A90004
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
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C14H8O2
化学文摘社编号:
分子量:
208.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-549-0
Beilstein/REAXYS Number:
390030
MDL number:
产品名称
蒽醌, 97%
InChI key
RZVHIXYEVGDQDX-UHFFFAOYSA-N
InChI
1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
SMILES string
O=C1c2ccccc2C(=O)c3ccccc13
vapor density
7.16 (vs air)
vapor pressure
1 mmHg ( 190 °C)
assay
97%
form
powder
bp
379-381 °C (lit.)
mp
284-286 °C (lit.)
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
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。
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Skin Sens. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
482.0 °F - closed cup
flash_point_c
250 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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)
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)
Anthraquinone-A review of the rise and fall of a pulping catalyst.
Hart PW and Rudie AW
Tappi Journal, 13(10), 23-31 (2014)
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
Witold Nowik et al.
Journal of chromatography. A, 1218(23), 3636-3647 (2011-05-03)
A series of reversed phases bonded with several functional groups was investigated for separation of anthraquinone derivatives, following the previous work, dedicated to the selectivity of octadecyl silica bonded phases. Considering wide diversity of substitutions in hydrophobic anthraquinone skeleton, interactions
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持