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この商品について
実験式(ヒル表記法):
C23H34O5
CAS番号:
分子量:
390.51
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
216-806-2
Beilstein/REAXYS Number:
96479
MDL number:
製品名
ジゴキシゲニン, analytical standard
InChI key
SHIBSTMRCDJXLN-KCZCNTNESA-N
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
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 1 Oral - Acute Tox. 2 Dermal
保管分類
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
Identification and Quantification of Cardiac Glycosides in Blood and Urine Samples by HPLC/MS/MS
Guan F, et al.
American Chemical Science Journal (1999)
Suzanne E McGaugh et al.
Nature communications, 5, 5307-5307 (2014-10-21)
Natural populations subjected to strong environmental selection pressures offer a window into the genetic underpinnings of evolutionary change. Cavefish populations, Astyanax mexicanus (Teleostei: Characiphysi), exhibit repeated, independent evolution for a variety of traits including eye degeneration, pigment loss, increased size
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
François Redelsperger et al.
Journal of virology, 88(14), 7915-7928 (2014-05-03)
Syncytin genes are fusogenic envelope protein (env) genes of retroviral origin that have been captured for a function in placentation. Within rodents, two such genes have previously been identified in the mouse-related clade, allowing a demonstration of their essential role
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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