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Safety Information

542873

Sigma-Aldrich

Pyrene-1-boronic acid

≥95.0%

Synonym(s):

1-Pyreneboronic acid, 1-Pyrenylboronic acid

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About This Item

Empirical Formula (Hill Notation):
C16H11BO2
CAS Number:
164461-18-1
Molecular Weight:
246.07
MDL number:
MFCD04974062
UNSPSC Code:
12352103
PubChem Substance ID:
24878642
NACRES:
NA.22

Quality Level

100

Assay

≥95.0%

form

solid

mp

247-251 °C (lit.)

SMILES string

OB(O)c1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H11BO2/c18-17(19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9,18-19H

InChI key

MWEKPLLMFXIZOC-UHFFFAOYSA-N

Related Categories

Other Notes

Contains varying amounts of anhydride

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

542873-5G:
542873-BULK:
542873-1G:
542873-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN5079
SHBK4657
SHBH0774V
SHBB2013V
28796BM

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Mohamed E El-Khouly et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(10), 1512-1518 (2017-08-02)
A light harvesting subphthalocyanine-pyrene dyad has been synthesized and characterized by linking pyrene (Py) with subphthalocyanine (SubPc) at its axial position with the B-O bond through the para position of the benzene group. Upon photoexcitation at the pyrene unit of
Hailei Zhang et al.
ACS applied materials & interfaces, 7(42), 23805-23811 (2015-10-10)
A novel fluorescence probe based on modified halloysite nanotubes (HNTs) by using 1-pyrenylboronic acid selectively grafted onto the inner surface of lumen was successfully achieved. The solid-state nuclear magnetic resonance ((13)C and (11)B), X-ray photoelectron spectroscopy (XPS) and Fourier transform

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