3'-Sialyllactose Sodium Salt TCI S0885

Chemical Identity

CAS No.: 128596-80-5
PubChem: CID 91972064·SID 253659872
Formula: C23H38NNaO19
Molecular weight: 655.5 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: sodium 5-acetamido-2-[3,5-dihydroxy-2-(hydroxymethyl)-6-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-4-yl]oxy-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylate
SMILES: CC(=O)NC1C(CC(OC1[C@@H]([C@@H](CO)O)O)(C(=O)[O-])OC2C(C(OC(C2O)OC3C(OC(C(C3O)O)O)CO)CO)O)O.[Na+]
InChIKey: PUDLCEYWDTXZER-VWWFDWIGSA-M

Rp 4.399.500,00

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3'-Sialyllactose Sodium Salt is a chemical compound widely used in biochemical and molecular biology research within laboratories. This glycoside plays a crucial role in the study of glycan-protein interactions, which are fundamental to understanding cellular communication and disease mechanisms. Its complex structure makes it an essential component in various experimental setups, particularly in glycoscience research. As a sodium salt, it offers enhanced solubility and stability, which are critical for maintaining the integrity of experimental results.

The compound is favored for its high purity and solubility in organic solvents such as acetone and ethyl acetate. These properties make it ideal for use in chromatographic techniques, spectroscopic analyses, and chemical reactions that require precise control and reactivity. Its stability under certain conditions further supports its utility in long-term storage and repeated use in research settings. This reliability ensures consistent performance across different laboratory applications.

In Indonesian laboratories, 3'-Sialyllactose Sodium Salt is commonly utilized in metabolic disease research, immunology studies, and pharmacological investigations. Its role in glycan structure analysis and the development of glyco-based therapeutics highlights its importance in both academic and applied research. The compound's versatility and reliability make it a valuable resource for scientists working in diverse fields of chemical biology.

TCI brochures (PDF)

Cancer Research Reagents 2025-04-01 · p. 3
Reagents for Glyco Chemistry & Biology 5th Edition · p. 96

Related TCI products

Metabolic Disease Research: This compound is used to study the role of glycan structures in metabolic disorders, aiding in the development of targeted therapies.
Immunology Studies: It supports research on glycan-protein interactions that influence immune responses and disease progression.
Pharmacological Investigations: The compound is integral in drug development, particularly in the design of glycoconjugate-based therapeutics.
Glycan Structure Analysis: Its complex structure makes it a key reagent in analytical techniques such as mass spectrometry and NMR spectroscopy.
Biochemical Reactions: It serves as a substrate or reactant in synthetic pathways involving glycosylation and carbohydrate chemistry.

Brand	TCI
CAS number	128596-80-5
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Glycoscience
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Sodium salt of 3'-sialyllactose (solid)
Storage	Store in a cool, dry place away from moisture and light

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to humidity, which could affect its stability. Due to its solubility in organic solvents, it should be handled with care to avoid contamination. Proper labeling of containers is essential for safe storage and retrieval. In laboratory settings, it is important to ensure that the compound is stored in a secure location, away from incompatible materials. Regular inspection of storage conditions ensures the compound remains in optimal condition for research use.

References cited in the TCI brochure

Aurélie Cazet. Tumour-associated carbohydrate antigens in breast cancer Breast Cancer Research, 2010. doi:10.1186/bcr2577
Mark M. Fuster. The sweet and sour of cancer: glycans as novel therapeutic targets Nature Reviews Cancer, 2005. doi:10.1038/nrc1649