Octa-O-acetyl D-(+)-Sucrose TCI S0052

Chemical Identity

CAS No.: 126-14-7
PubChem: CID 31340·SID 87575676
Formula: C28H38O19
Molecular weight: 678.6 g/mol
Purity: >98.0%(T)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[(2S,3S,4R,5R)-3,4-diacetyloxy-2,5-bis(acetyloxymethyl)oxolan-2-yl]oxyoxan-2-yl]methyl acetate
SMILES: CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@]2([C@H]([C@@H]([C@H](O2)COC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C
InChIKey: ZIJKGAXBCRWEOL-SAXBRCJISA-N

Rp 505.050,00

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Berat 25g 500g

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Octa-O-acetyl D-(+)-Sucrose is a chemical compound widely used in laboratory experiments related to glycoscience and biochemical research. As a fully acetylated derivative of sucrose, it features acetyl groups on all hydroxyl groups, making it a highly functional molecule. This compound plays a crucial role in chemical reactions involving glycosylation and carbohydrate modification. Its unique structure allows it to act as a substrate or modifier in various biochemical processes, supporting the study of molecular interactions and biological activities of carbohydrates.

The chemical stability and controlled reactivity of Octa-O-acetyl D-(+)-Sucrose make it a preferred choice for precise laboratory applications. Its resistance to degradation under normal conditions ensures long-term storage and consistent performance. The compound’s well-defined molecular structure also facilitates spectroscopic analysis and molecular characterization, making it a reliable material for analytical and synthetic purposes. These properties contribute to its widespread use in advanced research settings.

In Indonesian laboratories, Octa-O-acetyl D-(+)-Sucrose is commonly utilized in biochemistry, pharmacology, and organic chemistry research. It is a key component in studies involving carbohydrate interactions, enzyme activity, and molecular modeling. Its availability through AMI Scientific ensures that researchers in Indonesia have access to this essential compound for their experimental needs.

TCI brochures (PDF)

Reagents for Glyco Chemistry & Biology 5th Edition · p. 87

Related TCI products

Biochemical research utilizes this compound for studying glycosylation reactions due to its acetylated structure.
Pharmacological studies benefit from its role as a substrate in carbohydrate-based drug development.
Organic chemistry experiments employ it as a versatile building block for synthetic carbohydrate derivatives.
Molecular characterization techniques rely on its stable structure for accurate spectroscopic analysis.
Carbohydrate interaction studies use it to model and analyze molecular behavior in biological systems.

Brand	TCI
CAS number	126-14-7
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Glycoscience
Pack sizes	Available in standard laboratory quantities
Physical form	White crystalline solid
Storage	Store in a cool, dry place away from moisture and light

Octa-O-acetyl D-(+)-Sucrose should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Due to its acetylated structure, it is advisable to use appropriate personal protective equipment when handling the material. The compound should be stored away from incompatible substances to avoid any potential chemical reactions. Regular inspection of storage conditions ensures the integrity of the material over time. Proper handling and storage practices help preserve its reactivity and usability in laboratory applications.

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