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Brilliant Blue R Staining Solution_Molecular_structure_CAS_6104-59-2)
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Brilliant Blue R Staining Solution

Catalog No. B6529 Name Sigma Aldrich
CAS Number 6104-59-2 Website http://www.sigmaaldrich.com
M. F. C45H44N3NaO7S2 Telephone 1-800-521-8956
M. W. 825.96653 Fax
Purity Email
Storage Chembase ID: 106686

SYNONYMS

IUPAC name
sodium 3-({[4-({4-[(4-ethoxyphenyl)amino]phenyl}(4-{ethyl[(3-sulfonatophenyl)methyl]iminiumyl}cyclohexa-2,5-dien-1-ylidene)methyl)phenyl](ethyl)amino}methyl)benzene-1-sulfonate
IUPAC Traditional name
sodium 3-({[4-({4-[(4-ethoxyphenyl)amino]phenyl}(4-{ethyl[(3-sulfonatophenyl)methyl]iminio}cyclohexa-2,5-dien-1-ylidene)methyl)phenyl](ethyl)amino}methyl)benzenesulfonate
Synonyms
Brilliant indocyanin 6B
Acid Blue 83
Coomassie Brilliant Blue R
Brilliant Blue R

DATABASE IDS

Color Index Number 42660
Beilstein Number 5718025
PubChem SID 24891914
CAS Number 6104-59-2
MDL Number MFCD00041762

PROPERTIES

Apperance ethanol solution
Flash Point 27 °C
Flash Point 80.6 °F
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H226-H315-H319
European Hazard Symbols Irritant Irritant (Xi)
Personal Protective Equipment Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P305 + P351 + P338
RID/ADR UN 1170 3/PG 3
Risk Statements 10-36/38
Safety Statements 26
Hazard Class 3
UN Number 1170
Packing Group 3
German water hazard class 2

DETAILS

Description (English)
Components
0.5% (w/v) Brilliant Blue R, 45% (v/v) ethanol and 10% (v/v) acetic acid.
Analysis Note
Tested for suitability on agarose gels following immunoelectrophoresis.
Application
Brilliant Blue R staining solution is especially designed for use in staining protein in agarose gels following immunoelectrophoresis and Ouchterlony gels. The stain contains ethanol and acetic acid so gels do not require fixing prior to staining. The immunoelectrophoresis or Ouchterlony gel is first washed with water and saline to remove non-precipitated proteins and then dried. The gel is then immersed in staining solution for 30 min and destained with 10% acetic acid.
For detection of protein bands following electrophoresis.

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