133310
Aniline hydrochloride
97%
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About This Item
Linear Formula:
C6H5NH2 · HCl
CAS Number:
Molecular Weight:
129.59
EC Number:
205-519-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3593823
MDL number:
vapor density
4.46 (vs air)
assay
97%
mp
196-198 °C (lit.)
SMILES string
Cl.Nc1ccccc1
InChI
1S/C6H7N.ClH/c7-6-4-2-1-3-5-6;/h1-5H,7H2;1H
InChI key
MMCPOSDMTGQNKG-UHFFFAOYSA-N
Application
Aniline hydrochloride was used in the preparation of polyaniline coated poly(styrene-co-styrene sulfonate) nanoparticles. It was used to study the induction of Nei-like DNA glycosylases (NEIL1/2)-mediated base excision repair(BER) in rat spleen and 8-oxoguanine glycosylase 1-mediated BER due to aniline exposure.
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.
Other Notes
This product has been replaced by A8524-ALDRICH | Aniline hydrochloride ≥99%
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
Storage Class
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
Regulatory Information
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Huaxian Ma et al.
Toxicology and applied pharmacology, 251(1), 1-7 (2010-12-15)
The mechanisms by which aniline exposure elicits splenotoxic response, especially the tumorigenic response, are not well-understood. Earlier, we have shown that aniline-induced oxidative stress is associated with increased oxidative DNA damage in rat spleen. The base excision repair (BER) pathway
Preparation of PANI-coated poly (styrene-co-styrene sulfonate) nanoparticles.
Kim BJ, et al.
Polymer, 43(1), 111-116 (2002)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E1641-2MG | 04061833602034 |
| E1641-10MG | 04061833602027 |