1,5-18,20-30H,2-4H2/t5-,6+,7+,8+,9+,10+,11+,12-,13-,14+,15+,16+,17-,18+/m0/s1 |
| Isomeric SMILES | C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@H](O2)O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)O)O)O)O)O)O)O |
| WGK Germany | 3 |
| PubChem CID | 94448 |
| Molecular Weight | 504.44 |
| Beilstein | 100481 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Oligosaccharides |
| Alternative Parents | Alkyl glycosides O-glycosyl compounds Fatty alcohols Oxanes Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Oligosaccharide - Fatty acyl glycoside - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Fatty alcohol - Beta-hydroxy aldehyde - Fatty acyl - Oxane - Alpha-hydroxyaldehyde - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Aldehyde - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Primary alcohol - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. |
| External Descriptors | trisaccharide |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 I2510524 | Certificate of Analysis | Jul 03, 2025 | P301896 |
| I2510525 | Certificate of Analysis | Jul 03, 2025 | P301896 |
| I2510526 | Certificate of Analysis | Jul 03, 2025 | P301896 |
| I2413131 | Certificate of Analysis | Sep 09, 2024 | P301896 |
| I2413132 | Certificate of Analysis | Sep 09, 2024 | P301896 |
| D2415122 | Certificate of Analysis | Mar 28, 2024 | P301896 |
| D2415123 | Certificate of Analysis | Mar 28, 2024 | P301896 |
| E2323630 | Certificate of Analysis | Apr 14, 2023 | P301896 |
| E2323644 | Certificate of Analysis | Apr 14, 2023 | P301896 |
| E2323647 | Certificate of Analysis | Apr 14, 2023 | P301896 |
| E2323651 | Certificate of Analysis | Apr 14, 2023 | P301896 |
| E2323675 | Certificate of Analysis | Apr 14, 2023 | P301896 |
| E2323677 | Certificate of Analysis | Apr 14, 2023 | P301896 |
| Sensitivity | Sensitivity to humidity; Sensitive to light |
|---|---|
| Specific Rotation[α] | 155 ° (C=2, H2O) |
| Melt Point(°C) | 223°C |
| Molecular Weight | 504.400 g/mol |
| XLogP3 | -7.200 |
| Hydrogen Bond Donor Count | 11 |
| Hydrogen Bond Acceptor Count | 16 |
| Rotatable Bond Count | 11 |
| Exact Mass | 504.169 Da |
| Monoisotopic Mass | 504.169 Da |
| Topological Polar Surface Area | 277.000 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 625.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 14 |
| 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 | 1 |
| 1. Liping Xu, Dandan Sha, Rongfan Ren, Hongli Li, David Da Yong Chen. (2025) Methylation in ambient ion source enables direct isomer differentiation of oligosaccharides by tandem mass spectrometry. CARBOHYDRATE POLYMERS, [PMID:41320349] [10.1016/j.carbpol.2025.124493] |
