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Triphenylene - 98%, high purity , CAS No.217-59-4

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Triphenylene - 98%, high purity , CAS No.217-59-4

5 Citations

COA

Grade & Purity:

≥98%

Cas Number: 217-59-4
Molecular Weight: 228.29
Beilstein Registry Number: 1342908
EC Number: 205-922-9
MDL number: MFCD00001108
PubChem CID: 9170
PubChem SID: 504751795

In stock

Item Number

T124123

Grouped product items
SKU	Size	Availability	Price
T124123-250mg	250mg	3	$9.90
T124123-1g	1g	3	$27.90
T124123-5g	5g	3	$123.90
T124123-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$223.90
T124123-25g	25g	3	$502.90
T124123-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,807.90

View related series

aromatic hydrocarbon (251) Non heterocyclic block (8163)

Basic Description

Synonyms	NSC 57455 \| OL10154 \| TRIPHENYLENE [MI] \| T0513 \| 18WX3373I0 \| BBL100122 \| Benzo[l]phenanthrene \| C19541 \| EINECS 205-922-9 \| AKOS004908298 \| Benzo(l)phenanthrene \| Isochrysene \| Q2975866 \| UNII-18WX3373I0 \| CCRIS 1301 \| 1,2:3,4-Dibenznaphthalene \| SB6686
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Separation of Aromatic Compounds Using Ascentis RP-Amide Separation of Aromatic Compounds Using Ascentis C18
Storage Temp	Room temperature
Shipped In	Normal
Product Description	A compound that fluoresces in the ultraviolet region.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenanthrenes and derivatives
    - Subclass Triphenylenes

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenanthrenes and derivatives
Subclass	Triphenylenes
Intermediate Tree Nodes	Not available
Direct Parent	Triphenylenes
Alternative Parents	Naphthalenes Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Triphenylene - Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as triphenylenes. These are compounds containing a triphenylene moiety, which consists of four fused benzene rings forming a 9,10-benzo[l]phenanthrene.
External Descriptors	ortho-fused polycyclic arene
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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504751795
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504751795
IUPAC Name	triphenylene
INCHI	InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H
InChIKey	SLGBZMMZGDRARJ-UHFFFAOYSA-N
Smiles	C1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24
Isomeric SMILES	C1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24
WGK Germany	3
RTECS	YK2925000
PubChem CID	9170
Molecular Weight	228.29
Beilstein	1342908
Reaxy-Rn	1342908

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

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

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number	Certificate Type	Date	Item
L1726064	Certificate of Analysis	Jul 09, 2025	T124123
E1522120	Certificate of Analysis	Feb 08, 2023	T124123
J1825114	Certificate of Analysis	Aug 12, 2022	T124123
J1825113	Certificate of Analysis	Aug 12, 2022	T124123
B2226172	Certificate of Analysis	Jan 03, 2022	T124123
B2226186	Certificate of Analysis	Jan 03, 2022	T124123
B2226175	Certificate of Analysis	Jan 03, 2022	T124123
B2226170	Certificate of Analysis	Jan 03, 2022	T124123

Chemical and Physical Properties

Boil Point(°C)	438°C
Melt Point(°C)	196.0-200.0°C
Molecular Weight	228.300 g/mol
XLogP3	4.900
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	0
Exact Mass	228.094 Da
Monoisotopic Mass	228.094 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	217.000
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

Documents & Articles

Preparation and functionalized design of novel graphene-based nanostructures

Categories: Technical articles

Tags:

exfoliated graphite perylene Pyrene Porphyrin fullerenes

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Houmei Liu, Zhan Li, Makoto Takafuji, Hirotaka Ihara, Hongdeng Qiu. (2017) Octadecylimidazolium ionic liquid-modified magnetic materials: Preparation, adsorption evaluation and their excellent application for honey and cinnamon. FOOD CHEMISTRY, 229 (208).
2. Fafu Yang, Jianwei Xie, Hongyu Guo, Bingting Xu, Congcong Li. (2012) Novel discotic liquid crystal oligomers: 1,3,5-triazine-based triphenylene dimer and trimer with wide mesophase. LIQUID CRYSTALS,
3. Ruting Xiao,Aijin Shen,Gaowa Jin,Wenyi Yu,Zhimou Guo,Jing Zeng. (2020-01-01) Synthesis and chromatographic evaluation of a new stationary phase based on mild thiol-Michael addition reaction.. Journal of chromatography. A, 1617 (460807-460807).
4. Yali Yang, Jia Chen, Xiaojing Liang, Bei Liu, Kaijun Quan, Xiuhui Liu, Hongdeng Qiu. (2024) Adjustable chromatographic performance of silica-based mixed-mode stationary phase through the control of co-grafting amounts of imidazole and C18 chain. JOURNAL OF CHROMATOGRAPHY A, 1722 (464889).
5. Jia-Xu Shuang, Jie Sheng, Yunzhong Wu, Manyu Liu, Changsheng Xing, Rui Liu, Tong Zhang, Bin Liu, Yekang Guan, Lidong Wang, Weidong Fei. (2025) In-situ synthesis of graphene/Cu powder and composite through mechanochemical route. JOURNAL OF ALLOYS AND COMPOUNDS, (178940).

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