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Merck

294438

Sigma-Aldrich

4-Nitrobenzenediazonium tetrafluoroborate

97%

Sinónimos:

Azoic Diazo No. 37, Fast Red GG salt

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About This Item

Fórmula lineal:
C6H4N3O2 · BF4
Número de CAS:
Peso molecular:
236.92
Beilstein/REAXYS Number:
3599869
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

assay

97%

form

powder

composition

Carbon 29.3-31.5%,Nitrogen 17.1-18.4%

color

light brown

mp

144-148 °C (dec.)

solubility

acetonitrile: 50 mg/mL

density

1.66 g/cm3 at 25 °C

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

2-8°C

SMILES string

F[B-](F)(F)F.[O-][N+](=O)c1ccc(cc1)[N+]#N

InChI

1S/C6H4N3O2.BF4/c7-8-5-1-3-6(4-2-5)9(10)11;2-1(3,4)5/h1-4H;/q+1;-1

InChI key

AFULQCYCQAHYIP-UHFFFAOYSA-N

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General description

4-Nitrobenzenediazonium tetrafluoroborate, also known as Fast Red GG is a Diazonium salt/diazo dye. It is commonly used for the histochemical detection of bilirubin and indolamines.

Application

4-Nitrobenzenediazonium tetrafluoroborate has been used in ellipsometry. It has also been used for surface modification of carbon nanotubes (CNTs).

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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A highly sensitive and simplified method for the differential determination of serum ketone bodies has been developed. Serum was deproteinized with perchloric acid, and acetoacetate contained in the supernate was reacted with newly synthesized p-nitrobenzene diazonium fluoroborate at 37 degrees
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Biokhimiia (Moscow, Russia), 46(2), 369-375 (1981-02-01)
p-Nitrophenyldiazonium chloride was found to modify the Tyr-75 and Tyr-189 residues in aspergillopepsin A. Incubation of the protein with a 45-fold molar excess of the reagent at pH 5,2 results in the attachment of 1,8 inhibitor residues, which leads to
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