Date published: 2025-12-15

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Carbohydrates

Santa Cruz Biotechnology now offers a broad range of carbohydrates for use in various applications. Carbohydrates, a fundamental category of biomolecules, encompass simple sugars, polysaccharides, and complex carbohydrates, playing critical roles in numerous biological processes and scientific research. In biochemistry, carbohydrates are essential for studying glycosylation patterns on proteins and lipids, which are crucial for understanding cell signaling, protein folding, and immune responses. Researchers utilize carbohydrates to investigate energy metabolism, as they are central to glycolysis, the citric acid cycle, and other metabolic pathways. In molecular biology, carbohydrates are employed to explore the structure and function of nucleic acids, as sugar moieties form the backbone of DNA and RNA. Additionally, carbohydrates are pivotal in microbiology for studying the composition and function of bacterial cell walls and biofilms, contributing to our understanding of microbial physiology and pathogenesis. Environmental scientists use carbohydrates to examine the carbon cycle and the role of polysaccharides in soil structure and fertility. In materials science, carbohydrates are used to develop biodegradable polymers and hydrogels, advancing sustainable materials and technologies. Analytical chemists rely on carbohydrates for developing and refining methods such as chromatography and mass spectrometry to analyze complex biological samples. By offering a diverse selection of carbohydrates, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate carbohydrate for their specific experimental needs. This extensive range of carbohydrates facilitates innovation and discovery across multiple scientific disciplines, including chemistry, biology, environmental science, and materials science. View detailed information on our available carbohydrates by clicking on the product name.

Items 11 to 20 of 185 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Hyaluronic Acid, Sodium Salt

9067-32-7sc-204004A
sc-204004B
sc-204004C
sc-204004D
sc-204004
100 mg
1 g
25 g
100 g
500 mg
$82.00
$360.00
$700.00
$1715.00
$235.00
1
(1)

Hyaluronic Acid, Sodium Salt is a polysaccharide renowned for its exceptional water retention capacity, enabling it to maintain hydration in various environments. Its unique structure allows for extensive hydrogen bonding, promoting viscoelasticity and contributing to its gel-like consistency. This compound interacts with cell membranes, facilitating cellular communication and influencing tissue hydration dynamics. Its high molecular weight enhances its ability to form stable complexes, impacting its behavior in diverse biochemical pathways.

Pirlimycin hydrochloride (Mixture of Diastereomers)

78822-40-9sc-212565
sc-212565A
500 µg
5 mg
$405.00
$2550.00
(3)

Pirlimycin hydrochloride, a mixture of diastereomers, exhibits intriguing molecular interactions due to its unique stereochemistry. This compound engages in specific hydrogen bonding and hydrophobic interactions, influencing its solubility and reactivity in various environments. Its distinct conformational flexibility allows for diverse binding affinities, which can modulate its kinetic behavior in biochemical pathways. Additionally, the presence of functional groups enhances its ability to participate in complexation reactions, affecting its overall stability and reactivity.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

5-Azacytidine is a nucleoside analog that exhibits unique interactions with nucleic acids, influencing gene expression and epigenetic regulation. Its structure allows for incorporation into RNA, disrupting normal base pairing and altering transcriptional dynamics. This compound can modulate cellular pathways by affecting RNA stability and processing, leading to distinct kinetic profiles in biochemical reactions. Its ability to mimic natural nucleotides enables it to engage in specific molecular interactions that impact cellular function.

λ-Carrageenan

9064-57-7sc-216084
sc-216084B
sc-216084A
sc-216084C
sc-216084D
5 g
10 g
25 g
50 g
100 g
$97.00
$173.00
$352.00
$520.00
$622.00
6
(1)

λ-Carrageenan is a sulfated polysaccharide known for its unique gel-forming properties, which arise from its helical structure and the presence of sulfate groups. These features facilitate strong intermolecular interactions, including ionic and hydrogen bonding, leading to the formation of stable gels in aqueous solutions. Its ability to undergo conformational changes in response to temperature and ionic strength allows for dynamic viscosity modulation, making it a versatile agent in various applications.

D-myo-Inositol-1-phosphate, sodium salt

sc-223909
sc-223909A
500 µg
1 mg
$77.00
$115.00
(0)

D-myo-Inositol-1-phosphate, sodium salt, is a carbohydrate derivative characterized by its role in cellular signaling and metabolic pathways. Its phosphate group facilitates interactions with proteins and lipids, influencing membrane dynamics and cellular communication. This compound participates in the inositol phosphate signaling cascade, impacting various physiological processes. Additionally, its solubility in aqueous environments enhances its reactivity and bioavailability, making it a key player in cellular metabolism.

H-Trisaccharide

sc-300786
1 mg
$250.00
(0)

H-Trisaccharide is a complex carbohydrate that exhibits unique structural properties, enabling it to form specific hydrogen bonds and hydrophobic interactions. Its branched configuration allows for diverse molecular recognition events, influencing enzyme-substrate interactions and facilitating glycosylation processes. The compound's solubility in polar solvents enhances its kinetic reactivity, promoting rapid participation in carbohydrate metabolism and energy transfer pathways within biological systems.

D-Mannose-6-phosphate, Disodium Salt

33068-18-7sc-203019
sc-203019A
50 mg
1 g
$154.00
$740.00
(1)

D-Mannose-6-phosphate, Disodium Salt is a phosphorylated sugar that plays a pivotal role in cellular metabolism. Its phosphate group enhances solubility and facilitates specific enzyme interactions, promoting efficient energy transfer. This compound participates in the mannose metabolic pathway, influencing glycoprotein synthesis and cellular signaling. Its unique structural conformation allows for effective binding with lectins, impacting cell recognition processes and intercellular communication.

D-myo-Inositol-1,2,3,5,6-pentaphosphate, sodium salt

sc-223913
sc-223913A
100 µg
500 µg
$220.00
$992.00
(0)

D-myo-Inositol-1,2,3,5,6-pentaphosphate, sodium salt is a highly phosphorylated carbohydrate that serves as a key regulator in various cellular processes. Its multiple phosphate groups confer a high degree of negative charge, enhancing its interaction with metal ions and proteins. This compound is integral in signaling pathways, particularly inositol phosphate signaling, where it modulates enzyme activity and influences cellular responses. Its unique structure allows for specific binding to proteins, impacting cellular dynamics and metabolic regulation.

D-myo-Inositol-1,2,4,5,6-pentaphosphate, sodium salt

sc-223916
sc-223916A
100 µg
500 µg
$220.00
$992.00
(0)

D-myo-Inositol-1,2,4,5,6-pentaphosphate, sodium salt is a complex carbohydrate characterized by its extensive phosphorylation, which facilitates intricate interactions with cellular components. The presence of multiple phosphate groups enhances its solubility and reactivity, allowing it to participate in diverse biochemical pathways. This compound plays a pivotal role in cellular signaling, influencing processes such as calcium mobilization and protein phosphorylation, thereby affecting metabolic pathways and cellular homeostasis. Its structural versatility enables it to act as a molecular scaffold, promoting specific protein interactions and modulating enzymatic functions.

DL-Glyceraldehyde

56-82-6sc-218255
sc-218255A
1 g
5 g
$148.00
$444.00
2
(1)

DL-Glyceraldehyde is a triose sugar that serves as a key intermediate in various metabolic pathways, particularly glycolysis. Its unique aldehyde functional group allows for rapid isomerization and participation in aldol reactions, influencing carbohydrate metabolism. The compound exhibits distinct stereochemistry, leading to different reactivity profiles in enzymatic processes. Additionally, its ability to form hemiacetals with alcohols enhances its role in carbohydrate chemistry, contributing to the formation of more complex sugars.