Glycoscience

Stability Hygroscopic, Light Sensitive, Temperature Sensitive
Applications 3-Deoxyglucosone-13C6, is the labeled anologue of 3-Deoxyglucosone (D239150), an intermediate in the Maillard reaction of proteins with glucose, which is metabolised to 3-Deoxyfructose. An intermediate in the formation of pyrraline, which might contribute to a pathological effect, such as carcinogenesis.
References Kato, H. et al.: Agric. Biol. Chem., 51, 683 (1987), Hayase, F. et al.: J. Biol. Chem., 264, 3758 (1989), Kato, H. et al.: Biochimica et Biophysica Acta, 1035, 71 (1990)

Stability Hygroscopic
Applications 4-O-α-D-Mannopyranosyl-D-mannose is used in the preparation of immunostimulants, useful as materials for foods as well.
References Imamura, L., et al.: Biol. Pharm. Bull., 17, 596 (1994), ,Perrin, S., et al.: J. Appl. Microbiol., 90, 859 (2001), Olano-Martin, E., et al.: J. Appl. Microbiol., 93, 505 (2002), Gibson, G., et al.: J. Food Sci., 69, 141 (2004),

Applications Protected Maltotriose.
References Brayer, G., et al.: Biochem., 39, 4778 (2000),

Applications Methyl 4-Deoxy-4-fluoro-α-D-glucose (cas# 56926-53-5) is a compound useful in organic synthesis.

Applications 5-Azido-6-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-Gulono-1,4-lactone (cas# 118464-49-6) is a compound useful in organic synthesis.

Applications Ethyl-2,2,2-d3-malonic Acid (CAS# 70907-93-6) is a useful isotopically labeled research compound.

Applications 5-Hydroxy-2’-deoxycytidine-13C,15N2 is the Isotope labelled analogue of 5-Hydroxy-2’-deoxycytidine (H946650), a substrate for uracil DNA N-glycosylase and has been used to study the oxidation of DNA due to exposure to reactive oxygen species.
References Ganguly, M., et al.: Biochem., 51, 2018 (2012); Foresta, M., et al.: Free. Rad. Biol. Med., 48, 681 (2010); Daviet, S., et al.: DNA Repair., 6, 8 (2007);

Stability Moisture Sensitive
Applications US Pat. 7033765

Methyl L-rhamnopyranoside is a sugar that is the product of the reaction between l-rhamnose and acetone. This compound has been used as a chiral building block for the synthesis of other sugars, such as D-arabinose and D-lyxose. The yield of this reaction depends on the concentration of potassium thioacetate and temperature. This compound can be obtained in two forms: (1) anomeric form, which is an intermediate in the synthesis of carbohydrates and (2) crystalline form, which is a white solid with melting point at 157.3°C. The anomeric form has a stereogenic center at carbon atom 3, whereas the crystalline form does not have any stereogenic centers. Methyl L-rhamnopyranoside also reacts with chlorination reagents to produce chlorinated derivatives, such as 2-chloro-3-(3′,4′-dimeth

Pentaric acid is a crystalline, monocarboxylic acid with a hydroxyl group. It is used as an inhibitor of corrosion in metal and as a disinfectant. Pentaric acid can be found in urine samples and has been shown to be an effective inhibitor of the enzymatic reaction that produces azobenzene, which is associated with the development of bladder cancer. This compound also inhibits the growth of bacteria. Pentaric acid is used as an additive in some detergents and soaps because it can inhibit the growth of bacteria on surfaces.
Pentaric acid was first synthesized by German chemist Otto Wohlert in 1834. Hydrogen ions are released when pentaric acid dissolves in water, lowering the pH level and causing corrosion to metal surfaces. The corrosion inhibition properties of pentaric acid have been known since its discovery, but its anti-bacterial properties were not discovered until recently when researchers found that pentar

Ezetimibe hydroxy-b-D-glucuronide is an oligosaccharide that can be synthesized from the modified sugar, L-glucuronic acid. It has a molecular weight of 536 and is soluble in water and methanol. This compound has been used in the synthesis of glycosides, saccharides, and polysaccharides. The chemical name for this compound is 1-(2-hydroxyethyl)-3-(((4'-carboxybenzyl)oxy)carbonyl)-2,6-diazaoctane glucuronide. Ezetimibe hydroxy-b-D-glucuronide has been shown to increase the absorption of cholesterol and decrease low density lipoprotein (LDL) levels in the blood by inhibiting intestinal cholesterol absorption.

Lacto-N-difucohexaose I-APD-KLH is a synthetic, high purity, custom synthesis carbohydrate that has been fluorinated with APD and KLH. The carbohydrate is methylated and glycosylated. Lacto-N-difucohexaose I-APD-KLH has a CAS number of 73387-87-8.

Sulpho Lewisa Na is a complex carbohydrate that has been modified with fluorination and methylation. This product is custom synthesized, high purity, and has a CAS number. It is available for synthesis in various lengths of saccharides with a variety of modifications. Sulpho Lewisa Na can be used in the following applications: glycosylations, click modification, and methylation.

Allyl 4,6-O-benzylidene-a-L-glucopyranoside is a glycosylation agent that is used in the synthesis of oligosaccharides. It is a synthetic compound that can be modified to produce complex carbohydrates. Allyl 4,6-O-benzylidene-a-L-glucopyranoside has been shown to be effective for the fluorination and methylation of sugar chains. It also has high purity and CAS number, which makes it an excellent choice for custom synthesis.

6-Chloro-6-deoxy-D-galactitol is a sugar with the molecular formula C6H12O6. It is a modification of galactose and has the same chemical structure as 6-chloro-D-mannitol. It can be used in the synthesis of complex carbohydrates, and it is also an intermediate for producing oligosaccharides or polysaccharides. 6-Chloro-6-deoxy-D-galactitol is also known as Lactotriose. This product has been modified by fluorination, which increases its stability and reduces its reactivity to other compounds.

UDP-2-ketopropyl-a-D-galactose is a synthetic compound that belongs to the group of oligosaccharides. It is an excellent candidate for glycosylation, methylation, and click modification. The product has a CAS number, which provides high purity and custom synthesis. The product is also a complex carbohydrate with a variety of modifications.