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A89804

Sigma-Aldrich

Anthranilamid

≥98%

Synonym(e):

2-AB, 2-Amino-benzamid, Anthranilsäure-amid

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About This Item

Lineare Formel:
2-(H2N)C6H4CONH2
CAS-Nummer:
88-68-6
Molekulargewicht:
136.15
Beilstein:
508509
EG-Nummer:
201-851-2
MDL-Nummer:
MFCD00007981
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24891390
NACRES:
NA.22

Assay

≥98%

Form

crystals

mp (Schmelzpunkt)

111-113 °C (lit.)

Fluoreszenz

λex 330 nm; λem 420 nm(lit.)

SMILES String

NC(=O)c1ccccc1N

InChI

1S/C7H8N2O/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H2,9,10)

InChIKey

PXBFMLJZNCDSMP-UHFFFAOYSA-N

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Anwendung

Fluorescently labels glycans containing a free reducing terminus.
Verwendet für nicht-selektive, wirksame Fluoreszenzmarkierung von Glycanen Leicht weniger empfindlich als Anthranilsäure (2-AA) für die Glycanmarkierung.

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Produkt-Nr.
Beschreibung
Preisangaben

PP0520

GlycoProfile™ 2-AB Labeling Kit

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H319

Gefahreneinstufungen

Eye Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

>365.0 °F

Flammpunkt (°C)

> 185 °C

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
WXBD4959V
WXBD2675V
WXBC6615V
WXBC9405V
WXBC8559V

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3-Aminobenzamid ≥99% (TLC)

Sigma-Aldrich

A0788

3-Aminobenzamid

Michael Melmer et al.
Analytical and bioanalytical chemistry, 398(2), 905-914 (2010-07-20)
In contrast with conventional drugs, biopharmaceuticals are highly complex molecules with remarkable heterogeneity. Protein glycosylation is an inherent source of this heterogeneity and also affects the safety, efficacy, and serum half-life of therapeutic glycoproteins. Therefore analysis of the glycan pattern
Jia Jia et al.
Organic & biomolecular chemistry, 10(31), 6279-6286 (2012-06-23)
Three fluorescent probes CdABA', CdABA and ZnABA', which are structural isomers of ZnABA, have been designed with N,N-bis(2-pyridylmethyl) ethylenediamine (BPEA) as chelator and 2-aminobenzamide as fluorophore. These probes can be divided into two groups: CdABA, CdABA' for Cd(2+) and ZnABA
Karina Mariño et al.
Glycobiology, 21(10), 1317-1330 (2011-05-14)
Although the properties of milk oligosaccharides have been of scientific interest for many years, their structural diversity presents a challenging analytical task. In the quest for a simple and robust technology to characterize the different oligosaccharides present in milk, we
Udayanath Aich et al.
The FEBS journal, 278(10), 1699-1712 (2011-03-18)
Agglutination of red blood cells (RBCs), including chicken RBCs (cRBCs), has been used extensively to estimate viral titer, to screen glycan-receptor binding preference, and to assess the protective response of vaccines. Although this assay enjoys widespread use, some virus strains
Maja Pucić et al.
Molecular & cellular proteomics : MCP, 10(10), M111-M111 (2011-06-10)
All immunoglobulin G molecules carry N-glycans, which modulate their biological activity. Changes in N-glycosylation of IgG associate with various diseases and affect the activity of therapeutic antibodies and intravenous immunoglobulins. We have developed a novel 96-well protein G monolithic plate
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Methods and Matrices for Mass Spectrometry of Glycans

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Methods and matrices for mass spectrometry of glycans

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Glycan Labeling

Structural modifications of proteins are essential to living cells. When aberrantly regulated they are often the basis of disease. Glycans are responsible for much of the structural variation in biologic systems, and their representation on cell surfaces is commonly called the “glycome.”

Protokolle

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