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Merck

Q906

Sigma-Aldrich

醌茜

96%

别名:

1,4-二羟基蒽醌

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About This Item

经验公式(希尔记法):
C14H8O4
CAS号:
分子量:
240.21
Beilstein:
1914036
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.23

蒸汽密度

8.3 (vs air)

蒸汽壓力

1 mmHg ( 196.7 °C)

化驗

96%

mp

198-199 °C (lit.)

SMILES 字串

Oc1ccc(O)c2C(=O)c3ccccc3C(=O)c12

InChI

1S/C14H8O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-16H

InChI 密鑰

GUEIZVNYDFNHJU-UHFFFAOYSA-N

象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

431.6 °F

閃點(°C)

222 °C

個人防護裝備

Eyeshields, Faceshields, Gloves, type N95 (US)


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Andrzej Blachecki et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(13), 1798-1810 (2017-04-28)
Titanium dioxide nanocomposites were synthesized in hierarchical architectures through the use of a 1,4-dihydroxyanthraquinone photosensitizer. In the first step, the dye was either incorporated into the TiO
Kunihiko Ishii et al.
The Journal of chemical physics, 131(4), 044512-044512 (2009-08-07)
We have studied IR-induced low-frequency coherent vibration of an intramolecularly hydrogen-bonded molecule, quinizarin, by an ultrashort IR-pump-visible-probe spectroscopy with approximately 60 fs time resolution. In this experiment, the IR excitation of the symmetric OH-stretching mode induced a low-frequency vibrational coherence
T S Koch et al.
Biophysical chemistry, 36(3), 187-199 (1990-08-15)
The visible absorption spectra of 1,4-(dihydroxy)-9,10-anthraquinone and of Co(II), Ni(II), Cu(II) and Zn(II) chelates have been studied in different organic solvents. This system provides a model for the anthracycline antibiotics and their metal chelates. The band structure of the spectrum
Meiling Wang et al.
Environmental science & technology, 46(1), 367-373 (2011-12-02)
1,4-Dihydroxyanthraquinone (1,4-DHAQ, a fluorophore) doped cellulose (CL) (denoted as 1,4-DHAQ@CL) microporous nanofiber film has been achieved via simple electrospinning and subsequent deacetylating, and used for highly sensitive and selective fluorescence detection of Cu(2+) in aqueous solution. As the resultant byproduct
Giorgio Cozza et al.
Bioorganic & medicinal chemistry letters, 18(20), 5672-5675 (2008-09-19)
In eukaryotes, protein phosphorylation of serine, threonine or tyrosine residues by protein kinases plays an important role in many cellular processes. Members of the protein kinase CK1 family usually phosphorylate residues of serine that are close to other phosphoserine in

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