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I5763

Sigma-Aldrich

Indophenol

Powder

Synonym(s):

Phenolindophenol

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About This Item

Empirical Formula (Hill Notation):
C12H9NO2
CAS Number:
500-85-6
Molecular Weight:
199.21
Beilstein/REAXYS Number:
2095656
EC Number:
207-913-5
MDL number:
MFCD00001621
UNSPSC Code:
12171500
PubChem Substance ID:
24896077
NACRES:
NA.47

product name

Indophenol,

form

powder

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

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General description

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.
Indophenol method is common for the determination of ammonia. The reaction gives a blue product, which is measured spectrophotometrically.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Marczenko Z and Balcerzak M
Separation, Preconcentration and Spectrophotometry in Inorganic Analysis (2000)
Handbook of Acid-Base Indicators (2007)
Sonia Senra-Ferreiro et al.
Talanta, 85(3), 1448-1452 (2011-08-03)
A miniaturized method based on liquid-phase microextraction (LPME) in combination with microvolume UV-vis spectrophotometry for monitoring ammonia in waters is proposed. The methodology is based on the extraction of the ion pair formed between the blue indophenol obtained according to
Analía Bortolozzi et al.
The European journal of neuroscience, 18(5), 1235-1246 (2003-09-06)
In the rat, postsynaptic 5-hydroxytryptamine2A receptors medial prefrontal cortex control the activity of the serotonergic system through changes in the activity of pyramidal neurons projecting to the dorsal raphe nucleus. Here we extend these observations to mouse brain. The prefrontal
M Olga Rojas-Corrales et al.
Psychopharmacology, 190(2), 221-231 (2006-11-15)
The selective serotonin (5-HT) reuptake inhibitors (SSRIs) represent the first-line pharmacotherapy for obsessive-compulsive disorder (OCD), and atypical antipsychotic drugs, which block 5-HT2A receptors, are used in augmentation strategies. Opiate drugs are also effective in treatment-refractory OCD and Tourette syndrome. The
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