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Merck

112666

Sigma-Aldrich

4-Butylaniline

97%

Sinónimos:

(4-Butylphenyl)amine, 4-Butylbenzenamine, 4-n-Butylaniline, p-Aminobutylbenzene, p-Butylaminobenzene, p-Butylaniline

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About This Item

Fórmula lineal:
CH3(CH2)3C6H4NH2
Número de CAS:
Peso molecular:
149.23
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39030465
PubChem Substance ID:
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.535 (lit.)

bp

133-134 °C/14 mmHg (lit.)

density

0.945 g/mL at 25 °C (lit.)

SMILES string

CCCCc1ccc(N)cc1

InChI

1S/C10H15N/c1-2-3-4-9-5-7-10(11)8-6-9/h5-8H,2-4,11H2,1H3

InChI key

OGIQUQKNJJTLSZ-UHFFFAOYSA-N

Application

4-Butylaniline is used in the fabrication of RP/ion-exchange, mixed-mode, monolithic materials for capillary LC.

Biochem/physiol Actions

4-Butylaniline is a mammalian retinoid cycle inhibitor that reversibly suppresses the recovery of the outward R(2) component of ERC (early receptor current) from Vitamin A and 11-cis-retinal-loaded cells.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

wgk_germany

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Rhodopsin activation is measured by the early receptor current (ERC), a conformation-associated charge motion, in human embryonic kidney cells (HEK293S) expressing opsins. After rhodopsin bleaching in cells loaded with 11-cis-retinal, ERC signals recover in minutes and recurrently over a period
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This paper describes the fabrication of RP/ion-exchange mixed-mode monolithic materials for capillary LC. Following deactivation of the capillary surface with 3-(trimethoxysilyl)propyl methacrylate (gamma-MAPS), monoliths were formed by copolymerisation of pentaerythritol diacrylate monostearate (PEDAS), 2-sulphoethyl methacrylate (SEMA) with/without ethylene glycol dimethacrylate
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Ring-opening reaction with synchronous hydrolysis was used to prepare 4-butylaniline-modified attapulgite (abbreviated as BA-ATP) for pre-concentration of bisphenol A (BPA) in trace quantity. The preparation was achieved under mild condition, and the material was characterized by Fourier transform infrared spectroscopy
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