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Merck

D9026

Digoxigenin

analytical standard

Synonyme(s) :

3β,12β,14β,21-Tetrahydroxy-20(22)-norcholenic acid lactone, 3β,12β,14-Trihydroxy-5β,20(22)-cardenolide, 5β,20(22)-Cardenolide-3β,12β,14-triol, Lanadigigenin

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About This Item

Formule empirique (notation de Hill) :
C23H34O5
Numéro CAS:
Poids moléculaire :
390.51
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
216-806-2
Beilstein/REAXYS Number:
96479
MDL number:

Nom du produit

Digoxigenin, analytical standard

InChI

1S/C23H34O5/c1-21-7-5-15(24)10-14(21)3-4-17-18(21)11-19(25)22(2)16(6-8-23(17,22)27)13-9-20(26)28-12-13/h9,14-19,24-25,27H,3-8,10-12H2,1-2H3/t14-,15+,16-,17-,18+,19-,21+,22+,23+/m1/s1

InChI key

SHIBSTMRCDJXLN-KCZCNTNESA-N

SMILES string

C[C@]12CC[C@H](O)C[C@H]1CC[C@@H]3[C@@H]2C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C5=CC(=O)OC5

grade

analytical standard

agency

EPA 1694

assay

≥98% (HPLC)

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

222 °C (lit.)

application(s)

environmental
food and beverages
forensics and toxicology
veterinary

format

neat

functional group

ketone

storage temp.

room temp

Quality Level

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Application

Digoxigenin is used as an analytical reference standard for the quantification of the analyte in biological samples using high-performance liquid chromatography couped to tandem mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Digoxigenin is a therapeutic drug belonging to the group of cardiac glycosides, widely used in the management of congestive heart failure and other cardiac diseases.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 1 Oral - Acute Tox. 2 Dermal

Classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3


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Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Identification and Quantification of Cardiac Glycosides in Blood and Urine Samples by HPLC/MS/MS
Guan F, et al.
American Chemical Science Journal (1999)
Christine E Tinberg et al.
Nature, 501(7466), 212-216 (2013-09-06)
The ability to design proteins with high affinity and selectivity for any given small molecule is a rigorous test of our understanding of the physiochemical principles that govern molecular recognition. Attempts to rationally design ligand-binding proteins have met with little
Joan Camunas-Soler et al.
Nucleic acids research, 43(5), 2767-2779 (2015-02-19)
DNA bis-intercalators are widely used in molecular biology with applications ranging from DNA imaging to anticancer pharmacology. Two fundamental aspects of these ligands are the lifetime of the bis-intercalated complexes and their sequence selectivity. Here, we perform single-molecule optical tweezers
Guillaume Cornelis et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(41), E4332-E4341 (2014-10-01)
Syncytins are fusogenic envelope (env) genes of retroviral origin that have been captured for a function in placentation. Syncytins have been identified in Euarchontoglires (primates, rodents, Leporidae) and Laurasiatheria (Carnivora, ruminants) placental mammals. Here, we searched for similar genes in
Vicki Adams et al.
Applied and environmental microbiology, 80(12), 3597-3603 (2014-04-01)
TnpX is a site-specific recombinase responsible for the excision and insertion of the transposons Tn4451 and Tn4453 in Clostridium perfringens and Clostridium difficile, respectively. Here, we exploit phenotypic features of TnpX to facilitate genetic mutagenesis and complementation studies. Genetic manipulation

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