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)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 36773-250MG-R | 04061831827569 |
| 144037-10G | 04061838735294 |
| 144037-50G | 04061838735300 |