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359556

Sigma-Aldrich

4-Azidoaniline hydrochloride

97%

Sinônimo(s):

4-Aminophenyl azide hydrochloride

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250 MG
R$ 843,00
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250 MG
R$ 843,00
1 G
R$ 2.504,00

About This Item

Fórmula linear:
N3C6H4NH2 · HCl
Número CAS:
91159-79-4
Peso molecular:
170.60
Beilstein:
7942921
Número MDL:
MFCD00043274
Código UNSPSC:
12352100
ID de substância PubChem:
24862089
NACRES:
NA.22

R$ 843,00

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Ensaio

97%

adequação da reação

reaction type: click chemistry

pf

165 °C (dec.) (lit.)

grupo funcional

azide

cadeia de caracteres SMILES

Cl.Nc1ccc(cc1)N=[N+]=[N-]

InChI

1S/C6H6N4.ClH/c7-5-1-3-6(4-2-5)9-10-8;/h1-4H,7H2;1H

chave InChI

SDYAJRBHPPWHSF-UHFFFAOYSA-N

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Aplicação

4-Azidoaniline hydrochloride is suitable for use in the preparation of photo-reactive polymers, poly(acrylic acid) having encorporated phenylazido groups.[1] It may be used in the preparation of 1-(4-aminophenyl)-1H-[1,2,3]-triazol-4-ylcarbonyl-Phe-Gly-Phe-Gly-OH.[2] It is suitable for use in the synthesis of photo-reactive polysaccharides.[3]

Pictogramas

FlameSkull and crossbones
GHS02,GHS06

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

4.1B - Flammable solid hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
STBH8829
STBG1960V
STBF0875V
STBD9378V
BCBG8985V

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R Barbucci et al.
Biomaterials, 24(6), 915-926 (2002-12-31)
Surface microfabrication techniques were widely utilised for the spatial control of in vitro cell behaviour. A photo-immobilisation procedure was utilised to create micropatterned surfaces: four different stripe patterns (100, 50, 25 and 10 microm) of hyaluronan (Hyal) and its sulphated
Y Ito et al.
Journal of biomaterials science. Polymer edition, 12(4), 367-378 (2001-07-05)
Heparin was immobilized on a polystyrene plate in a graded micropattern by photolithography. The micropattern was confirmed by staining with brilliant green. In the presence of basic fibroblast growth factor (bFGF), the growth of NIH3T3 cells was enhanced only in
D Stangl et al.
Biochemistry, 30(35), 8605-8611 (1991-09-03)
Calcitonin gene-related peptide (CGRP) receptors were solubilized from human (h) cerebellum with use of the zwitterionic detergent 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonic acid (CHAPS). Scatchard analysis of equilibrium binding data indicated that the soluble extract contained a single class of CGRP binding sites with
D R Nisbet et al.
Journal of biomedical materials research. Part A, 89(1), 24-35 (2008-04-12)
In this study, thermoresponsive xyloglucan hydrogel scaffolds were investigated as candidates for neural tissue engineering of the spinal cord. The hydrogels were optimized to provide similar mechanical properties to that of native spinal cord, although also being functionalized through the
Christian W Tornøe et al.
The Journal of organic chemistry, 67(9), 3057-3064 (2002-04-27)
The cycloaddition of azides to alkynes is one of the most important synthetic routes to 1H-[1,2,3]-triazoles. Here a novel regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes to azides on solid-phase is reported. Primary, secondary, and tertiary alkyl azides, aryl azides
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