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CAS RN: 9041-93-4 | Product Number: B3972

Bleomycin Sulfate (mixture)


Purity: >85.0%(HPLC)
Synonyms:
Product Documents:
10MG
€144.00
2   ≥100 
50MG
€561.00
2   ≥100 

*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).


Supplemental Product Information:

This product has not been tested for potency and is guaranteed for chemical purity.

Product Number B3972
Purity / Analysis Method >85.0%(HPLC)
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Hygroscopic,Heat Sensitive
CAS RN 9041-93-4
Related CAS RN 11056-06-7
PubChem Substance ID 253659941
Merck Index (14) 1318
MDL Number

MFCD00070310

Specifications
Appearance White to Light yellow powder to crystal
Purity(HPLC) min.85.0 area% (Sum of A2,B2)
BleomycinA2 55.0 to 70.0 area%
BleomycinB2 25.0 to 32.0 area%
Properties (reference)
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H351 : Suspected of causing cancer.
Precautionary Statements P501 : Dispose of contents/ container to an approved waste disposal plant.
P202 : Do not handle until all safety precautions have been read and understood.
P201 : Obtain special instructions before use.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P308 + P313 : IF exposed or concerned: Get medical advice/ attention.
P405 : Store locked up.
Related Laws:
EC Number 232-925-2
RTECS# EC5991990
Transport Information:
HS Number 2941900000
Application
Quorum sensing inhibitor

Reference


Application
Adeno-associated virus vector transduction enhancer

Bleomycin increases transduction by adeno-associated virus (AAV) vectors.1)

References


Application
Reagent for pneumonitis model

References


Application
Reagent for pulmonary fibrosis model

References


Application
Bleomycin: A Glycopeptide Antitumor Antibiotics Agent

Bleomycin, a glycopeptide antitumor antibiotic agent, was first discovered in 1966 when the Japanese bacteriologist Umezawa found anticancer activity while screening culture filtrates of Streptomyces verticillus. Activated bleomycin (Fe-bleomycin-O2 complex), the active species, forms in the reaction of bleomycin with Fe(II) and O2. It also forms in the reaction of bleomycin with Fe(III) and peroxide, or bleomycin with superoxide and either Fe(III) or Fe(II). The activated bleomycin produces DNA strand break at 3'-4' bond in a deoxyribose sugar moiety. The mechanism of this bond cleavage reaction and the nature of the active oxidizing species are still open issues.

References


PubMed Literature


TCIMAIL
Product Documents (Note: Some products will not have analytical charts available.)
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