Date published: 2026-5-7

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Carbohydrate Labeling

Santa Cruz Biotechnology now offers a broad range of Carbohydrate Labeling chemicals for use in various applications. Carbohydrate labeling chemicals are crucial for the study of complex carbohydrates and glycoconjugates in biological systems, providing insights into the structure, function, and dynamics of these essential biomolecules. These labeling agents enable the tagging of carbohydrates with detectable markers such as fluorescent tags or biotin, allowing scientists to track their presence and behavior in live cells, tissues, and other biological matrices. This capability is instrumental in research fields such as glycomics, where understanding the roles of carbohydrates in cell communication, pathogen interaction, and immune responses is key. Carbohydrate labeling is also fundamental in environmental science for tracing the movement and breakdown of carbohydrate-rich substances in ecosystems. Furthermore, these chemicals are used in material science to investigate the properties of carbohydrate-based materials and their applications in biotechnology and engineering. By facilitating the visualization and analysis of carbohydrates, these labeling agents aid in uncovering the mechanisms by which carbohydrates influence various biological and chemical processes, providing a deeper understanding of their roles across a wide range of scientific disciplines. They also contribute significantly to the development of advanced analytical techniques that improve the accuracy and efficiency of carbohydrate detection and characterization. This makes them an indispensable tool in laboratories focusing on the fundamental aspects of molecular biology and chemistry, where detailed and precise measurements are crucial. View detailed information on our available Carbohydrate Labeling chemicals by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

9-Fluorenylmethyl carbazate

35661-51-9sc-210709
250 mg
$122.00
(0)

9-Fluorenylmethyl carbazate is a versatile compound that exhibits unique reactivity as a carbamate derivative. Its structure allows for selective interactions with nucleophiles, facilitating the formation of stable adducts. The compound's ability to undergo hydrolysis under specific conditions highlights its kinetic properties, making it an interesting subject for studying reaction mechanisms. Additionally, its distinct optical characteristics contribute to its role in various analytical applications, enhancing detection sensitivity.

D-Glucose-6,6-d2

18991-62-3sc-257287
sc-257287A
sc-257287B
sc-257287C
500 mg
1 g
10 g
100 g
$139.00
$196.00
$1359.00
$10714.00
1
(0)

D-Glucose-6,6-d2 is a deuterated form of glucose that serves as a valuable tool in metabolic studies. Its unique isotopic labeling allows for precise tracking of metabolic pathways and flux analysis in biological systems. The presence of deuterium alters the vibrational frequencies of the molecule, providing insights into molecular dynamics and interactions. This isotopic substitution can also influence reaction kinetics, making it a key compound for investigating enzymatic processes and carbohydrate metabolism.

L-[UL-13C6]fucose

478518-52-4sc-295236
sc-295236A
10 mg
25 mg
$1000.00
$2000.00
(0)

L-[UL-13C6]fucose is a stable isotopically labeled fucose variant, distinguished by its six carbon atoms, each containing a carbon-13 isotope. This labeling facilitates advanced studies in carbohydrate metabolism, enabling researchers to trace fucose's incorporation into glycoproteins and glycolipids. Its unique carbon framework enhances NMR spectroscopy resolution, allowing for detailed analysis of molecular interactions and conformational dynamics in biological systems.

3-Methylglutaconic acid

5746-90-7sc-397062
sc-397062A
25 mg
50 mg
$194.00
$318.00
(0)

3-Methylglutaconic acid is a dicarboxylic acid characterized by its branched structure, which facilitates unique intramolecular hydrogen bonding. This feature enhances its solubility in polar solvents and influences its reactivity in esterification and decarboxylation reactions. The presence of multiple carboxyl groups allows for versatile interactions with other biomolecules, potentially affecting metabolic pathways. Its distinct stereochemistry can also impact its behavior in enzymatic processes, leading to varied kinetic profiles.