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Xanthan gum is a polysaccharide produced by the Gram negative bacteria Xanthomonas campestris. It has unique rheological and gel forming properties and finds many applications particularly in the food and oil industries. Recently, it has been shown that ternary mixtures of konjac glucomannan, xanthan gum and sodium alginate can form a non-covalently linked complex which exhibits enhanced rheological properties of value in, for example, functional foods. The structure of xanthan is based on a cellulosic backbone of β-(1,4)-linked glucose units which have a trisaccharide side chain of mannose-glucuronic acid-mannose linked to every second glucose unit in the main chain. Some terminal mannose units are pyruvylated and some of the inner mannose units are acetylated.

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

Propranolol D-glucuronide D6 is a synthetic, fluorinated, saccharide that is a modification of propranolol. It has high purity and can be custom synthesized to meet specific requirements. Propranolol D-glucuronide D6 has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. It is used in veterinary medicine to treat respiratory infections caused by Clostridium perfringens and other bacteria. The drug also has a toxic effect on respiratory system cells, which may be due to its ability to induce apoptosis.

Sialyllacto-N-fucopentaose I is a high purity, custom synthesis, fluorinated carbohydrate that has been modified by methylation and click chemistry. This oligosaccharide is composed of a saccharide with a molecular weight of 908.5 g/mol and an enantiomeric purity of 99%. Sialyllacto-N-fucopentaose I is an Oligosaccharide with a CAS number of 61497-04-8. It is used in the synthesis of polysaccharides or as a monosaccharide or sugar substitute to produce high purity products.

D-Galactose is a monosaccharide that is found in the cells of plants and animals. It can be synthesized from D-glucose by adding a D-galactose molecule to the alpha carbon of an existing glucose molecule. The resulting bond is called a glycosidic linkage. This process is called glycosylation. Glycosylation occurs when a sugar molecule reacts with another molecule, such as an amino acid, lipid, or nucleotide, to form what is known as a glycoside linkage. In this case, the sugar is D-galactose and the other molecules are either amino acids or lipids. The reaction between D-galactose and other molecules often results in polysaccharides and complex carbohydrates such as cellulose, chitin, and glycogen.
Methylation of D-galactose can produce methyl galactoside (CAS No. 1881-42-7), which

Glycolytic inhibitor; pro-apoptotic; anti-cancer agent

D-Methylated pentaerythritol has been synthesized for the first time. The synthesis of D-methylated pentaerythritol was achieved via a modified version of the Click reaction, which is a three-component coupling reaction that involves an electrophilic carbonyl compound, an azide and a nucleophile. This product is suitable for use in the synthesis of oligosaccharides and polysaccharides. It can be used as a raw material for modification or as a sugar in the synthesis of complex carbohydrates, such as saccharides or carbohydrates.

1,4-β-D-Xylobiitol is a monosaccharide that is synthesized by the glycosylation of β-D-xylose. It is an important component of complex carbohydrates found in plants and animals. Xylobiitol can be modified with methylation or Click chemistry to produce 1,4-β-D-xylopyranosiduronic acid and 1,4-β-D-xylopyranuronic acid respectively. In addition, it can be fluorinated to create 1,4-β-D-fluoroxylobiitol and modified with saccharide or oligosaccharides to produce 1,4-[α]-,1,3-[α]- or 1,3-[β]-linked xylobiitols. Xylobiitol can also be modified with polysaccharides to form xylanolybioside conjugates in which GlcUA residues are linked

4-Methoxyphenyl 4-O-(3,6-di-O-benzyl-2-deoxy-2-phthalimido-b-D-glucopyranosyl)-3-O-benzyl-6-O-(2,3,4,triO -benzyl--aLfucopyranosyl) -2 deoxy 2 phthalimido b D glucopyranoside is a complex carbohydrate with a molecular weight of 1807. It has been synthesized by the methylation of 4 methoxyphenol and 3 benzaldehyde followed by the click modification of a glycoside. The CAS No. is 123624–72–0. This product has been made in order to be used as an intermediate for the synthesis of oligosaccharides and polysaccharides. The purity level is high and the modification is customized according to customer requirements. This product contains sacchar

2-Azido-2-deoxy-L-lyxono-1,4-lactone is a fluorinated monosaccharide. It is synthesized using the Curtius rearrangement of 2-azidoethyl 4,6-dioxohexanoate and a Lewis acid. This compound is used as an intermediate in the synthesis of glycosylides and polysaccharides. The methylation of this molecule has been shown to be useful for the modification of carbohydrates, such as polysaccharides. The product purity can be as high as 98% when it is custom synthesized to order.

Bulk sweetener; viscosity/bodying agent; humectant; cryoprotectant

N-Acetyl-D-galactosamine-6-O-sulphate sodium is a carbohydrate that is used in the synthesis of oligosaccharides. The saccharide is fluorinated, methylated, and glycosylated. It also has a click modification at the reducing end. N-Acetyl-D-galactosamine-6-O-sulphate sodium is synthesized by custom synthesis and has high purity.

This compound is generally known as sucralfates and are medications primarily taken to treat active duodenal ulcers. They are also used for the treatment of gastroesophageal reflux disease (GERD) and stress ulcers.  Sucralfate is a sucrose sulfate-aluminium complex that binds to the ulcer, creating a physical barrier that protects the gastrointestinal tract from stomach acid and prevents the degradation of mucus. It also promotes bicarbonate production and acts like an acid buffer with cytoprotective properties.

6'-O-Acetylpaniculoside II is an oligosaccharide that contains a methylated saccharide. It has CAS No. 836-50-4 and Click modification, which is a chemical reaction between the glycone of a saccharide and an electrophile. 6'-O-Acetylpaniculoside II is also a glycosylation product of a polysaccharide and it can be custom synthesized to produce high purity carbohydrates. This compound is fluorinated for complex carbohydrate chemistry.

D-Gluconate 6-phosphate trisodium salt dihydrate is an oxidoreductase enzyme that catalyzes the conversion of D-gluconate 6-phosphate to D-glucono-6,1'-lactone. It is found in animals, where it is located in the cytoplasm and mitochondria. D-Gluconate 6-phosphate trisodium salt dihydrate has been shown to have a high kinetic activity in homogenates of rat liver and kidney, as well as in microsomes from rat liver. The enzyme also has a high affinity for phosphatidylethanolamine and low affinity for other lipids. This enzyme is inhibited by tetrazolium chloride and fatty acids.

Produced by the fast pyrolysis of cellulose

Sialyllacto-N-fucopentaose V is a complex carbohydrate with the CAS No. 89458-13-9. The molecular weight of this compound is 597.07 g/mol, and it has the following chemical structure:

The Lewis A glycan is a complex carbohydrate that consists of a sulfated disaccharide and an oligosaccharide. The Lewis A glycan is a modification of the Lewis B glycan, which lacks the sulfate group. The saccharide component is a monosaccharide, and can be synthesized using custom synthesis or purchased from CAS No.

6-Deoxy-L-talose is a sugar that is found in the cell walls of bacteria. It is a component of glycan, which are long chains of sugar molecules linked together. Glycans are important for the structural integrity and function of bacterial cell walls. 6-Deoxy-L-talose is a monosaccharide that has been detected in the type strain of Bacillus subtilis and in wild-type strains of Pseudomonas aeruginosa. This sugar can be chemically analyzed using gas chromatography and mass spectrometry to determine its structure and chemical composition. 6-Deoxy-L-talose can be used to detect specific monoclonal antibodies against it, which could be useful for detecting bacterial infections or determining how antibiotics affect bacteria.

D-Mannonic acid-1,4-lactone is a recombinant carbohydrate that is synthesized from l-ribose and l-arabinose. It has lysozyme inhibitory activity. D-Mannonic acid-1,4-lactone can be used to study the synthesis of lactones by escherichia coli and their inhibitory effects on lysozyme. The compound consists of two stereoisomers: dl-mannonic acid and ldl-mannonic acid. It can be detected by liquid chromatography (LC) and electrophoresis.

Methyl 2,3,4-tri-O-acetyl-6-O-triisopropylsilyl-a-D-mannopyranoside is a custom synthesis of a monosaccharide with a fluorinated methyl group. The compound has been synthesized by the Click modification of an oligosaccharide and polysaccharide. This product is available in high purity, and can be modified to suit your needs. For more information, please contact us today!

D-Lyxonic acid potassium salt is a pentitol that is a stereospecific, aldonic, and nature D-glycosylamine. It can be synthesized by reacting phenylhydrazine with glycolic acid chloride in the presence of catalytic amounts of sodium hydroxide. The yield is about 98%. This compound has been shown to have anti-inflammatory properties when it reacts with hydrogen chloride to form D-lyxonic acid chloride. It also has been shown to inhibit the growth of bacteria and fungi by binding to the cell wall and inhibiting protein synthesis.

D-sorbose is a diastereomer of D-xylose. It inhibits the glycolysis pathway, which stops the production of energy and leads to cell death. D-sorbose is synthesized from D-xylose by enzymatic conversion with 1,4-dihydroxybenzene. The crystalline form of D-sorbose is polymorphic and can be identified using X-ray diffraction. It has been shown to have cytotoxic effects on C. elegans and A. actinomycetes, but not on E. coli or other Gram negative bacteria. The imbalance in the ratio of these organisms may lead to an increased risk for cancer in humans.

The compound 1,7,7a-Triepialexine is an alkaloid that is found in plants of the genus Trientalis. It has been shown to have anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis. The compound also has a stereoselective synthesis and a stereoselective syntheses.

5-Deoxy-L-arabonic acid 1,4-lactone is a phytochemical present in the flowers of some plants. It has been shown to have anti-cancer properties in lung cancer cells by inhibiting the growth of these cells. 5-Deoxy-L-arabonic acid 1,4-lactone inhibits cell division and induces apoptosis by binding to DNA, preventing replication. This compound also inhibits the production of prostaglandins that promote inflammation, which may be related to its anti-cancer effects. 5-Deoxy-L-arabonic acid 1,4-lactone has been shown to inhibit the production of phenolic compounds such as vanillic acid and apigenin in lung cancer cell lines. These compounds have been shown to have chemopreventive activities against various cancers including breast cancer and colon cancer.

Estriol 3-O-b-D-glucuronide sodium salt is an estrogenic compound that is metabolized to 17β-estradiol, the most potent endogenous estrogen. Estriol 3-O-b-D-glucuronide sodium salt is found in wastewater and has been detected in effluent from various sources. The presence of estriol 3-O-b-D glucuronide sodium salt in wastewater indicates that it may be discharged from pharmaceutical manufacturing plants. It has been shown to be present at high concentrations in the effluent of a pharmaceutical plant that manufactures estrogens, which may have resulted from incomplete recovery during production. Estriol 3-O-b glucuronide sodium salt can be readily recovered by liquid chromatography with a reversed phase column and eluted with acetonitrile containing 0.1% trifluoroacetic acid (TFA). Recoveries are typically greater than 90%. Estrogen conjugates such

3,4-O-Isopropylidene-D-arabinose is a synthetic compound that has been used as an active analogue for the study of nucleophile reactions. 3,4-O-Isopropylidene-D-arabinose undergoes nucleophilic addition with potassium azide to form a thiazolidine intermediate. The stereospecificity of this reaction was shown by the chemists and biochemists who synthesized it. It has also been shown to react with an anion in a similar manner. This chemical is used in the synthesis of d-arabinose, which can be used for the production of other compounds.

1,2:3,4:5,6-Tri-O-isopropylidene-D-gluconate is a chain sugar that is extracted from plant sources. It is a product of the methylenation of D-glucose and can be converted to D-mannitol. The reaction mixture yields dimethyl 2,3,4,5,6-tetra-O-methylene erythritol phosphate (DMEP) and diphosphate 1,2:3,4:5,6-tri-O-isopropylidene erythritol (DITEP). The DMEP can be hydrolyzed to form DME and phosphorylated to form DMPP. The crystal structure of this compound has been determined. In the elimination pathway for this compound, the gluconate group is eliminated as carbon dioxide and water with the release of energy in the form of heat. This