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Merck
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주요 문서

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186368

Sigma-Aldrich

4-Aminoazobenzene

98%

동의어(들):

4-Phenylazoaniline

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모든 사진(1)

About This Item

Linear Formula:
C6H5N=NC6H4NH2
CAS Number:
60-09-3
Molecular Weight:
197.24
색상 지수 번호:
11000
Beilstein:
1913042
EC Number:
200-453-6
MDL number:
MFCD00007854
UNSPSC 코드:
12171500
PubChem Substance ID:
24851216
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분석

98%

bp

>360 °C (lit.)

mp

123-126 °C (lit.)

λmax

386 nm

SMILES string

Nc1ccc(cc1)\N=N/c2ccccc2

InChI

1S/C12H11N3/c13-10-6-8-12(9-7-10)15-14-11-4-2-1-3-5-11/h1-9H,13H2/b15-14+

InChI key

QPQKUYVSJWQSDY-CCEZHUSRSA-N

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픽토그램

Health hazardExclamation markEnvironment
GHS08,GHS07,GHS09

신호어

Danger

유해 및 위험 성명서

H302,H317,H350,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

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

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시험 성적서(COA)

Lot/Batch Number
MKBL6968V
08810AE
08128PD
18322DD
18503CB

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Kristina B Clark et al.
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Depression of the peripheral blood platelet count during acute infection is a hallmark of dengue. This thrombocytopenia has been attributed, in part, to an insufficient level of platelet production by megakaryocytes that reside in the bone marrow (BM). Interestingly, it
G Venkatesh et al.
Journal of fluorescence, 21(4), 1485-1497 (2011-02-03)
Spectral characteristics of 1-(2,4-diamino phenylazo) naphthalene (FBRR, fat brown RR) and 4-aminoazobenzene (AAB) have been studied in various solvents, varying hydrogen ion concentrations and in β-cyclodextrin (β-CD). The inclusion complex of FBRR and AAB with β-CD were analysed by UV-visible
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Journal of colloid and interface science, 384(1), 94-98 (2012-07-24)
A "light-triggerable" azobenzene amine derivative (additive 1) was synthesized and then introduced into organogels of 12-hydroxystearic acid (HSA) in the molar ratio of 1:3. The organogels (HSA/1) consisting of additive 1 and HSA were analyzed by (1)H nuclear magnetic resonance
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An account is presented of modeling and experimental work, which complements, in many useful ways, the excellent coverage, afforded by a recent dedicated issue edited by Siepmann and Peppas (Int. J. Pharm. 2011, 418(1)), of the theoretical background and many
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