Date published: 2025-10-18

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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 41 to 50 of 185 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

α-D-Glucosamine 1-phosphate

2152-75-2sc-214446
sc-214446A
sc-214446B
sc-214446C
sc-214446D
5 mg
25 mg
100 mg
250 mg
500 mg
$310.00
$948.00
$3019.00
$6808.00
$13270.00
(0)

α-D-Glucosamine 1-phosphate is a key intermediate in carbohydrate metabolism, playing a crucial role in the biosynthesis of glycoproteins and glycolipids. Its phosphate group enhances its reactivity, facilitating enzymatic phosphorylation and dephosphorylation processes. This compound participates in various metabolic pathways, influencing cellular signaling and energy transfer. The presence of the amino group allows for unique hydrogen bonding interactions, impacting its solubility and stability in biological systems.

Heparin disaccharide I-S sodium salt

136098-10-7sc-215132
sc-215132B
1 mg
25 mg
$249.00
$2879.00
(0)

Heparin disaccharide I-S sodium salt is a unique carbohydrate characterized by its intricate sulfation patterns, which enhance its affinity for various proteins and receptors. This compound plays a crucial role in modulating cell adhesion and migration through specific interactions with growth factors and extracellular matrix components. Its structural complexity allows for diverse conformational states, influencing its reactivity and interactions in biological systems, thereby impacting various cellular processes.

N-Glycolylneuraminic Acid

1113-83-3sc-202234
sc-202234A
sc-202234B
sc-202234C
sc-202234D
sc-202234E
sc-202234F
10 mg
25 mg
50 mg
100 mg
1 g
5 g
10 g
$299.00
$515.00
$821.00
$1484.00
$2555.00
$5105.00
$11735.00
2
(0)

N-Glycolylneuraminic Acid is a sialic acid derivative characterized by its unique acyl group, which enhances its interaction with glycoproteins and glycolipids. This compound plays a crucial role in cellular recognition and adhesion processes due to its ability to modulate receptor-ligand interactions. Its distinct structural features allow for specific enzymatic pathways, influencing glycosylation patterns and cellular signaling. The presence of the glycolyl group also affects its reactivity, making it a key player in various biochemical processes.

D-myo-Inositol-3-phosphate (sodium salt)

sc-221511
sc-221511A
100 µg
500 µg
$50.00
$176.00
(0)

D-myo-Inositol-3-phosphate (sodium salt) is a carbohydrate that serves as a key signaling molecule in cellular processes. Its unique phosphate group facilitates interactions with proteins involved in signal transduction pathways, influencing cellular responses to environmental stimuli. The compound's ability to form complexes with divalent cations enhances its stability and reactivity, allowing it to participate in various biochemical reactions and modulate metabolic pathways effectively.

D-Ribulose

488-84-6sc-221520
sc-221520A
25 mg
50 mg
$112.00
$155.00
1
(1)

D-Ribulose is a pentose sugar that serves as a key intermediate in the pentose phosphate pathway, crucial for cellular metabolism. Its unique structure allows for specific enzymatic interactions, particularly with ribulose-1,5-bisphosphate carboxylase/oxygenase, facilitating carbon fixation in photosynthesis. The compound's stereochemistry influences its reactivity and binding affinity, impacting metabolic flux and energy production in various biological systems.

D-myo-Inositol-1,4,5,6-tetraphosphate, sodium salt

157542-47-7sc-223926
sc-223926A
100 µg
500 µg
$165.00
$902.00
(0)

D-myo-Inositol-1,4,5,6-tetraphosphate, sodium salt, is a polyphosphate carbohydrate that plays a crucial role in cellular signaling pathways. Its unique tetraphosphate structure allows for multiple phosphorylation sites, enabling it to interact with various proteins and enzymes. This interaction can influence metabolic processes and cellular communication. The compound's high solubility enhances its mobility within the cytoplasm, promoting efficient signaling and rapid response to cellular stimuli.

N,N′,N″,N‴,N⁗,N⁗′-Hexaacetylchitohexaose

38854-46-5sc-222018
sc-222018A
sc-222018B
1 mg
5 mg
25 mg
$224.00
$408.00
$1846.00
3
(1)

N,N',N'',N''',N'''',N'''''-Hexaacetylchitohexaose is a highly acetylated derivative of chitohexaose, characterized by its multiple acetyl groups that enhance solubility and stability in various environments. This compound exhibits unique interactions with lectins and other carbohydrate-binding proteins, influencing binding affinities and selectivity. Its structural complexity allows for distinct conformational dynamics, which can affect its reactivity in glycosylation reactions and other carbohydrate-related processes.

Guar

9000-30-0sc-215114
sc-215114A
sc-215114B
250 g
500 g
1 kg
$34.00
$82.00
$163.00
(0)

Guar is a polysaccharide derived from the guar bean, characterized by its high viscosity and ability to form gels in aqueous solutions. Its unique galactomannan structure allows for specific hydrogen bonding interactions, enhancing its thickening properties. Guar's molecular weight variability influences its rheological behavior, making it a versatile agent in various applications. Additionally, its solubility in cold water and rapid hydration kinetics contribute to its effectiveness in modifying texture and stability in formulations.

1,3,4,6-Tetra-O-acetyl-2-amino-2-desoxy-β-D-glucopyranose hydrochloride

10034-20-5sc-282335
1 g
$130.00
(0)

1,3,4,6-Tetra-O-acetyl-2-amino-2-desoxy-β-D-glucopyranose hydrochloride is a modified carbohydrate featuring multiple acetyl groups that enhance its solubility and reactivity. The presence of the amino group introduces unique hydrogen bonding capabilities, facilitating specific interactions with other biomolecules. Its structural configuration allows for selective enzymatic pathways, influencing reaction kinetics and stability in various environments. This compound's ability to form stable complexes further underscores its distinctive behavior in carbohydrate chemistry.

PtdIns-(3,4,5)-P3 (1,2-dioctanoyl) (sodium salt)

sc-222207
sc-222207A
100 µg
500 µg
$91.00
$406.00
(0)

PtdIns-(3,4,5)-P3 (1,2-dioctanoyl) (sodium salt) is a phosphoinositide that plays a pivotal role in cellular signaling pathways. Its unique structure allows for specific interactions with proteins containing pleckstrin homology domains, facilitating membrane recruitment and activation of signaling cascades. The presence of octanoyl chains enhances membrane affinity and fluidity, promoting effective lipid-protein interactions. This compound's dynamic behavior in lipid bilayers influences cellular responses and signal transduction efficiency.