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M7753

Sigma-Aldrich

Maltoheptaose

≥60% (HPLC)

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About This Item

Formula empirica (notazione di Hill):
C42H72O36
Numero CAS:
34620-78-5
Peso molecolare:
1153.00
Numero CE:
252-119-4
Numero MDL:
MFCD00064605
Codice UNSPSC:
12352201
ID PubChem:
329817914
NACRES:
NA.25

Origine biologica

synthetic (organic)

Livello qualitativo

200

Stato

powder

Concentrazione

≥60% (HPLC)

tecniche

HPLC: suitable

Colore

white

Solubilità

water: 50 mg/mL, clear, colorless

Temperatura di conservazione

room temp

Stringa SMILE

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
BNABBHGYYMZMOA-QJBBZCPBSA-N

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Descrizione generale

Maltoheptaose is a glucose heptamer.

Applicazioni

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.

Altre note

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
SLCK0655
SLCJ3088
SLCJ0388
SLCC9281
MKBX0320V

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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

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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
Artaches A Kazarian et al.
Analytica chimica acta, 662(2), 206-213 (2010-02-23)
This study describes the development of a novel fluorescent tag, O-2-[aminoethyl]fluorescein, for the separation of sugars by capillary electrophoresis with fluorescence detection using an argon ion laser. The tag was synthesised using three consecutive steps namely: esterification, alkylation and hydrolysis
Issei Otsuka et al.
Langmuir : the ACS journal of surfaces and colloids, 26(4), 2325-2332 (2010-02-10)
This work discusses the self-assembly properties of thermoresponsive hybrid oligosaccharide-block-poly(N-isopropylacrylamide) copolymer systems: maltoheptaose-block-poly(N-isopropylacrylamide) (Mal(7)-b-PNIPAM(n)) copolymers. Those systems at different molar masses and volume fractions were synthesized using Cu(I)-catalyzed 1,3-dipolar azide/alkyne cycloaddition, so-called "click" chemistry, between an alkynyl-functionalized maltoheptaose (1) and
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