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Idarubicin hydrochloride_Molecular_structure_CAS_57852-57-0)
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Idarubicin hydrochloride

Catalog No. I1656 Name Sigma Aldrich
CAS Number 57852-57-0 Website http://www.sigmaaldrich.com
M. F. C26H27NO9 Telephone 1-800-521-8956
M. W. 497.49388 Fax
Purity Email
Storage Chembase ID: 1048

SYNONYMS

IUPAC name
(7S,9S)-9-acetyl-7-{[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy}-6,9,11-trihydroxy-5,7,8,9,10,12-hexahydrotetracene-5,12-dione
IUPAC Traditional name
idarubicin
Synonyms
(7S-cis)-9-Acetyl-7-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-5,12-naphthacenedione
DMDR
IMI-30
Idamycin

DATABASE IDS

EC Number 260-990-7
CAS Number 57852-57-0
PubChem SID 24278488
MDL Number MFCD00866457

PROPERTIES

Empirical Formula (Hill Notation) C26H27NO9 · HCl
Shipped in wet ice
Apperance solid
GHS Pictograms GHS06
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H300-H351-H360
European Hazard Symbols Highly toxic Highly toxic (T+)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P201-P264-P281-P301 + P310-P308 + P313
RID/ADR UN 2811 6.1/PG 2
Risk Statements 60-61-28-40
RTECS HB7877000
Safety Statements 53-45
Storage Temperature 2-8°C
Hazard Class 6.1
UN Number 2811
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
Idarubicin is an anthracycline antibiotic that is an anti-leukemia agent with higher DNA binding capacity and greater cytotoxicity than daunorubicin.
Biochem/physiol Actions
Topoisomerase II inhibitor
Description (简体中文)
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
Idarubicin is an anthracycline antibiotic that is an anti-leukemia agent with higher DNA binding capacity and greater cytotoxicity than daunorubicin.
Biochem/physiol Actions
Topoisomerase II inhibitor

REFERENCES