Heparin disaccharide II-H sodium salt(α-ΔUA-[1→4]-GlcN-6S) - ≥95% , CAS No.136098-02-7

CAS: 136098-02-7 Cat. No.: H759977 Molecular Weight: 461.31
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Size
Status
Price
Qty
1mg
H759977-1mg
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

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.

Specifications

Specifications & Purity
≥95%
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥95%
Names and Identifiers
Canonical SmilesC1=C(OC(C(C1O)O)OC(C(COS(=O)(=O)O)O)C(C(C=O)N)O)C(=O)O.[Na]
InChIKeyPZZOMOYPUZNPJJ-UHFFFAOYSA-N
INCHI1S/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

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides
Direct ParentMonosaccharide 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 FrameworkAliphatic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
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Chemical and Physical Properties
SensitivityMoisture sensitive
Documents & Articles
Solution Calculators
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