Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Heparin disaccharide III-S sodium salt is a product of the digestion of heparan sulfate and heparin by various heparinases. Heparin disaccharide III-S sodium salt, a complex carbohydrate, possesses notable anticoagulant and anti-inflammatory properties. Research has revealed its interactions with a diverse array of proteins and enzymes, rendering it valuable for investigating protein-protein interactions and enzymatic activity.
| Canonical Smiles | C1=C(OC(C(C1O)OS(=O)(=O)[O-])OC2C(OC(C(C2O)NS(=O)(=O)[O-])O)CO)C(=O)[O-].[Na+].[Na+].[Na+] |
|---|---|
| IUPAC Name | trisodium;(2R,3R,4S)-2-[(2R,3S,4R,5R)-4,6-dihydroxy-2-(hydroxymethyl)-5-(sulfonatoamino)oxan-3-yl]oxy-4-hydroxy-3-sulfonatooxy-3,4-dihydro-2H-pyran-6-carboxylate |
| InChIKey | KNWWWYJQBVFLQC-LXROVJCJSA-K |
| INCHI | 1S/C12H19NO16S2.3Na/c14-2-5-9(7(16)6(11(19)26-5)13-30(20,21)22)28-12-8(29-31(23,24)25)3(15)1-4(27-12)10(17)18;;;/h1,3,5-9,11-16,19H,2H2,(H,17,18)(H,20,21,22)(H,23,24,25);;;/q;3*+1/p-3/t3-,5+,6+,7+,8+,9+,11?,12-;;;/m0.../s1 |
| Isomeric SMILES | C1=C(O[C@H]([C@@H]([C@H]1O)OS(=O)(=O)[O-])O[C@@H]2[C@H](OC([C@@H]([C@H]2O)NS(=O)(=O)[O-])O)CO)C(=O)[O-].[Na+].[Na+].[Na+] |
| Molecular Weight | 563.35 |
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 | Disaccharides |
| Alternative Parents | Sulfuric acid monoesters Sulfuric acid monoamides Alkyl sulfates Oxanes Secondary alcohols Carboxylic acid salts Hemiacetals Acetals Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Primary alcohols Hydrocarbon derivatives Organopnictogen compounds Carbonyl compounds Organic oxides Organic sodium salts Organonitrogen compounds Organic cations |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Disaccharide - Sulfuric acid monoamide - Oxane - Sulfuric acid monoester - Sulfate-ester - Alkyl sulfate - Sulfuric acid ester - Organic sulfuric acid or derivatives - Carboxylic acid salt - Hemiacetal - Secondary alcohol - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Organic alkali metal salt - Organic oxide - Organopnictogen compound - Alcohol - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Primary alcohol - Organic salt - Carbonyl group - Organic sodium salt - Organic cation - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as disaccharides. These are compounds containing two carbohydrate moieties linked to each to each other through a glycosidic bond, no set of three or more glycosidically linked carbohydrate units. |
| External Descriptors | Not available |
| Sensitivity | Moisture sensitive |
|---|