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A38002

4′-Aminoacetophenone

Name: 4′-Aminoacetophenone
Brand: ALDRICH

99%

Synonym(s):

4-Acetylaniline

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About This Item

Linear Formula:

H₂NC₆H₄COCH₃

CAS Number:

99-92-3

Molecular Weight:

135.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24890814

EC Number:

202-801-2

Beilstein/REAXYS Number:

471493

MDL number:

MFCD00007896

Assay:

99%

Form:

powder

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Properties

Quality Level

200

assay

99%

form

powder

bp

293 °C (lit.)

mp

103-107 °C (lit.)

SMILES string

CC(=O)c1ccc(N)cc1

InChI

1S/C8H9NO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,9H2,1H3

InChI key

GPRYKVSEZCQIHD-UHFFFAOYSA-N

Description

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pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Identification of aromatic moieties and mycosamine in antifungal heptaenes with high-performance liquid chromatography, high-performance liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry.

O Raatikainen et al.

Journal of chromatography, 585(2), 247-254 (1991-11-01)

A high-performance liquid chromatographic (HPLC) method for the determination of the aromaticity of heptaene polyene antibiotics has been developed. The released aromatic moiety of the heptaene polyenes aureofungin, candicidin, candimycin, hamycin and trichomycin was assayed after alkaline hydrolysis. The presence

[Determination of p-aminoacetophenone and changes in its levels in a levorin producer depending on culture conditions].

O A Aleksintseva et al.

Antibiotiki, 26(8), 566-570 (1981-08-01)

A method for spectrophotometric determination of p-aminoacetophenone (p-AAP) in the mycelium and fermentation broth filtrates of organisms producing polyenic macrolide antibiotics is described. The level of p-AAP accumulation was studied as applicable to the biosynthesis of levorin, a polyenic antibiotic

Involvement of proton transfer in the reductive repair of DNA guanyl radicals by aniline derivatives.

Anne Ly et al.

Organic & biomolecular chemistry, 3(5), 917-923 (2005-02-26)

The most easily oxidized sites in DNA are the guanine bases, and major intermediates produced by the direct effect of ionizing radiation (ionization of the DNA itself) are electron deficient guanine species. By means of a radiation chemical method (gamma-irradiation

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Global Trade Item Number

SKU	GTIN
A38002-100G	04061833367995
A38002-25G	04061833368008