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Key Documents

M7753

Sigma-Aldrich

Maltoheptaose

≥60% (HPLC)

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About This Item

Empirical Formula (Hill Notation):
C42H72O36
CAS Number:
Molecular Weight:
1153.00
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic (organic)

Quality Level

form

powder

concentration

≥60% (HPLC)

technique(s)

HPLC: suitable

color

white

solubility

water: 50 mg/mL, clear, colorless

storage temp.

room temp

SMILES string

OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O[C@@H]2CO)O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@@H]3CO)O[C@H]4[C@H](O)[C@@H](O)[C@H](O[C@@H]4CO)O[C@H]5[C@H](O)[C@@H](O)[C@H](O[C@@H]5CO)O[C@H]6[C@H](O)[C@@H](O)[C@H](O[C@@H]6CO)O[C@H]7[C@H](O)[C@@H](O)C(O)O[C@@H]7CO)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C42H72O36/c43-1-8-15(50)16(51)24(59)37(67-8)74-31-10(3-45)69-39(26(61)18(31)53)76-33-12(5-47)71-41(28(63)20(33)55)78-35-14(7-49)72-42(29(64)22(35)57)77-34-13(6-48)70-40(27(62)21(34)56)75-32-11(4-46)68-38(25(60)19(32)54)73-30-9(2-44)66-36(65)23(58)17(30)52/h8-65H,1-7H2/t8-,9-,10-,11-,12-,13-,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

InChI key

BNABBHGYYMZMOA-QJBBZCPBSA-N

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General description

Maltoheptaose is a glucose heptamer.

Application

A partial hydrolysis of maltoheptaose has been used to prepare a dextran ladder in a study that assessed cationic labeling of oligosaccharides. The sensitivity of O-2-[aminoethyl]fluorescein was evaluated using maltoheptaose in a study that investigated the development of a novel fluorescent tag for the electrophoretic separation of oligosaccharides.

Other Notes

To gain a comprehensive understanding of our extensive range of Polysaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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Jan Partyka et al.
Journal of chromatography. A, 1267, 116-120 (2012-07-10)
Cationic derivatization of oligosaccharides by quaternary ammonium label was investigated for capillary electrophoretic separation with transient isotachophoretic preconcentration (t-ITP) as detected by capacitively coupled contactless conductivity detection (C4D). Dextran ladder, prepared by partial hydrolysis of dextran, isomaltotriose, maltopentaose and maltoheptaose
Structure of maltoheptaose by difference Fourier methods and a model for glycogen.
E Goldsmith et al.
Journal of molecular biology, 156(2), 411-427 (1982-04-05)
Svetlana E Soboleva et al.
Biomolecules, 9(6) (2019-05-31)
Lactoferrin (LF) is a Fe3+-binding glycoprotein, that was first recognized in milk and then in other epithelial secretions and barrier body fluids to which many different functions have been attributed to LF including protection from iron-induced lipid peroxidation, immunomodulation, cell
Nicole M Koropatkin et al.
Structure (London, England : 1993), 16(7), 1105-1115 (2008-07-10)
The human gut microbiota performs functions that are not encoded in our Homo sapiens genome, including the processing of otherwise undigestible dietary polysaccharides. Defining the structures of proteins involved in the import and degradation of specific glycans by saccharolytic bacteria
Slavko Kralj et al.
Applied and environmental microbiology, 77(22), 8154-8163 (2011-09-29)
Lactobacillus reuteri 121 uses the glucosyltransferase A (GTFA) enzyme to convert sucrose into large amounts of the α-D-glucan reuteran, an exopolysaccharide. Upstream of gtfA lies another putative glucansucrase gene, designated gtfB. Previously, we have shown that the purified recombinant GTFB

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