Skip to Content
Merck

D9026

Digoxigenin

analytical standard

Synonym(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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C23H34O5
CAS Number:
1672-46-4
Molecular Weight:
390.51
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329798887
EC Number:
216-806-2
Beilstein/REAXYS Number:
96479
MDL number:
MFCD00871861

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

analytical standard

Quality Level

100

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

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

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

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.

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.

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

Storage Class

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000147209
0000147208
0000147208
0000147209
0000147210

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Identification and Quantification of Cardiac Glycosides in Blood and Urine Samples by HPLC/MS/MS
Guan F, et al.
American Chemical Science Journal (1999)
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
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
Simone Dealtry et al.
Applied and environmental microbiology, 80(13), 4012-4020 (2014-04-29)
Biopurification systems (BPS) are used on farms to control pollution by treating pesticide-contaminated water. It is assumed that mobile genetic elements (MGEs) carrying genes coding for enzymes involved in degradation might contribute to the degradation of pesticides. Therefore, the composition
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
View All Related Papers

Global Trade Item Number

SKUGTIN
D9026-25MG04061838343895
D9026-500MG04061833651605
D9026-100MG04061833590140

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service