Methyl (Phenyl 5-Acetamido-4,7,8-tri-O-acetyl-9-azido-3,5,9-trideoxy-2-thio-D-glycero-beta-D-galacto-2-nonulopyranosid)onate TCI M2695

Chemical Identity

CAS No.: 219814-65-0
PubChem: CID 91972126·SID 253661413
Formula: C24H30N4O10S
Molecular weight: 566.6 g/mol
Purity: >92.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 5-acetamido-4-acetyloxy-6-[(1R,2R)-1,2-diacetyloxy-3-azidopropyl]-2-phenylsulfanyloxane-2-carboxylate
SMILES: CC(=O)NC1C(CC(OC1[C@@H]([C@@H](CN=[N+]=[N-])OC(=O)C)OC(=O)C)(C(=O)OC)SC2=CC=CC=C2)OC(=O)C
InChIKey: YCUSQTURLGBYSS-FBTHOKQTSA-N

Rp 24.035.550,00

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Berat 100mg

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This complex chemical compound is widely used in the field of chemical biology, particularly in conjugation and click chemistry applications. It serves as a versatile linker or binder, enabling the construction of complex molecules such as proteins, nucleic acids, and lipids. Its role in the laboratory is critical for enhancing molecular functionality and stability through precise chemical reactions. Due to its high reactivity, it is ideal for applications requiring rapid and accurate chemical transformations.

The compound's unique molecular structure, featuring multiple functional groups such as azido and amino groups, allows for efficient and selective chemical reactions. These properties make it a preferred choice for researchers aiming to create complex molecular systems with high specificity. Its ability to form stable covalent bonds under controlled conditions ensures reliable results in various biochemical experiments. The compound's stability and reactivity further support its use in demanding laboratory environments.

In Indonesian laboratories, this compound is commonly used in biochemistry research, especially in the development of conjugated molecules and functionalized biomolecules. It is a key reagent in studies involving molecular labeling, drug conjugation, and bioconjugate synthesis. Its application is particularly relevant in academic and industrial research settings where precision and efficiency are essential.

TCI brochures (PDF)

Glycosidation 2026-04-14 · p. 6
Click Chemistry 2026-09-08 · p. 10
Reagents for Glyco Chemistry & Biology 5th Edition · p. 69

Related TCI products

Bioconjugate synthesis for creating targeted drug delivery systems due to its ability to form stable covalent bonds with biomolecules.
Molecular labeling applications where precise and efficient chemical reactions are required for attaching functional groups to biomolecules.
Click chemistry experiments that rely on the compound's azido and amino groups for rapid and selective coupling reactions.
Protein and nucleic acid modification studies that benefit from its high reactivity and specificity in forming conjugates.
Development of functionalized lipids for use in membrane research and drug delivery systems requiring controlled molecular interactions.

Brand	TCI
CAS number	219814-65-0
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Conjugation Chemistry/Click Chemistry
Pack sizes	Available in various quantities as per standard laboratory supply options
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

Data from the TCI brochure

Purity	>97.0%(HPLC)

Source: TCI brochure reagent_for_glyco_chemistry_&_biology_5th_ed ()

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical properties. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its high reactivity, it should be used in a well-ventilated area to minimize any potential risks. Proper storage and handling ensure the compound remains effective for its intended applications in biochemical research.

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