4-Nitrophenyl α-D-maltohexaoside - ≥97% , CAS No.74173-30-1

CAS: 74173-30-1 Cat. No.: N343349 Molecular Weight: 1111.95 Beilstein Registry Number: 3586152 EC Number: 635-209-1 PubChem CID: 16218488

GRADE & PURITY ≥97%

Synonyms

4-Nitrophenyl alpha -D-maltohexaoside | 4-NITROPHENYL-ALPHA-D-MALTOHEXAOSIDE | 4-Nitrophenyl alpha-D-hexa-(1->4)-glucopyranoside | 4-Nitrophenyl-alpha-D-maltohexaoside, 97% | 4-Nitrophenyl alpha-D-maltohexaoside, >=98.0% (HPLC) | MFCD00065704 | 4-Nitrophe

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Overview

4-Nitrophenyl α-D-maltohexaoside is a substrate used in the determination of α-amylase activity.

Specifications

Synonyms

4-Nitrophenyl alpha -D-maltohexaoside | 4-NITROPHENYL-ALPHA-D-MALTOHEXAOSIDE | 4-Nitrophenyl alpha-D-hexa-(1->4)-glucopyranoside | 4-Nitrophenyl-alpha-D-maltohexaoside, 97% | 4-Nitrophenyl alpha-D-maltohexaoside, >=98.0% (HPLC) | MFCD00065704 | 4-Nitrophe

Specifications & Purity

≥97%

Biochemical and Physiological Mechanisms

4-Nitrophenyl ǥ-D-maltohexaoside serves as a chromogenic substrate for ǥ-amylases and yields a yellow product upon cleavage，that can be spectrophotometrically measured at 44 nm.

Storage

Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Canonical Smiles: C1=CC(=CC=C1[N+](=O)[O-])OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)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)O)O)O)O)O)O)O)O)O)O)O)O)O
• IUPAC Name: (2R,3R,4S,5S,6R)-2-[(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-6-(hydroxymethyl)oxane-3,4,5-triol
• InChIKey: GNFSLPRCTKUSTG-UYDBUFRNSA-N
• INCHI: 1S/C42H65NO33/c44-5-13-19(50)20(51)26(57)38(66-13)72-33-15(7-46)68-40(28(59)22(33)53)74-35-17(9-48)70-42(30(61)24(35)55)76-36-18(10-49)71-41(31(62)25(36)56)75-34-16(8-47)69-39(29(60)23(34)54)73-32-14(6-45)67-37(27(58)21(32)52)65-12-3-1-11(2-4-12)43(63)64/h1-4,13-42,44-62H,5-10H2/t13-,14-,15-,16-,17-,18-,19-,20+,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37+,38-,39-,40-,41-,42-/m1/s1
• Isomeric SMILES: C1=CC(=CC=C1[N+](=O)[O-])O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O[C@@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O[C@@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O[C@@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)O)O)O)O)O)O)O)O)O)O
• WGK Germany: 3
• PubChem CID: 16218488
• Molecular Weight: 1111.95
• Beilstein: 3586152

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Fatty Acyls
      • Subclass Fatty acyl glycosides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty acyl glycosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acyl glycosides of mono- and disaccharides
• Alternative Parents: Alkyl glycosides Nitrobenzenes Phenoxy compounds Phenol ethers Nitroaromatic compounds Oxanes Monosaccharides Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxoanionic compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Organic nitro compound - Secondary alcohol - C-nitro compound - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Organic hyponitrite - Alcohol - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water.
• Refractive Index: n20D1.71 (Predicted)
• Boil Point(°C): ~1383.4° C at 760 mmHg (Predicted)
• Molecular Weight: 1112.000 g/mol
• XLogP3: -11.200
• Hydrogen Bond Donor Count: 19
• Hydrogen Bond Acceptor Count: 33
• Rotatable Bond Count: 18
• Exact Mass: 1111.34 Da
• Monoisotopic Mass: 1111.34 Da
• Topological Polar Surface Area: 541.000 Ų
• Heavy Atom Count: 76
• Formal Charge: 0
• Complexity: 1790.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 30
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1