Basic Description

Synonyms	AKOS003620496 \| 1,3,6,8-Tetrabromopyrene, 97% \| EINECS 204-900-6 \| Q27265604 \| FT-0755634 \| AS-59009 \| 1,3,6,8- Tetrabromopyrene \| SY052723 \| 1,3,6,8-Tetrabromopyrene \| SCHEMBL1005904 \| A921470 \| DTXSID2029165 \| YSZC173 \| 6VWU1E395N \| Pyrene, 1,3,6,8-tetr
Specifications & Purity	≥98%
Storage Temp	Argon charged
Shipped In	Normal
Product Description	Synthetic building block for the creation of blue to green OLED emitters. Application 1,3,6,8-Tetrabromopyrene is used as a reactant in the synthesis of pyrene-centered starburst oligofluorenes which display good film forming ability and sky blue fluroescence and used in electroluminescent devices.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Pyrenes

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Pyrenes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Pyrenes
Alternative Parents	Polybrominated biphenyls Phenanthrenes and derivatives Naphthalenes Aryl bromides Organobromides Hydrocarbon derivatives
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Pyrene - Polybrominated biphenyl - Phenanthrene - Naphthalene - Aryl halide - Aryl bromide - Hydrocarbon derivative - Organobromide - Organohalogen compound - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as pyrenes. These are compounds containing a pyrene moiety, which consists four fused benzene rings, resulting in a flat aromatic system.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488183908
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488183908
IUPAC Name	1,3,6,8-tetrabromopyrene
INCHI	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
InChIKey	ZKBKRTZIYOKNRG-UHFFFAOYSA-N
Smiles	C1=CC2=C3C(=C(C=C2Br)Br)C=CC4=C(C=C(C1=C43)Br)Br
Isomeric SMILES	C1=CC2=C3C(=C(C=C2Br)Br)C=CC4=C(C=C(C1=C43)Br)Br
WGK Germany	3
PubChem CID	67188
Molecular Weight	517.84
Beilstein	5(3)2286
Reaxy-Rn	2287262

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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6 results found

Lot Number	Certificate Type	Date	Item
D1916175	Certificate of Analysis	Feb 08, 2023	T162338
H2205574	Certificate of Analysis	Jun 21, 2022	T162338
H2205573	Certificate of Analysis	Jun 21, 2022	T162338
H2205572	Certificate of Analysis	Jun 21, 2022	T162338
I2402432	Certificate of Analysis	Dec 16, 2021	T162338
A2310449	Certificate of Analysis	Dec 16, 2021	T162338

Chemical and Physical Properties

Solubility	Nitrobenzene (Very Slightly, Heated, Partially Soluble)
Melt Point(°C)	416-420℃
Molecular Weight	517.799 g/mol
XLogP3	7.800
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	0
Exact Mass	517.716 Da
Monoisotopic Mass	513.72 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	319.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Qiu Zhuang, Hao Chen, Chaofan Zhang, Siyao Cheng, Wei Dong, Aming Xie. (2022) Rapid chromium reduction by metal-free organic polymer photocatalysis via molecular engineering. JOURNAL OF HAZARDOUS MATERIALS, 434 (128938).
2. Can Lang, Hao Gong, Gang Ye, Pachaiyappan Murugan, Zheng-Hui Xie, Yi-Fan Dai, Kai Yang, Changlin Yu, Shi-Yong Liu. (2025) D1-D2-A ternary conjugated microporous polymers synthesized via direct CH arylation for enhancing photocatalytic hydrogen evolution. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 688 (818).

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SKU	Size	Availability	Price
T162338-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$23.90
T162338-5g	5g	3	$91.90
T162338-25g	25g	Available within 1-2 weeks(?) Item is derived from our semi-finished stock and is processed in 1-2 weeks.	$410.90
T162338-100g	100g	1	$1,477.90

1,3,6,8-Tetrabromopyrene - >98.0%, high purity , CAS No.128-63-2