Oligosaccharides
Chitosan (200-600mPa.s, 0.5% in 0.5% Acetic Acid at 20°C), TCI America™
CAS: 9012-76-4 Molecular Formula: C56H103N9O39 Molecular Weight (g/mol): 1526.464 MDL Number: MFCD00161512 InChI Key: FLASNYPZGWUPSU-SICDJOISSA-N Synonym: chitosan,poliglusam,deacetylchitin,chicol,flonac c,flonac n,sea cure plus,kytex h,kytex m,kimitsu chitosan f PubChem CID: 71853 IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hy SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O
Chitosan (5-20mPa.s, 0.5% in 0.5% Acetic Acid at 20°C), TCI America™
CAS: 9012-76-4 Molecular Formula: C56H103N9O39 Molecular Weight (g/mol): 1526.464 MDL Number: MFCD00161512 InChI Key: FLASNYPZGWUPSU-SICDJOISSA-N Synonym: chitosan,poliglusam,deacetylchitin,chicol,flonac c,flonac n,sea cure plus,kytex h,kytex m,kimitsu chitosan f PubChem CID: 71853 IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hy SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O
Chitosan (20-100mPa.s, 0.5% in 0.5% Acetic Acid at 20°C), TCI America™
CAS: 9012-76-4 Molecular Formula: C56H103N9O39 Molecular Weight (g/mol): 1526.464 MDL Number: MFCD00161512 InChI Key: FLASNYPZGWUPSU-SICDJOISSA-N Synonym: chitosan,poliglusam,deacetylchitin,chicol,flonac c,flonac n,sea cure plus,kytex h,kytex m,kimitsu chitosan f PubChem CID: 71853 IUPAC Name: methyl N-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-5-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-6-(hy SMILES: COC(=O)NC1C(C(C(OC1OC2C(OC(C(C2O)N)OC3C(OC(C(C3O)N)O)CO)CO)CO)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)N)O)N)O)N)O)N)O)N)O)N)O
eMolecules 2-(4-(2-Hydroxyethyl)piperazin-1-yl)ethanesulfonic acid | 7365-45-9 | MFCD00006158 | 25g
Ambeed | 2-(4-(2-Hydroxyethyl)piperazin-1-yl)ethanesulfonic acid | 25g | 490553609 | A318293 | | 7365-45-9 | MFCD00006158 | 238.300 | C8H18N2O4S
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eMolecules Building Block Tool
ALADDIN SCIENTIFIC CORPORATION a-Cyclodextrin, 100g
a-Cyclodextrin can be used- In fabricating reversible supramolecular assemblies As a modifier to enhance the solubility of oleic acid stabilized nanoparticles In the preparation of polyrotaxanes with ply(ethylene glycol) In the synthesis of cationic star polymers with oligoethylenimine
Medchemexpress LLC Gum ghatti | 9000-28-6 | ≈12,000 g/mol | 50 G
Gum ghatti is a natural exudate polysaccharide supplied as a dry powder for research use. It serves as a biochemical reagent and excipient for assays, formulations, and other laboratory applications requiring a water-soluble gum. The material is a complex mixture of calcium/magnesium salts of ghattic acids and mixed monosaccharides (CAS 9000-28-6); the water-soluble fraction has an approximate molecular weight of 12,000 Da.
ALADDIN SCIENTIFIC CORPORATION B-Cyclodextrin, 100g
Useful for forming water-soluble complexes for fluorescent labeling of proteins Product Application-Use to solubilize non-polar compounds such as fatty acids lipids and cholesterol Reported useful for the selective precipitation of enantiomeric positional or structural isomers-Cyclodextrin is used with dansyl chloride to form water-soluble complexes for fluorescent labeling of proteins It is an active ingredient of household odor eliminator It is also used in personal care products like toothpastes skin creams and dusting powders It finds applications in the cosmetic industry for products like detergents and perfumes for the controlled release of fragrances Further it is used to produce HPLC columns allowing chiral enantiomers separation In addition to this it is used to decrease the level of cholesterol in milk fat
Medchemexpress LLC Glycogen (from rabbit liver) | 9005-79-2 | MFCD00081547 | 91.0% | Not specified (polymeric, variable molecular weight) | (C6H10O5)n | 5 MG
Glycogen from rabbit liver is a highly branched glucose polysaccharide provided as a solid for research use. It functions as the animal storage form of glucose and is used as a reagent, standard, or carrier in various biochemical and molecular biology assays. Certificate of analysis and safety data are available to confirm lot-specific properties.
- High branching and biological relevance for metabolism studies.
- Suitable as a reagent or standard in enzymatic and biochemical assays.
- Provides a reliable carrier for nucleic acid precipitation and detection assays.
- Supplied as a stable powdered solid for ease of handling and storage.
- Lot-specific purity and analytical data available via certificate of analysis.
AdipoGen N-Acetyl-D-glucosamine
Chemical. CAS 7512-17-6. Formula C8H15NO6. MW 221.2. Prepared by using chitin as a substrate. N-Acetyl-D-glucosamine D-GlcNAc is a non-toxic derivatized glucose monosaccharide found in polymers Peptidoglycan PGN of bacterial cell walls, chitin e.g. fungi, invertebrates, crustaceans, hyaluronic acids and various glycans. It is also synthesized in the glycosylation pathway as uridine diphosphate UDP-GlcNAc, which can then be released following degradation of glycosylated proteins. Atypical microbial danger signal that acts as a new activator of NLRP3 inflammasome by dissociating the enzyme hexokinase from the mitochondria. D-GlcNAc inhibits purified hexokinase, which is also involved in the glucose metabolism and obesity in mM range. For hexokinase dissociation from the mitochondria much higher concentrations are needed. Acceptor substrate for galactosyltransferases.