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Merck

A8524

Aniline hydrochloride

≥99%

Sinónimos:

Anilinium chloride, Benzenamine hydrochloride, Phenylamine hydrochloride, Phenylammonium chloride

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5 G

MXP 1,979.00

50 G

MXP 2,364.00

MXP 1,979.00

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Fórmula lineal:
C6H5NH2 · HCl
Número CAS:
142-04-1
Peso molecular:
129.59
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57653890
EC Number:
205-519-8
Beilstein/REAXYS Number:
3593823
MDL number:
MFCD00012958

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Nombre del producto

Aniline hydrochloride, ≥99%

InChI key

MMCPOSDMTGQNKG-UHFFFAOYSA-N

InChI

1S/C6H7N.ClH/c7-6-4-2-1-3-5-6;/h1-5H,7H2;1H

SMILES string

Cl.Nc1ccccc1

vapor density

4.46 (vs air)

assay

≥99%

form

crystals

mp

196-198 °C (lit.)

Quality Level

200

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1 of 4

Este artículo
222100331546A41607
Aniline hydrochloride ≥99%

Sigma-Aldrich

A8524

Aniline hydrochloride

4-(Hexyloxy)aniline 99%

Sigma-Aldrich

222100

4-(Hexyloxy)aniline

2,5-Bis(trifluoromethyl)aniline 99%

Sigma-Aldrich

331546

2,5-Bis(trifluoromethyl)aniline

2-(Trifluoromethyl)aniline 99%

Sigma-Aldrich

A41607

2-(Trifluoromethyl)aniline

assay

≥99%

assay

99%

assay

99%

assay

99%

Quality Level

200

Quality Level

100

Quality Level

200

Quality Level

100

form

crystals

form

-

form

liquid

form

liquid

mp

196-198 °C (lit.)

mp

43-45 °C (lit.)

mp

-

mp

34 °C (lit.)

vapor density

4.46 (vs air)

vapor density

-

vapor density

-

vapor density

-

Biochem/physiol Actions

The acute toxicity of aniline involves its activation in vivo to 4-hydroxyaniline and the formation of adducts with hemoglobin. In erythrocytes, this is associated with the release of iron and the accumulation of methemoglobin and the development of hemolytic anemia and inflammation of the spleen. Tumor formation is often observed in the spleen on prolonged administration.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Skin Sens. 1 - STOT RE 1

Clase de almacenamiento

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

wgk

WGK 3

flash_point_f

381.2 °F - closed cup

flash_point_c

194 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCB4501
BCCB4481
BCCB4502
BCBZ4920
BCBV1466

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Noor Mohammad et al.
Scientific reports, 10(1), 13412-13412 (2020-08-10)
This study presents the preparation of membranes of polylactic acid (PLLA), polyacrylonitrile (PAN) and their corresponding membranes coated with polyaniline (PANI) for the adsorption of methylene blue (MB). Scanning electron microscopy micrographs reveal that all the membranes exhibit nanofibrous morphology.
Conghui Tang et al.
Journal of the American Chemical Society, 134(46), 18924-18927 (2012-11-08)
A novel and efficient copper-catalyzed azidation reaction of anilines via C-H activation has been developed. This method, in which the primary amine acts as a directing group by coordinating to the metal center, provides ortho azidation products regioselectively under mild
Huihui Yang et al.
Electrophoresis, 34(4), 510-517 (2012-11-23)
A novel (3-sulfopropyl methacrylate potassium)-silica hybrid monolithic column for CEC has been prepared by a simple one-pot approach based on efficient thiol-ene click chemistry. In this process, the polycondensation of hydrolyzed alkoxysilanes and in situ click reaction of vinyl groups
Roman Spesyvtsev et al.
Faraday discussions, 157, 165-179 (2012-12-13)
Femtosecond time-resolved photoelectron imaging is employed to investigate ultrafast electronic relaxation in aniline, a prototypical aromatic amine. The molecule is excited at wavelengths between 269 and 238 nm. We observe that the S2(pi3s/pi sigma*) state is populated directly during the
Wen Chen et al.
Journal of the American Chemical Society, 135(11), 4438-4449 (2013-03-02)
A series of linear and cyclic, sequence controlled, DNA-conjoined copolymers of aniline (ANi) and 2,5-bis(2-thienyl)pyrrole (SNS) were synthesized. In one approach, linear copolymers were prepared from complementary DNA oligomers containing covalently attached SNS and ANi monomers. Hybridization of the oligomers
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