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46130

Supelco

4-Aminoazobenzene

analytical standard

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Synonym(s):
4-Phenylazoaniline
Linear Formula:
C6H5N=NC6H4NH2
CAS Number:
60-09-3
Molecular Weight:
197.24
Colour Index Number:
11000
Beilstein:
1913042
EC Number:
200-453-6
MDL number:
MFCD00007854
UNSPSC Code:
41116107
PubChem Substance ID:
329757079
NACRES:
NA.24

grade

analytical standard

Quality Level

100

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

>360 °C (lit.)

mp

123-126 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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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Related Categories

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Statements

H302,H317,H350,H410

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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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John H Petropoulos et al.
International journal of pharmaceutics, 437(1-2), 178-191 (2012-08-28)
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
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
Frederic Delbecq et al.
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
Ana Neto et al.
Development (Cambridge, England), 139(2), 301-311 (2011-12-02)
Vertebrate odd-skipped related genes (Osr) have an essential function during the formation of the intermediate mesoderm (IM) and the kidney structures derived from it. Here, we show that these genes are also crucial for limb bud formation in the adjacent
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