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Sigma-Aldrich

1-Pyrenecarboxaldehyde

99%

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Synonym(s):
1-Formylpyrene, 1-Pyrenealdehyde, 1-Pyrenecarbaldehyde, 3-Pyrenylaldehyde
Empirical Formula (Hill Notation):
C17H10O
CAS Number:
3029-19-4
Molecular Weight:
230.26
Beilstein:
1874889
EC Number:
221-196-6
MDL number:
MFCD00004139
PubChem Substance ID:
24848624
NACRES:
NA.23

Quality Level

100

Assay

99%

form

liquid

mp

123-126 °C (lit.)

SMILES string

[H]C(=O)c1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C17H10O/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12/h1-10H

InChI key

RCYFOPUXRMOLQM-UHFFFAOYSA-N

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General description

1-Pyrenecarboxaldehyde (PCA) is a bifunctional molecule with pyrene moiety and one aldehyde group. The pyrene moiety interacts with the side walls of carbon nanotubes(CNT) through π-π stacking which leads to the uniform immobilization of PCA on the CNT surface. Therefore, it is widely used for the surface functionalization of CNTs. It can also be used to fabricate fluorescent chemosensors.

Features and Benefits

Exhibits reversible tuning properties with temperature and the properties depend upon the solvent environment.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Ashutosh Ghosh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 204, 425-431 (2018-07-04)
Edge-oxidized graphene oxide (EOGO) nanosheets are good acceptors of electrons. We have employed a suitably designed pyrene-tailed fluorescent probe to establish that the electron acceptability of EOGO can be tuned by undulation of the GO sheet. Comparison between EOGO and
A fluorescence probe study of gemini surfactants in aqueous solution: a comparison between n-2-n and n-6-n series of the alkanediyl-a, w-bis (dimethyl alkylammonium bromides)
Silveira Junior, P. B., V. A. O. Tiera, and M. J. Tiera
Ecletica Quimica , 32(2), 47-54 (2007)
Yunyan Gao et al.
Talanta, 178, 663-669 (2017-11-16)
This work reports a facile strategy for the synthesis of water-soluble fluorescent probes Pyr1 and Pyr2, which have carboxyl and hydroxyl group in the side chain of thioacetal moiety, respectively. Pyr1-2 exhibit exclusively selective turn-on fluorescence response towards Hg
Tamara Zoltan et al.
Scientia pharmaceutica, 78(4), 767-789 (2010-12-24)
The synthesis of the meso-tetra(pyren-1-yl)porphyrin (1) was successfully accomplished by means of the pyrrole condensation with pyrene-1-carb-aldehyde in acidic media. Its metallization was carried out in an almost quantitative yield to obtain the corresponding complexes of Ni(II) (2), Cu(II) (3)
Aqueous Dispersion and Temperature Induced Reversible Fluorescence Properties of 1-Pyrenecarboxaldehyde
Ashaduzzaman, Md, and Masashi Kunitake
International Letters of Chemistry, Physics and Astronomy, 1, 55-62 (2013)
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