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Merck
CN

N10970

蒽醌

analytical standard

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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
EC Number:
201-549-0
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
390030
MDL number:
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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

grade

analytical standard

vapor density

7.16 (vs air)

vapor pressure

1 mmHg ( 190 °C)

packaging

ampule of 1 g

manufacturer/tradename

Chem Service, Inc. PS-926

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

bp

379-381 °C (lit.)

mp

284-286 °C (lit.)

format

neat

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Health hazardExclamation mark

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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C Ma et al.
Journal of applied microbiology, 112(5), 883-891 (2012-03-06)
To isolate an alkaliphilic bacterium and to investigate its ability of extracellular reduction. An alkaliphilic and halotolerant humus-reducing anaerobe, Bacillus pseudofirmus MC02, was successfully isolated from a pH 10·0 microbial fuel cell. To examine its ability of extracellular reduction, AQDS
Rakesh Kumar et al.
Molecular diversity, 15(3), 687-695 (2010-11-30)
H(2)O(2) mediated oxidation of alcohols in ionic liquid is revisited, wherein, ionic liquids under the influence of microwave irradiation have been found to facilitate activation of H(2)O(2) without any metal catalyst in aqueous condition. The method utilizes a neutral ionic
Hai-Yu Hu et al.
Organic letters, 10(21), 5035-5038 (2008-10-11)
The first selective catalytic hydrogenation induced by the artificial helix based on oligo(phenanthroline dicarboxamide)s containing a 9,10-anthraquinone subunit is described. Due to the steric hindrance within the helically folded oligomers, the selective reductions of the anthraquinone units were completely different
B Hemmateenejad et al.
Talanta, 77(1), 351-359 (2008-09-23)
The retention behavior of 28 synthesized 9,10-anthraquinone derivatives in a reversed-phase (RP) high performance liquid chromatography (HPLC) system has been studied on a C18-RP column using acetonitrile-water mixtures as mobile phase. The influences of the composition of mobile phase and
Seyed Hadi Ebrahimia et al.
Archives of animal nutrition, 65(4), 267-277 (2011-09-06)
The objective of the present study was to investigate the hypothesis that 9,10-anthraquinone (AQ) in combination with fumaric acid (FMA) may provide complementary effects to inhibit methanogens and enhance rumen's capacity for better utilisation of FMA towards propionate production. Three

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