2-CHLORO-4-NITROPHENYL-BETA-D-MALTOTRIOSIDE

• CAT Number: M041785
• CAS Number: 165522-16-7
• Molecular Formula: C24H34ClNO18
• Molecular Weight: 659.98
• Purity: ≥95%
• Storage: -20°C
• IUPAC Name: (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6S)-6-(2-chloro-4-nitrophenoxy)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
• InChI: InChI=1S/C24H34ClNO18/c25-8-3-7(26(37)38)1-2-9(8)39-22-18(35)15(32)20(11(5-28)41-22)44-24-19(36)16(33)21(12(6-29)42-24)43-23-17(34)14(31)13(30)10(4-27)40-23/h1-3,10-24,27-36H,4-6H2/t10-,11-,12-,13-,14+,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-/m1/s1
• InChIKey: KMYYNUOXSFGLNX-KKFBLJMZSA-N
• SMILES: C1=CC(=C(C=C1[N+](=O)[O-])Cl)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O

2-Chloro-4-nitrophenyl-beta-D-maltotrioside（Cat No.:M041785） is a specialized synthetic glycoside that combines a 2-chloro-4-nitrophenyl aglycone with a maltotrioside, a trisaccharide composed of three glucose units linked by glycosidic bonds. This compound is particularly useful in biochemical assays as a chromogenic or fluorogenic substrate. The presence of the nitrophenyl group allows it to release a chromophore upon enzymatic cleavage, which can be easily detected and measured. It is primarily used in enzymology to study glycosidase activity, where the cleavage of the glycosidic bond by specific enzymes leads to a measurable color change, facilitating enzyme characterization and kinetics studies.