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 31 to 40 of 185 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

D-myo-Inositol-4-phosphate (ammonium salt)

142760-33-6sc-205287
sc-205287A
100 µg
500 µg
$220.00
$650.00
(0)

D-myo-Inositol-4-phosphate (ammonium salt) is a phosphorylated carbohydrate that plays a pivotal role in cellular signaling pathways. Its unique phosphate group facilitates interactions with various proteins, influencing signal transduction and metabolic processes. The compound exhibits distinct solubility characteristics, allowing it to participate in diverse biochemical reactions. Its structural conformation can modulate enzyme activity, impacting the kinetics of phosphorylation and dephosphorylation events within cellular systems.

myo-Inositol

87-89-8sc-202714
sc-202714A
sc-202714B
sc-202714C
100 g
250 g
1 kg
5 kg
$78.00
$148.00
$270.00
$821.00
(1)

Myo-Inositol is a cyclic sugar alcohol that serves as a versatile carbohydrate, integral to cellular processes. Its unique stereochemistry allows for multiple hydroxyl groups to engage in hydrogen bonding, enhancing its solubility in aqueous environments. This property facilitates its role in forming phospholipids and inositol phosphates, which are crucial for membrane dynamics and intracellular signaling. Additionally, myo-Inositol's ability to act as a secondary messenger underscores its importance in regulating various metabolic pathways.

Trehalose dihydrate, cell culture

6138-23-4sc-394303
sc-394303A
sc-394303B
10 g
25 g
100 g
$76.00
$135.00
$355.00
1
(1)

Trehalose dihydrate is a disaccharide composed of two glucose units linked by an α,α-1,1-glycosidic bond, exhibiting unique properties in cellular environments. Its ability to form hydrogen bonds contributes to its high solubility and stability, making it an effective osmoprotectant. Trehalose dihydrate influences cellular signaling pathways and stress responses, enhancing cell viability under adverse conditions. Its distinct molecular interactions facilitate the preservation of protein structure and function.

DL-Glyceraldehyde 3-phosphate solution

591-59-3 (free acid)sc-507252
25 mg
$221.00
(0)

DL-Glyceraldehyde 3-phosphate is a triose phosphate that serves as a pivotal intermediate in glycolysis and the Calvin cycle. Its aldehyde group allows for rapid oxidation and reduction reactions, facilitating energy transfer within cells. The compound's ability to form stable enolates enhances its reactivity in various biochemical pathways. Additionally, its role in the synthesis of amino acids and nucleotides underscores its importance in metabolic networks, influencing cellular energy dynamics.

PLC Thio-PIP2 (sodium salt)

sc-224207
sc-224207A
100 µg
500 µg
$188.00
$846.00
(0)

PLC Thio-PIP2 (sodium salt) is a sophisticated carbohydrate derivative known for its unique thiophosphate group, which enhances its reactivity and interaction with biological macromolecules. This compound exhibits distinct binding affinities, influencing cellular signaling pathways and modulating enzyme activities. Its structural flexibility allows for dynamic conformational changes, facilitating interactions with lipid membranes and contributing to its role in cellular communication and metabolic regulation.

Gum guaiac

9000-29-7sc-215116B
sc-215116
sc-215116A
25 g
1 kg
100 g
$82.00
$1574.00
$305.00
(0)

Gum guaiac is a complex carbohydrate known for its unique structural properties, including its ability to form hydrogen bonds and engage in hydrophobic interactions. These characteristics contribute to its solubility in organic solvents and its role in stabilizing various molecular structures. The compound's intricate polymerization pathways allow for diverse interactions within biological systems, influencing its reactivity and participation in metabolic processes. Its distinct physical properties, such as viscosity and texture, further enhance its functional versatility.

Phytic acid calcium salt

23183-60-0sc-253275
sc-253275A
5 g
25 g
$220.00
$925.00
(0)

Phytic acid calcium salt is notable for its ability to chelate metal ions, forming stable complexes that influence nutrient bioavailability. Its unique structure allows for multiple phosphate groups to engage in electrostatic interactions, enhancing its solubility in aqueous environments. This compound also participates in various biochemical pathways, modulating enzymatic activities and influencing metabolic processes. Its distinct physical properties, such as viscosity and texture, further affect its behavior in different systems.

N-Acetyl-α-D-glucosamine 1-phosphate disodium salt

31281-59-1sc-215434
sc-215434A
5 mg
25 mg
$260.00
$650.00
(0)

N-Acetyl-α-D-glucosamine 1-phosphate disodium salt exhibits unique properties as a carbohydrate, particularly in its role as a substrate in glycosylation reactions. Its phosphorylated structure enhances its reactivity, facilitating interactions with enzymes and other biomolecules. This compound can influence cellular signaling pathways through its participation in the synthesis of glycoproteins and glycolipids, impacting cellular communication and structural integrity. Its solubility and stability in physiological conditions further contribute to its functional versatility in biological systems.

IPTG, Dioxane-Free

367-93-1sc-202185
sc-202185A
sc-202185B
sc-202185C
sc-202185D
sc-202185E
sc-202185F
1 g
5 g
100 g
500 g
1 kg
10 kg
25 kg
$50.00
$115.00
$500.00
$1750.00
$2000.00
$16320.00
$32130.00
27
(1)

IPTG, dioxane-free, is a synthetic compound that acts as a potent inducer of gene expression by mimicking lactose. Its unique structure facilitates specific interactions with the lac repressor protein, effectively releasing it from the operator site on DNA. This interaction initiates transcriptional activation, leading to enhanced protein production. The compound's stability and solubility in aqueous environments contribute to its effectiveness in promoting controlled gene expression in various biological systems.

2,7-Dimethyloctane

1072-16-8sc-266238
1 g
$47.00
(0)

2,7-Dimethyloctane is a branched alkane characterized by its unique hydrophobic interactions, which influence its behavior in various chemical environments. Its structure allows for distinct packing in liquid phases, affecting viscosity and diffusion rates. The compound's non-polar nature leads to minimal solubility in polar solvents, impacting its reactivity in organic synthesis. Additionally, its steric hindrance can influence reaction pathways, making it a subject of interest in studies of hydrocarbon behavior.