Substance
ID:348280
Names and Identifiers
IUPAC Traditional name
carvedilol
IUPAC name
[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl][2-(2-methoxyphenoxy)ethyl]amine
Synonyms
BM-141901-(9H-Carbazol-4-yloxy)-3-[[2-(2-methoxyphenoxy)ethyl]amino]-2-propanolCarvedilol
Properties
Safety Information
GHS Hazard statements
H411
GHS Precautionary statements
P273
European Hazard Symbols
Nature polluting (N)Personal Protective Equipment
Eyeshields, Gloves
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
RID/ADR
UN 3077 9/PG 3
Safety Statements
61
German water hazard class
3
RTECS
UA8670000
Hazard Class
9
MSDS Link
Risk Statements
51/53
UN Number
3077
Packing Group
3
Physical Property
Solubility
DMSO: >20 mg/mL
Apperance
white to off-white solid
Product Information
Empirical Formula (Hill Notation)
C24H26N2O4
Purity
≥98% (HPLC)
Molecule Details
Biochem/physiol Actions
Cavedilol is a non-selective β-adrenergic blocker with α1 blocking activity. Carvedilol is used specifically for the treatment of heart failure and high blood pressure. It has been shown to improve left ventricular ejection fraction and may reduce mortality.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C3993.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Cavedilol is a non-selective β-adrenergic blocker with α1 blocking activity. Carvedilol is used specifically for the treatment of heart failure and high blood pressure. It has been shown to improve left ventricular ejection fraction and may reduce mortality.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C3993.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Molecular Spectra
No Data Available
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References
No Data Available
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