Stachyose Hydrate TCI S0397

Chemical Identity

CAS No.: 54261-98-2
PubChem: CID 439531·SID 87575904
Formula: C24H42O21
Molecular weight: 666.6 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,3R,4S,5R,6R)-2-[[(2R,3R,4S,5R,6S)-6-[[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES: C([C@@H]1[C@@H]([C@@H]([C@H]([C@H](O1)OC[C@@H]2[C@@H]([C@@H]([C@H]([C@H](O2)OC[C@@H]3[C@H]([C@@H]([C@H]([C@H](O3)O[C@]4([C@H]([C@@H]([C@H](O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O
InChIKey: UQZIYBXSHAGNOE-XNSRJBNMSA-N

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Stachyose Hydrate is a carbohydrate compound widely used in chemical and biochemical experiments. It is a complex glycoside composed of four monosaccharide units—glucose, fructose, and two galactose molecules. This compound plays a crucial role in laboratory settings, particularly in enzymatic reactions and the synthesis of other glycosidic compounds. Its structural complexity makes it a valuable tool for studying carbohydrate metabolism and biological interactions. Due to its stability and availability, it is a common choice for researchers in various scientific disciplines.

Stachyose Hydrate is chemically neutral and does not readily react with other chemical substances, making it easy to handle in laboratory environments. It dissolves well in water, which simplifies the preparation of solutions for experiments. Its consistent quality and high availability further enhance its appeal for scientific research. These properties ensure that it remains a reliable and versatile material for both basic and advanced biochemical investigations.

In Indonesian laboratories, Stachyose Hydrate is frequently used in biochemistry and pharmacology research. It is commonly found in studies related to carbohydrate metabolism, enzyme activity, and the development of pharmaceutical compounds. Its role in supporting scientific inquiry makes it an essential component in the research toolkit of Indonesian scientists and researchers.

TCI brochures (PDF)

Reagents for Glyco Chemistry & Biology 5th Edition · p. 99

Related TCI products

Enzymatic Reaction Studies - Stachyose Hydrate serves as a substrate for enzymatic reactions, allowing researchers to study enzyme activity and substrate specificity in biochemical processes.
Glycoside Synthesis - Its complex glycosidic structure makes it ideal for the synthesis of other glycosidic compounds, supporting research in organic chemistry and medicinal chemistry.
Carbohydrate Metabolism Research - It is used to investigate metabolic pathways involving carbohydrates, aiding in the understanding of cellular energy processes.
Pharmaceutical Compound Development - Its structural properties are valuable in the development of pharmaceuticals, particularly those involving glycosidic linkages.
Biochemical Analysis - Stachyose Hydrate is used in various analytical techniques to study the behavior and interactions of carbohydrates in biological systems.

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Brand - TCI
CAS Number - 54261-98-2
Category - Chemistry > Chemical Biology > Glycoscience
Pack Sizes - Available in various quantities as per supplier specifications
Physical Form - White crystalline powder
Storage Note - Store in a cool, dry place away from moisture and direct sunlight

Stachyose Hydrate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture, which could affect its solubility and purity. Due to its neutral chemical nature, it does not react with most common laboratory reagents, making it relatively safe to handle. However, standard laboratory safety practices should still be followed, including the use of appropriate personal protective equipment. The compound is stable under normal storage conditions and does not require refrigeration unless specified by the supplier. Proper labeling and storage are essential to ensure its integrity and safe use in research settings.

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