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I5763

Indophenol

Powder

Synonym(s):

Phenolindophenol

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Pack SizeSKUAvailabilityPrice
1 g
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CZK 2,660.00

About This Item

Empirical Formula (Hill Notation):
C12H9NO2
CAS Number:
Molecular Weight:
199.21
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
207-913-5
MDL number:
Beilstein/REAXYS Number:
2095656

CZK 2,660.00


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Product Name

Indophenol,

form

powder

Quality Segment

color

dark green to black

mp

>300 °C (lit.)

solubility

1 M NaOH: 10 mg/mL, clear, blue to very deep blue

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Oc1ccc(cc1)N=C2C=CC(=O)C=C2

InChI

1S/C12H9NO2/c14-11-5-1-9(2-6-11)13-10-3-7-12(15)8-4-10/h1-8,14H

InChI key

RSAZYXZUJROYKR-UHFFFAOYSA-N

General description

Indophenol method is common for the determination of ammonia. The reaction gives a blue product, which is measured spectrophotometrically.
Indophenol is used in hair dyes, redox materials, lubricants, liquid crystal displays, biosensor and fuel cells. It is toxic to fishes and is implicated in environmental pollution.

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This Item
330574D1878215643
color

dark green to black

color

-

color

-

color

-

solubility

1 M NaOH: 10 mg/mL, clear, blue to very deep blue

solubility

-

solubility

H2O: soluble 10 mg/mL, clear, blue to very deep blue

solubility

1 M NH4OH: 10 mg/mL, opaque, blue

form

powder

form

powder

form

powder

form

powder

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
food and beverages
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

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

-


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



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Handbook of Acid-Base Indicators (2007)
Marczenko Z and Balcerzak M
Separation, Preconcentration and Spectrophotometry in Inorganic Analysis (2000)
C Bishop et al.
Neuroscience, 121(3), 649-657 (2003-10-22)
Loss of dopaminergic innervation to the striatum increases the sensitivity of dopamine (DA) D1 and serotonin (5-HT) 5-HT2 receptor signaling. Previous work from our laboratory has shown that systemic co-administration of D1 and 5-HT2 receptor agonists leads to the synergistic



Global Trade Item Number

SKUGTIN
I5763-5G04061833857564
I5763-1G04061833857557

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