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1-Bromopyrene

1-Bromopyrene Structure
1-Bromopyrene structure
CAS No.
1714-29-0
Chemical Name:
1-Bromopyrene
Synonyms
2-Bromopyrene;DK4994;1-Bromopyene;1-BROMOPYRENE;Pyrene, 1-bromo-;1-Pyrenyl bromide;1-Bromopyrene >1-Bromopyrene 96%;1714-29-0 1-Bromopyrene;1-Bromopyrene in toluene
CBNumber:
CB3285442
Molecular Formula:
C16H9Br
Molecular Weight:
281.15
MDL Number:
MFCD00015767
MOL File:
1714-29-0.mol
MSDS File:
SDS
Last updated:2026-05-28 01:10:26
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1-Bromopyrene Properties

Melting point 102-105 °C (lit.)
Boiling point 255 °C / 7mmHg
Density 1.4316 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Soluble), DMSO (Slightly, Heated, Sonicated), Methanol (Slightly)
form Crystalline
color White to Pale Yellow
InChI InChI=1S/C16H9Br/c17-14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H
InChIKey HYGLETVERPVXOS-UHFFFAOYSA-N
SMILES C1(Br)=C2C3=C4C(C=C2)=CC=CC4=CC=C3C=C1
CAS DataBase Reference 1714-29-0(CAS DataBase Reference)
NIST Chemistry Reference 1-Bromopyrene(1714-29-0)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29039990
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

1-Bromopyrene price More Price(82)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 391573 1-Bromopyrene 96% 1714-29-0 1g $73.1 2026-04-30 Buy
TCI Chemical B1495 1-Bromopyrene >95.0%(GC) 1714-29-0 5g $69 2026-04-30 Buy
TCI Chemical B1495 1-Bromopyrene >95.0%(GC) 1714-29-0 25g $207 2026-04-30 Buy
AstaTech 54602 1-BROMO-PYRENE 97% 1714-29-0 5G $30 2026-04-30 Buy
AstaTech 54602 1-BROMO-PYRENE 97% 1714-29-0 25G $63 2026-04-30 Buy
Product number Packaging Price Buy
391573 1g $73.1 Buy
B1495 5g $69 Buy
B1495 25g $207 Buy
54602 5G $30 Buy
54602 25G $63 Buy

1-Bromopyrene Chemical Properties,Uses,Production

Chemical Properties

White to yellow to light brown powder

Uses

1-Bromopyrene is used in the cleavage of DNA in studies. It is also used in the preparation of DNA base analogs.

Uses

1-Bromopyrene is suitable reagent used in the comparative study of effect of substituents of some pyrene derivatives in inducing phototoxicity, DNA damage and repair in human skin keratinocytes and light-induced lipid peroxidation in methanol. It is suitable reagent used in the study to investigate the UV photon-assisted thermal decomposition of PAHs at elevated temperature.
1-Bromopyrene may be used as a standard to compare its spectral properties with that of pyrene based fluorescence probe. It may be used to study the effects of the addition of halogen hetero-atoms on the vapor pressures and thermodynamics of polycyclic aromatic hydrocarbons.
It may be used in the synthesis of the following:
2-methyl-4-pyren-1-yl-but-3-yn-2-ol
1-ethynylpyrene
silsesquioxane (SSQ) based hybrid
ruthenium nanoparticles functionalized with pyrene moiety
mono- and di-pyrenyl perfluoroalkanes
oligo(1-bromopyrene)(OBrP) films
dinitropyrene-derived DNA adduct

Preparation

1-Bromopyrene is an important intermediate in the OLED material industry. The synthesis method is as follows: pyrene is dissolved in an organic solvent dichloromethane, and dibromohydantoin is added for reaction, filtered, and the obtained solid is recrystallized to obtain 1-bromopyrene.

Synthesis Reference(s)

Synthetic Communications, 18, p. 2207, 1988 DOI: 10.1080/00397918808082362
Synthesis of 1-Bromopyrene and 1-Pyrenecarbaldehyde

General Description

1-Bromopyrene, a polycyclic aromatic hydrocarbon (PAH), is a mono bromo substituted pyrene derivative. Its synthesis has been reported. Its gas phase UV-absorption spectra in the UV wavelength range at elevated temperature has been studied. Electron affinitiy (EA) of 1-bromopyrene has been investigated using electron attachment desorption chemical ionization mass spectrometry (DCI-MS) and triple quadrupole tandem mass spectrometry. It participates in the synthesis of novel ruthenium (II) bipyridine or terpyridine complexes bearing pyrene moiety. The reaction of 1-bromopyrene cation radical with water in acetonitrile has been analyzed using the electron transfer stopped-flow (ETSF) method.

Synthesis

Pyrene

129-00-0

1-Bromopyrene

1714-29-0

The general procedure for the synthesis of 1-bromopyrene from pyrene was as follows: anhydrous N,N-dimethylformamide (DMF, 5 mL) solution of N-bromosuccinimide (NBS, 187 mg, 1.05 mmol) was slowly added dropwise to anhydrous DMF (10 mL) solution of pyrene (252 mg, 1.0 mmol) and the reaction mixture was stirred at room temperature for 24 hours. After completion of the reaction, the mixture was poured into deionized water (50 mL) and extracted three times with dichloromethane (100 mL). The organic phases were combined, washed thoroughly with deionized water, dried over anhydrous magnesium sulfate (MgSO4), and concentrated under reduced pressure to remove the solvent to give the crude product 1-bromopyrene (332 mg, 85% yield) as a light yellow solid. The crude product was recrystallized with hexane to obtain pure 1-bromopyrene as light yellow powder, melting point 103-104°C (literature value: 102-104°C).

References

[1] Tetrahedron Letters, 2010, vol. 51, # 9, p. 1317 - 1321
[2] Journal of the Chinese Chemical Society, 2012, vol. 59, # 3, p. 289 - 296
[3] Tetrahedron Letters, 2003, vol. 44, # 21, p. 4085 - 4088
[4] European Journal of Organic Chemistry, 2011, # 27, p. 5261 - 5271
[5] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2013, vol. 68, # 4, p. 367 - 377

1-Bromopyrene Preparation Products And Raw materials

Raw materials

Pyrene N-Bromosuccinimide N,N-Dimethylformamide

Preparation Products

1-Pyrenecarboxaldehyde Pyrene, 1,3-dibromo- 1-Hydroxypyrene 1-Pyrenylboronic acid 1,6-Dibromopyrene
1-Methoxypyrene

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1-Bromopyrene Suppliers

Global( 369)Suppliers
Supplier Tel Email Country ProdList Advantage
Zhengzhou Jicheng Chemical Technology Co., Ltd 15639929870 15639929870 1811685958@qq.com China 305 58
Zhengzhou HQ Material Co., Ltd. 67759225 13526468238 sales@hqmat.com China 812 55
Henan Research New Material Co., Ltd. 86-18903931531 18903931628 sales036@researchvip.com China 180 58
Yurui (Shanghai) Chemical Co., Ltd. 02150456736 18602143071 Jenny@riyngroup.com China 500 30
Changzhou Kafule Environmental Protection Materials Co., Ltd 13839301681 1370806610@qq.com China 272 58
TIANJIAYI (BEIJING) TECHNOLOGY DEVELOPMENT CO., LTD 01080109118 18515310203 tianjiayi20200518@163.com China 11 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Beijing Donghualituo Techonlogy Development Co.,Ltd. 010-88425576 sales@dhltchem.com China 793 59
INTATRADE GmbH +49 3493/605464 sales@intatrade.de Germany 3563 66
Supplier Advantage
Zhengzhou Jicheng Chemical Technology Co., Ltd 58
Zhengzhou HQ Material Co., Ltd. 55
Henan Research New Material Co., Ltd. 58
Yurui (Shanghai) Chemical Co., Ltd. 30
Changzhou Kafule Environmental Protection Materials Co., Ltd 58
TIANJIAYI (BEIJING) TECHNOLOGY DEVELOPMENT CO., LTD 58
J & K SCIENTIFIC LTD. 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 62
Beijing Donghualituo Techonlogy Development Co.,Ltd. 59
INTATRADE GmbH 66

Related Questions

Ask a question
Q:What are the primary applications of 1-Bromopyrene ?wipes - Oct 17,2025
A:1-Bromopyrene is a crucial building block primarily used in the synthesis of pyrene-based derivatives for advanced functional materials. Its main application lies in organic and materials chemistry, where it serves as a key intermediate for creating larger, more complex polycyclic aromatic hydrocarbons (PAHs) and fluorescent probes. Through metal-catalyzed cross-coupling reactions, such as Suzuki or Sonogashira couplings, the bromo-group can be replaced to attach various functional groups, enabling the construction of molecules with tailored photophysical properties. These resulting compounds are widely investigated for their use in organic light-emitting diodes (OLEDs), fluorescent sensors for detecting molecules like glucose, and as components in solar cells and other electronic devices.

View Lastest Price from 1-Bromopyrene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1-Bromopyrene pictures 2026-09-02 1-Bromopyrene
1714-29-0
 $1.00-100.00 1KG 99% Henan Fengda Chemical Co., Ltd
1-Bromopyrene pictures 2026-03-20 1-Bromopyrene
1714-29-0
 $10.00 1KG 99% 5tons Hebei Chuanghai Biotechnology Co., Ltd
1-Bromopyrene pictures 2025-06-20 1-Bromopyrene
1714-29-0
 1kg 98%?min 20tons Hebei Yanxi Chemical Co., Ltd.
  • 1-Bromopyrene pictures
  • 1-Bromopyrene
    1714-29-0
  • $1.00-100.00
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • 1-Bromopyrene pictures
  • 1-Bromopyrene
    1714-29-0
  • $10.00
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd
  • 1-Bromopyrene pictures
  • 1-Bromopyrene
    1714-29-0
  • $0.00
  • 98%?min
  • Hebei Yanxi Chemical Co., Ltd.

1-Bromopyrene Spectrum

1-Bromopyrene(1714-29-0)MS1-Bromopyrene(1714-29-0)1HNMR1-Bromopyrene(1714-29-0)13CNMR1-Bromopyrene(1714-29-0)IR11-Bromopyrene(1714-29-0)IR21-Bromopyrene(1714-29-0)Raman

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1-BROMOPYRENE Pyrene, 1-bromo- 1-Pyrenyl bromide 1-Bromopyene 1-Bromopyrene 96% 1-Bromopyrene > 1-Bromopyrene, 95%, for synthesis 1-Bromopyrene ISO 9001：2015 REACH DK4994 1714-29-0 1-Bromopyrene Hlddsa（n-dodecylsuccinic anhydride） 1-Bromopyrene in toluene 2-Bromopyrene 1714-29-0 C16H9Br C13 to C37+ Aryl Building Blocks Halogenated Hydrocarbons Organic Building Blocks Pyrenes OLED materrials OLED materials,pharm chemical,electronic fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis OLED Electronic Chemicals Pyrenes Aryl C13 to C37+ Halogenated Hydrocarbons Aromatic Compounds