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B1064

Cibacron Blue 3G-A

Dye content ≥55 %, Powder

Synonym(s):

Cibacron Blue; 1-amino-4-[4-[[4-chloro-6-(2-sulfoanilino)-1,3,5-triazin-2-yl]amino]-3-sulfoanilino]-9,10-dioxoanthracene-2-sulfonic acid

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About This Item

Empirical Formula (Hill Notation):
C29H20ClN7O11S3
CAS Number:
Molecular Weight:
774.16
MDL number:
UNSPSC Code:
12171500
NACRES:
NA.47
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Product Name

Cibacron Blue 3G-A, Dye content ≥55 %

form

powder

Quality Level

composition

Dye content, ≥55%

color

dark blue

solubility

H2O: 10 mg/mL, blue

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Nc1c(cc(Nc2ccc(Nc3nc(Cl)nc(Nc4ccccc4S(O)(=O)=O)n3)c(c2)S(O)(=O)=O)c5C(=O)c6ccccc6C(=O)c15)S(O)(=O)=O

InChI

1S/C29H20ClN7O11S3/c30-27-35-28(33-16-7-3-4-8-19(16)49(40,41)42)37-29(36-27)34-17-10-9-13(11-20(17)50(43,44)45)32-18-12-21(51(46,47)48)24(31)23-22(18)25(38)14-5-1-2-6-15(14)26(23)39/h1-12,32H,31H2,(H,40,41,42)(H,43,44,45)(H,46,47,48)(H2,33,34,35,36,37)

InChI key

YKCWQPZFAFZLBI-UHFFFAOYSA-N

Application

When immobilized using an insoluble porous support matrix such as agarose, Cibacron Blue 3GA is used for affinity chromatography purification of enzymes.[1] This affinity has been attributed to a structural similarity between the dye and the natural ligands for proteins with cofactor binding domains.[2]

Biochem/physiol Actions

Cibacron Blue 3GA is an anionic anthraquinone dye. It acts as a P2-purinoceptor antagonist[3] and inhibits stimulus-evoked glutamate release by rat brain cortical tissue.[4] Cibacron Blue 3GA inhibits OXA-1[5] and OXA-2 β-lactamases[6] and was used to observe the binding of ligands to OXA-1 β-lactamase by monitoring tryptophan fluorescence.

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This Item
A315716030B5388
color

dark blue

color

dark blue

color

-

color

-

solubility

H2O: 10 mg/mL, blue

solubility

water: 1 mg/mL, blue

solubility

methanol: 0.01 g/10 mL, blue to very deep blue

solubility

water: 1 mg/mL, blue to very deep blue

form

powder

form

powder or crystals

form

powder

form

powder

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

composition

Dye content, ≥55%

composition

Dye content, ≥50%

composition

-

composition

Dye content, ≥60%


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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W O Smith et al.
Plant physiology, 68(2), 443-446 (1981-08-01)
The binding of phytochrome to Cibacron Blue 3GA was utilized to develop a new affinity purification procedure for phytochrome. Brushite-purified phytochrome from rye (Secale cereale c.v. Cougar) was bound to agarose-immobilized blue dye in 0.1 molar potassium phosphate (pH 7.8)
S T Thompson et al.
Proceedings of the National Academy of Sciences of the United States of America, 72(2), 669-672 (1975-02-01)
A procedure is described to utilize blue dextran-Sepharose as an affinity chromatographic column specific for the super-secondary structure called the dinucleotide fold, which forms the binding sites for substrates and effectors on a wide range of proteins. The procedure can
I von Kügelgen et al.
British journal of pharmacology, 113(3), 815-822 (1994-11-01)
1. Some postganglionic sympathetic axons possess P2Y-like P2-purinoceptors which, when activated, decrease the release of noradrenaline. We examined the question of whether such receptors also occur at the noradrenergic axons in the rat brain cortex. Slices of the brain cortex



Global Trade Item Number

SKUGTIN
B1064-1G04061832340036

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