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Merck
CN

392049

1-芘磺酸 水合物

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经验公式(希尔记法):
C16H10O3S · xH2O
化学文摘社编号:
分子量:
282.31 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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InChI

1S/C16H10O3S.H2O/c17-20(18,19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11;/h1-9H,(H,17,18,19);1H2

SMILES string

[H]O[H].OS(=O)(=O)c1ccc2ccc3cccc4ccc1c2c34

InChI key

RRDYFCSDPUHYDA-UHFFFAOYSA-N

mp

125-129 °C (lit.)

solubility

DMSO: soluble 250 mg/10 mL, clear to slightly hazy, yellow to brown

functional group

sulfonic acid

Quality Level

Application

1-芘磺酸(PSA)水合物可作为反应剂,与四(4-羟基苯基)卟啉(THPP)反应修饰氧化石墨烯表面。合成的氧化石墨烯纳米杂化材料(GO/THPP/PSA)具有出色的制氢光催化活性。也可用作分子砌块,与各种有机锡前体制备含芘的organostannoxanes。

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Subrata Kundu et al.
Chemistry, an Asian journal, 9(5), 1403-1412 (2014-03-13)
Organostannoxanes have been used as scaffolds for the preparation of multi-chromophore assemblies. A single-step synthesis procedure allows the preparation of compounds in which the number of chromophore units can be varied from two to six. Thus, the reactions of pyrene
Fabrication mechanism and photocatalytic activity for a novel graphene oxide hybrid functionalized with tetrakis-(4-hydroxylphenyl) porphyrin and 1-pyrenesulfonic acid
Luo Q, et al.
Applied Surface Science, 427, 15-23 (2018)
Keun-Hwan Oh et al.
ACS applied materials & interfaces, 6(10), 7751-7758 (2014-04-09)
We report boron nitride nanoflakes (BNNFs), for the first time, as a nanofiller for polymer electrolyte membranes in fuel cells. Utilizing the intrinsic mechanical strength of two-dimensional (2D) BN, addition of BNNFs even at a marginal content (0.3 wt %)
Pyrene sulfonate functionalised single-walled carbon nanotubes for mediatorless dioxygen bioelectrocatalysis.
JN Martin, et al.
Electrochemical Communications, 11(5), 1042-1044 (2009)
Preparation of Free 1-Pyrenesulfonic Acid
Abe Y and Hsu PC.
Yuki Gosei Kaguku Kyokaishi, 33(4), 277-278 (1975)

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