Skip to Content
Merck
CN

R115

Reactive Blue 2

Synonym(s):

1-Amino-4-[[4-[[4-chloro-6-[[3 (or 4)-sulfophenyl]amino]-1,3,5-triazin-2-yl]amino]-3-sulfophenyl]amino]-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid, Basilen Blue E-3G, Cibacron Blue F3G-A, Cibacron Blue F3GA, GST Inhibitor-1, Procion® Blue H-B

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C29H17ClN7Na3O11S3
CAS Number:
Molecular Weight:
840.10
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
249-524-3
Beilstein/REAXYS Number:
6561550
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

SMILES string

[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].Nc1c(cc(Nc2ccc(Nc3nc(Cl)nc(Nc4ccc(cc4)S([O-])(=O)=O)n3)c(c2)S([O-])(=O)=O)c5C(=O)c6ccccc6C(=O)c15)S([O-])(=O)=O.Nc7c(cc(Nc8ccc(Nc9nc(Cl)nc(Nc%10cccc(c%10)S([O-])(=O)=O)n9)c(c8)S([O-])(=O)=O)c%11C(=O)c%12ccccc%12C(=O)c7%11)S([O-])(=O)=O

color

dark blue

solubility

H2O: soluble

Biochem/physiol Actions

P2Y purinoceptor antagonist; most potent antagonist for ATP-activated channels.

Legal Information

Procion is a registered trademark of Dystar Textilfarben GmbH & Co.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

T A Anikina et al.
Bulletin of experimental biology and medicine, 152(6), 672-674 (2012-07-18)
We studied the effect of uridine 5'-triphosphate in concentrations of 10(-10)-10(-6) M on myocardial contractile activity in 7-100-day-old rats. Analysis of isometric contraction of myocardial strips showed that uridine 5'-triphosphate reduced the strength of myocardial contraction in rats of all
Mehmet Odabası
Preparative biochemistry & biotechnology, 41(3), 287-304 (2011-06-11)
Cibacron Blue F3GA was covalently attached onto magnetic poly(vinyl alcohol) (mPVAL) beads (100-150 μm in diameter) for human serum albumin (HSA) adsorption from human plasma. Despite low nonspecific adsorption of HSA on mPVAL beads, Cibacron Blue F3GA attachment significantly increased
Miao Li et al.
Protein and peptide letters, 20(4), 459-466 (2012-09-29)
From the fresh fruiting bodies of the mushroom Pleurotus eryngii a phytase with a molecular mass of 14 kDa was isolated. The isolation protocol entailed ion exchange chromatography on DEAE-cellulose and CM-cellulose, affinity chromatography on Affi-gel blue gel, and ion
K Nakazawa et al.
Pflugers Archiv : European journal of physiology, 418(3), 214-219 (1991-04-01)
The effects of suramin, reactive blue 2 (RB2) and d-tubocurarine (d-TC) were investigated electrophysiologically to elucidate the mechanisms underlying their antagonism of P2 purinoceptor-mediated responses. All three compounds inhibited an adenosine triphosphate (ATP)-activated inward current in rat phaeochromocytoma PC12 cells
Yuji Kado et al.
Journal of biochemistry, 151(4), 447-455 (2012-03-16)
In mast and Th2 cells, hematopoietic prostaglandin (PG) D synthase (H-PGDS) catalyses the isomerization of PGH(2) in the presence of glutathione (GSH) to produce the allergic and inflammatory mediator PGD(2). We determined the X-ray structures of human H-PGDS inhibitor complexes

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service