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About This Item
Empirical Formula (Hill Notation):
C12H9NO2
CAS Number:
Molecular Weight:
199.21
Beilstein:
2095656
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47
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Product Name
Indophenol,
form
powder
Quality Level
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Marczenko Z and Balcerzak M
Separation, Preconcentration and Spectrophotometry in Inorganic Analysis (2000)
Handbook of Acid-Base Indicators (2007)
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
Martin Hadamitzky et al.
Behavioural brain research, 204(1), 88-92 (2009-05-27)
Impulsivity or diminished inhibitory control of behavior (impulse control) is a prominent feature of several neuropsychiatric diseases. Serotonin (5-HT) plays an important role in impulse control. In order to examine the role of 5-HT2 receptors in a network comprising the
Roberto Amici et al.
Brain research, 996(1), 9-18 (2003-12-13)
Serotonin [5-hydroxytryptamine (5-HT)] plays an inhibitory role in rapid-eye-movement (REM) sleep although the exact mechanism(s) and site(s) of action are not known. It is commonly assumed that 5-HT exerts its influence on REM sleep via input from the dorsal raphe
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