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Merck
모든 사진(3)

Key Documents

I5763

Sigma-Aldrich

Indophenol

Powder

동의어(들):

Phenolindophenol

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C12H9NO2
CAS Number:
Molecular Weight:
199.21
Beilstein:
2095656
EC Number:
MDL number:
UNSPSC 코드:
12171500
PubChem Substance ID:
NACRES:
NA.47

product name

Indophenol,

형태

powder

색상

dark green to black

mp

>300 °C (lit.)

solubility

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

응용 분야

diagnostic assay manufacturing
hematology
histology

저장 온도

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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일반 설명

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

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
M Hassanain et al.
Brain research, 981(1-2), 201-209 (2003-07-30)
Previous studies have established that the expression of defensive rage behavior in the cat is mediated over reciprocal pathways that link the medial hypothalamus and the dorsolateral quadrant of the midbrain periaqueductal gray matter (PAG). The present study was designed
Bríd Aine Nic Dhonnchadha et al.
Behavioural brain research, 147(1-2), 175-184 (2003-12-09)
DOI [(+/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane] displays a high affinity for the rat 5-HT2A, 5-HT2B and 5-HT2C receptors (pKi 7.3, 7.4 and 7.8, respectively) and acts as an agonist. DOI (0.5-4 mg/kg, i.p. 30 min pre-test) increased the number of punished passages in the

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