Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Heparin disaccharide II-H sodium salt, a derivative of heparin, plays a crucial role in scientific research, particularly in the realm of glycobiology and biomedicine. This chemical entity consists of a disaccharide unit derived from heparin, a complex polysaccharide known for its anticoagulant properties. Researchers have focused on elucidating the structural and functional properties of heparin disaccharides, including their interactions with proteins, cells, and biological matrices. Specifically, studies have investigated the molecular mechanisms underlying the interactions between heparin disaccharide II-H and various biomolecules, such as growth factors, cytokines, and extracellular matrix proteins. These investigations have revealed the ability of heparin disaccharides to modulate signaling pathways involved in cell proliferation, differentiation, and tissue repair. Moreover, heparin disaccharide II-H has been employed as a molecular probe to study carbohydrate-protein interactions, glycosaminoglycan-mediated cell adhesion, and heparin-binding protein functions. Additionally, researchers have explored the incorporation of heparin disaccharide II-H into biomaterials and scaffolds for tissue engineering applications. By harnessing the unique structural features and biological activities of heparin disaccharide II-H, scientists aim to develop innovative strategies for drug delivery, regenerative medicine, and biomolecular sensing. Furthermore, ongoing research efforts continue to unravel the multifaceted roles of heparin disaccharide II-H in various physiological and pathological processes, providing insights into its potential applications in basic and translational research.
| Canonical Smiles | C1=C(OC(C(C1O)O)OC(C(COS(=O)(=O)O)O)C(C(C=O)N)O)C(=O)O.[Na] |
|---|---|
| InChIKey | PZZOMOYPUZNPJJ-UHFFFAOYSA-N |
| INCHI | 1S/C12H19NO13S.Na/c13-4(2-14)8(17)10(6(16)3-24-27(21,22)23)26-12-9(18)5(15)1-7(25-12)11(19)20;/h1-2,4-6,8-10,12,15-18H,3,13H2,(H,19,20)(H,21,22,23); |
| Isomeric SMILES | C1=C(OC(C(C1O)O)OC(C(COS(=O)(=O)O)O)C(C(C=O)N)O)C(=O)O.[Na] |
| Molecular Weight | 461.31 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Monosaccharides |
| Direct Parent | Monosaccharide sulfates |
| Alternative Parents | Sugar acids and derivatives Aminosaccharides Sulfuric acid monoesters Alkyl sulfates Beta-hydroxy aldehydes Secondary alcohols Amino acids Acetals Oxacyclic compounds Organic alkali metal salts Carboxylic acids Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Monoalkylamines Organopnictogen compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Monosaccharide sulfate - Sugar acid - Amino saccharide - Beta-hydroxy aldehyde - Sulfuric acid monoester - Sulfate-ester - Sulfuric acid ester - Alkyl sulfate - Organic sulfuric acid or derivatives - Amino acid or derivatives - Amino acid - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic oxide - Primary aliphatic amine - Aldehyde - Alcohol - Carbonyl group - Organonitrogen compound - Primary amine - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organopnictogen compound - Organic salt - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as monosaccharide sulfates. These are monosaccharides that contain a sulfate group linked to the sugar moiety. |
| External Descriptors | Not available |
| Sensitivity | Moisture sensitive |
|---|