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Merck
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Key Documents

717274

Sigma-Aldrich

1,3,6,8-Tetrabromopyrene

97%

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About This Item

Empirical Formula (Hill Notation):
C16H6Br4
CAS Number:
Molecular Weight:
517.83
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

97%

form

solid

mp

416-420 °C

SMILES string

Brc1cc(Br)c2ccc3c(Br)cc(Br)c4ccc1c2c34

InChI

1S/C16H6Br4/c17-11-5-13(19)9-3-4-10-14(20)6-12(18)8-2-1-7(11)15(9)16(8)10/h1-6H

InChI key

ZKBKRTZIYOKNRG-UHFFFAOYSA-N

Application

Synthetic building block for the creation of blue to green OLED emitters

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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


Certificates of Analysis (COA)

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You Zhou et al.
The Analyst, 143(15), 3628-3634 (2018-07-04)
1-Hydroxypyrene (1-HP) is a urinary metabolite of polycyclic aromatic hydrocarbons (PAHs), and can function as a convenient biomarker for human intoxication of PAH carcinogens. The development of simple 1-HP sensors with high sensitivity and fast response is highly desirable. Herein
Yasuchika Hasegawa et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(53), 12308-12315 (2019-07-23)
Oxygen-sensitive and near-infrared (NIR) luminescent YbIII coordination polymers incorporating ligands based on pyrene derivatives were synthesized: YbIII -TBAPy and YbIII -TIAPy (TBAPy: 1,3,6,8-tetrakis(p-benzoate)pyrene; TIAPy: 1,3,6,8-tetrakis(3,5-isophthalic acid)pyrene). The coordination structures of these materials have been characterized by means of electrospray ionization

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