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Merck
CN

A90004

Sigma-Aldrich

蒽醌

97%

别名:

1,4,11,12-四氢-9,10-蒽醌, 9,10-蒽醌, 蒽-9,10-醌, 蒽醌

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关于此项目

经验公式(希尔记法):
C14H8O2
CAS Number:
分子量:
208.21
Beilstein:
390030
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽密度

7.16 (vs air)

质量水平

蒸汽压

1 mmHg ( 190 °C)

方案

97%

表单

powder

沸点

379-381 °C (lit.)

mp

284-286 °C (lit.)

SMILES字符串

O=C1c2ccccc2C(=O)c3ccccc13

InChI

1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H

InChI key

RZVHIXYEVGDQDX-UHFFFAOYSA-N

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应用

蒽醌(AQ)可用于:
  • 合成水溶性蒽醌衍生物,如9,10-蒽醌-2,6-二磺酸二钠盐(AQ-2,6)和9,10-蒽醌-2-磺酸钠盐(AQ-2)。这些蒽醌衍生物可用作Becher工艺充气锈蚀步骤的氧化还原催化剂。
  • 作为指示剂测定聚(4-乙烯基吡啶)硫酸氢盐(P(4-VPH)HSO4)催化剂的酸强度。
  • 作为制浆催化剂。

象形图

Health hazardExclamation mark

警示用语:

Danger

危险声明

危险分类

Carc. 1B - Skin Sens. 1

储存分类代码

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

WGK

WGK 1

闪点(°F)

482.0 °F - closed cup

闪点(°C)

250 °C - closed cup

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The application of anthraquinone redox catalysts for accelerating the aeration step in the becher process.
Bruckard WJ, et al.
Hydrometallurgy, 73(1-2), 111-121 (2004)
Anthraquinone-A review of the rise and fall of a pulping catalyst.
Hart PW and Rudie AW
Tappi Journal, 13(10), 23-31 (2014)
Preparation, characterization and use of poly (4-vinylpyridinium) hydrogen sulfate salt as an eco-benign, efficient and reusable solid acid catalyst for the chemoselective 1, 1-diacetate protection and deprotection of aldehydes.
Khaligh NG and Shirini F
J. Mol. Catal. A: Chem., 348(1-2), 20-29 (2011)
Emilio M Ungerfeld et al.
Microorganisms, 8(6) (2020-05-30)
Ameliorating methane (CH4) emissions from ruminants would have environmental benefits, but it is necessary to redirect metabolic hydrogen ([H]) toward useful sinks to also benefit animal productivity. We hypothesized that inhibiting rumen methanogenesis would increase de novo synthesis of microbial
A A Stepanov et al.
The Journal of organic chemistry, 76(21), 8737-8748 (2011-09-14)
The nature of products in the diazotization of 1-amino-2-acetylenyl-9,10-anthraquinones strongly depends on the nature of substituents at both the alkyne and at the anthraquinone core. Donor substitution (NHAr, OH) at the fourth position stabilizes the diazonium salt at C1, decelerating

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