4-Nitrophenyl4,6-ethylidene-a-D-maltoheptaoside

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Catalog No: A10GD-4178
Cas No: 96597-16-9
Properties: Mol Formula: C50H77NO38, Mol Weight: 1300.1
IUPAC Name: (4aR,6R,7R,8R,8aS)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-2-methyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol
Synonym: Ethylidene-4-nitrophenyl-a-D-Maltoheptaoside, HY-112835, CS-0066482

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4-Nitrophenyl 4,6-ethylidene-a-D-maltoheptaoside

4-Nitrophenyl 4,6-ethylidene-?-D-maltoheptaoside is a substrate used in a reference measurement method for ?-amylase activity in the diagnosis of acute pancreatitis, approved by the International Federation of Clinical Chemistry (IFCC). The substrate is hydrolysed by serum ?-amylase into shorter 4-nitrophenylated oligosaccharides and their free counterparts. These reaction products are channeled into an indicator reaction with ?-glucosidase and are degraded into glucose and the chromophore, 4-nitrophenol.

CAS No 96597-16-9
Synonyms pNP-G7
Chemical Formula C50H77NO38
Molecular Weight 1,300.13 g/mol
Smiles CC1OCC2O[C@H](O[C@H]3[C@H](O)C(O)[C@@H](O[C@H]4[C@H](O)C(O)[C@@H](O[C@H]5[C@H](O)C(O)[C@@H](O[C@H]6[C@H](O)C(O)[C@@H](O[C@H]7[C@H](O)C(O)[C@@H](O[C@H]8[C@H](O)C(O)[C@@H](Oc9ccc(cc9)[N+](=O)[O-])OC8CO)OC7CO)OC6CO)OC5CO)OC4CO)OC3CO)C(O)[C@@H](O)[C@@H]2O1
Storage store at 2?C – 8?C
Harmonized Tariff Codes

Switzerland: 29389090 – USA: 2938900000 – Slovakia: 2938909090 – UK: 2938909000 – China: 2938909090

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Size

1 G, 100 MG, 5 G, Other

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