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1-Bromopyrene

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:2026-01-13 11:19:46

Product description	Number	Pack Size	Price
1-Bromopyrene 96%	391573	1g	$73.1
1-Bromopyrene >95.0%(GC)	B1495	5g	$69
1-Bromopyrene >95.0%(GC)	B1495	25g	$207
1-Bromopyrene	B686980	10g	$250
1-Bromopyrene	OR315404	25g	$221
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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)

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

Risk Statements

36/37/38

Safety Statements

26-36

WGK Germany

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(40)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich	391573	1-Bromopyrene 96%	1714-29-0	1g	$73.1	2026-03-19	Buy
TCI Chemical	B1495	1-Bromopyrene >95.0%(GC)	1714-29-0	5g	$69	2026-03-19	Buy
TCI Chemical	B1495	1-Bromopyrene >95.0%(GC)	1714-29-0	25g	$207	2026-03-19	Buy
TRC	B686980	1-Bromopyrene	1714-29-0	10g	$250	2021-12-16	Buy
Apolloscientific	OR315404	1-Bromopyrene	1714-29-0	25g	$221	2021-12-16	Buy

Product number	Packaging	Price	Buy
391573	1g	$73.1	Buy
B1495	5g	$69	Buy
B1495	25g	$207	Buy
B686980	10g	$250	Buy
OR315404	25g	$221	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

129-00-0

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

1of2

1-Bromopyrene Suppliers

Global( 357)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
Hebei Chuanghai Biotechnology Co., Ltd	+8615350571055	Sibel@chuanghaibio.com	China	8738	58
Hebei Xinsheng New Material Technology Co., LTD.	+86-16632316109	xinshengkeji@xsmaterial.com	China	1085	58
Henan Fengda Chemical Co., Ltd	+86-371-86557731 +86-13613820652	info@fdachem.com	China	20124	58
Springchem New Material Technology Co.,Limited	+86-021-62885108 +8613917661608	info@spring-chem.com	China	2068	57
Capot Chemical Co.,Ltd.	+86-（0）57185586718; +8613336195806	sales@capot.com	China	29640	60
Shanghai Daken Advanced Materials Co.,Ltd	+86-2158073036	info@dakenam.com	China	13815	58
Henan Tianfu Chemical Co.,Ltd.	+86-0371-55170693 +86-19937530512	info@tianfuchem.com	China	21592	55
ATK CHEMICAL COMPANY LIMITED	+undefined-21-51877795	ivan@atkchemical.com	China	33024	60
AB PharmaTech,LLC	323-480-4688	sales@acrospharmatech.com	United States	989	55
Beijing Green Guardee Technology Co., Ltd	86-010-69706062	sales2@greenguardee.com	CHINA	650	58

Supplier	Advantage
Hebei Chuanghai Biotechnology Co., Ltd	58
Hebei Xinsheng New Material Technology Co., LTD.	58
Henan Fengda Chemical Co., Ltd	58
Springchem New Material Technology Co.,Limited	57
Capot Chemical Co.,Ltd.	60
Shanghai Daken Advanced Materials Co.,Ltd	58
Henan Tianfu Chemical Co.,Ltd.	55
ATK CHEMICAL COMPANY LIMITED	60
AB PharmaTech,LLC	55
Beijing Green Guardee Technology Co., Ltd	58

Related Qustion

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

Update time	Product	Price	Min. Order	Purity	Supply Ability	Manufacturer
2026-03-20	1-Bromopyrene 1714-29-0	US $10.00 / KG	1KG	99%	5tons	Hebei Chuanghai Biotechnology Co., Ltd
2025-09-25	1-Bromopyrene 1714-29-0	US $100.00-1.00 / KG	1KG	99%	g-kg-tons, free sample is available	Henan Fengda Chemical Co., Ltd
2025-06-20	1-Bromopyrene 1714-29-0	US $0.00 / kg	1kg	98%?min	20tons	Hebei Yanxi Chemical Co., Ltd.

1-Bromopyrene
1714-29-0
US $10.00 / KG
99%
Hebei Chuanghai Biotechnology Co., Ltd

1-Bromopyrene
1714-29-0
US $100.00-1.00 / KG
99%
Henan Fengda Chemical Co., Ltd

1-Bromopyrene
1714-29-0
US $0.00 / kg
98%?min
Hebei Yanxi Chemical Co., Ltd.

1-Bromopyrene Spectrum

1-Bromopyrene(1714-29-0)MS 1-Bromopyrene(1714-29-0)¹HNMR 1-Bromopyrene(1714-29-0)¹³CNMR 1-Bromopyrene(1714-29-0)IR1 1-Bromopyrene(1714-29-0)IR2 1-Bromopyrene(1714-29-0)Raman

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1-BROMOPYRENE Pyrene, 1-bromo- 2-Bromopyrene 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 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