144037
1-Pyrenecarboxaldehyde
99%
Synonym(s):
1-Formylpyrene, 1-Pyrenealdehyde, 1-Pyrenecarbaldehyde, 3-Pyrenylaldehyde
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About This Item
Empirical Formula (Hill Notation):
C17H10O
CAS Number:
Molecular Weight:
230.26
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
221-196-6
Beilstein/REAXYS Number:
1874889
MDL number:
Quality Level
assay
99%
form
liquid
mp
123-126 °C (lit.)
density
±1.326 g/cm3 at 25 °C (Predicted)
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
General description
1-Pyrenecarboxaldehyde is a high-purity fluorescent compound (99%) used extensively in fluorescence spectroscopy and organic synthesis. With a molecular weight of 230.26 g/mol, it serves as a critical tool in research involving pyrene derivatives and biological imaging.
Application
- Fluorescence Spectroscopy: Ideal for use as a fluorescent probe in various analytical applications.
- Organic Synthesis: Utilized in the synthesis of pyrene-based compounds for research and industrial applications.
Features and Benefits
- High Purity: Ensures reliable results in sensitive experiments.
- Effective Fluorescence: Exhibits strong fluorescence properties, enhancing detection in analytical applications.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 36773-250MG-R | 04061831827569 |
| 144037-10G | 04061838735294 |
| 144037-50G | 04061838735300 |