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Merck
모든 사진(2)

주요 문서

129364

Sigma-Aldrich

4-Iodoaniline

98%

동의어(들):

p-Iodoaniline

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About This Item

Linear Formula:
IC6H4NH2
CAS Number:
Molecular Weight:
219.02
Beilstein:
774101
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

양식

solid

mp

61-63 °C (lit.)

solubility

H2O: slightly soluble
alcohol: freely soluble
chloroform: freely soluble
diethyl ether: freely soluble

작용기

iodo

SMILES string

Nc1ccc(I)cc1

InChI

1S/C6H6IN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

InChI key

VLVCDUSVTXIWGW-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

4-Iodoaniline is the most potent methaemoglobin former.

애플리케이션

4-Iodoaniline was used to prepare phenyl functionalized graphene oxide (I-Ph-GO).

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

R Mahmud et al.
Toxicology, 117(1), 1-11 (1997-02-14)
The structural basis of dapsone (4,4'-diaminodiphenyl sulphone) haemotoxicity has been determined by investigation of the in vitro bioactivation of a series of 4-substituted arylamines. In the presence of rat liver microsomes, dapsone (100 microM) was the most potent former of
Ok-Kyung Park et al.
Nano letters, 12(4), 1789-1793 (2012-01-21)
Highly conductive reduced graphene oxide (GO) polymer nanocomposites are synthesized by a well-organized in situ thermochemical synthesis technique. The surface functionalization of GO was carried out with aryl diazonium salt including 4-iodoaniline to form phenyl functionalized GO (I-Ph-GO). The thermochemically
Iain J McManus et al.
Faraday discussions, 188, 451-466 (2016-04-21)
Porous manganese oxide (OMS-2) and platinum supported on OMS-2 catalysts have been shown to facilitate the hydrogenation of the nitro group in chloronitrobenzene to give chloroaniline with no dehalogenation. Complete conversion was obtained within 2 h at 25 °C and
H Yoshida et al.
The Biochemical journal, 248(1), 79-84 (1987-11-15)
Azopigments were obtained from the delta fraction of bilirubin (mammalian biliprotein) in cholestatic sera of men, rats and guinea pigs by diazo reaction with diazotized p-iodoaniline and analysed by t.l.c. Delta bilirubin of men and rats generated both unconjugated and
Huong T Pham et al.
Analytical chemistry, 84(17), 7525-7532 (2012-08-14)
Contemporary lipidomics protocols are dependent on conventional tandem mass spectrometry for lipid identification. This approach is extremely powerful for determining lipid class and identifying the number of carbons and the degree of unsaturation of any acyl-chain substituents. Such analyses are

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