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Merck

35620

Supelco

2,6-Dichloroquinone-4-chloroimide

for spectrophotometric det. of vitamin B6, ≥99.0%

Sinónimos:

N,2,6-Trichloro-p-benzoquinoneimide, Gibb’s reagent

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About This Item

Fórmula empírica (notación de Hill):
C6H2Cl3NO
Número de CAS:
Peso molecular:
210.45
Beilstein:
2364249
Número CE:
Número MDL:
Código UNSPSC:
41116105
ID de la sustancia en PubChem:
NACRES:
NA.21

Nivel de calidad

Análisis

≥99.0% (AT)
≥99.0%

calidad

for spectrophotometric det. of vitamin B6

técnicas

UV/Vis spectroscopy: suitable

mp

65-67 °C (lit.)
65-68 °C

aplicaciones

food and beverages
vitamins, nutraceuticals, and natural products

temp. de almacenamiento

2-8°C

cadena SMILES

Cl\N=C1\C=C(Cl)C(=O)C(Cl)=C1

InChI

1S/C6H2Cl3NO/c7-4-1-3(10-9)2-5(8)6(4)11/h1-2H

Clave InChI

YHUMTHWQGWPJOQ-UHFFFAOYSA-N

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Descripción general

2,6-Dichloroquinone-4-chloroimide generally find application in being used as spot test and chromatographic spray reagents, mainly for phenols, though it can be used in detection of other types of compounds such as antioxidants, few primary and secondary amines, on silica gel chromatographic plates. Its decomposition rate is directly proportional to pressure.

Aplicación

Gibb′s reagent was used in paper chromatography, in an experiment conducted to semi-quantitatively estimate tyramine and octopamine.

Pictogramas

FlameExclamation mark

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Eye Irrit. 2 - Self-react. C - Skin Irrit. 2

Código de clase de almacenamiento

4.1A - Other explosive hazardous materials

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 P3 (EN 143) respirator cartridges


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Colour reaction of phenols with the gibbs reagent. The reaction mechanism and decomposition and stabilisation of the reagent.
Svobodova D
Microchimica Acta, 67 (3-4), 251-264 (1977)
P Miller et al.
Clinical chemistry, 36(4), 668-669 (1990-04-01)
In this nonenzymatic colorimetric method, dichlorobenzoquinone chloroimine is used as a color reagent to measure uric acid in urine. This method is less subject to the interferences that make enzymatic methods unreliable and is inexpensive, simple, and fast.
Colorimetric determination of prenalterol hydrochloride in dosage forms.
F A Aly et al.
Journal of pharmaceutical and biomedical analysis, 12(7), 955-958 (1994-07-01)
G G Mohamed et al.
Journal of pharmaceutical and biomedical analysis, 28(6), 1127-1133 (2002-06-07)
A simple, rapid and sensitive spectrophotometric method for the determination of sulbutamol in pure form and in different pharmaceutical preparations has been developed. The charge transfer (CT) reaction between salbutamol as electron donor and 2,6-dichloroquinone chlorimide (DCQ) and 7,7,8,8-tetracyanoquinodimethane (TCNQ)
Mohammad-Wadud Bhuiya et al.
Analytical biochemistry, 384(1), 151-158 (2008-10-18)
S-adenosyl-L-methionine (AdoMet)-dependent O-methyltransferases (OMTs) catalyze the transmethylation of a variety of phenolics in bacteria, plants, and humans. To rapidly characterize phenolic OMT activities, we adapted Gibbs' reagent, the dye originally used for detecting phenols, to develop a convenient assay method

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