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Merck
CN

A39009

1-氨基蒽醌

≥96.5% purity, powder, crystals or chunks

别名:

冰染重氮组分 36, 坚牢红 AL

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关于此项目

经验公式(希尔记法):
C14H9NO2
化学文摘社编号:
分子量:
223.23
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
Colour Index Number:
37275
EC Number:
201-423-5
MDL number:
Beilstein/REAXYS Number:
396360
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产品名称

1-氨基蒽醌, ≥96.5% (HPLC)

InChI

1S/C14H9NO2/c15-11-7-3-6-10-12(11)14(17)9-5-2-1-4-8(9)13(10)16/h1-7H,15H2

InChI key

KHUFHLFHOQVFGB-UHFFFAOYSA-N

SMILES string

Nc1cccc2C(=O)c3ccccc3C(=O)c12

assay

≥96.5% (HPLC)

form

powder, crystals or chunks

color

dark brown

mp

253-255 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

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Biochem/physiol Actions

1-氨基蒽醌具有增加蒽醌衍生物在超临界二氧化碳中溶解度的能力。

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Aneta Hałka-Grysińska et al.
Journal of chromatography. A, 1610, 460516-460516 (2019-09-19)
The new approach to the development of planar chromatogram with controlled developing solvent velocity was implemented for gradient reversed-phase chromatography of a test mixture of dyes. The developing solvent components were directly delivered onto the surface of the C18 type
Song Zhang et al.
Scientific reports, 7, 43419-43419 (2017-02-25)
We investigated the mechanism of intramolecular charge transfer and the following radiationless dynamics of the excited states of 1-aminoanthraquinone using steady state and time-resolved absorption spectroscopy combined with quantum chemical calculations. Following photoexcitation with 460 nm, conformational relaxation via twisting of
Solubility of 1-aminoanthraquinone and 1-nitroanthraquinone in supercritical carbon dioxide
Tamura K, et al.
The Journal of Chemical Thermodynamics, 104, 162-168 (2017)
Sarah J Schmidtke et al.
The journal of physical chemistry. A, 109(32), 7033-7045 (2006-07-13)
The dynamics of a series of 1-acylaminoanthraquinones with varying degrees of excited-state intramolecular proton transfer are studied in acetonitrile and dichloromethane. Events are followed via changes in the third-order intermolecular Raman response as a function of time after resonant excitation
S Pflugmacher et al.
The Science of the total environment, 357(1-3), 169-175 (2005-05-12)
Dissolved natural organic matter (NOM) is dead organic matter exceeding, in freshwater systems, the concentration of organic carbon in all living organisms by far. 80-90% (w/w) of the NOM is made up of humic substances (HS). Although NOM possesses several

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