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Merck

114367

Sigma-Aldrich

Bromocresol Green sodium salt

ACS reagent, 90% (HPLC), Dye content 90 %

Sinónimos:

3′,3″,5′,5″-Tetrabromo-m-cresolsulfonphthalein sodium salt

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About This Item

Fórmula empírica (notación de Hill):
C21H13Br4NaO5S
Número de CAS:
Peso molecular:
720.00
Número CE:
Número MDL:
Código UNSPSC:
12171500
ID de la sustancia en PubChem:
NACRES:
NA.47

grado

ACS reagent

Nivel de calidad

Agency

suitable for SM 2310
suitable for SM 2320

Ensayo

90% (HPLC)

Formulario

powder or crystals

composición

Dye content, 90%

visual transition interval

3.8, yellow(Visual Interval Pass)
3.8-5.2, yellow to blue
4.5, green
5.4, blue(Visual Interval Pass)

mp

230 °C (dec.) (lit.)

aplicaciones

diagnostic assay manufacturing
hematology
histology

temp. de almacenamiento

room temp

cadena SMILES

[Na+].Cc1c(Br)c(O)c(Br)cc1\C(=C2\C=C(Br)C(=O)C(Br)=C2C)c3ccccc3S([O-])(=O)=O

InChI

1S/C21H14Br4O5S.Na/c1-9-12(7-14(22)19(26)17(9)24)21(13-8-15(23)20(27)18(25)10(13)2)11-5-3-4-6-16(11)31(28,29)30-21;/h3-8,26-27H,1-2H3;/q;+1/p-1

Clave InChI

HEFSGAHJDGZCHA-UHFFFAOYSA-M

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Descripción general

Bromocresol Green (BCG), also known as bromcresol green, is a synthetic, anionic, triphenylmethane dye belonging to the phthalein and sulphonphthalein dyes group. It is commonly used as a pH indicator as it changes color from yellow to blue-green at pH 3.8-5.4. The monosodium salt of bromocresol green is highly ionizable in water. The dye at a higher pH level produces a large and weakly lipophilic dianion.

Aplicación

Bromocresol green serves as a pH indicator in biology and medicinal experiments.
  • It is used widely as a vital stain to study blood-brain permeability.
  • It is used as a tracking dye for DNA agarose gel electrophoresis, in protein determinations, and in charge-transfer complexation processes.
  • It is used in TLC for the visualization of compounds with functional groups whose pKa is below 5.0.
  • It has been used in the pH-sensitive colorimetric determination of glutamate decarboxylase activity.
  • It has also been employed in the evaluation of paper-analytical devices for colorimetric analysis of serum samples.
  • It is suitable as a selective inhibitor in kidney physiology studies.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Visite la Librería de documentos

Azo-functionalized superparamagnetic Fe3O4 nanoparticles: an efficient adsorbent for the removal of bromocresol green from contaminated water
Saad, et al.
Royal Society of Chemistry Advances, 12 (2022)
A high-throughput colorimetric assay to measure the activity of glutamate decarboxylase
Yu, et al.
Enzyme and Microbial Technology, 49(3) (2011)
Conn?s Biological Stains: A Handbook of Dyes, Stains and Fluorochromes for Use in Biology and Medicine (10th ed.)
RW Horobin, JA Kiernan (Eds.)
Conn?s Biological Stains (2002)
Preparation of Chitosan Poly(methacrylate) Composites for Adsorption of Bromocresol Green
Liu, et al.
ACS Omega, 4(7) (2019)
N Alizadeh et al.
Die Pharmazie, 63(11), 791-795 (2008-12-17)
Rapid and sensitive spectrophotometric methods are developed for the determination of lamotrigine (LTG) in pharmaceutical dosage forms and urine samples, based on the formation of the charge-transfer (CT) complexes between LTG as an n-donor and the acceptors: bromocresol green (BCG)

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